Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Louise M. McKenzie"'
Autor:
Michele H. Mokrzycki, Paul L. Kimmel, David Vlahov, Jeffrey S. Berns, Cheryl A. Winkler, Taras K. Oleksyk, Donald W. Bowden, William A. Briggs, Jeffrey B. Kopp, Stephen M. Korbet, Michael W. Smith, Barry I. Freedman, Eric E. Simon, Tejinder S. Ahuja, Louise M. McKenzie, Jeffrey R. Schelling, Richard A. Dart, George W. Nelson, Hiroshi Kajiyama, Randall C. Johnson, Monique E. Cho, Howard Trachtman, Donna M. Michel
Publikováno v:
Nature Genetics. 40:1175-1184
The increased burden of chronic kidney and end-stage kidney diseases (ESKD) in populations of African ancestry has been largely unexplained. To identify genetic variants predisposing to idiopathic and HIV-1–associated focal segmental glomeruloscler
Autor:
Michelle H. Mokrzycki, Jeffrey B. Kopp, Michael C. Smith, Stephen M. Korbet, Jeffrey S. Berns, Sher L. Hendrickson, Howard Trachtman, Donna M. Michel, Jeffrey R. Schelling, Yu C. Zhou, Monique E. Cho, Elizabeth Binns-Roemer, Eric E. Simon, Richard A. Dart, Paul L. Kimmel, Cheryl A. Winkler, Gregory D. Kirk, William A. Briggs, Louise M. McKenzie, Tejinder S. Ahuja
Publikováno v:
Journal of the American Society of Nephrology. 18:2987-2995
Mutations in NPHS2, the gene that encodes podocin, are well-established causes of both familial and sporadic steroid-resistant focal segmental glomerulosclerosis (FSGS) in the pediatric population, but have not been well-characterized in late-onset d
Autor:
Joel E. Richardson, Lois J. Maltais, Donna Maglott, Richard M. Baldarelli, Martin Ringwald, Benjamin L. King, Deanna M. Church, James A. Kadin, Lynn M. Schriml, Lori E. Corbani, Janan T. Eppig, Jun Adachi, Takeya Kasukawa, Louise M. McKenzie, Kim D. Pruitt, Longlong Yang, Yunxia Zhu, David P. Hill, Sharon Cousins, Deborah J Reed, Masaaki Furuno, Dong Qi, Sridhar Ramachandran, Judith A. Blake, Kenneth S. Frazer, Dirck W. Bradt, Carol J. Bult
Publikováno v:
Genome Research. 13:1505-1519
The Mouse Genome Sequencing Consortium and the RIKEN Genome Exploration Research grouphave generated large sets of sequence data representing the mouse genome and transcriptome, respectively. These data provide a valuable foundation for genomic resea
Autor:
Yuka Imamura Kawasawa, David P. Hill, Masashi Yanagisawa, Hidemasa Bono, Louise M McKenzie, Gsl Members
Publikováno v:
Genome Research. 13:1466-1477
G protein-coupled receptors (GPCRs) comprise the largest family of receptor proteins in mammals and play important roles in many physiological and pathological processes. Gene expression of GPCRs is temporally and spatially regulated, and many splici
Autor:
Jerry Ware, Phillip J. Robinson, Barbara Zieger, Richard M. Baldarelli, John R. Pringle, Manami Tanaka, Elizabeth M. Petty, Dagmar Roth, Lois J. Maltais, S. E. Hilary Russell, Shu Chan Hsu, Claudia Low, Christine M. Field, Makoto Kinoshita, Heidi Stuhlmann, Louise M. McKenzie, Tanaka Tomoo, Mary B. Kennedy, Yasuhide Hayashi, Nancy J. Zeleznik-Le, William S. Trimble, Timothy J. Mitchison, Mark Peifer, Toru Nishikawa, Mark S. Longtine, Makoto Noda, Michael Glotzer, Ian G. Macara
Publikováno v:
Molecular Biology of the Cell. 13:4111-4113
There are 10 known mammalian septin genes, some of which produce multiple splice variants. The current nomenclature for the genes and gene products is very confusing, with several different names having been given to the same gene product and distinc
Autor:
Lisa R. Yanek, Louise M. McKenzie, Lewis C. Becker, Diane M. Becker, Paul A. Nyquist, Cherie Winkler
Background: Monocyte chemoattractant protein 1 (MCP-1), acting in concert with its receptor chemokine receptor 2 (CCR2), promotes recruitment of macrophages into atherosclerotic plaque. We examined whether single nucleotide polymorphism (SNP) variant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a55b4defc2d8af7266e8ec7664ac79
https://europepmc.org/articles/PMC2914430/
https://europepmc.org/articles/PMC2914430/
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 8(2)
Nephrotic syndrome, characterized by edema, proteinuria, hyperlipidemia and low serum albumin, is a manifestation of kidney disease involving the glomeruli. Nephrotic syndrome may be caused by primary kidney disease such as focal segmental glomerulos
Publikováno v:
Publons
The production of a marsupial genetic linkage map is perhaps one of the most important objectives in marsupial research. This study used a total of 353 informative meioses and 64 genetic markers to construct a framework genetic linkage map for the ta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8015832613471d5ed4843af72b059fc7
https://europepmc.org/articles/PMC1462270/
https://europepmc.org/articles/PMC1462270/