Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Pei Tee Huan"'
Publikováno v:
The Journal of Molecular Diagnostics. 24:655-665
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2d0b2674fc301165924b9c2beb9658b
https://doi.org/10.1016/j.jmoldx.2022.03.004
https://doi.org/10.1016/j.jmoldx.2022.03.004
Autor:
Yi, Lu, Zhenhua, Li, Evelyn Huizi, Lim, Pei Tee, Huan, Shirley Kow Yin, Kham, Allen Eng-Juh, Yeoh
Publikováno v:
The Journal of molecular diagnostics : JMD. 24(6)
In minimal residual disease (MRD), where there are exceedingly low target copy numbers, digital PCR (dPCR) can improve MRD quantitation. However, standards for dPCR MRD interpretation in acute lymphoblastic leukemia are lacking. Here, for immunoglobu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bc03bff7a4a6a5feef59715f62922fce
https://pubmed.ncbi.nlm.nih.gov/35390515
https://pubmed.ncbi.nlm.nih.gov/35390515
Rapid prenatal diagnosis of common beta-thalassemia mutations in Southeast Asia using pyrosequencing
Autor:
Gek Har Leow, Evelyn Siew-Chuan Koay, Leng Kee Ching, Sherry Sze Yee Ho, Lily Chiu, Hai Yang Law, Pei Tee Huan
Publikováno v:
Prenatal Diagnosis. 33:1017-1022
Objective Current methods of prenatal diagnosis to detect beta-thalassemia are Sanger sequencing and reverse dot blot. These methods are time-consuming and can prolong assay turnaround time. We aim to develop a sensitive and rapid method to detect 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3159af118c74cb22f4365228e17e01b7
https://doi.org/10.1002/pd.4183
https://doi.org/10.1002/pd.4183
Autor:
Tin Wee Tan, Lily Chiu, Chin Hin Ng, Wee Joo Chng, Pei Tee Huan, Peak-Ling Lee, Evelyn Siew-Chuan Koay, Kenneth Ban, Yongli Hu, Benedict Yan, Elaine Seah, Christopher Ng
Publikováno v:
Journal of clinical pathology. 69(9)
AimsPCR amplicon-based next-generation sequencing (NGS) panels are increasingly used for clinical diagnostic assays. Amplification bias is a well-known limitation of PCR amplicon-based approaches. We sought to characterise lower-performance amplicons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f2a3224554178a7f1ae7b47400b9969
https://pubmed.ncbi.nlm.nih.gov/26896490
https://pubmed.ncbi.nlm.nih.gov/26896490
Publikováno v:
Clinical chemistry and laboratory medicine. 54(10)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83603e8ba409c375f01cf2713f959eb0
https://pubmed.ncbi.nlm.nih.gov/26974142
https://pubmed.ncbi.nlm.nih.gov/26974142
Rapid prenatal diagnosis of common beta-thalassemia mutations in Southeast Asia using pyrosequencing
Autor:
Sherry Sze Yee, Ho, Pei Tee, Huan, Gek Har, Leow, Leng Kee, Ching, Lily, Chiu, Hai Yang, Law, Evelyn S C, Koay
Publikováno v:
Prenatal diagnosis. 33(11)
Current methods of prenatal diagnosis to detect beta-thalassemia are Sanger sequencing and reverse dot blot. These methods are time-consuming and can prolong assay turnaround time. We aim to develop a sensitive and rapid method to detect 27 beta-thal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::cddd4805d666b9a7520ce104c399070f
https://pubmed.ncbi.nlm.nih.gov/23794144
https://pubmed.ncbi.nlm.nih.gov/23794144
Autor:
Pei-Tee Huan, E-Shyong Tai, Agus Salim, Huay-Cheem Tan, Mark Y. Chan, Bei Li, Richard C. Becker, Karen Tan, Mark Richards, Qian-Hui Phua, Wen-Chong Ong, Evelyn Siew-Chuan Koay, Adrian F. Low, H. Lee, Chi-Hang Lee
Publikováno v:
Pharmacogenomics. 13(5)
Aim, materials & methods: We investigated the functional significance of CYP2C19*2, *3, *17 and PON1 Q192R SNPs in 89 consecutive Asian patients on clopidogrel treatment and the prevalence of functionally significant polymorphisms among 300 Chinese,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dd19b37c16e52e8727de4a09374fa93
https://pubmed.ncbi.nlm.nih.gov/22462746
https://pubmed.ncbi.nlm.nih.gov/22462746
Autor:
Evelyn Siew-Chuan Koay, Chun Kiat Lee, Lily-Lily Chiu, H. Lee, Tze Ping Loh, Soon Tee Wong, Pei Tee Huan
Publikováno v:
Drug metabolism and pharmacokinetics. 27(5)
Summary: A 62-year-old Chinese patient with recurrent pompholyx submitted his blood sample for pre-treatment thiopurine S-methyltransferase (TPMT) pharmacogenetic profiling, and it was found to harbour a novel single nucleotide polymorphism (SNP). Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9da2e57e7e3b35d34d13a432bbf005dd
https://pubmed.ncbi.nlm.nih.gov/22447118
https://pubmed.ncbi.nlm.nih.gov/22447118
Autor:
Benedict Yan, Yongli Hu, Christopher Ng, Ban, Kenneth H. K., Tin Wee Tan, Pei Tee Huan, Peak-Ling Lee, Lily Chiu, Elaine Seah, Chin Hin Ng, Evelyn Siew-Chuan Koay, Wee-Joo Chng
Publikováno v:
Journal of Clinical Pathology; Sep2016, Vol. 69 Issue 9, p801-804, 4p, 1 Chart, 3 Graphs
Autor:
Chan, Mark Y., Tan, Karen, Huay-Cheem Tan, Pei-Tee Huan, Bei Li, Qian-Hui Phua, Hong-Kai Lee, Chi-Hang Lee, Low, Adrian, Becker, Richard C., Wen-Chong Ong, Richards, Mark A., Salim, Agus, E-Shyong Tai, Koay, Evelyn
Publikováno v:
Pharmacogenomics; Apr2012, Vol. 13 Issue 5, p533-542, 10p