Wu L - Search Results

1

Analysis of UGT1A1 genotype-phenotype correlation in Chinese patients with gilbert and crigler-Najjar II syndrome.

Wu L, Li Z, Song Y, Li Y, Zhang W, Zhong X, Wang X, Huang J, Ou X. Wu L, et al. Eur J Med Genet. 2024 Oct;71:104962. doi: 10.1016/j.ejmg.2024.104962. Epub 2024 Jul 26. Eur J Med Genet. 2024. PMID: 39069255 Free article.

2

Mutation analysis of the ABCC2 gene in Chinese patients with Dubin-Johnson syndrome.

Wu L, Zhang W, Jia S, Zhao X, Zhou D, Xu A, Duan W, Wu Z, Li H, Zheng S, Nan Y, Jia J, Huang J, Ou X. Wu L, et al. Among authors: wu z. Exp Ther Med. 2018 Nov;16(5):4201-4206. doi: 10.3892/etm.2018.6682. Epub 2018 Sep 3. Exp Ther Med. 2018. PMID: 30344695 Free PMC article.

3

Insertion of LINE-1 Retrotransposon Inducing Exon Inversion Causes a Rotor Syndrome Phenotype.

Zhou D, Qi S, Zhang W, Wu L, Xu A, Li X, Zhang B, Li Y, Jia S, Wang H, Jia J, Ou X, Huang J, You H. Zhou D, et al. Among authors: wu l. Front Genet. 2020 Jan 31;10:1399. doi: 10.3389/fgene.2019.01399. eCollection 2019. Front Genet. 2020. PMID: 32082363 Free PMC article.

4

A recurrent ABCC2 p.G693R mutation resulting in loss of function of MRP2 and hyperbilirubinemia in Dubin-Johnson syndrome in China.

Wu L, Li Y, Song Y, Zhou D, Jia S, Xu A, Zhang W, You H, Jia J, Huang J, Ou X. Wu L, et al. Orphanet J Rare Dis. 2020 Mar 18;15(1):74. doi: 10.1186/s13023-020-1346-4. Orphanet J Rare Dis. 2020. PMID: 32183854 Free PMC article.

5

Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China.

Wu L, Zhang W, Li Y, Zhou D, Zhang B, Xu A, Wu Z, Wu L, Li S, Wang X, Zhao X, Wang Q, Li M, Wang Y, You H, Huang J, Ou X, Jia J. Wu L, et al. Among authors: wu z. Orphanet J Rare Dis. 2021 Sep 28;16(1):398. doi: 10.1186/s13023-021-02020-y. Orphanet J Rare Dis. 2021. PMID: 34583728 Free PMC article.

6

Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis.

Zhang W, Li Y, Xu A, Ouyang Q, Wu L, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, You H, Huang J, Ou X, Jia J; China Registry of Genetic/Metabolic Liver Diseases (CR-GMLD) Group. Zhang W, et al. Among authors: wu l. Orphanet J Rare Dis. 2022 Jun 6;17(1):216. doi: 10.1186/s13023-022-02349-y. Orphanet J Rare Dis. 2022. PMID: 35668470 Free PMC article.

7

"Haemochromatotic" characteristics of the human BEL-7402 cell line.

Xu A, Li Y, Chen W, Li X, Zhang W, Li S, Wu L, Wu Z, Zhang B, Ou X, Huang J. Xu A, et al. Among authors: wu l, wu z. Br J Haematol. 2018 Oct;183(2):302-306. doi: 10.1111/bjh.14952. Epub 2017 Sep 29. Br J Haematol. 2018. PMID: 28961311 Free article. No abstract available.

8

A novel SLC40A1 p.Y333H mutation with gain of function of ferroportin: A recurrent cause of haemochromatosis in China.

Zhang W, Xu A, Li Y, Zhao S, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, Nan Y, You H, Jia J, Ou X, Huang J; China Registry of Genetic/Metabolic Liver Diseases (CR-GMLD) Group. Zhang W, et al. Among authors: wu l. Liver Int. 2019 Jun;39(6):1120-1127. doi: 10.1111/liv.14013. Epub 2018 Dec 28. Liver Int. 2019. PMID: 30500107

9

Electro-acupuncture reduced steatosis on MRI-PDFF in patients with non-alcoholic steatohepatitis: a randomized controlled pilot clinical trial.

Zhao J, Wang Q, Zhao X, Wu L, Li J, Zhang W, Xu S, Han C, Du Y, Tong X, Duan W, Cao D, Ren H, Zhao X, Ou X, Jia J, You H. Zhao J, et al. Among authors: wu l. Chin Med. 2023 Feb 24;18(1):19. doi: 10.1186/s13020-023-00724-w. Chin Med. 2023. PMID: 36829229 Free PMC article.

10

Genetic Factors and Their Role in the Pathogenesis of Biliary Atresia.

Wu LN, Zhu ZJ, Sun LY. Wu LN, et al. Front Pediatr. 2022 Jun 29;10:912154. doi: 10.3389/fped.2022.912154. eCollection 2022. Front Pediatr. 2022. PMID: 35844731 Free PMC article. Review.

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