Hao C - Search Results

1

BLOS1 mediates kinesin switch during endosomal recycling of LDL receptor.

Zhang C, Hao C, Shui G, Li W. Zhang C, et al. Among authors: hao c. Elife. 2020 Nov 12;9:e58069. doi: 10.7554/eLife.58069. Elife. 2020. PMID: 33179593 Free PMC article.

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. Among authors: hao c. 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. 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

DTNBP1, a schizophrenia susceptibility gene, affects kinetics of transmitter release.

Chen XW, Feng YQ, Hao CJ, Guo XL, He X, Zhou ZY, Guo N, Huang HP, Xiong W, Zheng H, Zuo PL, Zhang CX, Li W, Zhou Z. Chen XW, et al. J Cell Biol. 2008 Jun 2;181(5):791-801. doi: 10.1083/jcb.200711021. Epub 2008 May 26. J Cell Biol. 2008. PMID: 18504299 Free PMC article.

5

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. 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

6

Mutation of SLC35D3 causes metabolic syndrome by impairing dopamine signaling in striatal D1 neurons.

Zhang Z, Hao CJ, Li CG, Zang DJ, Zhao J, Li XN, Wei AH, Wei ZB, Yang L, He X, Zhen XC, Gao X, Speakman JR, Li W. Zhang Z, et al. PLoS Genet. 2014 Feb 13;10(2):e1004124. doi: 10.1371/journal.pgen.1004124. eCollection 2014 Feb. PLoS Genet. 2014. PMID: 24550737 Free PMC article.

7

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: hao cj. 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.

8

A novel de novo CASZ1 heterozygous frameshift variant causes dilated cardiomyopathy and left ventricular noncompaction cardiomyopathy.

Guo J, Li Z, Hao C, Guo R, Hu X, Qian S, Zeng J, Gao H, Li W. Guo J, et al. Among authors: hao c. Mol Genet Genomic Med. 2019 Aug;7(8):e828. doi: 10.1002/mgg3.828. Epub 2019 Jul 3. Mol Genet Genomic Med. 2019. PMID: 31268246 Free PMC article.

9

Whole-exome sequencing identifies a novel compound heterozygous mutation of ANKS6 gene in a Chinese nephronophthisis patient.

Fang B, Guo J, Hao C, Guo R, Qian S, Li W, Jia X. Fang B, et al. Among authors: hao c. Clin Chim Acta. 2020 Feb;501:131-135. doi: 10.1016/j.cca.2019.10.030. Epub 2019 Oct 31. Clin Chim Acta. 2020. PMID: 31678577

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. 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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