embryonic lethality phenotype

Aliases

dying on embryonic day 10

Related entities (1)

Mentioned in (49)

Papers in which this entity is mentioned.

• Epsin Nanotherapy Regulates Cholesterol Transport to Fortify Atheroma Regression. (2023)
• Impact of alcohol exposure on neural development and network formation in human cortical organoids. (2023)
• Pathogenesis of Alcohol-Associated Fatty Liver: Lessons From Transgenic Mice. (2022)
• Transcriptomic analyses of gastrulation-stage mouse embryos with differential susceptibility to alcohol. (2021)
• Unveiling Complexity and Multipotentiality of Early Heart Fields. (2021)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• Modification of stem cell states by alcohol and acetaldehyde. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells. (2018)
• Knockdown of Mns1 Increases Susceptibility to Craniofacial Defects Following Gastrulation-Stage Alcohol Exposure in Mice. (2018)
• Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. (2018)
• One-Carbon Metabolism in Health and Disease. (2017)
• Alternative Polyadenylation Directs Tissue-Specific miRNA Targeting in Somatic Tissues. (2017)
• TGF-β Signaling Is Necessary and Sufficient for Pharyngeal Arch Artery Angioblast Formation. (2017)
• What is the DNA repair defect underlying Fanconi anemia? (2015)
• Lead exposure induces changes in 5-hydroxymethylcytosine clusters in CpG islands in human embryonic stem cells and umbilical cord blood. (2015)
• Mechanisms of retinoic acid signalling and its roles in organ and limb development. (2015)
• The role of BAF (mSWI/SNF) complexes in mammalian neural development. (2014)
• Pre-administration of G9a/GLP inhibitor during synaptogenesis prevents postnatal ethanol-induced LTP deficits and neurobehavioral abnormalities in adult mice. (2014)
• Alcohol modulates expression of DNA methyltranferases and methyl CpG-/CpG domain-binding proteins in murine embryonic fibroblasts. (2013)
• Prenatal ethanol exposure disrupts intraneocortical circuitry, cortical gene expression, and behavior in a mouse model of FASD. (2013)
• DNA methylation program in developing hippocampus and its alteration by alcohol. (2013)
• Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
• Zebrafish models of human liver development and disease. (2013)
• SOX2 hypomorphism disrupts development of the prechordal floor and optic cup. (2012)
• Mutations in Hedgehog acyltransferase (Hhat) perturb Hedgehog signaling, resulting in severe acrania-holoprosencephaly-agnathia craniofacial defects. (2012)
• BRCA1 and BRCA2: different roles in a common pathway of genome protection. (2011)
• Cranial neural crest cells on the move: their roles in craniofacial development. (2011)
• The role of DYRK1A in neurodegenerative diseases. (2011)
• Platelet-derived growth factor receptor beta is critical for zebrafish intersegmental vessel formation. (2010)
• The plausibility of maternal nutritional status being a contributing factor to the risk for fetal alcohol spectrum disorders: the potential influence of zinc status as an example. (2010)
• Forkhead box, class O transcription factors in brain: regulation and behavioral manifestation. (2009)
• The histone gene activator HINFP is a nonredundant cyclin E/CDK2 effector during early embryonic cell cycles. (2009)
• Fetal effects of psychoactive drugs. (2009)
• Sonic hedgehog ligand partners with caveolin-1 for intracellular transport. (2009)
• Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation. (2009)
• Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. (2009)
• DNA methylation and methyl-CpG binding proteins: developmental requirements and function. (2009)
• Regulation and function of Zip4, the acrodermatitis enteropathica gene. (2008)
• Neuregulin 1 in neural development, synaptic plasticity and schizophrenia. (2008)
• A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development. (2008)
• Repression of smoothened by patched-dependent (pro-)vitamin D3 secretion. (2006)
• Mutations within Sox2/SOX2 are associated with abnormalities in the hypothalamo-pituitary-gonadal axis in mice and humans. (2006)
• Distinct effectors of platelet-derived growth factor receptor-alpha signaling are required for cell survival during embryogenesis. (2005)
• Autoamplification of NFATc1 expression determines its essential role in bone homeostasis. (2005)
• Temporal perturbations in sonic hedgehog signaling elicit the spectrum of holoprosencephaly phenotypes. (2004)
• Evolutionary divergence of platelet-derived growth factor alpha receptor signaling mechanisms. (2003)
• Extreme hydrops fetalis and cardiovascular abnormalities in mice lacking a functional Adrenomedullin gene. (2001)
• Disruption of hyaluronan synthase-2 abrogates normal cardiac morphogenesis and hyaluronan-mediated transformation of epithelium to mesenchyme. (2000)

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