TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes

por Henkhaus, Rebecca S., Bittel, Douglas C., Butler, Merlin G.
Publicado 2010

MicroRNA-421 Dysregulation is Associated with Tetralogy of Fallot

por Bittel, Douglas C., Kibiryeva, Nataliya, Marshall, Jennifer A., O’Brien, James E.
Publicado 2014

Snord94 expression level alters methylation at C(62) in snRNA U6

por Ogren, Allison, Kibiryeva, Nataliya, Marshall, Jennifer, O’Brien, James E., Bittel, Douglas C.
Publicado 2019

A tissue-specific gene expression template portrays heart development and pathology

por Rodemoyer, Amy, Kibiryeva, Nataliya, Bair, Alexis, Marshall, Jennifer, O’Brien, James E, Bittel, Douglas C
Publicado 2014

Viability, yield and expansion capability of feline MSCs obtained from subcutaneous and reproductive organ adipose depots

por Wysong, Amy, Ortiz, Priscilla, Bittel, Douglas, Ott, Lindsey, Karanu, Francis, Filla, Michael, Stehno-Bittel, Lisa
Publicado 2021

The Role of scaRNAs in Adjusting Alternative mRNA Splicing in Heart Development

por Nagasawa, Chloe, Ogren, Allison, Kibiryeva, Nataliya, Marshall, Jennifer, O’Brien, James E., Kenmochi, Naoya, Bittel, Douglas C.
Publicado 2018

Gene expression in cardiac tissues from infants with idiopathic conotruncal defects

por Bittel, Douglas C, Butler, Merlin G, Kibiryeva, Nataliya, Marshall, Jennifer A, Chen, Jie, Lofland, Gary K, O'Brien, James E
Publicado 2011

Ultra High-Resolution Gene Centric Genomic Structural Analysis of a Non-Syndromic Congenital Heart Defect, Tetralogy of Fallot

por Bittel, Douglas C., Zhou, Xin-Gang, Kibiryeva, Nataliya, Fiedler, Stephanie, O’Brien, James E., Marshall, Jennifer, Yu, Shihui, Liu, Hong-Yu
Publicado 2014

microRNA Expression Levels Change in Neonatal Patients During and After Exposure to Cardiopulmonary Bypass

por Hsieh, Lance, Tu, Lan N., Paquette, Alison, Sheng, Quanhu, Zhao, Shilin, Bittel, Douglas, O’Brien, James, Vickers, Kasey, Pastuszko, Peter, Nigam, Vishal
Publicado 2022

Genetic Subtype Differences in Neural Circuitry of Food Motivation in Prader-Willi Syndrome

por Holsen, Laura M., Zarcone, Jennifer R., Chambers, Rebecca, Butler, Merlin G., Bittel, Douglas C., Brooks, William M., Thompson, Travis I., Savage, Cary R.
Publicado 2008

A Hypothesis for Using Pathway Genetic Load Analysis for Understanding Complex Outcomes in Bilirubin Encephalopathy

por Riordan, Sean M., Bittel, Douglas C., Le Pichon, Jean-Baptiste, Gazzin, Silvia, Tiribelli, Claudio, Watchko, Jon F., Wennberg, Richard P., Shapiro, Steven M.
Publicado 2016

Hyperactivity in the Gunn rat model of neonatal jaundice: age-related attenuation and emergence of gait deficits

por Stanford, John A., Shuler, Jeffrey M., Fowler, Stephen C., Stanford, Kimberly G., Ma, Delin, Bittel, Douglas C., Le Pichon, Jean-Baptiste, Shapiro, Steven M.
Publicado 2014

Shear stress associated with cardiopulmonary bypass induces expression of inflammatory cytokines and necroptosis in monocytes

por Tu, Lan N., Hsieh, Lance, Kajimoto, Masaki, Charette, Kevin, Kibiryeva, Nataliya, Forero, Adriana, Hampson, Sarah, Marshall, Jennifer A., O’Brien, James, Scatena, Marta, Portman, Michael A., Savan, Ram, Benner, Chris, Aliseda, Alberto, Nuri, Muhammad, Bittel, Douglas, Pastuszko, Peter, Nigam, Vishal
Publicado 2021

Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

por Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A.J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.
Publicado 2020

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome

por Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A. J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.
Publicado 2021