Li W - Search Results

1

Exome sequencing as the first-tier test for pediatric respiratory diseases: A single-center study.

Hao C, Guo R, Liu J, Hu X, Guo J, Yao Y, Zhao Z, Qi Z, Yin J, Chen L, Wang H, Xu B, Li W. Hao C, et al. Among authors: li w. Hum Mutat. 2021 Jul;42(7):891-900. doi: 10.1002/humu.24216. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33942430

2

The BLOC interactomes form a network in endosomal transport.

Li W, Feng Y, Hao C, Guo X, Cui Y, He M, He X. Li W, et al. J Genet Genomics. 2007 Aug;34(8):669-82. doi: 10.1016/S1673-8527(07)60076-9. J Genet Genomics. 2007. PMID: 17707211 Review.

3

JNK activation mediates the apoptosis of xCT-deficient cells.

Qiao HX, Hao CJ, Li Y, He X, Chen RS, Cui J, Xu ZH, Li W. Qiao HX, et al. Among authors: li y, li w. Biochem Biophys Res Commun. 2008 Jun 13;370(4):584-8. doi: 10.1016/j.bbrc.2008.03.134. Epub 2008 Apr 3. Biochem Biophys Res Commun. 2008. PMID: 18395005

4

Dysbindin deficiency in sandy mice causes reduction of snapin and displays behaviors related to schizophrenia.

Feng YQ, Zhou ZY, He X, Wang H, Guo XL, Hao CJ, Guo Y, Zhen XC, Li W. Feng YQ, et al. Among authors: li w. Schizophr Res. 2008 Dec;106(2-3):218-28. doi: 10.1016/j.schres.2008.07.018. Epub 2008 Sep 5. Schizophr Res. 2008. PMID: 18774265

5

Impaired autophagy in hilar mossy cells of the dentate gyrus and its implication in schizophrenia.

Yuan Y, Wang H, Wei Z, Li W. Yuan Y, et al. Among authors: li w. J Genet Genomics. 2015 Jan 20;42(1):1-8. doi: 10.1016/j.jgg.2014.12.001. Epub 2014 Dec 23. J Genet Genomics. 2015. PMID: 25619597

6

SLC35D3 increases autophagic activity in midbrain dopaminergic neurons by enhancing BECN1-ATG14-PIK3C3 complex formation.

Wei ZB, Yuan YF, Jaouen F, Ma MS, Hao CJ, Zhang Z, Chen Q, Yuan Z, Yu L, Beurrier C, Li W. Wei ZB, et al. Among authors: li w. Autophagy. 2016 Jul 2;12(7):1168-79. doi: 10.1080/15548627.2016.1179402. Epub 2016 May 12. Autophagy. 2016. PMID: 27171858 Free PMC article.

7

Clinical feature and waveform in infantile nystagmus syndrome in children with FRMD7 gene mutations.

Bai D, Shi W, Qi Z, Li W, Wei A, Cui Y, Li C, Li L. Bai D, et al. Among authors: li c, li w, li l. Sci China Life Sci. 2017 Jul;60(7):707-713. doi: 10.1007/s11427-017-9089-5. Epub 2017 Jun 14. Sci China Life Sci. 2017. PMID: 28623544

8

Brain white matter microstructural alterations in children of type I Gaucher disease characterized with diffusion tensor MR imaging.

Kang H, Zhang M, Ouyang M, Guo R, Yu Q, Peng Q, Zhang N, Zhang Y, Duan Y, Tang X, Mishra V, Fang F, Li W, Huang H, Peng Y. Kang H, et al. Among authors: li w. Eur J Radiol. 2018 May;102:22-29. doi: 10.1016/j.ejrad.2018.02.014. Epub 2018 Feb 15. Eur J Radiol. 2018. PMID: 29685539

9

Application of multiplex ligation-dependent probe amplification in the genetic testing of oculocutaneous albinism.

Zhang YZ, Bai DY, Qi Z, Zhao SZ, Yang XM, Li W, Wei AH. Zhang YZ, et al. Among authors: li w. Chin Med J (Engl). 2019 Aug 20;132(16):2011-2012. doi: 10.1097/CM9.0000000000000356. Chin Med J (Engl). 2019. PMID: 31356463 Free PMC article. No abstract available.

10

Compound heterozygous LPIN2 pathogenic variants in a patient with Majeed syndrome with recurrent fever and severe neutropenia: case report.

Liu J, Hu XY, Zhao ZP, Guo RL, Guo J, Li W, Hao CJ, Xu BP. Liu J, et al. Among authors: li w. BMC Med Genet. 2019 Nov 14;20(1):182. doi: 10.1186/s12881-019-0919-3. BMC Med Genet. 2019. PMID: 31727123 Free PMC article.

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