| scholarly article | Q13442814 |
| P50 | author | Alessandro Vitriolo | Q57237358 |
| Pedro T Martins | Q58568198 | ||
| Sebastiano Trattaro | Q90678132 | ||
| Alejandro Andirko | Q91995526 | ||
| Stefanie Sturm | Q91995529 | ||
| Thomas O'Rourke | Q91995532 | ||
| Adrianos Skaros | Q91995535 | ||
| Cedric Boeckx | Q42533957 | ||
| Marija Mihailovich | Q47503354 | ||
| Matteo Zanella | Q48356687 | ||
| Pierre-Luc Germain | Q48356693 | ||
| Giuseppe Testa | Q48356701 | ||
| Giuseppe Merla | Q57076747 | ||
| P2093 | author name string | Natascia Malerba | |
| Magdalena Laugsch | |||
| Alvaro Rada-Iglesias | |||
| P2860 | cites work | Evaluating the self-domestication hypothesis of human evolution | Q92785489 |
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| CHD7 cooperates with PBAF to control multipotent neural crest formation | Q24630725 | ||
| Tumor necrosis factor receptor family member RANK mediates osteoclast differentiation and activation induced by osteoprotegerin ligand | Q24653311 | ||
| RUNX3, EGR1 and SOX9B form a regulatory cascade required to modulate BMP-signaling during cranial cartilage development in zebrafish | Q27334714 | ||
| Slug antagonizes p53-mediated apoptosis of hematopoietic progenitors by repressing puma | Q28281602 | ||
| The complete genome sequence of a Neanderthal from the Altai Mountains | Q28304347 | ||
| GLI2 promotes cell proliferation and migration through transcriptional activation of ARHGEF16 in human glioma cells | Q57280907 | ||
| NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly | Q58618789 | ||
| Red fox genome assembly identifies genomic regions associated with tame and aggressive behaviours | Q60112184 | ||
| The evolutionary history of the human face | Q63170520 | ||
| A catalog of single nucleotide changes distinguishing modern humans from archaic hominins. | Q64972623 | ||
| A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disability | Q85676342 | ||
| Directed differentiation of human pluripotent cells to neural crest stem cells | Q85839043 | ||
| Defects in pathfinding by cranial neural crest cells in mice lacking the neuregulin receptor ErbB4 | Q28506344 | ||
| periostin null mice exhibit dwarfism, incisor enamel defects, and an early-onset periodontal disease-like phenotype | Q28588837 | ||
| TGFβ2 knockout mice have multiple developmental defects that are non-overlapping with other TGFβ knockout phenotypes | Q28592444 | ||
| Convergent differential regulation of SLIT-ROBO axon guidance genes in the brains of vocal learners | Q28649912 | ||
| Signals and switches in Mammalian neural crest cell differentiation | Q28709598 | ||
| Cell-fate determination by ubiquitin-dependent regulation of translation | Q28975777 | ||
| Regulation of the CUL3 Ubiquitin Ligase by a Calcium-Dependent Co-adaptor | Q28975781 | ||
| AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis | Q28975784 | ||
| Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism | Q29013643 | ||
| Hierarchical mechanisms for direct reprogramming of fibroblasts to neurons | Q29871108 | ||
| Loss of WSTF results in spontaneous fluctuations of heterochromatin formation and resolution, combined with substantial changes to gene expression | Q30560450 | ||
| TGFB2 mutations cause familial thoracic aortic aneurysms and dissections associated with mild systemic features of Marfan syndrome | Q33662519 | ||
| Taming Human Genetic Variability: Transcriptomic Meta-Analysis Guides the Experimental Design and Interpretation of iPSC-Based Disease Modeling | Q33795908 | ||
| Neural crest cell signaling pathways critical to cranial bone development and pathology | Q33813000 | ||
| Analysis of early human neural crest development | Q34080990 | ||
| Enhancers as information integration hubs in development: lessons from genomics. | Q34266848 | ||
| Neuregulins and their receptors: a versatile signaling module in organogenesis and oncogenesis | Q34431223 | ||
| Reiterative AP2a activity controls sequential steps in the neural crest gene regulatory network | Q34471732 | ||
| High-throughput chromatin immunoprecipitation for genome-wide mapping of in vivo protein-DNA interactions and epigenomic states | Q34594554 | ||
| Williams-Beuren syndrome. | Q34615997 | ||
| TBX15 mutations cause craniofacial dysmorphism, hypoplasia of scapula and pelvis, and short stature in Cousin syndrome | Q34899527 | ||
| A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development | Q34909016 | ||
| Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfecta | Q35221699 | ||
| Cranial neural crest and the building of the vertebrate head | Q35549127 | ||
| Roles of collagen and periostin expression by cranial neural crest cells during soft palate development | Q35768123 | ||
| The mechanism of TGF‐β signaling during palate development | Q35896486 | ||
| RNAontheBENCH: computational and empirical resources for benchmarking RNAseq quantification and differential expression methods | Q36020652 | ||
| The human-induced pluripotent stem cell initiative-data resources for cellular genetics | Q36161963 | ||
| Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis | Q36282251 | ||
| Testing for Ancient Selection Using Cross-population Allele Frequency Differentiation | Q36677342 | ||
| Loss-of-function variants in HIVEP2 are a cause of intellectual disability | Q37058019 | ||
| Epigenomic annotation of enhancers predicts transcriptional regulators of human neural crest | Q37115627 | ||
| Smad4 is required to regulate the fate of cranial neural crest cells | Q37247522 | ||
| Transcription factor GATA-3 regulates the transcriptional activity of dopamine beta-hydroxylase by interacting with Sp1 and AP4 | Q37267550 | ||
| Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits | Q37397610 | ||
| Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans | Q37415443 | ||
| Novel Col12A1 variant expands the clinical picture of congenital myopathies with extracellular matrix defects | Q37585978 | ||
| WSTF does it all: a multifunctional protein in transcription, repair, and replication | Q37843469 | ||
| Human genetic variation within neural crest enhancers: molecular and phenotypic implications | Q38104719 | ||
| YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction | Q38432867 | ||
| Detecting ancient positive selection in humans using extended lineage sorting. | Q38636121 | ||
| Structural variants in genes associated with human Williams-Beuren syndrome underlie stereotypical hypersociability in domestic dogs | Q38641866 | ||
| Axon guidance pathways served as common targets for human speech/language evolution and related disorders | Q38686186 | ||
| Survival of the Friendliest: Homo sapiens Evolved via Selection for Prosociality | Q38812338 | ||
| Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. | Q38820711 | ||
| An essential role of discoidin domain receptor 2 (DDR2) in osteoblast differentiation and chondrocyte maturation via modulation of Runx2 activation | Q39664032 | ||
| TFBSTools: an R/bioconductor package for transcription factor binding site analysis. | Q40078817 | ||
| Pax5-deficient mice exhibit early onset osteopenia with increased osteoclast progenitors | Q40489394 | ||
| Noelin-1 is a secreted glycoprotein involved in generation of the neural crest | Q41732581 | ||
| Self-domestication in Homo sapiens: Insights from comparative genomics. | Q42680482 | ||
| Common genetic variation drives molecular heterogeneity in human iPSCs | Q42830893 | ||
| The transcription factor Sox9 is required for cranial neural crest development in Xenopus. | Q43863973 | ||
| Developmental expression of the putative transcription factor Egr-1 suggests that Egr-1 and c-fos are coregulated in some tissues | Q44325733 | ||
| A high-coverage Neandertal genome from Vindija Cave in Croatia. | Q46270621 | ||
| DISC1 Regulates the Proliferation and Migration of Mouse Neural Stem/Progenitor Cells through Pax5, Sox2, Dll1 and Neurog2. | Q47142446 | ||
| The chromatin basis of neurodevelopmental disorders: Rethinking dysfunction along the molecular and temporal axes. | Q47878488 | ||
| Phenotype comparison confirms ZMYND11 as a critical gene for 10p15.3 microdeletion syndrome. | Q47950653 | ||
| 7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages | Q48246014 | ||
| Genome-wide mapping of global-to-local genetic effects on human facial shape. | Q49830752 | ||
| WSTF promotes proliferation and invasion of lung cancer cells by inducing EMT via PI3K/Akt and IL-6/STAT3 signaling pathways | Q51622540 | ||
| Semaphorin-3A guides radial migration of cortical neurons during development. | Q51970500 | ||
| Slug expression during organogenesis in mice | Q52109798 | ||
| High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development. | Q55154023 | ||
| Activity of Genes with Functions in Human Williams-Beuren Syndrome Is Impacted by Mobile Element Insertions in the Gray Wolf Genome. | Q55340147 | ||
| P4510 | describes a project that uses | ImageJ | Q1659584 |
| P433 | issue | 12 | |
| P921 | main subject | self-domestication | Q7448074 |
| P304 | page(s) | eaaw7908 | |
| P577 | publication date | 2019-12-04 | |
| P1433 | published in | Science Advances | Q19881044 |
| P1476 | title | Dosage analysis of the 7q11.23 Williams region identifies BAZ1B as a major human gene patterning the modern human face and underlying self-domestication | |
| P478 | volume | 5 |
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