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Literature DB >> 12417743

Varitint-waddler: a double whammy for hearing.

Karen P Steel¹.

Abstract

Mesh：

Substances：
Membrane Proteins

Year: 2002 PMID： 12417743 PMCID： PMC133623 DOI： 10.1073/pnas.232585699

Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN： 0027-8424 Impact factor: 11.205

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28 in total

Review 1. A genetic approach to understanding auditory function.

Authors: K P Steel; C J Kros
Journal: Nat Genet Date: 2001-02 Impact factor: 38.330

2. Two mechanisms for transducer adaptation in vertebrate hair cells.

Authors: J R Holt; D P Corey
Journal: Proc Natl Acad Sci U S A Date: 2000-10-24 Impact factor: 11.205

Review 3. Molecular basis of mechanosensory transduction.

Authors: P G Gillespie; R G Walker
Journal: Nature Date: 2001-09-13 Impact factor: 49.962

4. Regulation of endocytosis by CUP-5, the Caenorhabditis elegans mucolipin-1 homolog.

Authors: H Fares; I Greenwald
Journal: Nat Genet Date: 2001-05 Impact factor: 38.330

5. Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations.

Authors: C J Kros; W Marcotti; S M van Netten; T J Self; R T Libby; S D M Brown; G P Richardson; K P Steel
Journal: Nat Neurosci Date: 2002-01 Impact factor: 24.884

6. Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

Authors: A E Kiernan; M Zalzman; H Fuchs; M Hrabe de Angelis; R Balling; K P Steel; K B Avraham
Journal: J Neurocytol Date: 1999 Oct-Nov

7. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

Authors: F Di Palma; R H Holme; E C Bryda; I A Belyantseva; R Pellegrino; B Kachar; K P Steel; K Noben-Trauth
Journal: Nat Genet Date: 2001-01 Impact factor: 38.330

4. Congenital sensorineural deafness in Australian stumpy-tail cattle dogs is an autosomal recessive trait that maps to CFA10.

Authors: Susan Sommerlad; Allan F McRae; Brenda McDonald; Isobel Johnstone; Leigh Cuttell; Jennifer M Seddon; Caroline A O'Leary
Journal: PLoS One Date: 2010-10-12 Impact factor: 3.240

4 in total

Varitint-waddler: a double whammy for hearing.

Review 1. A genetic approach to understanding auditory function.

2. Two mechanisms for transducer adaptation in vertebrate hair cells.

Review 3. Molecular basis of mechanosensory transduction.

4. Regulation of endocytosis by CUP-5, the Caenorhabditis elegans mucolipin-1 homolog.

5. Reduced climbing and increased slipping adaptation in cochlear hair cells of mice with Myo7a mutations.

6. Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

7. Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

8. The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.

9. Identification of the gene causing mucolipidosis type IV.

10. Mucolipidosis type IV is caused by mutations in a gene encoding a novel transient receptor potential channel.

Review 1. TRP channels as candidates for hearing and balance abnormalities in vertebrates.

Review 2. Transient Receptor Potential Channels and Auditory Functions.

Review 3. The varitint-waddler mouse phenotypes and the TRPML3 ion channel mutation: cause and consequence.

4. Congenital sensorineural deafness in Australian stumpy-tail cattle dogs is an autosomal recessive trait that maps to CFA10.