(Q22009151)

GOA release 2020-03-11

membrane fusion

1 reference

GOA release 2020-03-11

1 reference

M Cohen-Salmon

3

Martine

Cohen-Salmon

1 reference

12 September 2022

C Petit

9

Christine

Petit

1 reference

12 September 2022

M Grati

2

M'hamed

Grati

1 reference

12 September 2022

S Yasunaga

1

Shin'ichiro

Yasunaga

1 reference

12 September 2022

A El-Amraoui

4

Aziz

El-Amraoui

1 reference

12 September 2022

M Mustapha

5

Mirna

Mustapha

1 reference

12 September 2022

N Salem

6

Nabiha

Salem

1 reference

12 September 2022

E El-Zir

7

Elie

El-Zir

1 reference

12 September 2022

J Loiselet

8

Jacques

Loiselet

1 reference

Genes responsible for human hereditary deafness: symphony of a thousand

12 September 2022

language of work or name

English

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publication date

April 1999

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published in

Nature Genetics

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volume

21

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page(s)

363-9

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issue

4

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cites work

1 reference

7 January 2021

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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7 January 2021

Mutations in the myosin VIIA gene cause non-syndromic recessive deafness

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7 January 2021

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

1 reference

7 January 2021

Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

1 reference

7 January 2021

A mutation in PDS causes non-syndromic recessive deafness

1 reference

7 January 2021

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

1 reference

7 January 2021

Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.

1 reference

7 January 2021

Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene

1 reference

7 January 2021

Connexin 26 gene linked to a dominant deafness.

1 reference

7 January 2021

Otogelin: a glycoprotein specific to the acellular membranes of the inner ear

1 reference

7 January 2021

Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals

1 reference

7 January 2021

A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22-23

1 reference

7 January 2021

Interpreting cDNA sequences: some insights from studies on translation

1 reference

7 January 2021

A second middle eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9.

1 reference

7 January 2021

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

1 reference

7 January 2021

1 reference

7 January 2021

Structure of the first C2 domain of synaptotagmin I: a novel Ca2+/phospholipid-binding fold

1 reference

7 January 2021

C2-domains, structure and function of a universal Ca2+-binding domain

1 reference

7 January 2021

Identification of a synaptic vesicle-specific membrane protein with a wide distribution in neuronal and neurosecretory tissue

1 reference

7 January 2021

Phospholipid binding by a synaptic vesicle protein homologous to the regulatory region of protein kinase C

1 reference

7 January 2021

A novel arachidonic acid-selective cytosolic PLA2 contains a Ca(2+)-dependent translocation domain with homology to PKC and GAP

1 reference

7 January 2021

Rabphilin-3A, a putative target protein for smg p25A/rab3A p25 small GTP-binding protein related to synaptotagmin

1 reference

7 January 2021

Synaptic targeting of rabphilin-3A, a synaptic vesicle Ca2+/phospholipid-binding protein, depends on rab3A/3C

1 reference

7 January 2021

Mammalian homologues of Caenorhabditis elegans unc-13 gene define novel family of C2-domain proteins

1 reference

7 January 2021

DOC2 proteins in rat brain: complementary distribution and proposed function as vesicular adapter proteins in early stages of secretion

1 reference

7 January 2021

Rim is a putative Rab3 effector in regulating synaptic-vesicle fusion

1 reference

7 January 2021

Synaptotagmin-syntaxin interaction: the C2 domain as a Ca2+-dependent electrostatic switch

1 reference

7 January 2021

SNARE complex at the ribbon synapses of cochlear hair cells: analysis of synaptic vesicle- and synaptic membrane-associated proteins

1 reference

7 January 2021

Calcium-triggered exocytosis and endocytosis in an isolated presynaptic cell: capacitance measurements in saccular hair cells

1 reference

7 January 2021

Ca(2+)-dependent and -independent activities of neural and non-neural synaptotagmins

1 reference

7 January 2021

Synaptotagmins: C2-domain proteins that regulate membrane traffic

1 reference

7 January 2021

Hear come more genes!

1 reference

7 January 2021

The fundamental and medical impacts of recent progress in research on hereditary hearing loss.

1 reference

7 January 2021

Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development

1 reference

7 January 2021

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans

1 reference

7 January 2021

Evidence for a medial K+ recycling pathway from inner hair cells.

1 reference

7 January 2021

Inner ear defects induced by null mutation of the isk gene

1 reference

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

7 January 2021

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

7 January 2021

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

1 reference

7 January 2021

The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system

1 reference

7 January 2021

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1 reference

7 January 2021

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells

1 reference

7 January 2021

Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cells

1 reference

7 January 2021

A single protocol to detect transcripts of various types and expression levels in neural tissue and cultured cells: in situ hybridization using digoxigenin-labelled cRNA probes

1 reference

7 January 2021

Identifiers

DOI

10.1038/7693

1 reference

Consolidated OpenCitations Corpus – April 2017

2528470

release_kqwy4hd3kjhernkbgfvjnn5wke

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Fatcat ID

0 references

2528470

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference