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Showing results (661-670 of 786) with videos related to

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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 9, 2017
Acute genetic ablation of pendrin lowers blood pressure in miceFrancesco Trepiccione, Christelle Soukaseum, Veronique Baudrie, et al.
Advanced Materials (Deerfield Beach, Fla.)|January 11, 2024
Enhanced Photocatalytic and Photovoltaic Performance Arising from Unconventionally Low Donor-Y6 RatiosAndrew Dolan, Xun Pan, Matthew J Griffith, et al.
Research Square|October 27, 2023
Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria VascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Scientific Reports|February 6, 2024
Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Inorganic Chemistry|June 23, 2022
Two Distinct Cu(II)-V(IV) Superexchange Interactions with Similar Bond Angles in a Triangular "CuV<sub>2</sub>" FragmentYiran Wang, Masayuki Fukuda, Sergey Nikolaev, et al.
Frontiers in Sports and Active Living|June 18, 2025
<i>Parkinson's Elevated</i>: improving healthspanKathleen E McKee, Miriam R Rafferty, Theadora W Sakata, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domainTomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
BMC Medical Genetics|February 11, 2011
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndromeSaima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, et al.
European Journal of Human Genetics : EJHG|July 16, 2009
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, et al.
The Journal of Clinical Investigation|November 23, 2011
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genesYoshiyuki Kawashima, Gwenaëlle S G Géléoc, Kiyoto Kurima, et al.
Pageof 79

Showing results (661-670 of 786) with videos related to

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Pageof 79
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 9, 2017
Acute genetic ablation of pendrin lowers blood pressure in miceFrancesco Trepiccione, Christelle Soukaseum, Veronique Baudrie, et al.
Advanced Materials (Deerfield Beach, Fla.)|January 11, 2024
Enhanced Photocatalytic and Photovoltaic Performance Arising from Unconventionally Low Donor-Y6 RatiosAndrew Dolan, Xun Pan, Matthew J Griffith, et al.
Research Square|October 27, 2023
Transgenic Tg(Kcnj10-ZsGreen) Fluorescent Reporter Mice Allow Visualization of Intermediate Cells in the Stria VascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Scientific Reports|February 6, 2024
Transgenic Tg(Kcnj10-ZsGreen) fluorescent reporter mice allow visualization of intermediate cells in the stria vascularisDillon Strepay, Rafal T Olszewski, Sydney Nixon, et al.
Inorganic Chemistry|June 23, 2022
Two Distinct Cu(II)-V(IV) Superexchange Interactions with Similar Bond Angles in a Triangular "CuV<sub>2</sub>" FragmentYiran Wang, Masayuki Fukuda, Sergey Nikolaev, et al.
Frontiers in Sports and Active Living|June 18, 2025
<i>Parkinson's Elevated</i>: improving healthspanKathleen E McKee, Miriam R Rafferty, Theadora W Sakata, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domainTomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
BMC Medical Genetics|February 11, 2011
Variable expressivity of FGF3 mutations associated with deafness and LAMM syndromeSaima Riazuddin, Zubair M Ahmed, Rashmi S Hegde, et al.
European Journal of Human Genetics : EJHG|July 16, 2009
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3Shahid Yar Khan, Saima Riazuddin, Mohsin Shahzad, et al.
The Journal of Clinical Investigation|November 23, 2011
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genesYoshiyuki Kawashima, Gwenaëlle S G Géléoc, Kiyoto Kurima, et al.
Pageof 79