SMN1 dosage analysis in spinal muscular atrophy from India

por Kesari, Akanchha, Rennert, Hanna, Leonard, Debra GB, Mittal, Balraj
Publicado 2005

Molecular Diagnostics

por Kesari, Akanchha, Dalal, Ashwin, Lal, Girdhari, Pandey, Sachchida Nand
Publicado 2013

Muscular Dystrophy: Disease Mechanisms and Therapies

por Pandey, Sachchida Nand, Kesari, Akanchha, Yokota, Toshifumi, Pandey, Gouri Shankar
Publicado 2015

Reply: Autosomal dominant segregation of CAPN3 c.598_612del15 associated with a mild form of calpainopathy

por Nallamilli, Babi Ramesh Reddy, Chakravorty, Samya, Kesari, Akanchha, Bean, Lora, Hegde, Madhuri
Publicado 2020

Somatic mosaicism for Duchenne dystrophy: Evidence for genetic normalization mitigating muscle symptoms

por Kesari, Akanchha, Neel, Robert, Wagoner, Lynne, Harmon, Brennan, Spurney, Christopher, Hoffman, Eric P
Publicado 2009

Non-invasive Optical Imaging of Muscle Pathology in mdx Mice Using Cathepsin Caged Near-Infrared Imaging

por Baudy, Andreas R., Sali, Arpana, Jordan, Sarah, Kesari, Akanchha, Johnston, Helen K., Hoffman, Eric P., Nagaraju, Kanneboyina
Publicado 2010

Lamin A/C–mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy

por Méjat, Alexandre, Decostre, Valérie, Li, Juan, Renou, Laure, Kesari, Akanchha, Hantaï, Daniel, Stewart, Colin L., Xiao, Xiao, Hoffman, Eric, Bonne, Gisèle, Misteli, Tom
Publicado 2009

Genetic modifiers of ambulation in the cooperative international Neuromuscular research group Duchenne natural history study

por Bello, Luca, Kesari, Akanchha, Gordish-Dressman, Heather, Cnaan, Avital, Morgenroth, Lauren P, Punetha, Jaya, Duong, Tina, Henricson, Erik K, Pegoraro, Elena, McDonald, Craig M, Hoffman, Eric P
Publicado 2015

Osteopontin is linked with AKT, FoxO1, and myostatin in skeletal muscle cells

por Nghiem, Peter P., Kornegay, Joe N., Uaesoontrachoon, Kitipong, Bello, Luca, Yin, Ying, Kesari, Akanchha, Mittal, Priya, Schatzberg, Scott J., Many, Gina M., Lee, Norman H., Hoffman, Eric P.
Publicado 2017

Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy

por Dadgar, Sherry, Wang, Zuyi, Johnston, Helen, Kesari, Akanchha, Nagaraju, Kanneboyina, Chen, Yi-Wen, Hill, D. Ashley, Partridge, Terence A., Giri, Mamta, Freishtat, Robert J., Nazarian, Javad, Xuan, Jianhua, Wang, Yue, Hoffman, Eric P.
Publicado 2014

Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients

por Nallamilli, Babi Ramesh Reddy, Chakravorty, Samya, Kesari, Akanchha, Tanner, Alice, Ankala, Arunkanth, Schneider, Thomas, da Silva, Cristina, Beadling, Randall, Alexander, John J., Askree, Syed Hussain, Whitt, Zachary, Bean, Lora, Collins, Christin, Khadilkar, Satish, Gaitonde, Pradnya, Dastur, Rashna, Wicklund, Matthew, Mozaffar, Tahseen, Harms, Matthew, Rufibach, Laura, Mittal, Plavi, Hegde, Madhuri
Publicado 2018