Zobrazeno 1 - 10
of 189
pro vyhledávání: '"Wollmann Robert"'
Autor:
Hwang Jong-Hee, Roberts Craig W, Ferguson David JP, Wollmann Robert, Kirisits Michael J, Mayr Thomas, Kasza Kristen, Roberts Fiona, Mui Ernest, Kelly Krystyna A, Ajioka James W, Hermes Gretchen, Trendler Toria, Kennan Richard P, Suzuki Yasuhiro, Reardon Catherine, Hickey William F, Chen Lieping, McLeod Rima
Publikováno v:
Journal of Neuroinflammation, Vol 5, Iss 1, p 48 (2008)
Abstract Background Worldwide, approximately two billion people are chronically infected with Toxoplasma gondii with largely unknown consequences. Methods To better understand long-term effects and pathogenesis of this common, persistent brain infect
Externí odkaz:
https://doaj.org/article/8bcccbee78fc409db75633d68266e9c6
Publikováno v:
Science, 2002 Nov . 298(5599), 1781-1785.
Externí odkaz:
https://www.jstor.org/stable/3833012
Autor:
Hack, Andrew A., Ly, Chantal T., Jiang, Fang, Clendenin, Cynthia J., Sigrist, Kirsten S., Wollmann, Robert L., McNally, Elizabeth M.
Publikováno v:
The Journal of Cell Biology, 1998 Sep 01. 142(5), 1279-1287.
Externí odkaz:
https://www.jstor.org/stable/1618820
Autor:
Kim, Hye-Jung, Jung, Cha-Gyun, Dukala, Danuta, Bae, Hyun, Kakazu, Rafael, Wollmann, Robert, Soliven, Betty
Publikováno v:
In Journal of Neuroimmunology 2009 214(1):93-100
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1992 May . 89(10), 4524-4528.
Externí odkaz:
https://www.jstor.org/stable/2359361
Autor:
Vohra, Bhupinder P.S., Groshong, Jason S., Zayas, Roberto, Wollmann, Robert L., Gomez, Christopher M.
Publikováno v:
In Neurobiology of Disease 2006 23(2):462-470
Autor:
Maselli, Ricardo A, Vázquez, Jessica, Schrumpf, Leah, Arredondo, Juan, Lara, Marian, Strober, Jonathan B, Pytel, Peter, Wollmann, Robert L, Ferns, Michael
Publikováno v:
Molecular genetics & genomic medicine, vol 6, iss 3
BackgroundMonogenic defects of synaptic vesicle (SV) homeostasis have been implicated in many neurologic diseases, including autism, epilepsy, and movement disorders. In addition, abnormal vesicle exocytosis has been associated with several endocrine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::77e4b5f10821a699a48e484ad487324d
https://escholarship.org/uc/item/75c1g7vh
https://escholarship.org/uc/item/75c1g7vh
Publikováno v:
Tuberous Sclerosis Complex.
Externí odkaz:
https://doi.org/10.1093/oso/9780195122107.003.0018
Akademický článek
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Autor:
Maselli, Ricardo A, Arredondo, Juan, Cagney, Orla, Ng, Jarae J, Anderson, Jennifer A, Williams, Colette, Gerke, Bae J, Soliven, Betty, Wollmann, Robert L
Publikováno v:
Human molecular genetics, vol 19, iss 12
We describe a severe congenital myasthenic syndrome (CMS) caused by two missense mutations in the gene encoding the muscle specific receptor tyrosine kinase (MUSK). The identified MUSK mutations M605I and A727V are both located in the kinase domain o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::c88bcbe00ba9e919febd34e4fb9a38e5
https://escholarship.org/uc/item/1v90v314
https://escholarship.org/uc/item/1v90v314