Zhang CQ - Search Results

1

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: zhang cq, zhang zl. 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

2

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: zhang cq, zhang zl, zhang h. 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

3

Identification of one novel mutation in the EVC2 gene in a Chinese family with Ellis-van Creveld syndrome.

Zhang Z, Bao K, He JW, Fu WZ, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: zhang cq, zhang zl. Gene. 2012 Dec 15;511(2):380-2. doi: 10.1016/j.gene.2012.09.071. Epub 2012 Sep 29. Gene. 2012. PMID: 23026208

4

High prevalence of vitamin D insufficiency in China: relationship with the levels of parathyroid hormone and markers of bone turnover.

Lu HK, Zhang Z, Ke YH, He JW, Fu WZ, Zhang CQ, Zhang ZL. Lu HK, et al. Among authors: zhang cq, zhang z, zhang zl. PLoS One. 2012;7(11):e47264. doi: 10.1371/journal.pone.0047264. Epub 2012 Nov 8. PLoS One. 2012. PMID: 23144810 Free PMC article. Clinical Trial.

5

Primary hypertrophic osteoarthropathy: an update.

Zhang Z, Zhang C, Zhang Z. Zhang Z, et al. Front Med. 2013 Mar;7(1):60-4. doi: 10.1007/s11684-013-0246-6. Epub 2013 Jan 23. Front Med. 2013. PMID: 23345113 Review.

6

An analysis of the association between the vitamin D pathway and serum 25-hydroxyvitamin D levels in a healthy Chinese population.

Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: zhang cq, zhang zl. J Bone Miner Res. 2013 Aug;28(8):1784-92. doi: 10.1002/jbmr.1926. J Bone Miner Res. 2013. PMID: 23505139 Free article.

7

Mutations in the SLCO2A1 gene and primary hypertrophic osteoarthropathy: a clinical and biochemical characterization.

Zhang Z, He JW, Fu WZ, Zhang CQ, Zhang ZL. Zhang Z, et al. Among authors: zhang cq, zhang zl. J Clin Endocrinol Metab. 2013 May;98(5):E923-33. doi: 10.1210/jc.2012-3568. Epub 2013 Mar 18. J Clin Endocrinol Metab. 2013. PMID: 23509104

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: zhang cq, zhang zl. 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: zhang cq, zhang zl. 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

Association of serum 25-hydroxyvitamin D with insulin resistance and β-cell function in a healthy Chinese female population.

Tao MF, Zhang Z, Ke YH, He JW, Fu WZ, Zhang CQ, Zhang ZL. Tao MF, et al. Among authors: zhang cq, zhang z, zhang zl. Acta Pharmacol Sin. 2013 Aug;34(8):1070-4. doi: 10.1038/aps.2013.13. Epub 2013 Jun 17. Acta Pharmacol Sin. 2013. PMID: 23770983 Free PMC article.

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