Recent advances in understanding the genetics of congenital heart defects

Por Gelb, Bruce D.
Publicado em 2013

History of Our Understanding of the Causes of Congenital Heart Disease

Por Gelb, Bruce D.
Publicado no Circ Cardiovasc Genet (2015)

The Hole and the Whole: Lessons from Manipulation of Nipbl Deficiency

Por Gelb, Bruce D.
Publicado no PLoS Biol (2016)

Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms

Por Tartaglia, Marco, Gelb, Bruce D.
Publicado em 2010

RAS signaling pathway mutations and hypertrophic cardiomyopathy: getting into and out of the thick of it

Por Gelb, Bruce D., Tartaglia, Marco
Publicado em 2011

The Good SHP2 Association: A Porthole into the Genetics of Congenital Heart Disease

Por Gelb, Bruce D., Seidman, Christine E.
Publicado em 2012

Concise Review: Drug Discovery in the Age of the Induced Pluripotent Stem Cell

Por Ko, Huaising C., Gelb, Bruce D.
Publicado em 2014

Complex Genetics and the Etiology of Human Congenital Heart Disease

Por Gelb, Bruce D., Chung, Wendy K.
Publicado em 2014

Genetics of congenital heart disease

Por Edwards, Jonathan J., Gelb, Bruce D.
Publicado no Curr Opin Cardiol (2016)

Noonan syndrome and clinically related disorders

Por Tartaglia, Marco, Gelb, Bruce D., Zenker, Martin
Publicado em 2011

Cardiomyopathies in Noonan syndrome and the other RASopathies

Por Gelb, Bruce D., Roberts, Amy E., Tartaglia, Marco
Publicado no Prog Pediatr Cardiol (2015)

Fgfr3 Is a Transcriptional Target of Ap2δ and Ash2l-Containing Histone Methyltransferase Complexes

Por Tan, Cheryl C., Walsh, Martin J., Gelb, Bruce D.
Publicado em 2009

Spacing Effect: SHP2 Phosphatase Regulates Resting Intervals Between Learning Trials in Long-Term Memory Induction

Por Pagani, Mario R., Oishi, Kimihiko, Gelb, Bruce D., Zhong, Yi
Publicado em 2009

Frequency of and Consequences of Aortic Dilation in Noonan Syndrome

Por Cornwall, James W., Green, Robert S., Nielsen, James C., Gelb, Bruce D.
Publicado em 2013

Noonan syndrome

Por Roberts, Amy E, Allanson, Judith E, Tartaglia, Marco, Gelb, Bruce D
Publicado no Lancet (2013)

Genetics of Congenital Heart Disease: The Glass Half Empty

Por Fahed, Akl C., Gelb, Bruce D., Seidman, J. G., Seidman, Christine E.
Publicado em 2013

Signaling to Cardiac Hypertrophy: Insights from Human and Mouse RASopathies

Por Sala, Valentina, Gallo, Simona, Leo, Christian, Gatti, Stefano, Gelb, Bruce D, Crepaldi, Tiziana
Publicado em 2012

Human Engineered Cardiac Tissues Created Using Induced Pluripotent Stem Cells Reveal Functional Characteristics of BRAF-Mediated Hypertrophic Cardiomyopathy

Por Cashman, Timothy J., Josowitz, Rebecca, Johnson, Bryce V., Gelb, Bruce D., Costa, Kevin D.
Publicado no PLoS One (2016)

Age-Dependent Germline Mosaicism of the Most Common Noonan Syndrome Mutation Shows the Signature of Germline Selection

Por Yoon, Song-Ro, Choi, Soo-Kung, Eboreime, Jordan, Gelb, Bruce D., Calabrese, Peter, Arnheim, Norman
Publicado em 2013

Construction of Defined Human Engineered Cardiac Tissues to Study Mechanisms of Cardiac Cell Therapy

Por Cashman, Timothy J., Josowitz, Rebecca, Gelb, Bruce D., Li, Ronald A., Dubois, Nicole C., Costa, Kevin D.
Publicado no J Vis Exp (2016)