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Introduction:
馬偕醫學院生物醫學研究所於民國101年成立並開始招生。
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Date
Title
Authors
2004-11-01
Nitroreductase: a Prodrug-activating enzyme for cancer gene therapy
Peter F Searle
;
Ming-Jen Chen
;
Longqin Hu
;
Paul R Race
;
Andrew L Lovering
;
Jane I Grove
;
Chris Guise
;
Mansooreh Jaberipour
;
Nicholas D James
;
Vivien Mautner
;
Lawrence S Young
;
David J Kerr
;
Andrew Mountain
;
Scott A White
;
Eva I Hyde
2009-01-01
Noonan syndrome caused by germline KRAS mutation in Taiwan: report of two patients and a review of the literature.
Lo FS
;
Lin JL
;
Kuo MT
;
Chiu PC
;
Shu SG
;
Chao MC
;
Lee YJ
;
Lin SP
2013-04-01
A Novel Endogenous Induction of ColE7 Expression in a csrA Mutant of Escherichia coli
Hao-Wei Chang
;
Guang-Sheng Lei
;
Tsung-Yeh Yang
;
Kin-Fu Chak
2007-01-01
A novel HLA-DRB1 allele, DRB1*0832, identified by sequence-based typing method.
Dang CW
;
Chu CC
;
Liu TY
;
Lin M
;
Lee YJ
2005-04-01
Novel missense mutations, GCC [Ala306]- > GTC [Val] and ACG [Thr318]- > CCG [Pro], in the CYP11B1 gene cause steroid 11beta-hydroxylase deficiency in the Chinese
Hsien-Hsiung Lee
;
Ging-Shing Won
;
Hsiang Tai Chao
;
Yann-Jinn Lee
;
Bon-Chu Chung
2008-03-01
Occipital encephalocele associated with iniencephaly mimicking an unilateral nuchal tumor on prenatal ultrasound
Chih-Ping Chen
;
Yuh-Ming Hwu
;
Fuu-Jen Tsai
;
Wayseen Wang
2008-06-01
Omental trophoblastic implant with hemoperitoneum as a sequela of suction dilatation and curettage
Hong-Ming Wu
;
Chih-Ping Chen
;
Kuo-Ming Chang
;
Shing-Jyh Chang
2006-02-01
Only two amino acid substitutions of I236N and V237E in exon 6 are converted to the CYP21 gene in a Chinese patient with congenital adrenal hyperplasia
Hsien-Hsiung Lee
;
Mei-Chyn Chao
;
Yann-Jinn Lee
2012-06-01
Osteogenesis imperfecta type I: second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the asymptomatic father
Chih-Ping Chen
;
Yi-Ning Su
;
Tung-Yao Chang
;
Schu-Rern Chern
;
Chen-Yu Chen
;
Jun-Wei Su
;
Wayseen Wang
2012-06-01
Osteogenesis imperfecta type II: prenatal diagnosis and association with increased nuchal translucency and hypoechogenicity of the cranium
Chih-Ping Chen
;
Yi-Ning Su
;
Tung-Yao Chang
;
Ming-Chao Huang
;
Chun-Heng Pan
;
Schu-Rern Chern
;
Jun-Wei Su
;
Wayseen Wang
2012-06-01
Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Ming-Huei Lin
;
Jun-Wei Su
;
Wayseen Wang
2012-02-01
Outbreak of imipenem-resistant Acinetobacter calcoaceticus-Acinetobacter baumannii complex harboring different carbapenemase gene-associated genetic structures in an intensive care unit
Lee YT, Fung CP, Wang FD, Chen CP, Chen TL, Cho WL;
2009-03-01
The p21 codon 31*C- and DRD2 codon 313*T-related genotypes/alleles, but not XRCC1 codon 399, hOGG1 codon 326, and DRD1-48 polymorphisms, are correlated with the presence of leiomyoma
Yao-Yuan Hsieh
;
Chi-Chen Chang
;
Da-Tian Bau
;
Fuu-Jen Tsai
;
Chang-Hai Tsai
;
Chih-Ping Chen
2007-06-01
A p38 MAP kinase regulates the expression of the Aedes aegypti defensin gene in mosquito cells
Wu, R.C.C., Shaio, M.F., and Cho, W. L.;
2009-01-01
PAL31 may play an important role as inflammatory modulator in the repair process of the spinal cord injury rat
Li-Fen Shen
;
Henrich Cheng
;
Ming-Chu Tsai
;
Huai-Sheng Kuo
;
Kin-Fu Chak
2005-04-01
Partial androgen insensitivity syndrome with R840H mutation in androgen receptor: report of one case
Jui-Lung Yen
;
Kuang-Huey Chang
;
Jin-Cherng Sheu
;
Yann-Jinn Lee
;
Li-Ping Tsai
2011-06-01
Partial monosomy 13q (13q21.32→qter) and partial trisomy 8p (8p12→pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization
Chih-Ping Chen
;
Yi-Ning Su
;
Fuu-Jen Tsai
;
Ming-Huei Lin
;
Pei-Chen Wu
;
Schu-Rern Chern
;
Chen-Chi Lee
;
Chen-Wen Pan
;
Wayseen Wang
2012-09-01
Partial monosomy 3p (3p26.2->pter) and partial trisomy 5q (5q34->qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Ming-Ren Chen
;
Yi-Ning Su
;
Schu-Rern Chern
;
Yu-Peng Liu
;
Jun-Wei Su
;
Meng-Shan Lee
;
Wayseen Wang
2012-06-01
Partial monosomy 9p (9p22.2->pter) and partial trisomy 18q (18q21.32->qter) in a female infant with anorectal malformations
Chih-Ping Chen
;
Hsien-Ming Lin
;
Cheung Leung
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Jun-Wei Su
;
Yu-Ting Chen
;
Wayseen Wang
2010-12-01
Partial trisomy 10q (10q25.1→qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization
Chih-Ping Chen
;
Yi-Ning Su
;
Fuu-Jen Tsai
;
Schu-Rern Chern
;
Chin-Yuan Hsu
;
Pei-Chen Wu
;
Chen-Chi Lee
;
Wen-Lin Chen
;
Wayseen Wang
2010-12-01
Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization
Chih-Ping Chen
;
Yi-Ning Su
;
Richard Shih-Hung Young
;
Fuu-Jen Tsai
;
Pei-Chen Wu
;
Schu-Rern Chern
;
Dai-Dyi Town
;
Chen-Wen Pan
;
Wayseen Wang
2012-12-01
Partial trisomy 1q (1q42.13->qter) and partial monosomy 6q (6q27->qter) in a girl with single median maxillary central incisor, dysgenesis of corpus callosum and developmental delay
Chih-Ping Chen
;
Shuan-Pei Lin
;
Yi-Ning Su
;
Schu-Rern Chern
;
Jun-Wei Su
;
Chen-Chi Lee
;
Wayseen Wang
2011-03-01
Pathological characterization of a malformed umbilical cord associated with body stalk anomaly
Chih-Ping Chen
;
Tao-Yeuan Wang
;
Pei-Chen Wu
;
Fuu-Jen Tsai
;
Wayseen Wang
2010-06-01
Pathophysiology of increased fetal nuchal translucency thickness
Chih-Ping Chen;
2004-05-01
PCR-based detection of the CYP21 deletion and TNXA/TNXB hybrid in the RCCX module
Hsien-Hsiung Lee
;
Yann-Jinn Lee
;
Ching-Yu Lin
Showing items 276-300 of 499. (20 Page(s) Totally)
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