Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ezzatollah T. Shivapour"'
Autor:
Sushmita Sinha, Pranav S Renavikar, Michael P Crawford, Scott M Steward-Tharp, Ashley Brate, Eva Tsalikian, Michael Tansey, Ezzatollah T Shivapour, Tracey Cho, John Kamholz, Nitin J Karandikar
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0238070 (2020)
Factors regulating self-antigen directed immune-responses in autoimmunity are poorly understood. Signal regulatory protein gamma (SIRPγ) is a human T-cell specific protein with genetic variants associated with type 1 diabetes (T1D). SIRPγ's functio
Externí odkaz:
https://doaj.org/article/1e55512d7b8a45a5a6a12f43ec8393a6
Autor:
Nitin J. Karandikar, Michael Tansey, John Kamholz, Pranav S Renavikar, Ashley A. Brate, Sushmita Sinha, Tracey Cho, Ezzatollah T. Shivapour, Scott M. Steward-Tharp, Eva Tsalikian, Michael P. Crawford
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0238070 (2020)
PLoS ONE
PLoS ONE
Factors regulating self-antigen directed immune-responses in autoimmunity are poorly understood. Signal regulatory protein gamma (SIRPγ) is a human T-cell specific protein with genetic variants associated with type 1 diabetes (T1D). SIRPγ's functio
Autor:
Emilee Gibson, Michael Tansey, Nicholas Borcherding, Nitin J. Karandikar, Pranav S Renavikar, Heena Olalde, Ezzatollah T. Shivapour, John Kamholz, Michael P. Crawford, Frank Bittner, Sushmita Sinha, Eva Tsalikian
Publikováno v:
Scientific Reports
Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
Multiple GWAS studies have shown that the SNP rs2281808 TT variant, present within the SIRPG gene, is associated with autoimmune diseases, such as type 1 diabetes. However, the role of SIRPγ in human T-cells is not known, neither is the functional s
Autor:
Thomas R. Vidic, Nimish J. Thakore, Alexander Sherman, Stephen S. Rich, Jau-Shin Lou, Leo McCluskey, James B. Caress, Bryan J. Traynor, Tulio E. Bertorini, Roderick A. Corriveau, David Lacomis, Catherine Lomen-Hoerth, George Sachs, Richard Bedlack, Brian A. Crum, Paul E. Barkhaus, Erik P. Pioro, Laurie Gutmann, J. M. Shefner, Kate Bednarz, John E. Chapin, Jonathan D. Glass, Elham Bayat, Jaya Trivedi, Jeffery Rosenfeld, James Wymer, Nicholas J. Maragakis, John Hardy, Daragh Heitzman, Carlayne E. Jackson, Paul H. Gordon, Harris T. Brent, Dale J. Lange, Petra Kaufmann, Michael C. Graves, James Ostell, Merit Cudkowicz, Charles Cho, Gregory S. Carter, Larry Refolo, Katrina Gwinn, David A. Chad, Eric J. Sorenson, Laura Sams, Terry Heiman-Patterson, Michael D. Weiss, David Walk, Stephen N. Scelsa, Hiroshi Mitsumoto, Ghazala Hayat, Jaime Andrews, Robert G. Miller, Tahseen Mozaffar, Charles A. Thornton, Ashok Verma, Matthew D. Mailman, Kourosh Rezania, J. Clarke Stevens, Mark B. Bromberg, Josefina Nash, Robert H. Brown, Jerry M. Belsh, Praful Kelkar, Valerie Cwik, Rup Tandan, Amanda Peltier, Kimberly L. Goslin, Alan Pestronk, Ran Zhang, Richard J. Barohn, John J. Kelly, Stacy A. Rudnicki, Robin Conwit, Zachary Simmons, Andrew B. Singleton, Kevin Boylan, E. Peter Bosch, Edward J. Kasarskis, Carmel Armon, Ezzatollah T. Shivapour, Margaret A. Keller, Allitia DiBernardo, Benjamin Rix Brooks, Sandeep Rana, Lucie Bruijn, Yadollah Harati, James A. Russell, Daniel Newman, Ericka Simpson
Publikováno v:
PLoS ONE
PLoS ONE, Vol 2, Iss 12, p e1254 (2007)
PLoS ONE, Vol 2, Iss 12, p e1254 (2007)
Amyotrophic lateral sclerosis (ALS) is the most common form of motor neuron disease (MND). It is currently incurable and treatment is largely limited to supportive care. Family history is associated with an increased risk of ALS, and many Mendelian c