Zobrazeno 1 - 10
of 40
pro vyhledávání: '"Kuldip D Dave"'
Autor:
Nicole K Polinski, Terina N Martinez, Alexander Gorodinsky, Ralph Gareus, Michael Sasner, Mark Herberth, Robert Switzer, Syed O Ahmad, Mali Cosden, Monika Kandebo, Robert E Drolet, Peter D Buckett, Weisong Shan, Yi Chen, Lee J Pellegrino, Gregory D Ellsworth, Leo B Dungan, Warren D Hirst, Sean W Clark, Kuldip D Dave
Publikováno v:
PLoS ONE, Vol 16, Iss 6, p e0252325 (2021)
Multiple mutations have been described in the human GBA1 gene, which encodes the lysosomal enzyme beta-glucocerebrosidase (GCase) that degrades glucosylceramide and is pivotal in glycosphingolipid substrate metabolism. Depletion of GCase, typically b
Externí odkaz:
https://doaj.org/article/294b88f9cc54498d84ccf437a6bd2775
Autor:
Lorraine Iacovitti, Xiaotao Wei, Jingli Cai, Eric W Kostuk, Ruihe Lin, Alexander Gorodinsky, Philip Roman, Gretchen Kusek, Sonal S Das, Audrey Dufour, Terina N Martinez, Kuldip D Dave
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e113151 (2014)
Parkinson disease (PD) is the second leading neurodegenerative disease in the US. As there is no known cause or cure for PD, researchers continue to investigate disease mechanisms and potential new therapies in cell culture and in animal models of PD
Externí odkaz:
https://doaj.org/article/4d2f73f4e1f9464c9023cd5e0d39b7ae
Autor:
Marco A S Baptista, Kuldip D Dave, Mark A Frasier, Todd B Sherer, Melanie Greeley, Melissa J Beck, Julie S Varsho, George A Parker, Cindy Moore, Madeline J Churchill, Charles K Meshul, Brian K Fiske
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e80705 (2013)
The objective of this study was to evaluate the pathology time course of the LRRK2 knockout rat model of Parkinson's disease at 1-, 2-, 4-, 8-, 12-, and 16-months of age. The evaluation consisted of histopathology and ultrastructure examination of se
Externí odkaz:
https://doaj.org/article/91c01268d8074bafbcbd4a7729d3872b
Autor:
Nicole K. Polinski, Terina N. Martinez, Sylvie Ramboz, Michael Sasner, Mark Herberth, Robert Switzer, Syed O. Ahmad, Lee J. Pelligrino, Sean W. Clark, Jacob N. Marcus, Sean M. Smith, Kuldip D. Dave, Mark A. Frasier
Publikováno v:
Disease Models & Mechanisms, Vol 15, Iss 6 (2022)
Heterozygous mutations in the GBA1 gene – encoding lysosomal glucocerebrosidase (GCase) – are the most common genetic risk factors for Parkinson's disease (PD). Experimental evidence suggests a correlation between decreased GCase activity and acc
Externí odkaz:
https://doaj.org/article/2ff4a4f7438a460f8a91ec3fc7c58bc4
Autor:
Michael Benatar, Stephen A Goutman, Kim A Staats, Eva L Feldman, Marc Weisskopf, Evelyn Talbott, Kuldip D Dave, Neil M Thakur, Ammar Al-Chalabi
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 94:399-402
Autor:
Kuldip D. Dave, Shehan De Silva, Niketa P. Sheth, Sylvie Ramboz, Melissa J. Beck, Changyu Quang, Robert C. Switzer, III, Syed O. Ahmad, Susan M. Sunkin, Dan Walker, Xiaoxia Cui, Daniel A. Fisher, Aaron M. McCoy, Kevin Gamber, Xiaodong Ding, Matthew S. Goldberg, Stanley A. Benkovic, Meredith Haupt, Marco A.S. Baptista, Brian K. Fiske, Todd B. Sherer, Mark A. Frasier
Publikováno v:
Neurobiology of Disease, Vol 70, Iss , Pp 190-203 (2014)
Recessively inherited loss-of-function mutations in the PTEN-induced putative kinase 1(Pink1), DJ-1 (Park7) and Parkin (Park2) genes are linked to familial cases of early-onset Parkinson's disease (PD). As part of its strategy to provide more tools f
Externí odkaz:
https://doaj.org/article/3b4ee316f83d4fc3bf43bea037f0fae8
Autor:
Maxim Signaevsky, Bahram Marami, Marcel Prastawa, Nabil Tabish, Megan A. Iida, Xiang Fu Zhang, Mary Sawyer, Israel Duran, Daniel G. Koenigsberg, Clare H. Bryce, Lana M. Chahine, Brit Mollenhauer, Sherri Mosovsky, Lindsey Riley, Kuldip D. Dave, Jamie Eberling, Chris S. Coffey, Charles H. Adler, Geidy E. Serrano, Charles L. White, John Koll, Gerardo Fernandez, Jack Zeineh, Carlos Cordon-Cardo, Thomas G. Beach, John F. Crary
Publikováno v:
Acta neuropathologica communications. 10(1)
The diagnosis of Parkinson’s disease (PD) is challenging at all stages due to variable symptomatology, comorbidities, and mimicking conditions. Postmortem assessment remains the gold standard for a definitive diagnosis. While it is well recognized
Autor:
Lee Pellegrino, Monika Kandebo, Nicole K. Polinski, Mark Herberth, Leo B. Dungan, Robert Switzer, Gregory D. Ellsworth, Sean W. Clark, Alexander Gorodinsky, Robert E. Drolet, Peter D. Buckett, Mali Cosden, Michael Sasner, Ralph Gareus, Syed Omar Ahmad, Weisong Shan, Terina N. Martinez, Kuldip D. Dave, Warren D. Hirst, Yi Chen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 6, p e0252325 (2021)
PLoS ONE, Vol 16, Iss 6, p e0252325 (2021)
Multiple mutations have been described in the human GBA1 gene, which encodes the lysosomal enzyme beta-glucocerebrosidase (GCase) that degrades glucosylceramide and is pivotal in glycosphingolipid substrate metabolism. Depletion of GCase, typically b
Autor:
Erik Stoops, Brit Mollenhauer, Hugo Vanderstichele, Jing Zhang, Charlotte E. Teunissen, Henrik Zetterberg, Niels Kruse, Adrian W. Schmid, Kuldip D. Dave, Leslie M. Shaw, Jill Dunty, Robert M. Umek, Frederick Du Bois Bowman, Samantha J. Hutten, Tanja Schubert, Kaj Blennow, Marc Moniatte, Omar M. A. El-Agnaf, Daniel Drake, Chris L. Smith, Jennifer Masucci, Peggy Taylor, Hilal A. Lashuel, Jimmy Duong
Publikováno v:
Journal of Neurochemistry
Journal of Neurochemistry, 149(1), 126-138. Wiley-Blackwell
Mollenhauer, B, Bowman, F D, Drake, D, Duong, J, Blennow, K, el-Agnaf, O, Shaw, L M, Masucci, J, Taylor, P, Umek, R M, Dunty, J M, Smith, C L, Stoops, E, Vanderstichele, H, Schmid, A W, Moniatte, M, Zhang, J, Kruse, N, Lashuel, H A, Teunissen, C, Schubert, T, Dave, K D, Hutten, S J & Zetterberg, H 2019, ' Antibody-based methods for the measurement of α-synuclein concentration in human cerebrospinal fluid – method comparison and round robin study ', Journal of Neurochemistry, vol. 149, no. 1, pp. 126-138 . https://doi.org/10.1111/jnc.14569
Journal of Neurochemistry, 149(1), 126-138. Wiley-Blackwell
Mollenhauer, B, Bowman, F D, Drake, D, Duong, J, Blennow, K, el-Agnaf, O, Shaw, L M, Masucci, J, Taylor, P, Umek, R M, Dunty, J M, Smith, C L, Stoops, E, Vanderstichele, H, Schmid, A W, Moniatte, M, Zhang, J, Kruse, N, Lashuel, H A, Teunissen, C, Schubert, T, Dave, K D, Hutten, S J & Zetterberg, H 2019, ' Antibody-based methods for the measurement of α-synuclein concentration in human cerebrospinal fluid – method comparison and round robin study ', Journal of Neurochemistry, vol. 149, no. 1, pp. 126-138 . https://doi.org/10.1111/jnc.14569
α-Synuclein is the major component of Lewy bodies and a candidate biomarker for neurodegenerative diseases in which Lewy bodies are common, including Parkinson's disease and dementia with Lewy bodies. A large body of literature suggests that these d