Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Angamuthu K. Meena"'
Autor:
Angamuthu K. Meena, Sanjiban Chakrabarty, Sandeep Mallya, Hanumanthapura R. Arivinda, Madhu Nagappa, Kumarasamy Thangaraj, Sekar Deepha, Bindu Parayil Sankaran, Shama Prasada Kabekkodu, Narayanappa Gayathri, Pradyumna Jayaram, Arun B Taly, Periyasamy Govindaraj, J.N. Jessiena Ponmalar, Kapaettu Satyamoorthy, Sanjib Sinha, Rajan Kumar Jha
Publikováno v:
Journal of Neurology
Background Mitochondrial disorders are clinically complex and have highly variable phenotypes among all inherited disorders. Mutations in mitochon drial DNA (mtDNA) and nuclear genome or both have been reported in mitochondrial diseases suggesting co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33e70669f8562e895fbad10d98964809
https://doi.org/10.1007/s00415-020-10390-9
https://doi.org/10.1007/s00415-020-10390-9
Autor:
Arumugam Paramasivam, Kumarasamy Thangaraj, Angamuthu K. Meena, Robert D S Pitceathly, Challa Venkatapathi
Publikováno v:
Journal of Molecular Neuroscience
Epitranscriptomic systems enable post-transcriptional modifications of cellular RNA that are essential for regulating gene expression. Of the ~ 170 known RNA chemical modifications, methylation is among the most common. Loss of function mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f45f62064d1de4e85e06b23722ca1338
http://europepmc.org/articles/PMC7658056
http://europepmc.org/articles/PMC7658056
Autor:
Challa Venkatapathi, Kumarasamy Thangaraj, Arumugam Paramasivam, Robert D S Pitceathly, Angamuthu K. Meena
Publikováno v:
Journal of Molecular Neuroscience
Epitranscriptomic systems enable post-transcriptional modifications of cellular RNA that are essential for regulating gene expression. Of the ~ 170 known RNA chemical modifications, methylation is among the most common. Loss of function mutations in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb965f6184f73a17744dfaca72dbf735
http://europepmc.org/articles/PMC7658060
http://europepmc.org/articles/PMC7658060
Autor:
Gampa Sandeep, Megha S Uppin, Kumarasamy Thangaraj, Robert D S Pitceathly, Arumugam Paramasivam, Angamuthu K. Meena, Swati Mohapatra, Challa Venkatapathi
Publikováno v:
Mitochondrion. 48
Mutations in the mitochondrial DNA maintenance gene POLG (DNA Polymerase Gamma, Catalytic Subunit), encoding mitochondrial DNA polymerase gamma (pol γ), are associated with an extremely broad phenotypic spectrum. We identified homozygous POLG c.1879
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d8f44333fb226d7706707b3576e995
https://pubmed.ncbi.nlm.nih.gov/31425757
https://pubmed.ncbi.nlm.nih.gov/31425757
Autor:
Sonika Sharma, Kumarasamy Thangaraj, Arun B Taly, Megha S Uppin, Selvakumar Ambika, Challa Sundaram, Ayyasamy Vanniarajan, Angamuthu K. Meena, Parayil Sankaran Bindu, Narayanappa Gayathri, Nahid Akhtar Khan, Periyasamy Govindaraj, Nagasamy Soumittra, Sundaramoorthy Srilekha
Publikováno v:
Investigative Opthalmology & Visual Science. 59:382
We appreciate the effort shown by the authors and their comments on our article ‘‘Leber’s Hereditary Optic Neuropathy-Specific Mutation m.11778G>A Exists on Diverse Mitochondrial Haplogroups in India.’’ Leber’s hereditary optic neuropathy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f3ab48519b86d0228c0519b106c5f8
https://doi.org/10.1167/iovs.17-23468
https://doi.org/10.1167/iovs.17-23468
Autor:
Subhash Kaul, B. P. Sahu, Surath Mohandas, Angamuthu K. Meena, V. S. S. V. Prasad, A. K. Purohit, J. M. K. Murthy, C Sundaram, Sita Jayalakshmi, V. Laxmi, P Umabala, A. Suvarna, M V Sarathi, R Borghain, Manas Panigrahi
Publikováno v:
Histopathology. 49:396-405
Aims: To describe the pathology of central nervous system (CNS) fungal infections with particular reference to India. Methods and results: This was a retrospective study from 1988 to 2004 constituting 130 cases. The diagnosis was based on morphology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0e77ab25ecb8e0cd0bc6f7701f99e36
https://doi.org/10.1111/j.1365-2559.2006.02515.x
https://doi.org/10.1111/j.1365-2559.2006.02515.x
Autor:
Jagan Mohan Reddy, Malladi Umadevi, Suvarna Alladi, Angamuthu K. Meena, Subhash Kaul, Shanmukhi Somayajula
Publikováno v:
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association. 15(2)
Vascular dementia (VaD) is heterogeneous in its clinical, imaging, and etiological characteristics. Although VaD is common in India, its pattern is not completely known. In a hospital-based cohort, we aimed to characterize VaD by its subtypes and stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ee1969f4a5a9e757f1896a89a15d13
https://pubmed.ncbi.nlm.nih.gov/17904048
https://pubmed.ncbi.nlm.nih.gov/17904048
Autor:
Megha S Uppin, Nahid Akhtar Khan, Selvakumar Ambika, Periyasamy Govindaraj, Nagasamy Soumittra, Ayyasamy Vanniarajan, Kumarasamy Thangaraj, Challa Sundaram, Angamuthu K. Meena, Parayil Sankaran Bindu, Arun B Taly, Sundaramoorthy Srilekha, Narayanappa Gayathri
Publikováno v:
Investigative Opthalmology & Visual Science. 54:3999
Purpose To investigate the clinical and mitochondrial DNA (mtDNA) haplogroup background of Indian Leber hereditary optic neuropathy (LHON) patients carrying the m.14484T>C mutation. Methods Detailed clinical investigation and complete mtDNA sequencin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c335598d45be69295bca50137181172
https://doi.org/10.1167/iovs.13-11925
https://doi.org/10.1167/iovs.13-11925
Autor:
Angamuthu K. Meena, Rammohan Vadapalli, Yerasu Muralidhar Reddy, Megha S Uppin, Sundaram Challa
Publikováno v:
Neurology India. 61:660
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a33b2c86d493fbe4898ff7f81712af21
https://doi.org/10.4103/0028-3886.125280
https://doi.org/10.4103/0028-3886.125280
Publikováno v:
Clinical Neurophysiology. 117:203
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ad683969d07ab34b04219bbf594d686
https://doi.org/10.1016/j.clinph.2006.06.675
https://doi.org/10.1016/j.clinph.2006.06.675