Li G - Search Results

1

Analysis of the correlation between lipotoxicity and pituitary-thyroid axis hormone levels in men and male rats.

Yang J, Zhou X, Zhang X, Hu J, Gao L, Song Y, Yu C, Shao S, Yuan Z, Sun Y, Yan H, Li G, Zhao J. Yang J, et al. Among authors: li g. Oncotarget. 2016 Jun 28;7(26):39332-39344. doi: 10.18632/oncotarget.10045. Oncotarget. 2016. PMID: 27322428 Free PMC article.

2

Growth hormone-IGF-I axis and growth velocity in Chinese children with type 1 diabetes mellitus.

Li G, Mick G, Wang X, Xue J, McCormick K. Li G, et al. J Pediatr Endocrinol Metab. 2006 Nov;19(11):1313-8. doi: 10.1515/jpem.2006.19.11.1313. J Pediatr Endocrinol Metab. 2006. PMID: 17220059

3

Novel RNASET2 Pathogenic Variants in an East Asian Child with Delayed Psychomotor Development.

Sun Y, Hu X, Song J, Hu Y, Liu C, Li G. Sun Y, et al. Among authors: li g. Fetal Pediatr Pathol. 2018 Feb;37(1):15-21. doi: 10.1080/15513815.2017.1388456. Epub 2018 Jan 16. Fetal Pediatr Pathol. 2018. PMID: 29336640

4

CYP24A1 Variants in Two Chinese Patients with Idiopathic Infantile Hypercalcemia.

Sun Y, Shen J, Hu X, Qiao Y, Yang J, Shen Y, Li G. Sun Y, et al. Among authors: li g. Fetal Pediatr Pathol. 2019 Feb;38(1):44-56. doi: 10.1080/15513815.2018.1492052. Epub 2019 Jan 11. Fetal Pediatr Pathol. 2019. PMID: 30633617

5

Genotype-phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21-hydroxylase deficiency.

Xu C, Jia W, Cheng X, Ying H, Chen J, Xu J, Guan Q, Zhou X, Zheng D, Li G, Zhao J. Xu C, et al. Among authors: li g. Mol Genet Genomic Med. 2019 Jun;7(6):e671. doi: 10.1002/mgg3.671. Epub 2019 Apr 9. Mol Genet Genomic Med. 2019. PMID: 30968594 Free PMC article.

6

Novel compound variants of the AR and MAP3K1 genes are related to the clinical heterogeneity of androgen insensitivity syndrome.

Cheng Y, Sun Y, Ji Y, Jiang D, Teng G, Zhou X, Zhou X, Li G, Xu C. Cheng Y, et al. Among authors: li g. Biosci Rep. 2020 May 29;40(5):BSR20200616. doi: 10.1042/BSR20200616. Biosci Rep. 2020. PMID: 32338288 Free PMC article.

7

Identification of Oliver-McFarlane syndrome caused by novel compound heterozygous variants of PNPLA6.

Liu F, Ji Y, Li G, Xu C, Sun Y. Liu F, et al. Among authors: li g. Gene. 2020 Nov 30;761:145027. doi: 10.1016/j.gene.2020.145027. Epub 2020 Aug 3. Gene. 2020. PMID: 32758583

8

Posttranslational Modification Defects in Fibroblast Growth Factor Receptor 1 as a Reason for Normosmic Isolated Hypogonadotropic Hypogonadism.

Ying H, Sun Y, Wu H, Jia W, Guan Q, He Z, Gao L, Zhao J, Ji Y, Li G, Xu C. Ying H, et al. Among authors: li g. Oxid Med Cell Longev. 2020 Nov 21;2020:2358719. doi: 10.1155/2020/2358719. eCollection 2020. Oxid Med Cell Longev. 2020. PMID: 33299522 Free PMC article.

9

Identification of novel compound heterozygous variants in SLC19A2 and the genotype-phenotype associations in thiamine-responsive megaloblastic anemia.

Zhang S, Qiao Y, Wang Z, Zhuang J, Sun Y, Shang X, Li G. Zhang S, et al. Among authors: li g. Clin Chim Acta. 2021 May;516:157-168. doi: 10.1016/j.cca.2021.01.025. Epub 2021 Feb 9. Clin Chim Acta. 2021. PMID: 33571483 Free article.

10

[Analysis of pathogenic variants in a Chinese pedigree affected with hyaline fibromatosis syndrome].

Yang J, Shang X, Liu F, Wang Q, Liu C, Sun Y, Li G. Yang J, et al. Among authors: li g. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Mar 10;38(3):232-237. doi: 10.3760/cma.j.cn511374-20200625-00472. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33751531 Chinese.

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