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Showing items 251-300 of 499. (10 Page(s) Totally)
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DateTitleAuthors
2011-12-01 Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy Chih-Ping Chen; Yi-Ning Su; Chin-Yuan Hsu; Schu-Rern Chern; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Wayseen Wang
2012-12-01 Mosaic isochromosome 20q detected at amniocentesis may be a cell culture artifact Chih-Ping Chen; Shuenn-Dyh Chang; Yu-Ting Chen; Jun-Wei Su; Dai-Dyi Town; Wayseen Wang
2010-09-01 Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and dsomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization Chih-Ping Chen; Yung-Ting Guo; Shuan-Pei Lin; Yi-Ning Su; Yann-Jang Chen; Rui-Yuan Hseuh; Yi-Hui Lin; Pei-Chen Wu; Chen-Chi Lee,; Yu-Ting Chen; Wayseen Wang
2012-03-01 Mosaic ring chromosome 21, monosomy 21 and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3 Chih-Ping Chen; Yi-Hui Lin; Szu-Yuan Chou; Yi-Ning Su; Schu-Rern Chern; Yu-Ting Chen; Dai-Dyi Town; Wen-Lin Chen; Chen-Wen Pan; Wayseen Wang
2011-09-01 Mosaic ring chromosome 4 in a child with mild dysmorphisms, congenital heart defects and developmental delay Chih-Ping Chen; Shuan-Pei Lin; Yi-Ning Su; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang
2011-09-01 Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses Chih-Ping Chen; Shuan-Pei Lin; Ming Chen; Yi-Ning Su; Schu-Rern Chern,; Tao-Yeuan Wang; Yu-Peng Liu; Fuu-Jen Tsai; Chen-Chi Lee; Yen-Jiun Chen; Wayseen Wang
2010-06-01 Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Hsaio-En Cindy Chen; Shu-Shien Chiang; Wayseen Wang
2012-12-01 Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Ting Chen; Peih-Shan Wu; Jun-Wei Su; Chen-Wen Pan; Wayseen Wang
2010-09-01 Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yu-Ming Hwu; Shuan-Pei Lin; Chyong-Hsin Hsu; Fuu-Jen Tsai; Tao-Yeuan Wang; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Li-Feng Chen; Wayseen Wang
2010-09-01 Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses Chih-Ping Chen; Hsien-Ming Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
2008-01-01 Mothers’ experience supporting life adjustment in children with T1DM. Lin HP; Mu PF; Lee YJ
2011-02-01 MUC4 gene polymorphisms associate with endometriosis development and endometriosis-related infertility Cherry Yin-Yi Chang; Hui-Wen Chang; Chih-Mei Chen; Chia-Ying Lin; Chih-Ping Chen; Chih-Ho Lai; Wei-Yong Lin; Hsing-Ping Liu; Jim Jinn-Chyuan Sheu; Fuu-Jen Tsai
2001-07-01 Multiple endocrine neoplasia 2B (MEN 2B) Lee YJ; Liu HC; Lee HC; Tzen CY; Huang CY; Yang TL
2009-11-01 Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome Chia-Cheng Hung; Shin-Yu Lin; Chien-Nan Lee; Hui-Yu Cheng; Shuan-Pei Lin; Ming-Ren Chen; Chih-Ping Chen; Chien-Hui Chang; Chiou-Ya Lin; Chih-Chieh Yu; Hsin-Hui Chiu,; Wen-Fang Cheng; Hong-Nerng Ho; Dau-Ming Niu; Yi-Ning Su
2007-01-01 Mutational Analysis of PTPN11 Gene in Taiwanese Children with Noonan Syndrome. Hung CS; Lin JL; Lee YJ; Lin SP; Chao MC; Lo FS
2014-03-01 Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese Wu YL; Hwang DW; Hsiao HP; Ting WH; Huang CY; Tsai WY; Chen HC; Chao MC; Lo FS; Tsai JD; Yang S; Shih SL; Lin CL; Lee YJ
2007-05-01 Neck abscess and necrotizing fasciitis caused by Salmonella infection: a report of 2 cases. Luo CW; Liu CJ
2000-06-01 Neonatal adrenal hemorrhage Huang CY; Lee YJ; Lee HC; Huang FY
2002-06-01 Neonatal adrenal hemorrhage: 4-year experience Chang HY; Yeung CY; Hsu CH; Lee HC; Lee YJ; Lin DS; Lin CC
2012-12-01 Neural Stem Cells and Cell-based Approaches in Neurodegeneration and Peripheral Nerve Injuries Hsu YC; Chiu IM
1995-04-01 Neurogenic diabetes insipidus in a child with fatal Coxsackie virus B1 encephalitis ann-Jinn Lee; Dine Yang; Shyh-Dar Shyur; Nan-Chang Chiu
1996-03-01 Neurogenic diabetes insipidus in children with hypoxic encephalopathy Lee YJ; Huang FY; Shen EY; Kao HA; Ho MY; Shyur SD; Chiu NC
2013-08-01 The new face of the old molecules: crustin Pm4 and transglutaminase type I serving as rnps down-regulate astakine-mediated hematopoiesis Yun-Tsan Chang; Cheng-Yung Lin; Che-Yiang Tsai; Vinu S Siva; Chia-Ying Chu; Huai-Jen Tsai; Yen-Ling Song
2001-02-01 Newborns with ambiguous genitalia, impalpable gonads, and hyperpigmentation Chang HY; Lee YJ; Lin SP; Lee HH
2008-04-01 NFkB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1→qter) Chih-Ping Chen; Yann-Jang Chen; Fuu-Jen Tsai; Schu-Rern Chern; Wayseen Wang
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 251-300 of 499. (10 Page(s) Totally)
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