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J H Smith

Showing results (461-470 of 588) with videos related to

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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 21, 2024
Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working GroupNora Franceschini, David L Feldman, Jonathan S Berg, et al.
Stem Cell Reports|May 22, 2018
Identification and Single-Cell Functional Characterization of an Endodermally Biased Pluripotent Substate in Human Embryonic Stem CellsThomas F Allison, Andrew J H Smith, Konstantinos Anastassiadis, et al.
Journal of Medical Genetics|December 24, 2005
OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy alleleR Varga, M R Avenarius, P M Kelley, et al.
The Journal of Cell Biology|September 24, 2008
Association between active genes occurs at nuclear speckles and is modulated by chromatin environmentJill M Brown, Joanne Green, Ricardo Pires das Neves, et al.
Cold Spring Harbor Molecular Case Studies|December 28, 2022
Rapid genome sequencing identifies novel variants in complement factor IKatherine M Rodriguez, Jordan Vaught, Michelle Dilley, et al.
The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, et al.
Human Mutation|September 5, 2003
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric diseaseKim Cryns, Theru A Sivakumaran, Jody M W Van den Ouweland, et al.
American Journal of Medical Genetics|April 27, 2002
Performance of cochlear implant recipients with GJB2-related deafnessGlenn E Green, Daryl A Scott, Joshua M McDonald, et al.
American Journal of Human Genetics|March 16, 2007
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndromeBethan E Hoskins, Carl H Cramer, Derek Silvius, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 6, 2008
Deletion of the mouse RegIIIbeta (Reg2) gene disrupts ciliary neurotrophic factor signaling and delays myelination of mouse cranial motor neuronsL A Tebar, S M Géranton, C Parsons-Perez, et al.
Pageof 59

Showing results (461-470 of 588) with videos related to

Sort By:
Pageof 59
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 21, 2024
Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working GroupNora Franceschini, David L Feldman, Jonathan S Berg, et al.
Stem Cell Reports|May 22, 2018
Identification and Single-Cell Functional Characterization of an Endodermally Biased Pluripotent Substate in Human Embryonic Stem CellsThomas F Allison, Andrew J H Smith, Konstantinos Anastassiadis, et al.
Journal of Medical Genetics|December 24, 2005
OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy alleleR Varga, M R Avenarius, P M Kelley, et al.
The Journal of Cell Biology|September 24, 2008
Association between active genes occurs at nuclear speckles and is modulated by chromatin environmentJill M Brown, Joanne Green, Ricardo Pires das Neves, et al.
Cold Spring Harbor Molecular Case Studies|December 28, 2022
Rapid genome sequencing identifies novel variants in complement factor IKatherine M Rodriguez, Jordan Vaught, Michelle Dilley, et al.
The Annals of Otology, Rhinology, and Laryngology|July 30, 2016
Detection and Confirmation of Deafness-Causing Copy Number Variations in the STRC Gene by Massively Parallel Sequencing and Comparative Genomic HybridizationHideaki Moteki, Hela Azaiez, Christina M Sloan-Heggen, et al.
Human Mutation|September 5, 2003
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric diseaseKim Cryns, Theru A Sivakumaran, Jody M W Van den Ouweland, et al.
American Journal of Medical Genetics|April 27, 2002
Performance of cochlear implant recipients with GJB2-related deafnessGlenn E Green, Daryl A Scott, Joshua M McDonald, et al.
American Journal of Human Genetics|March 16, 2007
Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndromeBethan E Hoskins, Carl H Cramer, Derek Silvius, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 6, 2008
Deletion of the mouse RegIIIbeta (Reg2) gene disrupts ciliary neurotrophic factor signaling and delays myelination of mouse cranial motor neuronsL A Tebar, S M Géranton, C Parsons-Perez, et al.
Pageof 59