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J H Smith

Showing results (431-440 of 588) with videos related to

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Molecular and Cellular Probes|October 1, 1996
Detection of rRNA from four respiratory pathogens using an automated Q beta replicase assayB B Stone, S P Cohen, G L Breton, et al.
Journal of the Reticuloendothelial Society|August 1, 1983
Leprosy in wild armadillos (Dasypus novemcinctus) of the Texas Gulf Coast: epidemiology and mycobacteriologyJ H Smith, D S Folse, E G Long, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 21, 2005
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafnessAbram P Vore, Eugene H Chang, Jane E Hoppe, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 26, 2017
C4 Nephritic Factors in C3 Glomerulopathy: A Case SeriesYuzhou Zhang, Nicole C Meyer, Fernando C Fervenza, et al.
Annals of Human Genetics|July 21, 2010
Genetic variants in RELN are associated with otosclerosis in a non-European population from TunisiaAyda Khalfallah, Isabelle Schrauwen, Malek Mnaja, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutationHideaki Moteki, Hela Azaiez, Kevin T Booth, et al.
Frontiers in Immunology|January 1, 2021
Factor H Autoantibodies and Complement-Mediated DiseasesYuzhou Zhang, Nicolo Ghiringhelli Borsa, Dingwu Shao, et al.
Journal of the American Society of Nephrology : JASN|November 1, 2018
Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic SyndromeFengxiao Bu, Yuzhou Zhang, Kai Wang, et al.
Genome Medicine|June 26, 2014
Copy number variants are a common cause of non-syndromic hearing lossA Eliot Shearer, Diana L Kolbe, Hela Azaiez, et al.
Journal of Clinical Microbiology|June 1, 1997
Detection of Mycobacterium tuberculosis directly from sputum by using a prototype automated Q-beta replicase assayJ H Smith, D Buxton, P Cahill, et al.
Pageof 59

Showing results (431-440 of 588) with videos related to

Sort By:
Pageof 59
Molecular and Cellular Probes|October 1, 1996
Detection of rRNA from four respiratory pathogens using an automated Q beta replicase assayB B Stone, S P Cohen, G L Breton, et al.
Journal of the Reticuloendothelial Society|August 1, 1983
Leprosy in wild armadillos (Dasypus novemcinctus) of the Texas Gulf Coast: epidemiology and mycobacteriologyJ H Smith, D S Folse, E G Long, et al.
Archives of Otolaryngology--Head & Neck Surgery|December 21, 2005
Deletion of and novel missense mutation in POU3F4 in 2 families segregating X-linked nonsyndromic deafnessAbram P Vore, Eugene H Chang, Jane E Hoppe, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|August 26, 2017
C4 Nephritic Factors in C3 Glomerulopathy: A Case SeriesYuzhou Zhang, Nicole C Meyer, Fernando C Fervenza, et al.
Annals of Human Genetics|July 21, 2010
Genetic variants in RELN are associated with otosclerosis in a non-European population from TunisiaAyda Khalfallah, Isabelle Schrauwen, Malek Mnaja, et al.
The Annals of Otology, Rhinology, and Laryngology|March 20, 2015
Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutationHideaki Moteki, Hela Azaiez, Kevin T Booth, et al.
Frontiers in Immunology|January 1, 2021
Factor H Autoantibodies and Complement-Mediated DiseasesYuzhou Zhang, Nicolo Ghiringhelli Borsa, Dingwu Shao, et al.
Journal of the American Society of Nephrology : JASN|November 1, 2018
Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic SyndromeFengxiao Bu, Yuzhou Zhang, Kai Wang, et al.
Genome Medicine|June 26, 2014
Copy number variants are a common cause of non-syndromic hearing lossA Eliot Shearer, Diana L Kolbe, Hela Azaiez, et al.
Journal of Clinical Microbiology|June 1, 1997
Detection of Mycobacterium tuberculosis directly from sputum by using a prototype automated Q-beta replicase assayJ H Smith, D Buxton, P Cahill, et al.
Pageof 59