Ye L - Search Results

1

Mutation analysis of SCNN1B in a family with Liddle's syndrome.

Wang W, Zhou W, Jiang L, Cui B, Ye L, Su T, Wang J, Li X, Ning G. Wang W, et al. Among authors: ye l. Endocrine. 2006 Jun;29(3):385-90. doi: 10.1385/ENDO:29:3:385. Endocrine. 2006. PMID: 16943574

2

Autosomal dominant neurohypophyseal diabetes insipidus with linkage to chromosome 20p13 but without mutations in the AVP-NPII gene.

Ye L, Li X, Chen Y, Sun H, Wang W, Su T, Jiang L, Cui B, Ning G. Ye L, et al. J Clin Endocrinol Metab. 2005 Jul;90(7):4388-93. doi: 10.1210/jc.2004-2000. Epub 2005 Apr 5. J Clin Endocrinol Metab. 2005. PMID: 15811933

3

Hypomethylation in the promoter region of POMC gene correlates with ectopic overexpression in thymic carcinoids.

Ye L, Li X, Kong X, Wang W, Bi Y, Hu L, Cui B, Li X, Ning G. Ye L, et al. J Endocrinol. 2005 May;185(2):337-43. doi: 10.1677/joe.1.05963. J Endocrinol. 2005. PMID: 15845926

4

[Hereditary spinocerebellar ataxia--a family pedigree with SCA3 gene mutation].

Jiang XH, Ye L, Fu Y, Yu HZ, Yu GP, Zhao YJ, Ning G, Li XY. Jiang XH, et al. Among authors: ye l. Zhonghua Yi Xue Za Zhi. 2005 Mar 30;85(12):848-9. Zhonghua Yi Xue Za Zhi. 2005. PMID: 15949406 Chinese. No abstract available.

5

Mutation screening in Chinese hypokalemic periodic paralysis patients.

Wang W, Jiang L, Ye L, Zhu N, Su T, Guan L, Li X, Ning G. Wang W, et al. Among authors: ye l. Mol Genet Metab. 2006 Apr;87(4):359-63. doi: 10.1016/j.ymgme.2005.10.020. Epub 2006 Jan 4. Mol Genet Metab. 2006. PMID: 16386935

6

[Leprechaunism: an inherited insulin resistance syndrome caused by the defect of insulin receptor].

Jiang L, Liu C, Wang WQ, Ye L, Zhu N, Zhou WW, Su TW, Li XY, Ning G. Jiang L, et al. Among authors: ye l. Zhonghua Nei Ke Za Zhi. 2006 Sep;45(9):730-3. Zhonghua Nei Ke Za Zhi. 2006. PMID: 17166446 Chinese.

7

Globular adiponectin augments insulin secretion from pancreatic islet beta cells at high glucose concentrations.

Gu W, Li X, Liu C, Yang J, Ye L, Tang J, Gu Y, Yang Y, Hong J, Zhang Y, Chen M, Ning G. Gu W, et al. Among authors: ye l. Endocrine. 2006 Oct;30(2):217-21. doi: 10.1385/ENDO:30:2:217. Endocrine. 2006. PMID: 17322583

8

Characteristics of ectopic adrenocorticotropic hormone syndrome due to thymic carcinoid and analysis of the molecular mechanism.

Bi YF, Ye L, Chen YH, Ning G, Sun SY, Jiang L, Zhu N, Zhou WW, Wang WQ. Bi YF, et al. Among authors: ye l. Chin Med J (Engl). 2008 Apr 5;121(7):667-70. Chin Med J (Engl). 2008. PMID: 18466691 No abstract available.

9

Clinical and genetic analysis for four Chinese families with Prader-Willi syndrome.

Zhang YW, Jia HY, Hong J, Ge Y, Zhang HJ, Shen CF, Ye L, Cui B, Li XY, Gu WQ, Zhang YF, Wang WQ, Ning G. Zhang YW, et al. Among authors: ye l. Endocrine. 2009 Aug;36(1):37-44. doi: 10.1007/s12020-009-9203-1. Epub 2009 May 7. Endocrine. 2009. PMID: 19421899

10

Gene expression profiles of thymic neuroendocrine tumors (carcinoids) with ectopic ACTH syndrome reveal novel molecular mechanism.

Bi YF, Liu RX, Ye L, Fang H, Li XY, Wang WQ, Zhang J, Wang KK, Jiang L, Su TW, Chen ZY, Ning G. Bi YF, et al. Among authors: ye l. Endocr Relat Cancer. 2009 Dec;16(4):1273-82. doi: 10.1677/ERC-08-0325. Epub 2009 Jul 22. Endocr Relat Cancer. 2009. PMID: 19625467

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