Toward an Understanding of the Cause of Mitral Valve Prolapse

Por Towbin, Jeffrey A.
Publicado em 1999

INHERITED CARDIOMYOPATHIES

Por Towbin, Jeffrey A.
Publicado no Circ J (2014)

Ion Channel Dysfunction Associated With Arrhythmia, Ventricular Noncompaction, and Mitral Valve Prolapse: A New Overlapping Phenotype

Por Towbin, Jeffrey A.
Publicado no J Am Coll Cardiol (2014)

Sarcoglycan, the heart, and skeletal muscles: new treatment, old drug?

Por Towbin , Jeffrey A., Bowles, Neil E.
Publicado em 2001

Left Ventricular Noncompaction in a Family with Lamin A/C Gene Mutation

Por Parent, John J., Towbin, Jeffrey A., Jefferies, John L.
Publicado no Tex Heart Inst J (2015)

A Woman with Incidental Findings of Ventricular Aneurysms and a Desmosomal Cardiomyopathy

Por Ly, Suntharo, Marcus, Frank I., Xu, Tianhong, Towbin, Jeffrey A.
Publicado em 2008

Idiopathic and Primary Cardiomyopathies in Children

Por Lipshultz, Steven E., Colan, Steven D., Towbin, Jeffrey A., Wilkinson, James D.
Publicado em 2008

Transcription factor neuromancer/TBX20 is required for cardiac function in Drosophila with implications for human heart disease

Por Qian, Li, Mohapatra, Bhagyalaxmi, Akasaka, Takeshi, Liu, Jiandong, Ocorr, Karen, Towbin, Jeffrey A., Bodmer, Rolf
Publicado em 2008

Neonatal presentation of ventricular tachycardia and a Reye-like syndrome episode associated with disturbed mitochondrial energy metabolism

Por Scaglia, Fernando, Scheuerle, Angela E, Towbin, Jeffrey A, Armstrong, Dawna L, Sweetman, Lawrence, Wong, Lee-Jun C
Publicado em 2002

Identification and Functional Analysis of ZIC3 Mutations in Heterotaxy and Related Congenital Heart Defects

Por Ware, Stephanie M., Peng, Jianlan, Zhu, Lirong, Fernbach, Susan, Colicos, Suzanne, Casey, Brett, Towbin, Jeffrey, Belmont, John W.
Publicado em 2004

GSK3- and PRMT-1–dependent modifications of desmoplakin control desmoplakin–cytoskeleton dynamics

Por Albrecht, Lauren V., Zhang, Lichao, Shabanowitz, Jeffrey, Purevjav, Enkhsaikhan, Towbin, Jeffrey A., Hunt, Donald F., Green, Kathleen J.
Publicado no J Cell Biol (2015)

Dissection of Z-disc myopalladin gene network involved in the development of restrictive cardiomyopathy using system genetics approach

Por Gu, Qingqing, Mendsaikhan, Uzmee, Khuchua, Zaza, Jones, Byron C, Lu, Lu, Towbin, Jeffrey A, Xu, Biao, Purevjav, Enkhsaikhan
Publicado no World J Cardiol (2017)

Mutations in the human δ-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

Por Tsubata, Shinichi, Bowles, Karla R., Vatta, Matteo, Zintz, Carmelann, Titus, Jack, Muhonen, Linda, Bowles, Neil E., Towbin, Jeffrey A.
Publicado em 2000

A nonsense SCN5A mutation associated with Brugada type ECG and intraventricular conduction defects

Por Samani, Kaveh, Ai, Tomohiko, Towbin, Jeffrey A., Brugada, Ramon, Shuraih, Mossaab, Xi, Yutao, Wu, Geru, Cheng, Jie, Vatta, Matteo
Publicado em 2009

Association between diffuse myocardial fibrosis and diastolic dysfunction in sickle cell anemia

Por Niss, Omar, Fleck, Robert, Makue, Fowe, Alsaied, Tarek, Desai, Payal, Towbin, Jeffrey A., Malik, Punam, Taylor, Michael D., Quinn, Charles T.
Publicado no Blood (2017)

Pediatric and adult dilated cardiomyopathy represent distinct pathological entities

Por Patel, Meghna D., Mohan, Jayaram, Schneider, Caralin, Bajpai, Geetika, Purevjav, Enkhsaikhan, Canter, Charles E., Towbin, Jeffrey, Bredemeyer, Andrea, Lavine, Kory J.
Publicado no JCI Insight (2017)

Rare copy number variations in congenital heart disease patients identify unique genes in left-right patterning

Por Fakhro, Khalid A., Choi, Murim, Ware, Stephanie M., Belmont, John W., Towbin, Jeffrey A., Lifton, Richard P., Khokha, Mustafa K., Brueckner, Martina
Publicado em 2011

Accelerated cardiac remodeling in desmoplakin transgenic mice in response to endurance exercise is associated with perturbed Wnt/β-catenin signaling

Por Martherus, Ruben, Jain, Rahul, Takagi, Ken, Mendsaikhan, Uzmee, Turdi, Subat, Osinska, Hanna, James, Jeanne F., Kramer, Kristen, Purevjav, Enkhsaikhan, Towbin, Jeffrey A.
Publicado no Am J Physiol Heart Circ Physiol (2015)

NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling

Por McBride, Kim L., Riley, Maurisa F., Zender, Gloria A., Fitzgerald-Butt, Sara M., Towbin, Jeffrey A., Belmont, John W., Cole, Susan E.
Publicado em 2008

Modification of a Volume-Overload Heart Failure Model to Track Myocardial Remodeling and Device-Related Reverse Remodeling

Por Tuzun, Egemen, Bick, Roger, Kadipasaoglu, Cihan, Conger, Jeffrey L., Poindexter, Brian J., Gregoric, Igor D., Frazier, O. H., Towbin, Jeffrey A., Radovancevic, Branislav
Publicado em 2011