Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1) (Q28138049)

inferred from title

Bardet-Biedl syndrome 1

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N B Haider

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C Searby

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E Galperin

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L Mintz

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M Horowitz

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E M Stone

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V C Sheffield

Fast and sensitive silver staining of DNA in polyacrylamide gels

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language of work or name

English

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publication date

15 November 1999

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published in

Gene

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volume

240

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issue

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page(s)

227-32

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cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2899%2900395-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2899%2900395-9

7 January 2021

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/10.1016%2FS0378-1119%2899%2900395-9

7 January 2021

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

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7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0378-1119%2899%2900395-9

7 January 2021

Developmental selection of var gene expression in Plasmodium falciparum

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7 January 2021

EH: a novel protein-protein interaction domain potentially involved in intracellular sorting

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7 January 2021

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

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7 January 2021

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

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7 January 2021

A Transcript Map for the 2.8-Mb Region Containing the Multiple Endocrine Neoplasia Type 1 Locus

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7 January 2021

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

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7 January 2021

The human forkhead protein FREAC-2 contains two functionally redundant activation domains and interacts with TBP and TFIIB

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2899%2900395-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2899%2900395-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0378-1119%2899%2900395-9

7 January 2021

EHD1--an EH-domain-containing protein with a specific expression pattern

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7 January 2021

The novel ATM-related protein TRRAP is an essential cofactor for the c-Myc and E2F oncoproteins

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7 January 2021

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

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7 January 2021

Intrafamilial variation of the phenotype in Bardet-Biedl syndrome

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7 January 2021

Bardet-Biedl syndrome and related disorders

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7 January 2021

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

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7 January 2021

A method for constructing radiation hybrid maps of whole genomes

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7 January 2021

Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.

1 reference

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7 January 2021