Fu WZ - Search Results

1

Seven novel and six de novo PHEX gene mutations in patients with hypophosphatemic rickets.

Li SS, Gu JM, Yu WJ, He JW, Fu WZ, Zhang ZL. Li SS, et al. Among authors: fu wz. Int J Mol Med. 2016 Dec;38(6):1703-1714. doi: 10.3892/ijmm.2016.2796. Epub 2016 Nov 7. Int J Mol Med. 2016. PMID: 27840894 Free PMC article.

2

Identification of the CLCN7 gene mutations in two Chinese families with autosomal dominant osteopetrosis (type II).

Zhang ZL, He JW, Zhang H, Hu WW, Fu WZ, Gu JM, Yu JB, Gao G, Hu YQ, Li M, Liu YJ. Zhang ZL, et al. Among authors: fu wz. J Bone Miner Metab. 2009;27(4):444-51. doi: 10.1007/s00774-009-0051-0. Epub 2009 Mar 14. J Bone Miner Metab. 2009. PMID: 19288050

3

Association between VDR and ESR1 gene polymorphisms with bone and obesity phenotypes in Chinese male nuclear families.

Gu JM, Xiao WJ, He JW, Zhang H, Hu WW, Hu YQ, Li M, Liu YJ, Fu WZ, Yu JB, Gao G, Yue H, Ke YH, Zhang ZL. Gu JM, et al. Among authors: fu wz. Acta Pharmacol Sin. 2009 Dec;30(12):1634-42. doi: 10.1038/aps.2009.169. Acta Pharmacol Sin. 2009. PMID: 19960008 Free PMC article.

4

No association of the polymorphisms of the frizzled-related protein gene with peak bone mineral density in Chinese nuclear families.

Gao G, Zhang ZL, He JW, Zhang H, Yue H, Hu WW, Gu JM, Fu WZ, Hu YQ, Li M, Liu YJ, Yu JB. Gao G, et al. Among authors: fu wz. BMC Med Genet. 2010 Jan 1;11:1. doi: 10.1186/1471-2350-11-1. BMC Med Genet. 2010. PMID: 20043861 Free PMC article.

5

Polymorphisms in the HOXD4 gene are not associated with peak bone mineral density in Chinese nuclear families.

Zhang H, He JW, Gao G, Yue H, Yu JB, Hu WW, Gu JM, Hu YQ, Li M, Fu WZ, Liu YJ, Zhang ZL. Zhang H, et al. Among authors: fu wz. Acta Pharmacol Sin. 2010 Aug;31(8):977-83. doi: 10.1038/aps.2010.91. Acta Pharmacol Sin. 2010. PMID: 20686522 Free PMC article.

6

No association between LRP5 gene polymorphisms and bone and obesity phenotypes in Chinese male-offspring nuclear families.

Yu JB, Ke YH, He JW, Zhang H, Hu WW, Hu YQ, Li M, Liu YJ, Gu JM, Fu WZ, Gao G, Yue H, Xiao WJ, Zhang ZL. Yu JB, et al. Among authors: fu wz. Acta Pharmacol Sin. 2010 Nov;31(11):1464-9. doi: 10.1038/aps.2010.92. Epub 2010 Oct 18. Acta Pharmacol Sin. 2010. PMID: 20953208 Free PMC article.

7

No association between polymorphisms and haplotypes of COL1A1 and COL1A2 genes and osteoporotic fracture in postmenopausal Chinese women.

Hu WW, He JW, Zhang H, Wang C, Gu JM, Yue H, Ke YH, Hu YQ, Fu WZ, Li M, Liu YJ, Zhang ZL. Hu WW, et al. Among authors: fu wz. Acta Pharmacol Sin. 2011 Jul;32(7):947-55. doi: 10.1038/aps.2011.37. Epub 2011 May 23. Acta Pharmacol Sin. 2011. PMID: 21602843 Free PMC article.

8

The identification of novel mutations in COL1A1, COL1A2, and LEPRE1 genes in Chinese patients with osteogenesis imperfecta.

Zhang ZL, Zhang H, Ke YH, Yue H, Xiao WJ, Yu JB, Gu JM, Hu WW, Wang C, He JW, Fu WZ. Zhang ZL, et al. Among authors: fu wz. J Bone Miner Metab. 2012 Jan;30(1):69-77. doi: 10.1007/s00774-011-0284-6. Epub 2011 Jun 14. J Bone Miner Metab. 2012. PMID: 21667357

9

Identification of two novel mutations in the OCRL1 gene in two Chinese families with Lowe syndrome.

Ke YH, He JW, Fu WZ, Zhang ZL. Ke YH, et al. Among authors: fu wz. Nephrology (Carlton). 2012 Jan;17(1):20-5. doi: 10.1111/j.1440-1797.2011.01514.x. Nephrology (Carlton). 2012. PMID: 21854507

10

Identification of three novel mutations in the COL2A1 gene in four unrelated Chinese families with spondyloepiphyseal dysplasia congenita.

Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: fu wz. Biochem Biophys Res Commun. 2011 Oct 7;413(4):504-8. doi: 10.1016/j.bbrc.2011.08.090. Epub 2011 Sep 6. Biochem Biophys Res Commun. 2011. PMID: 21924244

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