Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Lori C. Gowen"'
Autor:
Jennifer A. Griffiths, Lori C. Gowen, Keith D. Anderson, Niels C. Adams, George D. Yancopoulos, Stephanie M. Zabski, Jeffrey Vercollone, David M. Valenzuela, Stanley J. Wiegand, Mark W. Sleeman, Joel C. Reinhardt, Susan D. Croll, Andrew J. Murphy, Richard Torres
Publikováno v:
Pain. 130:267-278
Neuromedin U (NMU) has recently been reported to have a role in nociception and inflammation. To clarify the function of the two known NMU receptors, NMU receptor 1 (NMUR1) and NMU receptor 2 (NMUR2), during nociception and inflammation in vivo, we g
Autor:
Roger B. Davis, Lori C. Gowen, Hiroya Hashizume, Matthew L. Springer, Shaun O'Brien, Amy Haskell, Donald M. McDonald, Betty Y. Y. Tam, Barbara Sennino, Scott M. Norberg, Gavin Thurston, Calvin J. Kuo, Shuji Joho, Tomomi Kamba, Keith D. Anderson, Michael R. Mancuso
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 290:H560-H576
Unlike during development, blood vessels in the adult are generally thought not to require VEGF for normal function. However, VEGF is a survival factor for many tumor vessels, and there are clues that some normal blood vessels may also depend on VEGF
Autor:
Jane D. Murray, Andrew J. Murphy, David M. Valenzuela, George D. Yancopoulos, Aris N. Economides, Stanley J. Wiegand, Katherine E. Wortley, Macdonald Lynn, Keith D. Anderson, Lori C. Gowen, Mark W. Sleeman, William Poueymirou, Mary V. Simmons, Dianna Barber
Publikováno v:
Proceedings of the National Academy of Sciences. 102:2496-2501
We identified a glycoprotein hormone β-subunit (OGH, also called GPB5) that, as a heterodimer with the α-subunit GPA2, serves as a second ligand for the thyroid-stimulating hormone receptor. Mice in which the OGH gene is deleted (OGH-/-) are indist
Autor:
David J. Glass, George D. Yancopoulos, William O. Kline, Mark W. Sleeman, Karen Garcia, Katherine E. Wortley, Jennifer Kintner, Ka-Man V. Lai, Lori C. Gowen, Stanley J. Wiegand, Trevor Stitt
Publikováno v:
Nature Medicine. 11:199-205
Genetic ablation of Inppl1, which encodes SHIP2 (SH2-domain containing inositol 5-phosphatase 2), was previously reported to induce severe insulin sensitivity, leading to early postnatal death. In the previous study, the targeting construct left the
Autor:
Amy L. Mansolf, Hua Zhu Ke, Lori C. Gowen, Hollis A. Simmons, George T. Tkalcevic, John D. McNeish, Thomas A. Brown, Kristen L. Chidsey-Frink, D.T. Crawford, Hong Qi, Jeffrey L. Stock, Donna N. Petersen
Publikováno v:
Journal of Biological Chemistry. 278:1998-2007
We have previously described osteoblast/osteocyte factor 45 (OF45), a novel bone-specific extracellular matrix protein, and demonstrated that its expression is tightly linked to mineralization and bone formation. In this report, we have cloned and ch
Autor:
Andrew Xiao, Amy R. Mohn, John N. Snouwaert, Anne M. Latour, Beverly H. Koller, Lauren M. DiBiase, Lori C. Gowen
Publikováno v:
Oncogene. 18:7900-7907
BRCA1 is a nuclear phosphoprotein that has been classified as a tumor suppressor based on the fact that women carrying a mutated copy of the BRCA1 gene are at increased risk of developing breast and ovarian cancer. The association of BRCA1 with RAD51
Publikováno v:
Science. 281:1009-1012
The breast and ovarian cancer susceptibility geneBRCA1encodes a zinc finger protein of unknown function. Association of the BRCA1 protein with the DNA repair protein Rad51 and changes in the phosphorylation and cellular localization of the protein af
Brca1 deficiency results in early embryonic lethality characterized by neuroepithelial abnormalities
Publikováno v:
Nature Genetics. 12:191-194
The breast and ovarian cancer susceptibility gene, BRCA1, has been cloned and shown to encode a zinc-finger protein of unknown function. Mutations in BRCA1 account for at least 80% of families with both breast and ovarian cancer, as well as some non-
Autor:
Harakiran Nistala, David M. Valenzuela, George D. Yancopoulos, Lisa Stadmeyer, Elizabetta Gazzerro, Florian Witte, Renata C. Pereira, Lori C. Gowen, Regina Raz, Stefan Mundlos, Stephanie M. Zabski, Julie L. Clor, Mark W. Sleeman, Ernesto Canalis, Sigmar Stricker, Xiangmin Wang, Aris N. Economides
Publikováno v:
Development (Cambridge, England). 135(9)
Mutations in ROR2 result in a spectrum of genetic disorders in humans that are classified, depending on the nature of the mutation and the clinical phenotype, as either autosomal dominant brachydactyly type B (BDB,MIM 113000) or recessive Robinow syn
Autor:
Jason G. Weinger, Katrina K. Hoyer, Joshua J. Troke, Michael A. Teitell, Christian Raphalides, Jun Xu, Mark W. Sleeman, Irwin J. Kurland, Mathilde Renard, W.N. Paul Lee, Mohammed F. Saad, Bhavapriya Vaitheesyaran, Lori C. Gowen
Publikováno v:
Diabetes. 55(12)
Despite altered regulation of insulin signaling, Pten(+/-) heterodeficient standard diet-fed mice, approximately 4 months old, exhibit normal fasting glucose and insulin levels. We report here a stable isotope flux phenotyping study of this "silent"