Literature DB >> 35960848

Emerging complexities of the mouse as a model for human hearing loss.

Ryan J Carlson1,2, Karen B Avraham3.   

Abstract

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Year:  2022        PMID： 35960848      PMCID： PMC9436342          DOI： 10.1073/pnas.2211351119

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN： 0027-8424            Impact factor:   12.779


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  24 in total

1.  Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.

Authors:  D P Kelsell; J Dunlop; H P Stevens; N J Lench; J N Liang; G Parry; R F Mueller; I M Leigh
Journal:  Nature       Date:  1997-05-01       Impact factor: 49.962

2.  Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

Authors:  A Wang; Y Liang; R A Fridell; F J Probst; E R Wilcox; J W Touchman; C C Morton; R J Morell; K Noben-Trauth; S A Camper; T B Friedman
Journal:  Science       Date:  1998-05-29       Impact factor: 47.728

3.  Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

Authors:  Sarah Vreugde; Alexandra Erven; Corné J Kros; Walter Marcotti; Helmut Fuchs; Kiyoto Kurima; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith; Rudi Balling; Martin Hrabé De Angelis; Karen B Avraham; Karen P Steel
Journal:  Nat Genet       Date:  2002-02-19       Impact factor: 38.330

Review 4.  Hearing loss: mechanisms revealed by genetics and cell biology.

Authors:  Amiel A Dror; Karen B Avraham
Journal:  Annu Rev Genet       Date:  2009       Impact factor: 16.830

5.  The LINC complex is essential for hearing.

Authors:  Henning F Horn; Zippora Brownstein; Danielle R Lenz; Shaked Shivatzki; Amiel A Dror; Orit Dagan-Rosenfeld; Lilach M Friedman; Kyle J Roux; Serguei Kozlov; Kuan-Teh Jeang; Moshe Frydman; Brian Burke; Colin L Stewart; Karen B Avraham
Journal:  J Clin Invest       Date:  2013-01-25       Impact factor: 14.808

6.  The nature of inherited deafness in deafness mice.

Authors:  K P Steel; G R Bock
Journal:  Nature       Date:  1980-11-13       Impact factor: 49.962

7.  Impairment of Vision in a Mouse Model of Usher Syndrome Type III.

Authors:  Guilian Tian; Richard Lee; Philip Ropelewski; Yoshikazu Imanishi
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-03       Impact factor: 4.799

8.  Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice.

Authors:  H D Gabriel; D Jung; C Bützler; A Temme; O Traub; E Winterhager; K Willecke
Journal:  J Cell Biol       Date:  1998-03-23       Impact factor: 10.539

9.  Allele-specific gene editing prevents deafness in a model of dominant progressive hearing loss.

Authors:  Bence György; Carl Nist-Lund; Bifeng Pan; Yukako Asai; K Domenica Karavitaki; Benjamin P Kleinstiver; Sara P Garcia; Mikołaj P Zaborowski; Paola Solanes; Sofia Spataro; Bernard L Schneider; J Keith Joung; Gwenaëlle S G Géléoc; Jeffrey R Holt; David P Corey
Journal:  Nat Med       Date:  2019-07-03       Impact factor: 53.440

10.  Mouse Models of Human Pathogenic Variants of TBC1D24 Associated with Non-Syndromic Deafness DFNB86 and DFNA65 and Syndromes Involving Deafness.

Authors:  Risa Tona; Ivan A Lopez; Cristina Fenollar-Ferrer; Rabia Faridi; Claudio Anselmi; Asma A Khan; Mohsin Shahzad; Robert J Morell; Shoujun Gu; Michael Hoa; Lijin Dong; Akira Ishiyama; Inna A Belyantseva; Sheikh Riazuddin; Thomas B Friedman
Journal:  Genes (Basel)       Date:  2020-09-24       Impact factor: 4.096
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