(Q28141267)

2

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H Ding

3

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A De Vriese

4

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S Plaisance

5

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S M van der Maarel

6

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G W Padberg

7

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R R Frants

8

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J E Hewitt

9

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D Collen

10

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A Belayew

Prediction of complete gene structures in human genomic DNA

11

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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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page(s)

25-32

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issue

1

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cites work

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A comprehensive set of sequence analysis programs for the VAX

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CpG islands in vertebrate genomes

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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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An alternative promoter in the mouse major histocompatibility complex class II I-Abeta gene: implications for the origin of CpG islands

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

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Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy

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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

2577394

2577394

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference