(Q28141267)

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H Ding

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A De Vriese

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S Plaisance

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S M van der Maarel

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G W Padberg

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R R Frants

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J E Hewitt

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D Collen

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A Belayew

Prediction of complete gene structures in human genomic DNA

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language of work or name

English

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publication date

5 August 1999

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published in

Gene

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volume

236

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issue

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page(s)

25-32

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cites work

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A comprehensive set of sequence analysis programs for the VAX

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Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy

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Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35

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Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis

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The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes

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Transcription from a TATA-less promoter requires a multisubunit TFIID complex

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FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

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The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.

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Yeast and human TATA-binding proteins have nearly identical DNA sequence requirements for transcription in vitro

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Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

10433963

1 reference

Consolidated OpenCitations Corpus – April 2017