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J Morell

Showing results (71-80 of 118) with videos related to

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Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, 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.
Genes|July 27, 2024
Deafness DFNB128 Associated with a Recessive Variant of Human <i>MAP3K1</i> Recapitulates Hearing Loss of <i>Map3k1</i>-Deficient MiceRabia Faridi, Rizwan Yousaf, Sayaka Inagaki, et al.
Science (New York, N.Y.)|June 20, 1998
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, 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.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2017
Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouseJianguo Fan, Li Jia, Yan Li, et al.
European Journal of Human Genetics : EJHG|November 27, 2021
Genomic analysis of childhood hearing loss in the Yoruba population of NigeriaAdebolajo Adeyemo, Rabia Faridi, Parna Chattaraj, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Clinical Genetics|October 22, 2020
Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndromeTalah T Wafa, Rabia Faridi, Kelly A King, et al.
Genes|September 29, 2020
Mouse Models of Human Pathogenic Variants of <i>TBC1D24</i> Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving DeafnessRisa Tona, Ivan A Lopez, Cristina Fenollar-Ferrer, et al.
Pageof 12

Showing results (71-80 of 118) with videos related to

Sort By:
Pageof 12
Science (New York, N.Y.)|June 20, 1998
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3A Wang, Y Liang, R A Fridell, 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.
Genes|July 27, 2024
Deafness DFNB128 Associated with a Recessive Variant of Human <i>MAP3K1</i> Recapitulates Hearing Loss of <i>Map3k1</i>-Deficient MiceRabia Faridi, Rizwan Yousaf, Sayaka Inagaki, et al.
Science (New York, N.Y.)|June 20, 1998
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgeneF J Probst, R A Fridell, Y Raphael, 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.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2017
Maturation arrest in early postnatal sensory receptors by deletion of the miR-183/96/182 cluster in mouseJianguo Fan, Li Jia, Yan Li, et al.
European Journal of Human Genetics : EJHG|November 27, 2021
Genomic analysis of childhood hearing loss in the Yoruba population of NigeriaAdebolajo Adeyemo, Rabia Faridi, Parna Chattaraj, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Clinical Genetics|October 22, 2020
Vestibular phenotype-genotype correlation in a cohort of 90 patients with Usher syndromeTalah T Wafa, Rabia Faridi, Kelly A King, et al.
Genes|September 29, 2020
Mouse Models of Human Pathogenic Variants of <i>TBC1D24</i> Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving DeafnessRisa Tona, Ivan A Lopez, Cristina Fenollar-Ferrer, et al.
Pageof 12