Αποτελέσματα αναζήτησης - Konrad Noben‐Trauth
- Εμφανίζονται 1 - 7 Αποτελέσματα από 7
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TRPML3 mutations cause impaired mechano‐electrical transduction and depolarization by an inward‐rectifier cation current in auditory hair cells of varitint‐waddler mice από 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
Έκδοση 2008Artigo -
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Association of Unconventional Myosin <i>MYO15</i> Mutations with Human Nonsyndromic Deafness <i>DFNB3</i> από Aihui Wang, Yong Liang, Robert A. Fridell, Frank J. Probst, Edward R. Wilcox, Jeffrey W. Touchman, Cynthia C. Morton, Robert J. Morell, Konrad Noben‐Trauth, Sally A. Camper, Thomas B. Friedman
Έκδοση 1998Artigo -
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Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human από Nikoletta Charizopoulou, Andrea Lelli, Margit Schraders, Kausik K. Ray, Michael S. Hildebrand, Arabandi Ramesh, C. R. Srikumari Srisailapathy, Jaap Oostrik, R.J.C. Admiraal, Harold R. Neely, Joseph R. Latoche, Richard J. Smith, John K. Northup, Hannie Kremer, Jeffrey R. Holt, Konrad Noben‐Trauth
Έκδοση 2011Artigo
Εργαλεία αναζήτησης:
Σχετικά θέματα
Biology
Gene
Genetics
Mutation
Audiology
Cochlea
Hair cell
Hearing loss
Medicine
Missense mutation
Mutant
Stereocilia (inner ear)
Allele
Anatomy
Cell biology
Chromosome
Exon
Inner ear
Locus (genetics)
Phenotype
Biochemistry
Biophysics
Candidate gene
Centimorgan
Chemistry
Congenic
Conserved sequence
Depolarization
Endocochlear potential
Frameshift mutation