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1

Single nucleotide polymorphisms in the cadherin 23 (CDH23) gene in Polish workers exposed to industrial noise

Mariola Sliwinska-Kowalska, Konrad Noben-Trauth, Malgorzata Pawelczyk, Tomasz Jarema Kowalski

Journal:

American Journal of Human Biology

Year:

2008

Language:

english

File:

PDF, 66 KB

english, 2008

2

Balanced levels of Espin are critical for stereociliary growth and length maintenance

Agnieszka Rzadzinska, Mark Schneider, Konrad Noben-Trauth, James R. Bartles, Bechara Kachar

Journal:

Year:

2005

Language:

english

File:

PDF, 468 KB

english, 2005

3

Enhancement of β-Adrenergic-induced cAMP accumulation in activated T-Cells

Dr. Sonia L. Carlson, Konrad Trauth, William H. Brooks, Thomas L. Roszman

Journal:

Journal of Cellular Physiology

Year:

1994

Language:

english

File:

PDF, 1011 KB

english, 1994

4

Mouse chromosome 10

Margit Burmeister, Elizabeth C. Bryda, Jean-François Bureau, Konrad Noben-Trauth

Journal:

Mammalian Genome

Year:

1998

Language:

english

File:

PDF, 970 KB

english, 1998

5

Mouse Chromosome 10

Margit Burmeister, Elizabeth C. Bryda, Jean-Francois Bureau, Konrad Noben-Trauth

Journal:

Mammalian Genome

Year:

1999

Language:

english

File:

PDF, 21 KB

english, 1999

6

Cellular and molecular function of mucolipins (TRPML) and polycystin 2 (TRPP2)

Feng Qian, Konrad Noben-Trauth

Journal:

Pflügers Archiv European Journal of Physiology

Year:

2005

Language:

english

File:

PDF, 347 KB

english, 2005

7

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

Hung J. Kim, Torrance Jackson, Konrad Noben–Trauth

Journal:

Journal of the Association for Research in Otolaryngology

Year:

2003

Language:

english

File:

PDF, 227 KB

english, 2003

8

High-Frequency Sensorineural Hearing Loss and Its Underlying Genetics (Hfhl1andHfhl2) in NIH Swiss Mice

James M. Keller, Harold R. Neely, Joseph R. Latoche, Konrad Noben-Trauth

Journal:

Journal of the Association for Research in Otolaryngology

Year:

2011

Language:

english

File:

PDF, 977 KB

english, 2011

9

Loss of GLUR2 α-amino-3-hydroxy-5-methyl-4-isoxazoleproprionic acid receptor subunit differentially affects remaining synaptic glutamate receptors in cerebellum and cochlear nuclei

Ronald S. Petralia, Nathalie Sans, Ya-Xian Wang, Bryce Vissel, Kai Chang, Konrad Noben-Trauth, Stephen F. Heinemann, Robert J. Wenthold

Journal:

European Journal of Neuroscience

Year:

2004

Language:

english

File:

PDF, 698 KB

english, 2004

10

10.1038/1284

Tempel, Bruce L., Street, Valerie A., McKee-Johnson, Jennifer W., Fonseca, Rosalia C., Noben-Trauth, Konrad

Journal:

Nature Genetics

Year:

1998

Language:

english

File:

PDF, 321 KB

english, 1998

11

A candidate gene for the mouse mutation tubby

Noben-Trauth, Konrad, Naggert, Juergen K., North, Michael A., Nishina, Patsy M.

Journal:

Year:

1996

File:

PDF, 1.32 MB

1996

12

10.1038/83660

Noben-Trauth, Konrad, Palma, Federica Di, Holme, Ralph H., Bryda, Elizabeth C., Belyantseva, Inna A., Pellegrino, Richard, Kachar, Bechara, Steel, Karen P.

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 783 KB

english, 2001

13

Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss

Noben-Trauth, Konrad, Zheng, Qing Yin, Johnson, Kenneth R

Journal:

Nature Genetics

Year:

2003

Language:

english

File:

PDF, 544 KB

english, 2003

14

10.1038/ng710

Parkinson, Nicholas J., Olsson, Christine L., Hallows, Janice L., McKee-Johnson, Jennifer, Keogh, Bart P., Noben-Trauth, Konrad, Kujawa, Sharon G., Tempel, Bruce L

Journal:

Nature Genetics

Year:

2001

Language:

english

File:

PDF, 2.01 MB

english, 2001

15

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

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

Journal:

The Journal of Physiology

Year:

2008

Language:

english

File:

PDF, 1.08 MB

english, 2008

16

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

Efrat Birk, Adi Har-Zahav, Chiara M. Manzini, Metsada Pasmanik-Chor, Liora Kornreich, Christopher A. Walsh, Konrad Noben-Trauth, Adi Albin, Amos J. Simon, Laurence Colleaux, Yair Morad, Limor Rainshte

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 972 KB

english, 2010

17

Strain background effects and genetic modifiers of hearing in mice

Kenneth R. Johnson, Qing Yin Zheng, Konrad Noben-Trauth

Journal:

Year:

2006

Language:

english

File:

PDF, 303 KB

english, 2006

18

Inheritance patterns of progressive hearing loss in laboratory strains of mice

Konrad Noben-Trauth, Kenneth R. Johnson

Journal:

Year:

2009

Language:

english

File:

PDF, 216 KB

english, 2009

19

Cloning and expression analysis of mouse Cclp1, a new gene encoding a coiled-coil-like protein

Konrad Noben-Trauth, Jürgen K. Naggert, Patsy M. Nishina

Journal:

Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression

Year:

1997

Language:

english

File:

PDF, 361 KB

english, 1997

20

Modifier genes of hereditary hearing loss

Thomas Friedman, James Battey, Bechara Kachar, Sheikh Riazuddin, Konrad Noben-Trauth, Andrew Griffith, Edward Wilcox

Journal:

Current Opinion in Neurobiology

Year:

2000

Language:

english

File:

PDF, 442 KB

english, 2000

21

Mybl2(Bmyb) Maps to Mouse Chromosome 2 and Human Chromosome 20q13.1

Konrad Noben-Trauth, Neal G. Copeland, Debra J. Gilbert, Nancy A. Jenkins, Gonosuke Sonoda, Joseph R. Testa, Karl-Heinz Klempnauer

Journal:

Year:

1996

Language:

english

File:

PDF, 136 KB

english, 1996

22

mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)

Konrad Noben-Trauth, Qing Yin Zheng, Kenneth R. Johnson, Patsy M. Nishina

Journal:

Year:

1997

Language:

english

File:

PDF, 145 KB

english, 1997

23

Dok1Encoding p62dokMaps to Mouse Chromosome 6 and Human Chromosome 2 in a Region of Translocation in Chronic Lymphocytic Leukemia

Keats Nelms, Andrew J. Snow, Konrad Noben-Trauth

Journal:

Year:

1998

Language:

english

File:

PDF, 61 KB

english, 1998

24

Tectorin-β (Tectb)Maps to Mouse Chromosome 19

Hung Jeff Kim, Konrad Noben-Trauth, Robert J. Morell

Journal:

Year:

1998

Language:

english

File:

PDF, 62 KB

english, 1998

25

High-Resolution Genetic and Physical Mapping of Modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v)

Elizabeth C. Bryda, Hung J. Kim, Marie E. Legare, Wayne N. Frankel, Konrad Noben-Trauth

Journal:

Year:

2001

Language:

english

File:

PDF, 204 KB

english, 2001

26

TRPML3 and hearing loss in the varitint-waddler mouse

Margaret Atiba-Davies, Konrad Noben-Trauth

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Year:

2007

Language:

english

File:

PDF, 624 KB

english, 2007

27

Sustained cadherin 23 expression in young and adult cochlea of normal and hearing-impaired mice

Agnieszka K. Rzadzinska, Adam Derr, Bechara Kachar, Konrad Noben-Trauth

Journal:

Hearing Research

Year:

2005

Language:

english

File:

PDF, 531 KB

english, 2005

28

Mapping quantitative trait loci for hearing loss in Black Swiss mice

Meghan Drayton, Konrad Noben-Trauth

Journal:

Hearing Research

Year:

2006

Language:

english

File:

PDF, 458 KB

english, 2006

29

Cochlear developmental defect and background-dependent hearing thresholds in the Jackson circler (jc) mutant mouse

Alfredo Calderon, Adam Derr, Barden B. Stagner, Kenneth R. Johnson, Glen Martin, Konrad Noben-Trauth

Journal:

Hearing Research

Year:

2006

Language:

english

File:

PDF, 1.13 MB

english, 2006

30

Normal hearing in α-galactosidase A-deficient mice, the mouse model for Fabry disease

Konrad Noben-Trauth, Harold Neely, Roscoe O. Brady

Journal:

Hearing Research

Year:

2007

Language:

english

File:

PDF, 456 KB

english, 2007

31

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

Joseph R. Latoche, Harold R. Neely, Konrad Noben-Trauth

Journal:

Hearing Research

Year:

2011

Language:

english

File:

PDF, 1.63 MB

english, 2011

32

Gene Expression Profile of the Mouse Organ of Corti at the Onset of Hearing

Celine Pompeia, Belen Hurle, Inna A. Belyantseva, Konrad Noben-Trauth, Kirk Beisel, James Gao, Patee Buchoff, Graeme Wistow, Bechara Kachar

Journal:

Year:

2004

Language:

english

File:

PDF, 344 KB

english, 2004

33

Genetic and physical maps of jerker (Espnje) on mouse chromosome 4

Torrance Jackson, James Thomas, Eric D Green, Konrad Noben-Trauth

Journal:

Biochemical and Biophysical Research Communications

Year:

2002

Language:

english

File:

PDF, 202 KB

english, 2002

34

Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23)

Federica Di Palma, Richard Pellegrino, Konrad Noben-Trauth

Journal:

Year:

2001

Language:

english

File:

PDF, 1.09 MB

english, 2001

35

A new spontaneous mutation in the mouse Ames waltzer gene, Pcdh15

Lori L. Hampton, Charles G. Wright, Kumar N. Alagramam, James F. Battey, Konrad Noben-Trauth

Journal:

Hearing Research

Year:

2003

Language:

english

File:

PDF, 634 KB

english, 2003

36

Genome-wide linkage analyses identifyHfhl1andHfhl3with frequency-specific effects on the hearing spectrum of NIH Swiss mice

James M Keller, Konrad Noben-Trauth

Journal:

Year:

2012

Language:

english

File:

PDF, 511 KB

english, 2012

37

Molecular Characterization of TUB, TULP1, and TULP2, Members of the Novel Tubby Gene Family and their Possible Relation to Ocular Diseases

Michael A. North, Juergen K. Naggert, Yingzhuo Yan, Konrad Noben-Trauth and Patsy M. Nishina

Journal:

Proceedings of the National Academy of Sciences

Year:

1997

Language:

english

File:

PDF, 1.70 MB

english, 1997