E-LIB Suche - Ergebnisse für: Binner, Priska

1

Clinical characterization and mutation spectrum of patients..:

Bardey, Frieda ; Rieck, Lorenz ; Spira, Dominik...
Journal of Lipid Research. , 2024

Link: https://doi.org/10.1016/..

2

FH ALERT: efficacy of a novel approach to identify patients..:

Fath, Felix ; Bengeser, Andreas ; Barresi, Mathias...
Scientific Reports. 11 (2021) 1 - p. , 2021

Link: https://doi.org/10.1038/..

3

Clinical characterization and mutation spectrum of German p..:

Grenkowitz, Thomas ; Kassner, Ursula ; Wühle-Demuth, Marion...
Atherosclerosis. 253 (2016) - p. 88-93 , 2016

Link: https://doi.org/10.1016/..

4

High-density oligonucleotide-based resequencing assay for m..:

Kathiravel, Ushanthine ; Keyser, Britta ; Hoffjan, Sabine...
Molecular and Cellular Probes. 27 (2013) 2 - p. 103-108 , 2013

Link: https://doi.org/10.1016/..

5

Novel correlations between the genotype and the phenotype o..:

Waldmüller, Stephan ; Erdmann, Jeanette ; Binner, Priska...
European Journal of Heart Failure. 13 (2011) 11 - p. 1185-1192 , 2011

Link: https://doi.org/10.1093/..

6

Six sequence variants on chromosome 9p21.3 are associated w..:

Forschungsverbund Herz-Kreislauf in NRW (Research Consortium Heart and Circulation in North Rhine-Westphalia) ; Scheffold, Thomas ; Kullmann, Silke...
BMC Cardiovascular Disorders. 11 (2011) 1 - p. , 2011

Link: https://doi.org/10.1186/..

7

Variation in the human soluble epoxide hydrolase gene and r..:

Kullmann, Silke ; Binner, Priska ; Rackebrandt, Kirsten...
BMC Cardiovascular Disorders. 9 (2009) 1 - p. , 2009

Link: https://doi.org/10.1186/..

8

Array-Based Resequencing Assay for Mutations Causing Hypert..:

Scheffold, Thomas ; Bonin, Michael ; Poths, Sven...
Clinical Chemistry. 54 (2008) 4 - p. 682-687 , 2008

Link: https://doi.org/10.1373/..

9

Noncompaction of the Ventricular Myocardium Is Associated w..:

Budde, Birgit S. ; Binner, Priska ; Waldmüller, Stephan...
PLoS ONE. 2 (2007) 12 - p. e1362 , 2007

Link: https://doi.org/10.1371/..

10

Hypertrophe Kardiomyopathie:

Scheffold, Thomas ; Binner, Priska ; Erdmann, Jeanette..
Herz Kardiovaskuläre Erkrankungen. 30 (2005) 6 - p. 550-557 , 2005

Link: https://doi.org/10.1007/..

11

Mutations in the Human Muscle LIM Protein Gene in Families ..:

Geier, Christian ; Perrot, Andreas ; Özcelik, Cemil...
Circulation. 107 (2003) 10 - p. 1390-1395 , 2003

Link: https://doi.org/10.1161/..

12

MHC class I antigen processing pathway defects, ras mutatio..:

Atkins, Derek ; Breuckmann, Aldona ; Schmahl, Gerd E....
International Journal of Cancer. 109 (2003) 2 - p. 265-273 , 2003

Link: https://doi.org/10.1002/..

13

Three novel mutations in the ACTA2 gene in German patients ..:

Hoffjan, Sabine ; Waldmüller, Stephan ; Blankenfeldt, Wulf...
info:eu-repo/semantics/altIdentifier/doi/10.1038/ejhg.2010.239. , 2011

Link: https://hal.archives-ouv..

14

Three novel mutations in the ACTA2 gene in German patients ..:

Hoffjan, Sabine ; Waldmüller, Stephan ; Blankenfeldt, Wulf...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3083620. , 2011

Link: http://www.ncbi.nlm.nih...

15

Six sequence variants on chromosome 9p21.3 are associated w..:

Stellbrink Christoph ; Hegge Franz ; Motz Wolfgang...
http://www.biomedcentral.com/1471-2261/11/9. , 2011

Link: https://doi.org/10.1186/..