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...
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...
Software support for improving technology infusion (2005)
Feather, Martin S., Hicks, Kenneth A., Johnson, Kenneth R., Cornford, Steven L.
NASA
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...
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...
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...
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...
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"...
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...
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"...
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...
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)
Thesis (M. Div.)--St. Vladimir's Orthodox Theological Seminary, 1992.
The Christian ideal in the seven letters of St. Anthony the Great (1992)
Thesis (M. Div.)--St. Vladimir's Orthodox Theological Seminary, 1992.
The Christian ideal in the seven letters of St. Anthony the Great (1992)
Thesis (M. Div.)--St. Vladimir's Orthodox Theological Seminary, 1992.
Thesis (M.A.)--St. Vladimir's Orthodox Theological Seminary, 1989.
Reception of converts into the Orthodox Church three case studies / (1989)
Thesis (M.A.)--St. Vladimir's Orthodox Theological Seminary, 1989.
Reception of converts into the Orthodox Church three case studies / (1989)
Thesis (M.A.)--St. Vladimir's Orthodox Theological Seminary, 1989.
Photocopy of typescript.
Thesis (Ph. D.)--Pennsylvania State University, 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...
Reciprocity and multiplicativity in a class of arithmetic functions /--by Kenneth R. Johnson. (1980)
Thesis (Ph. D.)--University of Colorado at Boulder, 1980.
A driving simulation technique for the investigation of gap acceptance behaviour / (1976)
Thesis (M. Sc.)--University of Newcastle upon Tyne. 1976.
Audiological manifestations in juvenile-onset diabetics [microform] / (1970)
Thesis (Ph. D.)--Michigan State University, 1970.
Thesis--University of Southern California.
Thesis (Ed.D.)--University of Southern California, 1969.
The woman suffrage movement in Florida / (1966)
Thesis (Ph. D.)--Florida State University, 1966.
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...
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...
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...
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...