Các bài viết có thể truy cập công khai - Nahid KhanTìm hiểu thêm
Không có ở bất kỳ nơi nào: 4
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
Các cơ quan ủy nhiệm: Council of Scientific and Industrial Research, India, Department of …
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
Các cơ quan ủy nhiệm: Department of Biotechnology, India
Mitochondrial genome variations in idiopathic dilated cardiomyopathy
P Govindaraj, B Rani, P Sundaravadivel, A Vanniarajan, KP Indumathi, ...
Mitochondrion 48, 51-59, 2019
Các cơ quan ủy nhiệm: Council of Scientific and Industrial Research, India, Department of Science …
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
Các cơ quan ủy nhiệm: Department of Biotechnology, India
Có tại một số nơi: 16
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
Các cơ quan ủy nhiệm: Swiss National Science Foundation, US National Institutes of Health …
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
Các cơ quan ủy nhiệm: Swiss National Science Foundation, Academy of Finland, European Commission
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
Các cơ quan ủy nhiệm: US National Institutes of Health, Academy of Finland, European Commission
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
Các cơ quan ủy nhiệm: Academy of Finland
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
Các cơ quan ủy nhiệm: Swiss National Science Foundation, Academy of Finland, European Commission
Mitochondrial disorders: challenges in diagnosis & treatment
NA Khan, P Govindaraj, AK Meena, K Thangaraj
Indian Journal of Medical Research 141 (1), 13-26, 2015
Các cơ quan ủy nhiệm: Council of Scientific and Industrial Research, India, Department of …
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
Các cơ quan ủy nhiệm: Academy of Finland, UK Biotechnology and Biological Sciences Research …
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
Các cơ quan ủy nhiệm: Department of Biotechnology, India
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
Các cơ quan ủy nhiệm: Council of Scientific and Industrial Research, India, Department of …
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
Các cơ quan ủy nhiệm: Department of Biotechnology, India
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
Các cơ quan ủy nhiệm: Council of Scientific and Industrial Research, India, Department of …
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
Các cơ quan ủy nhiệm: Council of Scientific and Industrial Research, India, Department of …
Phenotypic effects of dietary stress in combination with a respiratory chain bypass in mice
PK Dhandapani, AM Lyyski, L Paulin, NA Khan, A Suomalainen, ...
Physiological reports 7 (13), e14159, 2019
Các cơ quan ủy nhiệm: Academy of Finland, European Commission
Clinical and neuroimaging features in two children with mutations in the mitochondrial ND5 gene
K Sonam, PS Bindu, AB Taly, C Govindaraju, N Gayathri, HR Arvinda, ...
Neuropediatrics 46 (04), 277-281, 2015
Các cơ quan ủy nhiệm: Department of Biotechnology, India
Mitochondrial DNA variations in Madras motor neuron disease
P Govindaraj, A Nalini, N Krishna, A Sharath, NA Khan, R Tamang, ...
Mitochondrion 13 (6), 721-728, 2013
Các cơ quan ủy nhiệm: US National Institutes of Health, Council of Scientific and Industrial …
Author Response: Penetrance of the LHON Mutation m. 11778G> A May Depend on Factors Other Than Haplotype or Heteroplasmy Rate
NA Khan, P Govindaraj, N Soumittra, S Sharma, S Srilekha, S Ambika, ...
Investigative Ophthalmology & Visual Science 59 (1), 382-382, 2018
Các cơ quan ủy nhiệm: Council of Scientific and Industrial Research, India, Department of …
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