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Nature Genetics, ISSN 1061-4036, 09/2000, Volume 26, Issue 1, pp. 56 - 60
Journal Article
Human Genetics, ISSN 0340-6717, 3/2005, Volume 116, Issue 4, pp. 292 - 299
Usher syndrome type I (USH1), the most severe form of this syndrome, is characterized by profound congenital sensorineural deafness, vestibular dysfunction,... 
LifeSciences | HETEROGENEITY | HAPLOTYPE ANALYSIS | PROTEIN | SYNDROME TYPE 1D | FAMILIES | GENETICS & HEREDITY | CDH23 | USH1C | MYOSIN VIIA GENE | RECESSIVE DEAFNESS | ALLELIC MUTATIONS | Carrier Proteins - genetics | Adaptor Proteins, Signal Transducing | Humans | Mutation | Abnormalities, Multiple - genetics | Syndrome | Cohort Studies | Index Medicus
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2013, Volume 8, Issue 11, pp. e79791 - e79791
Atoh1 is a transcription factor that regulates neural development in multiple tissues and is conserved among species. Prior mouse models of Atoh1, though... 
MATH1 | MULTIDISCIPLINARY SCIENCES | COCHLEAR HAIR-CELLS | IN-VIVO | MOUSE | USH1C GENE | NEURONS | GENERATION | DIFFERENTIATION | EXPRESSION | REQUIREMENT | Amino Acid Sequence | Hearing Loss - diagnosis | Basic Helix-Loop-Helix Transcription Factors - genetics | Cerebellum - metabolism | RNA, Messenger - genetics | Gene Expression Regulation | Hair Cells, Auditory, Inner - ultrastructure | Chromosome Mapping | Hearing Loss - pathology | Longevity - genetics | RNA, Messenger - metabolism | Cerebellum - pathology | Hair Cells, Auditory, Inner - pathology | Hearing Loss - genetics | Ear, Inner - metabolism | Phenotype | Sequence Alignment | Animals | Aging - genetics | DNA Mutational Analysis | Mice | Mutation | Hearing Tests | Basic Helix-Loop-Helix Transcription Factors - chemistry | Brain | Wildlife conservation | Gene mutations | Genetic research | Evolution | Genetic aspects | Cerebellum | Neurosciences | Animal models | Transcription factors | Gait | Laboratories | Brain stem | Central nervous system | Otolaryngology | Lethality | Biochemistry | Tissues | Neurogenesis | Inner ear | Atrophy | Genotype & phenotype | Rodents | Aging | Hair | Phenotypes | Abnormalities | Histology | Hearing impairment | Gene expression | Hearing loss | Hearing | Otology | Life span | Point mutation | Ear | Ears & hearing | Fecundity | Cancer | Index Medicus
Journal Article
Journal Article
Nature Genetics, ISSN 1061-4036, 09/2000, Volume 26, Issue 1, pp. 51 - 55
Journal Article
Journal Article
PLOS ONE, ISSN 1932-6203, 12/2016, Volume 11, Issue 12
Otitis media (OM), inflammation of the middle ear, is a common cause of hearing loss in children and in patients with many different syndromic diseases.... 
OSTEOMALACIA | MULTIDISCIPLINARY SCIENCES | VASCULAR CALCIFICATION | MUTATION | DISEASE | USH1C GENE | MIDDLE-EAR | DEAFNESS | GENERALIZED ARTERIAL CALCIFICATION | KNOCKOUT MOUSE | INFANCY
Journal Article