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L Narayanan

Showing results (31-40 of 91) with videos related to

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Drug Design and Discovery|March 1, 1996
Synthesis and cytotoxic activities of the amine-exchange products of 2-dimethylaminomethyl-5-(E)-substituted arylidene cyclopentanones with anilines: 2-arylaminomethyl-5-(E)-arylidene cyclopentanonesH Chen, Z Ji, L K Wong, et al.
Pharmaceutical Research|October 1, 1996
Synthesis, antiinflammatory, and cytotoxic activities of 2-alkyl and 2-benzyl-2-dimethylaminomethyl-5-(E)-arylidene cyclopentanone hydrochloridesH Chen, Z Ji, L K Wong, et al.
Cancer Research|April 28, 2001
Hypermutability to ionizing radiation in mismatch repair-deficient, Pms2 knockout miceX S Xu, L Narayanan, B Dunklee, et al.
Bioorganic & Medicinal Chemistry|October 1, 1994
Synthesis and anti-cancer activity of 2-alkylaminomethyl-5-(E)-alkylidene cyclopentanone hydrochloridesH Chen, Z Ji, L K Wong, et al.
Neuroscience|January 11, 2014
Functional characterization of rare variants in human dopamine receptor D4 gene by genotype-phenotype correlationsK A Michealraj, N Jatana, Jafurulla, et al.
Journal of Biomolecular NMR|October 5, 2015
Improved validation of IDP ensembles by one-bond Cα-Hα scalar couplingsVytautas Gapsys, Raghavendran L Narayanan, ShengQi Xiang, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
Familial choreoathetosis due to novel heterozygous mutation in PDE10ADhanya L Narayanan, Dipti Deshpande, Aneek Das Bhowmik, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2L Narayanan, J A Fritzell, S M Baker, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|April 23, 2003
Sensitive high-performance liquid chromatography method for the determination of low levels of perchlorate in biological samplesL Narayanan, G W Buttler, K O Yu, et al.
Clinical Genetics|July 11, 2018
Report of second case and clinical and molecular characterization of Eiken syndromeA Moirangthem, D L Narayanan, P Jacob, et al.
Pageof 10

Showing results (31-40 of 91) with videos related to

Sort By:
Pageof 10
Drug Design and Discovery|March 1, 1996
Synthesis and cytotoxic activities of the amine-exchange products of 2-dimethylaminomethyl-5-(E)-substituted arylidene cyclopentanones with anilines: 2-arylaminomethyl-5-(E)-arylidene cyclopentanonesH Chen, Z Ji, L K Wong, et al.
Pharmaceutical Research|October 1, 1996
Synthesis, antiinflammatory, and cytotoxic activities of 2-alkyl and 2-benzyl-2-dimethylaminomethyl-5-(E)-arylidene cyclopentanone hydrochloridesH Chen, Z Ji, L K Wong, et al.
Cancer Research|April 28, 2001
Hypermutability to ionizing radiation in mismatch repair-deficient, Pms2 knockout miceX S Xu, L Narayanan, B Dunklee, et al.
Bioorganic & Medicinal Chemistry|October 1, 1994
Synthesis and anti-cancer activity of 2-alkylaminomethyl-5-(E)-alkylidene cyclopentanone hydrochloridesH Chen, Z Ji, L K Wong, et al.
Neuroscience|January 11, 2014
Functional characterization of rare variants in human dopamine receptor D4 gene by genotype-phenotype correlationsK A Michealraj, N Jatana, Jafurulla, et al.
Journal of Biomolecular NMR|October 5, 2015
Improved validation of IDP ensembles by one-bond Cα-Hα scalar couplingsVytautas Gapsys, Raghavendran L Narayanan, ShengQi Xiang, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
Familial choreoathetosis due to novel heterozygous mutation in PDE10ADhanya L Narayanan, Dipti Deshpande, Aneek Das Bhowmik, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1997
Elevated levels of mutation in multiple tissues of mice deficient in the DNA mismatch repair gene Pms2L Narayanan, J A Fritzell, S M Baker, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|April 23, 2003
Sensitive high-performance liquid chromatography method for the determination of low levels of perchlorate in biological samplesL Narayanan, G W Buttler, K O Yu, et al.
Clinical Genetics|July 11, 2018
Report of second case and clinical and molecular characterization of Eiken syndromeA Moirangthem, D L Narayanan, P Jacob, et al.
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