Bilirubin metabolism and UDP‐glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response von Huang, May‐Jen, Chen, Pei‐Lain, Huang, Ching‐Shan

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Effect of UDP‐glucuronosyltransferase 1A1 activity on risk for developing Gilbert's syndrome von Huang, May‐Jen, Chen, Yi‐Chun, Huang, Yang‐Yang, Yang, Sien‐Sing, Chen, Pei‐Lain, Huang, Ching‐Shan

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Effects of variation status and enzyme activity for UDP-glucuronosyltransferase 1A1 gene on neonatal hyperbilirubinemia von Huang, May-Jen, Lin, Yu-Cheng, Liu, Kevin, Chang, Pi-Feng, Huang, Ching-Shan

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Analysis of double-stranded DNA by microchip capillary electrophoresis using polymer solutions containing gold nanoparticles von Lin, Yang-Wei, Huang, May-Jen, Chang, Huan-Tsung

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Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia von Huang, Ching–Shan, Huang, May–Jen, Chen, En–Sung, Chang, Pi–Feng, Chen, Wu–Charng

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Bilirubin concentrations in thalassemia heterozygotes in university students von Huang, Yang-Yang, Huang, May-Jen, Wang, Hai-Lung, Chan, Cung-Cuan, Huang, Ching-Shan

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Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia von HUANG, Ching-Shan, CHANG, Pi-Feng, HUANG, May-Jen, CHEN, En-Sung, HUNG, Kun-Long, TSOU, Kuo-Inn

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Risk factors for severe hyperbilirubinemia in neonates von Huang, May-Jen, Kua, Ka-Em, Teng, Hsiu-Chen, Tang, Kung-Sheng, Weng, Hui-Wen, Huang, Ching-Shan

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Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis von Huang, Yang-Yang, Huang, Ching-Shui, Yang, Sien-Sing, Lin, Min-Shung, Huang, May-Jen, Huang, Ching-Shan

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Polymorphisms of uridine-diphosphoglucuronosyltransferase 1A7 gene in Taiwan Chinese von Huang, May-Jen, Yang, Sien-Sing, Lin, Min-Shung, Huang, Ching-Shan

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Crigler-Najjar Syndrome Type 2 von Huang, Ching-Shan, Tan, Nancy, Yang, Sien-Sing, Sung, Yung-Chan, Huang, May-Jen

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Genetic factors related to unconjugated hyperbilirubinemia amongst adults von Huang, Ching-Shan, Huang, May-Jen, Lin, Min-Shung, Yang, Sien-Sing, Teng, Hsiu-Chen, Tang, Kung-Sheng

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Neonatal jaundice and molecular mutations in glucose‐6‐phosphate dehydrogenase deficient newborn infants von Huang, Ching‐Shan, Hung, Kun‐Long, Huang, May‐Jen, Li, Yi‐Ching, Liu, Te‐Hui, Tang, Tang K.

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UDP-glucuronosyltransferase 1A7 polymorphisms are associated with liver cirrhosis von Tang, Kung-Sheng, Lee, Chuan-Mo, Teng, Hsiu-Chen, Huang, May-Jen, Huang, Ching-Shan

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Multiple variants in UGT1A1 gene are factors to develop indirect hyper-bilirubinemia von Hu, Rei-Ting, Wang, Nai-Yuan, Huang, May-Jen, Huang, Ching-Shan, Chen, Ding-Shinn, Yang, Sien-Sing

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Diverse Point Mutations Result in Glucose-6-Phosphate Dehydrogenase (G6PD) Polymorphism in Taiwan von Tang, Tang K., Huang, Ching-Shan, Huang, May-Jen, Tam, Ka-Bik, Yeh, Chiao-Hwa, Tang, Chieh-Ju C.

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Content of reduced glutathione and consequences in recipients of glucose‐6‐phosphate dehydrogenase deficient red blood cells von Huang, Ching‐Shan, Sung, Yung‐Chan, Huang, May‐Jen, Yang, Chung‐Shi, Shei, Wei‐Shang, Tang, Tang K.

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Crigler-Najjar Syndrome Type 2 von Huang, Ching-Shan, Tan, Nancy, Yang, Sien-Sing, Sung, Yung-Chan, Huang, May-Jen

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G6PD NanKang (517 T→C; 173 Phe→Leu): A New Chinese G6PD Variant Associated with Neonatal Jaundice von Chen, Hua-Ling, Huang, May-Jen, Huang, Ching-Shan, Tang, Tang K.

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Bilirubin concentrations in thalassemia heterozygotes in university students: Bilirubin and thalassemia heterozygotes von Huang, Yang-Yang, Huang, May-Jen, Wang, Hai-Lung, Chan, Cung-Cuan, Huang, Ching-Shan

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