Results 181 to 190 of about 7,387 (194)

Genetic, Clinical, Molecular, and Pathogenic Aspects of the South Asian–Specific Polymorphic MYBPC3Δ25bp Variant

Biophysical Reviews, 2020
Yigang Wang, Mohammed Arif, Taejeong Song   +2 more
exaly  

Two Novel Mutations of the MYBPC3 Gene Identified in Chinese Families With Hypertrophic Cardiomyopathy

Canadian Journal of Cardiology, 2010
Xiang-Jun Yang, Ting-Bo Jiang, Wen-Ping Jiang   +2 more
exaly  

MicroRNA Transcriptome Profiling in Cardiac Tissue of Hypertrophic Cardiomyopathy Patients With MYBPC3 Mutations

Journal of Molecular and Cellular Cardiology, 2013
Jolanda van der Velden, Paula A da Costa Martins   +1 more
exaly  

Biallelic Mutation in MYH7 and MYBPC3 Leads to Severe Cardiomyopathy With Left Ventricular Noncompaction Phenotype

Human Mutation, 2019
Sabine Klaassen, Lucie Carrier, Brenda Gerull   +2 more
exaly  

MYBPC3 AS A BIOMARKER FOR PPARA MODULATORS

2008
GOLZ STEFAN, SUMMER HOLGER, GEERTS ANDREAS, WILMEN ANDREAS, GRUSDAT GERDA, BRUEGGEMEIER ULF   +5 more
openaire   +1 more source

Novel Deletions in MYH7 and MYBPC3 Identified in Indian Families With Familial Hypertrophic Cardiomyopathy

Journal of Molecular and Cellular Cardiology, 2003
Maria Golubenko, Ketty Schwartz, Hans-Peter Vosberg   +2 more
exaly  

Clinical Outcome of Hypertrophic Cardiomyopathy in Probands With the Founder Variant c.913_914del in MYBPC3: A Slovenian Cohort Study

Journal of Cardiovascular Translational Research
Borut Peterlin, Aleš Maver
exaly  

MYBPC3 In Hypertrophic Cardiomyopathy: From Mutation Identification to RNA-Based Correction

Pflugers Archiv European Journal of Physiology, 2014
Lucie Carrier, Giulia Mearini, Christina Gedicke-Hornung   +2 more
exaly  

Gene symbol: MYBPC3. Disease: Cardiomyopathy, hypertrophic.

Human genetics, 2008
Volker, Ruppert, Thomas, Meyer, Sabine, Pankuweit, Bernhard, Maisch, Reinhard C, Funck   +4 more
openaire   +1 more source

Left ventricular noncompaction associated with a compound heterozygous MYBPC3 mutation

European Journal of Medical Genetics, 2014
Josef, Finsterer, Sinda, Zarrouk-Mahjoub
openaire   +2 more sources