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Article
Bilateral thermal capsulotomy with MR-guided focused ultrasound for patients with treatment-refractory obsessive-compulsive disorder: a proof-of-concept study
Despite optimal pharmacotherapy and cognitive-behavioral treatments, a proportion of patients with obsessive-compulsive disorder (OCD) remain refractory to treatment. Neurosurgical ablative or nondestructive s...
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Article
Induction of CD45 expression on bone marrow-derived mesenchymal stem cells
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Article
Mesenchymal stem cells can be easily isolated from bone marrow of patients with various haematological malignancies but the surface antigens expression may be changed after prolonged ex vivo culture
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Article
Molecular basis of weak D in Taiwanese
Two genes, RHD and RHCE, encode the antigens of the RH blood group system. The weak D phenotype is caused by many different RHD alleles encoding aberrant RhD proteins, resulting in distinct serologic phenotype...
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Article
Association between apolipoprotein E genotype and outcome of traumatic brain injury
¶Background. The prognosis of traumatic brain injury is quite variable and not fully explained by the known factors. This study is to examine if the polymorphism of apolipoprotein E (apoE) influences the outcome ...
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Article
Molecular characterization of deletional forms of β-thalassemia in Taiwan
β-Thalassemia is one of the most common genetic diseases in Taiwan. The most common mutations of β-globin are point mutations, and six mutations account for over 90% of cases. Less than 5% of the cases with β...
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Article
Molecular analysis of mutations and polymorphisms of the Lewis secretor type α(1,2)-fucosyltransferase gene reveals that Taiwan aborigines are of Austronesian derivation
The origins of the Taiwan aborigines have not been fully resolved. Anthropological and linguistic studies have indicated that their ancestry is mainly Austronesian or Malayopolynesian. Some polymorphisms and ...
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Article
Lewis (FUT3) genotypes in Taiwanese, Thai, and Filipino populations
The Lewis (Le) blood type comprises two major antigens, Lea and Leb, which are encoded by α (1,2)-fucosyltransferase (FUT2) and α (1,3/1,4)-fucosyltransferase (FUT3). In this study, we analyzed the mutations of ...
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Article
Molecular characterization of secretor type α(1,2)-fucosyltransferase gene deficiency in the Philippine population
We analyzed the seven mutations which are responsible for the deficiency of the secretor type α(1,2)-fucosyltransferase gene product, Se enzyme, in the Philippine population. One hundred and one unrelated Fil...
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Article
Open AccessAnalysis of TSG101 tumour susceptibility gene transcripts in cervical and endometrial cancers
Carcinoma of the uterine cervix is a common malignancy among women that has been found to show loss of heterozygosity in the chromosome 11p. Recent studies have localized the TSG101 gene in this region, and also ...
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Article
Aberrant FHIT transcripts in hepatocellular carcinomas
To study abnormalities of the FHIT gene in human hepatocellular carcinoma (HCC), eight liver cancer cell lines, 18 matched tumorous and non-tumorous tissues from patients with HCC and three normal liver tissue...
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Article
Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents
We have assayed deletions of two candidate genes for spinal muscular atrophy (SMA), the survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes, in 101 patients from 86 Chinese SMA ...
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Article
Rapid detection of hemoglobin variants by mutagenically separate polymerase chain reaction (MS-PCR)
The detection of molecular defects of hemoglobin variants using mutagenically separated polymerase chain reaction (MS-PCR) was applied in this study. Using different lengths of allele-specific mutagenic primer...
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Article
Rapid detection of −α 4.2 deletion of α-thalassemia-2 by polymerase chain reaction
We sequenced part of the X boxes ofα-thalassemia-1 of Southeast Asia type (- -SEA) with−α 4.2,−α 3.7,−α G-Taichung, andα CSα. We found the X box of−α 3.7 belonged to the X box of α2 globin gene and the X box ofα
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Article
Rapid molecular characterization of Hb H disease in Chinese by polymerase chain reaction
We have developed a rapid method to molecularly distinguish different types of Hb H disease. The study depended on (a) most of the Hb H disease in Taiwan having anα-thalassemia-1 of the Southeast Asia type (-SEA)...