Torthaí cuardaigh - Sweetser, David

Sympathoadrenal Hyperplasia Causes Renal Malformations in Ret(MEN2B)-Transgenic Mice de réir Gestblom, Carolina, Sweetser, David A., Doggett, Barbara, Kapur, Raj P.

Faigh an téacs iomlán Faigh an téacs iomlán

Training the Future Leaders in Personalized Medicine de réir Mason-Suares, Heather, Sweetser, David A., Lindeman, Neal I., Morton, Cynthia C.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

TLE4 regulation of wnt-mediated inflammation underlies its role as a tumor suppressor in myeloid leukemia de réir Shin, Thomas H., Brynczka, Christopher, Dayyani, Farshid, Rivera, Miguel N., Sweetser, David A.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

IQSEC2 and X-linked Syndromal Intellectual Disability de réir Alexander-Bloch, Aaron F., McDougle, Christopher J., Ullman, Zhanna, Sweetser, David A.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Discovering chemical modifiers of oncogene-regulated hematopoietic differentiation de réir Yeh, Jing-Ruey J., Munson, Kathleen M., Elagib, Kamaleldin E., Goldfarb, Adam N., Sweetser, David A., Peterson, Randall T.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

TLE4 Is a Critical Mediator of Osteoblast and Runx2-Dependent Bone Development de réir Shin, Thomas H., Theodorou, Evangelos, Holland, Carl, Yamin, Rae’e, Raggio, Cathleen L., Giampietro, Philip F., Sweetser, David A.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

The Corepressor Tle4 Is a Novel Regulator of Murine Hematopoiesis and Bone Development de réir Wheat, Justin C., Krause, Daniela S., Shin, Thomas H., Chen, Xi, Wang, Jianfeng, Ding, Dacheng, Yamin, Rae’e, Sweetser, David A.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Novel compound heterozygous mutations expand the recognized phenotypes of FARS2-linked disease de réir Walker, Melissa A., Mohler, Kyle P., Hopkins, Kyle W., Oakley, Derek H., Sweetser, David A., Ibba, Michael, Frosch, Matthew P., Thibert, Ronald L.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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 de réir 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.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Tle corepressors are differentially partitioned to instruct CD8(+) T cell lineage choice and identity de réir Xing, Shaojun, Shao, Peng, Li, Fengyin, Zhao, Xudong, Seo, Wooseok, Wheat, Justin C., Ramasamy, Selvi, Wang, Jianfeng, Li, Xiang, Peng, Weiqun, Yu, Shuyang, Liu, Chengyu, Taniuchi, Ichiro, Sweetser, David A., Xue, Hai-Hui

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene TCF4 de réir Hennig, Krista M., Fass, Daniel M., Zhao, Wen-Ning, Sheridan, Steven D., Fu, Ting, Erdin, Serkan, Stortchevoi, Alexei, Lucente, Diane, Cody, Jannine D., Sweetser, David, Gusella, James F., Talkowski, Michael E., Haggarty, Stephen J.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment de réir Dutta, Debdeep, Briere, Lauren C, Kanca, Oguz, Marcogliese, Paul C, Walker, Melissa A, High, Frances A, Vanderver, Adeline, Krier, Joel, Carmichael, Nikkola, Callahan, Christine, Taft, Ryan J, Simons, Cas, Helman, Guy, Network, Undiagnosed Diseases, Wangler, Michael F, Yamamoto, Shinya, Sweetser, David A, Bellen, Hugo J

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

Missense variants in CTNNB1 can be associated with vitreoretinopathy—Seven new cases of CTNNB1‐associated neurodevelopmental disorder including a previously unreported retinal phen... de réir Rossetti, Linda Z., Bekheirnia, Mir Reza, Lewis, Andrea M., Mefford, Heather C., Golden‐Grant, Katie, Tarczy‐Hornoch, Kristina, Briere, Lauren C., Sweetser, David A., Walker, Melissa A., Kravets, Elijah, Stevenson, David A., Bruenner, Georgette, Sebastian, Jessica, Knapo, Julia, Rosenfeld, Jill A., Marcogliese, Paul C., Wangler, Michael F.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy de réir Briere, Lauren C., Walker, Melissa A., High, Frances A., Cooper, Cynthia, Rogers, Cassandra A., Callahan, Christine J., Ishimura, Ryosuke, Ichimura, Yoshinobu, Caruso, Paul A., Sharma, Nutan, Brokamp, Elly, Koziura, Mary E., Mohammad, Shekeeb S., Dale, Russell C., Riley, Lisa G., Phillips, John A., Komatsu, Masaaki, Sweetser, David A.

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán

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

Faigh an téacs iomlán Faigh an téacs iomlán Faigh an téacs iomlán