Cargando…
Mutational Analysis of EYA1, SIX1 and SIX5 Genes and Strategies for Management of Hearing Loss in Patients with BOR/BO Syndrome
BACKGROUND: Branchio-oto-renal (BOR) or branchio-otic (BO) syndrome is one of the most common forms of autosomal dominant syndromic hearing loss. Mutations in EYA1, SIX1 and SIX5 genes have been associated with BOR syndrome. In this study, clinical and genetic analyses were performed in patients wit...
Autores principales: | Song, Mee Hyun, Kwon, Tae-Jun, Kim, Hui Ram, Jeon, Ju Hyun, Baek, Jeong-In, Lee, Won-Sang, Kim, Un-Kyung, Choi, Jae Young |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3696009/ https://www.ncbi.nlm.nih.gov/pubmed/23840632 http://dx.doi.org/10.1371/journal.pone.0067236 |
Ejemplares similares
-
Structure-Function Analyses of the Human SIX1–EYA2 Complex Reveal Insights into Metastasis and BOR Syndrome
por: Patrick, Aaron N, et al.
Publicado: (2013) -
BOR-Syndrome-Associated Eya1 Mutations Lead to Enhanced Proteasomal Degradation of Eya1 Protein
por: Musharraf, Amna, et al.
Publicado: (2014) -
Evaluation of the Contribution of the EYA4 and GRHL2 Genes in Korean Patients with Autosomal Dominant Non-Syndromic Hearing Loss
por: Kim, Ye-Ri, et al.
Publicado: (2015) -
Evolution of the Pax-Six-Eya-Dach network: the calcisponge case study
por: Fortunato, Sofia AV, et al.
Publicado: (2014) -
SIX1 Activates STAT3 Signaling to Promote the Proliferation of Thyroid Carcinoma via EYA1
por: Kong, Deguang, et al.
Publicado: (2019)