Lu L - Search Results

1

Leukocyte telomere length and bipolar disorder risk: evidence from Mendelian randomization analysis.

Lu L, Zeng H, Wan B, Sun M. Lu L, et al. PeerJ. 2023 Mar 31;11:e15129. doi: 10.7717/peerj.15129. eCollection 2023. PeerJ. 2023. PMID: 37020849 Free PMC article.

2

Methylation-reprogrammed Wnt/β-catenin signalling mediated prenatal hypoxia-induced brain injury in foetal and offspring rats.

Zhang Y, Zhang M, Li L, Wei B, He A, Lu L, Li X, Zhang L, Xu Z, Sun M. Zhang Y, et al. Among authors: lu l. J Cell Mol Med. 2018 Aug;22(8):3866-3874. doi: 10.1111/jcmm.13660. Epub 2018 May 28. J Cell Mol Med. 2018. PMID: 29808608 Free PMC article.

3

Prenatal hypoxia plus postnatal high-fat diet exacerbated vascular dysfunction via up-regulated vascular Cav1.2 channels in offspring rats.

Li X, Feng X, Lu L, He A, Liu B, Zhang Y, Shi R, Liu Y, Chen X, Sun M, Xu Z. Li X, et al. Among authors: lu l. J Cell Mol Med. 2019 Feb;23(2):1183-1196. doi: 10.1111/jcmm.14020. Epub 2018 Dec 16. J Cell Mol Med. 2019. PMID: 30556291 Free PMC article.

4

Methylation-reprogrammed AGTR1 results in increased vasoconstriction by angiotensin II in human umbilical cord vessel following in vitro fertilization-embryo transfer.

Zhang M, Lu L, Zhang Y, Li X, Fan X, Chen X, Tang J, Han B, Li M, Tao J, Gao Q, Xu Z, Sun M. Zhang M, et al. Among authors: lu l. Life Sci. 2019 Oct 1;234:116792. doi: 10.1016/j.lfs.2019.116792. Epub 2019 Aug 26. Life Sci. 2019. PMID: 31465733

5

AURKB: a promising biomarker in clear cell renal cell carcinoma.

Wan B, Huang Y, Liu B, Lu L, Lv C. Wan B, et al. Among authors: lu l. PeerJ. 2019 Sep 16;7:e7718. doi: 10.7717/peerj.7718. eCollection 2019. PeerJ. 2019. PMID: 31576249 Free PMC article.

6

A novel dominant-negative mutation of the CSF1R gene causes adult-onset leukoencephalopathy with axonal spheroids and pigmented glia.

Leng C, Lu L, Wang G, Zhang Y, Xu Y, Lin X, Shen N, Xu X, Qun S, Sun M, Ge W. Leng C, et al. Among authors: lu l. Am J Transl Res. 2019 Sep 15;11(9):6093-6101. eCollection 2019. Am J Transl Res. 2019. PMID: 31632577 Free PMC article.

7

Essential tremor as the early symptom of NOTCH2NLC gene-related repeat expansion disorder.

Chen H, Lu L, Wang B, Hua X, Wan B, Sun M, Xu X. Chen H, et al. Among authors: lu l. Brain. 2020 Jul 1;143(7):e56. doi: 10.1093/brain/awaa142. Brain. 2020. PMID: 32449905 No abstract available.

8

Brachydactyly type A3 is caused by a novel 13 bp HOXD13 frameshift deletion in a Chinese family.

Zhang M, Lu L, Wei B, Zhang Y, Li X, Shi Y, Ge W, Sun M. Zhang M, et al. Among authors: lu l. Am J Med Genet A. 2020 Oct;182(10):2432-2436. doi: 10.1002/ajmg.a.61788. Epub 2020 Aug 13. Am J Med Genet A. 2020. PMID: 32789964

9

Re-defining the clinicopathological spectrum of neuronal intranuclear inclusion disease.

Chen H, Lu L, Wang B, Cui G, Wang X, Wang Y, Raza HK, Min Y, Li K, Cui Y, Miao Z, Wan B, Sun M, Xu X. Chen H, et al. Among authors: lu l. Ann Clin Transl Neurol. 2020 Oct;7(10):1930-1941. doi: 10.1002/acn3.51189. Epub 2020 Sep 15. Ann Clin Transl Neurol. 2020. PMID: 32931652 Free PMC article.

10

Methylation-reprogrammed CHRM3 results in vascular dysfunction in the human umbilical vein following IVF-ET†.

Shi Y, Liu J, Zhu D, Lu L, Zhang M, Li W, Zeng H, Yu X, Guo J, Zhang Y, Zhou X, Gao Q, Xia F, Chen Y, Li M, Sun M. Shi Y, et al. Among authors: lu l. Biol Reprod. 2022 Apr 26;106(4):687-698. doi: 10.1093/biolre/ioab234. Biol Reprod. 2022. PMID: 34935917

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