Song HD - Search Results

1

The genetic characteristics of congenital hypothyroidism in China by comprehensive screening of 21 candidate genes.

Sun F, Zhang JX, Yang CY, Gao GQ, Zhu WB, Han B, Zhang LL, Wan YY, Ye XP, Ma YR, Zhang MM, Yang L, Zhang QY, Liu W, Guo CC, Chen G, Zhao SX, Song KY, Song HD. Sun F, et al. Among authors: song hd, song ky. Eur J Endocrinol. 2018 Jun;178(6):623-633. doi: 10.1530/EJE-17-1017. Epub 2018 Apr 12. Eur J Endocrinol. 2018. PMID: 29650690 Free PMC article.

2

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: song hd. 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

3

Influence of visceral adiposity on ghrelin secretion and expression in rats during fasting.

Li RY, Li XS, Shao L, Wu ZY, Du WH, Li SX, Zhao SX, Chen KM, Chen MD, Song HD. Li RY, et al. Among authors: song hd. J Mol Endocrinol. 2009 Jan;42(1):67-74. doi: 10.1677/JME-08-0111. Epub 2008 Oct 30. J Mol Endocrinol. 2009. PMID: 18974228

4

Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.

Song HD, Liang J, Shi JY, Zhao SX, Liu Z, Zhao JJ, Peng YD, Gao GQ, Tao J, Pan CM, Shao L, Cheng F, Wang Y, Yuan GY, Xu C, Han B, Huang W, Chu X, Chen Y, Sheng Y, Li RY, Su Q, Gao L, Jia WP, Jin L, Chen MD, Chen SJ, Chen Z, Chen JL. Song HD, et al. Hum Mol Genet. 2009 Mar 15;18(6):1156-70. doi: 10.1093/hmg/ddn442. Epub 2009 Jan 6. Hum Mol Genet. 2009. PMID: 19126779

5

Clinical associations of the genetic variants of CTLA-4, Tg, TSHR, PTPN22, PTPN12 and FCRL3 in patients with Graves' disease.

Gu LQ, Zhu W, Zhao SX, Zhao L, Zhang MJ, Cui B, Song HD, Ning G, Zhao YJ. Gu LQ, et al. Among authors: song hd. Clin Endocrinol (Oxf). 2010 Feb;72(2):248-55. doi: 10.1111/j.1365-2265.2009.03617.x. Epub 2009 Apr 27. Clin Endocrinol (Oxf). 2010. PMID: 19438904

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: song hd. 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

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. Among authors: song hd. Hum Mutat. 2009 Sep;30(9):E855-65. doi: 10.1002/humu.21072. Hum Mutat. 2009. PMID: 19551906

8

Different expression of mimecan as a marker for differential diagnosis between NSCLC and SCLC.

Zheng CX, Zhao SX, Wang P, Yu HM, Wang CF, Han B, Su B, Xiang Y, Li XS, Li SX, Ma QY, Zhang RX, Wan HY, Song HD. Zheng CX, et al. Among authors: song hd. Oncol Rep. 2009 Nov;22(5):1057-61. doi: 10.3892/or_00000536. Oncol Rep. 2009. PMID: 19787221

9

Association of the CTLA4 gene with Graves' disease in the Chinese Han population.

Zhao SX, Pan CM, Cao HM, Han B, Shi JY, Liang J, Gao GQ, Peng YD, Su Q, Chen JL, Zhao JJ, Song HD. Zhao SX, et al. Among authors: song hd. PLoS One. 2010 Mar 23;5(3):e9821. doi: 10.1371/journal.pone.0009821. PLoS One. 2010. PMID: 20352109 Free PMC article.

10

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: song hd. Mutagenesis. 2011 Mar;26(2):283-9. doi: 10.1093/mutage/geq086. Epub 2010 Nov 10. Mutagenesis. 2011. PMID: 21068205

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