Zobrazeno 1 - 10
of 292
pro vyhledávání: '"S K, Shankar"'
Autor:
S K Shankar, Anita Mahadevan
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 65, Iss 5, Pp 218-225 (2022)
Biobanks are set to become the norm. The explosion of new and powerful technologies like genomics and other multiomics has catapulted research from individual laboratories to multi-institutional and international partners. Today, with increasing life
Externí odkaz:
https://doaj.org/article/e0901c416b204800946b5e4c2075922b
Autor:
B R Vijaykumar, R Sai Kant, C Rajendran, Swathi U Lekshmi, Sundar Keerthana, Anita Mahadevan, S K Shankar, R S Jayshree
Publikováno v:
Annals of Indian Academy of Neurology, Vol 21, Iss 4, Pp 250-255 (2018)
Context: Published data on genetic characterization of Toxoplasma gondii (T.gondii) from clinical cases of toxoplasmosis from India is lacking. Aims: The present study was aimed at identifying genetic types of T. gondii in fatal cases of cerebral tox
Externí odkaz:
https://doaj.org/article/d2c63387c1d045048443e245f4eb2620
Autor:
Debpali Sur, Raj Kishor Kustwar, Savita Budania, Anita Mahadevan, Dustin C. Hancks, Vijay Yadav, S. K. Shankar, Prabhat K. Mandal
Publikováno v:
Mobile DNA, Vol 8, Iss 1, Pp 1-12 (2017)
Abstract Background Recent reports indicate that retrotransposons – a type of mobile DNA – can contribute to neuronal genetic diversity in mammals. Retrotransposons are genetic elements that mobilize via an RNA intermediate by a “copy-and-paste
Externí odkaz:
https://doaj.org/article/b8c2f1819ef54497b71c0e4e74164b25
Publikováno v:
Annals of Indian Academy of Neurology, Vol 22, Iss 4, Pp 462-463 (2019)
Externí odkaz:
https://doaj.org/article/6759e87121494956aa71ce3d99e64bd3
Autor:
Özlem Atlı, Sabina Yasmin, Antonio Lavecchia, Susanta Kumar Mondal, Fulvio Loiodice, S K Shankar, Merve Baysal, Mohd Usman Mohd Siddique, Fabrizio Dal Piaz, Ravi Pratap Singh, Venkatesan Jayaprakash, Carmen Cerchia, Sankaran Vadivelan, Ashok Kumar Pattnaik, Antonio Laghezza, Vishnu Nayak Badavath
Publikováno v:
ChemMedChem. 16:484-498
Insulin resistance is a major pathophysiological feature in the development of type 2 diabetes (T2DM). Ferulic acid is known for attenuating the insulin resistance and reducing the blood glucose in T2DM rats. In this work, we designed and synthesized
Publikováno v:
The Biology of Glial Cells: Recent Advances ISBN: 9789811683121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::71393db33efc99fe7fd6ae10d45381a2
https://doi.org/10.1007/978-981-16-8313-8_8
https://doi.org/10.1007/978-981-16-8313-8_8
Publikováno v:
International Conference on Computing, Communication, Electrical and Biomedical Systems ISBN: 9783030861643
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c633be001651ff5c745f3fcc2352f504
https://doi.org/10.1007/978-3-030-86165-0_33
https://doi.org/10.1007/978-3-030-86165-0_33
Autor:
Thomas Mathew, Sushanth Aroor, Anup J Devasia, Anita Mahadevan, Vineeta Shobha, Raghunandan Nadig, Raji Varghese, S K Shankar, G. R. K. Sarma
Publikováno v:
Annals of Indian Academy of Neurology, Vol 15, Iss 1, Pp 27-30 (2012)
Objective: To study the clinical, pathological and prognostic profile of patients with temporal arteritis in India. Materials and Methods: The study was conducted in a tertiary care center from south India from 2005 to 2010 in the departments of neur
Externí odkaz:
https://doaj.org/article/54047a6c13814411a7622b6649669a7f
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 54, Iss 2, Pp 350-354 (2011)
Background: Dysferlinopathy is an autosomal recessive-limb girdle muscular dystrophy (AR-LGMD) caused due to the defect in gene encoding dysferlin, a sarcolemmal protein. Awareness of the variants and their relative frequency is essential for accurat
Externí odkaz:
https://doaj.org/article/99d23f46a2784caa8ca58e253404a5ec
Autor:
S K Shankar, Anita Mahadevan, Silvano Dias Sapico, M. S. G. Ghodkirekar, R. G. W. Pinto, S N Madhusudana
Publikováno v:
Annals of Indian Academy of Neurology, Vol 15, Iss 3, Pp 221-223 (2012)
We report a case of rabies viral encephalitis in a 48-year-old male with an unusually long incubation period, historically suspected to be more than 20 years. The case was referred for histological diagnosis following alleged medical negligence to th
Externí odkaz:
https://doaj.org/article/2b83cb412e2d4970ab5e0cb4a310c7a8