Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Anil Gwal"'
Autor:
Shweta Shrivas, Madhav Patel, Rajat Kumar, Anil Gwal, Ramswaroop Uikey, Shashi Kant Tiwari, Anil Kumar Verma, Priyaleela Thota, Aparup Das, Praveen Kumar Bharti, Rajasubramaniam Shanmugam
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Sickle cell disease is a major public health problem in India. Lack of rapid and reliable diagnostic methods result in many avoidable deaths in affected population. Current diagnostic tools are laboratory based, expensive and need trained manpower. H
Externí odkaz:
https://doaj.org/article/4556210461d7447aaccad93af60fd66a
Autor:
Rajiv Yadav, M. P. Singh, Ravindra Kumar, Shanmugam Rajasubramaniam, Praveen K. Bharti, Anil Gwal, Sweta Mishra
Publikováno v:
Annals of Hematology. 100:365-373
Sickle cell disease has varied clinical symptoms, and patients having high fetal hemoglobin (HbF) have milder symptoms. Various genetic factors are known to modulate the HbF levels. Kruppel-like factor 1 (KLF1) is a transcription factor that regulate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7fc184cad168b32cf8163bacafcf5cb
https://doi.org/10.1007/s00277-020-04381-z
https://doi.org/10.1007/s00277-020-04381-z
Autor:
Madhav Patel, Anil Kumar Verma, Rajasubramaniam Shanmugam, Shweta Shrivas, Ramswaroop Uikey, Praveen K. Bharti, Priyaleela Thota, Aparup Das, Rajat Kumar, Anil Gwal, Shashikant Tiwari
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Frontiers in Medicine
Frontiers in Medicine
Sickle cell disease is a major public health problem in India. Lack of rapid and reliable diagnostic methods result in many avoidable deaths in affected population. Current diagnostic tools are laboratory based, expensive and need trained manpower. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fdf614286c298423e40d4a3124f0e94
https://www.frontiersin.org/articles/10.3389/fmed.2021.639208/full
https://www.frontiersin.org/articles/10.3389/fmed.2021.639208/full
Autor:
Anil Gwal, Amol Mun, Rajasubramaniam Shanmugam, Sweta Mishra, Praveen K. Bharti, Ravindra Kumar, Ram Swaroop Uikey
Publikováno v:
Journal of Clinical Pathology. 74:336-338
Haemoglobinopathies (thalassaemia and haemoglobin (Hb) variants) are the most common of all inherited monogenic disorders. More than 1800 mutations in alpha or beta globin genes are known to be responsible for haemoglobinopathies.1 The clinical spect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03c0214145139450a362a492c0edd049
https://doi.org/10.1136/jclinpath-2020-206589
https://doi.org/10.1136/jclinpath-2020-206589
Publikováno v:
Indian J Clin Biochem
The aim of the study is to evaluate the stability and longevity of the paper-based screening test for the sickle cell disease in relation to different temperatures and storage time. Blood stain patterns were interpreted after spotting the blood-buffe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7a503d190f9013a1ec8a3eba58e7ffc
https://pubmed.ncbi.nlm.nih.gov/35463103
https://pubmed.ncbi.nlm.nih.gov/35463103
Autor:
Shanmugam Rajasubramaniam, Ravindra Kumar, Anil Gwal, Praveen K. Bharti, Roshan B. Colah, Purushottam Patel
Publikováno v:
Indian J Hematol Blood Transfus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46580f4852d011cc9dc51c0854fb490a
https://doi.org/10.1007/s12288-019-01125-6
https://doi.org/10.1007/s12288-019-01125-6
Autor:
Purushottam Patel, Rajiv Yadav, Rajasubramaniam Shanmugam, Harsha Lad, Anil Gwal, Pawan Ghanghoria
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 34:185-187
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e183e2a135fa7e3f3fa2d4b16c845093
https://doi.org/10.1007/s12288-017-0806-z
https://doi.org/10.1007/s12288-017-0806-z
Autor:
Sudhansu Sekhar Nishank, Mendi Prema Shyam Sunder Singh, Rajiv Yadav, Gupta R, Anil Gwal, Vijay Sadashiv Gadge
Publikováno v:
Journal of Human Genetics. 58:775-779
Patients with sickle cell disease (SCD) produce significantly low levels of plasma nitric oxide (NO) during acute vaso-occlusive crisis. In transgenic sickle cell mice, NO synthesized by endothelial nitric oxide synthase (eNOS) enzyme of vascular end
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a909a8e01585214948fb36af3be9a8f
https://doi.org/10.1038/jhg.2013.99
https://doi.org/10.1038/jhg.2013.99
Autor:
Harsha, Lad, Pawan, Ghanghoria, Rajiv, Yadav, Purushottam, Patel, Anil, Gwal, Rajasubramaniam, Shanmugam
Publikováno v:
Indian journal of hematologyblood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion. 34(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b43f3ffedc611744e41e6944e5e749a9
https://pubmed.ncbi.nlm.nih.gov/29398830
https://pubmed.ncbi.nlm.nih.gov/29398830