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J Morell

Showing results (51-60 of 118) with videos related to

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Frontiers in Cellular Neuroscience|June 13, 2020
Cell-Specific Transcriptional Responses to Heat Shock in the Mouse Utricle EpitheliumErica Sadler, Matthew M Ryals, Lindsey A May, et al.
Clinical Genetics|March 8, 2024
Homozygous novel truncating variant of CLPP associated with severe Perrault syndromeRabia Faridi, Pamela Stratton, Noemi Salmeri, et al.
Frontiers in Cell and Developmental Biology|September 28, 2020
Single-Cell RNA-Sequencing From Mouse Incisor Reveals Dental Epithelial Cell-Type Specific GenesYuta Chiba, Kan Saito, Daniel Martin, et al.
The Journal of Clinical Investigation|February 7, 2018
Modifier variant of METTL13 suppresses human GAB1-associated profound deafnessRizwan Yousaf, Zubair M Ahmed, Arnaud Pj Giese, et al.
Clinical Genetics|February 19, 2008
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1L M Peters, R A Fridell, E T Boger, et al.
Human Molecular Genetics|October 24, 2002
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28Linda M Peters, David W Anderson, Andrew J Griffith, et al.
The Journal of Biological Chemistry|September 8, 2012
The transcription factors Grainyhead-like 2 and NK2-homeobox 1 form a regulatory loop that coordinates lung epithelial cell morphogenesis and differentiationSaaket Varma, Yuxia Cao, Jean-Bosco Tagne, et al.
Frontiers in Molecular Neuroscience|September 27, 2021
Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene TargetsIan A Taukulis, Rafal T Olszewski, Soumya Korrapati, et al.
BMC Genomics|September 23, 2018
A comparative analysis of library prep approaches for sequencing low input translatome samplesYang Song, Beatrice Milon, Sandra Ott, et al.
American Journal of Human Genetics|June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZ M Ahmed, S Riazuddin, S L Bernstein, et al.
Pageof 12

Showing results (51-60 of 118) with videos related to

Sort By:
Pageof 12
Frontiers in Cellular Neuroscience|June 13, 2020
Cell-Specific Transcriptional Responses to Heat Shock in the Mouse Utricle EpitheliumErica Sadler, Matthew M Ryals, Lindsey A May, et al.
Clinical Genetics|March 8, 2024
Homozygous novel truncating variant of CLPP associated with severe Perrault syndromeRabia Faridi, Pamela Stratton, Noemi Salmeri, et al.
Frontiers in Cell and Developmental Biology|September 28, 2020
Single-Cell RNA-Sequencing From Mouse Incisor Reveals Dental Epithelial Cell-Type Specific GenesYuta Chiba, Kan Saito, Daniel Martin, et al.
The Journal of Clinical Investigation|February 7, 2018
Modifier variant of METTL13 suppresses human GAB1-associated profound deafnessRizwan Yousaf, Zubair M Ahmed, Arnaud Pj Giese, et al.
Clinical Genetics|February 19, 2008
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1L M Peters, R A Fridell, E T Boger, et al.
Human Molecular Genetics|October 24, 2002
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28Linda M Peters, David W Anderson, Andrew J Griffith, et al.
The Journal of Biological Chemistry|September 8, 2012
The transcription factors Grainyhead-like 2 and NK2-homeobox 1 form a regulatory loop that coordinates lung epithelial cell morphogenesis and differentiationSaaket Varma, Yuxia Cao, Jean-Bosco Tagne, et al.
Frontiers in Molecular Neuroscience|September 27, 2021
Single-Cell RNA-Seq of Cisplatin-Treated Adult Stria Vascularis Identifies Cell Type-Specific Regulatory Networks and Novel Therapeutic Gene TargetsIan A Taukulis, Rafal T Olszewski, Soumya Korrapati, et al.
BMC Genomics|September 23, 2018
A comparative analysis of library prep approaches for sequencing low input translatome samplesYang Song, Beatrice Milon, Sandra Ott, et al.
American Journal of Human Genetics|June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZ M Ahmed, S Riazuddin, S L Bernstein, et al.
Pageof 12