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Tjin-Shing Jap

Showing results (11-20 of 32) with videos related to

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Journal of Cellular Biochemistry|January 26, 2005
Insulin-like growth factor-1 increases endothelin receptor A levels and action in cultured rat aortic smooth muscle cellsChing Fai Kwok, Chi-Chang Juan, Kuang-Chung Shih, et al.
Metabolism: Clinical and Experimental|March 24, 2007
A compound heterozygous mutation in the CYP17 (17alpha-hydroxylase/17,20-lyase) gene in a Chinese subject with congenital adrenal hyperplasiaGin-Sing Won, Chih-Yang Chiu, Yi-Chu Tso, et al.
Diabetes Care|June 17, 2008
Beneficial effects of insulin on glycemic control and beta-cell function in newly diagnosed type 2 diabetes with severe hyperglycemia after short-term intensive insulin therapyHarn-Shen Chen, Tzu-En Wu, Tjin-Shing Jap, et al.
Diabetes Research and Clinical Practice|January 29, 2014
A novel mutation of KCNJ11 gene in a patient with permanent neonatal diabetes mellitusWei-Lun Chang, Chun-Jui Huang, Tsun-Hsiang Lei, et al.
Journal of the Chinese Medical Association : JCMA|September 6, 2008
Analysis of the RET gene in subjects with sporadic Hirschsprung's diseaseTai-Wai Chin, Chih-Yang Chiu, Hsin-Lin Tsai, et al.
Metabolism: Clinical and Experimental|August 19, 2007
Analysis of the SLC26A4 gene in patients with Pendred syndrome in TaiwanChien-Chung Lai, Chih-Yang Chiu, An-Suey Shiao, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 6, 2010
Hemoglobin A(1c) and fructosamine for assessing glycemic control in diabetic patients with CKD stages 3 and 4Harn-Shen Chen, Tzu-En Wu, Hong-Da Lin, et al.
International Journal of Pediatric Otorhinolaryngology|July 11, 2013
A Novel mutation in the SLC26A4 gene in a Chinese family with Pendred syndromeChun-Jui Huang, Tsun-Hsing Lei, Wei-Lun Chang, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 2009
A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemiaSteven A Lietman, Yardena Tenenbaum-Rakover, Tjin Shing Jap, et al.
Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|January 14, 2003
A reappraisal of the ovine corticotropin-releasing hormone stimulation test in the differential diagnosis of Cushing's syndrome: a comparison with the standard high-dose dexamethasone suppression testTing-I Lee, Shih-Yi Lin, Justin Ging-Shing Won, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Journal of Cellular Biochemistry|January 26, 2005
Insulin-like growth factor-1 increases endothelin receptor A levels and action in cultured rat aortic smooth muscle cellsChing Fai Kwok, Chi-Chang Juan, Kuang-Chung Shih, et al.
Metabolism: Clinical and Experimental|March 24, 2007
A compound heterozygous mutation in the CYP17 (17alpha-hydroxylase/17,20-lyase) gene in a Chinese subject with congenital adrenal hyperplasiaGin-Sing Won, Chih-Yang Chiu, Yi-Chu Tso, et al.
Diabetes Care|June 17, 2008
Beneficial effects of insulin on glycemic control and beta-cell function in newly diagnosed type 2 diabetes with severe hyperglycemia after short-term intensive insulin therapyHarn-Shen Chen, Tzu-En Wu, Tjin-Shing Jap, et al.
Diabetes Research and Clinical Practice|January 29, 2014
A novel mutation of KCNJ11 gene in a patient with permanent neonatal diabetes mellitusWei-Lun Chang, Chun-Jui Huang, Tsun-Hsiang Lei, et al.
Journal of the Chinese Medical Association : JCMA|September 6, 2008
Analysis of the RET gene in subjects with sporadic Hirschsprung's diseaseTai-Wai Chin, Chih-Yang Chiu, Hsin-Lin Tsai, et al.
Metabolism: Clinical and Experimental|August 19, 2007
Analysis of the SLC26A4 gene in patients with Pendred syndrome in TaiwanChien-Chung Lai, Chih-Yang Chiu, An-Suey Shiao, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|March 6, 2010
Hemoglobin A(1c) and fructosamine for assessing glycemic control in diabetic patients with CKD stages 3 and 4Harn-Shen Chen, Tzu-En Wu, Hong-Da Lin, et al.
International Journal of Pediatric Otorhinolaryngology|July 11, 2013
A Novel mutation in the SLC26A4 gene in a Chinese family with Pendred syndromeChun-Jui Huang, Tsun-Hsing Lei, Wei-Lun Chang, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 2009
A novel loss-of-function mutation, Gln459Arg, of the calcium-sensing receptor gene associated with apparent autosomal recessive inheritance of familial hypocalciuric hypercalcemiaSteven A Lietman, Yardena Tenenbaum-Rakover, Tjin Shing Jap, et al.
Zhonghua Yi Xue Za Zhi = Chinese Medical Journal; Free China Ed|January 14, 2003
A reappraisal of the ovine corticotropin-releasing hormone stimulation test in the differential diagnosis of Cushing's syndrome: a comparison with the standard high-dose dexamethasone suppression testTing-I Lee, Shih-Yi Lin, Justin Ging-Shing Won, et al.
Pageof 4