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Year Number of Results
1995 2
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Page 1
The TRPML3 channel: from gene to function.
Noben-Trauth K. Noben-Trauth K. Adv Exp Med Biol. 2011;704:229-37. doi: 10.1007/978-94-007-0265-3_13. Adv Exp Med Biol. 2011. PMID: 21290299 Review.
Modifier genes of hereditary hearing loss.
Friedman T, Battey J, Kachar B, Riazuddin S, Noben-Trauth K, Griffith A, Wilcox E. Friedman T, et al. Among authors: noben trauth k. Curr Opin Neurobiol. 2000 Aug;10(4):487-93. doi: 10.1016/s0959-4388(00)00120-3. Curr Opin Neurobiol. 2000. PMID: 10981618 Review.
TRPML3 and hearing loss in the varitint-waddler mouse.
Atiba-Davies M, Noben-Trauth K. Atiba-Davies M, et al. Among authors: noben trauth k. Biochim Biophys Acta. 2007 Aug;1772(8):1028-31. doi: 10.1016/j.bbadis.2007.01.007. Epub 2007 Jan 23. Biochim Biophys Acta. 2007. PMID: 17329082 Free article. Review.
Strain background effects and genetic modifiers of hearing in mice.
Johnson KR, Zheng QY, Noben-Trauth K. Johnson KR, et al. Among authors: noben trauth k. Brain Res. 2006 May 26;1091(1):79-88. doi: 10.1016/j.brainres.2006.02.021. Epub 2006 Mar 31. Brain Res. 2006. PMID: 16579977 Free PMC article. Review.
A candidate gene for the mouse mutation tubby.
Noben-Trauth K, Naggert JK, North MA, Nishina PM. Noben-Trauth K, et al. Nature. 1996 Apr 11;380(6574):534-8. doi: 10.1038/380534a0. Nature. 1996. PMID: 8606774
Mouse chromosome 10.
Burmeister M, Bryda EC, Bureau JF, Noben-Trauth K. Burmeister M, et al. Among authors: noben trauth k. Mamm Genome. 1999 Oct;10(10):950-1. doi: 10.1007/s003359901129. Mamm Genome. 1999. PMID: 10501952 Free article. No abstract available.
50 results