Qiao J - Search Results

1

C-reactive protein inhibits adiponectin gene expression and secretion in 3T3-L1 adipocytes.

Yuan G, Chen X, Ma Q, Qiao J, Li R, Li X, Li S, Tang J, Zhou L, Song H, Chen M. Yuan G, et al. Among authors: qiao j. J Endocrinol. 2007 Aug;194(2):275-81. doi: 10.1677/JOE-07-0133. J Endocrinol. 2007. PMID: 17641277

2

A complex heterozygous mutation of His373Leu and Asp487-Ser488-Phe489 deletion in human cytochrome P450c17 causes 17alpha-hydroxylase/17,20-lyase deficiency in three Chinese sisters.

Qiao J, Hu RM, Peng YD, Song HD, Peng YW, Gao GF, Hao JH, Hu NY, Xu MY, Chen JL. Qiao J, et al. Mol Cell Endocrinol. 2003 Mar 28;201(1-2):189-95. doi: 10.1016/s0303-7207(02)00156-9. Mol Cell Endocrinol. 2003. PMID: 12706306

3

Effect of short-term and long-term fasting on transcriptional regulation of metabolic genes in rat tissues.

Li RY, Zhang QH, Liu Z, Qiao J, Zhao SX, Shao L, Xiao HS, Chen JL, Chen MD, Song HD. Li RY, et al. Among authors: qiao j. Biochem Biophys Res Commun. 2006 Jun 2;344(2):562-70. doi: 10.1016/j.bbrc.2006.03.155. Epub 2006 Apr 3. Biochem Biophys Res Commun. 2006. PMID: 16620784

4

[A clinical and genetic analysis of a pedigree with two 46,XY patients suffering from 17alpha-hydroxylase deficiency].

Liang J, Qiao J, Chen X, Wu QQ, Heng H, Zhang T, Zhao JJ, Song HD. Liang J, et al. Among authors: qiao j. Zhonghua Nei Ke Za Zhi. 2008 Jun;47(6):482-5. Zhonghua Nei Ke Za Zhi. 2008. PMID: 19040066 Chinese.

5

Inhibitory effect of paeoniflorin on the inflammatory vicious cycle between adipocytes and macrophages.

Jiang B, Qiao J, Yang Y, Lu Y. Jiang B, et al. Among authors: qiao j. J Cell Biochem. 2012 Aug;113(8):2560-6. doi: 10.1002/jcb.22173. Epub 2009 Apr 24. J Cell Biochem. 2012. PMID: 19396840

6

[Clinical and molecular genetic analysis for 7 patients from 5 pedigrees with 17a-hydroxylase/17, 20 lyase deficiency].

Liu BL, Qiao J, Chen X, Liang J, Zuo CL, Gu YY, Han B, Gong J, Ru Y, Lu YL, Wu WL, Chen MD, Song HD. Liu BL, et al. Among authors: qiao j. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Jun;26(3):282-7. doi: 10.3760/cma.j.issn.1003-9406.2009.03.010. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19504440 Chinese.

7

Identification of steroid biosynthetic defects in genotype-proven heterozygous individuals for 17alpha-hydroxylase/17,20-lyase deficiency.

Qiao J, Chen X, Zuo CL, Gu YY, Liu BL, Liang J, Lu YL, Tang JF, Wu YX, Chen MD, Chen JL, Wu WL, Song HD. Qiao J, et al. Clin Endocrinol (Oxf). 2010 Mar;72(3):312-9. doi: 10.1111/j.1365-2265.2009.03607.x. Epub 2009 Apr 17. Clin Endocrinol (Oxf). 2010. PMID: 19508587

8

A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditism.

Qiao J, Han B, Liu BL, Chen X, Ru Y, Cheng KX, Chen FG, Zhao SX, Liang J, Lu YL, Tang JF, Wu YX, Wu WL, Chen JL, Chen MD, Song HD. Qiao J, et al. Hum Mutat. 2009 Sep;30(9):E855-65. doi: 10.1002/humu.21072. Hum Mutat. 2009. PMID: 19551906

9

Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).

Fan JY, Han B, Qiao J, Liu BL, Ji YR, Ge SF, Song HD, Fan XQ. Fan JY, et al. Among authors: qiao j. Mutagenesis. 2011 Mar;26(2):283-9. doi: 10.1093/mutage/geq086. Epub 2010 Nov 10. Mutagenesis. 2011. PMID: 21068205

10

A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17{alpha}-hydroxylase deficiency.

Qiao J, Han B, Liu BL, Liu W, Wu JJ, Pan CM, Jiang H, Gu T, Jiang BR, Zhu H, Lu YL, Wu WL, Chen MD, Song HD. Qiao J, et al. Eur J Endocrinol. 2011 Apr;164(4):627-33. doi: 10.1530/EJE-10-0933. Epub 2011 Jan 31. Eur J Endocrinol. 2011. PMID: 21282350

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