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Shehnaaz S M Manji

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The American Journal of Pathology|February 15, 2012
Identification of three novel hearing loss mouse strains with mutations in the Tmc1 geneShehnaaz S M Manji, Kerry A Miller, Louise H Williams, et al.
Hearing Research|March 15, 2013
Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunctionLouise H Williams, Kerry A Miller, Hans-Henrik M Dahl, et al.
Plos One|October 3, 2013
Eeyore: a novel mouse model of hereditary deafnessKerry A Miller, Louise H Williams, Hans-Henrik M Dahl, et al.
Journal of Neuroscience Research|December 13, 2005
Molecular characterization and expression of maternally expressed gene 3 (Meg3/Gtl2) RNA in the mouse inner earShehnaaz S M Manji, Brita S Sørensen, Tuomas Klockars, et al.
The Journal of Molecular Diagnostics : JMD|August 26, 2006
Detection of mutations in genes associated with hearing loss using a microarray-based approachKirby Siemering, Shehnaaz S M Manji, Wendy M Hutchison, et al.
Plos One|December 20, 2012
Inner ear morphology is perturbed in two novel mouse models of recessive deafnessKerry A Miller, Louise H Williams, Elizabeth Rose, et al.
Archives of Neurology|December 14, 2005
Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) geneWendy M Hutchison, Dominic Thyagarajan, Joanna Poulton, et al.
International Journal of Cancer|January 25, 2002
Expression and mutation analysis of the Wilms' tumor 1 gene in human neural tumorsSally L Dennis, Shehnaaz S M Manji, Darryl P Carrington, et al.
Plos One|March 23, 2011
A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain MozartShehnaaz S M Manji, Louise H Williams, Kerry A Miller, et al.
The American Journal of Pathology|June 22, 2011
An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in miceShehnaaz S M Manji, Kerry A Miller, Louise H Williams, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
The American Journal of Pathology|February 15, 2012
Identification of three novel hearing loss mouse strains with mutations in the Tmc1 geneShehnaaz S M Manji, Kerry A Miller, Louise H Williams, et al.
Hearing Research|March 15, 2013
Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunctionLouise H Williams, Kerry A Miller, Hans-Henrik M Dahl, et al.
Plos One|October 3, 2013
Eeyore: a novel mouse model of hereditary deafnessKerry A Miller, Louise H Williams, Hans-Henrik M Dahl, et al.
Journal of Neuroscience Research|December 13, 2005
Molecular characterization and expression of maternally expressed gene 3 (Meg3/Gtl2) RNA in the mouse inner earShehnaaz S M Manji, Brita S Sørensen, Tuomas Klockars, et al.
The Journal of Molecular Diagnostics : JMD|August 26, 2006
Detection of mutations in genes associated with hearing loss using a microarray-based approachKirby Siemering, Shehnaaz S M Manji, Wendy M Hutchison, et al.
Plos One|December 20, 2012
Inner ear morphology is perturbed in two novel mouse models of recessive deafnessKerry A Miller, Louise H Williams, Elizabeth Rose, et al.
Archives of Neurology|December 14, 2005
Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) geneWendy M Hutchison, Dominic Thyagarajan, Joanna Poulton, et al.
International Journal of Cancer|January 25, 2002
Expression and mutation analysis of the Wilms' tumor 1 gene in human neural tumorsSally L Dennis, Shehnaaz S M Manji, Darryl P Carrington, et al.
Plos One|March 23, 2011
A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain MozartShehnaaz S M Manji, Louise H Williams, Kerry A Miller, et al.
The American Journal of Pathology|June 22, 2011
An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in miceShehnaaz S M Manji, Kerry A Miller, Louise H Williams, et al.
Pageof 2