검색결과 : 7건
| No. | Article |
|---|---|
| 1 |
7,8,3'-Trihydroxyflavone, a potent small molecule TrkB receptor agonist, protects spiral ganglion neurons from degeneration both in vitro and in vivo Yu Q, Chang Q, Liu X, Gong SS, Ye KQ, Lin X Biochemical and Biophysical Research Communications, 422(3), 387, 2012 |
| 2 |
A South African family with the mitochondrial A1555G mutation on haplogroup L0d Human H, Lombard D, de Jong G, Bardien S Biochemical and Biophysical Research Communications, 382(2), 390, 2009 |
| 3 |
Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M Biochemical and Biophysical Research Communications, 385(3), 445, 2009 |
| 4 |
The digenic hypothesis unraveled: The GJB6 del(GJB6-D13S1830) mutation causes allele-specific loss of GJB2 expression in cis Rodriguez-Paris J, Schrijver I Biochemical and Biophysical Research Communications, 389(2), 354, 2009 |
| 5 |
The analysis of three markers flanking GJB2 gene suggests a single origin of the most common 35delG mutation in the Moroccan population Abidi O, Boulouiz R, Nahili H, Imken L, Rouba H, Chafik A, Barakat A Biochemical and Biophysical Research Communications, 377(3), 971, 2008 |
| 6 |
Maternally inherited non-syndromic hearing loss associated with mitochondrial 12S rRNA A827G mutation in a Chinese family Xing GQ, Chen ZB, Wei QJ, Tian HQ, Li XL, Zhou AD, Bu XK, Cao X Biochemical and Biophysical Research Communications, 344(4), 1253, 2006 |
| 7 |
Maternally inherited nonsyndromic hearing loss is associated with the T7511C mutation in the mitochondrial tRNA (Ser(UCN)) gene in a Japanese family Li RH, Ishikawa K, Deng JH, Heman-Ackah S, Tamagawa Y, Yang L, Bai YD, Ichimura K, Guan MX Biochemical and Biophysical Research Communications, 328(1), 32, 2005 |