Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Thomas J Fielder"'
Autor:
Elyse K Paterson, Thomas J Fielder, Grant R MacGregor, Shosuke Ito, Kazumasa Wakamatsu, Daniel L Gillen, Victoria Eby, Raymond E Boissy, Anand K Ganesan
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0143702 (2015)
The mechanisms that lead to variation in human skin and hair color are not fully understood. To better understand the molecular control of skin and hair color variation, we modulated the expression of Tyrosinase (Tyr), which controls the rate-limitin
Externí odkaz:
https://doaj.org/article/f686141cdd10446dbe864532116f42bf
Autor:
Victoria Eby, Kazumasa Wakamatsu, Thomas J. Fielder, Anand K. Ganesan, Daniel L. Gillen, Grant R. MacGregor, Shosuke Ito, Raymond E. Boissy, Elyse K. Paterson
Publikováno v:
Paterson, EK; Fielder, TJ; MacGregor, GR; Ito, S; Wakamatsu, K; Gillen, DL; et al.(2015). Tyrosinase Depletion Prevents the Maturation of Melanosomes in the Mouse Hair Follicle. PLOS ONE, 10(11). doi: 10.1371/journal.pone.0143702. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3k80t4w2
PLoS ONE, Vol 10, Iss 11, p e0143702 (2015)
PloS one, vol 10, iss 11
PLoS ONE
PLoS ONE, Vol 10, Iss 11, p e0143702 (2015)
PloS one, vol 10, iss 11
PLoS ONE
The mechanisms that lead to variation in human skin and hair color are not fully understood. To better understand the molecular control of skin and hair color variation, we modulated the expression of Tyrosinase (Tyr), which controls the rate-limitin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f335adc872654d80da9f17bd7299ff5a
http://www.escholarship.org/uc/item/3k80t4w2
http://www.escholarship.org/uc/item/3k80t4w2
Autor:
Douglas C. Wallace, Shuling Wang, Kai-Xuan Shi, Charles S. Yi, Hsiao-Wen Chen, Katrina G. Waymire, Juliet Masumi, Grant R. MacGregor, Thomas J. Fielder
To identify ways to improve the efficiency of generating chimeric mice via microinjection of blastocysts with ES cells, we compared production and performance of ES-cell derived chimeric mice using blastocysts from two closely related and commonly us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3384a9c8f405f5af07b2174d8a3bab24
https://europepmc.org/articles/PMC3445772/
https://europepmc.org/articles/PMC3445772/
Autor:
Rita Shiang, Thomas J. Fielder, Maureen Bocian, Ya-Zhen Zhu, Leslie M. Thompson, Sara T. Winokur, Deanna M. Church, John J. Wasmuth
Publikováno v:
Cell. 78:335-342
Achondroplasia (ACH) is the most common genetic form of dwarfism. This disorder is inherited as an autosomal dominant trait, although the majority of cases are sporadic. A gene for ACH was recently localized to 4p16.3 by linkage analyses. The ACH can
Autor:
Lisa A. McConnachie, Ulrike Luderer, Yvonne D. Hoang, Terrance J. Kavanagh, Thomas J. Fielder, Jinhwan Lim, Brooke N. Nakamura
Publikováno v:
Nakamura, BN; Fielder, TJ; Hoang, YD; Lim, J; McConnachie, LA; Kavanagh, TJ; et al.(2011). Lack of maternal glutamate cysteine ligase modifier subunit (Gclm) decreases oocyte glutathione concentrations and disrupts preimplantation development in mice. Endocrinology, 152(7), 2806-2815. doi: 10.1210/en.2011-0207. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/3443c48z
Glutathione (GSH) is the most abundant intracellular thiol and an important regulator of cellular redox status. Mice that lack the modifier subunit of glutamate cysteine ligase (Gclm), the rate-limiting enzyme in GSH synthesis, have decreased GSH syn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1273c253d5d452cffa62a95a0ff40704
http://www.escholarship.org/uc/item/3443c48z
http://www.escholarship.org/uc/item/3443c48z
Autor:
Lluis Montoliu, Thomas J. Fielder
Publikováno v:
Springer Protocols Handbooks ISBN: 9783642207914
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56b2c1a3935e38f22526919fc0c96102
https://doi.org/10.1007/978-3-662-45763-4_5
https://doi.org/10.1007/978-3-662-45763-4_5
Autor:
Glenn Barnes, James F. Gusella, Francis S. Collins, Annemarie Poustka, S. Youngman, Sarah Baxendale, Duncan Shaw, Richard H. Myers, John Valdes, Barbara Jenkins, Marcy E. MacDonald, Karen M. Draths, Sherryl A.M. Taylor, Gillian P. Bates, Lucio H. Castilla, Alan Buckler, Thomas J. Fielder, John J. Wasmuth, Carol Lin, Lakshmi Srinidhi, Nicole A. Datson, Mabel P. Duyao, Christine Ambrose, Susan F. Kirby, Michael R. Altherr, Manju Swaroop, Peter S. Harper, Zdenek Sedlacek, Marc W. Allard, Mike North, Russell G. Snell, Rita Shiang, David E. Housman, Lawrence W. Elmer, Marianne James, Richard Mott, Kathleen Gillespie, Leslie M. Thompson, Laura Riba-Ramirez, Nancy S. Wexler, Deanna M. Church, Günther Zehetner, Scott A. Strobel, Heather MacFarlane, Anna-Maria Frischauf, Mary Anne Anderson, Hans Lehrach, Michael Conlon O'Donovan, Vincent P. Stanton, Kris Blanchard, Danilo A. Tagle, Lynn Doucette-Stamm, Holger Hummerich, Tracey Holloway, Manish A. Shah, Jennifer L. Wales, Nicolet Groot, Peter B. Dervan
Publikováno v:
Cell. 72:971-983
The Huntington's disease (HD) gene has been mapped in 4p16.3 but has eluded identification. We have used haplotype analysis of linkage disequilibrium to spotlight a small segment of 4p16.3 as the likely location of the defect. A new gene, 1715, isola
Publikováno v:
Transgenic research. 19(4)
The generation of transgenic mice by microinjection of DNA into the pronuclei of fertilized oocytes was described in the early 1980s. A number of parameters affecting the efficiency of the technique were soon identified, including the type of DNA con
Publikováno v:
Infection and Immunity. 59:4147-4153
Three monoclonal antibodies (MAbs), E4, L1-4, and L1-24, to the major outer membrane protein (MOMP) of Chlamydia trachomatis were identified that neutralized in vitro the infectivity of members of the B- and C-related complex as well as the mouse pne
Autor:
Jorge N. Artaza, Ruoqing Shen, Nestor F. Gonzalez-Cadavid, Indrani Sinha-Hikim, Suzanne Reisz-Porszasz, Shalender Bhasin, Aimee Hogue, Thomas J. Fielder
Publikováno v:
American journal of physiology. Endocrinology and metabolism. 285(4)
Mutations in the myostatin gene are associated with hypermuscularity, suggesting that myostatin inhibits skeletal muscle growth. We postulated that increased tissue-specific expression of myostatin protein in skeletal muscle would induce muscle loss.