nucleotide in the 30 direction. cDNA analysis confirmed a p. chromosome 8q22.3 (NCBI 37/hg19) and contains 16 exons, which cysts, reduced or absent otoliths, malformed semicircular canals, insensitivities to sound stimulation, and abnormal swimming position despite the normal appearance of hair cells in the inner ear. Upon wild type human GRHL2 mRNA injection, the inner ear defects in the zebrafish were rescued, whereas injection with mutant human GRHL2 was unable to rescue otic defects [Han et al., 2011]. This suggests a conserved structure and function of GRHL2 in vertebrate inner ear development. s-Maximilians-4 Wuerzburg, Article first published online in Wiley Online Librar
The ear is essential to maintaining balance and hearing; both of which can be linked to one another ...
Contains fulltext : 155391.PDF (publisher's version ) (Open Access)Hereditary hear...
Recessive mutations at the mouse pirouette (pi) locus result in hearing loss and vestibular dysfunct...
Hearing loss is one of the most prevalent human birth defects. Genetic factors contribute to the pat...
AbstractZebrafish holds great potential as a model system for studying inner ear development because...
The inner ear is a complex organ containing sensory tissue, including hair cells, the development of...
Zebrafish has become an excellent model for studying the development and function of inner ear. We r...
Hearing loss is one of the most prevalent human birth defects. Genetic factors contribute to the pat...
Contains fulltext : 196393.pdf (publisher's version ) (Open Access)Hearing and bal...
In a large scale screen for genetic defects in zebrafish embryogenesis we identified mutations affec...
Hereditary hearing loss is characterized by a high degree of genetic heterogeneity. Here we presentO...
<div><p>Hearing loss is one of the most prevalent human birth defects. Genetic factors contribute to...
Approximately 1 in 500 infants are diagnosed with hearing loss, and about half of these cases can be...
9Age-related hearing loss (ARHL) is the most common sensory impairment in the elderly affecting mill...
(A) Regions of mouse chromosomes 5 and 18 that contain the Grxcr1 and Grxcr2, respectively, also con...
The ear is essential to maintaining balance and hearing; both of which can be linked to one another ...
Contains fulltext : 155391.PDF (publisher's version ) (Open Access)Hereditary hear...
Recessive mutations at the mouse pirouette (pi) locus result in hearing loss and vestibular dysfunct...
Hearing loss is one of the most prevalent human birth defects. Genetic factors contribute to the pat...
AbstractZebrafish holds great potential as a model system for studying inner ear development because...
The inner ear is a complex organ containing sensory tissue, including hair cells, the development of...
Zebrafish has become an excellent model for studying the development and function of inner ear. We r...
Hearing loss is one of the most prevalent human birth defects. Genetic factors contribute to the pat...
Contains fulltext : 196393.pdf (publisher's version ) (Open Access)Hearing and bal...
In a large scale screen for genetic defects in zebrafish embryogenesis we identified mutations affec...
Hereditary hearing loss is characterized by a high degree of genetic heterogeneity. Here we presentO...
<div><p>Hearing loss is one of the most prevalent human birth defects. Genetic factors contribute to...
Approximately 1 in 500 infants are diagnosed with hearing loss, and about half of these cases can be...
9Age-related hearing loss (ARHL) is the most common sensory impairment in the elderly affecting mill...
(A) Regions of mouse chromosomes 5 and 18 that contain the Grxcr1 and Grxcr2, respectively, also con...
The ear is essential to maintaining balance and hearing; both of which can be linked to one another ...
Contains fulltext : 155391.PDF (publisher's version ) (Open Access)Hereditary hear...
Recessive mutations at the mouse pirouette (pi) locus result in hearing loss and vestibular dysfunct...