| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1016/S0168-9525(96)80020-5 |
| P698 | PubMed publication ID | 8855667 |
| P2093 | author name string | Fryxell KJ | |
| P2860 | cites work | A novel IL-1 receptor, cloned from B cells by mammalian expression, is expressed in many cell types | Q24309431 |
| Targeted mutation in the neurotrophin-3 gene results in loss of muscle sensory neurons | Q24564570 | ||
| Homeobox genes and axial patterning | Q28181571 | ||
| Molecular evolution of the human interleukin-8 receptor gene cluster | Q28208052 | ||
| Function and evolution in the NGF family and its receptors | Q28211906 | ||
| Mapping of genes for the human C5a receptor (C5AR), human FMLP receptor (FPR), and two FMLP receptor homologue orphan receptors (FPRH1, FPRH2) to chromosome 19 | Q28269315 | ||
| Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage | Q28272540 | ||
| A novel multigene family may encode odorant receptors: a molecular basis for odor recognition | Q28276183 | ||
| T cell antigen receptors and the immunoglobulin supergene family | Q28306996 | ||
| Cloning and expression of odorant receptors | Q28567936 | ||
| Critical role for lysines 21 and 22 in signal-induced, ubiquitin-mediated proteolysis of I kappa B-alpha | Q28618972 | ||
| Late Precambrian bilaterians: grades and clades | Q28775959 | ||
| Diversity of G proteins in signal transduction | Q29618841 | ||
| NF-kappa B: a pleiotropic mediator of inducible and tissue-specific gene control | Q29620172 | ||
| Searching through sequence databases | Q31106631 | ||
| Severe sensory and sympathetic neuropathies in mice carrying a disrupted Trk/NGF receptor gene. | Q34338664 | ||
| Punctuated equilibrium comes of age. | Q34344229 | ||
| Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse | Q34364325 | ||
| Structure and evolution of insulins: implications for receptor binding | Q35230812 | ||
| Evolution of the vertebrate Hox homeobox genes | Q35256407 | ||
| Gene amplification and insecticide resistance | Q37672953 | ||
| Cactus protein degradation mediates Drosophila dorsal-ventral signaling | Q38297088 | ||
| Dif, a dorsal-related gene that mediates an immune response in Drosophila. | Q38314185 | ||
| Tandem genetic duplications in phage and bacteria | Q39707701 | ||
| Methotrexate resistance and gene amplification. Mechanisms and implications | Q39729478 | ||
| The appearance of new structures and functions in proteins during evolution. | Q40470932 | ||
| Evolution of Hox genes | Q40614030 | ||
| Functional analysis and regulation of nuclear import of dorsal during the immune response in Drosophila. | Q40805661 | ||
| The area-code hypothesis: the immune system provides clues to understanding the genetic and molecular basis of cell recognition during development | Q41037625 | ||
| Signals from the IL-1 receptor homolog, Toll, can activate an immune response in a Drosophila hemocyte cell line. | Q41351317 | ||
| kappa B-like motifs regulate the induction of immune genes in Drosophila | Q41541544 | ||
| Identification of effector-activating residues of Gs alpha | Q41927516 | ||
| Macrophage differentiation marker MyD88 is a member of the Toll/IL-1 receptor family | Q42602845 | ||
| Conservation of ligand specificity between the mammalian and amphibian fibroblast growth factor receptors | Q42820193 | ||
| Nerve Growth Factor and Insulin | Q46305123 | ||
| The evolution of rhodopsins and neurotransmitter receptors | Q46616948 | ||
| The evolutionary divergence of neurotransmitter receptors and second-messenger pathways | Q46633856 | ||
| Insect immunology. Ancient relationships | Q47239211 | ||
| cactus, a gene involved in dorsoventral pattern formation of Drosophila, is related to the I kappa B gene family of vertebrates | Q48148826 | ||
| The characterization of somatomedin A, isolated by microcomputer-controlled chromatography, reveals an apparent identity to insulin-like growth factor 1. | Q50921080 | ||
| Molecular drive in multigene families: How biological novelties arise, spread and are assimilated | Q56533481 | ||
| P433 | issue | 9 | |
| P921 | main subject | co-evolution | Q208841 |
| P304 | page(s) | 364-369 | |
| P577 | publication date | 1996-09-01 | |
| P1433 | published in | Trends in Genetics | Q2451468 |
| P1476 | title | The coevolution of gene family trees | |
| P478 | volume | 12 |
| Q33368522 | A homolog of NO APICAL MERISTEM is an immediate target of the floral homeotic genes APETALA3/PISTILLATA. |
| Q48331609 | A site-specific measure for rate difference after gene duplication or speciation |
| Q33337467 | AtSKtheta, a plant homologue of SGG/GSK-3 marks developing tissues in Arabidopsis thaliana |
| Q34407655 | Basis for substrate recognition and distinction by matrix metalloproteinases |
| Q34539656 | Chapter 4: Protein interactions and disease |
| Q39749049 | Characterization of the Double-Partitioning Modules of R27: Correlating Plasmid Stability with Plasmid Localization |
| Q64085466 | Characterizing human genomic coevolution in locus-gene regulatory interactions |
| Q30352387 | Co-evolution analysis on endocrine research: a methodological approach. |
| Q37087528 | Co-evolution and co-adaptation in protein networks |
| Q41954144 | Co-evolution of RNA polymerase with RbpA in the phylum Actinobacteria |
| Q33572801 | Coevolution of axon guidance molecule Slit and its receptor Robo |
| Q41830334 | Comparable rates of gene loss and functional divergence after genome duplications early in vertebrate evolution |
| Q34537153 | Comparative genomics of the vertebrate insulin/TOR signal transduction pathway: a network-level analysis of selective pressures |
| Q33518047 | Comparison of phylogenetic trees through alignment of embedded evolutionary distances |
| Q34139922 | Computational methods for the prediction of protein interactions |
| Q47388509 | Conflicting phylogenetic signals at the base of the metazoan tree |
| Q35003145 | Correlated evolution among six gene families in Drosophila revealed by parallel change of gene numbers. |
| Q28749543 | Covariation of branch lengths in phylogenies of functionally related genes |
| Q47126316 | Divergent evolutionary patterns of the MAPK cascade genes in Brassica rapa and plant phylogenetics |
| Q53394729 | Dynamic sensitivity and nonlinear interactions influence the system-level evolutionary patterns of phototransduction proteins. |
| Q38086348 | Emerging methods in protein co-evolution |
| Q33316210 | Enhancing the prediction of protein pairings between interacting families using orthology information |
| Q41818711 | Evidence that the E4 and FE4 esterase genes responsible for insecticide resistance in the aphid Myzus persicae (Sulzer) are part of a gene family |
| Q43114543 | Evolution of animal and plant dicers: early parallel duplications and recurrent adaptation of antiviral RNA binding in plants |
| Q41876083 | Evolution of multigene families by gene duplication. A haploid model |
| Q34606438 | Evolution of the RECQ family of helicases: A drosophila homolog, Dmblm, is similar to the human bloom syndrome gene |
| Q33945071 | Evolution of vertebrate steroid receptors from an ancestral estrogen receptor by ligand exploitation and serial genome expansions |
| Q21245454 | Evolutionary divergence and functions of the human interleukin (IL) gene family |
| Q73073424 | Exploiting the co-evolution of interacting proteins to discover interaction specificity |
| Q46665970 | Fifty years of co-evolution and beyond: integrating co-evolution from molecules to species |
| Q35536256 | G Protein-coupled Receptor Kinases of the GRK4 Protein Subfamily Phosphorylate Inactive G Protein-coupled Receptors (GPCRs). |
| Q30493003 | Gene divergence and pathway duplication in the metabolic network of yeast and digital organisms |
| Q59269359 | Gene duplication plays a major role in gene co-option: Studies into the evolution of the motilin/ghrelin family and their receptors |
| Q33665075 | Generation of evolutionary novelty by functional shift |
| Q28475165 | Genome-wide functional divergence after the symbiosis of proteobacteria with insects unraveled through a novel computational approach |
| Q28366747 | Genomic organization of plant terpene synthases and molecular evolutionary implications |
| Q36458869 | High-confidence prediction of global interactomes based on genome-wide coevolutionary networks |
| Q51892474 | Homology and phylogeny and their automated inference. |
| Q33972814 | Identification of two different 14-alpha sterol demethylase-related genes (cyp51A and cyp51B) in Aspergillus fumigatus and other Aspergillus species |
| Q87370078 | Investigating co-evolution of functionally associated phosphosites in human |
| Q35101729 | Mapping proteins in the presence of paralogs using units of coevolution |
| Q37119623 | Network-level molecular evolutionary analysis of the insulin/TOR signal transduction pathway across 12 Drosophila genomes |
| Q47861102 | Organization and structural evolution of four multigene families in Arabidopsis thaliana: AtLCAD, AtLGT, AtMYST and AtHD-GL2. |
| Q90694220 | Phylogenetic correlations can suffice to infer protein partners from sequences |
| Q34391358 | Practical aspects of protein co-evolution |
| Q30002397 | Predicting biological networks from genomic data |
| Q47637567 | Prediction of protein-protein interaction networks. |
| Q36914675 | Protein co-evolution, co-adaptation and interactions |
| Q30002405 | Protein-protein interactions: analysis and prediction |
| Q34560926 | Receptor kinase signalling in plants and animals: distinct molecular systems with mechanistic similarities |
| Q55035526 | Similarity of phylogenetic trees as indicator of protein-protein interaction. |
| Q35084983 | Slow co-evolution of the MAGO and Y14 protein families is required for the maintenance of their obligate heterodimerization mode |
| Q48000292 | Structure and polymorphism of the Chironomus thummi gene encoding special lobe-specific silk protein, ssp160. |
| Q34974100 | TSEMA: interactive prediction of protein pairings between interacting families |
| Q35804136 | Tex19 and Sectm1 concordant molecular phylogenies support co-evolution of both eutherian-specific genes |
| Q48049064 | The Arabidopsis downy mildew resistance gene RPP5 shares similarity to the toll and interleukin-1 receptors with N and L6. |
| Q36709556 | The diversity and evolutionary relationships of the pregnancy-associated glycoproteins, an aspartic proteinase subfamily consisting of many trophoblast-expressed genes. |
| Q35037659 | The evolution of signalling pathways in animal development |
| Q37395221 | The human protein coevolution network. |
| Q34503048 | The origins of the evolutionary signal used to predict protein-protein interactions |
| Q24792242 | The prolactin and growth hormone families: pregnancy-specific hormones/cytokines at the maternal-fetal interface |
| Q48355459 | Two large Arabidopsis thaliana gene families are homologous to the Brassica gene superfamily that encodes pollen coat proteins and the male component of the self-incompatibility response |
| Q34610467 | Two medfly promoters that have originated by recent gene duplication drive distinct sex, tissue and temporal expression patterns |
| Q82880690 | Two-component signal transduction systems of Desulfovibrio vulgaris: structural and phylogenetic analysis and deduction of putative cognate pairs |
| Q34005823 | Virulence plasmid of Rhodococcus equi contains inducible gene family encoding secreted proteins |
| Q37037782 | Why should we care about molecular coevolution? |
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