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Akademický článek

Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease.

Autor: Min Peng, Marni J Falk, Volker H Haase, Rhonda King, Erzsebet Polyak, Mary Selak, Marc Yudkoff, Wayne W Hancock, Ray Meade, Ryoichi Saiki, Adam L Lunceford, Catherine F Clarke, David L Gasser

Publikováno v: PLoS Genetics, Vol 4, Iss 4, p e1000061 (2008)

Coenzyme Q (CoQ) is an essential electron carrier in the respiratory chain whose deficiency has been implicated in a wide variety of human mitochondrial disease manifestations. Its multi-step biosynthesis involves production of polyisoprenoid diphosp

Externí odkaz: https://doaj.org/article/4b0727f4f27f4e6eb1b2ffd376c6dd98

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Glomerular and Tubular Epithelial Defects in kd/kd Mice Lead to Progressive Renal Failure

Autor: Rexford S. Ahima, Min Peng, Wayne W. Hancock, Ray Meade, Daniel J. Rader, John E. Tomaszewski, Michael P. Madaio, David L. Gasser, Alberto Mendoza

Publikováno v: American Journal of Nephrology. 25:604-610

Background/Aim: The kd/kd mouse spontaneously develops severe and progressive nephritis leading to renal failure, characterized by cellular infiltration, tubular destruction and glomerular sclerosis. Recent identification of the mutant gene and the o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4774d3ef934bc6314506d4976baa3f42
https://doi.org/10.1159/000089709

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Contents Vol. 25, 2005

Autor: Melvin R. Hayden, Natan Cohen, Andrea Galassi, Pamela Schinleber, Marco Antonio P. Leite, David L. Gasser, Michael Rapoport, Hongqi Ren, Shai Efrati, Daniel J. Rader, Zhihong Liu, Barry I. Freedman, Laurie Roberts, David Modai, Wayne W. Hancock, James R. Sowers, Ahuva Golik, Federica Cecchini, Jin Kim, Caihong Zeng, Frederic Clayton, John E. Tomaszewski, Krystyna Pawlak, Joshua Weissgarten, Renata C. Santos, In San Kim, Leishi Li, Cristianne L. Fabris, Michael P. Madaio, Jung Ho Cha, Huiping Chen, Adam Whaley-Connell, Walid Ghantous, James M. Bates, Guillermo Coca Velarde, Can Li, Stuart M. Sprague, Min Peng, Vernon L. Tesh, Chul Woo Yang, Claudine Jurkovitz, F.M. Ribeiro, William M. McClellan, Michal Mysliwiec, Jolanta Malyszko, Hajamohideen S. Raffi, Mordechay Aladjem, Guang Yang, Jacek S. Malyszko, Donald E. Kohan, Nataliya V. Volkova, Domenico Russo, Satish Kumar, Zoltan Laszik, Jocemir Ronaldo Lugon, Olivia Turri, Suk Hee Lee, Alberto Mendoza, Ray Meade, Elena Galperin, Scott G. Satko, Nathaniel D. Denkers, J. Michael Soucie, Rexford S. Ahima, Maria Luisa Biondi, Tomasz Hryszko, Anna L. Zisman, Fletcher B. Taylor, Richard L. Siegler, Sun Woo Lim, Bum Soon Choi, Theodore J. Pysher, Vittorio E. Andreucci, Hong Zhou, Maurizio Gallieni, Jenna Krisher, Diego Brancaccio, Mario Cozzolino, Sylvia Berman, Zhan Averbukh, Randall Lou, Zheng Tang

Publikováno v: American Journal of Nephrology. 25:627-630

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2bd57c9798dcabc871200418ce3daa8a
https://doi.org/10.1159/000090454

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Purification of Her-2 extracellular domain and identification of its cleavage site

Autor: Amy L Lasut, Mark J Rupar, Michael Ramaker, Chao-Xing Yuan, Phillip C Liu, Gregory F Hollis, Ray Meade, Richard Wynn, Nicola T. Neff

Publikováno v: Protein Expression and Purification. 29:217-222

The EGF family of receptors belongs to the tyrosine kinase receptor (TKR) family and plays an important role during embryonic and postnatal development and also in the progression of tumors. Her-2/neu/c-erbB-2, a member of the epidermal growth factor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e7b8b8e1481fdaae71ac78e058485c8
https://doi.org/10.1016/s1046-5928(03)00058-5

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Primary coenzyme Q deficiency in Pdss2 mutant mice causes isolated renal disease

Autor: Volker H. Haase, Marc Yudkoff, Marni J. Falk, Mary A. Selak, Erzsebet Polyak, Min Peng, Ray Meade, Wayne W. Hancock, David L. Gasser, Catherine F. Clarke, Rhonda King, Adam L. Lunceford, Ryoichi Saiki

Publikováno v: PLoS genetics, vol 4, iss 4
PLoS Genetics
PLoS Genetics, Vol 4, Iss 4, p e1000061 (2008)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bb182c03fabe1e3087f857a3248a6a5
https://escholarship.org/uc/item/2g96r43r

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The mitochondrial and kidney disease phenotypes of kd/kd mice under germfree conditions

Autor: Wayne W. Hancock, Min Peng, Ray Meade, Troy Hallman, David L. Gasser, Michael P. Madaio

Publikováno v: Journal of autoimmunity. 26(1)

Interstitial nephritis occurs spontaneously in kd/kd mice, but the mechanisms leading to this disease have not been fully elucidated. The earliest manifestation of a phenotype is the appearance of ultrastructural defects in the mitochondria of mice a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d2e02e8fd64931c921316aea8fa9a0c
https://pubmed.ncbi.nlm.nih.gov/16337774

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