Search Results - "Chao, T H"

Etiology of a genetically complex seizure disorder in Celf4 mutant mice by Wagnon, J. L., Mahaffey, C. L., Sun, W., Yang, Y., Chao, H.‐T., Frankel, W. N.

“…Mice deficient for the gene encoding the RNA‐binding protein CELF4 (CUGBP, ELAV‐like family member 4) have a complex seizure phenotype that includes both…”
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Effects of estrogen on cognition, mood, and cerebral blood flow in AD: a controlled study by Wang, P N, Liao, S Q, Liu, R S, Liu, C Y, Chao, H T, Lu, S R, Yu, H Y, Wang, S J, Liu, H C

“…To examine the effects of estrogen therapy on cognition, mood, and cerebral blood flow in patients with AD. Some studies have suggested estrogen may be…”
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Platelet‐activating factor‐acetylhydrolase A379V (exon 11) gene polymorphism is an independent and functional risk factor for premature myocardial infarction by LIU, P.‐Y., LI, Y.‐H., WU, H.‐L., CHAO, T.‐H., TSAI, L.‐M., LIN, L.‐J., SHI, G.‐Y., CHEN, J.‐H.

“…Background: Oxidation of low density lipoproteins is an initial step of atherogenesis that generates pro‐inflammatory phospholipids, including…”
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Mitochondrial deoxyribonucleic acid 4977-bp deletion is associated with diminished fertility and motility of human sperm by Kao, S, Chao, H T, Wei, Y H

“…The accumulation of mitochondrial DNA (mtDNA) mutations has been suggested to be an important contributor to human aging and degenerative diseases. In previous…”
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Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa by KAO, S.-H, CHAO, H.-T, WEI, Y.-H

“…Sperm motility is one of the major determinants of male fertility and is required for successful fertilization. In a previous study, we demonstrated that the…”
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Direct molecular diagnosis of CYP21 mutations in congenital adrenal hyperplasia by Lee, H H, Chao, H T, Ng, H T, Choo, K B

“…The majority of congenital adrenal hyperplasia (CAH) cases arise from mutations in the steroid 21-hydroxylase (CYP21) gene. Without reliance on HLA gene…”
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Stromelysin‐1 promoter 5A/6A polymorphism is an independent genetic prognostic risk factor and interacts with smoking cessation after index premature myocardial infarction by LIU, P.‐Y., LI, Y.‐H., TSAI, W.‐C., TSAI, L.‐M., CHAO, T.‐H., WU, H.‐L., CHEN, J.‐H.

“…Objective: To evaluate the prognostic roles of multiple polymorphisms and smoking cessation for premature myocardial infarction (MI). Methods: We studied 170…”
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Risk Factors Contributing to Early Occurrence of Port Site Metastases of Laparoscopic Surgery for Malignancy by Wang, Peng-Hui, Yuan, Chiou-Chung, Lin, Grace, Ng, Heung-Tat, Chao, Hsiang-Tai

“…In this article, the authors present an up-to-date review of our experience and that of the medical literature encompassing all important aspects of port site…”
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High prevalence of incidental brain findings in primary dysmenorrhoea by Li, W.C., Tu, C.H., Chao, H.T., Yeh, T.C., Chen, L.F., Hsieh, J.C.

“…Background Primary dysmenorrhoea (PDM) is inexorably common. PDM women suffer from cramping pain in the lower abdomen that starts with menstruation and lasts…”
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Role of BMK1 in regulation of growth factor-induced cellular responses by Kato, Y, Chao, T H, Hayashi, M, Tapping, R I, Lee, J D

“…Big mitogen-activated protein kinase (MAPK) 1 (BMK1), also known as ERK5, is a recently identified member of the mammalian MAPK family. Cellular stimulation of…”
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Port Site Metastasis after Laparoscopic-Assisted Vaginal Hysterectomy for Endometrial Cancer: Possible Mechanisms and Prevention by Wang, Peng-Hui, Yen, Ming-Shyen, Yuan, Chiou-Chung, Chao, Kuan-Chong, Ng, Heung-Tat, Lee, Wen-Ling, Chao, Hsiang-Tai

“…Only 19 cases of metastases at the cannula insertion site after laparoscopy for gynecological malignancy have been reported in the literature. One case has…”
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Gonadotropin-releasing hormone-agonist as a neoadjuvant therapy for Sertoli–Leydig cell tumors of the ovary by Chao, H.T., Wang, P.H., Lin, H.D.

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G-33a mutation in the promoter region of thrombomodulin gene and its association with coronary artery disease and plasma soluble thrombomodulin levels by Li, Yi-Heng, Chen, Jyh-Hong, Wu, Hua-Lin, Shi, Guey-Yueh, Huang, Huey-Chun, Chao, Ting-Hsing, Tsai, Wei-Chuan, Tsai, Liang-Miin, Guo, How-Ran, Wu, Wen-Shiann, Chen, Zhih-Cherng

“…Thrombomodulin is an endothelial glycoprotein that decreases thrombin activity and activates protein C. A recent study has shown that G-33A promoter mutation…”
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Structure−Activity Relationship Studies of Salinosporamide A (NPI-0052), a Novel Marine Derived Proteasome Inhibitor by Macherla, Venkat R, Mitchell, Scott S, Manam, Rama Rao, Reed, Katherine A, Chao, Ta-Hsiang, Nicholson, Benjamin, Deyanat-Yazdi, Gordafaried, Mai, Bao, Jensen, Paul R, Fenical, William F, Neuteboom, Saskia T. C, Lam, Kin S, Palladino, Michael A, Potts, Barbara C. M

“…Salinosporamide A (1, NPI-0052) is a potent proteasome inhibitor in development for treating cancer. In this study, a series of analogues was assayed for…”
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Identification of four novel mutations in the CYP21 gene in congenital adrenal hyperplasia in the Chinese by LEE, H.-H, CHAO, H.-T, LEE, Y.-J, SHU, S.-G, CHAO, M.-C, KUO, J.-M, CHUNG, B.-C

“…Congenital adrenal hyperplasia (CAH) is a common autosomal recessive disorder mainly caused by defects in the steroid 21-hydroxylase (CYP21) gene. We have…”
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A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib by Chauhan, Dharminder, Catley, Laurence, Li, Guilan, Podar, Klaus, Hideshima, Teru, Velankar, Mugdha, Mitsiades, Constantine, Mitsiades, Nicolas, Yasui, Hiroshi, Letai, Anthony, Ovaa, Huib, Berkers, Celia, Nicholson, Benjamin, Chao, Ta-Hsiang, Neuteboom, Saskia T.C., Richardson, Paul, Palladino, Michael A., Anderson, Kenneth C.

“…Bortezomib therapy has proven successful for the treatment of relapsed and/or refractory multiple myeloma (MM); however, prolonged treatment is associated with…”
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Carrier analysis and prenatal diagnosis of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in Chinese by LEE, H.-H, KUO, J.-M, CHAO, H.-T, LEE, Y.-J, CHANG, J.-G, TSAI, C.-H, CHUNG, B.-C

“…Congenital adrenal hyperplasia (CAH) is a common autosomal recessive disorder mainly caused by defects in the steroid 21-hydroxylase (CYP21) gene. We screened…”
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Use of a long-acting gonadotropin-releasing hormone agonist for treatment of steroid cell tumors of the ovary by Wang, P H, Chao, H T, Lee, W L

“…To report a complete serologic response in a 50-year-old women who received long-acting gonadotropin-releasing hormone agonist (GnRH-A) therapy for steroid…”
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Association Between FRAX Without BMD and Incidence of Falls in Middle-Aged and Old People: An Epidemiological Cohort Survey by Ou, L.-C, Chang, Y.-F, Chang, C.-S, Chiu, C.-J, Chao, T.-H, Lin, R.-M, Sun, Z.-J, Wu, C.-H

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Analysis of the Chimeric CYP21P/CYP21 Gene in Steroid 21-Hydroxylase Deficiency by Lee, Hsien-Hsiung, Chang, Jan-Gowth, Tsai, Chang-Hai, Tsai, Fuu-Jen, Chao, Hsiang-Tai, Chung, Bon-chu

“…A single nonfunctional chimeric gene with its 5' and 3' ends corresponding to CYP21P and CYP21, respectively, is caused by unequal gene crossover in the CYP21…”
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