(Q34360936)

1 August 2017

title

Cloning and characterization of a splice variant of human Bardet-Biedl syndrome 4 gene (BBS4). (English)

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1 August 2017

main subject

Bardet-Biedl syndrome

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based on heuristic

inferred from title

Bardet-Biedl syndrome 4

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Xin Ye

1

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1 August 2017

Jianliang Dai

2

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1 August 2017

Weiqun Fang

3

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1 August 2017

Wei Jin

4

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1 August 2017

Yi Guo

5

1 reference

1 August 2017

Jiaping Song

6

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1 August 2017

Chaoneng Ji

7

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1 August 2017

Shaohua Gu

8

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1 August 2017

Yi Xie

9

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1 August 2017

Yumin Mao

10

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1 August 2017

publication date

1 June 2004

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1 August 2017

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1 August 2017

volume

15

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1 August 2017

issue

3

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1 August 2017

page(s)

213-218

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

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

Alu repeats and human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

SPINDLY, a tetratricopeptide repeat protein involved in gibberellin signal transduction in Arabidopsis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

O-Linked GlcNAc transferase is a conserved nucleocytoplasmic protein containing tetratricopeptide repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

The glucocorticoid attenuated response genes GARG-16, GARG-39, and GARG-49/IRG2 encode inducible proteins containing multiple tetratricopeptide repeat domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

Isolation and characterization of a human putative receptor protein kinase cDNA STYK1

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F10425170410001679165

10.1080/10425170410001679165

21 January 2018

Identifiers

DOI

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1 August 2017

1 reference