J. G. Seidman

发表

Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog.

N. Copeland, D. Gilbert, N. Jenkins, 1995, Genomics.

A mouse model of human familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism

J. Seidman, E. Brown, C. Seidman, 1995, Nature Genetics.

QTL influencing autoimmune diabetes and encephalomyelitis map to a 0.15-cM region containing Il2

J. Seidman, H. Weiner, V. Kuchroo, 1999, Nature Genetics.

Single-Cell Resolution of Temporal Gene Expression during Heart Development.

J. Seidman, B. Bruneau, W. Pu, 2016, Developmental cell.

Gene Mutations in Apical Hypertrophic Cardiomyopathy

J. Seidman, B. Maron, C. Seidman, 2005, Circulation.

Genetic Basis of Hypertrophic Cardiomyopathy: From Bench to the Clinics

J. Seidman, C. Seidman, R. Alcalai, 2007, Journal of cardiovascular electrophysiology.

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1.

S. Solomon, J. Seidman, R. Holcombe, 1989, The New England journal of medicine.

A Tension-Based Model Distinguishes Hypertrophic versus Dilated Cardiomyopathy

J. Seidman, S. Houser, M. Regnier, 2016, Cell.

A-Band Titin Truncation in Zebrafish Causes Dilated Cardiomyopathy and Hemodynamic Stress Intolerance

J. Seidman, F. Braet, C. Hayward, 2018, Circulation. Genomic and precision medicine.

Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy.

Birgit Funke, Christine E Seidman, S. Colan, 2010, Journal of the American College of Cardiology.

Tbx5-dependent rheostatic control of cardiac gene expression and morphogenesis.

Kazuko Koshiba-Takeuchi, R Mark Henkelman, Christine E Seidman, 2006, Developmental biology.

Characterization of endoglin and identification of novel mutations in hereditary hemorrhagic telangiectasia.

J. Hughes, J. Seidman, C. Seidman, 1997, American journal of human genetics.

Tbx5 maintains atrial identity in postnatal cardiomyocytes by regulating an atrial-specific enhancer network

Vassilios J. Bezzerides, H. Wakimoto, Carlos Perez-Cervantes, 2023, Nature Cardiovascular Research.

CD36 overexpression predisposes to arrhythmias but reduces infarct size in spontaneously hypertensive rats: gene expression profile analysis.

T. Kurtz, C. Seidman, V. Zídek, 2012, Physiological genomics.

A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13.

J. Seidman, C. Seidman, M. Haas, 1998, Kidney international.

Cao-sensing receptor (CaR)-mediated activation of K+ channels is blunted in CaR gene-deficient mouse neurons.

J. Seidman, E. Brown, C. Seidman, 1997, Neuroreport.

Exercise Training Improves Cardiac Function and Attenuates Arrhythmia in Cpvt Mice Experimental Protocol

J. Seidman, C. Seidman, M. Eldar, 2022 .

Neonatal atria and ventricles secrete atrial natriuretic factor via tissue-specific secretory pathways

J. Seidman, J. Fallon, C. Seidman, 1986, Cell.

Cellular Polycomb Repressive Complex 2 Regulates Normal Development of the Mouse Heart

Aibin He, Danos C. Christodoulou, Huafeng Xie, 2012 .

Subtle Abnormalities in Contractile Function Are an Early Manifestation of Sarcomere Mutations in Dilated Cardiomyopathy

S. Colan, J. Seidman, E. Orav, 2012, Circulation. Cardiovascular genetics.

Somatic events modify hypertrophic cardiomyopathy pathology and link hypertrophy to arrhythmia.

Christopher Semsarian, Christine E Seidman, J. Seidman, 2005, Proceedings of the National Academy of Sciences of the United States of America.

A gene for hereditary haemorrhagic telangiectasia maps to chromosome 9q3

J. Hughes, J. Seidman, C. Seidman, 1994, Nature Genetics.

Allele-Specific Silencing of Mutant Myh6 Transcripts in Mice Suppresses Hypertrophic Cardiomyopathy

Christine E. Seidman, J. Seidman, C. Seidman, 2013, Science.

Hypertrophic cardiomyopathy: Translating cellular cross talk into therapeutics

Christine E. Seidman, J. Seidman, C. Seidman, 2012, The Journal of cell biology.

Mutations in genes related to myocyte contraction and ventricular septum development in non-syndromic tetralogy of Fallot

Drayton C Harvey, J. G. Seidman, Riya Verma, 2023, Frontiers in Cardiovascular Medicine.

Tbx5 Is Required for Avian and Mammalian Epicardial Formation and Coronary Vasculogenesis

O. Elemento, C. Seidman, C. Basson, 2014, Circulation research.

Tbx 5 Is Required for Avian and Mammalian Epicardial Formation and Coronary Vasculogenesis

O. Elemento, C. Seidman, C. Basson, 2022 .

Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia.

J. Seidman, C. Seidman, C. Berul, 2007, The Journal of clinical investigation.

Reduced cross-bridge dependent stiffness of skinned myocardium from mice lacking cardiac myosin binding protein-C

J. Seidman, N. Alpert, T. Irving, 2004, Molecular and Cellular Biochemistry.

Dilated cardiomyopathy in homozygous myosin-binding protein-C mutant mice.

D. Kass, J. Seidman, D. Turnbull, 1999, The Journal of clinical investigation.

Role of Cardiac Myosin Binding Protein C in Sustaining Left Ventricular Systolic Stiffening

D. Kass, J. Seidman, Y. Wang, 2004, Circulation research.

Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart Transplantation

C. Seidman, S. DePalma, B. McDonough, 2023, Circulation. Genomic and precision medicine.

The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome.

J. Seidman, M. Bamshad, L. Jorde, 1999, American journal of human genetics.

Cytoskeletal Changes in the Brains of Mice Lacking Calcineurin Aα

J. Seidman, H. Potter, U. Kayyali, 1997, Journal of neurochemistry.

Effects of two familial hypertrophic cardiomyopathy-causing mutations on alpha-tropomyosin structure and function

Lehrer, S. Hitchcock-DeGregori, S. Lehrer, 1999, Biochemistry.

FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY: CLINICAL AND GENETIC DIAGNOSIS

S. DePalma, F. She, Yuanwei Liu, 2023 .

DMD-Associated Dilated Cardiomyopathy: Genotypes, Phenotypes, and Phenocopies

Emma M. Rath, D. Fatkin, C. Seidman, 2023, Circulation. Genomic and precision medicine.

cis-dominance of rat atrial natriuretic factor gene regulatory sequences in transgenic mice.

J. Seidman, C. Seidman, E. V. Schmidt, 1991, Canadian journal of physiology and pharmacology.

Eya4-deficient mice are a model for heritable otitis media.

J. Seidman, R. Eavey, M. Liberman, 2008, The Journal of clinical investigation.

Identification of genetic loci associated with paralysis, inflammation and weight loss in mouse experimental autoimmune encephalomyelitis.

J. Seidman, H. Weiner, V. Kuchroo, 2001, International immunology.

Atrial natriuretic factor: assessment of its structure in atria and regulation of its biosynthesis with volume depletion.

J. Seidman, J. Fallon, C. Seidman, 1986, Journal of molecular and cellular cardiology.

Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection

J. Seidman, H. Rehm, R. Kucherlapati, 2009, Nature Methods.

Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.

J. Seidman, D. Fatkin, R. Eavey, 2000, Circulation.

Calcium-ion-sensing cell-surface receptors.

J. Seidman, E. Brown, C. Seidman, 1995, The New England journal of medicine.

Dynamic Cellular Integration Drives Functional Assembly of the Heart’s Pacemaker Complex

Christine E. Seidman, Trevor Henley, Michael Bressan, 2018, Cell reports.

The H2Bub1-deposition complex is required for human and mouse cardiogenesis

Sidi Chen, Syndi Barish, Lauren K. Wasson, 2023, Development.

Functional dissection of human cardiac enhancers and noncoding de novo variants in congenital heart disease

Xujie Liu, P. Zhou, Joshua M. Gorham, 2024, Nature genetics.

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

J A Osborne, H Niimura, S. Solomon, 1999, Circulation.

Identification of cDNA encoding an additional alpha subunit of a human GTP-binding protein: expression of three alpha i subtypes in human tissues and cell lines.

J. Seidman, E. Neer, S. Ang, 1988, Proceedings of the National Academy of Sciences of the United States of America.

Genetic analysis of susceptibility to experimental autoimmune encephalomyelitis in a cross between SJL/J and B10.S mice.

J. Seidman, H. Weiner, V. Kuchroo, 1996, Journal of immunology.

Elevated rates of force development and MgATP binding in F764L and S532P myosin mutations causing dilated cardiomyopathy.

J. Schmitt, J. Seidman, Y. Wang, 2013, Journal of molecular and cellular cardiology.

Cardiovascular homeostasis dependence on MICU2, a regulatory subunit of the mitochondrial calcium uniporter

V. Mootha, J. Seidman, C. Seidman, 2017, Proceedings of the National Academy of Sciences.

108 A NOVEL COL1A1 MUTATION IN INFANTILE CORTICAL HYPEROSTOSIS (CAFFEY DISEASE) EXPANDS THE SPECTRUM OF COLLAGEN-RELATED DISORDERS

D. Sillence, S. Mundlos, J. Seidman, 2005, Journal of Investigative Medicine.

Cardiac myosin binding protein-C is essential for thick-filament stability and flexural rigidity.

J. Seidman, C. Seidman, J. Vigoreaux, 2009, Biophysical journal.

Mutations in cardiac myosin heavy chain genes cause familial hypertrophic cardiomyopathy.

J. Seidman, C. Seidman, J. G. Seidman, 1991, Molecular biology & medicine.

Spatial transcriptional profile of the chick and mouse endocardial cushions identify novel regulators of endocardial EMT in vitro.

C. Seidman, Danos C. Christodoulou, H. Baldwin, 2013, Journal of molecular and cellular cardiology.

Molecular and Spatial Signatures of Mouse Embryonic Endothelial Cells at Single-Cell Resolution

P. Zhou, Daniel M. DeLaughter, Feng Xiao, 2024, Circulation research.

Causes of clinical diversity in human TBX5 mutations.

J. Seidman, C. Seidman, C. Basson, 2002, Cold Spring Harbor symposia on quantitative biology.