He JW - Search Results

1

Phenotype and genotype analysis of Chinese patients with osteogenesis imperfecta type V.

Zhang Z, Li M, He JW, Fu WZ, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: he jw. PLoS One. 2013 Aug 20;8(8):e72337. doi: 10.1371/journal.pone.0072337. eCollection 2013. PLoS One. 2013. PMID: 23977282 Free PMC article.

2

Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.

Zhang H, Yue H, Wang C, Hu W, Gu J, He J, Fu W, Hu Y, Li M, Zhang Z. Zhang H, et al. Mol Med Rep. 2016 Nov;14(5):4918-4926. doi: 10.3892/mmr.2016.5835. Epub 2016 Oct 12. Mol Med Rep. 2016. PMID: 27748872

3

Novel mutations of the SERPINF1 and FKBP10 genes in Chinese families with autosomal recessive osteogenesis imperfecta.

Zhang H, Xu Y, Yue H, Wang C, Gu J, He J, Fu W, Hu W, Zhang Z. Zhang H, et al. Int J Mol Med. 2018 Jun;41(6):3662-3670. doi: 10.3892/ijmm.2018.3542. Epub 2018 Mar 7. Int J Mol Med. 2018. PMID: 29512769

4

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: he jw. 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

5

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: he jw. 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

6

Identification of two novel mutations in the SLC4A1 gene in two unrelated Chinese families with distal renal tubular acidosis.

Zhang Z, Liu KX, He JW, Fu WZ, Yue H, Zhang H, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: he jw. Arch Med Res. 2012 May;43(4):298-304. doi: 10.1016/j.arcmed.2012.05.001. Epub 2012 May 16. Arch Med Res. 2012. PMID: 22609520

7

A novel mutation (R122Q) in the cathepsin K gene in a Chinese child with Pyknodysostosis.

Zheng H, Zhang Z, He JW, Fu WZ, Zhang ZL. Zheng H, et al. Among authors: he jw. Gene. 2013 May 25;521(1):176-9. doi: 10.1016/j.gene.2013.03.014. Epub 2013 Mar 16. Gene. 2013. PMID: 23506830

8

A novel mutation in the SLCO2A1 gene in a Chinese family with primary hypertrophic osteoarthropathy.

Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: he jw. Gene. 2013 May 25;521(1):191-4. doi: 10.1016/j.gene.2013.03.047. Epub 2013 Mar 24. Gene. 2013. PMID: 23531451

9

Identification of one novel mutation in the C-propeptide of COL2A1 in a Chinese family with spondyloperipheral dysplasia.

Zhang Z, Zhao SC, He JW, Fu WZ, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: he jw. Gene. 2013 Jun 10;522(1):107-10. doi: 10.1016/j.gene.2013.03.083. Epub 2013 Mar 29. Gene. 2013. PMID: 23545312

10

Mutation screening for the EXT1 and EXT2 genes in Chinese patients with multiple osteochondromas.

Kang QL, Xu J, Zhang Z, He JW, Fu WZ, Zhang ZL. Kang QL, et al. Among authors: he jw. Arch Med Res. 2013 Oct;44(7):542-8. doi: 10.1016/j.arcmed.2013.09.008. Epub 2013 Oct 10. Arch Med Res. 2013. PMID: 24120389

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