Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Sharmistha Mitra"'
Autor:
Sharmistha Mitra, Baozhi Chen, Peixiang Wang, Erin E. Chown, Mathew Dear, Dikran R. Guisso, Ummay Mariam, Jun Wu, Emrah Gumusgoz, Berge A. Minassian
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 1 (2023)
Externí odkaz:
https://doaj.org/article/24f6a47e51664198bbbbbe98bb91751b
Publikováno v:
Rev Neurol (Paris)
The ubiquitin system impacts most cellular processes and is altered in numerous neurodegenerative diseases . However, little is known about its role in neurodegenerative diseases due to disturbances of glycogen metabolism such as Lafora disease (LD).
Autor:
Silvia Nitschke, Mitchell A Sullivan, Sharmistha Mitra, Charlotte R Marchioni, Jennifer P Y Lee, Brandon H Smith, Saija Ahonen, Jun Wu, Erin E Chown, Peixiang Wang, Sara Petković, Xiaochu Zhao, Laura F DiGiovanni, Ami M Perri, Lori Israelian, Tamar R Grossman, Holly Kordasiewicz, Francisco Vilaplana, Kazuhiro Iwai, Felix Nitschke, Berge A Minassian
Publikováno v:
Brain
Longer glucan chains tend to precipitate. Glycogen, by far the largest mammalian glucan and the largest molecule in the cytosol with up to 55 000 glucoses, does not, due to a highly regularly branched spherical structure that allows it to be perfused
Publikováno v:
Biochemical Society Transactions
Altered protein ubiquitination is associated with the pathobiology of numerous diseases; however, its involvement in glycogen metabolism and associated polyglucosan body (PB) disease has not been investigated in depth. In PB disease, excessively long
Autor:
Dikran R Guisso, Silvia Nitschke, Berge A. Minassian, Jun Wu, Brandy Verhalen, Matthew Dear, Felix Nitschke, Emrah Gumusgoz, Sharmistha Mitra, Sahba Kasiri
Publikováno v:
Neurotherapeutics
Many adult and most childhood neurological diseases have a genetic basis. CRISPR/Cas9 biotechnology holds great promise in neurological therapy, pending the clearance of major delivery, efficiency, and specificity hurdles. We applied CRISPR/Cas9 geno
Publikováno v:
Nature Reviews Neurology. 14:606-617
Lafora disease is a severe, autosomal recessive, progressive myoclonus epilepsy. The disease usually manifests in previously healthy adolescents, and death commonly occurs within 10 years of symptom onset. Lafora disease is caused by loss-of-function
Publikováno v:
Statistical Quality Technologies ISBN: 9783030207083
In this paper, we design a decision theoretic sampling plan (DSP) based on Type-I and Type-I hybrid censored lifetime data from a one-parameter exponential distribution. The Bayes estimator of the mean lifetime is used to define a decision function.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18e275bc1a5ec1a6595edaab9cb92d69
https://doi.org/10.1007/978-3-030-20709-0_8
https://doi.org/10.1007/978-3-030-20709-0_8
Autor:
Jason G. McCoy, Ming Zhou, Wonpil Im, Jumin Lee, Sébastien F. Poget, Zhenning Ren, Sharmistha Mitra, Elena J. Levin, Vitali Stanevich, Matthias Quick
Publikováno v:
Structure. 24:956-964
The phosphoenolpyruvate:carbohydrate phosphotransferase systems are found in bacteria, where they play central roles in sugar uptake and regulation of cellular uptake processes. Little is known about how the membrane-embedded components (EIICs) selec
The study proposes a new decision theoretic sampling plan (DSP) for Type-I and Type-I hybrid censored samples when the lifetimes of individual items are exponentially distributed with a scale parameter. The DSP is based on an estimator of the scale p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f393bfca7bd8140bc164732abcbf8701
http://arxiv.org/abs/1807.00615
http://arxiv.org/abs/1807.00615
Autor:
Ami M. Perri, Saija Ahonen, Xiaochu Zhao, Lori Israelian, Felix Nitschke, Cameron Ackerley, Berge A. Minassian, Mitchell A. Sullivan, Sharmistha Mitra, Laura F. DiGiovanni, Erin E. Chown, Mackenzie Chown, Peixiang Wang
SUMMARYGlycogen synthesis is vital, malstructure resulting in precipitation and accumulation into neurotoxic polyglucosan bodies (PBs). One well-understood mechanism of PB generation is glycogen branching enzyme deficiency (GBED). Less understood is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de9c5e6cd2df8cccc6a673ffc341fb8f