Sreedharan H - Search Results

1

Acute myeloid leukemia patients with variant or unusual translocations involving chromosomes 8 and 21 - A comprehensive cytogenetic profiling of three cases with review of literature.

Akhila Raj TV, Gopinath P, Geetha Raj JA, Narayanan G, Nair SG, Joy Philip DS, Raveendran S, Geetha P, Sreedharan H. Akhila Raj TV, et al. Among authors: sreedharan h. J Cancer Res Ther. 2022 Apr-Jun;18(3):697-703. doi: 10.4103/jcrt.jcrt_190_21. J Cancer Res Ther. 2022. PMID: 35900542 Free article. Review.

2

Novel t(7;10)(p22;p24) along with NPM1 mutation in patient with relapsed acute myeloid leukemia.

Sarojam S, Raveendran S, Narayanan G, Sreedharan H. Sarojam S, et al. Among authors: sreedharan h. Ann Saudi Med. 2013 Nov-Dec;33(6):619-22. doi: 10.5144/0256-4947.2013.619. Ann Saudi Med. 2013. PMID: 24413869 Free PMC article.

3

A novel chromosomal abnormality t (9;14)(p24;q13) in B-acute lymphoblastic leukemia.

Raveendran S, Sarojam S, Narayanan G, Sreedharan H. Raveendran S, et al. Among authors: sreedharan h. Indian J Hum Genet. 2014 Jan;20(1):79-81. doi: 10.4103/0971-6866.132763. Indian J Hum Genet. 2014. PMID: 24959020 Free PMC article.

4

Characterization of CEBPA Mutations and Polymorphisms and their Prognostic Relevance in De Novo Acute Myeloid Leukemia Patients.

Sarojam S, Raveendran S, Vijay S, Sreedharan J, Narayanan G, Sreedharan H. Sarojam S, et al. Among authors: sreedharan j, sreedharan h. Asian Pac J Cancer Prev. 2015;16(9):3785-92. doi: 10.7314/apjcp.2015.16.9.3785. Asian Pac J Cancer Prev. 2015. PMID: 25987038 Free article.

5

Mutation Analysis of IDH1/2 Genes in Unselected De novo Acute Myeloid Leukaemia Patients in India - Identification of A Novel IDH2 Mutation.

Raveendran S, Sarojam S, Vijay S, Geetha AC, Sreedharan J, Narayanan G, Sreedharan H. Raveendran S, et al. Among authors: sreedharan j, sreedharan h. Asian Pac J Cancer Prev. 2015;16(9):4095-101. doi: 10.7314/apjcp.2015.16.9.4095. Asian Pac J Cancer Prev. 2015. PMID: 25987093 Free article.

6

Isodicentric Philadelphia Chromosome: A Rare Chromosomal Aberration in Imatinib-Resistant Chronic Myelogenous Leukemia Patients - Case Report with Review of the Literature.

Ramachandran KC, Narayanan G, Nair SG, Thambi SM, Kamala LH, Gopinath P, Sreedharan H. Ramachandran KC, et al. Among authors: sreedharan h. Cytogenet Genome Res. 2016;150(3-4):273-280. doi: 10.1159/000458164. Epub 2017 Mar 3. Cytogenet Genome Res. 2016. PMID: 28253493 Review.

7

Prognostic Implications of Derivative Chromosome 9 Deletions in Patients with Advanced-Stage Chronic Myelogenous Leukemia.

Chandran RK, Geetha N, Sakthivel KM, Aswathy CG, Gopinath P, Nair JKKM, Sreedharan H. Chandran RK, et al. Among authors: sreedharan h. J Environ Pathol Toxicol Oncol. 2018;37(2):117-126. doi: 10.1615/JEnvironPatholToxicolOncol.2018026023. J Environ Pathol Toxicol Oncol. 2018. PMID: 30055547

8

Genomic amplification of BCR-ABL1 fusion gene and its impact on the disease progression mechanism in patients with chronic myelogenous leukemia.

Chandran RK, Geetha N, Sakthivel KM, Aswathy CG, Gopinath P, Raj TVA, Priya G, Nair JKKM, Sreedharan H. Chandran RK, et al. Among authors: sreedharan h. Gene. 2019 Feb 20;686:85-91. doi: 10.1016/j.gene.2018.11.005. Epub 2018 Nov 3. Gene. 2019. PMID: 30399426 Clinical Trial.

9

A concise review on the molecular genetics of acute myeloid leukemia.

Padmakumar D, Chandraprabha VR, Gopinath P, Vimala Devi ART, Anitha GRJ, Sreelatha MM, Padmakumar A, Sreedharan H. Padmakumar D, et al. Among authors: sreedharan h. Leuk Res. 2021 Dec;111:106727. doi: 10.1016/j.leukres.2021.106727. Epub 2021 Oct 16. Leuk Res. 2021. PMID: 34700049 Review.

10

Double Philadelphia chromosome: a rare and sole abnormality in pediatric B-acute lymphoblastic leukemia.

Padmakumar A, Thankamony P, Vasudevan JA, Gopinath P, Chandraprabha VR, Devi ARTV, Anitha GRJ, Sreelatha MM, Padmakumar D, Sreedharan H. Padmakumar A, et al. Among authors: sreedharan h. 3 Biotech. 2024 Mar;14(3):75. doi: 10.1007/s13205-024-03935-6. Epub 2024 Feb 14. 3 Biotech. 2024. PMID: 38371902

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