D. Chu

发表

The use of real-time quantitative polymerase chain reaction to detect hypermethylation of the CpG islands in the promoter region flanking the GSTP1 gene to diagnose prostate carcinoma.

C. Tseng, C. Chuang, D. Chu, 2002, The Journal of urology.

Maternal serum α-fetoprotein and dimeric inhibin A detect aneuploidies other than Down syndrome ☆ ☆☆ ★

K. Wenstrom, L. Boots, J. Owen, 1998 .

High-resolution melting analysis is a more effective approach for screening TSC genes mutations.

Shih-Cheng Chang, Chung-Ming Chang, Shuan-Pei Lin, 2011, Genetic testing and molecular biomarkers.

Real‐time quantitative PCR analysis for α‐thalassemia‐1 of Southeast Asian type deletion in Taiwan

K. Tsao, Tsu‐Lan Wu, D. Chu, 2001, Clinical genetics.

Prenatal diagnosis of alpha-thalassemia of Southeast Asian deletion with non-radioactive southern hybridization.

D. Chu, P. Cheng, Chien-Hong Lee, 2003, Chang Gung medical journal.

Hypermethylation of the CpG islands in the promoter region flanking GSTP1 gene is a potential plasma DNA biomarker for detecting prostate carcinoma.

C. Chuang, D. Chu, Chien‐Feng Sun, 2007, Cancer detection and prevention.

The Use of Real‐Time Quantitative PCR to Detect Circulating Prostate‐Specific Membrane Antigen mRNA in Patients with Prostate Carcinoma

C. Chuang, D. Chu, Chien‐Feng Sun, 2004, Annals of the New York Academy of Sciences.

Elevated maternal midtrimester serum free beta-human chorionic gonadotropin levels in vegetarian pregnancies that cause increased false-positive Down syndrome screening results.

L. See, D. Chu, P. Cheng, 2004, American journal of obstetrics and gynecology.

Non-radioactive Southern hybridization for early diagnosis of alpha-thalassemia with southeast Asian-type deletion in Taiwan.

K. Tsao, C. H. Lee, D. Chu, 2000, American journal of medical genetics.

Maternal serum alpha-fetoprotein and dimeric inhibin A detect aneuploidies other than Down syndrome.

L. Boots, J. Owen, D. Chu, 1998, American journal of obstetrics and gynecology.

Free β‐hCG Subunit Versus Intact hCG in Down Syndrome Screening

K. Wenstrom, L. Boots, J. Owen, 1997 .

Free beta-hCG subunit versus intact hCG in Down syndrome screening.

L. Boots, J. Owen, D. Chu, 1997, Obstetrics and gynecology.

Prospective evaluation of free beta-subunit of human chorionic gonadotropin and dimeric inhibin A for aneuploidy detection.

L. Boots, J. Owen, D. Chu, 1999, American journal of obstetrics and gynecology.

Novel mutations, including a novel G659A missense mutation, of the FUT1 gene are responsible for the para-Bombay phenotype.

C. H. Lee, D. Chu, C. F. Sun, 2000, Annals of clinical and laboratory science.

Three missense mutations, including a novel 860C>T transition, and allelic enhancement phenomenon associated with ABO blood subgroups A in Taiwan

Lei Li, K. Chak, D. Chu, 2007, Transfusion.

Human chromosome 21-specific DNA markers are useful in prenatal detection of Down syndrome.

D. Chu, P. Cheng, Shuenn-Dyh Chang, 2004, Annals of clinical and laboratory science.

A unique 502C>T mutation in exon 7 of ABO gene associated with the Bel phenotype in Taiwan

D. Chu, K. Lin, Pi-Hsiang Lin, 2003, Transfusion.

Lack of STK11 gene expression in homozygous twins with Peutz-Jeghers syndrome.

D. Chu, C. Tseng, P. Cheng, 2004, Annals of clinical and laboratory science.

Lack of STK 11 Gene Expression in Homozygous Twins with Peutz-Jeghers Syndrome

D. Chu, C. Tseng, P. Cheng, 2004 .

α-Fetoprotein, free β-human chorionic gonadotropin, and dimeric inhibin A produce the best results in a three-analyte, multiple-marker screening test for fetal Down syndrome

K. Wenstrom, L. Boots, J. Owen, 1997 .

pten suppression on rheb expression through inhibition of mtorc1 s6k1 dependent protein translation in prostate cancer cells

C. Chuang, D. Chu, Tz-Shiu Tsai, 2018 .

Elevated second-trimester dimeric inhibin A levels identify Down syndrome pregnancies.

L. Boots, J. Owen, D. Chu, 1997, American journal of obstetrics and gynecology.

Alpha‐fetoprotein, free beta‐human chorionic gonadotropin, and dimeric inhibin A produce the best results in a three‐analyte, multiple‐marker screening test for fetal Down syndrome

L. Boots, J. Owen, D. Chu, 1998, American Journal of Obstetrics and Gynecology.

Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor

D. Chu, M H Yang, L Li, 2011, Transfusion medicine.