(Q22010266)

English

The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23

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The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23 (English)

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GOA release 2020-03-11

visual perception

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GOA release 2020-03-11

Bardet-Biedl syndrome

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author name string

S W Gorman

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S W

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Gorman

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PubMed publication ID

7 February 2023

N B Haider

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N B

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Haider

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PubMed publication ID

7 February 2023

U Grieshammer

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U

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Grieshammer

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PubMed publication ID

7 February 2023

R E Swiderski

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R E

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Swiderski

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PubMed publication ID

7 February 2023

E Kim

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E

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Kim

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PubMed publication ID

7 February 2023

J W Welch

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J W

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Welch

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PubMed publication ID

7 February 2023

C Searby

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C

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Searby

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PubMed publication ID

7 February 2023

S Leng

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S

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Leng

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PubMed publication ID

7 February 2023

R Carmi

9

author given names

R

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Carmi

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PubMed publication ID

7 February 2023

V C Sheffield

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author given names

V C

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Sheffield

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PubMed publication ID

7 February 2023

D M Duhl

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author given names

D M

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Duhl

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PubMed publication ID

7 February 2023

language of work or name

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publication date

15 July 1999

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59

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2

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150-60

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Bardet-Biedl syndrome and related disorders

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https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

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inferred from DOI database lookup

Cardiac abnormalities in the Bardet-Biedl syndrome: echocardiographic studies of 22 patients

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome loci.

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https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

A novel type of myosin implicated in signalling by rho family GTPases

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

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

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Maps from two interspecific backcross DNA panels available as a community genetic mapping resource

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Fast and sensitive silver staining of DNA in polyacrylamide gels

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Unconventional myosins

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Requirement for LIM homeobox gene Isl1 in motor neuron generation reveals a motor neuron-dependent step in interneuron differentiation

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for Usher syndrome type I (USH1A) maps to chromosome 14q

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Myosins on the move to signal transduction

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel myosin heavy chain encoded by murine dilute coat colour locus

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Defective myosin VIIA gene responsible for Usher syndrome type 1B

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

The Spectrum of Renal Disease in Laurence–Moon–Biedl Syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification and overlapping expression of multiple unconventional myosin genes in vertebrate cell types

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Adherence to the first-AUG rule when a second AUG codon follows closely upon the first

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of a Bardet-Biedl syndrome locus on chromosome 3 and evaluation of an efficient approach to homozygosity mapping

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of a DNA pooling strategy to identify a human obesity syndrome locus on chromosome 15

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Ocular findings in the Laurence-Moon-Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Function of myosin-V in filopodial extension of neuronal growth cones

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Three-dimensional structure of myosin subfragment-1: a molecular motor

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Intrafamilial variation of the phenotype in Bardet-Biedl syndrome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Bardet-Biedl syndrome: a molecular and phenotypic study of 18 families

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Unconventional Myosins

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1999.5867

7 January 2021

based on heuristic

inferred from DOI database lookup

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