Pages that link to "Q28209898"

The following pages link to Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28 (Q28209898):

Displaying 44 items.

• Mutations in GRHL2 result in an autosomal-recessive ectodermal Dysplasia syndrome (Q24302372) (← links)
• Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human. (Q24629226) (← links)
• A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss (Q24670142) (← links)
• Genetics of vestibular disorders: pathophysiological insights (Q26753131) (← links)
• Genetics of Nonsyndromic Congenital Hearing Loss (Q26753842) (← links)
• autosomal dominant nonsyndromic deafness 28 (Q28024685) (← links)
• (Q28176761) (redirect page) (← links)
• Grainyhead-like 2 regulates neural tube closure and adhesion molecule expression during neural fold fusion (Q28511638) (← links)
• The transcription factors Grainyhead-like 2 and NK2-homeobox 1 form a regulatory loop that coordinates lung epithelial cell morphogenesis and differentiation (Q28586709) (← links)
• Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse (Q28594231) (← links)
• Finding new genes for non-syndromic hearing loss through an in silico prioritization study (Q28749118) (← links)
• Association between genetic variations in GRHL2 and noise-induced hearing loss in Chinese high intensity noise exposed workers: a case-control analysis (Q30426446) (← links)
• Alleles that modulate late life hearing in genetically heterogeneous mice (Q30451621) (← links)
• Inheritance patterns of progressive hearing loss in laboratory strains of mice (Q30488782) (← links)
• Progress and prospects in human genetic research into age-related hearing impairment (Q34033991) (← links)
• A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1. (Q34366946) (← links)
• Phosphorylation of Grainy head by ERK is essential for wound-dependent regeneration but not for development of an epidermal barrier (Q34490793) (← links)
• Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss (Q35187716) (← links)
• Human Nonsyndromic Sensorineural Deafness (Q35550640) (← links)
• Lineage-specific and ubiquitous biological roles of the mammalian transcription factor LSF (Q35962753) (← links)
• Associations of genetic variations in EYA4, GRHL2 and DFNA5 with noise-induced hearing loss in Chinese population: a case- control study (Q36088920) (← links)
• Comprehensive Genetic Analysis of Japanese Autosomal Dominant Sensorineural Hearing Loss Patients (Q36211885) (← links)
• Grhl2 is required in nonneural tissues for neural progenitor survival and forebrain development (Q36464102) (← links)
• Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea. (Q36621165) (← links)
• Genetic Variation in POU4F3 and GRHL2 Associated with Noise-Induced Hearing Loss in Chinese Population: A Case-Control Study (Q37044745) (← links)
• USH1H, a novel locus for type I Usher syndrome, maps to chromosome 15q22-23. (Q37170113) (← links)
• Environmental and genetic factors in age-related hearing impairment (Q37866018) (← links)
• Molecular genetic epidemiology of age-related hearing impairment (Q37878038) (← links)
• Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness (Q38393019) (← links)
• Grainyhead-like Transcription Factors in Craniofacial Development. (Q38684025) (← links)
• A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family (Q38902635) (← links)
• Expression and role of grainyhead-like 2 in gastric cancer (Q39091704) (← links)
• Grainyhead-like 2 in development and cancer (Q39275026) (← links)
• Alternative splicing and start sites: Lessons from the Grainyhead-like family. (Q39384017) (← links)
• A microdeletion in the GRHL2 Gene in two unrelated patients with congenital fibrosis of the extra ocular muscles (Q45420195) (← links)
• Grhl2 deficiency impairs otic development and hearing ability in a zebrafish model of the progressive dominant hearing loss DFNA28. (Q47073283) (← links)
• Grainyhead-like 3 (Grhl3) deficiency in brain leads to altered locomotor activity and decreased anxiety-like behaviors in aged mice (Q48410341) (← links)
• Age-Related Hearing Impairment Associated NAT2, GRM7, GRHL2 Susceptibility Gene Polymorphisms and Haplotypes in Roma and Hungarian Populations (Q49891657) (← links)
• The grainyhead-like 2 gene (GRHL2) single nucleotide polymorphism is not associated with age-related hearing impairment in Han Chinese. (Q50434075) (← links)
• Confirmation of GRHL2 as the gene for the DFNA28 locus. (Q54253156) (← links)
• Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness (Q89671520) (← links)
• Gene therapy development in hearing research in China (Q97587562) (← links)
• Spotlight on the Granules (Grainyhead-Like Proteins) - From an Evolutionary Conserved Controller of Epithelial Trait to Pioneering the Chromatin Landscape (Q99712241) (← links)
• Synergistic effect of smoking on age-related hearing loss in patients with diabetes (Q101216898) (← links)