Pages that link to "Q34400476"
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The following pages link to Contribution of VANGL2 mutations to isolated neural tube defects (Q34400476):
Displaying 49 items.
- 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)
- Planar cell polarity signaling pathway in congenital heart diseases (Q26861173) (← links)
- Comparison of phenotypes between different vangl2 mutants demonstrates dominant effects of the Looptail mutation during hair cell development (Q27308779) (← links)
- Frizzled Receptors in Development and Disease (Q28071320) (← 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)
- PTK7 regulates myosin II activity to orient planar polarity in the mammalian auditory epithelium (Q30418906) (← 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)
- Detection of copy number variants reveals association of cilia genes with neural tube defects (Q34563191) (← links)
- Mutations in planar cell polarity gene SCRIB are associated with spina bifida (Q34902377) (← links)
- The roles of maternal Vangl2 and aPKC inXenopusoocyte and embryo patterning (Q35176660) (← links)
- Roles of planar cell polarity pathways in the development of neural [correction of neutral] tube defects (Q35218565) (← links)
- Planar cell polarity gene expression correlates with tumor cell viability and prognostic outcome in neuroblastoma (Q35976974) (← links)
- FZD6is a novel gene for human neural tube defects (Q36352681) (← 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)
- Van-Gogh-like 2 antagonises the canonical WNT pathway and is methylated in colorectal cancers (Q36889627) (← links)
- Planar Cell Polarity (PCP) Protein Vangl2 Regulates Ectoplasmic Specialization Dynamics via Its Effects on Actin Microfilaments in the Testes of Male Rats (Q36911532) (← links)
- SEC14 and spectrin domains 1 (Sestd1) and Dapper antagonist of catenin 1 (Dact1) scaffold proteins cooperatively regulate the Van Gogh-like 2 (Vangl2) four-pass transmembrane protein and planar cell polarity (PCP) pathway during embryonic developmen (Q37012349) (← 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)
- Alternative Wnt pathways and receptors (Q38039332) (← links)
- Wnt signaling in vertebrate neural development and function (Q38046770) (← 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 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)
- Prickle1 stunts limb growth through alteration of cell polarity and gene expression (Q38728039) (← links)
- Claudins are essential for cell shape changes and convergent extension movements during neural tube closure (Q38763085) (← links)
- Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. (Q38774722) (← links)
- Neurodevelopmental Perspectives on Wnt Signaling in Psychiatry (Q38917986) (← 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)
- Role of the planar cell polarity gene Protein tyrosine kinase 7 in neural tube defects in humans (Q40541258) (← 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)
- Mutations in the COPII vesicle component gene SEC24B are associated with human neural tube defects (Q47766184) (← links)
- Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young mice. (Q49789426) (← links)
- Regulation of spermatid polarity by the actin- and microtubule (MT)-based cytoskeletons (Q50150051) (← links)
- The planar cell polarity protein Vangl2 is required for retinal axon guidance. (Q50586276) (← links)
- Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos. (Q51733362) (← links)
- Genomic approaches to the assessment of human spina bifida risk. (Q54908931) (← links)
- Variants identified in PTK7 associated with neural tube defects (Q64229545) (← links)
- Polymorphisms in FZD3 and FZD6 genes and risk of neural tube defects in a northern Han Chinese population (Q87851392) (← links)
- Update on the Role of the Non-Canonical Wnt/Planar Cell Polarity Pathway in Neural Tube Defects (Q90567115) (← links)
- Mutations associated with human neural tube defects display disrupted planar cell polarity in Drosophila (Q90797904) (← links)
- Functional Validation of CLDN Variants Identified in a Neural Tube Defect Cohort Demonstrates Their Contribution to Neural Tube Defects (Q98224394) (← links)