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An Evaluation of Otopathology in the MOV-13 Transgenic Mutant Mousea.
Published in:
Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 249, doi. 10.1111/j.1749-6632.1991.tb19595.x
By:
- ALTSCHULER, RICHARD A.;
- DOLAN, DAVID F.;
- PTOK, MARTIN;
- GHOLIZADEH, GANJEI;
- BONADIO, JEFFREY;
- HAWKINS, JOSEPH E.
Publication type:
Article
A Modifier Gene Alleviates Hypothyroidism-Induced Hearing Impairment in Pou1f1dw Dwarf Mice.
Published in:
Genetics, 2011, v. 189, n. 2, p. 665, doi. 10.1534/genetics.111.130633
By:
- Fang, Qing;
- Longo-Guess, Chantal;
- Gagnon, Leona H.;
- Mortensen, Amanda H.;
- Dolan, David F.
Publication type:
Article
The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing.
Published in:
eLife, 2015, p. 1, doi. 10.7554/eLife.08627
By:
- Qing Fang;
- Indzhykulian, Artur A.;
- Mustapha, Mirna;
- Riordan, Gavin P.;
- Dolan, David F.;
- Friedman, Thomas B.;
- Belyantseva, Inna A.;
- Frolenkov, Gregory I.;
- Camper, Sally A.;
- Bird, Jonathan E.
Publication type:
Article
Generation and Characterization of α9 and α10 Nicotinic Acetylcholine Receptor Subunit Knockout Mice on a C57BL/6J Background.
Published in:
Frontiers in Neuroscience, 2017, p. 1, doi. 10.3389/fnins.2017.00516
By:
- Morley, Barbara J.;
- Dolan, David F.;
- Ohlemiller, Kevin K.;
- Simmons, Dwayne D.
Publication type:
Article
Auditory hair cell replacement and hearing improvement by Atoh1 gene therapy in deaf mammals.
Published in:
Nature Medicine, 2005, v. 11, n. 3, p. 271, doi. 10.1038/nm1193
By:
- Izumikawa, Masahiko;
- Minoda, Ryosei;
- Kawamoto, Kohei;
- Abrashkin, Karen A.;
- Swiderski, Donald L.;
- Dolan, David F.;
- Brough, Douglas E.;
- Raphael, Yehoash
Publication type:
Article
Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus.
Published in:
2004
By:
- Odeh, Hana;
- Hagiwara, Nobuko;
- Skynner, Michael;
- Mitchem, Kristina L.;
- Beyer, Lisa A.;
- Allen, Nicholas D.;
- Brilliant, Murray H.;
- Lebart, M. C.;
- Dolan, David F.;
- Raphael, Yehoash;
- Kohrman, David C.
Publication type:
journal article
Heat shock factor 1‐deficient mice exhibit decreased recovery of hearing following noise overstimulation.
Published in:
Journal of Neuroscience Research, 2005, v. 81, n. 4, p. 589, doi. 10.1002/jnr.20417
By:
- Damon A. Fairfield;
- Margaret I. Lomax;
- Gary A. Dootz;
- Shu Chen;
- Andrzej T. Galecki;
- Ivor J. Benjamin;
- David F. Dolan;
- Richard A. Altschuler
Publication type:
Article
Deafness and Permanently Reduced Potassium Channel Gene Expression and Function in Hypothyroid Pit1dw Mutants.
Published in:
Journal of Neuroscience, 2009, v. 29, n. 4, p. 1212, doi. 10.1523/JNEUROSCI.4957-08.2009
By:
- Mustapha, Mirna;
- Qing Fang;
- Tzy-Wen Gong;
- Dolan, David F.;
- Raphael, Yehoash;
- Camper, Sally A.;
- Duncan, R. Keith
Publication type:
Article
Conditioning the Cochlea to Facilitate Survival and Integration of Exogenous Cells into the Auditory Epithelium.
Published in:
Molecular Therapy, 2014, v. 22, n. 4, p. 873, doi. 10.1038/mt.2013.292
By:
- Park, Yong-Ho;
- Wilson, Kevin F.;
- Ueda, Yoshihisa;
- Tung Wong, Hiu;
- Beyer, Lisa A.;
- Swiderski, Donald L.;
- Dolan, David F.;
- Raphael, Yehoash
Publication type:
Article
Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.
Published in:
2012
By:
- Fang Q;
- Giordimaina AM;
- Dolan DF;
- Camper SA;
- Mustapha M;
- Fang, Qing;
- Giordimaina, Alicia M;
- Dolan, David F;
- Camper, Sally A;
- Mustapha, Mirna
Publication type:
journal article
Induction of heat shock proteins by hyperthermia and noise overstimulation in hsf1 -/- mice.
Published in:
2012
By:
- Gong TW;
- Fairfield DA;
- Fullarton L;
- Dolan DF;
- Altschuler RA;
- Kohrman DC;
- Lomax MI;
- Gong, Tzy-Wen;
- Fairfield, Damon A;
- Fullarton, Lynne;
- Dolan, David F;
- Altschuler, Richard A;
- Kohrman, David C;
- Lomax, Margaret I
Publication type:
journal article
Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.
Published in:
2007
By:
- Mustapha, Mirna;
- Beyer, Lisa;
- Izumikawa, Masahiko;
- Swiderski, Donald;
- Dolan, David;
- Raphael, Yehoash;
- Camper, Sally;
- Beyer, Lisa A;
- Swiderski, Donald L;
- Dolan, David F;
- Camper, Sally A
Publication type:
journal article
Long-term effects of acoustic trauma on electrically evoked otoacoustic emission.
Published in:
2005
By:
- Halsey, Kärin;
- Fegelman, Karen;
- Raphael, Yehoash;
- Grosh, Karl;
- Dolan, David F.;
- Halsey, Kirin
Publication type:
journal article
Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.
Published in:
Mammalian Genome, 2007, v. 18, n. 8, p. 596, doi. 10.1007/s00335-007-9038-0
By:
- Karolyi, I. Jill;
- Dootz, Gary A.;
- Halsey, Karin;
- Beyer, Lisa;
- Probst, Frank J.;
- Johnson, Kenneth R.;
- Parlow, Albert F.;
- Raphael, Yehoash;
- Dolan, David F.;
- Camper, Sally A.
Publication type:
Article
Genetic and phenotypic analysis of the mouse mutant mh2J, an Ap3d allele caused by IAP element insertion.
Published in:
Mammalian Genome, 2003, v. 14, n. 3, p. 157, doi. 10.1007/s00335-002-2238-8
By:
- Kantheti, Prameela;
- Diaz, Maria E.;
- Peden, Andrew E.;
- Seong, Eunju E.;
- Dolan, David F.;
- Robinson, Margaret S.;
- Noebels, Jeffrey L.;
- Burmeister, Margit L.
Publication type:
Article
Rapamycin Added to Diet in Late Mid-Life Delays Age-Related Hearing Loss in UMHET4 Mice.
Published in:
Frontiers in Cellular Neuroscience, 2021, v. 15, p. N.PAG, doi. 10.3389/fncel.2021.658972
By:
- Altschuler, Richard A.;
- Kabara, Lisa;
- Martin, Catherine;
- Kanicki, Ariane;
- Stewart, Courtney E.;
- Kohrman, David C.;
- Dolan, David F.
Publication type:
Article
Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.
Published in:
Human Molecular Genetics, 2003, v. 12, n. 21, p. 2797, doi. 10.1093/hmg/ddg308
By:
- Karolyi, I. Jill;
- Probst, Frank J.;
- Beyer, Lisa;
- Odeh, Hana;
- Dootz, Gary;
- Cha, Kelly B.;
- Martin, Donna M.;
- Avraham, Karen B.;
- Kohrman, David;
- Dolan, David F.;
- Raphael, Yehoash;
- Camper, Sally A.
Publication type:
Article
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.
Published in:
Human Molecular Genetics, 2003, v. 12, n. 16, p. 2049, doi. 10.1093/hmg/ddg210
By:
- Ben-Yosef, Tamar;
- Belyantseva, Inna A.;
- Saunders, Thomas L.;
- Hughes, Elizabeth D.;
- Kawamoto, Kohei;
- Van Itallie, Christina M.;
- Beyer, Lisa A.;
- Halsey, Kärin;
- Gardner, Donald J.;
- Wilcox, Edward R.;
- Rasmussen, Julia;
- Anderson, James M.;
- Dolan, David F.;
- Forge, Andrew;
- Raphael, Yehoash;
- Camper, Sally A.;
- Friedman, Thomas B.
Publication type:
Article
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.
Published in:
Human Molecular Genetics, 2002, v. 11, n. 16, p. 1887, doi. 10.1093/hmg/11.16.1887
By:
- Mitchem, Kristina L.;
- Hibbard, Ellen;
- Beyer, Lisa A.;
- Bosom, Ken;
- Dootz, Gary A.;
- Dolan, David F.;
- Johnson, Kenneth R.;
- Raphael, Yehoash;
- Kohrman, David C.
Publication type:
Article
Hearing dysfunction in heterozygous Mitf Mi-wh/+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome.
Published in:
Pigment Cell & Melanoma Research, 2013, v. 26, n. 1, p. 78, doi. 10.1111/pcmr.12030
By:
- Ni, Christina;
- Zhang, Deming;
- Beyer, Lisa A.;
- Halsey, Karin E.;
- Fukui, Hideto;
- Raphael, Yehoash;
- Dolan, David F.;
- Hornyak, Thomas J.
Publication type:
Article
Grxcr2 is required for stereocilia morphogenesis in the cochlea.
Published in:
PLoS ONE, 2018, v. 13, n. 8, p. 1, doi. 10.1371/journal.pone.0201713
By:
- Avenarius, Matthew R.;
- Jung, Jae-Yun;
- Askew, Charles;
- Jones, Sherri M.;
- Hunker, Kristina L.;
- Azaiez, Hela;
- Rehman, Atteeq U.;
- Schraders, Margit;
- Najmabadi, Hossein;
- Kremer, Hannie;
- Smith, Richard J. H.;
- Géléoc, Gwenaëlle S. G.;
- Dolan, David F.;
- Raphael, Yehoash;
- Kohrman, David C.
Publication type:
Article
Experimental model of immune-mediated hearing loss using cross-species immunization.
Published in:
Laryngoscope, 1990, v. 100, n. 9, p. 941, doi. 10.1288/00005537-199009000-00006
By:
- Orozco, Charles R.;
- Niparko, John K.;
- Richardson, Bruce C.;
- Dolan, David F.;
- Ptok, Martin U.;
- Altschuler, Richard A.
Publication type:
Article
Amelioration of Cisplatin-Induced ototoxicity by fosfomycin.
Published in:
Laryngoscope, 1986, v. 96, n. 9, p. 948, doi. 10.1288/00005537-198609000-00005
By:
- Schweitzer, Vanessa G.;
- Dolan, David F.;
- Davidson, Thomas;
- Abrams, Gerald E.;
- Bs, Ronald Snyder
Publication type:
Article
Vestibular morphological analysis of the effects of cisplatin VS. platinum analogs, CBDCA (JM-8).
Published in:
Laryngoscope, 1986, v. 96, n. 9, p. 959, doi. 10.1288/00005537-198609000-00006
By:
- Schweitzer, Vanessa G.;
- Rarey, Kyle E.;
- Abrams, Gerald E.;
- Dolan, David F.;
- Sheridan, Christine
Publication type:
Article

Found: 24

An Evaluation of Otopathology in the MOV-13 Transgenic Mutant Mouse<sup>a</sup>.

A Modifier Gene Alleviates Hypothyroidism-Induced Hearing Impairment in Pou1f1<sup>dw</sup> Dwarf Mice.

The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing.

Generation and Characterization of α9 and α10 Nicotinic Acetylcholine Receptor Subunit Knockout Mice on a C57BL/6J Background.

Auditory hair cell replacement and hearing improvement by Atoh1 gene therapy in deaf mammals.

Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus.

Heat shock factor 1‐deficient mice exhibit decreased recovery of hearing following noise overstimulation.

Deafness and Permanently Reduced Potassium Channel Gene Expression and Function in Hypothyroid Pit1<sup>dw</sup> Mutants.

Conditioning the Cochlea to Facilitate Survival and Integration of Exogenous Cells into the Auditory Epithelium.

Genetic background of Prop1(df) mutants provides remarkable protection against hypothyroidism-induced hearing impairment.

Induction of heat shock proteins by hyperthermia and noise overstimulation in hsf1 -/- mice.

Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants.

Long-term effects of acoustic trauma on electrically evoked otoacoustic emission.

Dietary thyroid hormone replacement ameliorates hearing deficits in hypothyroid mice.

Genetic and phenotypic analysis of the mouse mutant mh<sup>2J</sup>, an Ap3d allele caused by IAP element insertion.

Rapamycin Added to Diet in Late Mid-Life Delays Age-Related Hearing Loss in UMHET4 Mice.

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

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.

Hearing dysfunction in heterozygous Mitf<sup> Mi-wh</sup>/+ mice, a model for Waardenburg syndrome type 2 and Tietz syndrome.

Grxcr2 is required for stereocilia morphogenesis in the cochlea.

Experimental model of immune-mediated hearing loss using cross-species immunization.

Amelioration of Cisplatin-Induced ototoxicity by fosfomycin.

Vestibular morphological analysis of the effects of cisplatin VS. platinum analogs, CBDCA (JM-8).