(Q33194576)

English

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

scientific article published on November 5, 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Duchenne muscular dystrophy

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

genetic polymorphism

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14600829

29 March 2024

1 reference

10.1007/S00439-003-1041-2

https://api.crossref.org/works/10.1007/S00439-003-1041-2

29 March 2024

Marco Sifringer

1

object named as

Marco Sifringer

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

7

object named as

Ina Koch

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14600829

29 March 2024

author name string

Birgit Uhlenberg

2

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Stefanie Lammel

3

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Rita Hanke

4

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Benjamin Neumann

5

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Arpad von Moers

6

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Astrid Speer

8

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=14600829

29 March 2024

publication date

5 November 2003

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/s00439-003-1041-2.pdf

Portable Document Format

1 reference

10.1007/S00439-003-1041-2

https://api.crossref.org/works/10.1007/S00439-003-1041-2

29 March 2024

http://link.springer.com/article/10.1007/s00439-003-1041-2/fulltext.html

1 reference

10.1007/S00439-003-1041-2

https://api.crossref.org/works/10.1007/S00439-003-1041-2

29 March 2024

http://link.springer.com/content/pdf/10.1007/s00439-003-1041-2

1 reference

10.1007/S00439-003-1041-2

https://api.crossref.org/works/10.1007/S00439-003-1041-2

29 March 2024

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

114

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

149-156

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Full functional rescue of a complete muscle (TA) in dystrophic hamsters by adeno-associated virus vector-directed gene therapy

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rescue of dystrophin expression in mdx mouse muscle by RNA/DNA oligonucleotides

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathophysiology and targeted therapeutics for muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prestin is the motor protein of cochlear outer hair cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Non-isotopic analysis of single strand conformation polymorphism (SSCP) in the exon 13 region of the human dystrophin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene expression comparison of biopsies from Duchenne muscular dystrophy (DMD) and normal skeletal muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning and characterization of a novel gene, CORS26, encoding a putative secretory protein and its possible involvement in skeletal development

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and mapping of novel candidate genes for retinal disorders using suppression subtractive hybridization

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gentamicin treatment of Duchenne and Becker muscular dystrophy due to nonsense mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Basic local alignment search tool

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Suppression subtractive hybridization: a method for generating differentially regulated or tissue-specific cDNA probes and libraries

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

cDNA microarray analysis of individual Duchenne muscular dystrophy patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Undetectable dystrophin can still result in a relatively benign phenotype of dystrophinopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PERP, an apoptosis-associated target of p53, is a novel member of the PMP-22/gas3 family

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophin expression in a Duchenne muscular dystrophy patient with a frame shift deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second promoter provides an alternative target for therapeutic up-regulation of utrophin in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/14600829

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00439-003-1041-2

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

Dimensions Publication ID

0 references

release_iauli672kjhjrk6354zj2zx6e4

1 reference

https://api.fatcat.wiki/v0/release/iauli672kjhjrk6354zj2zx6e4

24 November 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 July 2017

ResearchGate publication ID

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