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Kenneth Johnson

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Vishnu Hosur; Kenneth R Johnson; Anoop Kavirayani; Bonnie L Lyons; Kimberly A Martin; Rebecca L Riding; Lynn Alley; Lisa M Burzenski; Gregory A Cox; Melissa L Cox; Leonard D Shultz
Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) mice.
Kenneth R Johnson; Leona H Gagnon; Chantal M Longo-Guess; Kelly L Kane
Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice.
Kenneth R Johnson; Chantal M Longo-Guess; Leona H Gagnon
Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia.

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2013: Vishnu Hosur; Kenneth R Johnson; Anoop Kavirayani; Bonnie L Lyons; Kimberly A Martin; Rebecca L Riding; Lynn Alley; Lisa M Burzenski; Gregory A Cox; Melissa L Cox; Leonard D Shultz
Retrotransposon insertion in the T-cell acute lymphocytic leukemia 1 (Tal1) gene is associated with severe renal disease and patchy alopecia in Hairpatches (Hpt) mice.
PloS one 2013;8(1):e53426.
2012: Kenneth R Johnson; Leona H Gagnon; Chantal M Longo-Guess; Kelly L Kane
Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice.
Neurobiology of aging 2012;33(8):1720-9.
2012: Kenneth R Johnson; Chantal M Longo-Guess; Leona H Gagnon
Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia.
PloS one 2012;7(4):e36074.
2012: Kelly L Kane; Chantal M Longo-Guess; Richard J Salvi; Dalian Ding; Leona H Gagnon; Kenneth R Johnson
Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice.
Hearing research 2012;283(1-2):80-8.
2010: Peter G Fuerst; Belinda S Harris; Kenneth R Johnson; Robert W Burgess
A novel null allele of mouse DSCAM survives to adulthood on an inbred C3H background with reduced phenotypic variability.
Genesis (New York, N.Y. : 2000) 2010;48(10):578-84.
2010: Kenneth R Johnson; Heping Yu; Dalian Ding; Haiyan Jiang; Leona H Gagnon; Richard J Salvi
Separate and combined effects of Sod1 and Cdh23 mutations on age-related hearing loss and cochlear pathology in C57BL/6J mice.
Hearing research 2010;268(1-2):85-92.
2010: Jung-Bum Shin; Chantal M Longo-Guess; Leona H Gagnon; Katherine W Saylor; Rachel A Dumont; Kateri J Spinelli; James M Pagana; Phillip A Wilmarth; Larry L David; Peter G Gillespie; Kenneth R Johnson
The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2010;30(29):9683-94.
2010: Victoria E DeMambro; Masanobu Kawai; Thomas Landes Clemens; Keertik Fulzele; Jane A Maynard; Caralina Marín de Evsikova; Kenneth R Johnson; Ernesto Canalis; Wesley G Beamer; Clifford J Rosen; Leah Rae Donahue
A novel spontaneous mutation of Irs1 in mice results in hyperinsulinemia, reduced growth, low bone mass and impaired adipogenesis.
The Journal of endocrinology 2010;204(3):241-53.
2010: Thomas H Chase; Bonnie L Lyons; Roderick T Bronson; Oded Foreman; Leah Rae Donahue; Lisa M Burzenski; Bruce Gott; Priscilla Lane; Belinda Harris; Uta Ceglarek; Joachim Thiery; Henning Wittenburg; Jonathan N Thon; Joseph E Italiano; Kenneth R Johnson; Leonard D Shultz
The mouse mutation "thrombocytopenia and cardiomyopathy" (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia.
Blood 2010;115(6):1267-76.
2008: Kenneth R Johnson; Chantal M Longo-Guess; Leona H Gagnon; Heping Yu; Qing Yin Zheng
A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice.
Genomics 2008;92(4):219-25.
2007: Chantal M Longo-Guess; Leona H Gagnon; David E Bergstrom; Kenneth R Johnson
A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9.
Hearing research 2007;234(1-2):21-8.
2007: Chantal M Longo-Guess; Leona H Gagnon; Bernd Fritzsch; Kenneth R Johnson
Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(9):646-56.
2007: Kenneth R Johnson; Coleen C Marden; Patricia Ward-Bailey; Leona H Gagnon; Roderick T Bronson; Leah Rae Donahue
Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2.
Molecular endocrinology (Baltimore, Md.) 2007;21(7):1593-602.
2006: Leona H Gagnon; Chantal M Longo-Guess; Mark Berryman; Jung-Bum Shin; Katherine W Saylor; Heping Yu; Peter G Gillespie; Kenneth R Johnson
The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear function.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(40):10188-98.
2006: Kenneth R Johnson; Qing Yin Zheng; Konrad Noben-Trauth
Strain background effects and genetic modifiers of hearing in mice.
Brain research 2006;1091(1):79-88.
2006: Sherri M Jones; Timothy A Jones; Kenneth R Johnson; Heping Yu; Lawrence C Erway; Qing Yin Zheng
A comparison of vestibular and auditory phenotypes in inbred mouse strains.
Brain research 2006;1091(1):40-6.
2005: Sherri M Jones; Kenneth R Johnson; Heping Yu; Lawrence C Erway; Kumar N Alagramam; Natasha Pollak; Timothy A Jones
A quantitative survey of gravity receptor function in mutant mouse strains.
Journal of the Association for Research in Otolaryngology : JARO 2005;6(4):297-310.
2005: Chantal M Longo-Guess; Leona H Gagnon; Susan A Cook; Jian Wu; Qing Yin Zheng; Kenneth R Johnson
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(22):7894-9.
2005: Kenneth R Johnson; Qing Yin Zheng; M D Weston; L J Ptacek; Konrad Noben-Trauth
The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.
Genomics 2005;85(5):582-90.
2004: Sherri M Jones; Lawrence C Erway; Kenneth R Johnson; Heping Yu; Timothy A Jones
Gravity receptor function in mice with graded otoconial deficiencies.
Hearing research 2004;191(1-2):34-40.
2004: Bettina Lorenz-Depiereux; Victoria E Guido; Kenneth R Johnson; Qing Yin Zheng; Leona H Gagnon; Joiel D Bauschatz; Muriel T Davisson; Linda L Washburn; Leah Rae Donahue; Tim M Strom; Eva M Eicher
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(3):151-61.
2003: Kenneth R Johnson; Leona H Gagnon; Lisa S Webb; Luanne L Peters; Norman L Hawes; Bo Chang; Qing Yin Zheng
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
Human molecular genetics 2003;12(23):3075-86.
2003: Leah Rae Donahue; Bo Chang; Subburaman Mohan; Naohisa Miyakoshi; Jon E Wergedal; David J Baylink; Norman L Hawes; Clifford J Rosen; Patricia Ward-Bailey; Qing Yin Zheng; Roderick T Bronson; Kenneth R Johnson; Muriel T Davisson
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003;18(9):1612-21.
2003: Kenneth R Johnson; Priscilla W Lane; Susan A Cook; Belinda S Harris; Patricia Ward-Bailey; Roderick T Bronson; Bonnie L Lyons; Leonard D Shultz; Muriel T Davisson
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.
Genomics 2003;81(1):6-14.
2002: Kenneth R Johnson; Qing Yin Zheng
Ahl2, a second locus affecting age-related hearing loss in mice.
Genomics 2002;80(5):461-4.
2002: Akihiro Ikeda; Qing Yin Zheng; Aamir Zuberi; Kenneth R Johnson; Jürgen K Naggert; Patsy M Nishina
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).
Nature genetics 2002;30(4):401-5.
2001: Qing Yin Zheng; Kenneth R Johnson
Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice.
Hearing research 2001;154(1-2):45-53.
2001: Kenneth R Johnson; Qing Yin Zheng; Yelena Bykhovskaya; O Spirina; N Fischel-Ghodsian
A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice.
Nature genetics 2001;27(2):191-4.
2001: Susan A Cook; Ellen C Akeson; CJ Calvano; Kenneth R Johnson; J Mandell; Norman L Hawes; Roderick T Bronson; TH Roderick; Muriel T Davisson
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene.
Cytogenetics and cell genetics 2001;93(1-2):77-82.
2000: Muriel T Davisson; Kenneth R Johnson; Roderick T Bronson; Patricia Ward-Bailey; Susan A Cook; Belinda S Harris; Leah Rae Donahue
Grey intense: a new mouse mutation affecting pigmentation.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(12):1139-41.
2000: Kenneth R Johnson; Qing Yin Zheng; Lawrence C Erway
A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.
Genomics 2000;70(2):171-80.
2000: Verity A Letts; A Valenzuela; C Dunbar; Qing Yin Zheng; Kenneth R Johnson; Wayne N Frankel
A new spontaneous mouse mutation in the Kcne1 gene.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):831-5.
2000: Patricia Ward-Bailey; B Wood; Kenneth R Johnson; Roderick T Bronson; Leah Rae Donahue; Muriel T Davisson
Neuromuscular ataxia: a new spontaneous mutation in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):820-3.
1999: Akihiro Ikeda; Qing Yin Zheng; Philip Rosenstiel; Terry P Maddatu; Aamir Zuberi; Derry C Roopenian; M A North; Jürgen K Naggert; Kenneth R Johnson; Patsy M Nishina
Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss.
Human molecular genetics 1999;8(9):1761-7.
1999: Qing Yin Zheng; Kenneth R Johnson; Lawrence C Erway
Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses.
Hearing research 1999;130(1-2):94-107.
1999: Kenneth R Johnson; Susan A Cook; Lawrence C Erway; A N Matthews; L P Sanford; NE Paradies; R A Friedman
Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome.
Human molecular genetics 1999;8(4):645-53.
1999: R S Smith; Kenneth R Johnson; Norman L Hawes; Belinda S Harris; John P Sundberg; Muriel T Davisson
Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(2):102-6.
1998: Hope O Sweet; Murray H Brilliant; Susan A Cook; Kenneth R Johnson; Muriel T Davisson
A new allelic series for the underwhite gene on mouse chromosome 15.
The Journal of heredity 1998;89(6):546-51.
1998: Kenneth R Johnson; Susan A Cook; Qing Yin Zheng
The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(11):889-92.
1998: Kenneth R Johnson; Hope O Sweet; Leah Rae Donahue; Patricia Ward-Bailey; Roderick T Bronson; Muriel T Davisson
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.
Human molecular genetics 1998;7(6):1033-8.
1998: Roderick T Bronson; Leah Rae Donahue; Kenneth R Johnson; A Tanner; Priscilla W Lane; J R Faust
Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.
American journal of medical genetics 1998;77(4):289-97.
1998: Kenneth R Johnson; Muriel T Davisson
Encyclopedia of the mouse genome VII. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;8 Spec No():S343-52.
1997: Kenneth R Johnson; Lawrence C Erway; Susan A Cook; James F Willott; Qing Yin Zheng
A major gene affecting age-related hearing loss in C57BL/6J mice.
Hearing research 1997;114(1-2):83-92.
1996: Leah Rae Donahue; Susan A Cook; Kenneth R Johnson; Roderick T Bronson; Muriel T Davisson
Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(12):871-6.
1996: Hope O Sweet; Roderick T Bronson; Kenneth R Johnson; Susan A Cook; Muriel T Davisson
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):798-802.
1996: Patricia Ward-Bailey; Kenneth R Johnson; M A Handel; B S Harris; Muriel T Davisson
A new mouse mutation causing male sterility and histoincompatibility.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):793-7.
1996: P A Schweitzer; N Noben-Trauth; S C Pelsue; Kenneth R Johnson; Stanley Wolf; L D Shultz
Genetic mapping of the IL-12 alpha chain gene (Il12a) on mouse chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(5):394-5.
1996: N Noben-Trauth; P A Schweitzer; Kenneth R Johnson; Stanley Wolf; Barbara B Knowles; L D Shultz
The interleukin-12 beta subunit (p40) maps to mouse chromosome 11.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(5):392.
1996: H O Sweet; S C Marks; C A MacKay; Kenneth R Johnson; Muriel T Davisson
Dense incisors (din): a new mouse mutation on chromosome 16 affecting tooth eruption and body size.
The Journal of heredity 1996;87(2):162-7.
1996: Kenneth R Johnson; Muriel T Davisson
Encyclopedia of the mouse genome V. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;6 Spec No():S300-8.
1995: Kenneth R Johnson; Priscilla W Lane; Patricia Ward-Bailey; Muriel T Davisson
Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac.
Genomics 1995;29(2):457-64.
1995: Dennis S Rice; Robert Williams; Patricia Ward-Bailey; Kenneth R Johnson; B S Harris; Muriel T Davisson; Dan Goldowitz
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(8):546-8.
1995: Susan A Cook; Kenneth R Johnson; Roderick T Bronson; Muriel T Davisson
Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(3):187-91.
1994: Kenneth R Johnson; Susan A Cook; Muriel T Davisson
Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(11):670-87.
1994: Kenneth R Johnson; Muriel T Davisson
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S259-65.
1993: Muriel T Davisson; Kenneth R Johnson
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4 Spec No():S253-60.
1993: Kenneth R Johnson; Susan A Cook; Patricia Ward-Bailey; M Bustin; Muriel T Davisson
Identification and genetic mapping of the murine gene and 20 related sequences encoding chromosomal protein HMG-17.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(2):83-9.
1993: Kenneth R Johnson; Susan A Cook; Patricia Ward-Bailey; Muriel T Davisson
Genetic mapping of variable length rDNA segments to centromeric regions of mouse chromosomes 11, 12, 15, 16, and 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(1):49-52.
1992: Kenneth R Johnson; S Lu; M T Murtha; F H Ruddle; Muriel T Davisson
Genetic mapping of a new homeobox gene to mouse chromosome 7.
Genomics 1992;14(4):1107-9.
1992: Kenneth R Johnson; Muriel T Davisson
A multipoint genetic linkage map of mouse chromosome 18.
Genomics 1992;13(4):1143-9.
1992: Kenneth R Johnson; Susan A Cook; Muriel T Davisson
Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins.
Genomics 1992;12(3):503-9.
1992: Muriel T Davisson; Kenneth R Johnson
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S261-5.
1992: Kenneth R Johnson; Susan A Cook; M Bustin; Muriel T Davisson
Genetic mapping of the murine gene and 14 related sequences encoding chromosomal protein HMG-14.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(11):625-32.
1991: Kenneth R Johnson
Improved oligonucleotide labeling and hybridization assay for endogenous nonecotropic murine leukemia proviruses.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(4):260-2.