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J H Smith

Showing results (361-370 of 588) with videos related to

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Nature|April 21, 2006
Critical role for the p110alpha phosphoinositide-3-OH kinase in growth and metabolic regulationLazaros C Foukas, Marc Claret, Wayne Pearce, et al.
Histochemistry and Cell Biology|March 22, 2003
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cellsKim Cryns, Sofie Thys, Lut Van Laer, et al.
International Journal of Pediatric Otorhinolaryngology|November 21, 2007
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment familiesFatemeh Alasti, Mohammad Hossein Sanati, Amir Hossein Behrouzifard, et al.
Clinical Genetics|May 11, 2007
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosisW Chen, N C Meyer, M J McKenna, et al.
Genes & Development|August 11, 2011
Polycomb eviction as a new distant enhancer functionDouglas Vernimmen, Magnus D Lynch, Marco De Gobbi, et al.
Human Genetics|September 29, 2025
Investigation of GSDME results in the identification of the first pathogenic synonymous variants and genotype-phenotype correlationsJoseph J Chin, W Daniel Walls, Kai Wang, et al.
Cell Reports|March 14, 2019
Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA SequencingPaul T Ranum, Alexander T Goodwin, Hidekane Yoshimura, et al.
Lancet (London, England)|October 22, 2002
Pre-eclampsia, antiretroviral therapy, and immune reconstitutionR C Wimalasundera, N Larbalestier, J H Smith, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|March 23, 2010
Mentoring in otolaryngology training programsRichard K Gurgel, Bradley A Schiff, John H Flint, et al.
American Journal of Medical Genetics|May 7, 2002
Searching for evidence of DFNB2Lisa M Astuto, Philip M Kelley, James W Askew, et al.
Pageof 59

Showing results (361-370 of 588) with videos related to

Sort By:
Pageof 59
Nature|April 21, 2006
Critical role for the p110alpha phosphoinositide-3-OH kinase in growth and metabolic regulationLazaros C Foukas, Marc Claret, Wayne Pearce, et al.
Histochemistry and Cell Biology|March 22, 2003
The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cellsKim Cryns, Sofie Thys, Lut Van Laer, et al.
International Journal of Pediatric Otorhinolaryngology|November 21, 2007
A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment familiesFatemeh Alasti, Mohammad Hossein Sanati, Amir Hossein Behrouzifard, et al.
Clinical Genetics|May 11, 2007
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosisW Chen, N C Meyer, M J McKenna, et al.
Genes & Development|August 11, 2011
Polycomb eviction as a new distant enhancer functionDouglas Vernimmen, Magnus D Lynch, Marco De Gobbi, et al.
Human Genetics|September 29, 2025
Investigation of GSDME results in the identification of the first pathogenic synonymous variants and genotype-phenotype correlationsJoseph J Chin, W Daniel Walls, Kai Wang, et al.
Cell Reports|March 14, 2019
Insights into the Biology of Hearing and Deafness Revealed by Single-Cell RNA SequencingPaul T Ranum, Alexander T Goodwin, Hidekane Yoshimura, et al.
Lancet (London, England)|October 22, 2002
Pre-eclampsia, antiretroviral therapy, and immune reconstitutionR C Wimalasundera, N Larbalestier, J H Smith, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|March 23, 2010
Mentoring in otolaryngology training programsRichard K Gurgel, Bradley A Schiff, John H Flint, et al.
American Journal of Medical Genetics|May 7, 2002
Searching for evidence of DFNB2Lisa M Astuto, Philip M Kelley, James W Askew, et al.
Pageof 59