Inheritance patterns of progressive hearing loss in laboratory strains of mice

Por Noben-Trauth, Konrad, Johnson, Kenneth R.
Publicado em 2009

Ahl2, a Second Locus Affecting Age-Related Hearing Loss in Mice

Por Johnson, Kenneth R., Zheng, Qing Yin
Publicado em 2002

Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice

Por Zheng, Qing Yin, Johnson, Kenneth R.
Publicado em 2001

Ectopic Mineralization and Conductive Hearing Loss in Enpp1(asj) Mutant Mice, a New Model for Otitis Media and Tympanosclerosis

Por Tian, Cong, Harris, Belinda S., Johnson, Kenneth R.
Publicado no PLoS One (2016)

A hypomorphic mutation of the gamma-1 adaptin gene (Ap1g1) causes inner ear, retina, thyroid, and testes abnormalities in mice

Por Johnson, Kenneth R., Gagnon, Leona H., Chang, Bo
Publicado no Mamm Genome (2016)

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

Por Zheng, Qing Yin, Johnson, Kenneth R., Erway, Lawrence C.
Publicado em 1999

The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome

Por Johnson, Kenneth R., Cook, Susan A., Zheng, Qing Yin
Publicado em 1998

Strain background effects and genetic modifiers of hearing in mice

Por Johnson, Kenneth R., Zheng, Qing Yin, Noben-Trauth, Konrad
Publicado em 2006

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

Por Noben-Trauth, Konrad, Zheng, Qing Yin, Johnson, Kenneth R
Publicado em 2003

Application of Mouse Models to Research in Hearing and Balance

Por Ohlemiller, Kevin K., Jones, Sherri M., Johnson, Kenneth R.
Publicado no J Assoc Res Otolaryngol (2016)

Mutations of the Mouse ELMO Domain Containing 1 Gene (Elmod1) Link Small GTPase Signaling to Actin Cytoskeleton Dynamics in Hair Cell Stereocilia

Por Johnson, Kenneth R., Longo-Guess, Chantal M., Gagnon, Leona H.
Publicado em 2012

A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice

Por Johnson, Kenneth R., Longo-Guess, Chantal M., Gagnon, Leona H.
Publicado no Mamm Genome (2015)

A novel null allele of mouse Dscam survives to adulthood on an inbred C3H background with reduced phenotypic variability

Por Fuerst, Peter G., Harris, Belinda S., Johnson, Kenneth R., Burgess, Robert W.
Publicado em 2010

Atlas en color de cirugia oral menor /

Por Koerner, Karl R., Tilt, Lloyd V., Johnson, Kenneth R., Castellví, Montserrat Boquera.
Publicado em 1995

A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9

Por Longo-Guess, Chantal, Gagnon, Leona H., Bergstrom, David E., Johnson, Kenneth R.
Publicado em 2007

Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation

Por Longo-Guess, Chantal M., Gagnon, Leona H., Fritzsch, Bernd, Johnson, Kenneth R.
Publicado em 2007

Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development

Por Schuster-Gossler, Karin, Harris, Belinda, Johnson, Kenneth R, Serth, Jürgen, Gossler, Achim
Publicado em 2009

Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice

Por Johnson, Kenneth R., Gagnon, Leona H., Longo-Guess, Chantal, Kane, Kelly L.
Publicado em 2011

A locus on distal Chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice

Por Zheng, Qing Yin, Ding, Dalian, Yu, Heping, Salvi, Richard J., Johnson, Kenneth R.
Publicado em 2008

A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

Por Johnson, Kenneth R., Zheng, Qing Yin, Bykhovskaya, Yelena, Spirina, Olga, Fischel-Ghodsian, Nathan
Publicado em 2001