Kenneth R. Johnson

Publication List Details

Period

1959 - 2009

Number

42

Co-Authors

Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass (2009)

Munroe, Robert J, Prabhu, Vinay, Acland, Greg M, Johnson, Kenneth R, Harris, Belinda S, O'Brien, Tim P, ...

Abstract Background The H6 homeobox genes Hmx1 , Hmx2 , and Hmx3 (also known as Nkx5-3 ; Nkx5-2 and Nkx5-1 , respectively), compose a family within the NKL subclass of the ANTP class of homeobox...

Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1levels during early mouse development (2009)

Schuster-Gossler, Karin, Harris, Belinda, Johnson, Kenneth R, Serth, Jürgen, Gossler, Achim

Abstract Background The evolutionarily conserved Notch signalling pathway regulates multiple developmental processes in a wide variety of organisms. One critical posttranslational modification of...

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans (2005)

Zheng, Qing Yin, Yan, Denise, Ouyang, Xiao Mei, Du, Li Lin, Yu, Heping, Chang, Bo, ...

Mutations in genes coding for cadherin 23 and protocadherin 15 cause deafness in both mice and humans. Here, we provide evidence that mutations at these two cadherin loci can interact to cause...

Graphic Three-Axes Presentation of Residual Gas Analyser Data (2004)

Johnson, Kenneth R., Levi, Alejandro G.

Residual gas analyzers (RGA) are commonly used to measure the composition of residual gases in thermal-vacuum test chambers. Measurements from RGAs are often used to identify and quantify outgassing...

Mars Pathfinder Spacecraft, Lander, and Rover Testing in Simulated Deep Space and Mars Surface Environments (2004)

Johnson, Kenneth R.

This paper describes the test program which was conducted to verify the Mars Pathfinder spacecraft thermal design. The testing program required subjecting the mission hardware to both deep space and...

Digenic inheritance of deafness caused by mutations in the genes encoding cadherin 23 and protocadherin 15 in mice and humans (2004)

Zheng, Qing Yin, Yan, Denise, Ouyang, Xiao Mei, Du, Li Lin, Yu, Heping, Chang, Bo, ...

Mutations in the genes coding for cadherin 23 and protocadherin 15 cause deafness in both mice and humans. Here we provide evidence that mutations at these two cadherin loci can interact to cause...

Digenic inheritance of deafness caused by mutations in the genes encoding cadherin 23 and protocadherin 15 in mice and humans (2004)

Zheng, Qing Yin, Yan, Denise, Ouyang, Xiao Mei, Du, Li Lin, Yu, Heping, Chang, Bo, ...

Mutations in the genes coding for cadherin 23 and protocadherin 15 cause deafness in both mice and humans. Here we provide evidence that mutations at these two cadherin loci can interact to cause...

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene (2003)

Johnson, Kenneth R., Gagnon, Leona H., Webb, Lisa S., Peters, Luanne L., Hawes, Norman L., Chang, Bo, ...

We mapped two new recessive mutations causing circling behavior and deafness to the same region on Chromosome 7 and showed they are allelic by complementation analysis. One was named "deaf circler"...

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene (2003)

Johnson, Kenneth R., Gagnon, Leona H., Webb, Lisa S., Peters, Luanne L., Hawes, Norman L., Chang, Bo, ...

We mapped two new recessive mutations causing circling behavior and deafness to the same region on chromosome 7 and showed they are allelic by complementation analysis. One was named ‘deaf...

Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene (2003)

Johnson, Kenneth R., Gagnon, Leona H., Webb, Lisa S., Peters, Luanne L., Hawes, Norman L., Chang, Bo, ...

We mapped two new recessive mutations causing circling behavior and deafness to the same region on Chromosome 7 and showed they are allelic by complementation analysis. One was named "deaf circler"...

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6 (2002)

Mitchem, Kristina L., Hibbard, Ellen, Beyer, Lisa A., Bosom, Ken, Dootz, Gary A., Dolan, David F., ...

The recessive mutation at the mouse spinner (sr) locus results in hearing loss and vestibular dysfunction due to neuroepithelial defects in the inner ear. Using a positional cloning strategy, we have...

Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss (1999)

Ikeda, Akihiro, Zheng, Qing Yin, Rosenstiel, Philip, Maddatu, Terry, Zuberi, Aamir R., Roopenian, Derry C., ...

Quantitative trait locus (QTL) analysis of genetic crosses has proven to be a useful tool for identifying loci associated with specific phenotypes and for dissecting genetic components of complex...

The Christian ideal in the seven letters of St. Anthony the Great [microform] / (1992)

Johnson, Kenneth R.

Thesis (M. Div.)--St. Vladimir's Orthodox Theological Seminary, 1992.

The Christian ideal in the seven letters of St. Anthony the Great (1992)

Johnson, Kenneth R.

Thesis (M. Div.)--St. Vladimir's Orthodox Theological Seminary, 1992.

The Christian ideal in the seven letters of St. Anthony the Great (1992)

Johnson, Kenneth R.

Thesis (M. Div.)--St. Vladimir's Orthodox Theological Seminary, 1992.

Reception of converts into the Orthodox Church three case studies / (1989)

Johnson, Kenneth R.

Thesis (M.A.)--St. Vladimir's Orthodox Theological Seminary, 1989.

Reception of converts into the Orthodox Church three case studies / (1989)

Johnson, Kenneth R.

Thesis (M.A.)--St. Vladimir's Orthodox Theological Seminary, 1989.

Linkage associations in hybridized Salvelinus genomes: The duplicate loci encoding pepidase-D and glucosephosphate isomerase and the unduplicated sorbitol dehydrogenase locus (1984)

Hollister, Annette, Johnson, Kenneth R., Wright, James E.

Electrophoresis was performed on parents and progeny of 21 families of tetraploid derivative Salvelinus species. Variable phenotypes were shown for the duplicate loci encoding the enzyme peptidase D...

The woman suffrage movement in Florida / (1966)

Johnson, Kenneth R.

Thesis (Ph. D.)--Florida State University, 1966.

Cloning, Characterization, and Mapping of a Murine Promiscuous Chemokine Receptor Gene: Homolog of the Human Duffy Gene

Luo, Hong, Chaudhuri, Asok, Johnson, Kenneth R., Neote, Kuldeep, Zbrzezna, Valerie, He, Yu, ...

We report here the isolation and genomic organization of the orthologous mouse Duffy gene, named Dfy. It is a single copy gene located in chromosome 1 in a region homologous to the human Duffy gene...

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

Longo-Guess, Chantal M., Gagnon, Leona H., Cook, Susan A., Wu, Jian, Zheng, Qing Y., Johnson, Kenneth R.

Mouse deafness mutations provide valuable models of human hearing disorders and entry points into molecular pathways important to the hearing process. A newly discovered mouse mutation named...

Cloning, Characterization, and Mapping of a Murine Promiscuous Chemokine Receptor Gene: Homolog of the Human Duffy Gene

Luo, Hong, Chaudhuri, Asok, Johnson, Kenneth R., Neote, Kuldeep, Zbrzezna, Valerie, He, Yu, ...

We report here the isolation and genomic organization of the orthologous mouse Duffy gene, named Dfy. It is a single copy gene located in chromosome 1 in a region homologous to the human Duffy gene...

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice

Longo-Guess, Chantal M., Gagnon, Leona H., Cook, Susan A., Wu, Jian, Zheng, Qing Y., Johnson, Kenneth R.

Mouse deafness mutations provide valuable models of human hearing disorders and entry points into molecular pathways important to the hearing process. A newly discovered mouse mutation named...

A Quantitative Survey of Gravity Receptor Function in Mutant Mouse Strains

Jones, Sherri M., Johnson, Kenneth R., Yu, Heping, Erway, Lawrence C., Alagramam, Kumar N., Pollak, Natasha, ...

The purpose of this research was to identify vestibular deficits in mice using linear vestibular evoked potentials (VsEPs). VsEP thresholds, peak latencies, and peak amplitudes from 24 strains with...