Pages that link to "Q33912301"
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The following pages link to Novel mutations in VANGL1 in neural tube defects (Q33912301):
Displaying 50 items.
- Genetics of human neural tube defects (Q22337140) (← links)
- Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis (Q24297844) (← links)
- Mutations in the planar cell polarity gene, Fuzzy, are associated with neural tube defects in humans (Q24322638) (← links)
- Identification and characterization of novel rare mutations in the planar cell polarity gene PRICKLE1 in human neural tube defects (Q24337438) (← links)
- Comparison of phenotypes between different vangl2 mutants demonstrates dominant effects of the Looptail mutation during hair cell development (Q27308779) (← links)
- Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans (Q27321031) (← links)
- Frizzled Receptors in Development and Disease (Q28071320) (← links)
- Frizzled 1 and frizzled 2 genes function in palate, ventricular septum and neural tube closure: general implications for tissue fusion processes (Q28586361) (← links)
- The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation (Q28586682) (← links)
- Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse (Q29144926) (← links)
- Rare missense variants in DVL1, one of the human counterparts of the Drosophila dishevelled gene, do not confer increased risk for neural tube defects. (Q30351950) (← links)
- Is LMNB1 a susceptibility gene for neural tube defects in humans? (Q30431444) (← links)
- Folate deficiency facilitates recruitment of upstream binding factor to hot spots of DNA double-strand breaks of rRNA genes and promotes its transcription (Q33558438) (← links)
- Neural tube defects: recent advances, unsolved questions, and controversies (Q33620909) (← links)
- Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice (Q34241126) (← links)
- Contribution of VANGL2 mutations to isolated neural tube defects (Q34400476) (← links)
- Missing genetic risk in neural tube defects: can exome sequencing yield an insight? (Q34429995) (← links)
- Detection of copy number variants reveals association of cilia genes with neural tube defects (Q34563191) (← links)
- Wnt signaling gradients establish planar cell polarity by inducing Vangl2 phosphorylation through Ror2 (Q34706774) (← links)
- Epigenetic profiles in children with a neural tube defect; a case-control study in two populations (Q35040928) (← links)
- The roles of maternal Vangl2 and aPKC in Xenopus oocyte and embryo patterning (Q35176660) (← links)
- Roles of planar cell polarity pathways in the development of neural [correction of neutral] tube defects (Q35218565) (← links)
- Neural tube defects: from a proteomic standpoint (Q35237613) (← links)
- Planar cell polarity in Drosophila (Q35624641) (← links)
- FZD6 is a novel gene for human neural tube defects (Q36352681) (← links)
- Wnt-Frizzled/planar cell polarity signaling: cellular orientation by facing the wind (Wnt) (Q36358270) (← links)
- Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects (Q36407760) (← links)
- Novel VANGL1 Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube Defects (Q36526064) (← links)
- Genetic analysis of disheveled 2 and disheveled 3 in human neural tube defects (Q36592686) (← links)
- A novel hypomorphic Looptail allele at the planar cell polarity Vangl2 gene (Q36670765) (← links)
- Single-Nucleotide Polymorphisms, Acute Rejection, and Severity of Tubulitis in Kidney Transplantation, Accounting for Center-to-Center Variation (Q36676420) (← links)
- Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans (Q37668913) (← links)
- Planar Cell Polarity Signaling in the Drosophila Eye (Q37801483) (← links)
- Human neural tube defects: genetic causes and prevention (Q37889823) (← links)
- Wnt signaling in mammalian development: lessons from mouse genetics (Q38006924) (← links)
- Mouse as a model for multifactorial inheritance of neural tube defects (Q38018292) (← links)
- A consideration of the evidence that genetic defects in planar cell polarity contribute to the etiology of human neural tube defects (Q38048237) (← links)
- Planar cell polarity signaling: coordination of cellular orientation across tissues (Q38052130) (← links)
- Planar cell polarity signaling in collective cell movements during morphogenesis and disease (Q38111369) (← links)
- Genetic evidence in planar cell polarity signaling pathway in human neural tube defects (Q38168793) (← links)
- Expanding the mutational spectrum associated to neural tube defects: literature revision and description of novel VANGL1 mutations. (Q38248134) (← links)
- The intracellular carboxyl terminal domain of Vangl proteins contains plasma membrane targeting signals (Q38570344) (← links)
- Frizzled 2 and frizzled 7 function redundantly in convergent extension and closure of the ventricular septum and palate: evidence for a network of interacting genes (Q39253940) (← links)
- Non-canonical WNT/PCP signalling in cancer: Fzd6 takes centre stage. (Q39454318) (← links)
- Patterning skin by planar cell polarity: the multi-talented hair designer (Q40375592) (← links)
- Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation (Q42502729) (← links)
- Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis (Q42638040) (← links)
- Identification and characterization of a novel chemically induced allele at the planar cell polarity gene Vangl2. (Q47611555) (← links)
- Wnt-induced Vangl2 phosphorylation is dose-dependently required for planar cell polarity in mammalian development. (Q47619354) (← links)
- Mutations in the COPII vesicle component gene SEC24B are associated with human neural tube defects (Q47766184) (← links)