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Konrad Noben-Trauth

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James M Keller; Konrad Noben-Trauth
Genome-wide linkage analyses identify Hfhl1 and Hfhl3 with frequency-specific effects on the hearing spectrum of NIH Swiss mice.
James M Keller; Joseph R Latoche; Harold R Neely; Konrad Noben-Trauth
High-frequency sensorineural hearing loss and its underlying genetics (Hfhl1 and Hfhl2) in NIH Swiss mice.
Joseph R Latoche; Harold R Neely; Konrad Noben-Trauth
Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain.

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All Publications

2012: James M Keller; Konrad Noben-Trauth
Genome-wide linkage analyses identify Hfhl1 and Hfhl3 with frequency-specific effects on the hearing spectrum of NIH Swiss mice.
BMC genetics 2012;13():32.
2011: James M Keller; Joseph R Latoche; Harold R Neely; Konrad Noben-Trauth
High-frequency sensorineural hearing loss and its underlying genetics (Hfhl1 and Hfhl2) in NIH Swiss mice.
Journal of the Association for Research in Otolaryngology : JARO 2011;12(5):617-31.
2011: Joseph R Latoche; Harold R Neely; Konrad Noben-Trauth
Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain.
Hearing research 2011;275(1-2):150-9.
2011: Konrad Noben-Trauth; Joseph R Latoche
Ectopic mineralization in the middle ear and chronic otitis media with effusion caused by RPL38 deficiency in the Tail-short (Ts) mouse.
The Journal of biological chemistry 2011;286(4):3079-93.
2011: Nikoletta Charizopoulou; Andrea Lelli; Margit Schraders; Kausik Ray; Michael S Hildebrand; Arabandi Ramesh; C R Srikumari Srisailapathy; Jaap Oostrik; Ronald J C Admiraal; Harold R Neely; Joseph R Latoche; Richard J H Smith; John K Northup; Hannie Kremer; Jeffrey R Holt; Konrad Noben-Trauth
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human.
Nature communications 2011;2():201.
2011: Konrad Noben-Trauth
The TRPML3 channel: from gene to function.
Advances in experimental medicine and biology 2011;704():229-37.
2010: Einat Birk; Adi Har-Zahav; Chiara M Manzini; Metsada Pasmanik-Chor; Liora Kornreich; Christopher Walsh; Konrad Noben-Trauth; Adi Albin; Amos J Simon; Laurence Colleaux; Yair Morad; Limor Rainshtein; David J Tischfield; Peter Wang; Nurit Magal; Idit Maya; Noa Shoshani; Gideon Rechavi; Doron Gothelf; Gal Maydan; Mordechai Shohat; Lina Basel-Vanagaite
SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system.
American journal of human genetics 2010;87(5):694-700.
2010: Konrad Noben-Trauth; Joseph R Latoche; Harold R Neely; Beth Bennett
Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.
PloS one 2010;5(7):e11459.
2009: Konrad Noben-Trauth; Kenneth R Johnson
Inheritance patterns of progressive hearing loss in laboratory strains of mice.
Brain research 2009;1277():42-51.
2008: Alexander F J van Aken; Margaret Atiba-Davies; Walter Marcotti; Richard J Goodyear; Jane E Bryant; Guy P Richardson; Konrad Noben-Trauth; Corné J Kros
TRPML3 mutations cause impaired mechano-electrical transduction and depolarization by an inward-rectifier cation current in auditory hair cells of varitint-waddler mice.
The Journal of physiology 2008;586(Pt 22):5403-18.
2008: Mariola Sliwinska-Kowalska; Konrad Noben-Trauth; Malgorzata Pawelczyk; Tomasz Jarema Kowalski
Single nucleotide polymorphisms in the cadherin 23 (CDH23) gene in Polish workers exposed to industrial noise.
American journal of human biology : the official journal of the Human Biology Council 2008;20(4):481-3.
2008: Zheng Chen; Mireille Montcouquiol; Rene Calderon; Nancy A Jenkins; Neal G Copeland; Matthew W Kelley; Konrad Noben-Trauth
Jxc1/Sobp, encoding a nuclear zinc finger protein, is critical for cochlear growth, cell fate, and patterning of the organ of corti.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008;28(26):6633-41.
2007: Konrad Noben-Trauth; Harold Neely; Roscoe O Brady
Normal hearing in alpha-galactosidase A-deficient mice, the mouse model for Fabry disease.
Hearing research 2007;234(1-2):10-4.
2007: Margaret Atiba-Davies; Konrad Noben-Trauth
TRPML3 and hearing loss in the varitint-waddler mouse.
Biochimica et biophysica acta 2007;1772(8):1028-31.
2006: Alfredo Calderon; Adam Derr; Barden B Stagner; Kenneth R Johnson; Glen Martin; Konrad Noben-Trauth
Cochlear developmental defect and background-dependent hearing thresholds in the Jackson circler (jc) mutant mouse.
Hearing research 2006;221(1-2):44-58.
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: Meghan Drayton; Konrad Noben-Trauth
Mapping quantitative trait loci for hearing loss in Black Swiss mice.
Hearing research 2006;212(1-2):128-39.
2005: Agnieszka Rzadzinska; Mark Schneider; Konrad Noben-Trauth; James R Bartles; Anne E White-Olson
Balanced levels of Espin are critical for stereociliary growth and length maintenance.
Cell motility and the cytoskeleton 2005;62(3):157-65.
2005: Agnieszka Rzadzinska; Adam Derr; Anne E White-Olson; Konrad Noben-Trauth
Sustained cadherin 23 expression in young and adult cochlea of normal and hearing-impaired mice.
Hearing research 2005;208(1-2):114-21.
2005: Feng Qian; Konrad Noben-Trauth
Cellular and molecular function of mucolipins (TRPML) and polycystin 2 (TRPP2).
Pflügers Archiv : European journal of physiology 2005;451(1):277-85.
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: Celine Pompeia; Belen Hurle; Inna A Belyantseva; Konrad Noben-Trauth; Kirk W Beisel; James Gao; Patee Buchoff; Graeme Wistow; Anne E White-Olson
Gene expression profile of the mouse organ of Corti at the onset of hearing.
Genomics 2004;83(6):1000-11.
2004: Ronald S Petralia; Nathalie Sans; Ya-Xian Wang; Bryce Vissel; Kai Chang; Konrad Noben-Trauth; Stephen F Heinemann; Robert Wenthold
Loss of GLUR2 alpha-amino-3-hydroxy-5-methyl-4-isoxazoleproprionic acid receptor subunit differentially affects remaining synaptic glutamate receptors in cerebellum and cochlear nuclei.
The European journal of neuroscience 2004;19(8):2017-29.
2003: Konrad Noben-Trauth; Qing Yin Zheng; Kenneth R Johnson
Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss.
Nature genetics 2003;35(1):21-3.
2003: Lori L Hampton; Charles G Wright; Kumar N Alagramam; James F Battey; Konrad Noben-Trauth
A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15.
Hearing research 2003;180(1-2):67-75.
2003: Hung J Kim; Torrance Jackson; Konrad Noben-Trauth
Genetic analyses of the mouse deafness mutations varitint-waddler (Va) and jerker (Espnje).
Journal of the Association for Research in Otolaryngology : JARO 2003;4(1):83-90.
2002: Federica Di Palma; Inna A Belyantseva; Hung J Kim; Thomas F Vogt; Anne E White-Olson; Konrad Noben-Trauth
Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(23):14994-9.
2002: Torrance Jackson; James Thomas; Eric Green; Konrad Noben-Trauth
Genetic and physical maps of jerker (Espn(je)) on mouse chromosome 4.
Biochemical and biophysical research communications 2002;296(5):1143-7.
2001: Federica Di Palma; R Pellegrino; Konrad Noben-Trauth
Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).
Gene 2001;281(1-2):31-41.
2001: EC Bryda; H J Kim; Marie E Legare; Wayne N Frankel; Konrad Noben-Trauth
High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v).
Genomics 2001;73(3):338-42.
2001: Lorraine A Everett; Inna A Belyantseva; Konrad Noben-Trauth; Raquel Cantos; Amy Chen; S I Thakkar; Shelley Hoogstraten-Miller; Anne E White-Olson; Doris K Wu; Eric Green
Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.
Human molecular genetics 2001;10(2):153-61.
2001: Federica Di Palma; Ralph H Holme; EC Bryda; Inna A Belyantseva; R Pellegrino; Anne E White-Olson; Karen P Steel; Konrad Noben-Trauth
Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.
Nature genetics 2001;27(1):103-7.
2000: T Friedman; James F Battey; Anne E White-Olson; Sheikh Amer Riazuddin; Konrad Noben-Trauth; Andrew J Griffith; Edward R Wilcox
Modifier genes of hereditary hearing loss.
Current opinion in neurobiology 2000;10(4):487-93.
1999: Margit Burmeister; EC Bryda; J F Bureau; Konrad Noben-Trauth
Mouse chromosome 10.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(10):950-1.
1998: H J Kim; Konrad Noben-Trauth; Robert J Morell
Tectorin-beta (Tectb) maps to mouse chromosome 19.
Genomics 1998;53(3):419-20.
1998: A Wang; Y Liang; RA Fridell; Frank J Probst; Edward R Wilcox; JW Touchman; C C Morton; Robert J Morell; Konrad Noben-Trauth; Sally A Camper; Thomas B Friedman
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.
Science (New York, N.Y.) 1998;280(5368):1447-51.
1998: Frank J Probst; RA Fridell; Yehoash Raphael; Thomas L Saunders; A Wang; Y Liang; Robert J Morell; JW Touchman; Robert H Lyons Jr; Konrad Noben-Trauth; Thomas B Friedman; Sally A Camper
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.
Science (New York, N.Y.) 1998;280(5368):1444-7.
1998: Margit Burmeister; EC Bryda; J F Bureau; Konrad Noben-Trauth
Encyclopedia of the mouse genome VII. Mouse chromosome 10.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;8 Spec No():S200-14.
1997: Konrad Noben-Trauth; Qing Yin Zheng; K R Johnson; Patsy M Nishina
mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw).
Genomics 1997;44(3):266-72.
1997: Konrad Noben-Trauth; Jürgen K Naggert; Patsy M Nishina
Cloning and expression analysis of mouse Cclp1, a new gene encoding a coiled-coil-like protein.
Biochimica et biophysica acta 1997;1352(2):133-7.
1997: M A North; Jürgen K Naggert; Y Yan; Konrad Noben-Trauth; Patsy M Nishina
Molecular characterization of TUB, TULP1, and TULP2, members of the novel tubby gene family and their possible relation to ocular diseases.
Proceedings of the National Academy of Sciences of the United States of America 1997;94(7):3128-33.
1996: Konrad Noben-Trauth; N G Copeland; D J Gilbert; N A Jenkins; G Sonoda; J R Testa; Karl-Heinz Klempnauer
Mybl2 (Bmyb) maps to mouse chromosome 2 and human chromosome 20q 13.1.
Genomics 1996;35(3):610-2.
1996: Konrad Noben-Trauth; Jürgen K Naggert; Patsy M Nishina
The ets-related mouse Pea3 gene maps to distal chromosome 11.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(7):551.
1996: J Sitzmann; Konrad Noben-Trauth; H Kamano; Karl-Heinz Klempnauer
Expression of B-Myb during mouse embryogenesis.
Oncogene 1996;12(9):1889-94.
1996: Konrad Noben-Trauth; Jürgen K Naggert; M A North; Patsy M Nishina
A candidate gene for the mouse mutation tubby.
Nature 1996;380(6574):534-8.
1995: H Kamano; B Burk; Konrad Noben-Trauth; Karl-Heinz Klempnauer
Differential splicing of the mouse B-myb gene.
Oncogene 1995;11(12):2575-82.
1995: J Sitzmann; Konrad Noben-Trauth; Karl-Heinz Klempnauer
Expression of mouse c-myb during embryonic development.
Oncogene 1995;11(11):2273-9.