Liu BL - Search Results

1

Identification of a novel mutation in CYP17A1 gene.

Xue LQ, Han B, Chen LB, Pan CM, Zhu H, Liu BL, Liu W, Wu WL, Chen MD, Lu YL, Qiao J, Song HD. Xue LQ, et al. Among authors: liu bl, liu w. Transl Res. 2013 Jan;161(1):44-9. doi: 10.1016/j.trsl.2012.08.007. Epub 2012 Oct 1. Transl Res. 2013. PMID: 23036723

2

[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. 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.

3

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. Among authors: liu bl. 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

4

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: liu bl. Hum Mutat. 2009 Sep;30(9):E855-65. doi: 10.1002/humu.21072. Hum Mutat. 2009. PMID: 19551906

5

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

6

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. Among authors: liu bl, liu w. 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

7

Identifying a novel mutation of CYP17A1 gene from five Chinese 17α-hydroxylase/17, 20-lyase deficiency patients.

Han B, Liu W, Zuo CL, Zhu H, Li L, Xu C, Wang XJ, Liu BL, Pan CM, Lu YL, Wu WL, Chen MD, Song HD, Cheng KX, Qiao J. Han B, et al. Among authors: liu bl, liu w. Gene. 2013 Mar 10;516(2):345-50. doi: 10.1016/j.gene.2012.12.010. Epub 2013 Jan 2. Gene. 2013. PMID: 23291414

8

Phenotypic Heterogeneity and Fertility Potential of Patients With 17-Hydroxylase/17,20-lyase Deficiency.

Xu Y, Jiang S, Yan Z, Niu Y, Du W, Liu B, Han B, Liu X, Zhao S, Song H, Kuang Y, Qiao J. Xu Y, et al. J Clin Endocrinol Metab. 2022 May 17;107(6):e2610-e2618. doi: 10.1210/clinem/dgac029. J Clin Endocrinol Metab. 2022. PMID: 35043964

9

Functional study of an aberrant splicing variant of the human luteinizing hormone (LH) receptor.

Han B, Wang ZQ, Xue LQ, Ma JH, Liu W, Liu BL, Wu JJ, Pan CM, Chen X, Zhao SX, Lu YL, Wu WL, Qiao J, Song HD. Han B, et al. Among authors: liu bl, liu w. Mol Hum Reprod. 2012 Mar;18(3):129-35. doi: 10.1093/molehr/gar065. Epub 2011 Oct 14. Mol Hum Reprod. 2012. PMID: 22002533 Free PMC article.

10

Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population.

Song ZY, Liu W, Xue LQ, Pan CM, Wang HN, Gu ZH, Yang SY, Cao HM, Zuo CL, Zhang XN, Jiang H, Liu BL, Bi YX, Zhang XM, Zhao SX, Song HD. Song ZY, et al. Among authors: liu bl, liu w. Clin Endocrinol (Oxf). 2013 Aug;79(2):267-74. doi: 10.1111/cen.12115. Epub 2013 Apr 27. Clin Endocrinol (Oxf). 2013. PMID: 23170961

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