Genome-wide linkage analyses identify <it>Hfhl1</it> and <it>Hfhl3</it> with frequency-specific effects on the hearing spectrum of NIH Swiss mice

Por Keller James M, Noben-Trauth Konrad
Publicado em 2012-04-01

Inheritance patterns of progressive hearing loss in laboratory strains of mice

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

Ectopic Mineralization in the Middle Ear and Chronic Otitis Media with Effusion Caused by RPL38 Deficiency in the Tail-short (Ts) Mouse

Por Noben-Trauth, Konrad, Latoche, Joseph R.
Publicado em 2011

Genome-wide linkage analyses identify Hfhl1 and Hfhl3 with frequency-specific effects on the hearing spectrum of NIH Swiss mice

Por Keller, James M, Noben-Trauth, Konrad
Publicado em 2012

Genetic Analyses of the Mouse Deafness Mutations Varitint-Waddler (Va) and Jerker (Espnje)

Por Kim, Hung J., Jackson, Torrance, Noben–Trauth, Konrad
Publicado em 2002

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

Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain

Por Latoche, Joseph R., Neely, Harold R., Noben-Trauth, Konrad
Publicado em 2010

Phenotype and Genetics of Progressive Sensorineural Hearing Loss (Snhl1) in the LXS Set of Recombinant Inbred Strains of Mice

Por Noben-Trauth, Konrad, Latoche, Joseph R., Neely, Harold R., Bennett, Beth
Publicado em 2010

High-Frequency Sensorineural Hearing Loss and Its Underlying Genetics (Hfhl1 and Hfhl2) in NIH Swiss Mice

Por Keller, James M., Neely, Harold R., Latoche, Joseph R., Noben-Trauth, Konrad
Publicado em 2011

Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases

Por North, Michael A., Naggert, Juergen K., Yan, Yingzhuo, Noben-Trauth, Konrad, Nishina, Patsy M.
Publicado em 1997

Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice

Por Di Palma, Federica, Belyantseva, Inna A., Kim, Hung J., Vogt, Thomas F., Kachar, Bechara, Noben-Trauth, Konrad
Publicado em 2002

Jxc1/Sobp, Encoding a Nuclear Zinc Finger Protein, Is Critical for Cochlear Growth, Cell Fate, and Patterning of the Organ of Corti

Por Chen, Zheng, Montcouquiol, Mireille, Calderon, Rene, Jenkins, Nancy A., Copeland, Neal G., Kelley, Matthew W., Noben-Trauth, Konrad
Publicado em 2008

TRPML3 mutations cause impaired mechano-electrical transduction and depolarization by an inward-rectifier cation current in auditory hair cells of varitint-waddler mice

Por van Aken, Alexander F J, Atiba-Davies, Margaret, Marcotti, Walter, Goodyear, Richard J, Bryant, Jane E, Richardson, Guy P, Noben-Trauth, Konrad, Kros, Corné J
Publicado em 2008

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

Por Charizopoulou, Nikoletta, Lelli, Andrea, Schraders, Margit, Ray, Kausik, Hildebrand, Michael S., Ramesh, Arabandi, Srisailapathy, C. R. Srikumari, Oostrik, Jaap, Admiraal, Ronald J. C., Neely, Harold R., Latoche, Joseph R., Smith, Richard J. H., Northup, John K., Kremer, Hannie, Holt, Jeffrey R., Noben-Trauth, Konrad
Publicado em 2011

SOBP Is Mutated in Syndromic and Nonsyndromic Intellectual Disability and Is Highly Expressed in the Brain Limbic System

Por Birk, Efrat, Har-Zahav, Adi, Manzini, Chiara M., Pasmanik-Chor, Metsada, Kornreich, Liora, Walsh, Christopher A., Noben-Trauth, Konrad, Albin, Adi, Simon, Amos J., Colleaux, Laurence, Morad, Yair, Rainshtein, Limor, Tischfield, David J., Wang, Peter, Magal, Nurit, Maya, Idit, Shoshani, Noa, Rechavi, Gideon, Gothelf, Doron, Maydan, Gal, Shohat, Mordechai, Basel-Vanagaite, Lina
Publicado em 2010