Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by N Overlack
Gene-Based Treatment Options for Usher Type 1C by Translational Read-Through of a Nonsense Mutation
Cilia
Cell Biology
The Usher Syndrome 1G Protein SANS Participates in the Transport of Ciliary Cargo in Photoreceptor Cells
Cilia
Cell Biology
Related publications
Gene Repair of an Usher Syndrome Causing Mutation by Zinc-Finger Nuclease Mediated Homologous Recombination
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Neurofilament Deficiency in Quail Caused by Nonsense Mutation in Neurofilament-L Gene
Journal of Cell Biology
Medicine
Cell Biology
Nonsense Mutation of Islet-1 Gene (Q310X) Found in a Type 2 Diabetic Patient With a Strong Family History
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
Identification of a Nonsense Mutation in the PAX9 Gene in Molar Oligodontia
European Journal of Human Genetics
Genetics
Lentiviral Gene Replacement Therapy of Retinas in a Mouse Model for Usher Syndrome Type 1B
Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Profound, Prelingual Nonsyndromic Deafness Maps to Chromosome 10q21 and Is Caused by a Novel Missense Mutation in the Usher Syndrome Type IF Gene PCDH15
European Journal of Human Genetics
Genetics
Read-Through Strategies for Suppression of Nonsense Mutations in Duchenne/ Becker Muscular Dystrophy: Aminoglycosides and Ataluren (PTC124)
Journal of Child Neurology
Child Health
Neurology
Pediatrics
Perinatology
A Nonsense Mutation in a Cinnamyl Alcohol Dehydrogenase Gene Is Responsible for the Sorghum Brown Midrib6 Phenotype
Plant Physiology
Plant Science
Genetics
Physiology
Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.
Journal of Medical Genetics
Genetics
