Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Santhi Sarojam"'
Autor:
Uma Thankam, Sankar Vaikom Hariharan, Santhi Sarojam, Remya Syamala, Sherrin Thomas Alex, Nandini V Ratnamma, Sujamol Jacob
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 16, Iss 11, Pp QC09-QC12 (2022)
Introduction: Primary amenorrhoea may be due to chromosomal abnormalities and identification of these abnormalities is important for counselling and management of these individuals. Aim: To identify the prevalence of chromosomal abnormalities in a c
Externí odkaz:
https://doaj.org/article/060ef32a296344c6a885057634c56016
Autor:
Santhi Sarojam, Sangeetha Vijay, Sureshkumar Raveendran, Jayadevan Sreedharan, Geetha Narayanan, Hariharan Sreedharan
Publikováno v:
Middle East Journal of Cancer, Vol 5, Iss 4, Pp 185-196 (2014)
Background: Fms-like tyrosine kinase 3 is a tyrosine kinase receptor that plays an important role in proliferation and differentiation of hematopoietic stem cells. Internal tandem duplication and tyrosine kinase domain mutation are the two most com
Externí odkaz:
https://doaj.org/article/3e6c0bcc7f254950a182360fa52e0ac7
Publikováno v:
Annals of Saudi Medicine, Vol 33, Iss 6, Pp 619-622 (2013)
Chromosomal abnormalities/genetic mutations associated with hematological malignancies alter the structure and function of genes controlling cell proliferation and differentiation through multiple and complex pathways, resulting different clinical ou
Externí odkaz:
https://doaj.org/article/678aa1b4cdde4a399d3ac73ea9d7836e
Publikováno v:
Annals of Saudi Medicine, Vol 33, Iss 6, Pp 619-622 (2013)
Chromosomal abnormalities/genetic mutations associated with hematological malignancies alter the structure and function of genes controlling cell proliferation and differentiation through multiple and complex pathways, resulting different clinical ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4671895b6f7609aab60a9afcc6e929b3
https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2013.619
https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2013.619
Autor:
Hariharan S, Sangeetha Vijay, Sureshkumar Raveendran, Leelakumari S, Syamala, Santhi Sarojam, Geetha Narayanan
Publikováno v:
Chinese Journal of Cancer
Acute myeloid leukemia (AML) is a phenotypically heterogeneous disorder. The M4 subtype of AML is frequently associated with the cytogenetic marker inversion 16 and/or the presence of eosinophilia. Blast crisis is the aggressive phase of the triphasi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaf611a8ffcbac3d81cd082d2d8a8372
https://doi.org/10.5732/cjc.011.10201
https://doi.org/10.5732/cjc.011.10201
Autor:
Suresh Kumar Raveendran, Sreedharan Hariharan, Santhi Sarojam, Sangeetha Vijay, Geetha Narayanan
Publikováno v:
Iranian Red Crescent Medical Journal
Introduction: Inversion of chromosome 9 had been widely discussed among geneticists and evolutionary biologists because of its significant impact on various hereditary disorders and in the evolution of man. The role of such inversions in human diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2953af71f223080daf856a593d79f484
https://doi.org/10.5812/ircmj.25062
https://doi.org/10.5812/ircmj.25062
Publikováno v:
Indian Journal of Human Genetics
Acute lymphoblastic leukemia is a malignant disease of the bone marrow in which early lymphoid precursors proliferate and replace the normal hematopoietic cells of the marrow. We describe the clinical, morphologic, immunophenotypic and cytogenetic fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0038dfc34b90e2f1b8e12a68869b6485
http://europepmc.org/articles/PMC4065485
http://europepmc.org/articles/PMC4065485
Autor:
Aswathy Chandran Geetha, Santhi Sarojam, Jayadevan Sreedharan, Geetha Narayanan, Hariharan Sreedharan, Sureshkumar Raveendran, Sangeetha Vijay
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 16(9)
IDH1/2 mutations which result in alternation in DNA methylation pattern are one of the most common methylation associated mutations in Acute myeloid leukaemia. IDH1/2 mutations frequently associated with higher platelet level, normal cytogentics and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dff73230ef4a5f2aeafded48be748ee0
https://pubmed.ncbi.nlm.nih.gov/25987093
https://pubmed.ncbi.nlm.nih.gov/25987093
Autor:
Sangeetha Vijay, Santhi Sarojam, Jayadevan Sreedharan, Hariharan Sreedharan, Geetha Narayanan, Sureshkumar Raveendran
Publikováno v:
Asian Pacific journal of cancer prevention : APJCP. 16(9)
The CCAAT/enhancer-binding protein-alpha (CEBPA) is a transcriptional factor that plays a crucial role in the control of proliferation and differentiation of myeloid precursors. This gene was recognized as the target of genetic alterations and were a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5edfb5945d34ff043fd0df7f520c1c88
https://pubmed.ncbi.nlm.nih.gov/25987038
https://pubmed.ncbi.nlm.nih.gov/25987038
Autor:
Fahad, Luay Attallah1 loaiattallah@gmail.com, Al-Omar, Zahraa Marwan1, AL-Kheroo, Khalid Naf’i2
Publikováno v:
Al-Anbar Medical Journal. Jun2024, Vol. 20 Issue 1, p74-79. 6p.