Ma L - Search Results

1

Caffeine Inhibits NLRP3 Inflammasome Activation by Suppressing MAPK/NF-κB and A2aR Signaling in LPS-Induced THP-1 Macrophages.

Zhao W, Ma L, Cai C, Gong X. Zhao W, et al. Among authors: ma l. Int J Biol Sci. 2019 Jun 2;15(8):1571-1581. doi: 10.7150/ijbs.34211. eCollection 2019. Int J Biol Sci. 2019. PMID: 31360100 Free PMC article.

2

[Expression of microRNA-495-5p in preterm infants with bronchopulmonary dysplasia: a bioinformatics analysis].

Sun YF, Ma L, Gong XH, Hong WC, Cai C. Sun YF, et al. Among authors: ma l. Zhongguo Dang Dai Er Ke Za Zhi. 2020 Jan;22(1):24-30. doi: 10.7499/j.issn.1008-8830.2020.01.006. Zhongguo Dang Dai Er Ke Za Zhi. 2020. PMID: 31948520 Free PMC article. Chinese.

3

Phenotypic spectrum of typical CHARGE syndrome in a Chinese male neonate: a case report.

Sun Y, Sun J, Li N, Cai C, Gong X, Ma L. Sun Y, et al. Among authors: ma l. Transl Pediatr. 2020 Apr;9(2):180-186. doi: 10.21037/tp.2020.03.09. Transl Pediatr. 2020. PMID: 32477919 Free PMC article.

4

Application of Next-Generation Sequencing for Genetic Diagnosis in Neonatal Intensive Care Units: Results of a Multicenter Study in China.

Zhu T, Gong X, Bei F, Ma L, Chen Y, Zhang Y, Wang X, Sun J, Wang J, Qiu G, Sun J, Sun Y, Zhang Y. Zhu T, et al. Among authors: ma l. Front Genet. 2020 Nov 6;11:565078. doi: 10.3389/fgene.2020.565078. eCollection 2020. Front Genet. 2020. PMID: 33240318 Free PMC article.

5

A Chinese newborn with Zellweger syndrome and compound heterozygous mutations novel in the PEX1 gene: a case report and literature review.

Lu P, Ma L, Sun J, Gong X, Cai C. Lu P, et al. Among authors: ma l. Transl Pediatr. 2021 Feb;10(2):446-453. doi: 10.21037/tp-20-167. Transl Pediatr. 2021. PMID: 33708531 Free PMC article.

6

Primary immunodeficiency-related genes in neonatal intensive care unit patients with various genetic immune abnormalities: a multicentre study in China.

Zhu T, Gong X, Bei F, Ma L, Sun J, Wang J, Qiu G, Sun J, Sun Y, Zhang Y. Zhu T, et al. Among authors: ma l. Clin Transl Immunology. 2021 Mar 22;10(3):e1266. doi: 10.1002/cti2.1266. eCollection 2021. Clin Transl Immunology. 2021. PMID: 33777394 Free PMC article.

7

Two novel variants in PLOD1 causing hydrocephalus in female newborn with kyphoscoliotic Ehlers-Danlos syndrome.

Zhao Y, Sun J, Chen Y, Hu Y, Gong X, Ma L. Zhao Y, et al. Among authors: ma l. Eur J Med Genet. 2021 Sep;64(9):104269. doi: 10.1016/j.ejmg.2021.104269. Epub 2021 Jun 20. Eur J Med Genet. 2021. PMID: 34161861

8

Severe hyperbilirubinemia in a neonate with hereditary spherocytosis due to a de novo ankyrin mutation: A case report.

Wang JF, Ma L, Gong XH, Cai C, Sun JJ. Wang JF, et al. Among authors: ma l. World J Clin Cases. 2021 Jul 6;9(19):5245-5251. doi: 10.12998/wjcc.v9.i19.5245. World J Clin Cases. 2021. PMID: 34307574 Free PMC article.

9

The neonatal onset diabetes mellitus of Chinese neonate with congenital generalized lipodystrophy 2: a case report.

Yang Y, Ma L, Sun J, Gong X, Cai C, Hong W. Yang Y, et al. Among authors: ma l. BMC Endocr Disord. 2022 Mar 29;22(1):83. doi: 10.1186/s12902-022-00992-x. BMC Endocr Disord. 2022. PMID: 35351089 Free PMC article.

10

Loss of Protein Function Causing Severe Phenotypes of Female-Restricted Wieacker Wolff Syndrome due to a Novel Nonsense Mutation in the ZC4H2 Gene.

Sun JJ, Cai Q, Xu M, Liu YN, Li WR, Li J, Ma L, Cai C, Gong XH, Zeng YT, Ren ZR, Zeng F. Sun JJ, et al. Among authors: ma l. Genes (Basel). 2022 Aug 29;13(9):1558. doi: 10.3390/genes13091558. Genes (Basel). 2022. PMID: 36140726 Free PMC article.

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