| 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 |
| 國立臺灣大學 |
2009 |
Chromosome 3p12.3-P14.2 and 3q26.2-Q26.32 Are Genomic Markers for Prognosis of Advanced Nasopharyngeal Carcinoma
|
許晉銓; 李家惠; 柯政郁; 吳仲峻; 方志宇; 蔡輔仁; 花俊宏; 陳志榮; 陳振陽; SHEU, JIM JINN-CHYUAN; LEE, CHIA-HUEI; KO, JENQ-YUH; WU, CHUNG-CHUN; FANG, CHIH-YEU; TSAI, FUU-JEN; HUA, CHUN-HUNG; CHEN, CHI- LONG; CHEN, JEN-YANG |
| 臺大學術典藏 |
2021-10-25T02:57:32Z |
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 |
2021-11-15T07:48:32Z |
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. |
| 中國醫藥大學 |
2009-10 |
Chromosome 3p12.3-p14.2 and 3q26.2-q26.32 are genomic markers for prognosis of advanced nasopharyngeal carcinoma.
|
許晉銓(Jinn-Chyuan Sheu); (Lee CH); (KoJYY); (Tsao G); (Wu CC); (Fang CY); 蔡輔仁(Fuu-Jen Tsai); 花俊宏(Chun-Hung Hua); (Chen CL); (Chen JY) |
| 國家衛生研究院 |
2011-04 |
Chromosome 8p23.2-pter: a critical region for mental retardation, autism and epilepsy? Response to Nucaro et al
|
Gau, SSF;Chen, CH |
| 高雄醫學大學 |
2011 |
Chromosome 9p21基因多型性與心肌梗塞相關但不與缺血性中風有關
|
林秀芬;蔡佩倩;廖翊筑;林宗憲;戴志達;卓夙航;林瑞泰 ; HF Lin;PC Tsai;YC Liao;TH Lin;CT Tai;SH Juo;RT Lin |
| 高雄醫學大學 |
2011 |
chromosome 9p21基因對動脈硬化之影響
|
林秀芬;蔡佩倩;林瑞泰;卓夙航 |
| 國立臺灣大學 |
2001 |
CHROMOSOME ABERRATIONS IN LYMPHOCYTES OF RESIDENTS LIVING IN BUILDINGS CONSTRUCTED WITH RADIOACTIVELY CONTAMINATED REBARS
|
SHENG, WANG-WUU; TAI, JOHN JEN; LIN, SHOW-YU; CHEN, WEI-LI; WUU, KUANG-DONG; 王昇; 戴政; 林秀玉; 陳偉勵; 武光東 |
| 臺大學術典藏 |
2018-09-10T15:01:41Z |
Chromosome abnormalities in embryos derived from microsurgical epididymal sperm aspiration and testicular sperm extraction
|
Weng, S. P. F. ; Surrey, M. W. ; Danzer, H. C. ; Hill, D. L. ; Chen, P. C. ; Wu, T. C. J.; Pau-Chung CHEN |
| 臺大學術典藏 |
2022-03-31T02:39:09Z |
Chromosome abnormalities in embryos derived from microsurgical epididymal sperm aspiration and testicular sperm extraction
|
Weng S.P.F.; Surrey M.W.; Danzer H.C.; Hill D.L.; PAU-CHUNG CHEN; Wu T.C.J. |
| 國立臺灣大學 |
1993 |
Chromosome Analysis in Patients with Cryptorchidism
|
陳世乾; Chuen, Shih-Chieh; 莊壽洺; 丘祖毅; 陳世乾; Chuen, Shih-Chieh; 莊壽洺; Chiu, Tsu-Yih |
