Works by Tsai, Shih-Feng

Results: 36

A Novel BTK Gene Mutation in a Child With Atypical X-Linked Agammaglobulinemia and Recurrent Hemophagocytosis: A Case Report.

Published in:

Frontiers in Immunology, 2019, p. 1, doi. 10.3389/fimmu.2019.01953

By:

Han, Shu-Ping;
Lin, Yung-Feng;
Weng, Hui-Ying;
Tsai, Shih-Feng;
Fu, Lin-Shien

Publication type:

Article

Rare APOE p.Gly4Glu: A putative disease-causing variant for early-onset Alzheimer's disease identified by next-generation sequencing.

Published in:

Tzu Chi Medical Journal, 2025, v. 37, n. 2, p. 175, doi. 10.4103/tcmj.tcmj_117_24

By:

Wu, Chu-Ting;
Hu, Liang-Hsuan;
Weng, Hui-Ying;
Liu, Yen-Ming;
Lin, Yung-Feng;
Tsai, Shih-Feng;
Lo, Raymond Y.;
Ching, Yung-Hao

Publication type:

Article

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.

Published in:

Nature Genetics, 2001, v. 28, n. 3, p. 232, doi. 10.1038/90067

By:

Bressler, Jan;
Tsai, Ting-Fen;
Wu, Mei-Yi;
Tsai, Shih-Feng;
Ramirez, Maricela A.;
Armstrong, Dawna;
Beaudet, Arthur L.

Publication type:

Article

Chromosomal aberrations in nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Published in:

Genes, Chromosomes & Cancer, 1999, v. 25, n. 2, p. 169, doi. 10.1002/(SICI)1098-2264(199906)25:2<169::AID-GCC13>3.0.CO;2-I

By:

Chen, Yann-Jang;
Ko, Jenq-Yuh;
Chen, Pei-Jer;
Shu, Chih-Hung;
Hsu, Ming-Ta;
Tsai, Shih-Feng;
Lin, Chi-Hung

Publication type:

Article

Identification of the common regulators for hepatocellular carcinoma induced by hepatitis B virus X antigen in a mouse model.

Published in:

Carcinogenesis, 2012, v. 33, n. 1, p. 209, doi. 10.1093/carcin/bgr224

By:

Lu, Jeng-Wei;
Hsia, Yu;
Yang, Wan-Yu;
Lin, Yu-I;
Li, Chao-Chin;
Tsai, Ting-Fen;
Chang, Ko-Wei;
Shieh, Grace S.;
Tsai, Shih-Feng;
Wang, Horng-Dar;
Yuh, Chiou-Hwa

Publication type:

Article

Generation and Analysis of the Expressed Sequence Tags from the Mycelium of Ganoderma lucidum

Published in:

PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0061127

By:

Huang, Yen-Hua;
Wu, Hung-Yi;
Wu, Keh-Ming;
Liu, Tze-Tze;
Liou, Ruey-Fen;
Tsai, Shih-Feng;
Shiao, Ming-Shi;
Ho, Low-Tone;
Tzean, Shean-Shong;
Yang, Ueng-Cheng

Publication type:

Article

Copy Number Change of the NDM-1 Sequence in a Multidrug-Resistant Klebsiella pneumoniae Clinical Isolate.

Published in:

PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0062774

By:

Huang, Tzu-Wen;
Chen, Te-Li;
Chen, Ying-Tsong;
Lauderdale, Tsai-Ling;
Liao, Tsai-Lien;
Lee, Yi-Tzu;
Chen, Chien-Pei;
Liu, Yen-Ming;
Lin, Ann-Chi;
Chang, Ya-Hui;
Wu, Keh-Ming;
Kirby, Ralph;
Lai, Jui-Fen;
Tan, Mei-Chen;
Siu, Leung-Kei;
Chang, Chung-Ming;
Fung, Chang-Phone;
Tsai, Shih-Feng

Publication type:

Article

Resonance assignments of a CoA binding protein from Klebsiella pneumoniae.

Published in:

2006

By:

Hung, Kuo-Wei;
Lin, Yi-Chao;
Cheng, Chun-Chia;
Fan, Pei-Ju;
Chang, Chi-Fon;
Tsai, Shih-Feng;
Huang, Tai-Huang

Publication type:

Letter

Unraveling the complex genetic landscape of OTOF-related hearing loss: a deep dive into cryptic variants and haplotype phasing.

Published in:

Molecular Medicine, 2025, v. 31, n. 1, p. 1, doi. 10.1186/s10020-025-01225-2

By:

Lin, Pei-Hsuan;
Tsai, Cheng-Yu;
Chiang, Yu-Ting;
Ho, Chang-Han;
Lu, Yue-Sheng;
Hsu, Jacob Shu-Jui;
Cheng, Yen-Fu;
Tsai, Shih-Feng;
Hsu, Chuan-Jen;
Chen, Pei-Lung;
Wu, Chen-Chi

Publication type:

Article

Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 5, p. 419, doi. 10.1007/s10038-008-0265-3

By:

Furuichi, Tatsuya;
Maeda, Koichi;
Chung-Tei Chou;
Yu-Fen Liu;
Ting-Chun Liu;
Miyamoto, Yoshinari;
Takahashi, Atsushi;
Mori, Kanji;
Ikari, Katsunori;
Kamatani, Naoyuki;
Kurosawa, Hisashi;
Inoue, Hisashi;
Tsai, Shih-Feng;
Ikegawa, Shiro

Publication type:

Article

Novel mutations involving the NF1 gene coding sequence in neurofibromatosis type 1 patients from Taiwan.

Published in:

Journal of Human Genetics, 2003, v. 48, n. 10, p. 545, doi. 10.1007/s10038-003-0066-7

By:

Liu, Ming-Tzen;
Su, Jih-Shyun;
Huang, Chun-Yu;
Tsai, Shih-Feng

Publication type:

Article

ARD1 Stabilization of TSC2 Suppresses Tumorigenesis Through the mTOR Signaling Pathway.

Published in:

Science Signaling, 2010, v. 3, n. 108, p. 1, doi. 10.1126/scisignal.2000590

By:

Hsu-Ping Kuo;
Dung-Fang Lee;
Chun-Te Chen;
Mo Liu;
Chao-Kai Chou;
Hong-Jen Lee;
Yi Du;
Xiaoming Xie;
Yongkun Wei;
Weiya Xia;
Zhang Weihua;
Jer-Yen Yang;
Chia-Jui Yen;
Tzu-Hsuan Huang;
Minjia Tan;
Gang Xing;
Yingming Zhao;
Chien-Hsing Lin;
Tsai, Shih-Feng;
Fidler, Isaiah J.

Publication type:

Article

Selective Retention of an Inactive Allele of the DKK2 Tumor Suppressor Gene in Hepatocellular Carcinoma.

Published in:

PLoS Genetics, 2016, v. 12, n. 5, p. 1, doi. 10.1371/journal.pgen.1006051

By:

Lin, Yung-Feng;
Li, Ling-Hui;
Lin, Chih-Hung;
Tsou, Mei-Hua;
Chuang, Ming-Tai Kiffer;
Wu, Keh-Ming;
Liao, Tsai-Lien;
Li, Jian-Chiuan;
Wang, Wei-Jie;
Tomita, Angela;
Tomita, Beverly;
Huang, Shiu-Feng;
Tsai, Shih-Feng

Publication type:

Article

Qualitative and comparative proteomic analysis of Xanthomonas campestris pv. campestris 17.

Published in:

Proteomics, 2007, v. 7, n. 12, p. 2047, doi. 10.1002/pmic.200600647

By:

Chung, Wei-Jen;
Shu, Hung-Yu;
Lu, Chi-Yu;
Wu, Chiu-Yi;
Tseng, Yi-Hsiung;
Tsai, Shih-Feng;
Lin, Chao-Hsiung

Publication type:

Article

Epigenetic Enhancement of the Post-replicative DNA Mismatch Repair of Mammalian Genomes by a Hemi-mCpG-Np95-Dnmt1 Axis.

Published in:

Scientific Reports, 2016, p. 37490, doi. 10.1038/srep37490

By:

Wang, Keh-Yang;
Chen, Chun-Chang;
Tsai, Shih-Feng;
Shen, Che-Kun James

Publication type:

Article

Network Signatures of IgG Immune Repertoires in Hepatitis B Associated Chronic Infection and Vaccination Responses.

Published in:

Scientific Reports, 2016, p. 26556, doi. 10.1038/srep26556

By:

Chang, Ya-Hui;
Kuan, Hui-Chung;
Hsieh, T. C.;
Ma, K. H.;
Yang, Chung-Hsiang;
Hsu, Wei-Bin;
Tsai, Shih-Feng;
Chao, Anne;
Liu, Hong-Hsing

Publication type:

Article

Next-Generation Integrated Sequencing Identifies Poor Prognostic Factors in Patients with MYD88-Mutated Chronic Lymphocytic Leukemia in Taiwan.

Published in:

Pathobiology, 2025, v. 92, n. 2, p. 77, doi. 10.1159/000541709

By:

Huang, Ying-Jung;
Lim, Jing Quan;
Hsu, Jacob Shujui;
Kuo, Ming-Chung;
Wang, Po-Nan;
Kao, Hsiao-Wen;
Wu, Jin-Hou;
Chen, Chiu-Chen;
Tsai, Shih-Feng;
Ong, Choon Kiat;
Shih, Lee-Yung

Publication type:

Article

Genetic Heterogeneity of Familial Primary Cutaneous Amyloidosis: Lack of Evidence for Linkage with the Chromosome 10 Pericentromeric Region in Chinese Families.

Published in:

Journal of Investigative Dermatology, 1996, v. 107, n. 1, p. 30, doi. 10.1111/1523-1747.ep12297840

By:

Lee, Ding-Dar;
Huang, Jiun-Yu;
Wong, Chu-Kwan;
Gagel, Robert F.;
Tsai, Shih-Feng

Publication type:

Article

Artificial-Intelligence-Assisted Discovery of Genetic Factors for Precision Medicine of Antiplatelet Therapy in Diabetic Peripheral Artery Disease.

Published in:

Biomedicines, 2022, v. 10, n. 1, p. 116, doi. 10.3390/biomedicines10010116

By:

Yeh, Chi-Hsiao;
Chou, Yi-Ju;
Tsai, Tsung-Hsien;
Hsu, Paul Wei-Che;
Li, Chun-Hsien;
Chan, Yun-Hsuan;
Tsai, Shih-Feng;
Ng, Soh-Ching;
Chou, Kuei-Mei;
Lin, Yu-Ching;
Juan, Yu-Hsiang;
Fu, Tieh-Cheng;
Lai, Chi-Chun;
Sytwu, Huey-Kang;
Tsai, Ting-Fen

Publication type:

Article

Integration of genome-wide association study and expression quantitative trait locus mapping for identification of endometriosis-associated genes.

Published in:

Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-020-79515-4

By:

Chou, Ya-Ching;
Chen, Ming-Jer;
Chen, Pi-Hua;
Chang, Ching-Wen;
Yu, Mu-Hsien;
Chen, Yi-Jen;
Tsai, Eing-Mei;
Tsai, Shih-Feng;
Kuo, Wun-Syuan;
Tzeng, Chii-Ruey

Publication type:

Article

ALPK1 genetic regulation and risk in relation to gout.

Published in:

International Journal of Epidemiology, 2013, v. 42, n. 2, p. 466, doi. 10.1093/ije/dyt028

By:

Min-Shan Ko, Albert;
Tu, Hung-Pin;
Liu, Tze-Tze;
Chang, Jan-Gowth;
Yuo, Chung-Yee;
Chiang, Shang-Lun;
Chang, Shun-Jen;
Liu, Yu-Fan;
Min-Jen Ko, Allen;
Lee, Chien-Hung;
Lee, Chi-Pin;
Chang, Chung-Ming;
Tsai, Shih-Feng;
Ko, Ying-Chin

Publication type:

Article

A persistent level of Cisd2 extends healthy lifespan and delays aging in mice.

Published in:

Human Molecular Genetics, 2012, v. 21, n. 18, p. 3956, doi. 10.1093/hmg/dds210

By:

Wu, Chia-Yu;
Chen, Yi-Fan;
Wang, Chih-Hao;
Kao, Cheng-Heng;
Zhuang, Hui-Wen;
Chen, Chih-Cheng;
Chen, Liang-Kung;
Kirby, Ralph;
Wei, Yau-Huei;
Tsai, Shih-Feng;
Tsai, Ting-Fen

Publication type:

Article

EGFR Mutation-Harboring Lung Cancer Cells Produce CLEC11A with Endothelial Trophic and Tumor-Promoting Activities.

Published in:

Cancers, 2022, v. 14, n. 5, p. 1356, doi. 10.3390/cancers14051356

By:

Lin, Tzu-Yin;
Yang, Chi-Hwa;
Chou, Hsiao-Chin;
Cheng, Chun-Mei;
Liu, Ya-Wen;
Wang, Jiz-Yuh;
Huang, Li-Rung;
Tsai, Shih-Feng;
Huang, Shiu-Feng;
Chen, Yi-Rong

Publication type:

Article

Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).

Published in:

Journal of Biomedical Science, 2021, v. 28, n. 1, p. 1, doi. 10.1186/s12929-021-00763-1

By:

Chen, Huan-Yun;
Hsu, Chia-Lang;
Lin, Han-Yi;
Lin, Yung-Feng;
Tsai, Shih-Feng;
Ho, Yu-Jung;
Li, Ye-Ru;
Tsai, Jin-Wu;
Teng, Shu-Chun;
Lin, Chin-Hsien

Publication type:

Article

The signaling role of feedback in the repeated public goods game: Experimental evidence from the laboratory.

Published in:

PLoS ONE, 2024, v. 19, n. 2, p. 1, doi. 10.1371/journal.pone.0299196

By:

Liu, Chi-Hsiang;
Tsai, Shih-Feng;
Chen, Ting-Cih;
Cheng, Hsiu-Wen

Publication type:

Article

Protein O-fucosyltransferase-1 mutation in familial Dowling-Degos Disease concomitant with atopic dermatitis.

Published in:

Dermatologica Sinica, 2022, v. 40, n. 4, p. 251, doi. 10.4103/1027-8117.359341

By:

Wu, Ro-Wei;
Weng, Hui-Ying;
Huang, Wei-Ping;
Lin, Yung-Feng;
Liu, Yen-Ming;
Tsai, Shih-Feng;
Chang, Chung-Hsing

Publication type:

Article

MCP-1 as an Effector of IL-31 Signaling in Familial Primary Cutaneous Amyloidosis.

Published in:

Journal of Investigative Dermatology, 2013, v. 133, n. 5, p. 1375, doi. 10.1038/jid.2012.484

By:

Shiao, Yu-Ming;
Chung, Hsiang-Ju;
Chen, Chih-Chiang;
Chiang, Keng-Nan;
Chang, Yun-Ting;
Lee, Ding-Dar;
Lin, Ming-Wei;
Tsai, Shih-Feng;
Matsuura, Isao

Publication type:

Article

High-Throughput Sequencing of Complementarity Determining Region 3 in the Heavy Chain of B-Cell Receptor in Renal Transplant Recipients: A Preliminary Report.

Published in:

Journal of Clinical Medicine, 2022, v. 11, n. 11, p. 2980, doi. 10.3390/jcm11112980

By:

Wu, Tsai-Hung;
Liao, Hsien-Tzung;
Li, Tzu-Hao;
Tsai, Hung-Cheng;
Lin, Niang-Cheng;
Chen, Cheng-Yen;
Tsai, Shih-Feng;
Huang, Tzu-Hao;
Tsai, Chang-Youh;
Yu, Chia-Li

Publication type:

Article

Mutation of epidermal growth factor receptor is associated with MIG6 expression.

Published in:

FEBS Journal, 2009, v. 276, n. 18, p. 5239, doi. 10.1111/j.1742-4658.2009.07220.x

By:

Nagashima, Takeshi;
Ushikoshi-Nakayama, Ryoko;
Suenaga, Atsushi;
Ide, Kaori;
Yumoto, Noriko;
Naruo, Yoshimi;
Takahashi, Kaoru;
Saeki, Yuko;
Taiji, Makoto;
Tanaka, Hiroshi;
Tsai, Shih-Feng;
Hatakeyama, Mariko

Publication type:

Article

TPMD: a database and resources of microsatellite marker genotyped in Taiwanese populations.

Published in:

Nucleic Acids Research, 2005, v. 33, n. suppl 1, p. d174

By:

Chang, Ya-Hui;
Su, Wen-Hui;
Lee, Tso-Ching;
Sun, Hsiao-Fang Sunny;
Chen, Chia-Hsiang;
Pan, Wen-Harn;
Tsai, Shih-Feng;
Jou, Yuh-Shan

Publication type:

Article

Genomic shotgun array: a procedure linking large‐scale DNA sequencing with regional transcript mapping.

Published in:

Nucleic Acids Research, 2004, v. 32, n. 3, p. e27

By:

Li, Ling‐Hui;
Li, Jian‐Chiuan;
Lin, Yung‐Feng;
Lin, Chung‐Yen;
Chen, Chung‐Yung;
Tsai, Shih‐Feng

Publication type:

Article

Disclosing an In-Frame Deletion of the Titin Gene as the Possible Predisposing Factor of Anthracycline-Induced Cardiomyopathy: A Case Report.

Published in:

International Journal of Molecular Sciences, 2022, v. 23, n. 16, p. 9261, doi. 10.3390/ijms23169261

By:

Chang, Yu-Wei;
Weng, Hui-Ying;
Tsai, Shih-Feng;
Fan, Frank Sheng

Publication type:

Article

Complex Movement Disorders in a Boy with PURA Syndrome.

Published in:

Movement Disorders Clinical Practice, 2021, v. 8, n. 7, p. 1137, doi. 10.1002/mdc3.13272

By:

Lin, Shan‐Ju;
Lin, Yung‐Feng;
Tsai, Cheng‐Hsien;
Huang, Chiung‐Hui;
Ho, Fangyi;
Tsai, Shih‐Feng;
Lin, Wei‐Sheng

Publication type:

Article

Clinical Relevance of Plasma DNA Methylation in Colorectal Cancer Patients Identified by Using a Genome-Wide High-Resolution Array.

Published in:

Annals of Surgical Oncology: An Oncology Journal for Surgeons, 2015, v. 22, p. 1419, doi. 10.1245/s10434-014-4277-2

By:

Lin, Pei-Ching;
Lin, Jen-Kou;
Lin, Chien-Hsing;
Lin, Hung-Hsin;
Yang, Shung-Haur;
Jiang, Jeng-Kai;
Chen, Wei-Shone;
Chou, Chih-Chi;
Tsai, Shih-Feng;
Chang, Shih-Ching

Publication type:

Article

Digital health literacy and its determinants among community dwelling elderly people in Taiwan.

Published in:

Digital Health, 2024, p. 1, doi. 10.1177/20552076241278926

By:

Tran, Tu T.;
Chang, Peter WS;
Yang, Jenn-Ming;
Chen, Tso-Hsiao;
Su, Chien-Tien;
Levin-Zamir, Diane;
Baron-Epel, Orna;
Neter, Efrat;
Tsai, Shih Feng;
Lo, Bryan;
Duong, Tuyen V;
Yang, Shwu-Huey

Publication type:

Article

HBV DNA Integration into Telomerase or MLL4 Genes and TERT Promoter Point Mutation as Three Independent Signatures in Subgrouping HBV-Related HCC with Distinct Features.

Published in:

Liver Cancer (2235-1795), 2024, v. 13, n. 1, p. 41, doi. 10.1159/000530699

By:

Li, Chiao-Ling;
Hsu, Chia-Lang;
Lin, You-Yu;
Ho, Ming-Chih;
Chen, Chi-Ling;
Ho, Tung-Ching;
Lin, Yung-Feng;
Tsai, Shih-Feng;
Tzeng, Sheng-Tai;
Huang, Chin-Fang;
Wang, Ya-Chun;
Yeh, Shiou-Hwei;
Chen, Pei-Jer

Publication type:

Article

Works by Tsai, Shih-Feng

A Novel BTK Gene Mutation in a Child With Atypical X-Linked Agammaglobulinemia and Recurrent Hemophagocytosis: A Case Report.

Rare APOE p.Gly4Glu: A putative disease-causing variant for early-onset Alzheimer's disease identified by next-generation sequencing.

The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.

Chromosomal aberrations in nasopharyngeal carcinoma analyzed by comparative genomic hybridization.

Identification of the common regulators for hepatocellular carcinoma induced by hepatitis B virus X antigen in a mouse model.

Generation and Analysis of the Expressed Sequence Tags from the Mycelium of <i>Ganoderma lucidum</i>

Copy Number Change of the NDM-1 Sequence in a Multidrug-Resistant <i>Klebsiella pneumoniae</i> Clinical Isolate.

Resonance assignments of a CoA binding protein from Klebsiella pneumoniae.

Unraveling the complex genetic landscape of OTOF-related hearing loss: a deep dive into cryptic variants and haplotype phasing.

Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese.

Novel mutations involving the NF1 gene coding sequence in neurofibromatosis type 1 patients from Taiwan.

ARD1 Stabilization of TSC2 Suppresses Tumorigenesis Through the mTOR Signaling Pathway.

Selective Retention of an Inactive Allele of the DKK2 Tumor Suppressor Gene in Hepatocellular Carcinoma.

Qualitative and comparative proteomic analysis of Xanthomonas campestris pv. campestris 17.

Epigenetic Enhancement of the Post-replicative DNA Mismatch Repair of Mammalian Genomes by a Hemi-<sup>m</sup>CpG-Np95-Dnmt1 Axis.

Network Signatures of IgG Immune Repertoires in Hepatitis B Associated Chronic Infection and Vaccination Responses.

Next-Generation Integrated Sequencing Identifies Poor Prognostic Factors in Patients with MYD88-Mutated Chronic Lymphocytic Leukemia in Taiwan.

Genetic Heterogeneity of Familial Primary Cutaneous Amyloidosis: Lack of Evidence for Linkage with the Chromosome 10 Pericentromeric Region in Chinese Families.

Artificial-Intelligence-Assisted Discovery of Genetic Factors for Precision Medicine of Antiplatelet Therapy in Diabetic Peripheral Artery Disease.

Integration of genome-wide association study and expression quantitative trait locus mapping for identification of endometriosis-associated genes.

ALPK1 genetic regulation and risk in relation to gout.

A persistent level of Cisd2 extends healthy lifespan and delays aging in mice.

EGFR Mutation-Harboring Lung Cancer Cells Produce CLEC11A with Endothelial Trophic and Tumor-Promoting Activities.

Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).

The signaling role of feedback in the repeated public goods game: Experimental evidence from the laboratory.

Protein O-fucosyltransferase-1 mutation in familial Dowling-Degos Disease concomitant with atopic dermatitis.

MCP-1 as an Effector of IL-31 Signaling in Familial Primary Cutaneous Amyloidosis.

High-Throughput Sequencing of Complementarity Determining Region 3 in the Heavy Chain of B-Cell Receptor in Renal Transplant Recipients: A Preliminary Report.

Mutation of epidermal growth factor receptor is associated with MIG6 expression.

TPMD: a database and resources of microsatellite marker genotyped in Taiwanese populations.

Genomic shotgun array: a procedure linking large‐scale DNA sequencing with regional transcript mapping.

Disclosing an In-Frame Deletion of the Titin Gene as the Possible Predisposing Factor of Anthracycline-Induced Cardiomyopathy: A Case Report.

Complex Movement Disorders in a Boy with PURA Syndrome.

Clinical Relevance of Plasma DNA Methylation in Colorectal Cancer Patients Identified by Using a Genome-Wide High-Resolution Array.

Digital health literacy and its determinants among community dwelling elderly people in Taiwan.

HBV DNA Integration into Telomerase or MLL4 Genes and TERT Promoter Point Mutation as Three Independent Signatures in Subgrouping HBV-Related HCC with Distinct Features.