Zobrazeno 1 - 10
of 63
pro vyhledávání: '"Behrouz, Bahareh"'
Autor:
Behrouz, Bahareh.
Publikováno v:
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Thesis (Ph. D.)--Michigan State University. Dept. of Neuroscience, 2008.
Title from PDF t.p. (viewed Sept. 11, 2009). Includes bibliographical references (p. 271-303). Also issued in print.
Title from PDF t.p. (viewed Sept. 11, 2009). Includes bibliographical references (p. 271-303). Also issued in print.
Design and high-throughput implementation of MALDI-TOF/MS-based assays for Parkin E3 ligase activity
Autor:
Traynor, Ryan, Moran, Jennifer, Stevens, Michael, Antico, Odetta, Knebel, Axel, Behrouz, Bahareh, Merchant, Kalpana, Hastie, C. James, Davies, Paul, Muqit, Miratul M.K., De Cesare, Virginia
Publikováno v:
In Cell Reports Methods 26 February 2024 4(2)
Autor:
Benskey, Matthew, Behrouz, Bahareh, Sunryd, Johan, Pappas, Samuel S., Baek, Seung-Hoon, Huebner, Marianne, Lookingland, Keith J., Goudreau, John L.
Publikováno v:
In Neurotoxicology June 2012 33(3):321-331
Autor:
Lee, Andrew, Fritzen, Edward, Campbell, Anahit, Romero, Donna, Yu, Jeremy, Pabla, Navjot, Behrouz, Bahareh (Spring)
Publikováno v:
In Kidney International Reports April 2024 9(4) Supplement:S47-S47
Autor:
Dächsel, Justus C., Behrouz, Bahareh, Yue, Mei, Beevers, Joel E., Melrose, Heather L., Farrer, Matthew J.
Publikováno v:
In Parkinsonism and Related Disorders 2010 16(10):650-655
Autor:
Vilariño-Güell, Carles, Ross, Owen A., Wider, Christian, Jasinska-Myga, Barbara, Cobb, Stephanie A., Soto-Ortolaza, Alexandra I., Kachergus, Jennifer M., Keeling, Brett H., Dachsel, Justus C., Melrose, Heather L., Behrouz, Bahareh, Wszolek, Zbigniew K., Uitti, Ryan J., Aasly, Jan O., Rajput, Alex, Farrer, Matthew J.
Publikováno v:
In Parkinsonism and Related Disorders 2010 16(2):109-111
Publikováno v:
In Neurotoxicology 2004 25(5):761-769
Autor:
Hinkle Kelly M, Yue Mei, Behrouz Bahareh, Dächsel Justus C, Lincoln Sarah J, Bowles Erin E, Beevers Joel E, Dugger Brittany, Winner Beate, Prots Iryna, Kent Caroline B, Nishioka Kenya, Lin Wen-Lang, Dickson Dennis W, Janus Christopher J, Farrer Matthew J, Melrose Heather L
Publikováno v:
Molecular Neurodegeneration, Vol 7, Iss 1, p 25 (2012)
Abstract Mutations in the LRRK2 gene are the most common cause of genetic Parkinson’s disease. Although the mechanisms behind the pathogenic effects of LRRK2 mutations are still not clear, data emerging from in vitro and in vivo models suggests rol
Externí odkaz:
https://doaj.org/article/6c25dd1f24ef43c6948b6a69831ef927
Autor:
Hinkle, Kelly M, Yue, Mei, Behrouz, Bahareh, Dachsel, Justus C, Lincoln, Sarah J, Bowles, Erin E, Beevers, Joel E, Dugger, Brittany, Winner, Beate, Prots, Iryna, Kent, Caroline B, Nishioka, Kenya, Wen-Lang Lin, Janus, Christopher, Dickson, Dennis W, Farrer, Matthew J, Melrose, Heather L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbc635db60fdcf0778e436934d031aa9
Autor:
Sarah Lincoln, Elizabeth Conibear, Behrouz Bahareh Behrouz, Ali H. Rajput, Joseph Ghika, Stephanie A. Cobb, Carles Vilariño-Güell, Greggory J. Wilhoite, Wyeth W. Wasserman, Jan O. Aasly, François Vingerhoets, Zbigniew K. Wszolek, Christian Wider, Anna Krygowska-Wajs, Alexandra I. Soto-Ortolaza, Ruth Djaldetti, Justus C. Dachsel, Fayçal Hentati, Ruey-Meei Wu, Andreas Puschmann, Heather L. Melrose, Owen A. Ross, Pierre R. Burkhard, Justin A. Bacon, Emna Hentati, Matthew J. Farrer, Alessandra Solida, Timothy Lynch, Daniel M. Evans, Alex Rajput, Jennifer M. Kachergus, Ryan J. Uitti, Eldad Melamed
Publikováno v:
American Journal of Human Genetics, Vol. 89, No 1 (2011) pp. 162-7
The identification of genetic causes for Mendelian disorders has been based on the collection of multi-incident families, linkage analysis, and sequencing of genes in candidate intervals. This study describes the application of next-generation sequen