화학공학소재연구정보센터
검색결과 : 6건
No. Article
1 Mutation of a gene encoding a protein with extracellular matrix motifs in usher syndrome type IIa
Eudy JD, Weston MD, Yao SF, Hoover DM, Rehm HL, Ma-Edmonds M, Yan D, Ahmad I, Cheng JJ, Ayuso C, Cremers C, Davenport S, Moller C, Talmadge CB, Beisel KW, Tamayo M, Morton CC, Swaroop A, Kimberling WJ, Sumegi J
Science, 280(5370), 1753, 1998
2 Pkd2, a Gene for Polycystic Kidney-Disease That Encodes an Integral Membrane-Protein
Mochizuki T, Wu GQ, Hayashi T, Xenophontos SL, Veldhuisen B, Saris JJ, Reynolds DM, Cai YQ, Gabow PA, Pierides A, Kimberling WJ, Breuning MH, Deltas CC, Peters DJ, Somlo S
Science, 272(5266), 1339, 1996
3 Defective Myosin VIIa Gene Responsible for Usher Syndrome Type 1B
Well D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levillers J, Weston MD, Kelley PM, Kimberling WJ, Wagenaar M, Leviacobas F, Largetpiet D, Munnich A, Steel KP, Brown SD, Petit C
Nature, 374(6517), 60, 1995
4 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
5 Quantitative Trait Locus for Reading-Disability (Vol 266, Pg 276, 1994)
Cardon LR, Smith SD, Fulker DW, Kimberling WJ, Pennington BF, Defries JC
Science, 268(5217), 1553, 1995
6 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