Zailong Qin[Author] - Search Results

Year	Number of Results
2013	1
2014	2
2015	2
2016	2
2017	4
2018	8
2019	5
2020	15
2021	9
2022	10
2023	8
2024	12

1

The function and mechanism of lactate and lactylation in tumor metabolism and microenvironment.

Zhang Y, Peng Q, Zheng J, Yang Y, Zhang X, Ma A, Qin Y, Qin Z, Zheng X. Zhang Y, et al. Among authors: qin z. Genes Dis. 2022 Oct 19;10(5):2029-2037. doi: 10.1016/j.gendis.2022.10.006. eCollection 2023 Sep. Genes Dis. 2022. PMID: 37492749 Free PMC article. Review.

2

Haplotype-specific MAPK3 expression in 16p11.2 deletion contributes to variable neurodevelopment.

Liu F, Liang C, Li Z, Zhao S, Yuan H, Yao R, Qin Z, Shangguan S, Zhang S, Zou LP, Chen Q, Gao Z, Wen S, Peng J, Yin F, Chen F, Qiu X, Luo J, Xie Y, Lu D, Zhang Y, Xie H, Li G, Zhang TJ, Luan P, Wang H, Cui X, Huang H, Liu R, Sun X, Chen C, Wu N, Wang J, Liu C, Shen Y, Gusella JF, Chen X. Liu F, et al. Among authors: qin z. Brain. 2023 Aug 1;146(8):3347-3363. doi: 10.1093/brain/awad071. Brain. 2023. PMID: 36869767

3

Phenotypic Spectrum of Trisomy 18 Mosaicism: a New Patient and Literature Review.

Sun W, Wang L, Liu T, Ouyang L, Qin W, Luo J, Qin Z. Sun W, et al. Among authors: qin z. Clin Lab. 2023 Mar 1;69(3). doi: 10.7754/Clin.Lab.2022.220610. Clin Lab. 2023. PMID: 36912299 Review.

4

Eph receptors: the bridge linking host and virus.

Wang J, Zheng X, Peng Q, Zhang X, Qin Z. Wang J, et al. Among authors: qin z. Cell Mol Life Sci. 2020 Jun;77(12):2355-2365. doi: 10.1007/s00018-019-03409-6. Epub 2019 Dec 31. Cell Mol Life Sci. 2020. PMID: 31893311 Free PMC article. Review.

5

Serine/arginine-rich splicing factors: the bridge linking alternative splicing and cancer.

Zheng X, Peng Q, Wang L, Zhang X, Huang L, Wang J, Qin Z. Zheng X, et al. Among authors: qin z. Int J Biol Sci. 2020 Jul 6;16(13):2442-2453. doi: 10.7150/ijbs.46751. eCollection 2020. Int J Biol Sci. 2020. PMID: 32760211 Free PMC article. Review.

6

Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing-site variant and a missense variant in the ROBO3 gene.

Yi S, Qin Z, Zhou X, Chen J, Yi S, Chen Q, Huang L, Zhang Q, Chen B, Luo J. Yi S, et al. Among authors: qin z. Mol Genet Genomic Med. 2023 Sep;11(9):e2215. doi: 10.1002/mgg3.2215. Epub 2023 Jun 18. Mol Genet Genomic Med. 2023. PMID: 37330975 Free PMC article. Review.

7

Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literature.

Zhang Q, Qin Z, Yi S, Wei H, Zhou XZ, Su J. Zhang Q, et al. Among authors: qin z. BMC Med Genomics. 2020 Dec 10;13(1):183. doi: 10.1186/s12920-020-00842-6. BMC Med Genomics. 2020. PMID: 33302946 Free PMC article. Review.

8

Novel SLC12A1 mutations cause Bartter syndrome in two patients with different prognoses.

Yi S, Li M, Yang Q, Zhang X, Chen F, Qin Z, Yi S, Huang L, Wei H, Zhang Q, Luo J. Yi S, et al. Among authors: qin z. Clin Chim Acta. 2022 Jun 1;531:120-125. doi: 10.1016/j.cca.2022.03.025. Epub 2022 Mar 28. Clin Chim Acta. 2022. PMID: 35358470 Review.

9

Epstein-Barr Virus MicroRNA miR-BART5-3p Inhibits p53 Expression.

Zheng X, Wang J, Wei L, Peng Q, Gao Y, Fu Y, Lu Y, Qin Z, Zhang X, Lu J, Ou C, Li Z, Zhang X, Liu P, Xiong W, Li G, Yan Q, Ma J. Zheng X, et al. Among authors: qin z. J Virol. 2018 Nov 12;92(23):e01022-18. doi: 10.1128/JVI.01022-18. Print 2018 Dec 1. J Virol. 2018. PMID: 30209170 Free PMC article.

10

Novel compound heterozygous variants in the RPL3L gene causing dilated cardiomyopathy type-2D: a case report and literature review.

Yang Q, Zhang Q, Qin Z, Zhang S, Yi S, Yi S, Zhang Q, Luo J. Yang Q, et al. Among authors: qin z. BMC Med Genomics. 2023 Jun 12;16(1):127. doi: 10.1186/s12920-023-01567-y. BMC Med Genomics. 2023. PMID: 37308880 Free PMC article. Review.

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