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J Morell

Showing results (41-50 of 118) with videos related to

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Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical presentation of DFNB12 and Usher syndrome type 1DJulie M Bork, Robert J Morell, Shaheen Khan, et al.
Journal of Medical Genetics|April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)S A Mohiddin, Z M Ahmed, A J Griffith, et al.
Allergologia Et Immunopathologia|December 24, 2005
How pediatricians in Spain manage the first acute wheezing episode in an atopic infant. Results from the TRAP studyJ A Castro-Rodríguez, A Escribano Montaner, J Garde Garde, et al.
Human Genetics|May 30, 2007
A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable traitRobert J Morell, Carmen C Brewer, Dongliang Ge, et al.
Journal of Structural Biology|September 2, 1998
A survey of the primary structure and the interspecies conservation of I-band titin's elastic elements in vertebratesC C Witt, N Olivieri, T Centner, et al.
American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.
Hearing Research|March 27, 2013
A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunctionSue I Lee, Travis Conrad, Sherri M Jones, et al.
Cell|July 3, 2018
Defects in the Alternative Splicing-Dependent Regulation of REST Cause DeafnessYoko Nakano, Michael C Kelly, Atteeq U Rehman, et al.
Anales Espanoles De Pediatria|January 1, 1990
[Schönlein-Henoch purpura and IgA nephropathy. A common pathogenetic cause?]D Barajas de Frutos, J Pedrero Vera, M J Martínez Gómez, et al.
Frontiers in Molecular Neuroscience|January 11, 2020
Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria VascularisSoumya Korrapati, Ian Taukulis, Rafal Olszewski, et al.
Pageof 12

Showing results (41-50 of 118) with videos related to

Sort By:
Pageof 12
Advances in Oto-Rhino-Laryngology|November 1, 2002
Clinical presentation of DFNB12 and Usher syndrome type 1DJulie M Bork, Robert J Morell, Shaheen Khan, et al.
Journal of Medical Genetics|April 3, 2004
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)S A Mohiddin, Z M Ahmed, A J Griffith, et al.
Allergologia Et Immunopathologia|December 24, 2005
How pediatricians in Spain manage the first acute wheezing episode in an atopic infant. Results from the TRAP studyJ A Castro-Rodríguez, A Escribano Montaner, J Garde Garde, et al.
Human Genetics|May 30, 2007
A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable traitRobert J Morell, Carmen C Brewer, Dongliang Ge, et al.
Journal of Structural Biology|September 2, 1998
A survey of the primary structure and the interspecies conservation of I-band titin's elastic elements in vertebratesC C Witt, N Olivieri, T Centner, et al.
American Journal of Human Genetics|July 21, 2000
Autosomal recessive nonsyndromic neurosensory deafness at DFNB1 not associated with the compound-heterozygous GJB2 (connexin 26) genotype M34T/167delTA J Griffith, A A Chowdhry, K Kurima, et al.
Hearing Research|March 27, 2013
A null mutation of mouse Kcna10 causes significant vestibular and mild hearing dysfunctionSue I Lee, Travis Conrad, Sherri M Jones, et al.
Cell|July 3, 2018
Defects in the Alternative Splicing-Dependent Regulation of REST Cause DeafnessYoko Nakano, Michael C Kelly, Atteeq U Rehman, et al.
Anales Espanoles De Pediatria|January 1, 1990
[Schönlein-Henoch purpura and IgA nephropathy. A common pathogenetic cause?]D Barajas de Frutos, J Pedrero Vera, M J Martínez Gómez, et al.
Frontiers in Molecular Neuroscience|January 11, 2020
Single Cell and Single Nucleus RNA-Seq Reveal Cellular Heterogeneity and Homeostatic Regulatory Networks in Adult Mouse Stria VascularisSoumya Korrapati, Ian Taukulis, Rafal Olszewski, et al.
Pageof 12