Patisiran treatment in patients with transthyretin cardiac amyloidosis

…, MT Sweetser, PY Jay, PP Garg, J Vest… - … England Journal of …, 2023 - Mass Medical Soc
Background Transthyretin amyloidosis, also called ATTR amyloidosis, is associated with
accumulation of ATTR amyloid deposits in the heart and commonly manifests as progressive …

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

…, T Shioi, A Buerger, S Izumo, PY Jay… - Proceedings of the …, 2007 - National Acad Sciences
Physical activity protects against cardiovascular disease, and physiological cardiac hypertrophy
associated with regular exercise is usually beneficial, in marked contrast to pathological …

Molecular genetics of congenital diaphragmatic defects

M Bielinska, PY Jay, JM Erlich, S Mannisto… - Annals of …, 2007 - Taylor & Francis
Congenital diaphragmatic hernia (CDH) is a severe birth defect that is accompanied by
malformations of the lung, heart, testis, and other organs. Patients with CDH may have any …

A mechanical function of myosin II in cell motility

PY Jay, PA Pham, SA Wong… - Journal of cell …, 1995 - journals.biologists.com
Myosin II mutant Dictyostelium amoebae crawl more slowly than wild-type cells. Thus, myosin
II must contribute to amoeboid locomotion. We propose that contractile forces generated …

[HTML][HTML] Nkx2-5 mutation causes anatomic hypoplasia of the cardiac conduction system

PY Jay, BS Harris, CT Maguire… - The Journal of …, 2004 - Am Soc Clin Investig
J. Barhanin kindly provided the minK in situ probe. This work is supported by grants from
the NIH (to PY Jay, RG Gourdie, and S. Izumo), the Marram and Carpenter Fund for Innovation …

[HTML][HTML] The complex genetic basis of congenital heart defects

E Akhirome, NA Walton, JM Nogee, PY Jay - Circulation Journal, 2017 - jstage.jst.go.jp
Twenty years ago, chromosomal abnormalities were the only identifiable genetic causes of
a small fraction of congenital heart defects (CHD). Today, a de novo or inherited genetic …

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

T Prendiville, PY Jay, WT Pu - Cold Spring …, 2014 - perspectivesinmedicine.cshlp.org
Study of monogenic congenital heart disease (CHD) has provided entry points to gain new
understanding of heart development and the molecular pathogenesis of CHD. In this review, …

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

PY Jay, M Bielinska, JM Erlich, S Mannisto, WT Pu… - Developmental …, 2007 - Elsevier
Congenital diaphragmatic hernia (CDH) is an often fatal birth defect that is commonly associated
with pulmonary hypoplasia and cardiac malformations. Some investigators hypothesize …

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

…, E Bisping, ED Abel, WT Pu, S Izumo, PY Jay - Journal of cardiac …, 2006 - Elsevier
BACKGROUND: Conditional gene inactivation in mice using the bacteriophage P1 Cre-loxP
recombination system requires transgenic expression of Cre-recombinase driven by a tissue…

Capping protein levels influence actin assembly and cell motility in Dictyostelium

C Hug, PY Jay, I Reddy, JG McNally, PC Bridgman… - Cell, 1995 - cell.com
Actin assembly is important for cell motility, but the mechanism of assembly and how it relates
to motility in vivo is largely unknown. In vitro, actin assembly can be controlled by proteins, …