BAT-26 and BAT-40 Instability in Colorectal Adenomas and Carcinomas and Germline Polymorphisms

Por Samowitz, Wade S., Slattery, Martha L., Potter, John D., Leppert, Mark F.
Publicado em 1999

Linkage Analysis of Tourette Syndrome in a Large Utah Pedigree

Por Knight, Stacey, Coon, Hilary, Johnson, Michael, Leppert, Mark F, Camp, Nicola J, McMahon, William M
Publicado em 2010

Mapping Approaches to Gene Identification in Humans

Por White, Raymond L., Lalouel, Jean-Marc, Lathrop, G. Mark, Leppert, Mark F., Nakamura, Yusuke, O'Connell, Peter
Publicado em 1987

High-Sensitivity NanoLC—MS/MS Analysis of Urinary Desmosine and Isodesmosine

Por Boutin, Michel, Berthelette, Carl, Gervais, François G., Scholand, Mary-Beth, Hoidal, John, Leppert, Mark F., Bateman, Kevin P., Thibault, Pierre
Publicado em 2009

American Founder Mutation for Attenuated Familial Adenomatous Polyposis

Por Neklason, Deborah W., Stevens, Jeffery, Boucher, Kenneth M., Kerber, Richard A., Matsunami, Nori, Barlow, Jahn, Mineau, Geraldine, Leppert, Mark F., Burt, Randall W.
Publicado em 2007

Toward targeting B cell cancers with CD4(+) CTLs: identification of a CD19-encoded minor histocompatibility antigen using a novel genome-wide analysis

Por Spaapen, Robbert M., Lokhorst, Henk M., van den Oudenalder, Kelly, Otterud, Brith E., Dolstra, Harry, Leppert, Mark F., Minnema, Monique C., Bloem, Andries C., Mutis, Tuna
Publicado em 2008

Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer

Por Neklason, Deborah W, Tuohy, Therese M, Stevens, Jeffery, Otterud, Brith, Baird, Lisa, Kerber, Richard A, Samowitz, Wade S, Kuwada, Scott K, Leppert, Mark F, Burt, Randall W
Publicado em 2010

Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer

Por Neklason, Deborah W., Tuohy, Thérèse M., Stevens, Jeffery, Otterud, Brith, Baird, Lisa, Kerber, Richard A., Samowitz, Wade S., Kuwada, Scott K., Leppert, Mark F., Burt, Randall W.
Publicado em 2010

Mouse models of human KCNQ2 and KCNQ3 mutations for benign familial neonatal convulsions show seizures and neuronal plasticity without synaptic reorganization

Por Singh, Nanda A, Otto, James F, Jill Dahle, E, Pappas, Chris, Leslie, Jonathan D, Vilaythong, Alex, Noebels, Jeffrey L, Steve White, H, Wilcox, Karen S, Leppert, Mark F
Publicado em 2008

Leukemia-associated minor histocompatibility antigen discovery using T-cell clones isolated by in vitro stimulation of naive CD8(+) T cells

Por Bleakley, Marie, Otterud, Brith E., Richardt, Julia L., Mollerup, Audrey D., Hudecek, Michael, Nishida, Tetsuya, Chaney, Colette N., Warren, Edus H., Leppert, Mark F., Riddell, Stanley R.
Publicado em 2010

Exome Analysis of a Family with Pleiotropic Congenital Heart Disease

Por Arrington, Cammon B., Bleyl, Steven B., Matsunami, Norisada, Bonnell, Gabriel D., Otterud, Brith E.M., Nielsen, Douglas C., Stevens, Jeffrey, Levy, Shawn, Leppert, Mark F., Bowles, Neil E.
Publicado em 2012

The 5q31 variants associated with psoriasis and Crohn's disease are distinct

Por Li, Yonghong, Chang, Monica, Schrodi, Steven J., Callis-Duffin, Kristina P., Matsunami, Nori, Civello, Daniel, Bui, Nam, Catanese, Joseph J., Leppert, Mark F., Krueger, Gerald G., Begovich, Ann B.
Publicado em 2008

Rapid Molecular Analysis of the STAT3 Gene in Job Syndrome of Hyper-IgE and Recurrent Infectious Diseases

Por Kumánovics, Attila, Wittwer, Carl T., Pryor, Robert J., Augustine, Nancy H., Leppert, Mark F., Carey, John C., Ochs, Hans D., Wedgwood, Ralph J., Faville, Ralph J., Quie, Paul G., Hill, Harry R.
Publicado em 2010

Hereditary Hyperparathyroidism–Jaw Tumor Syndrome: The Endocrine Tumor Gene HRPT2 Maps to Chromosome 1q21-q31

Por Szabó, József, Heath, Brett, Hill, Virginia M., Jackson, Charles E., Zarbo, Richard J., Mallette, Lawrence E., Chew, Shern L., Besser, Gordon M., Thakker, Rajesh V., Huff, Vicki, Leppert, Mark F., Heath, Hunter
Publicado em 1995

Polymorphisms in the Nonmuscle Myosin Heavy Chain 9 Gene (MYH9) Are Associated with Albuminuria in Hypertensive African Americans: The HyperGEN Study

Por Freedman, Barry I., Kopp, Jeffrey B., Winkler, Cheryl A., Nelson, George W., Rao, D.C., Eckfeldt, John H., Leppert, Mark F., Hicks, Pamela J., Divers, Jasmin, Langefeld, Carl D., Hunt, Steven C.
Publicado em 2009

Inverse Relationship between Microsatellite Instability and K-ras and p53 Gene Alterations in Colon Cancer

Por Samowitz, Wade S., Holden, Joseph A., Curtin, Karen, Edwards, Sandra L., Walker, Adrianne R., Lin, Heather A., Robertson, Margaret A., Nichols, Melanie F., Gruenthal, Kristin M., Lynch, Beverly J., Leppert, Mark F., Slattery, Martha L.
Publicado em 2001

A Role of SCN9A in Human Epilepsies, As a Cause of Febrile Seizures and As a Potential Modifier of Dravet Syndrome

Por Singh, Nanda A., Pappas, Chris, Dahle, E. Jill, Claes, Lieve R. F., Pruess, Timothy H., De Jonghe, Peter, Thompson, Joel, Dixon, Missy, Gurnett, Christina, Peiffer, Andy, White, H. Steve, Filloux, Francis, Leppert, Mark F.
Publicado em 2009

Carriers of rare missense variants in IFIH1 are protected from psoriasis

Por Li, Yonghong, Liao, Wilson, Cargill, Michele, Chang, Monica, Matsunami, Nori, Feng, Bingjian, Poon, Annie, Duffin, Kristina Callis, Catanese, Joseph J., Bowcock, Ann M., Leppert, Mark F., Kwok, Pui-Yan, Krueger, Gerald G., Begovich, Ann B.
Publicado em 2010

Colonic Adenoma Risk in Familial Colorectal Cancer – a Study of Six Extended Kindreds

Por Neklason, Deborah W., Thorpe, Brett L., Ferrandez, Angel, Tumbapura, Anil, Boucher, Kenneth, Garibotti, Gilda, Kerber, Richard A., Solomon, Cindy H., Samowitz, Wade S., Fang, John C., Mineau, Geraldine P., Leppert, Mark F., Burt, Randall W., Kuwada, Scott K.
Publicado em 2008

Further Genetic Evidence for Three Psoriasis-Risk Genes: ADAM33, CDKAL1, and PTPN22

Por Li, Yonghong, Liao, Wilson, Chang, Monica, Schrodi, Steven J., Bui, Nam, Catanese, Joseph J., Poon, Annie, Matsunami, Nori, Callis-Duffin, Kristina P., Leppert, Mark F., Bowcock, Anne M., Kwok, Pui-Yan, Krueger, Gerald G., Begovich, Ann B.
Publicado em 2008