Zobrazeno 1 - 10
of 10
pro vyhledávání: '"K. V. L. Narasingarao"'
Autor:
S. Arati, G. K. Chetan, M. K. Sibin, Dhananjaya I. Bhat, Vikas Vazhayil, K. V. L. Narasingarao
Publikováno v:
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-7 (2019)
Abstract Background Aneurysmal subarachnoid hemorrhage is a life- threatening condition with high rate of disability and mortality. Apolipoprotein E (APOE) and Factor XIIIA (F13A) genes are involved in the pathogenetic mechanism of aneurysmal subarac
Externí odkaz:
https://doaj.org/article/cee1d71e7f0a4ae3bc5d5730c8d1de0a
Autor:
Arati Suvatha, M. K. Sibin, Dhananjaya I. Bhat, K. V. L. Narasingarao, Vikas Vazhayil, G. K. Chetan
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
Abstract Background The rupture of a brain aneurysm causes bleeding in the subarachnoid space and is known as aneurysmal subarachnoid haemorrhage (aSAH). In our study, we evaluated the association of factor XIII polymorphism and the risk of Aneurysma
Externí odkaz:
https://doaj.org/article/6342d645c8314292a55603286977aa6a
Autor:
Vikas Vazhayil, A R Prabhuraj, K. V. L. Narasingarao, Bhanumathi Govindswamy, Somanna Sampath, Dwarakanath Srinivas, Dhananjaya I Bhat, Ujwal Yeole, Arimappamagan Arivazhagan
Publikováno v:
Journal of Neurological Surgery Part B: Skull Base. 83:e343-e352
Introduction Gamma Knife radiosurgery (GKRS) is an effective treatment for benign vestibular schwannomas (VSs). The established cutoffs have recently been challenged, as recent literature expanded the horizon of GKRS to larger tumors. Even though mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cfbd7070d3f7256b0eec5dfef3e072da
https://doi.org/10.1055/s-0041-1729977
https://doi.org/10.1055/s-0041-1729977
Autor:
Ujwal, Yeole, A R, Prabhuraj, Arimappamagan, Arivazhagan, K V L, Narasingarao, Vikas, Vazhayil, Dhananjaya, Bhat, Dwarakanath, Srinivas, Bhanumathi, Govindswamy, Somanna, Sampath
Publikováno v:
J Neurol Surg B Skull Base
Introduction Gamma Knife radiosurgery (GKRS) is an effective treatment for benign vestibular schwannomas (VSs). The established cutoffs have recently been challenged, as recent literature expanded the horizon of GKRS to larger tumors. Even though mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::abbc174d67e29cb9347365a3ba8da903
https://pubmed.ncbi.nlm.nih.gov/35832954
https://pubmed.ncbi.nlm.nih.gov/35832954
Autor:
K. V. L. Narasingarao, G. K. Chetan, Dhananjaya I Bhat, M. K. Sibin, S. Arati, Vikas Vazhayil
Publikováno v:
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-7 (2019)
BMC Cardiovascular Disorders, Vol 19, Iss 1, Pp 1-7 (2019)
Background Aneurysmal subarachnoid hemorrhage is a life- threatening condition with high rate of disability and mortality. Apolipoprotein E (APOE) and Factor XIIIA (F13A) genes are involved in the pathogenetic mechanism of aneurysmal subarachnoid hae
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::069dd9534a9d051c43acb8c0e02331c9
https://pubmed.ncbi.nlm.nih.gov/31315570
https://pubmed.ncbi.nlm.nih.gov/31315570
Publikováno v:
Meta Gene
Subarachnoid haemorrhage (SAH) is characterised by bleeding in the subarachnoid space in the brain. There are various polymorphisms in genes which are associated with this disease. We performed a systematic meta- analysis to investigate the relations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24eda27c17b59e92842477a248718ca0
https://doi.org/10.1016/j.mgene.2016.06.003
https://doi.org/10.1016/j.mgene.2016.06.003
Autor:
G. K. Chetan, K. V. L. Narasingarao, Dhananjaya I Bhat, Arati Suvatha, Vikas Vazhayil, M. K. Sibin
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-9 (2018)
Background The rupture of a brain aneurysm causes bleeding in the subarachnoid space and is known as aneurysmal subarachnoid haemorrhage (aSAH). In our study, we evaluated the association of factor XIII polymorphism and the risk of Aneurysmal subarac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cad988237a439b4d4ba68959c1e7b22
https://doi.org/10.1186/s12881-018-0674-x
https://doi.org/10.1186/s12881-018-0674-x
Autor:
I Bhat Dhananjaya, M. K. Sibin, S.M. Harshitha, P Shukla Dhaval, K. V. L. Narasingarao, G. K. Chetan
Publikováno v:
Journal of molecular neuroscience : MN. 61(2)
miRNA polymorphisms are recently identified as a risk factor for various cancers, and it is associated with change in the expression of target genes in vitro. rs11614913 polymorphism in miR196a2 was associated with risk of glioma in Chinese populatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a663ec36069cfc584707dab01a249193
https://pubmed.ncbi.nlm.nih.gov/27796868
https://pubmed.ncbi.nlm.nih.gov/27796868
Autor:
M. K. Sibin, M. Jeru-Manoj, I Bhat Dhananjaya, K. V. L. Narasingarao, S.M. Harshitha, G. K. Chetan
Publikováno v:
Meta Gene
Gliomas are most common neoplasms in the CNS with unknown aetiology. Gene polymorphisms have been studied in glioma to check its risk in different population. CDKN2A, commonly altered tumor suppressor gene polymorphisms were recently shown to be asso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::102357dbf6c6dbd8fccf7e4a7b5e5776
https://pubmed.ncbi.nlm.nih.gov/27617221
https://pubmed.ncbi.nlm.nih.gov/27617221
Publikováno v:
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine. 36(10)
Human high-grade glioma is heterogeneous in nature based on pathological and genetic profiling. Various tumour suppressor gene alterations are considered as prognostic markers in high-grade glioma. Gene expression of CDKN2A (p16) is used in various c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3ad3286aed1f8890ab850f0729bbbd9
https://pubmed.ncbi.nlm.nih.gov/25921285
https://pubmed.ncbi.nlm.nih.gov/25921285