Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Sanjay Chandriani"'
Autor:
Michael C. Babcock, Christina R. Mikulka, Bing Wang, Sanjay Chandriani, Sundeep Chandra, Yue Xu, Katherine Webster, Ying Feng, Hemanth R. Nelvagal, Alex Giaramita, Bryan K. Yip, Melanie Lo, Xuntian Jiang, Qi Chao, Josh C. Woloszynek, Yuqiao Shen, Shripad Bhagwat, Mark S. Sands, Brett E. Crawford
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021)
Abstract Krabbe disease (KD) and metachromatic leukodystrophy (MLD) are caused by accumulation of the glycolipids galactosylceramide (GalCer) and sulfatide and their toxic metabolites psychosine and lysosulfatide, respectively. We discovered a potent
Externí odkaz:
https://doaj.org/article/b4baa35aa3c440d78cac8c75d11ceb69
Autor:
Yuanbin Ru, Carley Corado, Russell K. Soon Jr, Andrew C. Melton, Adam Harris, Guoying K. Yu, Nancy Pryer, John R. Sinclair, Martin L. Katz, Temitayo Ajayi, David Jacoby, Chris B. Russell, Sanjay Chandriani
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 12, Pp 2437-2447 (2019)
Abstract Objective Neuronal ceroid lipofuscinosis type 2 (CLN2 disease) is a rare, progressive, fatal neurodegenerative pediatric disorder resulting from deficiencies of the lysosomal enzyme tripeptidyl peptidase 1 that are caused by mutations in TPP
Externí odkaz:
https://doaj.org/article/f1502f91d5a84d26a84b4e9377e1f3b7
Autor:
Roger Lawrence, Jeremy L. Van Vleet, Linley Mangini, Adam Harris, Nathan Martin, Wyatt Clark, Sanjay Chandriani, Jonathan H. LeBowitz, Roberto Giugliani, Alessandra d'Azzo, Gouri Yogalingam, Brett E. Crawford
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 21, Iss , Pp - (2019)
Introduction: GM1 gangliosidosis is a rare autosomal recessive genetic disorder caused by the disruption of the GLB1 gene that encodes β-galactosidase, a lysosomal hydrolase that removes β-linked galactose from the non-reducing end of glycans. Defi
Externí odkaz:
https://doaj.org/article/a0f6f939f66e4358b688b3cdde4ec8b2
Autor:
Sanjay Chandriani, Eirik Frengen, Victoria H Cowling, Sarah A Pendergrass, Charles M Perou, Michael L Whitfield, Michael D Cole
Publikováno v:
PLoS ONE, Vol 4, Iss 8, p e6693 (2009)
BACKGROUND:The MYC oncogene contributes to induction and growth of many cancers but the full spectrum of the MYC transcriptional response remains unclear. METHODOLOGY/PRINCIPAL FINDINGS:Using microarrays, we conducted a detailed kinetic study of gene
Externí odkaz:
https://doaj.org/article/69ff29d0c9f247e09bbe3c302719b746
Autor:
Sanjay Chandriani, Don Ganem
Publikováno v:
PLoS ONE, Vol 2, Iss 8, p e811 (2007)
Lytic infection by Kaposi's sarcoma-associated herpesvirus (KSHV) is associated with an extensive shutoff of host gene expression, mediated chiefly by accelerated mRNA turnover due to expression of the viral SOX protein. We have previously identified
Externí odkaz:
https://doaj.org/article/40744cab24dd4ac1872725d284bf2771
Autor:
Terrence F. Satterfield, Daniela Linzner, Poojan Suri, Samnang Tep, Rebeca M. Choy, Taru Gujral, Eva Situ, Yannan Xi, David Beattie, Sarah B. Noonberg, Sanjay Chandriani, Julie Ullman, Eric Green
Publikováno v:
Molecular Genetics and Metabolism. 138:107304
Autor:
Russell K. Soon, Temitayo Ajayi, Nancy Pryer, Guoying K. Yu, John Sinclair, Sanjay Chandriani, Andrew Melton, Carley R. Corado, Yuanbin Ru, Adam Harris, Chris B. Russell, David Jacoby, Martin L. Katz
Publikováno v:
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 6, Iss 12, Pp 2437-2447 (2019)
Annals of Clinical and Translational Neurology, Vol 6, Iss 12, Pp 2437-2447 (2019)
Objective Neuronal ceroid lipofuscinosis type 2 (CLN2 disease) is a rare, progressive, fatal neurodegenerative pediatric disorder resulting from deficiencies of the lysosomal enzyme tripeptidyl peptidase 1 that are caused by mutations in TPP1. Identi
Autor:
Katherine A. Webster, Bryan K. Yip, Yue Xu, Christina R. Mikulka, Alex Giaramita, Brett E. Crawford, Michael C. Babcock, Hemanth R. Nelvagal, Sanjay Chandriani, Xuntian Jiang, Ying Feng, Melanie Lo, Sundeep Chandra, Josh C. Woloszynek, Shripad Bhagwat, Qi Chao, Yuqiao Shen, Mark S. Sands, Bing Wang
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-17 (2021)
Krabbe disease (KD) and metachromatic leukodystrophy (MLD) are caused by accumulation of the glycolipids galactosylceramide (GalCer) and sulfatide and their toxic metabolites psychosine and lysosulfatide, respectively. We discovered a potent and sele
Autor:
Brett E. Crawford, Adam Harris, Jeremy L. Van Vleet, Roberto Giugliani, Sanjay Chandriani, Roger Lawrence, Gouri Yogalingam, Linley Mangini, Nathan T. Martin, Wyatt T. Clark, Alessandra d'Azzo, Jonathan H. LeBowitz
Publikováno v:
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 21, Iss, Pp-(2019)
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 21, Iss, Pp-(2019)
Introduction: GM1 gangliosidosis is a rare autosomal recessive genetic disorder caused by the disruption of the GLB1 gene that encodes β-galactosidase, a lysosomal hydrolase that removes β-linked galactose from the non-reducing end of glycans. Defi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fad1e65eec41e62a514a14a12ceec192
Publikováno v:
Journal of Virology. 84:7934-7942
Genomewide analyses of the mammalian transcriptome have revealed that large tracts of sequence previously annotated as noncoding are frequently transcribed and give rise to stable RNA. Although the transcription of individual genes of the Kaposi's sa