Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sameera Fatima Qureshi"'
Autor:
Sameera Fatima Qureshi, Altaf Ali, Ananthapur Venkateshwari, Hygriv Rao, M.P. Jayakrishnan, Calambur Narasimhan, Jayaprakash Shenthar, Kumarasamy Thangaraj, Pratibha Nallari
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 15, Iss 6, Pp 269-285 (2015)
Heterogeneity in clinical manifestations is a well-known feature in Long QT Syndrome (LQTS). The extent of this phenomenon became evident in families wherein both symptomatic and asymptomatic family members are reported. The study hence warrants gene
Externí odkaz:
https://doaj.org/article/a41bce3fdf334a31a569dac2febdd924
Autor:
Jayaprakash Shenthar, Kumarasamy Thangaraj, Sameera Fatima Qureshi, Machinary Puthenpurayil Jayakrishnan, Altaf Ali, Ananthapur Venkateshwari, Hygriv B. Rao, Pratibha Nallari, Narsimhan Calambur
Publikováno v:
Exploratory Research and Hypothesis in Medicine. 3:21-27
Long QT syndrome (LQTS) is a rare primary cardiac electrophysiological disorder with characteristic symptoms of syncope, tachyarrhythmia and torsades-de-pointes. It is the outcome of mutations in genes encoding ion channels that function as voltage r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eadd32dda62ac30ab2cf02e1cd82d783
https://doi.org/10.14218/erhm.2017.00004
https://doi.org/10.14218/erhm.2017.00004
Autor:
Altaf Ali, Sameera Fatima Qureshi, Pratibha Nallari, Hygriv B. Rao, Jayaprakash Shenthar, Kumarasamy Thangaraj, Veronica Medikare, Ananthapur Venkateshwari, M. P. Jayakrishnan, Narsimhan Calambur
Publikováno v:
Journal of Interventional Cardiac Electrophysiology. 45:119-130
Long QT syndrome (LQTS) is a rare cardiac disorder caused due to mutations in genes encoding ion channels responsible for generation of electrical impulses. The heat shock protein (HSP)-70 gene, expressed under conditions of stress, plays a cardiopro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4c6edc07ae6b231f3b05e3c432acf81
https://doi.org/10.1007/s10840-015-0082-5
https://doi.org/10.1007/s10840-015-0082-5
Autor:
Sameera Fatima Qureshi, Pratibha Nallari, Jayaprakash Shenthar, Kumarasamy Thangaraj, Amol P. Jadhav, Altaf Ali, Hygriv B. Rao, Calambur Narasimhan, Ananthapur Venkateshwari, M. P. Jayakrishnan, Princy John
Publikováno v:
Meta Gene
The SCN5A gene encodes for the INa channel implicated in long QT syndrome type-3 (LQTS-type-3). Clinical symptoms of this type are lethal as most patients had a sudden death during sleep. Screening of SCN5A in South Indian cohort by PCR-SSCP analyses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12c3b2a32c3678ff94740080be67ea4a
https://doi.org/10.1016/j.mgene.2015.07.010
https://doi.org/10.1016/j.mgene.2015.07.010
Autor:
Narasimhan Calambur, Kumarasamy Thangaraj, Pratibha Nallari, Sameera Fatima Qureshi, M. P. Jayakrishnan, Altaf Ali, Venkateshwari Ananthapur
Publikováno v:
Indian Heart Journal, Vol 65, Iss 5, Pp 552-560 (2013)
Background Autosomal recessive Long QT syndrome is characterized by prolonged QTc along with congenital bilateral deafness depends on mutations in K + channel genes. A family of a Long QT syndrome proband from India has been identified with novel ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7414a7692a55691b9b805bb23229a6a0
https://doi.org/10.1016/j.ihj.2013.08.025
https://doi.org/10.1016/j.ihj.2013.08.025
Publikováno v:
Lymphatic research and biology. 13(2)
Lymphatic filariasis is the leading cause of secondary lymphedema wherein lymph transport is impaired due to lymphatic damage. FLT4 signaling and transcription factors such as FOXC2 play an important role in this type of lymphangiogenesis process ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f39d39d69dfed6ec5032746901f79118
https://pubmed.ncbi.nlm.nih.gov/26091406
https://pubmed.ncbi.nlm.nih.gov/26091406
Autor:
C Sandeep, Kumar, Sameera Fatima, Qureshi, Altaf, Ali, M L, Satyanarayana, Advithi, Rangaraju, A, Venkateshwari, Pratibha, Nallari
Publikováno v:
The Indian Journal of Medical Research
Transposable elements (TEs) represent genome's dynamic component, causing mutations and genetic variations. Transposable elements can invade eukaryotic genomes in a short span; these are silenced by homology-dependent gene silencing and some function
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d2ee87f8f449fcb7af0ecb7166af0ed7
https://pubmed.ncbi.nlm.nih.gov/23852286
https://pubmed.ncbi.nlm.nih.gov/23852286
Autor:
Ananthapur Venkateshwari, M. P. Jayakrishnan, Sameera Fatima Qureshi, A. P. Jadhav, Calambur Narasimhan, Altaf Ali, Jayaprakash Shenthar, Pratibha Nallari, Kumarasamy Thangaraj
Long QT Syndrome (LQTS), a disorder of the cardiac repolarization process with prolongation of the QT interval (QTc ≥0.46 seconds), is an ion-channelopathy. Mutations in either KCNQ1 or KCNE1 genes are susceptible to LQTS. Hence, screening of KCNQ1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da228b461f07485a05295a734229e754
Autor:
Pratibha Nallari, Ananthapur Venkateshwari, Jayaprakash Shenthar, M. P. Jayakrishnan, Kumarasamy Thangaraj, Sameera Fatima Qureshi, Hygriv B. Rao, Calambur Narasimhan, Altaf Ali
Publikováno v:
Indian Pacing and Electrophysiology Journal, Vol 15, Iss 6, Pp 269-285 (2015)
Indian Pacing and Electrophysiology Journal
Indian Pacing and Electrophysiology Journal
Heterogeneity in clinical manifestations is a well-known feature in Long QT Syndrome (LQTS). The extent of this phenomenon became evident in families wherein both symptomatic and asymptomatic family members are reported. The study hence warrants gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c0248a066c0ae1751871ba430c3e93d