Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Saurabh Kumar Bhattacharya"'
Autor:
Shiba Ranjan Mishra, Leena Rawal, Moneeb A. K. Othman, Atul Thatai, Aditi Sarkar, Vandana Lal, Saurabh Kumar Bhattacharya
Publikováno v:
Molecular Cytogenetics, Vol 14, Iss 1, Pp 1-5 (2021)
Abstract Background The translocation t(8;21)(q22;q22) is one of the most frequent chromosomal abnormalities associated with acute myeloid leukemia (AML) sub type M2. About 3–5 % of cases with additional chromosomal abnormalities, including structu
Externí odkaz:
https://doaj.org/article/568317231d6c4e6e9a135e040aac856e
Publikováno v:
Journal of Human Reproductive Sciences, Vol 13, Iss 3, Pp 209-215 (2020)
Background: Human reproduction is the most intricate event as ~ 20% of human pregnancies end in miscarriages for which chromosomal anomalies are a common factor. The chromosomal variations associated with reproductive failures include translocations,
Externí odkaz:
https://doaj.org/article/0fdbd24b1c23423c9e9aaf2f1546b3b2
Autor:
Priya Thakur, Nupur Bhargava, Shashank Jaitly, Pragya Gupta, Saurabh Kumar Bhattacharya, G. Padma, Saroja Kondaveeti, Suman Jain, Sivaprakash Ramalingam
Publikováno v:
Stem Cell Research, Vol 50, Iss , Pp 102124- (2021)
β-thalassemia (BT) is a hereditary blood disorder caused by mutations in the β-globin (HBB) gene leading to severely reduced or no synthesis of the β-chain of adult hemoglobin. IVS1-5 (G > C) is the most common BT mutation in Indian population and
Externí odkaz:
https://doaj.org/article/795b1d055132407c8d882c92e1711f0b
Autor:
Vandana Kamath, Vivi M Srivastava, S Yuvarani, Mary Purna Chacko, Saurabh Kumar Bhattacharya, Samuel Phillip Oommen, Sumita Danda, George Korula
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 1, Pp GC01-GC04 (2019)
Introduction: The balanced translocation t(11;22) is one of the most common constitutional genetic abnormality detected in humans. Carriers of the t(11;22) are usually phenotypically normal and their carrier status is ascertained only if they present
Externí odkaz:
https://doaj.org/article/3cd83fb4195e45f4b36d48c103e90427
Autor:
Nupur Bhargava, Priya Thakur, Thulasi Priyadharshini Muruganandam, Shashank Jaitly, Pragya Gupta, Neelam Lohani, Sangam Giri Goswami, Vinodh Saravanakumar, Saurabh Kumar Bhattacharya, Suman Jain, Sivaprakash Ramalingam
Publikováno v:
Molecular Biology Reports. 49:7887-7898
Disease-specific human induced pluripotent stem cells (hiPSCs) can be generated directly from individuals with known disease characteristics or alternatively be modified using genome editing approaches to introduce disease causing genetic mutations t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b22970cfbdc4fe050c7fabd6bafd15b1
https://doi.org/10.1007/s11033-022-07621-9
https://doi.org/10.1007/s11033-022-07621-9
Autor:
George Korula, Vandana Kamath, Mary Purna Chacko, Samuel Phillip Oommen, Vivi M. Srivastava, Danda Sumita, S Yuvarani, Saurabh Kumar Bhattacharya
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 1, Pp GC01-GC04 (2019)
Introduction: The balanced translocation t(11;22) is one of the most common constitutional genetic abnormality detected in humans. Carriers of the t(11;22) are usually phenotypically normal and their carrier status is ascertained only if they present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfe67654a9a92e8e8610b638233b81d4
Publikováno v:
Human & Experimental Toxicology; Jul2011, Vol. 30 Issue 7, p636-648, 13p, 3 Charts, 4 Graphs