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Systematic evaluation of markers used for the identification of human induced pluripotent stem cells.
Biol Open. 2017 Jan 15;6(1):100-108. doi: 10.1242/bio.022111.
Biol Open. 2017.
PMID: 28089995
Free PMC article.
Understanding the Molecular Basis of Heterogeneity in Induced Pluripotent Stem Cells.
Manian KV, Aalam SM, Bharathan SP, Srivastava A, Velayudhan SR.
Manian KV, et al. Among authors: bharathan sp.
Cell Reprogram. 2015 Dec;17(6):427-40. doi: 10.1089/cell.2015.0013. Epub 2015 Nov 12.
Cell Reprogram. 2015.
PMID: 26562626
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Identification of Stable OCT4+NANOG- State in Somatic Cell Reprogramming.
Aalam SM, Manian KV, Bharathan SP, Mayuranathan T, Velayudhan SR.
Aalam SM, et al. Among authors: bharathan sp.
Cell Reprogram. 2016 Nov;18(6):367-368. doi: 10.1089/cell.2016.0018. Epub 2016 Sep 13.
Cell Reprogram. 2016.
PMID: 27622636
No abstract available.
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Generation of an induced pluripotent stem cell line that mimics the disease phenotypes from a patient with Fanconi anemia by conditional complementation.
Bharathan SP, Nandy K, Palani D, Janet A NB, Natarajan K, George B, Srivastava A, Velayudhan SR.
Bharathan SP, et al.
Stem Cell Res. 2017 Apr;20:54-57. doi: 10.1016/j.scr.2017.02.006. Epub 2017 Feb 22.
Stem Cell Res. 2017.
PMID: 28395741
Free article.
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Generation of an integration-free iPSC line (CSCRi005-A) from erythroid progenitor cells of a healthy Indian male individual.
Manian KV, Bharathan SP, Maddali M, Srivastava VM, Srivastava A, Velayudhan SR.
Manian KV, et al. Among authors: bharathan sp.
Stem Cell Res. 2018 May;29:148-151. doi: 10.1016/j.scr.2018.03.020. Epub 2018 Apr 3.
Stem Cell Res. 2018.
PMID: 29665501
Free article.
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HUMAN CELLULAR MODELS FOR RETINAL DISEASE: From Induced Pluripotent Stem Cells to Organoids.
Mustafi D, Bharathan SP, Calderon R, Nagiel A.
Mustafi D, et al. Among authors: bharathan sp.
Retina. 2022 Oct 1;42(10):1829-1835. doi: 10.1097/IAE.0000000000003571.
Retina. 2022.
PMID: 35858274
Free PMC article.
Review.
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Genetic association analysis of ATP binding cassette protein family reveals a novel association of ABCB1 genetic variants with epilepsy risk, but not with drug-resistance.
Balan S, Bharathan SP, Vellichiramal NN, Sathyan S, Joseph V, Radhakrishnan K, Banerjee M.
Balan S, et al. Among authors: bharathan sp.
PLoS One. 2014 Feb 21;9(2):e89253. doi: 10.1371/journal.pone.0089253. eCollection 2014.
PLoS One. 2014.
PMID: 24586633
Free PMC article.
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