검색결과 : 7건
| No. | Article |
|---|---|
| 1 |
Blood microRNAs in Low or No Risk Ischemic Stroke Patients Tan JR, Tan KS, Koo YX, Yong FL, Wang CW, Armugam A, Jeyaseelan K International Journal of Molecular Sciences, 14(1), 2072, 2013 |
| 2 |
Association of functional microsatellites in the human type I collagen alpha 2 chain (COL1A2) gene with systemic sclerosis Hata RI, Akai J, Kimura A, Ishikawa O, Kuwana M, Shinkai H Biochemical and Biophysical Research Communications, 272(1), 36, 2000 |
| 3 |
A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects Yamagishi H, Garg V, Matsuoka R, Thomas T, Srivastava D Science, 283(5405), 1158, 1999 |
| 4 |
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N Nature, 392(6676), 605, 1998 |
| 5 |
The Duesberg-Phenomenon - Duesberg and Other Voices Duesberg PH Science, 267(5196), 313, 1995 |
| 6 |
Reading-Disability, Attention-Deficit Hyperactivity Disorder, and the Immune-System - Response Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, Defries JC Science, 268(5212), 787, 1995 |
| 7 |
Quantitative Trait Locus for Reading-Disability on Chromosome-6 Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, Defries JC Science, 266(5183), 276, 1994 |