Zhou Q - Search Results

1

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. Front Pediatr. 2020 Jul 24;8:410. doi: 10.3389/fped.2020.00410. eCollection 2020. Front Pediatr. 2020. PMID: 32850530 Free PMC article.

2

GATA3 mutation in a family with hypoparathyroidism, deafness and renal dysplasia syndrome.

Zhu ZY, Zhou QL, Ni SN, Gu W. Zhu ZY, et al. World J Pediatr. 2014 Aug;10(3):278-80. doi: 10.1007/s12519-014-0505-x. Epub 2014 Aug 15. World J Pediatr. 2014. PMID: 25124981

3

Clinical and Functional Characterization of Novel INSR Variants in Two Families With Severe Insulin Resistance Syndrome.

Zhou Q, Yu J, Yuan X, Wang C, Zhu Z, Zhang A, Gu W. Zhou Q, et al. Front Endocrinol (Lausanne). 2021 Apr 29;12:606964. doi: 10.3389/fendo.2021.606964. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 33995269 Free PMC article.

4

Clinical and molecular characterization of a patient with MBTPS1 related spondyloepiphyseal dysplasia: Evidence of pathogenicity for a synonymous variant.

Yuan Y, Zhou Q, Wang C, Zhou W, Gu W, Zheng B. Yuan Y, et al. Among authors: zhou w, zhou q. Front Pediatr. 2023 Jan 11;10:1056141. doi: 10.3389/fped.2022.1056141. eCollection 2022. Front Pediatr. 2023. PMID: 36714646 Free PMC article.

5

From glucose sensing to exocytosis: takes from maturity onset diabetes of the young.

Samadli S, Zhou Q, Zheng B, Gu W, Zhang A. Samadli S, et al. Among authors: zhou q. Front Endocrinol (Lausanne). 2023 May 15;14:1188301. doi: 10.3389/fendo.2023.1188301. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37255971 Free PMC article. Review.

6

A novel gain-of-function STAT3 variant in infantile-onset diabetes associated with multiorgan autoimmunity.

Zhou Q, Chen D, Yu J, Zheng B, Zhou W, Jia Z, Zhang A, Gu W. Zhou Q, et al. Among authors: zhou w. Mol Genet Genomic Med. 2024 Feb;12(2):e2407. doi: 10.1002/mgg3.2407. Mol Genet Genomic Med. 2024. PMID: 38404237 Free PMC article.

7

Association between dietary behavior and puberty in girls.

Du Y, Yan W, Bigambo FM, Zhou Q, Ma C, Gu W, Wang X. Du Y, et al. Among authors: zhou q. BMC Pediatr. 2024 May 21;24(1):349. doi: 10.1186/s12887-024-04840-w. BMC Pediatr. 2024. PMID: 38773477 Free PMC article.

8

Molecular and clinical profiles of pediatric monogenic diabetes subtypes: comprehensive genetic analysis of 138 patients.

Zhou Q, Samadli S, Zhang H, Zheng X, Zheng B, Zhang A, Gu W. Zhou Q, et al. J Clin Endocrinol Metab. 2024 Nov 6:dgae779. doi: 10.1210/clinem/dgae779. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 39504571

9

46,XY disorders of sex development and muscular dystrophy caused by Xp21 duplication: a case report and literature review.

Zheng XQ, Zhou QL, Gu W. Zheng XQ, et al. Transl Pediatr. 2024 Nov 30;13(11):2088-2096. doi: 10.21037/tp-24-327. Epub 2024 Nov 26. Transl Pediatr. 2024. PMID: 39649651 Free PMC article.

10

Catalytic Asymmetric Oxidative Coupling between C(sp³)-H Bonds and Carboxylic Acids.

Liu XM, Li F, Wang T, Dai L, Yang Y, Jiang NQ, Xue LY, Liu JY, Xue XS, Xiao LJ, Zhou QL. Liu XM, et al. Among authors: zhou ql. J Am Chem Soc. 2024 Dec 17. doi: 10.1021/jacs.4c12544. Online ahead of print. J Am Chem Soc. 2024. PMID: 39690117

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