Pages that link to "Q28143612"
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The following pages link to Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus (Q28143612):
Displaying 50 items.
- Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice (Q21092155) (← links)
- A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice (Q24529109) (← links)
- The role of connexins in ear and skin physiology - functional insights from disease-associated mutations (Q26827294) (← links)
- Cellular and Deafness Mechanisms Underlying Connexin Mutation-Induced Hearing Loss - A Common Hereditary Deafness (Q27009501) (← links)
- autosomal dominant nonsyndromic deafness 3B (Q28024693) (← links)
- The unique electrical properties in an extracellular fluid of the mammalian cochlea; their functional roles, homeostatic processes, and pathological significance. (Q28076301) (← links)
- Mutations in GJB6 cause hidrotic ectodermal dysplasia (Q28140272) (← links)
- A mutation in the connexin 30 gene in Chinese Han patients with hidrotic ectodermal dysplasia (Q28176979) (← links)
- K cycling and the endocochlear potential (Q28198160) (← links)
- Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells (Q28206633) (← links)
- A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect? (Q28207515) (← links)
- Functional studies of human skin disease- and deafness-associated connexin 30 mutations (Q28213840) (← links)
- Expression of a connexin31 mutation causing erythrokeratodermia variabilis is lethal for HeLa cells (Q28217685) (← links)
- Gap junctions and cochlear homeostasis (Q28245955) (← links)
- Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea (Q28254582) (← links)
- Hearing is normal without connexin30 (Q28283001) (← links)
- Purinergic control of intercellular communication between Hensen's cells of the guinea-pig cochlea (Q28360316) (← links)
- Connexin29 is highly expressed in cochlear Schwann cells, and it is required for the normal development and function of the auditory nerve of mice (Q28511260) (← links)
- Targeted disruption of otog results in deafness and severe imbalance (Q28592378) (← links)
- The human deafness-associated connexin 30 T5M mutation causes mild hearing loss and reduces biochemical coupling among cochlear non-sensory cells in knock-in mice (Q28748215) (← links)
- Finding new genes for non-syndromic hearing loss through an in silico prioritization study (Q28749118) (← links)
- A study of deafness-related genetic mutations as a basis for strategies to prevent hereditary hearing loss in Hebei, China (Q30403140) (← links)
- A de novo 2.9 Mb interstitial deletion at 13q12.11 in a child with developmental delay accompanied by mild dysmorphic characteristics (Q30423021) (← links)
- Connexons and pannexons: newcomers in neurophysiology (Q30425814) (← links)
- Genetics of hearing loss: focus on DFNA2. (Q30453431) (← links)
- Calcium signaling in the cochlea - Molecular mechanisms and physiopathological implications. (Q30465350) (← links)
- BAAV mediated GJB2 gene transfer restores gap junction coupling in cochlear organotypic cultures from deaf Cx26Sox10Cre mice (Q30474429) (← links)
- Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness (Q30478884) (← links)
- Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis (Q30479250) (← links)
- Function and expression pattern of nonsyndromic deafness genes (Q30482629) (← links)
- Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China (Q30486353) (← links)
- Gap-junction channels dysfunction in deafness and hearing loss (Q30490087) (← links)
- At the speed of sound: gene discovery in the auditory system (Q30502974) (← links)
- Mouse otocyst transuterine gene transfer restores hearing in mice with connexin 30 deletion-associated hearing loss. (Q30540472) (← links)
- Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound (Q30543886) (← links)
- Advances in hereditary deafness (Q30665416) (← links)
- Expression of members of Wnt and Frizzled gene families in the postnatal rat cochlea (Q30717081) (← links)
- Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1. (Q30896514) (← links)
- Pannexins are new molecular candidates for assembling gap junctions in the cochlea (Q31171198) (← links)
- Human hereditary hearing impairment: mouse models can help to solve the puzzle (Q33346003) (← links)
- Science, medicine, and the future: New interventions in hearing impairment (Q33800062) (← links)
- Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study (Q33905363) (← links)
- Longitudinal gradients of KCNQ4 expression in spiral ganglion and cochlear hair cells correlate with progressive hearing loss in DFNA2. (Q33922424) (← links)
- Neurological diseases caused by ion-channel mutations (Q33941556) (← links)
- A Novel Missense Mutation in the Connexin30 Causes Nonsyndromic Hearing Loss (Q33952479) (← links)
- Modifier genes of hereditary hearing loss (Q34029118) (← links)
- Ionizing radiation and genetic risks. XII. The concept of "potential recoverability correction factor" (PRCF) and its use for predicting the risk of radiation-inducible genetic disease in human live births (Q34056666) (← links)
- Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions (Q34084948) (← links)
- Ectodermal dysplasias: a new clinical-genetic classification (Q34090412) (← links)
- Prospective variants screening of connexin genes in children with hearing impairment: genotype/phenotype correlation (Q34123564) (← links)