Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Devesh C. Pant"'
Publikováno v:
Neurobiology of Disease, Vol 143, Iss , Pp 105014- (2020)
In recent years, research on sphingolipids, particularly ceramides, has attracted increased attention, revealing the important roles and many functions of these molecules in several human neurological disorders. The nervous system is enriched with im
Externí odkaz:
https://doaj.org/article/46c10fc743a14b1a82c0d6126c554b0d
Autor:
Janani Parameswaran, Nancy Zhang, Elke Braems, Kedamawit Tilahun, Devesh C Pant, Keena Yin, Seneshaw Asress, Kara Heeren, Anwesha Banerjee, Emma Davis, Samantha L Schwartz, Graeme L Conn, Gary J Bassell, Ludo Van Den Bosch, Jie Jiang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::711038c3720bbc1e8b5b669bbcb076db
https://doi.org/10.7554/elife.85902.sa2
https://doi.org/10.7554/elife.85902.sa2
Autor:
Janani Parameswaran, Nancy Zhang, Kedamawit Tilahun, Devesh C. Pant, Ganesh Chilukuri, Seneshaw Asress, Anwesha Banerjee, Emma Davis, Samantha L. Schwartz, Graeme L. Conn, Gary J. Bassell, Jie Jiang
GGGGCC (G4C2) hexanucleotide repeat expansion in the C9orf72 gene is the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). The repeat is bidirectionally transcribed and confers gain of toxicity. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbe09d352dcd8f93266fc4bcf1474dc8
https://doi.org/10.1101/2022.06.06.495030
https://doi.org/10.1101/2022.06.06.495030
Autor:
Devesh C Pant, Janani Parameswaran, Lu Rao, Isabel Loss, Ganesh Chilukuri, Rosanna Parlato, Liang Shi, Jonathan D Glass, Gary J Bassell, Philipp Koch, Rüstem Yilmaz, Jochen H Weishaupt, Arne Gennerich, Jie Jiang
Publikováno v:
EMBO Rep
Mutations in the human kinesin family member 5A (KIF5A) gene were recently identified as a genetic cause of amyotrophic lateral sclerosis (ALS). Several KIF5A ALS variants cause exon 27 skipping and are predicted to produce motor proteins with an alt
Autor:
Devesh C. Pant, Janani Parameswaran, Lu Rao, Liang Shi, Ganesh Chilukuri, Zachary T. McEachin, Jonathan Glass, Gary J. Bassell, Arne Gennerich, Jie Jiang
Mutations in the human kinesin family member 5A (KIF5A) gene were recently identified as a genetic cause of amyotrophic lateral sclerosis (ALS). Several KIF5A ALS variants cause exon 27 skipping and produce motor proteins with an altered C-terminal t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6eec4fb3144f3806d75c3e9f74f32406
https://doi.org/10.1101/2022.03.05.483071
https://doi.org/10.1101/2022.03.05.483071
Autor:
Devesh C. Pant, Taras Y. Nazarko
Publikováno v:
Autophagy
Selective autophagy is a specific elimination of certain intracellular substrates by autophagic pathways. The most studied macroautophagy pathway involves tagging and recognition of a specific cargo by the autophagic membrane (phagophore) followed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c546a6b8dd8235c2c547f1626776916
https://europepmc.org/articles/PMC8632090/
https://europepmc.org/articles/PMC8632090/
Autor:
Montserrat Ruiz, Gholamreza Shariati, Cristina Pujades, Eric W. Klee, Odile Boespflug-Tanguy, Joseph G. Gleeson, Reza Maroofian, Filippo Vairo, Nathalie Launay, Stéphane Fourcade, Javier Joya, Lauren Brady, Mark A. Tarnopolsky, Nara Sobreira, Marc C. Patterson, Agatha Schlüter, Julie S. Cohen, Laurence Colleaux, Elizabeth Wohler, Carles Cornet, Jingmin Wang, Margit Burmeister, Neda Mazaheri, Isabelle Desguerre, Kiely N. James, Diana Rodriguez, Maria Eugenia Yoldi, Imen Dorboz, Huifang Yan, Dorothée Ville, Hamid Galehdari, Damir Musaev, Mary J H Willis, Ali Fatemi, Gaetan Lesca, Davide Rubbini, Maha S. Zaki, Aurora Pujol, Brendan C. Lanpher, Devesh C. Pant, Karine Siquier-Pernet, Javier Terriente, Carlos Casasnovas, Sergio Aguilera-Albesa
Publikováno v:
Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2019, 129 (3), pp.1240-1256. ⟨10.1172/JCI123959⟩
Journal of Clinical Investigation, 2019, 129 (3), pp.1240-1256. ⟨10.1172/JCI123959⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Journal of Clinical Investigation, American Society for Clinical Investigation, 2019, 129 (3), pp.1240-1256. ⟨10.1172/JCI123959⟩
Journal of Clinical Investigation, 2019, 129 (3), pp.1240-1256. ⟨10.1172/JCI123959⟩
Dipòsit Digital de la UB
Universidad de Barcelona
Sphingolipid imbalance is the culprit in a variety of neurological diseases, some affecting the myelin sheath. We have used whole-exome sequencing in patients with undetermined leukoencephalopathies to uncover the endoplasmic reticulum lipid desatura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bddcd779b5407da142cab5d42fb93e8
https://hal.archives-ouvertes.fr/hal-02087782
https://hal.archives-ouvertes.fr/hal-02087782
Publikováno v:
Toxicological & Environmental Chemistry. 95:635-645
Vinca rosea is a plant renowned for its medicinal value, belonging to the family Apocynaceae. Traditionally, the leaf juice of V. rosea is used for treatment of various diseases. In the present study, the effect of V. rosea leaf extract on the develo
Autor:
Janani Parameswaran, Nancy Zhang, Elke Braems, Kedamawit Tilahun, Devesh C Pant, Keena Yin, Seneshaw Asress, Kara Heeren, Anwesha Banerjee, Emma Davis, Samantha L Schwartz, Graeme L Conn, Gary J Bassell, Ludo Van Den Bosch, Jie Jiang
Publikováno v:
eLife, Vol 12 (2023)
GGGGCC (G4C2) hexanucleotide repeat expansion in the C9ORF72 gene is the most common genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS). The repeat is bidirectionally transcribed and confers gain of toxicity. Howev
Externí odkaz:
https://doaj.org/article/b5c4b7e784d04f559aa8ececa782ffe9