Yu L - Search Results

1

Establishment and characterization of ZJUCHi003: an induced pluripotent stem cell line from a patient with Temple-Baraitser/Zimmermann-Laband syndrome carrying KCNH1 c.1070G > A (p.R357Q) variant.

Chen D, Su J, Huang X, Chen H, Jiang T, Zhi C, Zhou Z, Zhang B, Yu L, Jiang X. Chen D, et al. Among authors: yu l. Hum Cell. 2024 May;37(3):832-839. doi: 10.1007/s13577-024-01031-8. Epub 2024 Feb 19. Hum Cell. 2024. PMID: 38372889

2

Mitochondrial DNA variant spectrum and the association with chronic tic disorders.

Jiang P, Zhu T, Liu J, Tao X, Xue Z, Tao Y, Chen H, Zeng X, Zhu W, Shu Q, Yu L. Jiang P, et al. Among authors: yu l. Eur J Neurol. 2022 Nov;29(11):3187-3196. doi: 10.1111/ene.15484. Epub 2022 Jul 20. Eur J Neurol. 2022. PMID: 35781907

3

NRAS p.Q61R/K allele load is correlated to different phenotypes of congenital melanocytic naevi.

Zhao X, Dai Y, Zhang L, Liu Y, Chen H, Yue X, Yu L. Zhao X, et al. Among authors: yu l. Clin Exp Dermatol. 2022 Dec;47(12):2201-2207. doi: 10.1111/ced.15369. Epub 2022 Oct 5. Clin Exp Dermatol. 2022. PMID: 35962610

4

Integrated bulk and single-cell RNA-sequencing reveals SPOCK2 as a novel biomarker gene in the development of congenital pulmonary airway malformation.

Tan Z, Li F, Chen Q, Chen H, Xue Z, Zhang J, Gao Y, Liang L, Huang T, Zhang S, Li J, Shu Q, Yu L. Tan Z, et al. Among authors: yu l. Respir Res. 2023 May 10;24(1):127. doi: 10.1186/s12931-023-02436-z. Respir Res. 2023. PMID: 37165378 Free PMC article.

5

A Systematic Review and Meta-Analysis of the R778L Mutation in ATP7B With Wilson Disease in China.

Xue Z, Chen H, Yu L, Jiang P. Xue Z, et al. Among authors: yu l. Pediatr Neurol. 2023 Aug;145:135-147. doi: 10.1016/j.pediatrneurol.2023.04.026. Epub 2023 May 8. Pediatr Neurol. 2023. PMID: 37354629

6

Integrative analysis of bulk and single-cell RNA sequencing reveals the gene expression profile and the critical signaling pathways of type II CPAM.

Li F, Tan Z, Chen H, Gao Y, Xia J, Huang T, Liang L, Zhang J, Zhang X, Shi X, Chen Q, Shu Q, Yu L. Li F, et al. Among authors: yu l. Cell Biosci. 2024 Jul 18;14(1):94. doi: 10.1186/s13578-024-01276-8. Cell Biosci. 2024. PMID: 39026356 Free PMC article.

7

Diminished GALNS activity in induced pluripotent stem cells of mucopolysaccharidosis IVA caused by compound p. S162Y and p. C165F mutation.

Jiang X, Chen S, Jiang Z, Chen D, Chen H, Bai G, Yu L, Chen W. Jiang X, et al. Among authors: yu l. QJM. 2024 Aug 26:hcae164. doi: 10.1093/qjmed/hcae164. Online ahead of print. QJM. 2024. PMID: 39186005

8

Application and insights of targeted next-generation sequencing in a large cohort of 46,XY disorders of sex development in Chinese.

Chen H, Chen G, Li F, Huang Y, Zhu L, Zhao Y, Jiang Z, Yan X, Yu L. Chen H, et al. Among authors: yu l. Biol Sex Differ. 2024 Sep 16;15(1):73. doi: 10.1186/s13293-024-00648-6. Biol Sex Differ. 2024. PMID: 39285472 Free PMC article.

9

A novel approach for breast cancer treatment: the multifaceted antitumor effects of rMeV-Hu191.

Zheng XY, Lv Y, Xu LY, Zhou DM, Yu L, Zhao ZY. Zheng XY, et al. Among authors: yu l. Hereditas. 2024 Sep 28;161(1):36. doi: 10.1186/s41065-024-00337-9. Hereditas. 2024. PMID: 39342391 Free PMC article.

10

Successful treatment of retinopathy of prematurity in oculocutaneous albinism with OCA2 variants: a case report and review of literature.

Zheng XY, Wu DW, Yu L, Zhao ZY. Zheng XY, et al. Among authors: yu l. BMC Pediatr. 2024 Jun 10;24(1):390. doi: 10.1186/s12887-024-04864-2. BMC Pediatr. 2024. PMID: 38858617 Free PMC article. Review.

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