Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sukeshi Vaishnav"'
Autor:
Sukeshi Vaishnav, Charles T. Caskey, Peter B. Jones, Maki Wakamiya, Robert S. Geske, Allan Bradley, Xiangwei Wu, Charles A. Montgomery
Publikováno v:
Proceedings of the National Academy of Sciences. 91:742-746
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 certain other primates. The loss of urate oxidase in the human during primate evolution pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fd19215fcfacbd4099acfbbc49d30f2
https://doi.org/10.1073/pnas.91.2.742
https://doi.org/10.1073/pnas.91.2.742
Autor:
Cheng Chi Lee, Qiu Li, Binhai Zheng, Allan Bradley, Weiqin Lu, Zhong Sheng Sun, Urs Albrecht, Gregor Eichele, Sukeshi Vaishnav, Krista Kaasik, Marijke Sage
Publikováno v:
Cell
Mice carrying a null mutation in the Period 1 (mPer1) gene were generated using embryonic stem cell technology. Homozygous mPer1 mutants display a shorter circadian period with reduced precision and stability. Mice deficient in both mPer1 and mPer2 d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f178a8b1906f799c0f226d18e4122fde
https://pubmed.ncbi.nlm.nih.gov/11389837
https://pubmed.ncbi.nlm.nih.gov/11389837
Autor:
Charles A. Montgomery, Michael R. Blackburn, John W. Belmont, Maki Wakamiya, C. Thomas Caskey, Sukeshi Vaishnav, Roland Jurecic, Mark J. McArthur, Rodney E. Kellems, Robert S. Geske, Kohnosuke Mitani, Allan Bradley, Milton J. Finegold, Joiner Cartwright
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 fetuses exhibited hepatocellular impairment and died perinatally. Their lymphoid tissues were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6ef9da007fe1733674b20f075daf063
https://europepmc.org/articles/PMC42023/
https://europepmc.org/articles/PMC42023/
Publikováno v:
Nucleic Acids Research. 32:e161-e161
Genetic ablation experiments are used to resolve problems regarding cell lineages and the in vivo function of certain groups of cells. We describe a two-component conditional ablation technology using a mouse carrying an X-linked puDeltatk transgene,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6759490469ecb016eb4cabd766ea0078
https://doi.org/10.1093/nar/gnh158
https://doi.org/10.1093/nar/gnh158
Autor:
Charles T. Caskey, K. Wager-Smith, Sukeshi Vaishnav, J. Henkel-Tigges, T. Y. Tsao, S. M. W. Chang
Publikováno v:
Molecular and Cellular Biology. 7:854-863
Defective ecotropic and amphotropic retroviral vectors containing the cDNA for human hypoxanthine phosphoribosyltransferase (HPRT) were developed for efficient gene transfer and high-level cellular expression of HPRT. Helper cell clones which produce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9515045453fae2863fcdcba6d9ec872a
https://doi.org/10.1128/mcb.7.2.854-863.1987
https://doi.org/10.1128/mcb.7.2.854-863.1987