검색결과 : 12건
| No. | Article |
|---|---|
| 1 |
Nitrogen, sulfur co-doped hierarchically porous carbon from rape pollen as high-performance supercapacitor electrode Wan L, Wei W, Xie MJ, Zhang Y, Li X, Xiao R, Che J, Du C Electrochimica Acta, 311, 72, 2019 |
| 2 |
Knockdown of poc1b causes abnormal photoreceptor sensory cilium and vision impairment in zebrafish Zhang CH, Zhang Q, Wang F, Liu Q Biochemical and Biophysical Research Communications, 465(4), 651, 2015 |
| 3 |
Cataract-linked mutation RI 88H promotes beta B2-crystallin aggregation and fibrillization during acid denaturation Xi YB, Zhang K, Dai AB, Ji SR, Yao K, Yan YB Biochemical and Biophysical Research Communications, 447(2), 244, 2014 |
| 4 |
A new Na(v)1.7 mutation in an erythromelalgia patient Estacion M, Yang Y, Dib-Hajj SD, Tyrrell L, Lin ZM, Yang Y, Waxman SG Biochemical and Biophysical Research Communications, 432(1), 99, 2013 |
| 5 |
Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T > C mutation Ronchi D, Bordoni A, Cosi A, Rizzuti M, Fassone E, Di Fonzo A, Servida M, Sciacco M, Collotta M, Ronzoni M, Lucchini V, Mattioli M, Moggio M, Bresolin N, Corti S, Comi GP Biochemical and Biophysical Research Communications, 412(2), 245, 2011 |
| 6 |
Maternally inherited hypertension is associated with the mitochondrial tRNA(Ile) A4295G mutation in a Chinese family Li ZB, Liu Y, Yang L, Wang SW, Guan MX Biochemical and Biophysical Research Communications, 367(4), 906, 2008 |
| 7 |
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 |
| 8 |
Mitochondrial 12S rRNA A827G mutation is involved in the genetic susceptibility to aminoglycoside ototoxicity Xing GQ, Chen ZB, Wei QJ, Tian HQ, Li XL, Zhou AD, Bu XK, Cao X Biochemical and Biophysical Research Communications, 346(4), 1131, 2006 |
| 9 |
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 |
| 10 |
Drastic Ca2+ sensitization of myofilament associated with a small structural change in troponin I in inherited restrictive cardiomyopathy Yumoto F, Lu QW, Morimoto S, Tanaka H, Kono N, Nagata K, Qjima T, Takahashi-Yanaga F, Miwa Y, Sasaguri T, Nishita K, Tanokura M, Ohtsuki I Biochemical and Biophysical Research Communications, 338(3), 1519, 2005 |