检索结果 - Leppert, Mark

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