Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Kriti Chaplot"'
Publikováno v:
PLoS ONE, Vol 16, Iss 1, p e0241161 (2021)
Alpha-synuclein pre-formed fibrils (PFFs) represent a promising model system for the study of cellular processes underlying cell-to-cell transmission of alpha-synuclein proteopathic aggregates. However, the ability to differentiate the fate of intern
Externí odkaz:
https://doaj.org/article/4452e22d31c74a0291550787dbd1036b
Publikováno v:
Frontiers in Aging Neuroscience, Vol 12 (2020)
Protein homeostasis, or proteostasis, is a combination of cellular processes that govern protein quality control, namely, protein translation, folding, processing, and degradation. Disruptions in these processes can lead to protein misfolding and agg
Externí odkaz:
https://doaj.org/article/f9a7df1afac049fcbbdc882fa918c758
Autor:
Kriti Chaplot, Lokesh Pimpale, Balaji Ramalingam, Senthilkumar Deivasigamani, Siddhesh S. Kamat, Girish S. Ratnaparkhi
Publikováno v:
Disease Models & Mechanisms, Vol 12, Iss 2 (2019)
Familial amyotrophic lateral sclerosis (ALS) is an incurable, late-onset motor neuron disease, linked strongly to various causative genetic loci. ALS8 codes for a missense mutation, P56S, in VAMP-associated protein B (VAPB) that causes the protein to
Externí odkaz:
https://doaj.org/article/3dd5f25ebd454506bed46a64f75f78b8
Autor:
Juan R. Peinado, Kriti Chaplot, Timothy S. Jarvela, Edward M. Barbieri, James Shorter, Iris Lindberg
Publikováno v:
ACS Chem Neurosci
As neurons age, protein homeostasis becomes less efficient, resulting in misfolding and aggregation. Chaperone proteins perform vital functions in the maintenance of cellular proteostasis, and chaperone-based therapies that promote sequestration of t
Publikováno v:
Frontiers in Aging Neuroscience
Frontiers in Aging Neuroscience, Vol 12 (2020)
Frontiers in Aging Neuroscience, Vol 12 (2020)
Protein homeostasis, or proteostasis, is a combination of cellular processes that govern protein quality control, namely, protein translation, folding, processing, and degradation. Disruptions in these processes can lead to protein misfolding and agg
Autor:
Juan R. Peinado, Edward M. Barbieri, Timothy S. Jarvela, Kriti Chaplot, James Shorter, Iris Lindberg
As neurons age, protein homeostasis becomes less efficient, resulting in misfolding and aggregation. Chaperone proteins perform vital functions in the maintenance of cellular proteostasis, and chaperone-based therapies that promote sequestration of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ba4b53e4f74ddd8bec5d67c4ce519bb
https://doi.org/10.1101/2020.04.15.039578
https://doi.org/10.1101/2020.04.15.039578
Autor:
Kriti Chaplot
Publikováno v:
Disease Models & Mechanisms
First Person is a series of interviews with the first authors of a selection of papers published in Disease Models & Mechanisms, helping early-career researchers promote themselves alongside their papers. Kriti Chaplot is first author on ‘SOD1 acti
Autor:
Lokesh Pimpale, Balaji Ramalingam, Siddhesh S. Kamat, Girish S. Ratnaparkhi, Senthilkumar Deivasigamani, Kriti Chaplot
Publikováno v:
Disease Models & Mechanisms.
Familial amyotrophic lateral sclerosis (ALS) is an incurable, late-onset motor neuron disease, linked strongly to various causative genetic loci. ALS8 codes for a missense mutation, P56S, in VAMP-associated protein B (VAPB) that causes the protein to
Publikováno v:
Insights into Human Neurodegeneration: Lessons Learnt from Drosophila ISBN: 9789811322174
The fruit fly, Drosophila melanogaster, is an attractive model for studying human disease. The popularity of the model is a consequence of its well-developed toolbox for genetic engineering and the finding that 75% of genes that cause human disease h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0f7395f28a6148aaace2ea2466432ae
https://doi.org/10.1007/978-981-13-2218-1_5
https://doi.org/10.1007/978-981-13-2218-1_5
Autor:
Kriti, Chaplot, Lokesh, Pimpale, Balaji, Ramalingam, Senthilkumar, Deivasigamani, Siddhesh S, Kamat, Girish S, Ratnaparkhi
Publikováno v:
Disease Models & Mechanisms
Familial amyotrophic lateral sclerosis (ALS) is an incurable, late-onset motor neuron disease, linked strongly to various causative genetic loci. ALS8 codes for a missense mutation, P56S, in VAMP-associated protein B (VAPB) that causes the protein to