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J H Smith

Showing results (531-540 of 588) with videos related to

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Nature Communications|January 25, 2025
The α-globin super-enhancer acts in an orientation-dependent mannerMira T Kassouf, Helena S Francis, Matthew Gosden, et al.
Human Molecular Genetics|June 26, 2007
The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populationsMelissa Thys, Isabelle Schrauwen, Kathleen Vanderstraeten, et al.
Nature Reviews. Nephrology|January 30, 2019
C3 glomerulopathy - understanding a rare complement-driven renal diseaseRichard J H Smith, Gerald B Appel, Anna M Blom, et al.
DNA and Cell Biology|May 27, 2011
Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian populationIrene Gazquez, Jose A Lopez-Escamez, Antonia Moreno, et al.
Clinical Genetics|March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expressionE Wilch, H Azaiez, R A Fisher, et al.
International Journal of Pediatric Otorhinolaryngology|January 4, 2020
International Pediatric ORL Group (IPOG) Robin Sequence consensus recommendationsPierre Fayoux, Sam J Daniel, Gregory Allen, et al.
The Annals of Otology, Rhinology, and Laryngology|November 5, 2015
Audioprofile Surfaces: The 21st Century AudiogramKyle R Taylor, Kevin T Booth, Hela Azaiez, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
PKMζ-PKCι/λ double-knockout demonstrates atypical PKC is crucial for the persistence of hippocampal LTP and spatial memoryPanayiotis Tsokas, Changchi Hsieh, Alejandro Grau-Perales, et al.
Kidney International|October 12, 2024
Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International ForumDavid Kavanagh, Gianluigi Ardissino, Vicky Brocklebank, et al.
Human Genetics|June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutationsKim Cryns, Markus Pfister, Ronald J E Pennings, et al.
Pageof 59

Showing results (531-540 of 588) with videos related to

Sort By:
Pageof 59
Nature Communications|January 25, 2025
The α-globin super-enhancer acts in an orientation-dependent mannerMira T Kassouf, Helena S Francis, Matthew Gosden, et al.
Human Molecular Genetics|June 26, 2007
The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populationsMelissa Thys, Isabelle Schrauwen, Kathleen Vanderstraeten, et al.
Nature Reviews. Nephrology|January 30, 2019
C3 glomerulopathy - understanding a rare complement-driven renal diseaseRichard J H Smith, Gerald B Appel, Anna M Blom, et al.
DNA and Cell Biology|May 27, 2011
Functional variants in NOS1 and NOS2A are not associated with progressive hearing loss in Ménière's disease in a European Caucasian populationIrene Gazquez, Jose A Lopez-Escamez, Antonia Moreno, et al.
Clinical Genetics|March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expressionE Wilch, H Azaiez, R A Fisher, et al.
International Journal of Pediatric Otorhinolaryngology|January 4, 2020
International Pediatric ORL Group (IPOG) Robin Sequence consensus recommendationsPierre Fayoux, Sam J Daniel, Gregory Allen, et al.
The Annals of Otology, Rhinology, and Laryngology|November 5, 2015
Audioprofile Surfaces: The 21st Century AudiogramKyle R Taylor, Kevin T Booth, Hela Azaiez, et al.
Biorxiv : the Preprint Server for Biology|March 27, 2026
PKMζ-PKCι/λ double-knockout demonstrates atypical PKC is crucial for the persistence of hippocampal LTP and spatial memoryPanayiotis Tsokas, Changchi Hsieh, Alejandro Grau-Perales, et al.
Kidney International|October 12, 2024
Outcomes from the International Society of Nephrology Hemolytic Uremic Syndromes International ForumDavid Kavanagh, Gianluigi Ardissino, Vicky Brocklebank, et al.
Human Genetics|June 20, 2002
Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutationsKim Cryns, Markus Pfister, Ronald J E Pennings, et al.
Pageof 59