Sympathoadrenal Hyperplasia Causes Renal Malformations in Ret(MEN2B)-Transgenic Mice

Por Gestblom, Carolina, Sweetser, David A., Doggett, Barbara, Kapur, Raj P.
Publicado em 1999

Training the Future Leaders in Personalized Medicine

Por Mason-Suares, Heather, Sweetser, David A., Lindeman, Neal I., Morton, Cynthia C.
Publicado no J Pers Med (2016)

TLE4 regulation of wnt-mediated inflammation underlies its role as a tumor suppressor in myeloid leukemia

Por Shin, Thomas H., Brynczka, Christopher, Dayyani, Farshid, Rivera, Miguel N., Sweetser, David A.
Publicado no Leuk Res (2016)

Discovering chemical modifiers of oncogene-regulated hematopoietic differentiation

Por Yeh, Jing-Ruey J., Munson, Kathleen M., Elagib, Kamaleldin E., Goldfarb, Adam N., Sweetser, David A., Peterson, Randall T.
Publicado em 2009

The Corepressor Tle4 Is a Novel Regulator of Murine Hematopoiesis and Bone Development

Por Wheat, Justin C., Krause, Daniela S., Shin, Thomas H., Chen, Xi, Wang, Jianfeng, Ding, Dacheng, Yamin, Rae’e, Sweetser, David A.
Publicado em 2014

Novel compound heterozygous mutations expand the recognized phenotypes of FARS2-linked disease

Por Walker, Melissa A., Mohler, Kyle P., Hopkins, Kyle W., Oakley, Derek H., Sweetser, David A., Ibba, Michael, Frosch, Matthew P., Thibert, Ronald L.
Publicado no J Child Neurol (2016)

Loss of TLE1 and TLE4 from the del(9q) commonly deleted region in AML cooperates with AML1-ETO to affect myeloid cell proliferation and survival

Por Dayyani, Farshid, Wang, Jianfeng, Yeh, Jing-Ruey J., Ahn, Eun-Young, Tobey, Erica, Zhang, Dong-Er, Bernstein, Irwin D., Peterson, Randall T., Sweetser, David A.
Publicado em 2008

FLT3 internal tandem duplication in CD34(+)/CD33(-) precursors predicts poor outcome in acute myeloid leukemia

Por Pollard, Jessica A., Alonzo, Todd A., Gerbing, Robert B., Woods, William G., Lange, Beverly J., Sweetser, David A., Radich, Jerald P., Bernstein, Irwin D., Meshinchi, Soheil
Publicado em 2006

AML1-ETO mediates hematopoietic self-renewal and leukemogenesis through a COX/β-catenin signaling pathway

Por Zhang, Yiyun, Wang, Jianfeng, Wheat, Justin, Chen, Xi, Jin, Shan, Sadrzadeh, Hossein, Fathi, Amir T., Peterson, Randall T., Kung, Andrew L., Sweetser, David A., Yeh, Jing-Ruey Joanna
Publicado em 2013

Tle1 tumor suppressor negatively regulates inflammation in vivo and modulates NF-κB inflammatory pathway

Por Ramasamy, Selvi, Saez, Borja, Mukhopadhyay, Subhankar, Ding, Daching, Ahmed, Alwiya M., Chen, Xi, Pucci, Ferdinando, Yamin, Rae’e, Wang, Jianfeng, Pittet, Mikael J., Kelleher, Cassandra M., Scadden, David T., Sweetser, David A.
Publicado no Proc Natl Acad Sci U S A (2016)

Mutations in the neutral sphingomyelinase gene SMPD3 implicate the ceramide pathway in human leukemias

Por Kim, Woo Jae, Okimoto, Ross A., Purton, Louise E., Goodwin, Meagan, Haserlat, Sara M., Dayyani, Farshid, Sweetser, David A., McClatchey, Andrea I., Bernard, Olivier A., Look, A. Thomas, Bell, Daphne W., Scadden, David T., Haber, Daniel A.
Publicado em 2008

De novo missense variants in HECW2 are associated with neurodevelopmental delay and hypotonia

Por Berko, Esther R, Cho, Megan T, Eng, Christine, Shao, Yunru, Sweetser, David A, Waxler, Jessica, Robin, Nathaniel H, Brewer, Fallon, Donkervoort, Sandra, Mohassel, Payam, Bönnemann, Carsten G, Bialer, Martin, Moore, Christine, Wolfe, Lynne A, Tifft, Cynthia J, Shen, Yufeng, Retterer, Kyle, Millan, Francisca, Chung, Wendy K
Publicado no J Med Genet (2016)

Panel-based Genetic Diagnostic Testing for Inherited Eye Diseases is Highly Accurate and Reproducible and More Sensitive for Variant Detection Than Exome Sequencing

Por Consugar, Mark B., Navarro-Gomez, Daniel, Place, Emily M., Bujakowska, Kinga M., Sousa, Maria E., Fonseca-Kelly, Zoë D., Taub, Daniel G., Janessian, Maria, Wang, Dan Yi, Au, Elizabeth D., Sims, Katherine B., Sweetser, David A., Fulton, Anne B., Liu, Qin, Wiggs, Janey L., Gai, Xiaowu, Pierce, Eric A.
Publicado no Genet Med (2014)

Health Care Infrastructure for Financially Sustainable Clinical Genomics

Por Lennerz, Jochen K., McLaughlin, Heather M., Baron, Jason M., Rasmussen, David, Sumbada Shin, Meini, Berners-Lee, Nancy, Miller Batten, Julie, Swoboda, Kathryn J., Gala, Manish K., Winter, Harland S., Schmahmann, Jeremy D., Sweetser, David A., Boswell, Marianne, Pacula, Maciej, Stenzinger, Albrecht, Le, Long P., Hynes, William, Rehm, Heidi L., Klibanski, Anne, Black-Schaffer, Stephen W., Golden, Jeffrey A., Louis, David N., Weiss, Scott T., Iafrate, A. John
Publicado no J Mol Diagn (2016)