Fem1b promotes ubiquitylation and suppresses transcriptional activity of Gli1

nork Gilder, Andrew S., Chen, Yong-Bin, Jackson, Ramon J., Jiang, Jin, Maher, Joseph F.
Argitaratua izan da Biochem Biophys Res Commun (2013)

Abnormal Glucose Homeostasis and Pancreatic Islet Function in Mice with Inactivation of the Fem1b Gene

nork Lu, Deyin, Ventura-Holman, Tereza, Li, Jing, McMurray, Robert W., Subauste, Jose S., Maher, Joseph F.
Argitaratua 2005

Clustering of sebaceous gland carcinoma, papillary thyroid carcinoma and breast cancer in a woman as a new cancer susceptibility disorder: a case report

nork Newman, Brian D, Maher, Joseph F, Subauste, Jose S, Uwaifo, Gabriel I, Bigler, Steven A, Koch, Christian A
Argitaratua 2009

HMG-I/Y, a New c-Myc Target Gene and Potential Oncogene

nork Wood, Lisa J., Mukherjee, Mita, Dolde, Christine E., Xu, Yi, Maher, Joseph F., Bunton, Tracie E., Williams, John B., Resar, Linda M. S.
Argitaratua 2000

Gene-environment interaction between SCN5A-1103Y and hypokalemia influences QT interval prolongation in African Americans: The Jackson Heart Study

nork Akylbekova, Ermeg L., Payne, John P., Newton-Cheh, Christopher, May, Warren L., Fox, Ervin R., Wilson, James G., Sarpong, Daniel F., Taylor, Herman A., Maher, Joseph F.
Argitaratua 2013

Resting Heart Rate and Long-Term Outcomes Among African Americans: Insights From the Jackson Heart Study

nork Parikh, Kishan S., Greiner, Melissa A., Suzuki, Takeki, DeVore, Adam D., Blackshear, Chad, Maher, Joseph F., Curtis, Lesley H., Hernandez, Adrian F., O’Brien, Emily C., Mentz, Robert J.
Argitaratua izan da JAMA Cardiol (2017)

De Novo ACTA2 Mutation Causes a Novel Syndrome of Multisystemic Smooth Muscle Dysfunction

nork Milewicz, Dianna M., Østergaard, John R., Ala-Kokko, Leena M., Khan, Nadia, Grange, Dorothy K., Mendoza-Londono, Roberto, Bradley, Timothy J., Olney, Ann Haskins, Adès, Lesley, Maher, Joseph F., Guo, Dongchuan, Buja, L. Maximilian, Kim, Dong, Hyland, James C., Regalado, Ellen S.
Argitaratua 2010

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

nork Evans, Daniel S., Avery, Christy L., Nalls, Mike A., Li, Guo, Barnard, John, Smith, Erin N., Tanaka, Toshiko, Butler, Anne M., Buxbaum, Sarah G., Alonso, Alvaro, Arking, Dan E., Berenson, Gerald S., Bis, Joshua C., Buyske, Steven, Carty, Cara L., Chen, Wei, Chung, Mina K., Cummings, Steven R., Deo, Rajat, Eaton, Charles B., Fox, Ervin R., Heckbert, Susan R., Heiss, Gerardo, Hindorff, Lucia A., Hsueh, Wen-Chi, Isaacs, Aaron, Jamshidi, Yalda, Kerr, Kathleen F., Liu, Felix, Liu, Yongmei, Lohman, Kurt K., Magnani, Jared W., Maher, Joseph F., Mehra, Reena, Meng, Yan A., Musani, Solomon K., Newton-Cheh, Christopher, North, Kari E., Psaty, Bruce M., Redline, Susan, Rotter, Jerome I., Schnabel, Renate B., Schork, Nicholas J., Shohet, Ralph V., Singleton, Andrew B., Smith, Jonathan D., Soliman, Elsayed Z., Srinivasan, Sathanur R., Taylor, Herman A., Van Wagoner, David R., Wilson, James G., Young, Taylor, Zhang, Zhu-Ming, Zonderman, Alan B., Evans, Michele K., Ferrucci, Luigi, Murray, Sarah S., Tranah, Gregory J., Whitsel, Eric A., Reiner, Alex P., Sotoodehnia, Nona
Argitaratua izan da Hum Mol Genet (2016)