4.6 Article

A Novel Mouse Model of MYO7A USH1B Reveals Auditory and Visual System Haploinsufficiencies

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Biotechnology & Applied Microbiology

Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and Macaque

K. Tyler McCullough et al.

HUMAN GENE THERAPY (2019)

Article Multidisciplinary Sciences

Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments

Alix Trouillet et al.

SCIENTIFIC REPORTS (2018)

Article Multidisciplinary Sciences

Molecular characterization and prospective isolation of human fetal cochlear hair cell progenitors

Marta Roccio et al.

NATURE COMMUNICATIONS (2018)

Article Biotechnology & Applied Microbiology

Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome

Kevin Isgrig et al.

MOLECULAR THERAPY (2017)

Article Multidisciplinary Sciences

Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G

Alice Emptoz et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2017)

Article Neurosciences

Effects of Long-Term Exercise on Age-Related Hearing Loss in Mice

Chul Han et al.

JOURNAL OF NEUROSCIENCE (2016)

Article Ophthalmology

Outer Retinal Changes Including the Ellipsoid Zone Band in Usher Syndrome 1B due to MYO7A Mutations

Alexander Sumaroka et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2016)

Article Otorhinolaryngology

Hearing decline in menopausal women - a 10-year follow-up

Johan Svedbrant et al.

ACTA OTO-LARYNGOLOGICA (2015)

Article Multidisciplinary Sciences

Three-dimensional organization of nascent rod outer segment disk membranes

Stefanie Volland et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)

Article Biotechnology & Applied Microbiology

Dual Adeno-Associated Virus Vectors Result in Efficient In Vitro and In Vivo Expression of an Oversized Gene, MYO7A

Frank M. Dyka et al.

HUMAN GENE THERAPY METHODS (2014)

Article Biochemistry & Molecular Biology

Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus

V. S. Lopes et al.

GENE THERAPY (2013)

Article Biochemistry & Molecular Biology

Molecular Characterization of Mutant Mouse Strains Generated from the EUCOMM/KOMP-CSD ES Cell Resource

Edward Ryder et al.

MAMMALIAN GENOME (2013)

Article Multidisciplinary Sciences

Myosin7a Deficiency Results in Reduced Retinal Activity Which Is Improved by Gene Therapy

Pasqualina Colella et al.

PLOS ONE (2013)

Article Biochemical Research Methods

Fiji: an open-source platform for biological-image analysis

Johannes Schindelin et al.

NATURE METHODS (2012)

Article Multidisciplinary Sciences

Inner Ear Morphology Is Perturbed in Two Novel Mouse Models of Recessive Deafness

Kerry A. Miller et al.

PLOS ONE (2012)

Article Multidisciplinary Sciences

A conditional knockout resource for the genome-wide study of mouse gene function

William C. Skarnes et al.

NATURE (2011)

Article Ophthalmology

Mislocalization and Degradation of Human P23H-Rhodopsin-GFP in a Knockin Mouse Model of Retinitis Pigmentosa

Brandee A. Price et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)

Article Ophthalmology

Retinal Disease Course in Usher Syndrome 1B Due to MYO7A Mutations

Samuel G. Jacobson et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)

Article Ophthalmology

Moderate Light-Induced Degeneration of Rod Photoreceptors with Delayed Transducin Translocation in shaker1 Mice

You-Wei Peng et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2011)

Review Cell Biology

Mitochondrial oxidative damage and apoptosis in age-related hearing loss

Shinichi Someya et al.

MECHANISMS OF AGEING AND DEVELOPMENT (2010)

Article Biochemistry & Molecular Biology

Novel Lipofuscin Bisretinoids Prominent in Human Retina and in a Model of Recessive Stargardt Disease

Yalin Wu et al.

JOURNAL OF BIOLOGICAL CHEMISTRY (2009)

Article Ophthalmology

Disease Boundaries in the Retina of Patients with Usher Syndrome Caused by MYO7A Gene Mutations

Samuel G. Jacobson et al.

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2009)

Article Biochemistry & Molecular Biology

Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism

Samuel G. Jacobson et al.

HUMAN MOLECULAR GENETICS (2008)

Article Medicine, General & Internal

Presbycusis

GA Gates et al.

LANCET (2005)

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 Multidisciplinary Sciences

Knock-in human rhodopsin-GFP fusions as mouse models for human disease and targets for gene therapy

F Chan et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)

Article Multidisciplinary Sciences

Abnormal phagocytosis by retinal pigmented epithelium that lacks myosin Vila, the Usher syndrome 1B protein

D Gibbs et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)

Article Genetics & Heredity

Genetic heterogeneity of Usher syndrome: Analysis of 151 families with Usher type I

LM Astuto et al.

AMERICAN JOURNAL OF HUMAN GENETICS (2000)

Article Ophthalmology

Evaluation of the myosin VIIA gene and visual function in patients with Usher syndrome type I

AK Bharadwaj et al.

EXPERIMENTAL EYE RESEARCH (2000)