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J Morell

Showing results (61-70 of 118) with videos related to

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Biorxiv : the Preprint Server for Biology|July 9, 2025
CASZ1 regulates the rate at which outer hair cells mature and is required for hearingYoko Nakano, Elizabeth C Driver, Susan C Wiechert, et al.
Anales Espanoles De Pediatria|October 1, 1989
[Parathyroid insufficiency syndrome. Two new cases: type Ia pseudohypoparathyroidism and pseudo-idiopathic hypoparathyroidism]D Barajas de Frutos, J Pedrero Vera, J E Bolívar Barrales, et al.
The Journal of Clinical Investigation|March 11, 2025
Activin A activation of Smad3 mitigates innate inflammation in mouse models of psoriasis and sepsisThierry Gauthier, Yun-Ji Lim, Wenwen Jin, et al.
Frontiers in Molecular Neuroscience|March 3, 2020
Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human CochleaMichael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
Frontiers in Molecular Neuroscience|June 21, 2021
Corrigendum: Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human CochleaMichael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
American Journal of Human Genetics|September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)M Zhu, T Yang, S Wei, 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.
Elife|October 11, 2017
Molecular architecture underlying fluid absorption by the developing inner earKeiji Honda, Sung Huhn Kim, Michael C Kelly, et al.
American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.
The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Pageof 12

Showing results (61-70 of 118) with videos related to

Sort By:
Pageof 12
Biorxiv : the Preprint Server for Biology|July 9, 2025
CASZ1 regulates the rate at which outer hair cells mature and is required for hearingYoko Nakano, Elizabeth C Driver, Susan C Wiechert, et al.
Anales Espanoles De Pediatria|October 1, 1989
[Parathyroid insufficiency syndrome. Two new cases: type Ia pseudohypoparathyroidism and pseudo-idiopathic hypoparathyroidism]D Barajas de Frutos, J Pedrero Vera, J E Bolívar Barrales, et al.
The Journal of Clinical Investigation|March 11, 2025
Activin A activation of Smad3 mitigates innate inflammation in mouse models of psoriasis and sepsisThierry Gauthier, Yun-Ji Lim, Wenwen Jin, et al.
Frontiers in Molecular Neuroscience|March 3, 2020
Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human CochleaMichael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
Frontiers in Molecular Neuroscience|June 21, 2021
Corrigendum: Characterizing Adult Cochlear Supporting Cell Transcriptional Diversity Using Single-Cell RNA-Seq: Validation in the Adult Mouse and Translational Implications for the Adult Human CochleaMichael Hoa, Rafal Olszewski, Xiaoyi Li, et al.
American Journal of Human Genetics|September 19, 2003
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26)M Zhu, T Yang, S Wei, 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.
Elife|October 11, 2017
Molecular architecture underlying fluid absorption by the developing inner earKeiji Honda, Sung Huhn Kim, Michael C Kelly, et al.
American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.
The New England Journal of Medicine|November 20, 1998
Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafnessR J Morell, H J Kim, L J Hood, et al.
Pageof 12