Search Results - "Vaishnav, Sukeshi"

Nonredundant Roles of the mPer1 and mPer2 Genes in the Mammalian Circadian Clock by Zheng, Binhai, Albrecht, Urs, Kaasik, Krista, Sage, Marijke, Lu, Weiqin, Vaishnav, Sukeshi, Li, Qiu, Sun, Zhong Sheng, Eichele, Gregor, Bradley, Allan, Lee, Cheng Chi

“…Mice carrying a null mutation in the Period 1 ( mPer1) gene were generated using embryonic stem cell technology. Homozygous mPer1 mutants display a shorter…”
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Bigenic Cre/loxP, puDeltatk conditional genetic ablation by Chen, You-Tzung, Levasseur, Regis, Vaishnav, Sukeshi, Karsenty, Gerard, Bradley, Allan

“…Genetic ablation experiments are used to resolve problems regarding cell lineages and the in vivo function of certain groups of cells. We describe a…”
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Bigenic Cre/loxP, pu tk conditional genetic ablation by Chen, You-Tzung, Levasseur, Regis, Vaishnav, Sukeshi, Karsenty, Gerard, Bradley, Allan

“…Genetic ablation experiments are used to resolve problems regarding cell lineages and the in vivo function of certain groups of cells. We describe a…”
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Hyperuricemia and urate nephropathy in urate oxidase-deficient mice by Wu, X, Wakamiya, M, Vaishnav, S, Geske, R, Montgomery, C. Jr, Jones, P, Bradley, A, Caskey, C.T

“…Urate oxidase, or uricase (EC 1.7.3.3), is a purine metabolic enzyme that catalyzes the conversion of uric acid to allantoin in most mammals except humans and…”
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Bigenic Cre/loxP, puΔtk conditional genetic ablation by Chen, You-Tzung, Levasseur, Regis, Vaishnav, Sukeshi, Karsenty, Gerard, Bradley, Allan

“…Genetic ablation experiments are used to resolve problems regarding cell lineages and the in vivo function of certain groups of cells. We describe a…”
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Disruption of the Adenosine Deaminase Gene Causes Hepatocellular Impairment and Perinatal Lethality in Mice by Wakamiya, Maki, Blackburn, Michael R., Jurecic, Roland, McArthur, Mark J., Geske, Robert S., Cartwright, Joiner, Mitani, Kohnosuke, Vaishnav, Sukeshi, Belmont, John W., Kellems, Rodney E., Finegold, Milton J., Montgomery, Charles A., Bradley, Allan, Caskey, C. Thomas

“…We have generated mice with a null mutation at the Ada locus, which encodes the purine catabolic enzyme adenosine deaminase (ADA, EC 3.5.4.4). ADA-deficient…”
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Instability of the Expanded (CTG)nRepeats in the Myotonin Protein Kinase Gene in Cultured Lymphoblastoid Cell Lines from Patients with Myotonic Dystrophy by Ashizawa, Tetsuo, Monckton, Darren G., Vaishnav, Sukeshi, Patel, Bhavna J., Voskova, Alica, Caskey, C.Thomas

“…The mutation associated with myotonic dystrophy (DM) is the expansion of an unstable trinucleotide repeat, (CTG)n, in the 3′-untranslated region of the…”
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Construction of a defective retrovirus containing the human hypoxanthine phosphoribosyltransferase cDNA and its expression in cultured cells and mouse bone marrow by S M Chang, K Wager-Smith, T Y Tsao, J Henkel-Tigges, S Vaishnav, C T Caskey

“…Article Usage Stats Services MCB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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Construction of a Defective Retrovirus Containing the Human Hypoxanthine Phosphoribosyltransferase cDNA and its Expression in Cultured Cells and Mouse Bone Marrow by Chang, Stephen M. W., Wager-Smith, Karen, Tsao, Twee Y., Henkel-Tigges, J., Vaishnav, Sukeshi, Caskey, C. T.

“…Defective ecotropic and amphotropic retroviral vectors containing the cDNA for human hypoxanthine phosphoribosyltransferase (HPRT) were developed for efficient…”
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