| Effective treatment of mitochondrial myopathy by nicotinamide riboside, a vitamin B 3 NA Khan, M Auranen, I Paetau, E Pirinen, L Euro, S Forsström, L Pasila, ... EMBO molecular medicine 6 (6), 721-731, 2014 | 437 | 2014 |
| mTORC1 regulates mitochondrial integrated stress response and mitochondrial myopathy progression NA Khan, J Nikkanen, S Yatsuga, C Jackson, L Wang, S Pradhan, ... Cell metabolism 26 (2), 419-428. e5, 2017 | 376 | 2017 |
| Mitochondrial DNA replication defects disturb cellular dNTP pools and remodel one-carbon metabolism J Nikkanen, S Forsström, L Euro, I Paetau, RA Kohnz, L Wang, D Chilov, ... Cell metabolism 23 (4), 635-648, 2016 | 280 | 2016 |
| Niacin cures systemic NAD+ deficiency and improves muscle performance in adult-onset mitochondrial myopathy E Pirinen, M Auranen, NA Khan, V Brilhante, N Urho, A Pessia, ... Cell metabolism 31 (6), 1078-1090. e5, 2020 | 273 | 2020 |
| Fibroblast growth factor 21 drives dynamics of local and systemic stress responses in mitochondrial myopathy with mtDNA deletions S Forsström, CB Jackson, CJ Carroll, M Kuronen, E Pirinen, S Pradhan, ... Cell metabolism 30 (6), 1040-1054. e7, 2019 | 207 | 2019 |
| Mitochondrial disorders: challenges in diagnosis & treatment NA Khan, P Govindaraj, AK Meena, K Thangaraj Indian Journal of Medical Research 141 (1), 13-26, 2015 | 125 | 2015 |
| Mitochondrial dysfunction and genetic heterogeneity in chronic periodontitis P Govindaraj, NA Khan, P Gopalakrishna, RV Chandra, A Vanniarajan, ... Mitochondrion 11 (3), 504-512, 2011 | 75 | 2011 |
| Mosaic dysfunction of mitophagy in mitochondrial muscle disease T Mito, AE Vincent, J Faitg, RW Taylor, NA Khan, TG McWilliams, ... Cell metabolism 34 (2), 197-208. e5, 2022 | 62 | 2022 |
| Mitochondrial DNA variations associated with hypertrophic cardiomyopathy P Govindaraj, NA Khan, B Rani, DS Rani, P Selvaraj, V Jyothi, A Bahl, ... Mitochondrion 16, 65-72, 2014 | 40 | 2014 |
| Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutations K Sonam, NA Khan, PS Bindu, AB Taly, N Gayathri, MMS Bharath, ... Brain and Development 36 (9), 807-812, 2014 | 35 | 2014 |
| Bilateral hypertrophic olivary nucleus degeneration on magnetic resonance imaging in children with Leigh and Leigh-like syndrome PS Bindu, AB Taly, K Sonam, C Govindaraju, HR Arvinda, N Gayathri, ... The British Journal of Radiology 87 (1034), 20130478, 2014 | 31 | 2014 |
| Mitochondrial oxidative phosphorylation disorders in children: phenotypic, genotypic and biochemical correlations in 85 patients from South India K Sonam, PS Bindu, MMS Bharath, P Govindaraj, N Gayathri, HR Arvinda, ... Mitochondrion 32, 42-49, 2017 | 30 | 2017 |
| Leber's hereditary optic neuropathy–specific mutation m. 11778G> A exists on diverse mitochondrial haplogroups in India NA Khan, P Govindaraj, N Soumittra, S Sharma, S Srilekha, S Ambika, ... Investigative ophthalmology & visual science 58 (10), 3923-3930, 2017 | 28 | 2017 |
| Magnetic resonance imaging correlates of genetically characterized patients with mitochondrial disorders: a study from south India PS Bindu, H Arvinda, AB Taly, C Govindaraju, K Sonam, S Chiplunkar, ... Mitochondrion 25, 6-16, 2015 | 27 | 2015 |
| Outcome of epilepsy in patients with mitochondrial disorders: Phenotype genotype and magnetic resonance imaging correlations PS Bindu, K Sonam, P Govindaraj, C Govindaraju, S Chiplunkar, ... Clinical Neurology and Neurosurgery 164, 182-189, 2018 | 26 | 2018 |
| Mitochondrial genome variations in idiopathic dilated cardiomyopathy P Govindaraj, B Rani, P Sundaravadivel, A Vanniarajan, KP Indumathi, ... Mitochondrion 48, 51-59, 2019 | 22 | 2019 |
| Co-occurrence of m. 1555A> G and m. 11778G> A mitochondrial DNA mutations in two Indian families with strikingly different clinical penetrance of Leber hereditary optic neuropathy NA Khan, P Govindaraj, V Jyothi, AK Meena, K Thangaraj Molecular Vision 19, 1282, 2013 | 21 | 2013 |
| Haplogroup heterogeneity of LHON patients carrying the m. 14484T> C mutation in India NA Khan, P Govindaraj, N Soumittra, S Srilekha, S Ambika, A Vanniarajan, ... Investigative ophthalmology & visual science 54 (6), 3999-4005, 2013 | 21 | 2013 |
| The “double panda” sign in Leigh disease K Sonam, PS Bindu, N Gayathri, NA Khan, C Govindaraju, HR Arvinda, ... Journal of Child Neurology 29 (7), 980-982, 2014 | 16 | 2014 |
| Peripheral neuropathy in genetically characterized patients with mitochondrial disorders: A study from south India PS Bindu, C Govindaraju, K Sonam, M Nagappa, S Chiplunkar, R Kumar, ... Mitochondrion 27, 1-5, 2016 | 13 | 2016 |
Kumarasamy ThangarajCentre for Cellular and Molecular BiologyEmail được xác minh tại ccmb.res.in