Loss of Omi mitochondrial protease activity causes the neuromuscular disorder of mnd2 mutant mice von Jones, Julie M., Datta, Pinaki, Srinivasula, Srinivasa M., Ji, Weizhen, Gupta, Sanjeev, Zhang, ZhiJia, Davies, Erika, Hajnóczky, György, Saunders, Thomas L., Van Keuren, Margaret L., Fernandes-Alnemri, Teresa, Meisler, Miriam H., Alnemri, Emad S.

Volltext

Generating transgenic mice from bacterial artificial chromosomes: transgenesis efficiency, integration and expression outcomes von Van Keuren, Margaret L, Gavrilina, Galina B, Filipiak, Wanda E, Zeidler, Michael G, Saunders, Thomas L

Volltext

Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line von Hughes, Elizabeth D, Qu, Yun Yan, Genik, Suzanne J, Lyons, Robert H, Pacheco, Christopher D, Lieberman, Andrew P, Samuelson, Linda C, Nasonkin, Igor O, Camper, Sally A, Van Keuren, Margaret L, Saunders, Thomas L

Volltext

A novel intergenic ETnII-β insertion mutation causes multiple malformations in polypodia mice von Lehoczky, Jessica A, Thomas, Peedikayil E, Patrie, Kevin M, Owens, Kailey M, Villarreal, Lisa M, Galbraith, Kenneth, Washburn, Joe, Johnson, Craig N, Gavino, Bryant, Borowsky, Alexander D, Millen, Kathleen J, Wakenight, Paul, Law, William, Van Keuren, Margaret L, Gavrilina, Galina, Hughes, Elizabeth D, Saunders, Thomas L, Brihn, Lesil, Nadeau, Joseph H, Innis, Jeffrey W

Volltext

Rederivation of transgenic and gene-targeted mice by embryo transfer von VAN KEUREN, Margaret L, SAUNDERS, Thomas L

Volltext

Amyloid $\beta $ Protein Gene: cDNA, mRNA Distribution, and Genetic Linkage near the Alzheimer Locus von Tanzi, Rudolph E., Gusella, James F., Watkins, Paul C., Gail A. P. Bruns, St George-Hyslop, Peter, Van Keuren, Margaret L., Patterson, David, Pagan, Susan, Kurnit, David M., Neve, Rachael L.

Volltext

A Novel Intergenic ETnII-[beta] Insertion Mutation Causes Multiple Malformations in Polypodia Mice: e1003967 von Lehoczky, Jessica A, Thomas, Peedikayil E, Patrie, Kevin M, Owens, Kailey M, Villarreal, Lisa M, Galbraith, Kenneth, Washburn, Joe, Johnson, Craig N, Gavino, Bryant, Borowsky, Alexander D, Millen, Kathleen J, Wakenight, Paul, Law, William, Keuren, Margaret LVan, Gavrilina, Galina, Hughes, Elizabeth D, Saunders, Thomas L, Brihn, Lesil, Nadeau, Joseph H, Innis, Jeffrey W

Volltext

Resistance to organophosphorus agent toxicity in transgenic mice expressing the G117H mutant of human butyrylcholinesterase von Wang, Yuxia, Ticu Boeck, Andreea, Duysen, Ellen G, Van Keuren, Margaret, Saunders, Thomas L, Lockridge, Oksana

Volltext

Isolation of human and murine homologues of the Drosophila minibrain gene : Human homologue maps to 21q22.2 in the Down syndrome critical region von SONG, W.-J, STERNBERG, L. R, KURNIT, D. M, KASTEN-SPORTES, C, VAN KEUREN, M. L, CHUNG, S.-H, SLACK, A. C, MILLER, D. E, GLOVER, T. W, CHIANG, P.-W, LOU, L

Volltext

Human chromosome 21-encoded cDNA clones von Neve, Rachael L, Stewart, Gordon D, Newcomb, Patricia, Van Keuren, Margaret L, Patterson, David, Drabkin, H.A, Kurnit, David M

Volltext

Isolation of Human and Murine Homologues of theDrosophilaMinibrain Gene: Human Homologue Maps to 21q22.2 in the Down Syndrome “Critical Region” von Song, Woo-Joo, Sternberg, Lawrence R., Kasten-Sportès, Carol, Keuren, Margaret L.Van, Chung, Sul-Hee, Slack, Alison C., Miller, Diane E., Glover, Thomas W., Chiang, Pei-Wen, Lou, Liandi, Kurnit, David M.

Volltext

Use of a fluorescent-PCR reaction to detect genomic sequence copy number and transcriptional abundance von Chiang, P W, Song, W J, Wu, K Y, Korenberg, J R, Fogel, E J, Van Keuren, M L, Lashkari, D, Kurnit, D M

Volltext

[30] Gel protein stains: Silver stain von Merril, Carl R., Goldman, David, Van Keuren, Margaret L.

Volltext

Protein Variations Associated with Down's Syndrome, Chromosome 21, and Alzheimer's Disease von VAN KEUREN, MARGARET L., GOLDMAN, DAVID, MERRIL, CARL R.

Volltext

Simplified silver protein detection and image enhancement methods in polyacrylamide gels von Merril, Carl R., Goldman, David, Van Keuren, Margaret L.

Volltext

Trace Polypeptides in Cellular Extracts and Human Body Fluids Detected by Two-Dimensional Electrophoresis and a Highly Sensitive Silver Stain von Merril, Carl R., Switzer, Robert C., Van Keuren, Margaret L.

Volltext

Identification and analysis of the human and murine putative chromatin structure regulator SUPT6H and Supt6h von CHIANG, P.-W, WANG, S, GLOVER, T. W, MILLER, D. E, TSAI, C.-H, BLACKBURN, C. C, CHEN, X.-N, SUN, Z, CHENG, J.-F, KORENBERG, J. R, KURNIT, D. M, SMITHIVAS, P, SONG, W.-J, RAMAMOORTHY, S, HILLMAN, J, PUETT, S, VAN KEUREN, M. L, CROMBEZ, E, KUMAR, A

Volltext

Molecular Mechanism in the Formation of a Human Ring Chromosome 21 von Wong, Corinne, Kazazian, Haig H., Stetten, Gail, Earnshaw, William C., Van Keuren, Margaret L., Antonarakis, Stylianos E.

Volltext

[17] Silver staining methods for polyacrylamide gel electrophoresis von Merril, Carl R., Goldman, David, Van Keuren, Margaret L.

Volltext

Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2 von BAUER, T. R, MCDERMID, H. E, BUDARF, M. L, VAN KEUREN, M. L, BLOMBERG, D. B

Volltext