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Showing results (731-740 of 786) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 19, 2001
Radioimmunotherapy with (111)In/(90)Y-2IT-BAD-m170 for metastatic prostate cancerR T O'Donnell, S J DeNardo, A Yuan, et al.
JAMA Otolaryngology-- Head & Neck Surgery|September 21, 2013
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueductParna Chattaraj, Fabian R Reimold, Julie A Muskett, et al.
The Cochrane Database of Systematic Reviews|November 2, 2018
Vitamin and mineral supplementation for preventing dementia or delaying cognitive decline in people with mild cognitive impairmentJenny McCleery, Rajesh P Abraham, David A Denton, et al.
Human Mutation|May 11, 2013
Chimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyXiaohui Tan, Sarah L Anzick, Sikandar G Khan, et al.
International Journal of Epidemiology|December 7, 2022
Exploring the impact of selection bias in observational studies of COVID-19: a simulation studyLouise A C Millard, Alba Fernández-Sanlés, Alice R Carter, et al.
American Journal of Human Genetics|April 11, 2003
Mutations of MYO6 are associated with recessive deafness, DFNB37Zubair M Ahmed, Robert J Morell, Saima Riazuddin, et al.
Cell Stem Cell|May 6, 2014
Trichostatin A enhances vascular repair by injected human endothelial progenitors through increasing the expression of TAL1-dependent genesCarmen G Palii, Branka Vulesevic, Sylvain Fraineau, et al.
Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
IET Systems Biology|October 3, 2007
Systems biology of the neurospora biological clockW Dong, X Tang, Y Yu, et al.
European Journal of Human Genetics : EJHG|February 18, 2016
Heritability of non-speech auditory processing skillsCarmen C Brewer, Christopher K Zalewski, Kelly A King, et al.
Pageof 79

Showing results (731-740 of 786) with videos related to

Sort By:
Pageof 79
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 19, 2001
Radioimmunotherapy with (111)In/(90)Y-2IT-BAD-m170 for metastatic prostate cancerR T O'Donnell, S J DeNardo, A Yuan, et al.
JAMA Otolaryngology-- Head & Neck Surgery|September 21, 2013
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueductParna Chattaraj, Fabian R Reimold, Julie A Muskett, et al.
The Cochrane Database of Systematic Reviews|November 2, 2018
Vitamin and mineral supplementation for preventing dementia or delaying cognitive decline in people with mild cognitive impairmentJenny McCleery, Rajesh P Abraham, David A Denton, et al.
Human Mutation|May 11, 2013
Chimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyXiaohui Tan, Sarah L Anzick, Sikandar G Khan, et al.
International Journal of Epidemiology|December 7, 2022
Exploring the impact of selection bias in observational studies of COVID-19: a simulation studyLouise A C Millard, Alba Fernández-Sanlés, Alice R Carter, et al.
American Journal of Human Genetics|April 11, 2003
Mutations of MYO6 are associated with recessive deafness, DFNB37Zubair M Ahmed, Robert J Morell, Saima Riazuddin, et al.
Cell Stem Cell|May 6, 2014
Trichostatin A enhances vascular repair by injected human endothelial progenitors through increasing the expression of TAL1-dependent genesCarmen G Palii, Branka Vulesevic, Sylvain Fraineau, et al.
Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
IET Systems Biology|October 3, 2007
Systems biology of the neurospora biological clockW Dong, X Tang, Y Yu, et al.
European Journal of Human Genetics : EJHG|February 18, 2016
Heritability of non-speech auditory processing skillsCarmen C Brewer, Christopher K Zalewski, Kelly A King, et al.
Pageof 79