| scholarly article | Q13442814 |
| P50 | author | Robert Tjian | Q906579 |
| Nicole King | Q4795064 | ||
| Daniel S. Rokhsar | Q5218667 | ||
| Peer Bork | Q7160367 | ||
| William McGinnis | Q8015418 | ||
| Asaf Salamov | Q28050892 | ||
| Uffe Hellsten | Q28050897 | ||
| Ivica Letunic | Q28833310 | ||
| Antonis Rokas | Q42352198 | ||
| Jessica B Lyons | Q53997385 | ||
| Daniel J Richter | Q59981982 | ||
| David Pincus | Q88731645 | ||
| Alan Kuo | Q96187093 | ||
| Harris Shapiro | Q96233911 | ||
| Jarrod Chapman | Q110244026 | ||
| Gerard Manning | Q28958324 | ||
| David M. Goodstein | Q30518918 | ||
| Igor V. Grigoriev | Q30519357 | ||
| Nicholas Putnam | Q30530377 | ||
| P2093 | author name string | W Todd Miller | |
| Monika Abedin | |||
| Derek Lemons | |||
| William Dirks | |||
| Wendell A Lim | |||
| Kevin J Wright | |||
| Wanqing Li | |||
| Yoh Isogai | |||
| Susan L Young | |||
| Scott Nichols | |||
| Stephen Fairclough | |||
| Matthew Good | |||
| Andrea Morris | |||
| M Jody Westbrook | |||
| Richard Zuzow | |||
| Michael Marr | |||
| J G I Sequencing | |||
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| P275 | copyright license | Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported | Q15643954 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 7180 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Monosiga | Q35131894 |
| P304 | page(s) | 783-8 | |
| P577 | publication date | 2008-02-14 | |
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| Q37579339 | Evolutionary genomics of the Fox genes: origin of gene families and the ancestry of gene clusters. |
| Q33381547 | Evolutionary genomics reveals lineage-specific gene loss and rapid evolution of a sperm-specific ion channel complex: CatSpers and CatSperbeta |
| Q44857501 | Evolutionary genomics reveals the premetazoan origin of opposite gating polarity in animal-type voltage-gated ion channels |
| Q33408890 | Evolutionary history of Na,K-ATPases and their osmoregulatory role. |
| Q84935770 | Evolutionary history of exon shuffling |
| Q112570562 | Evolutionary history of the p53 family DNA-binding domain: insights from an Alvinella pompejana homolog |
| Q90780978 | Evolutionary history of tissue bending |
| Q41849996 | Evolutionary insights into T-type Ca2+ channel structure, function, and ion selectivity from the Trichoplax adhaerens homologue. |
| Q34064854 | Evolutionary insights into premetazoan functions of the neuronal protein homer |
| Q37834772 | Evolutionary origins of STIM1 and STIM2 within ancient Ca2+ signaling systems |
| Q88737584 | Evolutionary transitions in controls reconcile adaptation with continuity of evolution |
| Q27646502 | Exon 6 of human JAG1 encodes a conserved structural unit |
| Q34516481 | Expanded functional diversity of shaker K(+) channels in cnidarians is driven by gene expansion |
| Q33517914 | Expansion of tandem repeats in sea anemone Nematostella vectensis proteome: A source for gene novelty? |
| Q47343395 | Expansion, diversification, and expression of T-box family genes in Porifera |
| Q37339477 | Exploring the early origins of the synapse by comparative genomics |
| Q57898860 | Expression of Fox genes in the cephalochordate Branchiostoma lanceolatum |
| Q33614186 | Expression of multiple Sox genes through embryonic development in the ctenophore Mnemiopsis leidyi is spatially restricted to zones of cell proliferation |
| Q30841479 | Extended phylogeny of the Craspedida (Choanomonada). |
| Q90347873 | FAIM Is a Non-redundant Defender of Cellular Viability in the Face of Heat and Oxidative Stress and Interferes With Accumulation of Stress-Induced Protein Aggregates |
| Q28603241 | FAM46 proteins are novel eukaryotic non-canonical poly(A) polymerases |
| Q54397483 | FGF signaling emerged concomitantly with the origin of Eumetazoans. |
| Q33501348 | FGFRL1 is a neglected putative actor of the FGF signalling pathway present in all major metazoan phyla |
| Q26866370 | Fibrinogen-Related Proteins in Tissue Repair: How a Unique Domain with a Common Structure Controls Diverse Aspects of Wound Healing |
| Q37481055 | Finding partners: how BMPs select their targets |
| Q58482878 | First evidence of miniature transposable elements in sponges (Porifera) |
| Q26752422 | Flagellar apparatus structure of choanoflagellates |
| Q34069585 | Flexibly deployed Pax genes in eye development at the early evolution of animals demonstrated by studies on a hydrozoan jellyfish |
| Q39857095 | Flow-Induced Crystallization of Collagen: A Potentially Critical Mechanism in Early Tissue Formation |
| Q28652743 | Forward genetics for back-in-time questions |
| Q55109409 | Freshwater sponge silicateins: Comparison of gene sequences and exon-intron structure |
| Q91620045 | From traveler to homebody: Which signaling mechanisms sponge larvae use to become adult sponges? |
| Q38060917 | From tumor prevention to therapy: empowering p53 to fight back |
| Q35837317 | Functional Characterization of Cnidarian HCN Channels Points to an Early Evolution of Ih. |
| Q38198555 | Functional conservation and divergence of J-domain-containing ZUO1/ZRF orthologs throughout evolution |
| Q38065993 | Functional diversity and pharmacological profiles of the FKBPs and their complexes with small natural ligands |
| Q45826237 | Functional insights into the core-TFIIH from a comparative survey |
| Q26853567 | Functional interactions among members of the MAX and MLX transcriptional network during oncogenesis |
| Q45924993 | Functional replacement of a primary metabolic pathway via multiple independent eukaryote-to-eukaryote gene transfers and selective retention. |
| Q42607613 | Functional roles of Notch signaling in the cnidarian Nematostella vectensis |
| Q43068640 | Functional transition of Pak proto-oncogene during early evolution of metazoans |
| Q60948018 | G Proteins and GPCRs in C. elegans Development: A Story of Mutual Infidelity |
| Q48122857 | Gene Regulatory Networks for the Haploid-to-Diploid Transition of Chlamydomonas reinhardtii |
| Q28751404 | Gene duplication and the origins of morphological complexity in pancrustacean eyes, a genomic approach |
| Q28654542 | Gene expansion shapes genome architecture in the human pathogen Lichtheimia corymbifera: an evolutionary genomics analysis in the ancient terrestrial mucorales (Mucoromycotina) |
| Q56890351 | Gene family innovation, conservation and loss on the animal stem lineage |
| Q35137456 | Gene splicing of an invertebrate beta subunit (LCavβ) in the N-terminal and HOOK domains and its regulation of LCav1 and LCav2 calcium channels |
| Q47071563 | Genetic, functional and evolutionary characterization of scox, the Drosophila melanogaster ortholog of the human SCO1 gene |
| Q57231609 | Genome Portal, Joint Genome Institute |
| Q36665790 | Genome analysis of the unicellular green alga Chlamydomonas reinhardtii Indicates an ancient evolutionary origin for key pattern recognition and cell-signaling protein families |
| Q96116465 | Genome editing enables reverse genetics of multicellular development in the choanoflagellate Salpingoeca rosetta |
| Q112611290 | Genome sequencing and de novo assembly of the giant unicellular alga Acetabularia acetabulum using droplet MDA |
| Q41258354 | Genome-wide analysis of the sox family in the calcareous sponge Sycon ciliatum: multiple genes with unique expression patterns |
| Q33333945 | Genomes of model organisms: know thy tools |
| Q22065894 | Genomic analysis of organismal complexity in the multicellular green alga Volvox carteri |
| Q34024217 | Genomic insights into Wnt signaling in an early diverging metazoan, the ctenophore Mnemiopsis leidyi |
| Q21245387 | Genomic organization, evolution, and expression of photoprotein and opsin genes in Mnemiopsis leidyi: a new view of ctenophore photocytes |
| Q47822018 | Genomic survey of premetazoans shows deep conservation of cytoplasmic tyrosine kinases and multiple radiations of receptor tyrosine kinases. |
| Q34555096 | Genomics and evolution of protein phosphatases |
| Q35411477 | Genomics of Volvocine Algae. |
| Q42718044 | Glycoprotein hormones and their receptors emerged at the origin of metazoans |
| Q56750618 | Glycosyltransferases promote development and prevent promiscuous cell aggregation in the choanoflagellateS. rosetta |
| Q28648296 | Green algae and the origins of multicellularity in the plant kingdom |
| Q90640387 | Growth and single cell kinetics of the loricate choanoflagellate Diaphanoeca grandis |
| Q37388142 | Harnessing genomics for evolutionary insights |
| Q99619633 | Hedgehog signaling is required for endomesodermal patterning and germ cell development in the sea anemone Nematostella vectensis |
| Q58377349 | Heparan Sulfate Surfaces to Probe the Functions of the Master Regulator of the Extracellular Space |
| Q34632074 | Higher level taxonomy and molecular phylogenetics of the Choanoflagellatea |
| Q38045275 | Horizontal gene transfer in choanoflagellates |
| Q37882048 | How do they do Wnt they do?: regulation of transcription by the Wnt/β-catenin pathway. |
| Q38047030 | How was the notochord born? |
| Q112293300 | Human tRNAs with inosine 34 are essential to efficiently translate eukarya-specific low-complexity proteins |
| Q28550424 | Hydrophobic Core Variations Provide a Structural Framework for Tyrosine Kinase Evolution and Functional Specialization |
| Q61229487 | IMCC: Quantitative Analysis of the Inter-module Connectivity for Bio-network |
| Q34778817 | Identification and analysis of putative homologues of mechanosensitive channels in pathogenic protozoa. |
| Q27320213 | Identification of 526 conserved metazoan genetic innovations exposes a new role for cofactor E-like in neuronal microtubule homeostasis |
| Q46312852 | Identification of Aldh1a, Cyp26 and RAR orthologs in protostomes pushes back the retinoic acid genetic machinery in evolutionary time to the bilaterian ancestor |
| Q42661149 | Identification of a human ABCC10 orthologue in Catharanthus roseus reveals a U12-type intron determinant for the N-terminal domain feature. |
| Q112700263 | Identification of collagen 1α3 in teleost fish species and typical collision induced internal fragmentations |
| Q24321548 | Identification of glycosyltransferase 8 family members as xylosyltransferases acting on O-glucosylated notch epidermal growth factor repeats |
| Q36094320 | Identification of the kinase that activates a nonmetazoan STAT gives insights into the evolution of phosphotyrosine-SH2 domain signaling. |
| Q39769086 | Identification, localization, and functional implications of the microdomain-forming stomatin family in the ciliated protozoan Paramecium tetraurelia |
| Q41574266 | Imaging collagen in scar tissue: developments in second harmonic generation microscopy for biomedical applications |
| Q37599019 | Immortality and the base of multicellular life: Lessons from cnidarian stem cells |
| Q33849582 | Improving animal phylogenies with genomic data |
| Q53013895 | In silico identification and characterization of the MAPK family members of unicellular model eukaryote Tetrahymena thermophila. |
| Q34157354 | Incorporation of a horizontally transferred gene into an operon during cnidarian evolution |
| Q28079314 | Independent evolution of genomic characters during major metazoan transitions |
| Q34286083 | Independent evolution of striated muscles in cnidarians and bilaterians. |
| Q91637658 | Inherency of Form and Function in Animal Development and Evolution |
| Q37642681 | Innovation and constraint leading to complex multicellularity in the Ascomycota. |
| Q35163675 | Insights into the early evolution of animal calcium signaling machinery: a unicellular point of view |
| Q91596473 | Insights into the evolution of digestive systems from studies of Trichoplax adhaerens |
| Q37107569 | Insights into the origin of metazoan filopodia and microvilli |
| Q91782414 | Insights into the origin of metazoan multicellularity from predatory unicellular relatives of animals |
| Q42135019 | Integrin-mediated adhesion complex: Cooption of signaling systems at the dawn of Metazoa |
| Q38113551 | Interactions of photosynthesis with genome size and function |
| Q37698269 | Intercellular junction assembly, dynamics, and homeostasis |
| Q26852861 | Intracellular calcium channels in protozoa |
| Q37528149 | Intrinsically disordered regions of p53 family are highly diversified in evolution |
| Q38770008 | Introduction: History of SH2 Domains and Their Applications |
| Q27351922 | Intron evolution: testing hypotheses of intron evolution using the phylogenomics of tetraspanins |
| Q37224844 | KF-1 Ubiquitin Ligase: An Anxiety Suppressor |
| Q44496171 | KF-1 ubiquitin ligase: anxiety suppressor model |
| Q36023280 | KLF/SP Transcription Factor Family Evolution: Expansion, Diversification, and Innovation in Eukaryotes. |
| Q28681520 | LBP/BPI proteins and their relatives: conservation over evolution and roles in mutualism |
| Q30010003 | Lack of Csk-mediated negative regulation in a unicellular SRC kinase |
| Q33675663 | Landscape of histone modifications in a sponge reveals the origin of animal cis-regulatory complexity. |
| Q58482881 | Large-Scale Parsimony Analysis of Metazoan Indels in Protein-Coding Genes |
| Q90781043 | Light-regulated collective contractility in a multicellular choanoflagellate |
| Q34118422 | Lineage-specific expansion of DNA-binding transcription factor families |
| Q34314862 | Linear motif-mediated interactions have contributed to the evolution of modularity in complex protein interaction networks |
| Q38841444 | Losing Complexity: The Role of Simplification in Macroevolution |
| Q98198778 | MICAL1 constrains cardiac stress responses and protects against disease by oxidizing CaMKII |
| Q103776588 | MOB: Pivotal Conserved Proteins in Cytokinesis, Cell Architecture and Tissue Homeostasis |
| Q35157106 | Major diversification of voltage-gated K+ channels occurred in ancestral parahoxozoans. |
| Q37785132 | Mannose 6-phosphate receptor homology domain-containing lectins in mammalian endoplasmic reticulum-associated degradation. |
| Q24647521 | Mapping the tree of life: progress and prospects |
| Q37998043 | Marine protistan diversity |
| Q45977392 | Mating in the Closest Living Relatives of Animals Is Induced by a Bacterial Chondroitinase. |
| Q33899466 | Mechanism and evolution of cytosolic Hedgehog signal transduction |
| Q28235875 | Mechanisms and functions of Hedgehog signalling across the metazoa |
| Q38592891 | Mechanotransduction's impact on animal development, evolution, and tumorigenesis |
| Q37432747 | Merlin and the ERM proteins--regulators of receptor distribution and signaling at the cell cortex |
| Q36967449 | Meta-Analysis of EMT Datasets Reveals Different Types of EMT. |
| Q27316581 | Metabolic and chaperone gene loss marks the origin of animals: evidence for Hsp104 and Hsp78 chaperones sharing mitochondrial enzymes as clients |
| Q58066414 | Metazoan Complexity |
| Q34582288 | Metazoan-like signaling in a unicellular receptor tyrosine kinase. |
| Q36972635 | Metazoans evolved by taking domains from soluble proteins to expand intercellular communication network |
| Q52794337 | Methods for analyzing the evolutionary relationship of NF-κB proteins using free, web-driven bioinformatics and phylogenetic tools. |
| Q28740823 | Microbial Pathogens in the Fungal Kingdom |
| Q90421599 | Miles to go (mtgo) encodes FNDC3 proteins that interact with the chaperonin subunit CCT3 and are required for NMJ branching and growth in Drosophila |
| Q116287593 | Mirroring the effect of geological evolution: Protist divergence in the Atacama Desert |
| Q33359181 | Missing pieces of an ancient puzzle: evolution of the eukaryotic membrane-trafficking system |
| Q37983305 | Mitochondrial carrier homolog 2 (MTCH2): the recruitment and evolution of a mitochondrial carrier protein to a critical player in apoptosis |
| Q51520370 | Mitogenomics at the base of Metazoa. |
| Q59798385 | Modular Proteoglycan Perlecan/: Mutations, Phenotypes, and Functions |
| Q36153880 | Modular evolution of phosphorylation-based signalling systems |
| Q57470143 | Molecular Evolution of the Major Arthropod Chemoreceptor Gene Families |
| Q24617046 | Molecular and functional properties of P2X receptors--recent progress and persisting challenges |
| Q41760477 | Molecular cloning and characterization of a tyrosine phosphatase from Monosiga brevicollis |
| Q33654331 | Molecular evolution of the Yap/Yorkie proto-oncogene and elucidation of its core transcriptional program |
| Q28296614 | Molecular evolution of the cadherin superfamily |
| Q33983673 | Molecular evolutionary and structural analysis of the cytosolic DNA sensor cGAS and STING |
| Q36879246 | Molecular mechanism of activation-triggered subunit exchange in Ca(2+)/calmodulin-dependent protein kinase II |
| Q90179710 | Molecular mechanistic insights: The emerging role of SOXF transcription factors in tumorigenesis and development |
| Q90623692 | MotifAnalyzer-PDZ: A computational program to investigate the evolution of PDZ-binding target specificity |
| Q42780575 | Multicellularity: From brief encounters to lifelong unions |
| Q21090093 | Multigene Phylogeny of Choanozoa and the Origin of Animals |
| Q44643253 | Multiple Wnts are involved in Hydra organizer formation and regeneration. |
| Q33988346 | Multiple independent fusions of glucose-6-phosphate dehydrogenase with enzymes in the pentose phosphate pathway |
| Q35924226 | Multiscale modeling of form and function |
| Q29031715 | My Oldest Sister Is a Sea Walnut? |
| Q41905980 | Myosin regulatory light chain diphosphorylation slows relaxation of arterial smooth muscle |
| Q43884710 | NK homeobox genes with choanocyte-specific expression in homoscleromorph sponges. |
| Q112291997 | Negative elongation factor regulates muscle progenitor expansion for efficient myofiber repair and stem cell pool repopulation |
| Q112618400 | Neural stemness contributes to cell tumorigenicity |
| Q55932456 | Never Ending Analysis of a Century Old Evolutionary Debate: “Unringing” the Urmetazoon Bell |
| Q99721733 | New Lineage of Microbial Predators Adds Complexity to Reconstructing the Evolutionary Origin of Animals |
| Q34535226 | New genes as drivers of phenotypic evolution |
| Q39939700 | New insights into the autoinhibition mechanism of glycogen synthase kinase-3beta |
| Q28652533 | New tricks for "old" domains: how novel architectures and promiscuous hubs contributed to the organization and evolution of the ECM |
| Q64068120 | Nomenclature and Comparative Morphology of the Teneurin/TCAP/ADGRL Protein Families |
| Q47798489 | Not only tendons: The other architecture of collagen fibrils |
| Q46795621 | Notch Signaling in Development, Tissue Homeostasis, and Disease |
| Q26771105 | Notch-Mediated Cell Adhesion |
| Q38937915 | Notch: A multi-functional integrating system of microenvironmental signals |
| Q84686003 | Novel GPS-containing G protein-coupled receptor from Monosiga brevicollis |
| Q47771870 | Novel Scenarios of Early Animal Evolution—Is It Time to Rewrite Textbooks? |
| Q41116989 | Novel family GH3 β-glucosidases or β-xylosidases of unknown function found in various animal groups, including birds and reptiles |
| Q37233430 | Novel types of Ca2+ release channels participate in the secretory cycle of Paramecium cells |
| Q42054319 | Nuclear receptor complement of the cnidarian Nematostella vectensis: phylogenetic relationships and developmental expression patterns |
| Q90879092 | Nutrient Transport Driven by Microbial Active Carpets |
| Q38239452 | Of early animals, anaerobic mitochondria, and a modern sponge. |
| Q37697331 | On growth and form: a Cartesian coordinate system of Wnt and BMP signaling specifies bilaterian body axes |
| Q49646997 | On the origin of biological construction, with a focus on multicellularity. |
| Q91346197 | Opposing Action of Hedgehog and Insulin Signaling Balances Proliferation and Autophagy to Determine Follicle Stem Cell Lifespan |
| Q21089699 | Origin and evolution of glutamyl-prolyl tRNA synthetase WHEP domains reveal evolutionary relationships within Holozoa |
| Q83410676 | Origin and evolution of laminin gene family diversity |
| Q40890233 | Origin and evolution of lysyl oxidases |
| Q61796370 | Origin and evolution of plexins, semaphorins, and Met receptor tyrosine kinases |
| Q33510261 | Origin and evolution of the Notch signalling pathway: an overview from eukaryotic genomes. |
| Q84372267 | Origin and evolution of ubiquitin-conjugating enzymes from Guillardia theta nucleomorph to hominoid |
| Q42469449 | Origin of Pax and Six gene families in sponges: Single PaxB and Six1/2 orthologs in Chalinula loosanoffi |
| Q42479211 | Origin of animal epithelia: insights from the sponge genome. |
| Q42435003 | Origin of chordate peptides by horizontal protozoan gene transfer in early metazoans and protists: evolution of the teneurin C-terminal associated peptides (TCAP). |
| Q58733217 | Origin of exon skipping-rich transcriptomes in animals driven by evolution of gene architecture |
| Q34353566 | Origin of metazoan cadherin diversity and the antiquity of the classical cadherin/β-catenin complex |
| Q35005363 | Origins of Myc proteins--using intrinsic protein disorder to trace distant relatives |
| Q44593074 | Origins of multicellular complexity: Volvox and the volvocine algae |
| Q22337303 | Origins of neurogenesis, a cnidarian view |
| Q24635071 | Orthology prediction methods: a quality assessment using curated protein families |
| Q89771836 | Overview of Basic Mechanisms of Notch Signaling in Development and Disease |
| Q28660752 | Oxygen requirements of the earliest animals |
| Q28477906 | PTB domain-directed substrate targeting in a tyrosine kinase from the unicellular choanoflagellate Monosiga brevicollis |
| Q33815949 | Parallel expansions of Sox transcription factor group B predating the diversifications of the arthropods and jawed vertebrates |
| Q37812093 | Parasite annexins--new molecules with potential for drug and vaccine development |
| Q33909288 | Pathological unfoldomics of uncontrolled chaos: intrinsically disordered proteins and human diseases |
| Q57166993 | Patterns of Ancestral Animal Codon Usage Bias Revealed Through Holozoan Protists |
| Q38361542 | Peptide-gated ion channels and the simple nervous system of Hydra |
| Q37392591 | Pharmacology of ciliated protozoa--drug (in)sensitivity and experimental drug (ab)use |
| Q52729364 | Phosphorylation control of the ubiquitin ligase Cbl is conserved in choanoflagellates. |
| Q42413402 | Phosphotyrosine signaling: evolving a new cellular communication system |
| Q53129316 | Phosphotyrosine signalling and the origin of animal multicellularity. |
| Q27333622 | Phylogenetic Patterns of Codon Evolution in the ACTIN-DEPOLYMERIZING FACTOR/COFILIN (ADF/CFL) Gene Family |
| Q35085360 | Phylogenetic analysis of CDK and cyclin proteins in premetazoan lineages. |
| Q41075690 | Phylogenetic analysis of the teneurins: conserved features and premetazoan ancestry |
| Q39043809 | Phylogenetic evidence for the modular evolution of metazoan signalling pathways |
| Q26741622 | Phylogenetic-Derived Insights into the Evolution of Sialylation in Eukaryotes: Comprehensive Analysis of Vertebrate β-Galactoside α2,3/6-Sialyltransferases (ST3Gal and ST6Gal) |
| Q45944195 | Phylogenetic-signal dissection of nuclear housekeeping genes supports the paraphyly of sponges and the monophyly of Eumetazoa. |
| Q38599960 | Phylogenomic Insights into Animal Evolution |
| Q55030863 | Phylogenomics demonstrates that breviate flagellates are related to opisthokonts and apusomonads |
| Q38024900 | Phylogenomics meets neuroscience: how many times might complex brains have evolved? |
| Q28240393 | Phylogenomics revives traditional views on deep animal relationships |
| Q30863609 | Phylogeny and evolution of Rab7 and Rab9 proteins |
| Q28751278 | Phylogeny and function of the invertebrate p53 superfamily |
| Q37375071 | Phylogeny of Tec family kinases identification of a premetazoan origin of Btk, Bmx, Itk, Tec, Txk, and the Btk regulator SH3BP5. |
| Q18776012 | Phylogeny of the “Forgotten” Cellular Slime Mold, Fonticula alba, Reveals a Key Evolutionary Branch within Opisthokonta |
| Q28708481 | Phylostratigraphic profiles reveal a deep evolutionary history of the vertebrate head sensory systems |
| Q21245316 | Phylostratigraphic tracking of cancer genes suggests a link to the emergence of multicellularity in metazoa |
| Q28277090 | Physico-genetic determinants in the evolution of development |
| Q37393080 | Physiology and Evolution of Voltage-Gated Calcium Channels in Early Diverging Animal Phyla: Cnidaria, Placozoa, Porifera and Ctenophora |
| Q51905964 | Piwi expression in archeocytes and choanocytes in demosponges: insights into the stem cell system in demosponges. |
| Q34014242 | Placozoa and the evolution of Metazoa and intrasomatic cell differentiation |
| Q38976301 | Plant NBR1 is a selective autophagy substrate and a functional hybrid of the mammalian autophagic adapters NBR1 and p62/SQSTM1. |
| Q38003524 | Plant Proteus: brown algal morphological plasticity and underlying developmental mechanisms |
| Q45911166 | Plant vegetative and animal cytoplasmic actins share functional competence for spatial development with protists. |
| Q92691115 | Pluripotency and the origin of animal multicellularity |
| Q42265701 | Polyploidy and the evolution of complex traits |
| Q42705317 | Positive selection of tyrosine loss in metazoan evolution. |
| Q37402345 | Postsynaptic regulation of synaptic plasticity by synaptotagmin 4 requires both C2 domains. |
| Q34447869 | Pre-metazoan origins and evolution of the cadherin adhesome |
| Q26739742 | Precambrian origins of the TNFR superfamily |
| Q60950822 | Predicted glycosyltransferases promote development and prevent spurious cell clumping in the choanoflagellate |
| Q35468637 | Premetazoan ancestry of the Myc-Max network |
| Q21183992 | Premetazoan genome evolution and the regulation of cell differentiation in the choanoflagellate Salpingoeca rosetta |
| Q36120898 | Premetazoan origin of the hippo signaling pathway |
| Q46002820 | Preparation of high-molecular-weight genomic DNA from Monosiga brevicollis and other choanoflagellates. |
| Q27672465 | Primordial neurosecretory apparatus identified in the choanoflagellate Monosiga brevicollis |
| Q35119485 | Processes of fungal proteome evolution and gain of function: gene duplication and domain rearrangement |
| Q88938266 | Programming self-organizing multicellular structures with synthetic cell-cell signaling |
| Q21145789 | Protein evolution by molecular tinkering: diversification of the nuclear receptor superfamily from a ligand-dependent ancestor |
| Q42845318 | Protein evolution in cell and tissue development: going beyond sequence and transcriptional analysis |
| Q33950954 | Protein functional links in Trypanosoma brucei, identified by gene fusion analysis. |
| Q33384109 | Protists are microbes too: a perspective |
| Q28661921 | Punctuated emergences of genetic and phenotypic innovations in eumetazoan, bilaterian, euteleostome, and hominidae ancestors |
| Q30502984 | RNA interference in marine and freshwater sponges: actin knockdown in Tethya wilhelma and Ephydatia muelleri by ingested dsRNA expressing bacteria |
| Q90521897 | Reconstruction of protein domain evolution using single-cell amplified genomes of uncultured choanoflagellates sheds light on the origin of animals |
| Q55121687 | Reconstruction of the ancestral metazoan genome reveals an increase in genomic novelty. |
| Q30157090 | Reengineering the signaling properties of a Src family kinase |
| Q100945033 | Regeneration in sponge Sycon ciliatum partly mimics postlarval development |
| Q37408606 | Regulated aggregative multicellularity in a close unicellular relative of metazoa |
| Q39946025 | Regulation of Src and Csk nonreceptor tyrosine kinases in the filasterean Ministeria vibrans |
| Q37876443 | Regulation of spatiotemporal expression of cell-cell adhesion molecules during development of Dictyostelium discoideum |
| Q33738188 | Regulation of the cholesterol biosynthetic pathway and its integration with fatty acid biosynthesis in the oleaginous microalga Nannochloropsis oceanica |
| Q34059249 | Regulatory Factor X (RFX)-mediated transcriptional rewiring of ciliary genes in animals |
| Q87712503 | Research perspectives of biomedical gerontology and brain aging research: longevity genes in the brain |
| Q38331475 | Retromer and sorting nexins in endosomal sorting |
| Q37043759 | Reverse transcriptase and intron number evolution |
| Q36794564 | Review of Ets1 structure, function, and roles in immunity |
| Q62570592 | Revision of the Capsaspora genome using read mating information adjusts the view on premetazoan genome |
| Q112722973 | Role of epigenetics in unicellular to multicellular transition in Dictyostelium |
| Q92225836 | Rosette Colonies of Choanoflagellates (Salpingoeca rosetta) Show Increased Food Vacuole Formation Compared with Single Swimming Cells |
| Q34326156 | SECOM: a novel hash seed and community detection based-approach for genome-scale protein domain identification |
| Q29038594 | SH2 Domains Recognize Contextual Peptide Sequence Information to Determine Selectivity |
| Q46487364 | SNAREing the basis of multicellularity: consequences of protein family expansion during evolution |
| Q26996018 | SRC-family tyrosine kinases in oogenesis, oocyte maturation and fertilization: an evolutionary perspective |
| Q90554408 | Selective factors in the evolution of multicellularity in choanoflagellates |
| Q37003103 | Sequence comparative analysis using networks: software for evaluating de novo transcript assembly from next-generation sequencing |
| Q38271438 | Serendipity or prepared mind? Recollections of the KOP translocation (1967) and of one form of Perrault syndrome |
| Q28757825 | Seventeen new complete mtDNA sequences reveal extensive mitochondrial genome evolution within the Demospongiae |
| Q28646166 | Sex is a ubiquitous, ancient, and inherent attribute of eukaryotic life |
| Q36432826 | Short toxin-like proteins abound in Cnidaria genomes |
| Q37954785 | Signaling pathways and axis formation in the lower metazoa |
| Q30157711 | Signaling properties of a non-metazoan Src kinase and the evolutionary history of Src negative regulation |
| Q38716994 | Similar Ratios of Introns to Intergenic Sequence across Animal Genomes |
| Q90521917 | Single cell ecology |
| Q34397362 | Single nucleus genome sequencing reveals high similarity among nuclei of an endomycorrhizal fungus |
| Q48042704 | Single-cell measurement of ammonium and bicarbonate uptake within a photosymbiotic bioeroding sponge |
| Q43823205 | Single-domain β-thymosins: the family history |
| Q37638325 | Sirtuin/Sir2 phylogeny, evolutionary considerations and structural conservation |
| Q38148534 | Sox proteins: regulators of cell fate specification and differentiation |
| Q35178248 | Spatiotemporal transcriptomics reveals the evolutionary history of the endoderm germ layer |
| Q38729293 | Spheres of Hope, Packets of Doom: the Good and Bad of Outer Membrane Vesicles in Interspecies and Ecological Dynamics |
| Q47665914 | Sponge genes provide new insight into the evolutionary origin of the neurogenic circuit. |
| Q34047051 | Sponges as models to study emergence of complex animals |
| Q47213998 | Sponges: A Reservoir of Genes Implicated in Human Cancer |
| Q38062396 | Stem cell dynamics in Cnidaria: are there unifying principles? |
| Q33732822 | Stem cell-specific activation of an ancestral myc protooncogene with conserved basic functions in the early metazoan Hydra |
| Q22337198 | Sterols in a unicellular relative of the metazoans |
| Q93101041 | Still Enigmatic: Innate Immunity in the Ctenophore Mnemiopsis leidyi |
| Q99352806 | Structural Characterization and Computational Analysis of PDZ domains in Monosiga brevicollis |
| Q27675829 | Structural Insights into Cellulolytic and Chitinolytic Enzymes Revealing Crucial Residues of Insect β-N-acetyl-D-hexosaminidase |
| Q90949258 | Structural Insights into the Regulation of Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII) |
| Q34233642 | Structural basis for conservation in the CYP51 family |
| Q50459741 | Structural molecular components of septate junctions in cnidarians point to the origin of epithelial junctions in eukaryotes. |
| Q50540049 | Structure and expression of conserved Wnt pathway components in the demosponge Amphimedon queenslandica. |
| Q28475452 | Synthesizing and salvaging NAD: lessons learned from Chlamydomonas reinhardtii |
| Q38048246 | TCF/LEFs and Wnt signaling in the nucleus. |
| Q38206430 | TRPV6 channels |
| Q97870153 | Tannins from senescent Rhizophora mangle mangrove leaves have a distinctive effect on prokaryotic and eukaryotic communities in a Distichlis spicata salt marsh soil |
| Q117427787 | Technical note: The silicon isotopic composition of choanoflagellates: implications for a mechanistic understanding of isotopic fractionation during biosilicification |
| Q96609005 | Temperature sensitivities of metazoan and pre-metazoan Src kinases |
| Q22122176 | The Amphimedon queenslandica genome and the evolution of animal complexity |
| Q38771269 | The Birth of Animal Development: Multicellularity and the Germline |
| Q24337583 | The CKK domain (DUF1781) binds microtubules and defines the CAMSAP/ssp4 family of animal proteins |
| Q34363810 | The Capsaspora genome reveals a complex unicellular prehistory of animals |
| Q28598278 | The Cosmic Zoo: The (Near) Inevitability of the Evolution of Complex, Macroscopic Life |
| Q34523527 | The Dynamic Regulatory Genome of Capsaspora and the Origin of Animal Multicellularity |
| Q28603054 | The Evolution of COP9 Signalosome in Unicellular and Multicellular Organisms |
| Q28642185 | The Evolution of the Secreted Regulatory Protein Progranulin |
| Q33879071 | The Evolutionary Landscape of Dbl-Like RhoGEF Families: Adapting Eukaryotic Cells to Environmental Signals |
| Q57220385 | The Evolutionary Origin of Animals and Fungi |
| Q28656451 | The Fox/Forkhead transcription factor family of the hemichordate Saccoglossus kowalevskii |
| Q38773345 | The Function and Evolution of Nuclear Receptors in Insect Embryonic Development |
| Q34997600 | The GPCR repertoire in the demosponge Amphimedon queenslandica: insights into the GPCR system at the early divergence of animals |
| Q21972829 | The Genome of Naegleria gruberi Illuminates Early Eukaryotic Versatility |
| Q35996462 | The Gonium pectorale genome demonstrates co-option of cell cycle regulation during the evolution of multicellularity. |
| Q47380403 | The Insect Chemoreceptor Superfamily Is Ancient in Animals |
| Q59405758 | The Multiple Origins of Complex Multicellularity |
| Q57179384 | The Nuclear Receptor Field: A Historical Overview and Future Challenges |
| Q46036492 | The Origin of Animal Multicellularity and Cell Differentiation. |
| Q37642606 | The Rh protein family: gene evolution, membrane biology, and disease association |
| Q35239082 | The Rosetteless gene controls development in the choanoflagellate S. rosetta |
| Q28255020 | The SH2 domain-containing proteins in 21 species establish the provenance and scope of phosphotyrosine signaling in eukaryotes |
| Q38029732 | The SOX family of genes in cancer development: biological relevance and opportunities for therapy |
| Q35964142 | The TALE face of Hox proteins in animal evolution |
| Q27681387 | The WAVE Regulatory Complex Links Diverse Receptors to the Actin Cytoskeleton |
| Q30662577 | The actinin family of actin cross-linking proteins - a genetic perspective. |
| Q42686796 | The adaptive evolution divergence of triosephosphate isomerases between parasitic and free-living flatworms and the discovery of a potential universal target against flatworm parasites |
| Q30318335 | The age of protein kinases |
| Q45734650 | The alternative NADH dehydrogenase is present in mitochondria of some animal taxa |
| Q38403959 | The analysis of eight transcriptomes from all poriferan classes reveals surprising genetic complexity in sponges |
| Q35575349 | The ancient function of RB-E2F pathway: insights from its evolutionary history |
| Q38345421 | The ancient roots of calcium signalling evolutionary tree |
| Q34473067 | The antiquity of chordate odorant receptors is revealed by the discovery of orthologs in the cnidarian Nematostella vectensis |
| Q21093626 | The backbone of the post-synaptic density originated in a unicellular ancestor of choanoflagellates and metazoans |
| Q84077561 | The cell adhesion molecule DdCAD-1 regulates morphogenesis through differential spatiotemporal expression in Dictyostelium discoideum |
| Q39018629 | The cellular and molecular basis of cnidarian neurogenesis. |
| Q43269380 | The choanoflagellate Monosiga brevicollis karyotype revealed by the genome sequence: telomere-linked helicase genes resemble those of some fungi |
| Q45979614 | The choanoflagellates: heterotrophic nanoflagellates and sister group of the metazoa. |
| Q37801332 | The cnidarian nematocyst: a miniature extracellular matrix within a secretory vesicle. |
| Q34999420 | The conserved metalloprotease invadolysin localizes to the surface of lipid droplets. |
| Q34029056 | The default state of the cell: quiescence or proliferation? |
| Q98196738 | The diversification and lineage-specific expansion of nitric oxide signaling in Placozoa: insights in the evolution of gaseous transmission |
| Q21560967 | The diversification of the LIM superclass at the base of the metazoa increased subcellular complexity and promoted multicellular specialization |
| Q59569369 | The earliest fossil record of the animals and its significance |
| Q35081193 | The eukaryotic ancestor had a complex ubiquitin signaling system of archaeal origin |
| Q47764464 | The evolution and function of the Pax/Six regulatory network in sponges |
| Q38262432 | The evolution of MDM2 family genes |
| Q33431470 | The evolution of Runx genes II. The C-terminal Groucho recruitment motif is present in both eumetazoans and homoscleromorphs but absent in a haplosclerid demosponge. |
| Q35771544 | The evolution of animal genomes |
| Q37301036 | The evolution of cell types in animals: emerging principles from molecular studies |
| Q59793167 | The evolution of ependymin-related proteins |
| Q33772478 | The evolution of extracellular matrix |
| Q37995158 | The evolution of metazoan extracellular matrix |
| Q37677301 | The evolution of the GPCR signaling system in eukaryotes: modularity, conservation, and the transition to metazoan multicellularity |
| Q28727852 | The evolution of the Wnt pathway |
| Q42950778 | The evolution of the four subunits of voltage-gated calcium channels: ancient roots, increasing complexity, and multiple losses |
| Q28744006 | The evolution of thrombospondins and their ligand-binding activities |
| Q30157512 | The evolutionarily conserved arrangement of domains in SRC family kinases is important for substrate recognition |
| Q46135590 | The evolutionary analysis reveals domain fusion of proteins with Frizzled-like CRD domain |
| Q42485451 | The evolutionary history of YAP and the hippo/YAP pathway |
| Q43294454 | The evolutionary history of lysine biosynthesis pathways within eukaryotes |
| Q39873154 | The evolutionary history of the E2F and DEL genes in Viridiplantae |
| Q33955921 | The evolutionary history of the catenin gene family during metazoan evolution |
| Q28752612 | The fibrillar collagen family |
| Q64087426 | The first identification of complete Eph-ephrin signalling in ctenophores and sponges reveals a role for neofunctionalization in the emergence of signalling domains |
| Q34270689 | The functions of grainy head-like proteins in animals and fungi and the evolution of apical extracellular barriers |
| Q30918699 | The gene complement of the ancestral bilaterian - was Urbilateria a monster? |
| Q22065604 | The genome of the ctenophore Mnemiopsis leidyi and its implications for cell type evolution |
| Q43809640 | The genome of the sponge Amphimedon queenslandica provides new perspectives into the origin of Toll-like and interleukin 1 receptor pathways. |
| Q35630989 | The genome portal of the Department of Energy Joint Genome Institute |
| Q38139494 | The genomic and cellular foundations of animal origins |
| Q37606400 | The granulin gene family: from cancer to dementia |
| Q21195912 | The homeodomain complement of the ctenophore Mnemiopsis leidyi suggests that Ctenophora and Porifera diverged prior to the ParaHoxozoa |
| Q36093876 | The human phosphotyrosine signaling network: evolution and hotspots of hijacking in cancer |
| Q28749058 | The initiation of metamorphosis as an ancient polyphenic trait and its role in metazoan life-cycle evolution |
| Q48041758 | The last common ancestor of animals lacked the HIF pathway and respired in low-oxygen environments |
| Q34056277 | The mammalian disaggregase machinery: Hsp110 synergizes with Hsp70 and Hsp40 to catalyze protein disaggregation and reactivation in a cell-free system |
| Q37300635 | The molecular origins of multicellular transitions |
| Q61460308 | The mouth, the anus, and the blastopore—open questions about questionable openings |
| Q35839976 | The origin and evolution of G protein-coupled receptor kinases |
| Q38361538 | The origin and evolution of synaptic proteins - choanoflagellates lead the way. |
| Q37497066 | The origin of Metazoa: a transition from temporal to spatial cell differentiation. |
| Q39289407 | The origin of Metazoa: a unicellular perspective. |
| Q89808107 | The origin of animal body plans: a view from fossil evidence and the regulatory genome |
| Q113186028 | The origin of animals: an ancestral reconstruction of the unicellular-to-multicellular transition |
| Q34045549 | The origin of the Hox/ParaHox genes, the Ghost Locus hypothesis and the complexity of the first animal |
| Q34502445 | The origin of the animals and a 'Savannah' hypothesis for early bilaterian evolution. |
| Q50459532 | The origins of developmental gene regulation. |
| Q37317007 | The origins of multicellularity and the early history of the genetic toolkit for animal development |
| Q56531721 | The other eukaryotes in light of evolutionary protistology |
| Q38825614 | The p53 Pathway: Origins, Inactivation in Cancer, and Emerging Therapeutic Approaches |
| Q91695083 | The p53 gene family in vertebrates: Evolutionary considerations |
| Q48479586 | The predictability of evolution: glimpses into a post-Darwinian world. |
| Q39246180 | The predicted secretomes of Monosiga brevicollis and Capsaspora owczarzaki, close unicellular relatives of metazoans, reveal new insights into the evolution of the metazoan extracellular matrix |
| Q37123067 | The primary cilium at the crossroads of mammalian hedgehog signaling |
| Q37808329 | The primary role of fibrinogen-related proteins in invertebrates is defense, not coagulation |
| Q36755352 | The protist, Monosiga brevicollis, has a tyrosine kinase signaling network more elaborate and diverse than found in any known metazoan |
| Q34041711 | The proto-MHC of placozoans, a region specialized in cellular stress and ubiquitination/proteasome pathways |
| Q28252420 | The regulation of protein phosphorylation |
| Q89029029 | The remembrance of the things past: Conserved signalling pathways link protozoa to mammalian nervous system |
| Q41436775 | The repertoires of ubiquitinating and deubiquitinating enzymes in eukaryotic genomes |
| Q85114455 | The rise of genomics sheds light on the dawn of animals |
| Q33787253 | The role of exon shuffling in shaping protein-protein interaction networks |
| Q38375711 | The role of fibrinogen-related proteins in the gastropod immune response |
| Q38960452 | The role of ficolin-like protein (PcFLP1) in the antibacterial immunity of red swamp crayfish (Procambarus clarkii). |
| Q33716090 | The scale and evolutionary significance of horizontal gene transfer in the choanoflagellate Monosiga brevicollis |
| Q92227516 | The significance of sponges for comparative studies of developmental evolution |
| Q28301865 | The solute carrier families have a remarkably long evolutionary history with the majority of the human families present before divergence of Bilaterian species |
| Q38071714 | The sox family of transcription factors: versatile regulators of stem and progenitor cell fate |
| Q37776425 | The spectrin-ankyrin-4.1-adducin membrane skeleton: adapting eukaryotic cells to the demands of animal life |
| Q37676279 | The stem cell system in demosponges: insights into the origin of somatic stem cells. |
| Q38051058 | The stem cell system in demosponges: suggested involvement of two types of cells: archeocytes (active stem cells) and choanocytes (food-entrapping flagellated cells). |
| Q112557535 | The structure of EXTL3 helps to explain the different roles of bi-domain exostosins in heparan sulfate synthesis |
| Q33527545 | The synapsin gene family in basal chordates: evolutionary perspectives in metazoans |
| Q52720562 | The triple helix of collagens - an ancient protein structure that enabled animal multicellularity and tissue evolution. |
| Q92318680 | The ventral epithelium of Trichoplax adhaerens deploys in distinct patterns cells that secrete digestive enzymes, mucus or diverse neuropeptides |
| Q33690172 | The voyage of the microbial eukaryote |
| Q34055251 | Thousands of rab GTPases for the cell biologist |
| Q42912620 | Three Dimensional Organization of Genome Might Have Guided the Dynamics of Gene Order Evolution in Eukaryotes |
| Q44310843 | Three families of LTR retrotransposons are present in the genome of the choanoflagellate Monosiga brevicollis |
| Q56889970 | Toward a systems level view of the ECM and related proteins: a framework for the systematic definition and analysis of biological systems |
| Q97088314 | Towards reconstructing the dipteran demise of an ancient essential gene: E3 ubiquitin ligase Murinedouble minute |
| Q104063284 | Towards understanding the origin of animal development |
| Q35968813 | Tracing the Evolutionary History of Inositol, 1, 4, 5-Trisphosphate Receptor: Insights from Analyses of Capsaspora owczarzaki Ca2+ Release Channel Orthologs |
| Q28656003 | Tracing the evolution of the p53 tetramerization domain |
| Q46710454 | Tracking the ancestry of a deeply conserved eumetazoan SINE domain |
| Q50625150 | Tracking the origin and divergence of cholinesterases and neuroligins: the evolution of synaptic proteins. |
| Q36358937 | Transcription factor networks directing the development, function, and evolution of innate lymphoid effectors |
| Q91744538 | Transcription factors in SOX family: Potent regulators for cancer initiation and development in the human body |
| Q97524917 | Transcriptomic and Ultrastructural Signatures of K+-Induced Aggregation in Phytophthora parasitica Zoospores |
| Q35051161 | Trask phosphorylation defines the reverse mode of a phosphotyrosine signaling switch that underlies cell anchorage state |
| Q42287488 | Trichoplax adhaerens reveals a network of nuclear receptors sensitive to 9-cis-retinoic acid at the base of metazoan evolution |
| Q47140201 | Tumorigenesis as a process of gradual loss of original cell identity and gain of properties of neural precursor/progenitor cells. |
| Q27692524 | Tyrosine kinase signaling and the emergence of multicellularity |
| Q34461401 | Understanding "green" multicellularity: do seaweeds hold the key? |
| Q34150586 | Unexpected repertoire of metazoan transcription factors in the unicellular holozoan Capsaspora owczarzaki |
| Q28274960 | Unicellular Ca2+ signaling 'toolkit' at the origin of metazoa |
| Q57479870 | Unicellular Origin of the Animal MicroRNA Machinery |
| Q38188212 | Unicellular eukaryotes as models in cell and molecular biology: critical appraisal of their past and future value. |
| Q43917078 | Unique genome of dicyemid mesozoan: highly shortened spliceosomal introns in conservative exon/intron structure |
| Q111195907 | Using the F/R-ratio for an evaluation of the ability of the demosponge Halichondria panicea to nourish solely on phytoplankton versus free-living bacteria in the sea |
| Q37944602 | Vascular smooth muscle myosin light chain diphosphorylation: mechanism, function, and pathological implications |
| Q37809303 | Volvox: simple steps to developmental complexity? |
| Q33463343 | WNT/beta-catenin signalling and epithelial patterning in the homoscleromorph sponge Oscarella |
| Q55452270 | We are not so special. |
| Q38712484 | What Defines the "Kingdom" Fungi? |
| Q88916801 | What Makes an Animal? The Molecular Quest for the Origin of the Animal Kingdom |
| Q28743958 | What are nuclear receptor ligands? |
| Q90549808 | What lies beneath: Hydra provides cnidarian perspectives into the evolution of FGFR docking proteins |
| Q37828883 | What sponges can tell us about the evolution of developmental processes. |
| Q30364669 | Where cell fate conversions meet Chinese philosophy. |
| Q42365202 | Whole-genome metabolic model of Trichoderma reesei built by comparative reconstruction |
| Q86155850 | Why flying dogs are rare: A general theory of luck in evolutionary transitions |
| Q88268314 | Wingless Signaling: A Genetic Journey from Morphogenesis to Metastasis |
| Q34011176 | Wnt gene loss in flatworms. |
| Q48503756 | Wnt signaling and polarity in freshwater sponges. |
| Q58794971 | Xenacoelomorpha Survey Reveals That All 11 Animal Homeobox Gene Classes Were Present in the First Bilaterians |
| Q54120973 | Yeast can accommodate phosphotyrosine: v-Src toxicity in yeast arises from a single disrupted pathway. |
| Q35698749 | dbHiMo: a web-based epigenomics platform for histone-modifying enzymes. |
| Q84583329 | p53 ancestry: gazing through an evolutionary lens |
| Q42833802 | p53 in the game of transposons |
| Q92459922 | α-Integrins dictate distinct modes of type IV collagen recruitment to basement membranes |
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