Editorial: Neurodegeneration: From Disease Mechanism to Therapeutic Advancement

por Sarkar, Partha S., Meola, Giovanni, Zhang, Nan
Publicado 2022

2nd International Conference on INformation Systems Design and Intelligent Applications

por Mandal, J, Satapathy, Suresh, Sanyal, Manas, Sarkar, Partha, Mukhopadhyay, Anirban
Publicado 2015

Design of a bioactive small molecule that targets r(AUUCU) repeats in spinocerebellar ataxia 10

por Yang, Wang-Yong, Gao, Rui, Southern, Mark, Sarkar, Partha S., Disney, Matthew D.
Publicado 2016

Polyglutamine Expansion in Huntingtin and Mechanism of DNA Damage Repair Defects in Huntington’s Disease

por Pradhan, Subrata, Gao, Rui, Bush, Keegan, Zhang, Nan, Wairkar, Yogesh P., Sarkar, Partha S.
Publicado 2022

Tailoring the Microstructure of a Solid Oxide Fuel Cell Anode Support by Calcination and Milling of YSZ

por Hanifi, Amir Reza, Laguna-Bercero, Miguel A., Sandhu, Navjot Kaur, Etsell, Thomas H., Sarkar, Partha
Publicado 2016

Ethanol Suppresses PGC-1α Expression by Interfering with the cAMP-CREB Pathway in Neuronal Cells

por Liu, Zilong, Liu, Yongping, Gao, Rui, Li, Haixia, Dunn, Tiffany, Wu, Ping, Smith, Robert G., Sarkar, Partha S., Fang, Xiang
Publicado 2014

Klotho Depletion Contributes to Increased Inflammation in Kidney of the db/db Mouse Model of Diabetes via RelA (Serine)(536) Phosphorylation

por Zhao, Yanhua, Banerjee, Srijita, Dey, Nilay, LeJeune, Wanda S., Sarkar, Partha S., Brobey, Reynolds, Rosenblatt, Kevin P., Tilton, Ronald G., Choudhary, Sanjeev
Publicado 2011

Classical non-homologous end-joining pathway utilizes nascent RNA for error-free double-strand break repair of transcribed genes

por Chakraborty, Anirban, Tapryal, Nisha, Venkova, Tatiana, Horikoshi, Nobuo, Pandita, Raj K., Sarker, Altaf H., Sarkar, Partha S., Pandita, Tej K., Hazra, Tapas K.
Publicado 2016

DNAzyme Cleavage of CAG Repeat RNA in Polyglutamine Diseases

por Zhang, Nan, Bewick, Brittani, Schultz, Jason, Tiwari, Anjana, Krencik, Robert, Zhang, Aijun, Adachi, Kaho, Xia, Guangbin, Yun, Kyuson, Sarkar, Partha, Ashizawa, Tetsuo
Publicado 2021

Glucocorticoids increase skeletal muscle NF‐κB inducing kinase (NIK): links to muscle atrophy

por Fry, Christopher S., Nayeem, Syed Z., Dillon, Edgar L., Sarkar, Partha S., Tumurbaatar, Batbayar, Urban, Randall J., Wright, Traver J., Sheffield‐Moore, Melinda, Tilton, Ronald G., Choudhary, Sanjeev
Publicado 2016

Cytoplasmic CUG RNA Foci Are Insufficient to Elicit Key DM1 Features

por Dansithong, Warunee, Wolf, Cordula M., Sarkar, Partha, Paul, Sharan, Chiang, Andy, Holt, Ian, Morris, Glenn E., Branco, Dorothy, Sherwood, Megan C., Comai, Lucio, Berul, Charles I., Reddy, Sita
Publicado 2008

Inactivation of PNKP by Mutant ATXN3 Triggers Apoptosis by Activating the DNA Damage-Response Pathway in SCA3

por Gao, Rui, Liu, Yongping, Silva-Fernandes, Anabela, Fang, Xiang, Paulucci-Holthauzen, Adriana, Chatterjee, Arpita, Zhang, Hang L., Matsuura, Tohru, Choudhary, Sanjeev, Ashizawa, Tetsuo, Koeppen, Arnulf H., Maciel, Patricia, Hazra, Tapas K., Sarkar, Partha S.
Publicado 2015

Inactivation of hnRNP K by Expanded Intronic AUUCU Repeat Induces Apoptosis Via Translocation of PKCδ to Mitochondria in Spinocerebellar Ataxia 10

por White, Misti C., Gao, Rui, Xu, Weidong, Mandal, Santi M., Lim, Jung G., Hazra, Tapas K., Wakamiya, Maki, Edwards, Sharon F., Raskin, Salmo, Teive, Hélio A. G., Zoghbi, Huda Y., Sarkar, Partha S., Ashizawa, Tetsuo
Publicado 2010

Mutant huntingtin impairs PNKP and ATXN3, disrupting DNA repair and transcription

por Gao, Rui, Chakraborty, Anirban, Geater, Charlene, Pradhan, Subrata, Gordon, Kara L, Snowden, Jeffrey, Yuan, Subo, Dickey, Audrey S, Choudhary, Sanjeev, Ashizawa, Tetsuo, Ellerby, Lisa M, La Spada, Albert R, Thompson, Leslie M, Hazra, Tapas K, Sarkar, Partha S
Publicado 2019

The Role of the Mammalian DNA End-processing Enzyme Polynucleotide Kinase 3’-Phosphatase in Spinocerebellar Ataxia Type 3 Pathogenesis

por Chatterjee, Arpita, Saha, Saikat, Chakraborty, Anirban, Silva-Fernandes, Anabela, Mandal, Santi M., Neves-Carvalho, Andreia, Liu, Yongping, Pandita, Raj K., Hegde, Muralidhar L., Hegde, Pavana M., Boldogh, Istvan, Ashizawa, Tetsuo, Koeppen, Arnulf H., Pandita, Tej K., Maciel, Patricia, Sarkar, Partha S., Hazra, Tapas K.
Publicado 2015

rbFOX1/MBNL1 competition for CCUG RNA repeats binding contributes to myotonic dystrophy type 1/type 2 differences

por Sellier, Chantal, Cerro-Herreros, Estefanía, Blatter, Markus, Freyermuth, Fernande, Gaucherot, Angeline, Ruffenach, Frank, Sarkar, Partha, Puymirat, Jack, Udd, Bjarne, Day, John W., Meola, Giovanni, Bassez, Guillaume, Fujimura, Harutoshi, Takahashi, Masanori P., Schoser, Benedikt, Furling, Denis, Artero, Ruben, Allain, Frédéric H. T., Llamusi, Beatriz, Charlet-Berguerand, Nicolas
Publicado 2018

PIAS1 modulates striatal transcription, DNA damage repair, and SUMOylation with relevance to Huntington’s disease

por Morozko, Eva L., Smith-Geater, Charlene, Monteys, Alejandro Mas, Pradhan, Subrata, Lim, Ryan G., Langfelder, Peter, Kachemov, Marketta, Hill, Austin, Stocksdale, Jennifer T., Cullis, Pieter R., Wu, Jie, Ochaba, Joseph, Miramontes, Ricardo, Chakraborty, Anirban, Hazra, Tapas K., Lau, Alice, St-cyr, Sophie, Orellana, Iliana, Kopan, Lexi, Wang, Keona Q., Yeung, Sylvia, Leavitt, Blair R., Reidling, Jack C., Yang, X. William, Steffan, Joan S., Davidson, Beverly L., Sarkar, Partha S., Thompson, Leslie M.
Publicado 2021