Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Marya S Sabir"'
Autor:
Aleksandra Grozić, Keaton Coker, Christopher M Dussik, Marya S Sabir, Zhela Sabir, Arianna Bradley, Lin Zhang, Jin Park, Steven Yale, Ichiro Kaneko, Maryam Hockley, Lucinda A Harris, Tisha N Lunsford, Todd R Sandrin, Peter W Jurutka
Publikováno v:
PLoS ONE, Vol 17, Iss 10, p e0275683 (2022)
Irritable bowel syndrome (IBS) is one of the most common gastrointestinal disorders and affects approximately 4% of the global population. The diagnosis of IBS can be made based on symptoms using the validated Rome criteria and ruling out commonly oc
Externí odkaz:
https://doaj.org/article/ecfd318ab7354af1bc157378b2504795
Autor:
Marya S. Sabir, Petcharat Leoyklang, Mary E. Hackbarth, Evgenia Pak, Amalia Dutra, Richard Tait, Laura Pollard, David R. Adams, William A. Gahl, Marjan Huizing, May Christine V. Malicdan
Publikováno v:
Stem Cell Research, Vol 81, Iss , Pp 103600- (2024)
Free sialic acid storage disorder (FSASD) is a rare, autosomal recessive, neurodegenerative disorder caused by biallelic mutations in SLC17A5, encoding the lysosomal transmembrane sialic acid exporter, SLC17A5. Defects in SLC17A5 lead to lysosomal ac
Externí odkaz:
https://doaj.org/article/4516a097c315411c89234a855ac39d44
Autor:
Marya S. Sabir, Cornelis Blauwendraat, Sarah Ahmed, Geidy E. Serrano, Thomas G. Beach, Matthew Perkins, Ann C. Rice, Eliezer Masliah, Christopher M. Morris, Lasse Pihlstrom, Alexander Pantelyat, Susan M. Resnick, Mark R. Cookson, Dena G. Hernandez, Marilyn Albert, Ted M. Dawson, Liana S. Rosenthal, Henry Houlden, Olga Pletnikova, Juan Troncoso, Sonja W. Scholz
Publikováno v:
Neurobiology of Disease, Vol 127, Iss , Pp 142-146 (2019)
Atypical parkinsonism syndromes are a heterogeneous group of neurodegenerative disorders that include corticobasal degeneration (CBD), Lewy body dementia (LBD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). The APOE ε4 all
Externí odkaz:
https://doaj.org/article/0b8f2037e2114d4bbffc089f1591cb20
Autor:
Sarah Livingston, Sanchita Mallick, Daniel A. Lucas, Marya S. Sabir, Zhela L. Sabir, Hespera Purdin, Sree Nidamanuri, Carol A. Haussler, Mark R. Haussler, Peter W. Jurutka
Publikováno v:
Biochemistry and Biophysics Reports, Vol 24, Iss , Pp 100825- (2020)
Mediated by the nuclear vitamin D receptor (VDR), the hormonally active vitamin D metabolite, 1,25-dihydroxyvitamin D3 (1,25D), is known to regulate expression of genes impacting calcium and phosphorus metabolism, the immune system, and behavior. Uro
Externí odkaz:
https://doaj.org/article/97eedda4d71a409f88143dc9029b252a
Autor:
Marya S. Sabir, Mark R. Haussler, Sanchita Mallick, Ichiro Kaneko, Daniel A. Lucas, Carol A. Haussler, G. Kerr Whitfield, Peter W. Jurutka
Publikováno v:
Genes & Nutrition, Vol 13, Iss 1, Pp 1-11 (2018)
Abstract Background Diminished brain levels of two neurohormones, 5-hydroxytryptamine (5-HT; serotonin) and 1,25-dihydroxyvitamin D3 (1,25D; active vitamin D metabolite), are proposed to play a role in the atypical social behaviors associated with ps
Externí odkaz:
https://doaj.org/article/e504b2f50ce6418ba2ba5000d168baf8
Autor:
Aleksandra Grozic, Zhela L. Sabir, Michael C. Heck, Ichiro Kaneko, Marya S. Sabir, Pamela A. Marshall, Sanchita Mallick, Carl E. Wagner, Christoper M. Dussik, Peter W. Jurutka
Publikováno v:
ACS Chemical Neuroscience. 12:857-871
There is considerable interest in identifying effective and safe drugs for neurodegenerative disorders. Cell culture and animal model work have demonstrated that modulating gene expression through RXR-mediated pathways may mitigate or reverse cogniti
Autor:
Marjan Huizing, Steven U. Walkley, Melissa Wasserstein, Christine Anne-Longin, Raymond Y. Wang, Richard Reimer, Laura Pollard, Liisa Paavola, May Christine Malicdan, Marya S. Sabir, Petcharat Leoyklang, David R. Adams, William A. Gahl
Publikováno v:
Molecular Genetics and Metabolism. 138:107160
Autor:
Marjan Huizing, Marya S. Sabir, Mary E. Hackbarth, Lynne A. Wolfe, Melissa P. Wasserstein, David R. Adams, May C. Malicdan, William A. Gahl, Steven U. Walkley, F.S.A.S.D. Consortium
Publikováno v:
Molecular Genetics and Metabolism. 135:S59-S60
Autor:
Thomas G. Beach, Mark R. Cookson, Dena G. Hernandez, Juan C. Troncoso, Eliezer Masliah, Lasse Pihlstrøm, Susan M. Resnick, Liana S. Rosenthal, Matthew H. Perkins, Olga Pletnikova, Alexander Pantelyat, Ted M. Dawson, Sarah A. Ahmed, Geidy E. Serrano, Marya S. Sabir, Marilyn S. Albert, Cornelis Blauwendraat, Henry Houlden, Ann C. Rice, Christopher Morris, Sonja W. Scholz
Publikováno v:
Neurobiology of Disease, Vol 127, Iss, Pp 142-146 (2019)
Neurobiol Dis
Neurobiol Dis
Atypical parkinsonism syndromes are a heterogeneous group of neurodegenerative disorders that include corticobasal degeneration (CBD), Lewy body dementia (LBD), multiple system atrophy (MSA), and progressive supranuclear palsy (PSP). The APOE e4 alle
Autor:
Sonja W. Scholz, Angela Kokkinis, William Zhu, Ellen Sidransky, Alice B. Schindler, Risa Isonaka, Marya S. Sabir, Esther Yoon, David S. Goldstein, Grisel Lopez, Pedro Gonzalez-Alegre, Sara Bandres-Ciga, Derek P. Narendra, Cornelis Blauwendraat, Debra Ehrlich
Publikováno v:
Mov Disord
BACKGROUND: Cytoplasmic inclusions of α-synuclein in brainstem neurons are characteristic of idiopathic Parkinson’ disease. Parkinson’s disease also entails α-synuclein buildup in sympathetic nerves. Among genetic forms of Parkinson’s disease