Luo S - Search Results

1

LncRNA GHET1 promotes cervical cancer progression through regulating AKT/mTOR and Wnt/β-catenin signaling pathways.

Liu Z, Luo S, Wu M, Huang C, Shi H, Song X. Liu Z, et al. Among authors: luo s. Biosci Rep. 2020 Jan 31;40(1):BSR20191265. doi: 10.1042/BSR20191265. Biosci Rep. 2020. PMID: 31682716 Free PMC article.

2

DDN-AS1-miR-15a/16-TCF3 feedback loop regulates tumor progression in cervical cancer.

Liu Z, Wu M, Shi H, Huang C, Luo S, Song X. Liu Z, et al. Among authors: luo s. J Cell Biochem. 2019 Jun;120(6):10228-10238. doi: 10.1002/jcb.28307. Epub 2018 Dec 23. J Cell Biochem. 2019. PMID: 30582201

3

miR-30a-3p inhibits the proliferation of liver cancer cells by targeting DNMT3a through the PI3K/AKT signaling pathway.

Chen Q, Gao Y, Yu Q, Tang F, Zhao PW, Luo SK, Lin JS, Mei H. Chen Q, et al. Oncol Lett. 2020 Jan;19(1):606-614. doi: 10.3892/ol.2019.11179. Epub 2019 Dec 3. Oncol Lett. 2020. PMID: 31897176 Free PMC article.

4

Identification and Characterization of a Germline Mutation in CARD11 From a Chinese Case of B Cell Expansion With NF-κB and T Cell Anergy.

Zhao P, Meng Q, Huang Y, Zhang L, Luo S, Zhang X, Tan L, Zhou A, Xiong H, He X. Zhao P, et al. Among authors: luo s. Front Immunol. 2021 Sep 7;12:676386. doi: 10.3389/fimmu.2021.676386. eCollection 2021. Front Immunol. 2021. PMID: 34557185 Free PMC article.

5

A 9-month-old Chinese patient with Gabriele-de Vries syndrome due to novel germline mutation in the YY1 gene.

Tan L, Li Y, Liu F, Huang Y, Luo S, Zhao P, Gu W, Lin J, Zhou A, He X. Tan L, et al. Among authors: luo s. Mol Genet Genomic Med. 2021 Feb;9(2):e1582. doi: 10.1002/mgg3.1582. Epub 2020 Dec 23. Mol Genet Genomic Med. 2021. PMID: 33369188 Free PMC article.

6

Infantile-onset CMT2D/dSMA-V in a Chinese family with parental germline mosaicism for a novel mutation in the GARS1 gene.

Huang Y, Bi B, Zhao P, Yu T, Luo S, Tan L, Liu Z, Liu J, He X. Huang Y, et al. Among authors: luo s. Mol Genet Genomic Med. 2022 Jan;10(1):e1846. doi: 10.1002/mgg3.1846. Epub 2021 Dec 12. Mol Genet Genomic Med. 2022. PMID: 34898052 Free PMC article.

7

Identification and characterization of novel mutations in MOGS in a Chinese patient with infantile spams.

Peiwei Zhao, Peng X, Luo S, Huang Y, Tan L, Shao J, He X. Peiwei Zhao, et al. Among authors: luo s. Neurogenetics. 2020 Apr;21(2):97-104. doi: 10.1007/s10048-019-00590-5. Epub 2020 Jan 10. Neurogenetics. 2020. PMID: 31925597

8

Analysis of epilepsy-associated variants in HCN3 - Functional implications and clinical observations.

Zhao P, Xiong H, Kuang G, Sun C, Zhang X, Huang Y, Luo S, Zhang L, Jiang J, He X. Zhao P, et al. Among authors: luo s. Epilepsia Open. 2024 Oct 3. doi: 10.1002/epi4.13049. Online ahead of print. Epilepsia Open. 2024. PMID: 39361439 Free article.

9

[Phenotypic and genotypic analysis of a girl carrying a 2q22.3 microduplication encompassing the MBD5 gene].

He X, Huang Y, Luo S, Cai X, Zeng C, Lin J. He X, et al. Among authors: luo s. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):624-627. doi: 10.3760/cma.j.issn.1003-9406.2019.06.024. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055822 Chinese.

10

Functional Analysis of a Novel CLN5 Mutation Identified in a Patient With Neuronal Ceroid Lipofuscinosis.

Luo S, Bi B, Zhu B, Tan L, Zhao P, Huang Y, Wu G, Zhou A, He X. Luo S, et al. Front Genet. 2020 Sep 2;11:536221. doi: 10.3389/fgene.2020.536221. eCollection 2020. Front Genet. 2020. PMID: 32983231 Free PMC article.

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