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Fertility and Sterility
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March 8, 2005
Estrogen receptor alpha dinucleotide repeat and cytochrome P450c17alpha gene polymorphisms are associated with susceptibility to endometriosis
Yao-Yuan Hsieh, Chi-Chen Chang, Fuu-Jen Tsai, et al.
Endocrine
|
February 16, 2005
Association between the TAP1 gene codon 637 polymorphism and Graves' disease
Rong-Hsing Chen, Wen-Chi Chen, Ching-Chu Chen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 3, 2011
Association study in Taiwanese girls with precocious puberty
I-Ching Chou, Chung-Hsing Wang, Wei-De Lin, et al.
Journal of Proteome Research
|
September 29, 2018
Identification of Urinary Metabolite Biomarkers of Type 2 Diabetes Nephropathy Using an Untargeted Metabolomic Approach
Chao-Jung Chen, Wen-Ling Liao, Chiz-Tzung Chang, et al.
Plos One
|
July 20, 2018
Urine proteome analysis by C18 plate-matrix-assisted laser desorption/ionization time-of-flight mass spectrometry allows noninvasive differential diagnosis and prediction of diabetic nephropathy
Chao-Jung Chen, Wen-Ling Liao, Chiz-Tzung Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
August 1, 2002
Monosomy of chromosome 10q26 with mild psychomotor retardation: report of one case
Kang-Hsi Wu, Ming-Tsung Yu, Fuu-Jen Tsai, et al.
Urologic Oncology
|
December 12, 2002
p21 gene codon 31 polymorphism is associated with bladder cancer
Wen-Chi Chen, Hsi-Chin Wu, Cheng-Der Hsu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
November 21, 2002
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers
Wei-De Lin, Jer-Yuarn Wu, Fuu-Jen Tsai, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 6, 2003
Mutation of IVS2 -12A/C>G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency
Hsien-Hsiung Lee, Shwu-Fen Chang, Fuu-Jen Tsai, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
August 20, 2004
Genetic and biochemical study in a patient with glutaric acidemia type I
Wei-De Lin, Chung-Hsing Wang, Chien-Chen Lai, et al.
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of 87
Search research articles
Search
Showing results (71-80 of 862) with videos related to
Sort By:
Page
of 87
Fertility and Sterility
|
March 8, 2005
Estrogen receptor alpha dinucleotide repeat and cytochrome P450c17alpha gene polymorphisms are associated with susceptibility to endometriosis
Yao-Yuan Hsieh, Chi-Chen Chang, Fuu-Jen Tsai, et al.
Endocrine
|
February 16, 2005
Association between the TAP1 gene codon 637 polymorphism and Graves' disease
Rong-Hsing Chen, Wen-Chi Chen, Ching-Chu Chen, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
May 3, 2011
Association study in Taiwanese girls with precocious puberty
I-Ching Chou, Chung-Hsing Wang, Wei-De Lin, et al.
Journal of Proteome Research
|
September 29, 2018
Identification of Urinary Metabolite Biomarkers of Type 2 Diabetes Nephropathy Using an Untargeted Metabolomic Approach
Chao-Jung Chen, Wen-Ling Liao, Chiz-Tzung Chang, et al.
Plos One
|
July 20, 2018
Urine proteome analysis by C18 plate-matrix-assisted laser desorption/ionization time-of-flight mass spectrometry allows noninvasive differential diagnosis and prediction of diabetic nephropathy
Chao-Jung Chen, Wen-Ling Liao, Chiz-Tzung Chang, et al.
Acta Paediatrica Taiwanica = Taiwan Er Ke Yi Xue Hui Za Zhi
|
August 1, 2002
Monosomy of chromosome 10q26 with mild psychomotor retardation: report of one case
Kang-Hsi Wu, Ming-Tsung Yu, Fuu-Jen Tsai, et al.
Urologic Oncology
|
December 12, 2002
p21 gene codon 31 polymorphism is associated with bladder cancer
Wen-Chi Chen, Hsi-Chin Wu, Cheng-Der Hsu, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
November 21, 2002
Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers
Wei-De Lin, Jer-Yuarn Wu, Fuu-Jen Tsai, et al.
The Journal of Clinical Endocrinology and Metabolism
|
June 6, 2003
Mutation of IVS2 -12A/C>G in combination with 707-714delGAGACTAC in the CYP21 gene is caused by deletion of the C4-CYP21 repeat module with steroid 21-hydroxylase deficiency
Hsien-Hsiung Lee, Shwu-Fen Chang, Fuu-Jen Tsai, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi
|
August 20, 2004
Genetic and biochemical study in a patient with glutaric acidemia type I
Wei-De Lin, Chung-Hsing Wang, Chien-Chen Lai, et al.
Page
of 87