Search Results - Leppert, Mark

BAT-26 and BAT-40 Instability in Colorectal Adenomas and Carcinomas and Germline Polymorphisms by Samowitz, Wade S., Slattery, Martha L., Potter, John D., Leppert, Mark F.

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Human Imprinted Chromosomal Regions Are Historical Hot-Spots of Recombination by Sandovici, Ionel, Kassovska-Bratinova, Sacha, Vaughan, Joe E, Stewart, Rae, Leppert, Mark, Sapienza, Carmen

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D7S449 detects a HindIII polymorphism tightly linked to the MET gene on chromosome 7 by Dean, Michael, Stewart, Claudia, Perry, Anjanette, Stauffer, Dora, Otterud, Brith, White, Ray, Leppert, Mark

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Linkage Analysis of Tourette Syndrome in a Large Utah Pedigree by Knight, Stacey, Coon, Hilary, Johnson, Michael, Leppert, Mark F, Camp, Nicola J, McMahon, William M

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Mapping Approaches to Gene Identification in Humans by White, Raymond L., Lalouel, Jean-Marc, Lathrop, G. Mark, Leppert, Mark F., Nakamura, Yusuke, O'Connell, Peter

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A Rare Variant in CACNA1D Segregates with 7 Bipolar I Disorder Cases in a Large Pedigree by Ross, Jessica, Gedvilaite, Erika, Badner, Judith A., Erdman, Carolyn, Baird, Lisa, Matsunami, Nori, Leppert, Mark, Xing, Jinchuan, Byerley, William

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High-Sensitivity NanoLC—MS/MS Analysis of Urinary Desmosine and Isodesmosine by Boutin, Michel, Berthelette, Carl, Gervais, François G., Scholand, Mary-Beth, Hoidal, John, Leppert, Mark F., Bateman, Kevin P., Thibault, Pierre

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Delineation of the Critical Interval of Bardet-Biedl Syndrome 1 (BBS1) to a Small Region of 11q13, through Linkage and Haplotype Analysis of 91 Pedigrees by Katsanis, Nicholas, Lewis, Richard A., Stockton, David W., Mai, Phuong M. T., Baird, Lisa, Beales, Philip L., Leppert, Mark, Lupski, James R.

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Quantitative-Trait Loci Influencing Body-Mass Index Reside on Chromosomes 7 and 13: The National Heart, Lung, and Blood Institute Family Heart Study by Feitosa, Mary F., Borecki, Ingrid B., Rich, Stephen S., Arnett, Donna K., Sholinsky, Phyliss, Myers, Richard H., Leppert, Mark, Province, Michael A.

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A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis by Jurynec, Michael J, Sawitzke, Allen D, Beals, Timothy C, Redd, Michael J, Stevens, Jeff, Otterud, Brith, Leppert, Mark F, Grunwald, David Jonah

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A hyperactivating proinflammatory RIPK2 allele associated with early-onset osteoarthritis by Jurynec, Michael J, Sawitzke, Allen D, Beals, Timothy C, Redd, Michael J, Stevens, Jeff, Otterud, Brith, Leppert, Mark F, Grunwald, David Jonah

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Ethnicity and Human Genetic Linkage Maps by Jorgenson, Eric, Tang, Hua, Gadde, Maya, Province, Mike, Leppert, Mark, Kardia, Sharon, Schork, Nicholas, Cooper, Richard, Rao, D. C., Boerwinkle, Eric, Risch, Neil

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American Founder Mutation for Attenuated Familial Adenomatous Polyposis by Neklason, Deborah W., Stevens, Jeffery, Boucher, Kenneth M., Kerber, Richard A., Matsunami, Nori, Barlow, Jahn, Mineau, Geraldine, Leppert, Mark F., Burt, Randall W.

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Mutational analysis of patients with adenomatous polyposis: Identical inactivating mutations in unrelated individuals by Groden, Joanna, Gelbert, Lawrence, Thliveris, Andrew, Nelson, Lesa, Robertson, Margaret, Joslyn, Geoff, Samowitz, Wade, Spirio, Lisa, Carlson, Mary, Burt, Randall, Leppert, Mark, White, Ray

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Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus by Spirio, Lisa, Otterud, Brith, Stauffer, Dora, Lynch, Henry, Lynch, Patrick, Watson, Patrice, Lanspa, Steven, Smyrk, Thomas, Cavalieri, Jennifer, Howard, Linda, Burt, Randall, White, Ray, Leppert, Mark

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Further linkage data on cystic fibrosis: The utah study by White, Ray, Leppert, Mark, O'Connell, Peter, Nakamura, Yusuke, Woodward, Scott, Hoff, Mark, Herbst, John, Dean, Michael, Woude, George Vande, Lathrop, G. Mark, Lalouel, Jean-Marc

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

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

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

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

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