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Lung-Chih Yu

Research Profile

Genes & Molecular Sequences

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Taiwan

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Publications

TOP 3
Yuh-Ching Twu; Chuang-Yi Hsieh; Marie Lin; Cheng-Hwai Tzeng; Chien-Feng Sun; Lung-Chih Yu
Phosphorylation status of transcription factor C/EBPalpha determines cell-surface poly-LacNAc branching (I antigen) formation in erythropoiesis and granulopoiesis.
Marie Lin; Lung-Chih Yu
Frequencies of the JKnull (IVS5-1g>a) allele in Taiwanese, Fujian, Filipino, and Indonesian populations.
Yao-Yun Fan; Shin-Yi Yu; Hiromi Ito; Akihiko Kameyama; Takashi Sato; Chi-Hung Lin; Lung-Chih Yu; Hisashi Narimatsu; Kay-Hooi Khoo
Identification of further elongation and branching of dimeric type 1 chain on lactosylceramides from colonic adenocarcinoma by tandem mass spectrometry sequencing analyses.

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All Publications

2010: Yuh-Ching Twu; Chuang-Yi Hsieh; Marie Lin; Cheng-Hwai Tzeng; Chien-Feng Sun; Lung-Chih Yu
Phosphorylation status of transcription factor C/EBPalpha determines cell-surface poly-LacNAc branching (I antigen) formation in erythropoiesis and granulopoiesis.
Blood 2010;115(12):2491-9.
2008: Marie Lin; Lung-Chih Yu
Frequencies of the JKnull (IVS5-1g>a) allele in Taiwanese, Fujian, Filipino, and Indonesian populations.
Transfusion 2008;48(8):1768.
2008: Yao-Yun Fan; Shin-Yi Yu; Hiromi Ito; Akihiko Kameyama; Takashi Sato; Chi-Hung Lin; Lung-Chih Yu; Hisashi Narimatsu; Kay-Hooi Khoo
Identification of further elongation and branching of dimeric type 1 chain on lactosylceramides from colonic adenocarcinoma by tandem mass spectrometry sequencing analyses.
The Journal of biological chemistry 2008;283(24):16455-68.
2008: Hou-Ren Wang; Chuang-Yi Hsieh; Yuh-Ching Twu; Lung-Chih Yu
Expression of the human Sd(a) beta-1,4-N-acetylgalactosaminyltransferase II gene is dependent on the promoter methylation status.
Glycobiology 2008;18(1):104-13.
2007: Yuh-Ching Twu; Chie-Pein Chen; Chuang-Yi Hsieh; Cheng-Hwai Tzeng; Chien-Feng Sun; Shih-Hsin Wang; Mau-Sun Chang; Lung-Chih Yu
I branching formation in erythroid differentiation is regulated by transcription factor C/EBPalpha.
Blood 2007;110(13):4526-34.
2006: Yuh-Ching Twu; Chuang-Yi Hsieh; Lung-Chih Yu
Expression of the histo-blood group B gene predominates in AB-genotype cells.
Transfusion 2006;46(11):1988-96.
2006: Marie Lin; Min-Ju Hou; Lung-Chih Yu
A novel IGnT allele responsible for the adult i phenotype.
Transfusion 2006;46(11):1982-7.
2006: Po-Chen Chu; Yuh-Cheng Yang; Yen-Ta Lu; Hsiang-Ting Chen; Lung-Chih Yu; Mau-Sun Chang
Silencing of p29 affects DNA damage responses with UV irradiation.
Cancer research 2006;66(17):8484-91.
2005: Marie Lin; Min-Ju Hou; Yuh-Ching Twu; Lung-Chih Yu
A novel A allele with 664G>A mutation identified in a family with the Am phenotype.
Transfusion 2005;45(1):63-9.
2003: Chien-Feng Sun; Ding-Ping Chen; Kuan-Tsou Lin; Wei-Ting Wang; Y-C Wang; Lung-Chih Yu
Molecular genetic analysis of the Bel phenotype.
Vox sanguinis 2003;85(3):216-20.
2003: Chien-Feng Sun; Lung-Chih Yu; Ing-Ping Chen; Ding-Lun Chou; Yuh-Ching Twu; Wei-Ting Wang; Marie Lin
Molecular genetic analysis for the Ae1 and A3 alleles.
Transfusion 2003;43(8):1138-44.
2003: Yuh-Ching Twu; Ming-Lun Chou; Lung-Chih Yu
The molecular genetics of the mouse I beta-1,6-N-acetylglucosaminyltransferase locus.
Biochemical and biophysical research communications 2003;303(3):868-76.
2003: Lung-Chih Yu; Yuh-Ching Twu; Ming-Lun Chou; Marion E Reid; Alan R Gray; Joann M Moulds; Ching-Yi Chang; Marie Lin
The molecular genetics of the human I locus and molecular background explain the partial association of the adult i phenotype with congenital cataracts.
Blood 2003;101(6):2081-8.
2002: Lung-Chih Yu; Yuh-Ching Twu; Ming-Lun Chou; Ching-Yi Chang; Chia-Ying Wu; Marie Lin
Molecular genetic analysis for the B(3) allele.
Blood 2002;100(4):1490-2.
2001: Lung-Chih Yu; Yuh-Ching Twu; Ching-Yi Chang; Marie Lin
Molecular basis of the adult i phenotype and the gene responsible for the expression of the human blood group I antigen.
Blood 2001;98(13):3840-5.
2001: Lung-Chih Yu; Chen-Chung Chu; Y S Chan; Ching-Yi Chang; Yuh-Ching Twu; Hui-Lin Lee; Marie Lin
Polymorphism and distribution of the Secretor alpha(1,2)-fucosyltransferase gene in various Taiwanese populations.
Transfusion 2001;41(10):1279-84.
2001: Lung-Chih Yu; Yuh-Ching Twu; Ching-Yi Chang; Marie Lin
Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens.
The Journal of biological chemistry 2001;276(13):10247-52.
2000: Lung-Chih Yu; Ching-Yi Chang; Yuh-Ching Twu; Marie Lin
Human histo-blood group ABO glycosyltransferase genes: different enhancer structures with different transcriptional activities.
Biochemical and biophysical research communications 2000;273(2):459-66.
1999: Lung-Chih Yu; Hui-Lin Lee; Y S Chan; Marie Lin
The molecular basis for the B(A) allele: an amino acid alteration in the human histoblood group B alpha-(1,3)-galactosyltransferase increases its intrinsic alpha-(1,3)-N-acetylgalactosaminyltransferase activity.
Biochemical and biophysical research communications 1999;262(2):487-93.
1999: Lung-Chih Yu; Hui-Lin Lee; Chen-Chung Chu; RE Broadberry; Marie Lin
A newly identified nonsecretor allele of the human histo-blood group alpha(1,2)fucosyltransferase gene (FUT2).
Vox sanguinis 1999;76(2):115-9.
1997: Lung-Chih Yu; Y L Hsiao; Y H Yang; Marie Lin; Y H Chen
The genomic structure of a mouse seminal vesicle autoantigen.
Biochemical and biophysical research communications 1997;231(1):106-10.
1997: Lung-Chih Yu; Y H Yang; RE Broadberry; Y H Chen; Marie Lin
Heterogeneity of the human H blood group alpha(1,2)fucosyltransferase gene among para-Bombay individuals.
Vox sanguinis 1997;72(1):36-40.
1996: Lung-Chih Yu; RE Broadberry; Y H Yang; Y H Chen; Marie Lin
Heterogeneity of the human Secretor alpha(1,2)fucosyltransferase gene among Lewis(a+b-) non-secretors.
Biochemical and biophysical research communications 1996;222(2):390-4.
1995: Lung-Chih Yu; Y H Yang; RE Broadberry; Y H Chen; Y S Chan; Marie Lin
Correlation of a missense mutation in the human Secretor alpha 1,2-fucosyltransferase gene with the Lewis(a+b+) phenotype: a potential molecular basis for the weak Secretor allele (Sew).
The Biochemical journal 1995;312 ( Pt 2)():329-32.