Yin X - Search Results

1

The EGFR-P38 MAPK axis up-regulates PD-L1 through miR-675-5p and down-regulates HLA-ABC via hexokinase-2 in hepatocellular carcinoma cells.

Liu Z, Ning F, Cai Y, Sheng H, Zheng R, Yin X, Lu Z, Su L, Chen X, Zeng C, Wang H, Liu L. Liu Z, et al. Among authors: yin x. Cancer Commun (Lond). 2021 Jan;41(1):62-78. doi: 10.1002/cac2.12117. Epub 2021 Jan 1. Cancer Commun (Lond). 2021. PMID: 34236149 Free PMC article.

2

[Gene mutations and clinical manifestations in children with glycogen storage disease type Ib].

Liang CL, Liu L, Sheng HY, Jiang MY, Yin X, Mei HF, Cheng J, Zhang W, Fan LP. Liang CL, et al. Among authors: yin x. Zhongguo Dang Dai Er Ke Za Zhi. 2013 Aug;15(8):661-5. Zhongguo Dang Dai Er Ke Za Zhi. 2013. PMID: 23965881 Free article. Chinese.

3

First case report of medium-chain acyl-coenzyme A dehydrogenase deficiency in China.

Liang C, Jiang M, Sheng H, Cai Y, Wu D, Yin X, Peng M, Liu L. Liang C, et al. Among authors: yin x. J Pediatr Endocrinol Metab. 2015 May;28(5-6):681-4. doi: 10.1515/jpem-2014-0058. J Pediatr Endocrinol Metab. 2015. PMID: 25503862

4

[Clinical features of pyruvate dehydrogenase complex deficiency and gene testing in one case].

Wu M, Liu L, Cai Y, Sheng H, Cheng J, Li X, Yin X, Lu Z, Lin R, Zhou Z, Fan L, Liu H. Wu M, et al. Among authors: yin x. Zhonghua Er Ke Za Zhi. 2014 Nov;52(11):863-6. Zhonghua Er Ke Za Zhi. 2014. PMID: 25582476 Chinese.

5

[Kniest dysplasia due to mutation of COL2A1 gene].

Wu M, Liu L, Zhou Z, Sheng H, Yin X, Li X, Cheng J, Huang Y, Cai Y, Li C, Fan L, Liu H. Wu M, et al. Among authors: yin x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Jun;32(3):323-6. doi: 10.3760/cma.j.issn.1003-9406.2015.03.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015. PMID: 26037341 Chinese.

6

Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China.

Su L, Cheng J, Yin X, Liu G, Lu Z, Sheng H, Cai Y, Shi Q, Liu L. Su L, et al. Among authors: yin x. Andrologia. 2017 Dec;49(10). doi: 10.1111/and.12763. Epub 2017 Mar 6. Andrologia. 2017. PMID: 28261839

7

Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China.

Liu Z, Zhao X, Sheng H, Cai Y, Yin X, Chen X, Su L, Lu Z, Zeng C, Li X, Liu L. Liu Z, et al. Among authors: yin x. Am J Med Genet A. 2018 Mar;176(3):589-596. doi: 10.1002/ajmg.a.38601. Epub 2018 Jan 23. Am J Med Genet A. 2018. PMID: 29359854

8

Early prenatal diagnosis of lysosomal storage disorders by enzymatic and molecular analysis.

Li D, Lin Y, Huang Y, Zhang W, Jiang M, Li X, Zhao X, Sheng H, Yin X, Su X, Shao Y, Liu Z, Li D, Li F, Liao C, Liu L. Li D, et al. Among authors: yin x. Prenat Diagn. 2018 Sep;38(10):779-787. doi: 10.1002/pd.5329. Epub 2018 Jul 17. Prenat Diagn. 2018. PMID: 29966168

9

Clinical presentation and mutational spectrum in a series of 166 patients with classical 21-hydroxylase deficiency from South China.

Su L, Yin X, Cheng J, Cai Y, Wu D, Feng Z, Liu L. Su L, et al. Among authors: yin x. Clin Chim Acta. 2018 Nov;486:142-150. doi: 10.1016/j.cca.2018.07.039. Epub 2018 Jul 24. Clin Chim Acta. 2018. PMID: 30048636

10

Corrigendum for Li D, Lin Y, Huang Y, et al (2018) https://doi.org/10.1002/pd.5329.

Li D, Lin Y, Huang Y, Zhang W, Jiang M, Li X, Zhao X, Sheng H, Yin X, Su X, Shao Y, Liu Z, Li D, Li F, Liao C, Liu L. Li D, et al. Among authors: yin x. Prenat Diagn. 2019 Jan;39(1):57. doi: 10.1002/pd.5387. Prenat Diagn. 2019. PMID: 30632198 No abstract available.

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