4.8 Article

Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness

Related references

Note: Only part of the references are listed.
Article Multidisciplinary Sciences

Targeting nuclear RNA for in vivo correction of myotonic dystrophy

Thurman M. Wheeler et al.

NATURE (2012)

Review Cell Biology

Towards Gene Therapy for Deafness

Marina Di Domenico et al.

JOURNAL OF CELLULAR PHYSIOLOGY (2011)

Review Neurosciences

Regulated Reprogramming in the Regeneration of Sensory Receptor Cells

Olivia Bermingham-McDonogh et al.

NEURON (2011)

Review Multidisciplinary Sciences

Integrating the biophysical and molecular mechanisms of auditory hair cell mechanotransduction

Anthony W. Peng et al.

NATURE COMMUNICATIONS (2011)

Article Obstetrics & Gynecology

Fetal transfusion: the spectrum of clinical research in the past year

Rebecca A. Uhlmann et al.

CURRENT OPINION IN OBSTETRICS & GYNECOLOGY (2010)

Article Developmental Biology

Deafness and Retinal Degeneration in a Novel USH1C Knock-In Mouse Model

Jennifer J. Lentz et al.

DEVELOPMENTAL NEUROBIOLOGY (2010)

Article Biochemical Research Methods

A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment

Rachel E. Hardisty-Hughes et al.

NATURE PROTOCOLS (2010)

Review Genetics & Heredity

Hearing Loss: Mechanisms Revealed by Genetics and Cell Biology

Amiel A. Dror et al.

ANNUAL REVIEW OF GENETICS (2009)

Review Neurosciences

Linking genes underlying deafness to hair-bundle development and function

Christine Petit et al.

NATURE NEUROSCIENCE (2009)

Article Cell Biology

Tetracyclines That Promote SMN2 Exon 7 Splicing as Therapeutics for Spinal Muscular Atrophy

Michelle L. Hastings et al.

SCIENCE TRANSLATIONAL MEDICINE (2009)

Article Biotechnology & Applied Microbiology

Ush1c216A knock-in mouse survives Katrina

Jennifer Lentz et al.

MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS (2007)

Review Medicine, General & Internal

Current concepts: Newborn hearing screening - A silent revolution

CC Morton et al.

NEW ENGLAND JOURNAL OF MEDICINE (2006)

Article Audiology & Speech-Language Pathology

A physiological place-frequency map of the cochlea in the CBA/J mouse

M Müller et al.

HEARING RESEARCH (2005)

Article Genetics & Heredity

The USH1C 216G→A splice-site mutation results in a 35-base-pair deletion

J Lentz et al.

HUMAN GENETICS (2005)