P. Jay

发表

Novel markers of gonadectomy-induced adrenocortical neoplasia in the mouse and ferret

R. Mitra, Maximiliaan Schillebeeckx, David B. Wilson, 2015, Molecular and Cellular Endocrinology.

Myocardial Induction of Type 3 Deiodinase in Dilated Cardiomyopathy.

D. Dorfman, R. Padera, A. Zavacki, 2017, Thyroid : official journal of the American Thyroid Association.

PI3K(p110alpha) inhibitors as anti-cancer agents: minding the heart.

J. McMullen, P. Jay, 2007, Cell cycle.

PI3K(p110α) Inhibitors as Anti-Cancer Agents: Minding the Heart

J. McMullen, P. Jay, 2007 .

Activation of Tolloid‐like 1 gene expression by the cardiac specific homeobox gene Nkx2–5

I. Sabirzhanova, B. Sabirzhanov, P. Jay, 2009, Development, growth & differentiation.

A mouse model of congenital heart disease: cardiac arrhythmias and atrial septal defect caused by haploinsufficiency of the cardiac transcription factor Csx/Nkx2.5.

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

Surface particle transport mechanism independent of myosin II in Dictyostelium

E. Elson, P. Jay, 1992, Nature.

Proper development of the outer longitudinal smooth muscle of the mouse pylorus requires Nkx2-5 and Gata3.

J. D. Engel, A. Prakash, J. Engel, 2014, Gastroenterology.

Association of genes with physiological functions by comparative analysis of pooled expression microarray data.

P. Jay, I. Chen, Vinay K Rathi, 2013, Physiological genomics.

Cardiac lipin 1 expression is regulated by the peroxisome proliferator activated receptor γ coactivator 1α/estrogen related receptor axis.

Xiaowei Wang, J. Huss, X. Su, 2011, Journal of molecular and cellular cardiology.

in BAL fluid after ANTU-induced edema in rats Fluorescein-labeled dextran concentration is increased

P. Auberger, P. Hruz, M. Halford, 2015 .

The Complex Genetic Basis of Congenital Heart Defects.

Nephi A. Walton, P. Jay, Ehiole Akhirome, 2017, Circulation journal : official journal of the Japanese Circulation Society.

Function follows form: cardiac conduction system defects in Nkx2-5 mutation.

C. Berul, S. Izumo, R. Gourdie, 2004, The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology.

Transcriptional regulation of cardiac conduction system development: 2004 FASEB cardiac conduction system minimeeting, Washington, DC.

S. Izumo, R. Gourdie, B. S. Harris, 2004, The anatomical record. Part A, Discoveries in molecular, cellular, and evolutionary biology.

Dilated cardiomyopathy resulting from high-level myocardial expression of Cre-recombinase.

W. Pu, S. Izumo, E. Abel, 2006, Journal of cardiac failure.

Gαi2 signaling: friend or foe in cardiac injury and heart failure?

R. Neubig, R. Charbeneau, K. Kaur, 2012, Naunyn-Schmiedeberg's Archives of Pharmacology.

The Maternal Age-Associated Risk of Congenital Heart Disease Is Modifiable

David B. Wilson, P. Jay, Claire E. Schulkey, 2015, Nature.

Loss of glypican-3 function causes growth factor-dependent defects in cardiac and coronary vascular development.

M. Wong, J. Erlich, P. Jay, 2009, Developmental biology.

Complex Trait Analysis of Ventricular Septal Defects Caused by Nkx2-5 Mutation

J. Erlich, P. Jay, Claire E. Schulkey, 2012, Circulation. Cardiovascular genetics.

Heterogeneity of Genetic Modifiers Ensures Normal Cardiac Development

R. Barlow, L. Janss, J. Erlich, 2010, Circulation.

GATA 4 Deficiency Impairs Ovarian Function in Adult Mice 1

M. Anttonen, David B. Wilson, M. Heikinheimo, 2019 .

GATA4 Deficiency Impairs Ovarian Function in Adult Mice1

M. Anttonen, David B. Wilson, M. Heikinheimo, 2011, Biology of reproduction.

A single misstep in cardiac development explains the co-occurrence of tetralogy of fallot and complete atrioventricular septal defect in Down syndrome.

P. Jay, Hoang H. Nguyen, 2014, The Journal of pediatrics.

Correction: Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies

I. Krantz, D. Dorsett, S. Kulkarni, 2009, PLoS ONE.

Dosage Effects of Cohesin Regulatory Factor PDS5 on Mammalian Development: Implications for Cohesinopathies

I. Krantz, D. Dorsett, J. Milbrandt, 2009, PloS one.

Saxagliptin improves glucose tolerance but not survival in a murine model of dilated cardiomyopathy

P. Hruz, M. Payne, P. Jay, 2012, Cardiovascular endocrinology.

Exenatide Improves Glucose Homeostasis and Prolongs Survival in a Murine Model of Dilated Cardiomyopathy

P. Hruz, Kai-Chien Yang, A. Tzekov, 2011, PloS one.

Rhythm genes sing more than one tune: noncanonical functions of cardiac ion channels.

P. Jay, Ehiole Akhirome, 2015, Circulation. Arrhythmia and electrophysiology.

Hereditary Supraventricular Tachycardias

C. Berul, P. Jay, 2000 .

Human Genetics of Atrial Septal Defect

P. Jay, R. Khan, 2016 .

Molecular Pathways and Animal Models of Atrial Septal Defect

Robert H. Anderson, K. Degenhardt, P. Jay, 2016 .

Elucidating the Molecular and Genetic Interactions Responsible for Congenital Heart Disease

S. Izumo, P. Jay, 2002, Pediatric Research.

Nkx 2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

D. Roden, C. Berul, H. Wakimoto, 2022 .

GATA4 is a critical regulator of gonadectomy-induced adrenocortical tumorigenesis in mice.

H. Parviainen, David B. Wilson, M. Heikinheimo, 2012, Endocrinology.

Metabolic and Cardiac Adaptation to Chronic Pharmacologic Blockade of Facilitative Glucose Transport in Murine Dilated Cardiomyopathy and Myocardial Ischemia

P. Hruz, R. Hresko, M. Payne, 2018, Scientific Reports.

Haploinsufficiency of the cardiac transcription factor Nkx2‐5 variably affects the expression of putative target genes

S. Izumo, A. Dorfman, P. Jay, 2005, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Absence of Msx2 Does Not Affect Cardiac Conduction or Rescue Conduction Defects Associated with Nkx2‐5 Mutation

C. Berul, H. Wakimoto, S. Izumo, 2005, Journal of cardiovascular electrophysiology.

Gαi2 signaling: friend or foe in cardiac injury and heart failure?

R. Neubig, R. Charbeneau, K. Kaur, 2012, Naunyn-Schmiedeberg's Archives of Pharmacology.

Genetic wiring diagram of the cardiac conduction system.

P. Jay, 2007, Circulation.

Molecular genetics of congenital diaphragmatic defects

J. Erlich, David B. Wilson, M. Heikinheimo, 2007, Annals of medicine.

Protective effects of exercise and phosphoinositide 3-kinase(p110α) signaling in dilated and hypertrophic cardiomyopathy

Yunyu Zhang, G. Jennings, E. Woodcock, 2007, Proceedings of the National Academy of Sciences.

Mice lacking sister chromatid cohesion protein PDS5B exhibit developmental abnormalities reminiscent of Cornelia de Lange syndrome

J. Milbrandt, R. Heuckeroth, Bin Zhang, 2007, Development.

The intracellular domains of Notch1 and Notch2 are functionally equivalent during development and carcinogenesis

Zhenyi Liu, Raphael Kopan, M. Morimoto, 2015, Development.

Capping protein levels influence actin assembly and cell motility in dictyostelium

E. Elson, J. Cooper, J. McNally, 1995, Cell.

Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defects.

W. Pu, J. Erlich, M. Heikinheimo, 2007, Developmental biology.

Somatic chromosomal translocation between Ewsr1 and Fli1 loci leads to dilated cardiomyopathy in a mouse model

K. Nakao, T. Noda, Takuro Nakamura, 2015, Scientific Reports.

Gene Silencing Therapeutics in Cardiology: A Review Article

M. Maier, J. Vest, Lisa Duarte, 2021, International Journal of Cardiovascular Sciences.

Enhanced cardiac PI3Kα signalling mitigates arrhythmogenic electrical remodelling in pathological hypertrophy and heart failure.

J. Nerbonne, Kai-Chien Yang, J. McMullen, 2012, Cardiovascular research.

Enhanced cardiac PI 3 K a signalling mitigates arrhythmogenic electrical remodelling in pathological hypertrophy and heart failure

J. Nerbonne, Kai-Chien Yang, J. McMullen, 2012 .

Homeostatic regulation of electrical excitability in physiological cardiac hypertrophy

J. Nerbonne, Céline Marionneau, Kai-Chien Yang, 2010, The Journal of physiology.

HIV protease inhibitors that block GLUT4 precipitate acute, decompensated heart failure in a mouse model of dilated cardiomyopathy

P. Hruz, P. Jay, H. Struthers, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

A mechanical function of myosin II in cell motility.

E. Elson, P. Jay, P. Pham, 1995, Journal of cell science.

The Heritable Basis of Congenital Heart Disease: Past, Present, and Future.

P. Jay, Julie M. Nogee, 2016, Circulation. Cardiovascular genetics.

The Genetic Architecture of a Congenital Heart Defect Is Related to Its Fitness Cost

J. Cheverud, P. Jay, Claire E. Schulkey, 2021, Genes.

The fitness cost of a congenital heart defect shapes its genetic architecture

J. Cheverud, P. Jay, Claire E. Schulkey, 2019, bioRxiv.

Role of ponticulin in pseudopod dynamics, cell-cell adhesion, and mechanical stability of an amoeboid membrane skeleton.

E. Elson, D. Soll, S. Block, 1998, The Biological bulletin.

Congenital Aneurysm of the Muscular Interventricular Septum Associated With Bifascicular Block

P. Jay, Hoang H. Nguyen, 2022, Cureus.

Nkx2-5 and Sarcospan genetically interact in the development of the muscular ventricular septum of the heart

Rebecca S. Cochran, P. Jay, Claire E. Schulkey, 2017, Scientific Reports.

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.

D. Roden, C. Berul, H. Wakimoto, 2004, The Journal of clinical investigation.

Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.

W. Pu, T. Prendiville, P. Jay, 2014, Cold Spring Harbor perspectives in medicine.

Patisiran treatment in patients with hereditary transthyretin‐mediated amyloidosis with polyneuropathy after liver transplantation

E. Nordh, R. Orrell, S. Ayache, 2022, American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons.

Ex vivo, microelectrode analysis of conduction through the AV node of wild‐type and Nkx2‐5 mutant mouse hearts as guided by a Cx40‐eGFP transgenic reporter

P. Jay, A. Gazit, L. Miquerol, 2014, Physiological reports.

Transgenerational cardiology: One way to a baby's heart is through the mother

J. Cheverud, P. Jay, Ehiole Akhirome, 2016, Molecular and Cellular Endocrinology.

Tissue Doppler Septal Tei Index Indicates Severity of Illness in Pediatric Patients With Congestive Heart Failure

C. Hildebolt, C. Canter, C. Rainey, 2013, Pediatric Cardiology.

Reprogramming the conduction system: Onward toward a biological pacemaker.

S. Rentschler, P. Jay, J. Meyers, 2016, Trends in cardiovascular medicine.

Forces in cell locomotion.

E. Elson, M. Kolodney, P. Jay, 1999, Biochemical Society symposium.

Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system.

D. Roden, C. Berul, H. Wakimoto, 2004, The Journal of clinical investigation.

Cardiac conduction and arrhythmia: insights from Nkx2.5 mutations in mouse and humans.

C. Berul, Y. Kurachi, S. Izumo, 2008, Novartis Foundation symposium.

Dichotomous roles of TBX3 in the establishment of atrioventricular conduction pathways in the human heart

G. V. Van Hare, D. Grange, P. Jay, 2018, HeartRhythm case reports.