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A Ramesh

Showing results (221-230 of 227) with videos related to

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Human Molecular Genetics|August 7, 2001
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1FK N Alagramam, H Yuan, M H Kuehn, et al.
Gene|October 3, 1998
Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19D A Scott, J H Greinwald, J R Marietta, et al.
American Journal of Human Genetics|November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.
MMWR. Morbidity and Mortality Weekly Report|January 31, 2015
Outbreaks of unexplained neurologic illness - Muzaffarpur, India, 2013-2014Aakash Shrivastava, Padmini Srikantiah, Anil Kumar, et al.
Nature Communications|March 31, 2022
Integrating central nervous system metagenomics and host response for diagnosis of tuberculosis meningitis and its mimicsP S Ramachandran, A Ramesh, F V Creswell, et al.
The Lancet. Global Health|February 4, 2017
Association of acute toxic encephalopathy with litchi consumption in an outbreak in Muzaffarpur, India, 2014: a case-control studyAakash Shrivastava, Anil Kumar, Jerry D Thomas, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 16, 2010
Insights into evolution of multicellular fungi from the assembled chromosomes of the mushroom Coprinopsis cinerea (Coprinus cinereus)Jason E Stajich, Sarah K Wilke, Dag Ahrén, et al.
Pageof 23

Showing results (221-230 of 227) with videos related to

Sort By:
Pageof 23
You have reached the last page of results.This site can display upto 227 results.
Human Molecular Genetics|August 7, 2001
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1FK N Alagramam, H Yuan, M H Kuehn, et al.
Gene|October 3, 1998
Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19D A Scott, J H Greinwald, J R Marietta, et al.
American Journal of Human Genetics|November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.
MMWR. Morbidity and Mortality Weekly Report|January 31, 2015
Outbreaks of unexplained neurologic illness - Muzaffarpur, India, 2013-2014Aakash Shrivastava, Padmini Srikantiah, Anil Kumar, et al.
Nature Communications|March 31, 2022
Integrating central nervous system metagenomics and host response for diagnosis of tuberculosis meningitis and its mimicsP S Ramachandran, A Ramesh, F V Creswell, et al.
The Lancet. Global Health|February 4, 2017
Association of acute toxic encephalopathy with litchi consumption in an outbreak in Muzaffarpur, India, 2014: a case-control studyAakash Shrivastava, Anil Kumar, Jerry D Thomas, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 16, 2010
Insights into evolution of multicellular fungi from the assembled chromosomes of the mushroom Coprinopsis cinerea (Coprinus cinereus)Jason E Stajich, Sarah K Wilke, Dag Ahrén, et al.
Pageof 23