馬偕醫學大學機構典藏(MacKay Medical University Institutional Repository):Browse by Title
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Showing items 661-670 of 1799. (180 Page(s) Totally)
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DateTitleAuthors
2013-05-01 Hypofunction of Glutamatergic Neurotransmission in the Periaqueductal Gray Contributes to Nerve-Injury-Induced Neuropathic Pain Yu-Cheng Ho; Jen-Kun Cheng; Lih-Chu Chiou
2007-10-01 Hypoplasia of the Cochlear Nerve in the Internal Auditory Canal Min-Tsan Shu; Hung-Ching Lin; Yu-Chun Chen; Jon-Kway Huang
2012-06-01 Hypothermia caused by slow and limited-volume fluid resuscitation decreases organ damage by hemorrhagic shock Yi-Maun Subeq; Bang-Gee Hsu; Nien-Tsung Lin; Fwu-Lin Yang; Yann-Fen C. Chao; Tai-Chu Peng; Ru-Ping Lee; Chia-Hua Kuo
2012-06-01 Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II Chih-Ping Chen; Yi-Ning Su; Fang-Yu Hung; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
2012-06-01 Identification of a deletion mutation in the short flanking repeat region of exon 44 of COL1A1 gene in a fetus with osteogenesis imperfecta type II Chih-Ping Chen; Yi-Ning Su; Tung-Yao Chang; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
2012-09-01 Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Schu-Rern Chern; Jun-Wei Su; Wayseen Wang
2005-05-01 Identification of an essential cleavage site in ColE7 required for import and killing of cells. Zhonghao Shi; Kin-Fu Chak; Hanna S. Yuan
2008-09-01 Identification of Chemical Inhibitors to Human Tissue Transglutaminase. Thung S Lai; Yusha Liu; T Tucker; K Daniel; DC. Sane; E Toone; JR. Burke; WJ. Strittmatter; CS. Greenberg
2009-09-01 Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR Chia-Cheng Hung; Shin-Yu Lin; Shuan-Pei Lin,; Dou-Ming Niu; Ni-Chung Lee; Wen-Fang Cheng; Chih-Ping Chen; Win-Li Lin; Chien-Nan Lee; Yi-Ning Su
1998-03-01 Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese H.-H. Lee; Hsiang-Tai Chao; Yann-Jinn Lee; San-Ging Shu; Mei-Chyn Chao; Jing-Mei Kuo; Bun-chu Chung
Showing items 661-670 of 1799. (180 Page(s) Totally)
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