Please note that PUB no longer supports Internet Explorer versions 8 or 9 (or earlier).

We recommend upgrading to the latest Internet Explorer, Google Chrome, or Firefox.

3 Publikationen

2018 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2916928
A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy
Schirmer I, Dieding M, Klauke B, Brodehl A, Gärtner-Rommel A, Walhorn V, Gummert J, Schulz U, Paluszkiewicz L, Anselmetti D, Milting H (2018)
Molecular Genetics & Genomic Medicine 6(2): 288-293.
PUB | DOI | Download (ext.) | WoS | PubMed | Europe PMC
 
2016 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 2902127
Functional characterization of the novel DES mutation p.L136P associated with dilated cardiomyopathy reveals a dominant filament assembly defect
Brodehl A, Dieding M, Biere N, Unger A, Klauke B, Walhorn V, Gummert J, Schulz U, Linke WA, Gerull B, Vorgert M, et al. (2016)
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY 91: 207-214.
PUB | DOI | WoS | PubMed | Europe PMC
 
2000 | Zeitschriftenaufsatz | Veröffentlicht | PUB-ID: 1618543
Generation of tension by skinned fibers and intact skeletal muscles from desmin-deficient mice
Wieneke S, Stehle R, Li ZL, Jockusch H (2000)
Biochemical and biophysical research communications 278(2): 419-425.
PUB | DOI | WoS | PubMed | Europe PMC
 

Filter und Suchbegriffe

keyword="myopathy"

Suche

Publikationen filtern

Darstellung / Sortierung

Export / Einbettung