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

	English \| 正體中文 \| 简体中文 \| Total items :2851802
	Visitors : 44733827 Online Users : 1490 Project Commissioned by the Ministry of Education Project Executed by National Taiwan University Library

Scope

Adv. Search

Login

Administrator

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

About TAIR
	About TAIR

Browse By
	Institution
	Author
	Title
	Date
	Statistics Chart
	Institution Facts
	Trend

News
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

Copyright
	Publisher & Journal Policy
	TAIR Copyright Conference Minutes

Related Links
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

"niu d m"

Return to Browse by Author
Sorting by Title	Sort by Date

Showing items 56-65 of 78 (8 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 > >>
View [10|25|50] records per page

Institution	Date	Title	Author
臺大學術典藏	2020-02-14T02:50:02Z	Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome	Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.
臺大學術典藏	2020-02-14T02:50:02Z	Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis	Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin C.-Y.; Chang C.-H.; Chiu H.-H.; Yu C.-C.; Lin S.-P.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.-N.
臺大學術典藏	2020-02-12T04:06:04Z	Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis	Su Y.-N.;Niu D.-M;Ho H.-N;Cheng W.-F;Lin S.-P;Yu C.-C;Chiu H.-H;Chang C.-H;Lin C.-Y;Cheng H.-Y;CHIEN-NAN LEE;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; CHIEN-NAN LEE; Cheng H.-Y; Lin C.-Y; Chang C.-H; Chiu H.-H; Yu C.-C; Lin S.-P; Cheng W.-F; Ho H.-N; Niu D.-M; Su Y.-N.
臺大學術典藏	2020-02-12T04:06:04Z	Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR	Lin S.-P; Niu D.-M; Lee N.-C; Cheng W.-F; Chen C.-P; Lin W.-L; CHIEN-NAN LEE; Su Y.-N.; Su Y.-N.;CHIEN-NAN LEE;Lin W.-L;Chen C.-P;Cheng W.-F;Lee N.-C;Niu D.-M;Lin S.-P;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y
臺大學術典藏	2020-02-12T04:06:00Z	Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome	Ho H.-N.;Su Y.-N;Lin C.-Y;Kuo P.-W;Tu M.-P;Fang M.-Y;Chen L.-Y;Hsu W.-M;Niu D.-M;Tung Y.-C;Hsieh W.-S;Li N.-C;Lin S.-P;Tsai W.-Y;Hung C.-C;CHIEN-NAN LEE;Lin S.-Y; Lin S.-Y; CHIEN-NAN LEE; Hung C.-C; Tsai W.-Y; Lin S.-P; Li N.-C; Hsieh W.-S; Tung Y.-C; Niu D.-M; Hsu W.-M; Chen L.-Y; Fang M.-Y; Tu M.-P; Kuo P.-W; Lin C.-Y; Su Y.-N; Ho H.-N.
臺大學術典藏	2020-02-12T04:05:56Z	A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity	Ho H.-N.;Su Y.-N;Niu D.-M;Hsieh W.S;Chen L.-Y;Hung C.-C;Chen P.-C;Chuang E.Y;Lai L.-C;Tsai M.-H;CHIEN-NAN LEE;Lin Y.-C;Hsieh S.-C;Lin S.-Y; Lin S.-Y; Hsieh S.-C; Lin Y.-C; CHIEN-NAN LEE; Tsai M.-H; Lai L.-C; Chuang E.Y; Chen P.-C; Hung C.-C; Chen L.-Y; Hsieh W.S; Niu D.-M; Su Y.-N; Ho H.-N.
臺大學術典藏	2020-02-10T06:49:24Z	Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome	Shin-Yu Lin;Lee C.-N;Hung C.-C;Tsai W.-Y;Lin S.-P;Li N.-C;Hsieh W.-S;Tung Y.-C;Niu D.-M;Hsu W.-M;Chen L.-Y;Fang M.-Y;Tu M.-P;Kuo P.-W;Lin C.-Y;Su Y.-N;Ho H.-N.; SHIN-YU LIN; Lee C.-N; Hung C.-C; Tsai W.-Y; Lin S.-P; Li N.-C; Hsieh W.-S; Tung Y.-C; Niu D.-M; Hsu W.-M; Chen L.-Y; Fang M.-Y; Tu M.-P; Kuo P.-W; Lin C.-Y; Su Y.-N; Ho H.-N.
臺大學術典藏	2020-02-06T05:22:17Z	Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR	Su Y.-N.;Lee C.-N.;Lin W.-L.;Chen C.-P.;WEN-FANG CHENG;Lee N.-C.;Niu D.-M.;Lin S.-P.;Lin S.-Y.;Hung C.-C.; Hung C.-C.; Lin S.-Y.; Lin S.-P.; Niu D.-M.; Lee N.-C.; WEN-FANG CHENG; Chen C.-P.; Lin W.-L.; Lee C.-N.; Su Y.-N.; Hung C.-C.; Lin S.-Y.; Lin S.-P.; Niu D.-M.; Lee N.-C.; WEN-FANG CHENG; Chen C.-P.; Lin W.-L.; Lee C.-N.; Su Y.-N.
臺大學術典藏	2020-02-06T05:22:16Z	Mutation spectrum of the fibrillin-1 (FBN1) gene in Taiwanese patients with Marfan syndrome	Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.; Chen M.-R.; Lin S.-P.; Cheng H.-Y.; Su Y.;Niu D.-M.;Ho H.-N.;WEN-FANG CHENG;Chiu H.-H.;Yu C.-C.;Lin C.-Y.;Chang C.-H.;Chen C.-P.;Chen M.-R.;Lin S.-P.;Cheng H.-Y.;Lee C.-N.;Lin S.-Y.;Hung C.-C.; Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin S.-P.; Chen M.-R.; Chen C.-P.; Chang C.-H.; Lin C.-Y.; Yu C.-C.; Chiu H.-H.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.; Hung C.-C.; Lin S.-Y.; Lee C.-N.
臺大學術典藏	2020-02-06T05:22:16Z	Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis	Su Y.-N.;Niu D.-M.;Ho H.-N.;WEN-FANG CHENG;Lin S.-P.;Yu C.-C.;Chiu H.-H.;Chang C.-H.;Lin C.-Y.;Cheng H.-Y.;Lee C.-N.;Lin S.-Y.;Hung C.-C.; Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin C.-Y.; Chang C.-H.; Chiu H.-H.; Yu C.-C.; Lin S.-P.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.-N.; Hung C.-C.; Lin S.-Y.; Lee C.-N.; Cheng H.-Y.; Lin C.-Y.; Chang C.-H.; Chiu H.-H.; Yu C.-C.; Lin S.-P.; WEN-FANG CHENG; Ho H.-N.; Niu D.-M.; Su Y.-N.

Showing items 56-65 of 78 (8 Page(s) Totally)
<< < 1 2 3 4 5 6 7 8 > >>
View [10|25|50] records per page