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A Ramesh

Showing results (211-220 of 227) with videos related to

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Annals of Human Genetics|December 16, 2004
DNA sequence variation and haplotype structure of the ICAM1 and TNF genes in 12 ethnic groups of India reveal patterns of importance in designing association studiesS Sengupta, S Farheen, N Mukherjee, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
Proteomics|February 10, 2016
Proteomic analysis of a compatible interaction between sugarcane and Sporisorium scitamineumLeonard Barnabas, N M R Ashwin, K Kaverinathan, et al.
Transboundary and Emerging Diseases|September 16, 2014
Emergence of Porcine Circovirus 2 Associated Reproductive Failure in Southern IndiaA K Karuppannan, A Ramesh, Y K Reddy, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
The Science of the Total Environment|May 31, 2024
Bioenergetic mapping of 'healthy microbiomes' via compound processing potential imprinted in gut and soil metagenomesCraig Liddicoat, Robert A Edwards, Michael Roach, et al.
American Journal of Human Genetics|January 10, 2006
Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralistsSanghamitra Sengupta, Lev A Zhivotovsky, Roy King, et al.
Genome Research|October 6, 1997
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21J H Greinwald, D A Scott, J R Marietta, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Pageof 23

Showing results (211-220 of 227) with videos related to

Sort By:
Pageof 23
Annals of Human Genetics|December 16, 2004
DNA sequence variation and haplotype structure of the ICAM1 and TNF genes in 12 ethnic groups of India reveal patterns of importance in designing association studiesS Sengupta, S Farheen, N Mukherjee, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Molecular Genetics|March 21, 1998
Localization of a gene for otosclerosis to chromosome 15q25-q26M S Tomek, M R Brown, S R Mani, et al.
Proteomics|February 10, 2016
Proteomic analysis of a compatible interaction between sugarcane and Sporisorium scitamineumLeonard Barnabas, N M R Ashwin, K Kaverinathan, et al.
Transboundary and Emerging Diseases|September 16, 2014
Emergence of Porcine Circovirus 2 Associated Reproductive Failure in Southern IndiaA K Karuppannan, A Ramesh, Y K Reddy, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
The Science of the Total Environment|May 31, 2024
Bioenergetic mapping of 'healthy microbiomes' via compound processing potential imprinted in gut and soil metagenomesCraig Liddicoat, Robert A Edwards, Michael Roach, et al.
American Journal of Human Genetics|January 10, 2006
Polarity and temporality of high-resolution y-chromosome distributions in India identify both indigenous and exogenous expansions and reveal minor genetic influence of Central Asian pastoralistsSanghamitra Sengupta, Lev A Zhivotovsky, Roy King, et al.
Genome Research|October 6, 1997
Construction of P1-derived artificial chromosome and yeast artificial chromosome contigs encompassing the DFNB7 and DFNB11 region of chromosome 9q13-21J H Greinwald, D A Scott, J R Marietta, et al.
Human Molecular Genetics|June 9, 1998
Two frequent missense mutations in Pendred syndromeP Van Hauwe, L A Everett, P Coucke, et al.
Pageof 23