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Spatiotemporal mapping of gene expression landscapes and developmental trajectories during zebrafish embryogenesis.
Liu C, Li R, Li Y, Lin X, Zhao K, Liu Q, Wang S, Yang X, Shi X, Ma Y, Pei C, Wang H, Bao W, Hui J, Yang T, Xu Z, Lai T, Berberoglu MA, Sahu SK, Esteban MA, Ma K, Fan G, Li Y, Liu S, Chen A, Xu X, Dong Z, Liu L. Liu C, et al. Among authors: ma k, ma y. Dev Cell. 2022 May 23;57(10):1284-1298.e5. doi: 10.1016/j.devcel.2022.04.009. Epub 2022 May 4. Dev Cell. 2022. PMID: 35512701 Free article.
Young and early-onset dilated cardiomyopathy with malignant ventricular arrhythmia and sudden cardiac death induced by the heterozygous LDB3, MYH6, and SYNE1 missense mutations.
Zhao T, Ma Y, Zhang Z, Xian J, Geng X, Wang F, Huang J, Yang Z, Luo Y, Lin Y. Zhao T, et al. Among authors: ma y. Ann Noninvasive Electrocardiol. 2021 Jul;26(4):e12840. doi: 10.1111/anec.12840. Epub 2021 May 5. Ann Noninvasive Electrocardiol. 2021. PMID: 33949037 Free PMC article.
SPEN induces miR-4652-3p to target HIPK2 in nasopharyngeal carcinoma.
Li Y, Lv Y, Cheng C, Huang Y, Yang L, He J, Tao X, Hu Y, Ma Y, Su Y, Wu L, Yu G, Jiang Q, Liu S, Liu X, Liu Z. Li Y, et al. Among authors: ma y. Cell Death Dis. 2020 Jul 2;11(7):509. doi: 10.1038/s41419-020-2699-2. Cell Death Dis. 2020. PMID: 32641685 Free PMC article.
Rare and potential pathogenic mutations of LMNA and LAMA4 associated with familial arrhythmogenic right ventricular cardiomyopathy/dysplasia with right ventricular heart failure, cerebral thromboembolism and hereditary electrocardiogram abnormality.
Chen J, Ma Y, Li H, Lin Z, Yang Z, Zhang Q, Wang F, Lin Y, Ye Z, Lin Y. Chen J, et al. Among authors: ma y. Orphanet J Rare Dis. 2022 May 7;17(1):183. doi: 10.1186/s13023-022-02348-z. Orphanet J Rare Dis. 2022. PMID: 35526016 Free PMC article.
39,342 results
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