Xu C - Search Results

1

Identification and Characteristics of Novel Mutations in Nonsyndromic Monogenic Obesity.

Shi P, Shi Y, Liu X, Wang S, Yuan J, Zhao W, Fang L, Wang R, Yan F, Xu C. Shi P, et al. Among authors: xu c. Adv Biol (Weinh). 2023 Aug;7(8):e2300061. doi: 10.1002/adbi.202300061. Epub 2023 Apr 21. Adv Biol (Weinh). 2023. PMID: 37083215

2

Characteristics and Follow-Up of 13 pedigrees with Gitelman syndrome.

Zhong F, Ying H, Jia W, Zhou X, Zhang H, Guan Q, Xu J, Fang L, Zhao J, Xu C. Zhong F, et al. Among authors: xu c, xu j. J Endocrinol Invest. 2019 Jun;42(6):653-665. doi: 10.1007/s40618-018-0966-1. Epub 2018 Nov 10. J Endocrinol Invest. 2019. PMID: 30413979 Free PMC article.

3

Bidirectional temporal relationship between obesity and hyperinsulinemia: longitudinal observation from a Chinese cohort.

Xu C, Zhou G, Zhao M, Zhang X, Fang L, Guan Q, Zhang H, Gao L, Zhang T, Zhao J. Xu C, et al. BMJ Open Diabetes Res Care. 2021 Feb;9(1):e002059. doi: 10.1136/bmjdrc-2020-002059. BMJ Open Diabetes Res Care. 2021. PMID: 33632707 Free PMC article.

4

Characterization of a novel COL10A1 variant associated with Schmid-type metaphyseal chondrodysplasia and a literature review.

Wu H, Wang S, Li G, Yao Y, Wang N, Sun X, Fang L, Jiang X, Zhao J, Wang Y, Xu C. Wu H, et al. Among authors: xu c. Mol Genet Genomic Med. 2021 May;9(5):e1668. doi: 10.1002/mgg3.1668. Epub 2021 Mar 25. Mol Genet Genomic Med. 2021. PMID: 33764685 Free PMC article. Review.

5

Mutations in GCK May Lead to MODY2 by Reducing Glycogen Synthesis.

Li Z, Li K, Sun Y, Jiang X, Liu J, Li J, Fang L, Li G, Guan Q, Xu C. Li Z, et al. Among authors: xu c. Adv Biol (Weinh). 2022 Nov;6(11):e2200097. doi: 10.1002/adbi.202200097. Epub 2022 Jun 30. Adv Biol (Weinh). 2022. PMID: 35770790

6

Cell-Dependent Pathogenic Roles of Filamin B in Different Skeletal Malformations.

Wu H, Wang Y, Chen X, Yao Y, Zhao W, Fang L, Sun X, Wang N, Jiang J, Gao L, Zhao J, Xu C. Wu H, et al. Among authors: xu c. Oxid Med Cell Longev. 2022 Jul 4;2022:8956636. doi: 10.1155/2022/8956636. eCollection 2022. Oxid Med Cell Longev. 2022. PMID: 35832491 Free PMC article.

7

Identification and Functional Characterization of a Novel Variant in the SEMA3A Gene in a Chinese Family with Kallmann Syndrome.

Shu M, Wu H, Wei S, Shi Y, Li Z, Cheng Y, Fang L, Xu C. Shu M, et al. Among authors: xu c. Int J Endocrinol. 2022 Oct 11;2022:2504660. doi: 10.1155/2022/2504660. eCollection 2022. Int J Endocrinol. 2022. PMID: 36267363 Free PMC article.

8

Identification and characterization of novel carboxyl ester lipase gene variants in patients with different subtypes of diabetes.

Wu H, Shu M, Liu C, Zhao W, Li Q, Song Y, Zhang T, Chen X, Shi Y, Shi P, Fang L, Wang R, Xu C. Wu H, et al. Among authors: xu c. BMJ Open Diabetes Res Care. 2023 Jan;11(1):e003127. doi: 10.1136/bmjdrc-2022-003127. BMJ Open Diabetes Res Care. 2023. PMID: 36634979 Free PMC article.

9

The health-care utilization and economic burden in patients with genetic skeletal disorders.

Liu L, Shi Y, Fan X, Yao Y, Wu W, Tian Y, Wu H, Li Z, Wang Y, Xu C. Liu L, et al. Among authors: xu c. Orphanet J Rare Dis. 2024 Mar 4;19(1):99. doi: 10.1186/s13023-024-03102-3. Orphanet J Rare Dis. 2024. PMID: 38438867 Free PMC article.

10

Characterization of novel PHEX variants in X-linked hypophosphatemic rickets and genotype-PHEX activity correlation.

Wu H, Ying H, Zhao W, Sun Y, Wang Y, Chen X, Li G, Yao Y, Xu S, Li T, Fang L, Sun X, Wang N, Xu J, Guan Q, Xia W, Wang L, Gao L, Zhao J, Xu C. Wu H, et al. Among authors: xu s, xu c, xu j. J Clin Endocrinol Metab. 2024 Mar 5:dgae120. doi: 10.1210/clinem/dgae120. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 38442738

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

24,732 results

Search Page