(Q40451838)

20 September 2017

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization. (English)

1 reference

20 September 2017

Blonden LA

1

1 reference

20 September 2017

den Dunnen JT

2

1 reference

20 September 2017

van Paassen HM

3

1 reference

20 September 2017

Wapenaar MC

4

1 reference

20 September 2017

Grootscholten PM

5

1 reference

20 September 2017

Ginjaar HB

6

1 reference

20 September 2017

Bakker E

7

1 reference

20 September 2017

Pearson PL

8

1 reference

20 September 2017

van Ommen GJ

9

1 reference

20 September 2017

language of work or name

1 reference

1 July 1989

1 reference

20 September 2017

Nucleic Acids Research

1 reference

20 September 2017

17

1 reference

20 September 2017

14

1 reference

20 September 2017

5611-5621

1 reference

Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention

20 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Double cos site vectors: simplified cosmid cloning.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Removal of repeated sequences from hybridisation probes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

A highly polymorphic locus in human DNA revealed by cosmid-derived probes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Mike, a chimeric filamentous phage designed for the separate production of either DNA strand of pKUN vector plasmids by F+ cells.

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresis

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Duchenne muscular dystrophy gene product is not identical in muscle and brain.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Duchenne muscular dystrophy gene expression in normal and diseased human muscle

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Acceleration of nucleic acid hybridization rate by polyethylene glycol

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=318183

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels

17 June 2018

1 reference

12 December 2020

Characterization of dystrophin in muscle-biopsy specimens from patients with Duchenne's or Becker's muscular dystrophy

1 reference

12 December 2020

Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA

1 reference

12 December 2020

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene

1 reference

12 December 2020

A deletion hot spot in the Duchenne muscular dystrophy gene

1 reference

12 December 2020

Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies

1 reference

12 December 2020

Identifiers

DOI

10.1093/NAR/17.14.5611

1 reference

20 September 2017

1 reference

20 September 2017

PubMed publication ID

2569720

1 reference