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Showing results (691-700 of 786) with videos related to

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Plos Genetics|October 8, 2011
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler miceKiyoto Kurima, Ronna Hertzano, Oksana Gavrilova, et al.
Human Genetics|September 5, 2023
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueductIsabelle Roux, Cristina Fenollar-Ferrer, Hyun Jae Lee, et al.
Journal of Medical Genetics|February 4, 2005
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entitiesS P Pryor, A C Madeo, J C Reynolds, et al.
Medical Physics|May 13, 2020
Characterization of an organic semiconductor diode for dosimetry in radiotherapyJessie A Posar, Jeremy Davis, Matthew J Large, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
The New England Journal of Medicine|April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
Frontiers in Cell and Developmental Biology|December 9, 2022
ALD-R491 regulates vimentin filament stability and solubility, cell contractile force, cell migration speed and directionalityHyejeong Rosemary Kim, Samantha J Warrington, Ana López-Guajardo, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Pageof 79

Showing results (691-700 of 786) with videos related to

Sort By:
Pageof 79
Plos Genetics|October 8, 2011
A noncoding point mutation of Zeb1 causes multiple developmental malformations and obesity in Twirler miceKiyoto Kurima, Ronna Hertzano, Oksana Gavrilova, et al.
Human Genetics|September 5, 2023
CHD7 variants associated with hearing loss and enlargement of the vestibular aqueductIsabelle Roux, Cristina Fenollar-Ferrer, Hyun Jae Lee, et al.
Journal of Medical Genetics|February 4, 2005
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entitiesS P Pryor, A C Madeo, J C Reynolds, et al.
Medical Physics|May 13, 2020
Characterization of an organic semiconductor diode for dosimetry in radiotherapyJessie A Posar, Jeremy Davis, Matthew J Large, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Ophthalmic Genetics|May 7, 2020
Atypical and ultra-rare Usher syndrome: a reviewRosalie M Nolen, Robert B Hufnagel, Thomas B Friedman, et al.
The New England Journal of Medicine|April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
Frontiers in Cell and Developmental Biology|December 9, 2022
ALD-R491 regulates vimentin filament stability and solubility, cell contractile force, cell migration speed and directionalityHyejeong Rosemary Kim, Samantha J Warrington, Ana López-Guajardo, et al.
World Journal of Otorhinolaryngology|May 12, 2015
<i>SLC26A4</i> mutation testing for hearing loss associated with enlargement of the vestibular aqueductTaku Ito, Julie Muskett, Parna Chattaraj, et al.
Pageof 79