(Q49045449)

18 February 2018

title

Genomic structure of the human unconventional myosin VI gene. (English)

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18 February 2018

author

Nadav Ahituv

1

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18 February 2018

author name string

Sobe T

2

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18 February 2018

Robertson NG

3

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18 February 2018

Morton CC

4

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18 February 2018

Taggart RT

5

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18 February 2018

Avraham KB

6

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18 February 2018

language of work or name

English

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publication date

1 December 2000

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18 February 2018

published in

Gene

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18 February 2018

volume

261

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18 February 2018

issue

2

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18 February 2018

page(s)

269-275

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18 February 2018

Vectorette PCR: a novel approach to genomic walking

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7 January 2021

The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

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7 January 2021

Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice

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7 January 2021

The localization of myosin VI at the golgi complex and leading edge of fibroblasts and its phosphorylation and recruitment into membrane ruffles of A431 cells after growth factor stimulation

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Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

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Connexin 26 gene linked to a dominant deafness

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Unconventional myosins and the genetics of hearing loss

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Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice

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Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).

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A type VII myosin encoded by the mouse deafness gene shaker-1

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Unconventional myosins in inner-ear sensory epithelia

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Characterization of isoform diversity in smooth muscle myosin heavy chains

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Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene

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Nonsyndromic deafness DFNA1 associated with mutation of a human homolog of the Drosophila gene diaphanous

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7 January 2021

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Unconventional Myosins

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Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

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A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

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7 January 2021

Role of myosin VI in the differentiation of cochlear hair cells

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7 January 2021

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

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Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome

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

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7 January 2021

Defective myosin VIIA gene responsible for Usher syndrome type 1B

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7 January 2021

Myosin VI is an actin-based motor that moves backwards

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7 January 2021

10.1016/S0378-1119(00)00535-7

Identifiers

DOI

1 reference

18 February 2018

1 reference

18 February 2018