臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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显示项目 255366-255415 / 2346260 (共46926页)
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机构	日期	题名	作者
國立臺灣大學	1989	Chromosomal Characterizations of Human Nasal and Nasopharyngeal Cells Immortalized by Human Papillomavirus Type 16 DNA	Debiec-Rychter, M.; Zukowski, K.; Wang, C. Y; 溫五男; Debiec-Rychter, M.; Zukowski, K.; Wang, C. Y; Wen, Wu-Nan
國立臺灣大學	1989	Chromosomal Charcteristics of Ph-Positive Chronic Myelogenous Leukemia in Transformation:A Study of 23 Chinese Patients in Taiwan	田蕙芬; 莊壽洺; Wang, C. H.; Lee, F. Y.; Chien, S. H.; 陳宜君; Shen, M. C.; Liu, C. H.; 田蕙芬; 莊壽洺; Wang, C. H.; Lee, F. Y.; Chien, S. H.; Chen, Yee-Chun; Shen, M. C.; Liu, C. H.
國立臺灣大學	2006-01	Chromosomal clustering and GATA transcriptional regulation of intestine-expressed genes in C-elegans	Pauli, F; Liu, YY; Kim, YA; Chen, PJ; Kim, SK
國家衛生研究院	2004-01-01	Chromosomal comparative genomic hybridization abnormalities in early- and late-onset human breast cancers: correlation with disease progression and TP53 mutations	Jong, YJ; Li, LH; Tsou, MH; Chen, YJ; Cheng, SH; Sheng, WW; Tsai, SF; Chen, CM; Huang, AT; Hsu, MT; Lin, CH
國家衛生研究院	2000-02-26	Chromosomal damage in long-term residents of houses contaminated with cobalt-60	Chen, FD; Chen, KY; Ngo, FQH; Lin, CH; Tsai, ST; Ling, TS; Whang-Peng, JJK; Edwards, AA; Lloyd, DC; Chen, WL
亞洲大學	2014-03	Chromosomal deletions detected at amniocentesis	Lin, Chen-Ju;Lin, Chen-Ju;陳持平;Chen, Chih-Ping;Chi, Shu-Chin;Chien, Shu-Chin;Lee, Chen-Chi;Chen-Chi Lee, ;Town, Dai-Dyi;Town, Dai-Dyi;Chen, Wen-Lin;Chen, Wen-Lin;Che, L i-Feng;Chen, L i-Feng;Le, Meng-Shan;Lee, Meng-Shan;Chen-Wen Pan, ;Ku-Chien Lin, ;Yeh, Tze-Tien;Yeh, Tze-Tien;
亞洲大學	2014-03	Chromosomal deletions detected at amniocentesis	Chen-Ju Lin(Chen-Ju Lin)*; 陳持平(Chih-Ping Chen); Shu-Chin Chi(Shu-Chin Chien); Chen-Chi Lee(Chen-Chi Lee, ); Dai-Dyi Town(Dai-Dyi Town); Wen-Lin Chen(Wen-Lin Chen); L i-Feng Che(L i-Feng Chen); Meng-Shan Le(Meng-Shan Lee); ,(Chen-Wen Pan,); ,(Ku-Chien Lin,); Tze-Tien Yeh(Tze-Tien Yeh); ; ;
中國醫藥大學	2014-03	Chromosomal deletions detected at amniocentesis	(Chen-Ju Lin)*;陳持平(Chih-Ping Chen);簡淑錦(Shu-Chin Chien);(Chen-Chi Lee);(Dai-Dyi Town);(Wen-Lin Chen);(L i-Feng Chen);(Meng-Shan Lee);(Chen-Wen Pan);(Ku-Chien Lin);(Tze-Tien Yeh)
中國醫藥大學	2006-01	Chromosomal distribution and organization of three cervid satellite DNAs in Chinese water deer(Hydropotes inermis)	林齊強(Chyi-Chyang Lin); 李月君(Yueh-Chun Li)*
國立臺灣大學	2002	Chromosomal fluorescence in situ hybridization: techniques and applications in plant genetics	Chen, C. C.; Kao, Y. Y.
臺北醫學大學	2007	Chromosomal gain of 3q and loss of 11q often associated with nodal metastasis in early stage cervical squamous cell carcinoma	林鈺山; Huang KF; Lee WY; Huang SC; Lin YS; Kang CY; Liou CP; Tzeng CC
臺大學術典藏	2019-08-30T01:08:18Z	Chromosomal integration of Epstein-Barr virus genomes in nasopharyngeal carcinoma cells	Chang Y;Cheng S.-D;Ching-Hwa Tsai; Chang Y; Cheng S.-D; CHING-HWA TSAI
臺大學術典藏	2022-04-08T09:23:22Z	Chromosomal integration of Epstein-Barr virus genomes in nasopharyngeal carcinoma cells	Chang Y.; Cheng S.-D.; CHING-HWA TSAI
國家衛生研究院	2008-02	Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates	Huang, WC; Chen, YYM; Teng, LJ; Lien, HT; Chen, JY; Chia, JS
國立臺灣大學	2008	Chromosomal Inversion between Rrn Operons among Streptococcus Mutans Serotype C Oral and Blood Isolates	黃紋娟; 鄧麗珍; 陳振陽; 賈景山; HUANG, WEN-CHUAN; TENG, LEE-JENE; CHEN, JEN-YANG; CHIA, JEAN-SAN
臺大學術典藏	2018-09-10T06:47:28Z	Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates	Huang, W.-C. and Chen, Y.-Y.M. and Teng, L.-J. and Lien, H.-T. and Chen, J.-Y. and Chia, J.-S.; 黃紋娟;鄧麗珍;陳振陽;賈景山; Huang, W. C.; Yi-Ywan, M.; Chen-Teng, L. J.; Lien, H. T.; Chen, J. Y.;Chia, J. S.*; HUANG, WEN-CHUAN;TENG, LEE-JENE;CHEN, JEN-YANG;CHIA, JEAN-SAN; LEE-JENE TENG; JEAN-SAN CHIA; HUANG, WEN-CHUAN; TENG, LEE-JENE; CHEN, JEN-YANG; CHIA, JEAN-SAN
臺大學術典藏	2020-06-30T06:13:35Z	Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates	Huang W.-C.;Chen Y.-Y.M.;Lee-Jene Teng;Lien H.-T.;Chen J.-Y.;Chia J.-S.; Huang W.-C.; Chen Y.-Y.M.; LEE-JENE TENG; Lien H.-T.; Chen J.-Y.; Chia J.-S.
國立臺灣大學	2008-02	Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates.	Huang, W. C.; Yi-Ywan, M.; Chen-Teng, L. J.; Lien, H. T.; Chen, J. Y.; Chia, J. S.*
國立臺灣大學	1998	Chromosomal inversion polymorphism in natural populations of Drosophila ruberrima	Fang, Shu; Lin, Fei-Jann; Chang, Hwei-yu
國立臺灣大學	1987	Chromosomal Inversions in Drosophila Albomicans in Taiwan	張慧羽; 林飛棧; Chang, Hwei-Yu; Lin, Fei-Jann
臺大學術典藏	2018-09-10T06:34:24Z	Chromosomal localization and partial genomic structure of the human peroxisome proliferator activated receptor-gamma (hPPARγ) gene	Beamer, B.A. and Negri, C. and Yen, C.-J. and Gavrilova, O. and Rumberger, J.M. and Durcan, M.J. and Yarnall, D.P. and Hawkins, A.L. and Griffin, C.A. and Burns, D.K. and Roth, J. and Reitman, M. and Shuldiner, A.R.; CHUNG-JEN YEN
臺大學術典藏	1997	Chromosomal localization and partial genomic structure of the human peroxisome proliferator activated receptor-gamma (hPPARγ) gene	Burns D.K.; Griffin C.A.; Hawkins A.L.; Yarnall D.P.; Rumberger J.M.; Durcan M.J.; Gavrilova O.; CHUNG-JEN YEN; Negri C.; Beamer B.A.; Roth J.; Reitman M.; Shuldiner A.R.
國立臺灣大學	2005	Chromosomal Organization, Evolutionary Relationship, and Expression of Zebrafish GnRH Family Members	Kuo, Ming-Wei; Lou, Show-Wan; Postlethwait, John; Chung, Bon-Chu
國立臺灣大學	2005-07	Chromosomal organization, evolutionary relationship, and expression of zebrafish GnRH family members	Kuo, MW; Lou, SW; Postlethwait, J; Chung, BC
東海大學	2001	Chromosomal polymorphism in the Gray Shrew Crocidura attenuata (Mammalia: Insectivora)	Motokawa, M., Harada, M., Wu, Y., Lin, L.-K., Suzuki, H.
臺大學術典藏	2021-11-22T02:27:28Z	Chromosomal polymorphism of ribosomal genes in the genus Oryza	Chung, M.-C.; Lee, Y.-I.; Cheng, Y.-Y.; Chou, Y.-J.; Lu, C.-F.
中國醫藥大學	2013-04	Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract	張鈺孜(chang, yu-tzu);Chou), 周宜卿(I-Ching;Wang), 王仲興(Chung-Hsing;Chin), 陳震南(Zheng-Nan;Kuo), 郭煌宗(Haung-Tsung;Lin), 林齊強(Chyi-Chyang;Tsai), 蔡長海(Chang-Hai;Tsai)*, 蔡輔仁(Fuu-Jen
亞洲大學	2011-09	Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)	陳持平;Chen, Chih-Ping;Li-Feng Chen, ;Adam Hwa-Ming Hsieh, ;Wang, Wayseen
中國醫藥大學	2011-09	Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)	陳持平(Chih-Ping Chen)*;(Yi-Hui Lin);(Heng-Kien Au);(Chin-Yuan Hsu);(Yu-Peng Liu);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Li-Feng Chen);(Adam Hwa-Ming Hsieh);(Wayseen Wang)
國立交通大學	2014-12-08T15:23:14Z	Chromosome 15q21-22-Related Polymorphisms and Haplotypes Are Associated with Susceptibility to Type-2 Diabetic Nonproliferative Retinopathy	Hsieh, Yao-Yuan; Huang, Yu-Chuen; Chang, Chi-Chen; Wang, Yu-Kuo; Lin, Wen-Hsin; Tsai, Fuu-Jen
中國醫藥大學	2012-05	Chromosome 15q21-22-related polymorphisms and haplotypes are associated with susceptibility to type-2 diabetic nonproliferative retinopathy	謝耀元(Hsieh Yao-Yuan);黃毓銓(Yu-Chuen Huang);(Chi-Chen Chang);(Yu-Kuo Wang);林文鑫(Wen-Hsin Lin);蔡輔仁(Fuu-Jen Tsai)*
中國醫藥大學	2013-12	Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review	陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Wan-Yuo Guo);(Pei-Chen Wu);(Liang-Kai Wang);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang)
亞洲大學	201309	Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes	陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen
臺大學術典藏	2018-09-10T06:00:32Z	Chromosome 1p aberrations are frequent in human primary hepatocellular carcinoma	Chen, H.-L., Chen, Y.-C., Chen, D.-S.; Hui-Ling Chen; DING-SHINN CHEN
亞洲大學	2011-09	Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia	陳持平;Chen, Chih-Ping
中國醫藥大學	2011-09	Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Yi-Yung Chen);(Schu-Rern Chern);(Yu-Peng Liu);(Pei-Chen Wu);(Chen-Chi Lee);(Yu-Ting Chen);(Wayseen Wang)
亞洲大學	2010-12	Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings	陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Wang, Wayseen
國立臺灣大學	2010	Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings	陳持平; 陳明; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 李貞?; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; LEE, CHEN-CHI
中國醫藥大學	2010-12	Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings	陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang)
國立政治大學	2014-11	Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations	Huang, H.-N.;Huang, W.-C.;Lin, C.-H.;Huang, Hsin Ying; 黃馨瑩
國立臺灣大學	2014	Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations	Huang, Hsien-Neng; Huang, Wen-Chih; Lin, Ching-Hung; Chiang, Ying-Cheng; Huang, Hsin-Ying; Kuo, Kuan-Ting; 林璟宏; 郭冠廷; 江盈澄; 林季宏
臺大學術典藏	2018-09-10T14:52:01Z	Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations	Huang, Hsien-Neng;Huang, Wen-Chih;Lin, Ching-Hung;Chiang, Ying-Cheng;Huang, Hsin-Ying;Kuo, Kuan-Ting; Huang, Hsien-Neng;Huang, Wen-Chih;Lin, Ching-Hung;Chiang, Ying-Cheng;Huang, Hsin-Ying;Kuo, Kuan-Ting; Huang, H.-N. and Huang, W.-C. and Lin, C.-H. and Chiang, Y.-C. and Huang, H.-Y. and Kuo, K.-T.; 林璟宏;郭冠廷;江盈澄;林季宏; 林璟宏;郭冠廷;江盈澄;林季宏; CHING-HUNG LIN; Huang, Hsien-Neng; Huang, Wen-Chih; KUAN-TING KUO; Lin, Ching-Hung; Chiang, Ying-Cheng; Huang, Hsin-Ying; Kuo, Kuan-Ting
臺大學術典藏	2020-02-14T08:50:34Z	Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations	Huang H.-N; Huang W.-C; Lin C.-H; YING-CHENG CHIANG; Huang H.-Y; Kuo K.-T.
臺大學術典藏	2020-03-05T07:52:34Z	Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations	Huang H.-N.; Huang W.-C.; Lin C.-H.; Chiang Y.-C.; Huang H.-Y.; KUAN-TING KUO
臺大學術典藏	2020-03-07T06:42:11Z	Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations	Huang H.-N.; Huang W.-C.; Lin C.-H.; Chiang Y.-C.; Huang H.-Y.; KUAN-TING KUO
臺大學術典藏	2021-02-04T07:44:56Z	Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations	Huang H.-N.;Huang W.-C.;Lin C.-H.;Ying-Cheng Chiang;Huang H.-Y.;Kuo K.-T.; Huang H.-N.; Huang W.-C.; Lin C.-H.; YING-CHENG CHIANG; Huang H.-Y.; Kuo K.-T.
亞洲大學	201309	Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review	陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen
國家衛生研究院	2009-10	Chromosome 3p12.3-p14.2 and 3q26.2-q26.32 are genomic markers for prognosis of advanced nasopharyngeal carcinoma	Sheu, JJC;Lee, CH;Ko, JY;Tsao, GSW;Wu, CC;Fang, CY;Tsai, FJ;Hua, CH;Chen, CL;Chen, JY
臺大學術典藏	2021-11-15T07:48:32Z	Chromosome 3p12.3-p14.2 and 3q26.2-q26.32 are genomic markers for prognosis of advanced nasopharyngeal carcinoma	Sheu J.J.-C; Lee C.-H; JENG-YUH KO; Tsao G.S.W; Wu C.-C; Fang C.-Y; Tsai F.-J; Hua C.-H; Chen C.-L; Chen J.-Y.
臺大學術典藏	2021-11-18T04:58:10Z	Chromosome 3p12.3-p14.2 and 3q26.2-q26.32 are genomic markers for prognosis of advanced nasopharyngeal carcinoma	Sheu J.J.-C; Lee C.-H; JENG-YUH KO; Tsao G.S.W; Wu C.-C; Fang C.-Y; Tsai F.-J; Hua C.-H; Chen C.-L; Chen J.-Y.

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