Jia Z - Search Results

1

A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.

Zheng B, Wang C, Jia Z, Liu Z, Li M, Jin Y, Pan J. Zheng B, et al. Among authors: jia z. J Pediatr Gastroenterol Nutr. 2017 Apr;64(4):559-564. doi: 10.1097/MPG.0000000000001316. J Pediatr Gastroenterol Nutr. 2017. PMID: 27467201

2

Novel compound heterozygous CLCNKB gene mutations (c.1755A>G/c.848_850delTCT) cause classic Bartter syndrome.

Wang C, Chen Y, Zheng B, Zhu M, Fan J, Wang J, Jia Z, Huang S, Zhang A. Wang C, et al. Among authors: jia z. Am J Physiol Renal Physiol. 2018 Oct 1;315(4):F844-F851. doi: 10.1152/ajprenal.00077.2017. Epub 2018 Feb 14. Am J Physiol Renal Physiol. 2018. PMID: 29442545 Free article.

3

COX-2 contributes to LPS-induced Stat3 activation and IL-6 production in microglial cells.

Zhu J, Li S, Zhang Y, Ding G, Zhu C, Huang S, Zhang A, Jia Z, Li M. Zhu J, et al. Among authors: jia z. Am J Transl Res. 2018 Mar 15;10(3):966-974. eCollection 2018. Am J Transl Res. 2018. PMID: 29636886 Free PMC article.

4

Presumed missense and synonymous mutations in ATP7B gene cause exon skipping in Wilson disease.

Wang C, Zhou W, Huang Y, Yin H, Jin Y, Jia Z, Zhang A, Liu Z, Zheng B. Wang C, et al. Among authors: jia z. Liver Int. 2018 Aug;38(8):1504-1513. doi: 10.1111/liv.13754. Epub 2018 May 2. Liver Int. 2018. PMID: 29637721

5

Whole-genome sequencing revealed an interstitial deletion encompassing OCRL and SMARCA1 gene in a patient with Lowe syndrome.

Zheng B, Chen Q, Wang C, Zhou W, Chen Y, Ding G, Jia Z, Zhang A, Huang S. Zheng B, et al. Among authors: jia z. Mol Genet Genomic Med. 2019 Sep;7(9):e876. doi: 10.1002/mgg3.876. Epub 2019 Aug 3. Mol Genet Genomic Med. 2019. PMID: 31376231 Free PMC article. Clinical Trial.

6

Splicing Characterization of CLCNKB Variants in Four Patients With Type III Bartter Syndrome.

Wang C, Han Y, Zhou J, Zheng B, Zhou W, Bao H, Jia Z, Zhang A, Huang S, Ding G, Zhao F. Wang C, et al. Among authors: jia z. Front Genet. 2020 Feb 21;11:81. doi: 10.3389/fgene.2020.00081. eCollection 2020. Front Genet. 2020. PMID: 32153641 Free PMC article.

7

A Synonymous Variant c.579A>G in the ETFDH Gene Caused Exon Skipping in a Patient With Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency: A Case Report.

Hu G, Zeng J, Wang C, Zhou W, Jia Z, Yang J, Zheng B. Hu G, et al. Among authors: jia z. Front Pediatr. 2020 Mar 27;8:118. doi: 10.3389/fped.2020.00118. eCollection 2020. Front Pediatr. 2020. PMID: 32292771 Free PMC article.

8

Functional Characterization of PHEX Gene Variants in Children With X-Linked Hypophosphatemic Rickets Shows No Evidence of Genotype-Phenotype Correlation.

Zheng B, Wang C, Chen Q, Che R, Sha Y, Zhao F, Ding G, Zhou W, Jia Z, Huang S, Chen Y, Zhang A. Zheng B, et al. Among authors: jia z. J Bone Miner Res. 2020 Sep;35(9):1718-1725. doi: 10.1002/jbmr.4035. Epub 2020 May 12. J Bone Miner Res. 2020. PMID: 32329911 Free article.

9

A rare case of pediatric recurrent rhabdomyolysis with compound heterogenous variants in the LPIN1.

Che R, Wang C, Zheng B, Zhang X, Ding G, Zhao F, Jia Z, Zhang A, Huang S, Feng Q. Che R, et al. Among authors: jia z. BMC Pediatr. 2020 May 14;20(1):218. doi: 10.1186/s12887-020-02134-5. BMC Pediatr. 2020. PMID: 32410653 Free PMC article.

10

Clinical and Molecular Analysis of Four Patients With 11β-Hydroxylase Deficiency.

Zhou Q, Wang D, Wang C, Zheng B, Liu Q, Zhu Z, Jia Z, Gu W. Zhou Q, et al. Among authors: jia z. Front Pediatr. 2020 Jul 24;8:410. doi: 10.3389/fped.2020.00410. eCollection 2020. Front Pediatr. 2020. PMID: 32850530 Free PMC article.

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