Zobrazeno 1 - 9
of 9
pro vyhledávání: '"K B, Avraham"'
Autor:
D. B. Chen, K. B. Avraham, Elizabeth L. Wagner, Y. Noy, George T. Hashisaki, D. W. Archer, Sihan Li, Jung-Bum Shin, J.-S. Im, T. E. Imbery, W. Xu, M. I. Nakahata
Prolonged exposure to loud noise has been shown to affect inner ear sensory hair cells in a variety of deleterious manners, including damaging the stereocilia core. The damaged sites can be visualized as “gaps” in phalloidin staining of F-actin,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::469927e322587fe5e62e316fc8c170e5
https://doi.org/10.1101/2021.08.10.455815
https://doi.org/10.1101/2021.08.10.455815
Autor:
K B, Avraham
Publikováno v:
Ernst Schering Research Foundation workshop. (36)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9e181eca5fd5d899af535091433f8819
https://pubmed.ncbi.nlm.nih.gov/11859565
https://pubmed.ncbi.nlm.nih.gov/11859565
Autor:
K B, Avraham
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 158
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d13feacccac5da10d5200fde85e9ffc0
https://pubmed.ncbi.nlm.nih.gov/11236668
https://pubmed.ncbi.nlm.nih.gov/11236668
Autor:
A E, Kiernan, M, Zalzman, H, Fuchs, M, Hrabe de Angelis, R, Balling, K P, Steel, K B, Avraham
Publikováno v:
Journal of neurocytology. 28(10-11)
We have undertaken a phenotypic approach in the mouse to identifying molecules involved in inner ear function by N-ethyl-N-nitrosourea mutagenesis followed by screening for new dominant mutations affecting hearing or balance. The pathology and geneti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5dcc8521ec23e2b522d8d0665f62308
https://pubmed.ncbi.nlm.nih.gov/10900098
https://pubmed.ncbi.nlm.nih.gov/10900098
Autor:
K B, Avraham
Publikováno v:
Advances in oto-rhino-laryngology. 56
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4af03ca7db92184417e6f1cb56099a1c
https://pubmed.ncbi.nlm.nih.gov/10868222
https://pubmed.ncbi.nlm.nih.gov/10868222
Publikováno v:
American journal of medical genetics. 89(3)
Mutations of the unconventional myosins genes encoding myosin VI, myosin VIIA and myosin XV cause hearing loss and thus these motor proteins perform fundamental functions in the auditory system. A null mutation in myosin VI in the congenitally deaf S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7729d004a3613dd703f05ad03e091632
https://pubmed.ncbi.nlm.nih.gov/10704189
https://pubmed.ncbi.nlm.nih.gov/10704189
Autor:
T, Sobe, P, Erlich, A, Berry, M, Korostichevsky, S, Vreugde, K B, Avraham, B, Bonné-Tamir, M, Shohat
Publikováno v:
American journal of medical genetics. 86(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7ddb30214bbe1817f43bbc98166b338
https://pubmed.ncbi.nlm.nih.gov/10508996
https://pubmed.ncbi.nlm.nih.gov/10508996
Publikováno v:
Progress in clinical and biological research. 360
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::29a9c7666f8d233de35bb102aa37122f
https://pubmed.ncbi.nlm.nih.gov/2147288
https://pubmed.ncbi.nlm.nih.gov/2147288
Autor:
K B Avraham, Santhosh Girirajan, Rajeev Jalvi, Anuranjan Anand, H M Ravi Shankar, R. Rangasayee, O Dagan, M. RamShankar
Publikováno v:
Scopus-Elsevier
Congenital hearing loss has been documented to occur in 1 of 1000 live births, with over half of these cases predicted to be hereditary in nature.1,2 Most hereditary hearing loss is inherited in a recessive manner, accounting for approximately 85% of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32eb41bc91a871a6f09f91816f04cba0
https://doi.org/10.1136/jmg.40.5.e68
https://doi.org/10.1136/jmg.40.5.e68