| RSK phosphorylates SOS1 creating 14-3-3 docking sites and negatively regulating MAPK activation S Madhurima, C Audrey, C Mujeeburahiman, Z Xiaocui, L Genevieve, ... Biochemical Journal, 2012 | 94 | 2012 |
| AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome S Suzuki-Hatano, M Saha, S Rizzo, R Witko, B Gosiker, M Ramanathan, ... Human Gene Therapy, 2019 | 52 | 2019 |
| Proteomic analysis of the cilia membrane of Paramecium tetraurelia J Yano, A Rajendran, MS Valentine, M Saha, BA Ballif, JL Van Houten Journal of proteomics 78, 113-122, 2013 | 43 | 2013 |
| Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions M Saha, S Mitsuhashi, MD Jones, K Manko, HM Reddy, C Bruels, KA Cho, ... Human Molecular Genetics, 2017 | 38 | 2017 |
| AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome S Suzuki-Hatano*, M Saha*, MS Soustek, PB Kang, BJ Byrne, WT Cade, ... Molecular Therapy - Methods & Clinical Development, 2019 | 23 | 2019 |
| Spinal mitogen-activated protein kinase phosphatase-3 (MKP-3) is necessary for the normal resolution of mechanical allodynia in a mouse model of acute postoperative pain M Saha, S Skopelja, E Martinez, DL Alvarez, BS Liponis, ... Journal of Neuroscience 33 (43), 17182-17187, 2013 | 22 | 2013 |
| The impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan M Saha*, HM Reddy*, M Salih*, E Estrella, MD Jones, S Mitsuhashi, ... Physiological Genomics, 2018 | 20 | 2018 |
| Mitogen-activated protein kinase (MAPK) phosphatase-3 (MKP-3) displays a p-JNK-MAPK substrate preference in astrocytes in vitro C Ndong, RP Landry, M Saha, EA Romero-Sandoval Neuroscience letters 575, 13-18, 2014 | 20 | 2014 |
| Megf10 deficiency impairs skeletal muscle stem cell migration and muscle regeneration C Li, D Vargas‐Franco, M Saha, RM Davis, KA Manko, I Draper, ... FEBS Open Bio 11 (1), 114-123, 2021 | 12 | 2021 |
| Mitogen activated protein kinase phosphatase-3 (MKP-3) in the surgical wound is necessary for the resolution of postoperative pain in mice S Skopelja*, M Saha*, PA Alvarado-Vazquez, BS Liponis, E Martinez, ... Journal of Pain Research 10, 763—774, 2017 | 11 | 2017 |
| hnRNP L is essential for myogenic differentiation and modulates myotonic dystrophy pathologies. MS Alexander, RM Hightower, AL Reid, DK Slonim, M Saha, G Kawahara, ... Mucsle and Nerve, 2021 | 10 | 2021 |
| Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy M Saha, SA Rizzo, M Ramanathan, RM Hightower, KE Santostefano, ... Human Molecular Genetics, 2019 | 10 | 2019 |
| The impact of Megf10/Drpr gain‐of‐function on muscle development in Drosophila I Draper, M Saha, H Stonebreaker, RN Salomon, B Matin, PB Kang FEBS letters 593 (7), 680-696, 2019 | 6 | 2019 |
| Pre-Clinical Development of AAV-Mediated TAZ Gene Delivery to Treat Barth Syndrome S Suzuki-Hatano, S Rizzo, M Saha, M Ramanathan, B Gosiker, M Soustek, ... MOLECULAR THERAPY 25 (5), 29-29, 2017 | 1 | 2017 |
| Identification and Characterization of Disease Mechanisms in MEGF10 Myopathy M Saha, S Mitsuhashi, P Kang The FASEB Journal 29, 1038.1, 2015 | 1 | 2015 |
| Immune Response to AAV Vector Capsid and Assessment of Eligibility for AAV Mediated Gene Therapy for Duchenne Muscular Dystrophy M Saha MOLECULAR THERAPY 30 (4), 76-76, 2022 | | 2022 |
| COMPOSITIONS AND METHODS FOR TREATMENT OF FRIEDREICH'S ATAXIA M Saha, E Rodriguez, D Falk WO Patent WO/2021/050,991, 2021 | | 2021 |
| Correction: RSK phosphorylates SOS1 creating 14-3-3-docking sites and negatively regulating MAPK activation M Saha, A Carriere, M Cheerathodi, X Zhang, G Lavoie, J Rush, PP Roux, ... Biochemical Journal 478 (5), 1137-1138, 2021 | | 2021 |
| -Omic Approaches to Understanding Muscle Biology: Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy … M Saha, HM Reddy, MA Salih, E Estrella, MD Jones, S Mitsuhashi, ... Physiological Genomics 50 (11), 929, 2018 | | 2018 |
| PYROXD1 is responsible for cellular functions in myoblasts and homozygous missense mutation in PYROXD1 causes limb-girdle muscular dystrophy among patients from Saudi Arabian … M Saha*, HM Reddy*, MA Salih, MD Jones, S Mitsuhashi, KA Cho, ... ASHG 2017 Annual Meeting, 2017 | | 2017 |
Philippe P. RouxProfessor of Pathology and Cell Biology, IRIC, University of MontrealDirección de correo verificada de umontreal.ca
