검색결과 : 6건
| No. | Article |
|---|---|
| 1 |
A novel frameshift variant of COCH supports the hypothesis that haploinsufficiency is not a cause of autosomal dominant nonsyndromic deafness 9 Masuda M, Mutai H, Arimoto Y, Nakano A, Matsunaga T Biochemical and Biophysical Research Communications, 469(2), 270, 2016 |
| 2 |
A novel frameshift mutation in KCNQ4 in a family with autosomal recessive non-syndromic hearing loss Wasano K, Mutai H, Obuchi C, Masuda S, Matsunaga T Biochemical and Biophysical Research Communications, 463(4), 582, 2015 |
| 3 |
A mutation in the heparin-binding site of noggin as a novel mechanism of proximal symphalangism and conductive hearing loss Masuda S, Namba K, Mutai H, Usui S, Miyanaga Y, Kaneko H, Matsunaga T Biochemical and Biophysical Research Communications, 447(3), 496, 2014 |
| 4 |
Moderate hearing loss associated with a novel KCNQ4 non-truncating mutation located near the N-terminus of the pore helix Watabe T, Matsunaga T, Namba K, Mutai H, Inoue Y, Ogawa K Biochemical and Biophysical Research Communications, 432(3), 475, 2013 |
| 5 |
PAL31, a nuclear protein required for progression to the S phase Sun WY, Hattori N, Mutai H, Toyoshima Y, Kimura H, Tanaka S, Shiota K Biochemical and Biophysical Research Communications, 280(4), 1048, 2001 |
| 6 |
PAL31, a novel nuclear protein, expressed in the developing brain Mutai H, Toyoshima Y, Sun WY, Hattori N, Tanaka S, Shiota K Biochemical and Biophysical Research Communications, 274(2), 427, 2000 |