G. Czernuszewicz

发表

Identification of a genetic locus for familial atrial fibrillation.

J. Brugada, R. Brugada, A. Marian, 1997, The New England journal of medicine.

Site-specific oligonucleotide binding represses transcription of the human c-myc gene in vitro.

S. J. Flint, M. Hogan, G. Czernuszewicz, 1988, Science.

Cardiac Fibro-Adipocyte Progenitors Express Desmosome Proteins and Preferentially Differentiate to Adipocytes Upon Deletion of the Desmoplakin Gene.

A. Marian, J. Willerson, Priyatansh Gurha, 2016, Circulation research.

Determinants of plasma vitamin D levels in patients with acute coronary syndromes

K. Mahaffey, A. Marian, N. Kleiman, 2011, European journal of clinical investigation.

The cloning, genomic organization and tissue expression profile of the human DLG5 gene

R. Gibbs, R. Brugada, R. Roberts, 2002, BMC Genomics.

MURC Variants in Cardiomyopathy

G. Dorn, H. Matsubara, A. Marian, 2011 .

Molecular Genetic and Functional Characterization Implicate Muscle-Restricted Coiled-Coil Gene (MURC) as a Causal Gene for Familial Dilated Cardiomyopathy

G. Dorn, H. Matsubara, A. Marian, 2011, Circulation. Cardiovascular genetics.

BET bromodomain inhibition attenuates cardiac phenotype in myocyte-specific Lamin A/C-deficient mice.

C. Coarfa, A. Marian, M. Robertson, 2020, The Journal of clinical investigation.

Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy.

Sanjay Shete, Raffaella Lombardi, Jianzhong Ma, 2007, Human molecular genetics.

Novel Cardiac Troponin T Mutation as a Cause of Familial Dilated Cardiomyopathy

R. Brugada, M. Quiñones, J. Durand, 2001, Circulation.

Human Molecular Genetic and Functional Studies Identify TRIM63, Encoding Muscle RING Finger Protein 1, as a Novel Gene for Human Hypertrophic Cardiomyopathy

Raffaella Lombardi, A. Marian, Jianping Jin, 2012, Circulation research.

Abstract 20201: Fibro-Adipocyte Progenitors are a Cell Source of Adipocytes in Arrhythmogenic Cardiomyopathy

A. Marian, J. Willerson, Priyatansh Gurha, 2014 .

Expression of a missense mutation in the messenger RNA for beta-myosin heavy chain in myocardial tissue in hypertrophic cardiomyopathy.

A. Marian, R. Roberts, G. Czernuszewicz, 1992, The Journal of clinical investigation.

Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

J. Towbin, S. Daiger, A. Marian, 1995, Circulation.