Pages that link to "Q24301501"

The following pages link to Multiple mutations of MYO1A, a cochlear-expressed gene, in sensorineural hearing loss (Q24301501):

Displaying 47 items.

• Myosin IA (Q21120913) (← links)
• An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss (Q24296636) (← links)
• Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4) (Q24533372) (← links)
• Dynamic length regulation of sensory stereocilia (Q24646242) (← links)
• Genetics of Nonsyndromic Congenital Hearing Loss (Q26753842) (← links)
• The myosin superfamily at a glance. (Q27011868) (← links)
• A Myo7a mutation cosegregates with stereocilia defects and low-frequency hearing impairment (Q28508053) (← links)
• Myosin-1a is critical for normal brush border structure and composition (Q28512472) (← links)
• Mice deficient for the type II transmembrane serine protease, TMPRSS1/hepsin, exhibit profound hearing loss (Q28590867) (← links)
• Finding new genes for non-syndromic hearing loss through an in silico prioritization study (Q28749118) (← links)
• The effect of novel mutations on the structure and enzymatic activity of unconventional myosins associated with autosomal dominant non-syndromic hearing loss. (Q30365318) (← links)
• Filling the silent void: genetic therapies for hearing impairment (Q30459235) (← links)
• Myosin-1a powers the sliding of apical membrane along microvillar actin bundles. (Q30480441) (← links)
• Function and expression pattern of nonsyndromic deafness genes (Q30482629) (← links)
• A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice (Q30490758) (← links)
• Myosin VI and VIIa distribution among inner ear epithelia in diverse fishes (Q30497077) (← links)
• Targeted and genomewide NGS data disqualify mutations in MYO1A, the "DFNA48 gene", as a cause of deafness (Q30774855) (← links)
• Predicting candidate genes for human deafness disorders: a bioinformatics approach (Q33251025) (← links)
• Deafness mutation mining using regular expression based pattern matching (Q33303929) (← links)
• Human hereditary hearing impairment: mouse models can help to solve the puzzle (Q33346003) (← links)
• Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing (Q33620800) (← links)
• The mapping of DFNB62, a new locus for autosomal recessive non-syndromic hearing impairment, to chromosome 12p13.2-p11.23 (Q34016266) (← links)
• Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations. (Q34675175) (← links)
• A hearing loss-associated myo1c mutation (R156W) decreases the myosin duty ratio and force sensitivity (Q34687221) (← links)
• Myosin motor function: the ins and outs of actin-based membrane protrusions. (Q34985570) (← links)
• Class I myosins have overlapping and specialized functions in left-right asymmetric development in Drosophila. (Q35342729) (← links)
• The genetic bases for syndromic and nonsyndromic deafness among Jews (Q35578676) (← links)
• Analysis of Low Frequency Protein Truncating Stop-Codon Variants and Fasting Concentration of Growth Hormone (Q35667413) (← links)
• Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing (Q36107256) (← links)
• Human deafness mutation E385D disrupts the mechanochemical coupling and subcellular targeting of myosin-1a (Q36303191) (← links)
• Identification of candidate regions for a novel Usher syndrome type II locus (Q36881902) (← links)
• In search of the DFNA11 myosin VIIA low- and mid-frequency auditory genetic modifier (Q37110827) (← links)
• Myosin-I molecular motors at a glance (Q37120373) (← links)
• Disruption of the ATE1 and SLC12A1 Genes by Balanced Translocation in a Boy with Non-Syndromic Hearing Loss. (Q37573604) (← links)
• Endocytosis and signaling: cell logistics shape the eukaryotic cell plan (Q37980726) (← links)
• Non-syndromic hereditary sensorineural hearing loss: review of the genes involved (Q38178411) (← links)
• New treatment options for hearing loss. (Q38384722) (← links)
• Improving hearing loss gene testing: a systematic review of gene evidence toward more efficient next-generation sequencing-based diagnostic testing and interpretation. (Q38631746) (← links)
• Unresolved questions regarding human hereditary deafness (Q38853306) (← links)
• A genotypic ascertainment approach to refute the association of MYO1A variants with non-syndromic deafness (Q39272235) (← links)
• Localization in stereocilia, plasma membrane, and mitochondria suggests diverse roles for NMHC-IIa within cochlear hair cells (Q42576575) (← links)
• Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss (Q47199341) (← links)
• Effects of human deafness gamma-actin mutations (DFNA20/26) on actin function (Q50464854) (← links)
• DFNB48, a new nonsyndromic recessive deafness locus, maps to chromosome 15q23-q25.1. (Q50474830) (← links)
• Site-Specific Evolutionary Rate Inference: Taking Phylogenetic Uncertainty into Account (Q56879928) (← links)
• The progression of the ClinGen gene clinical validity classification over time (Q57455599) (← links)
• Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome (Q57980301) (← links)