Yang L - Search Results

1

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. Among authors: yang l. 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.

2

Exome sequencing identifies SLC24A5 as a candidate gene for nonsyndromic oculocutaneous albinism.

Wei AH, Zang DJ, Zhang Z, Liu XZ, He X, Yang L, Wang Y, Zhou ZY, Zhang MR, Dai LL, Yang XM, Li W. Wei AH, et al. Among authors: yang xm, yang l. J Invest Dermatol. 2013 Jul;133(7):1834-40. doi: 10.1038/jid.2013.49. Epub 2013 Jan 30. J Invest Dermatol. 2013. PMID: 23364476 Free article.

3

HPS1 Regulates the Maturation of Large Dense Core Vesicles and Lysozyme Secretion in Paneth Cells.

Yu J, He X, Wei A, Liu T, Zhang Q, Pan Y, Hao Z, Yang L, Yuan Y, Zhang Z, Zhang C, Hao C, Liu Z, Li W. Yu J, et al. Among authors: yang l. Front Immunol. 2020 Nov 5;11:560110. doi: 10.3389/fimmu.2020.560110. eCollection 2020. Front Immunol. 2020. PMID: 33224134 Free PMC article.

4

The BLOS1-interacting protein KXD1 is involved in the biogenesis of lysosome-related organelles.

Yang Q, He X, Yang L, Zhou Z, Cullinane AR, Wei A, Zhang Z, Hao Z, Zhang A, He M, Feng Y, Gao X, Gahl WA, Huizing M, Li W. Yang Q, et al. Among authors: yang l. Traffic. 2012 Aug;13(8):1160-9. doi: 10.1111/j.1600-0854.2012.01375.x. Epub 2012 May 28. Traffic. 2012. PMID: 22554196 Free PMC article.

5

Biogenesis of lysosome-related organelles complex-1 subunit 1 (BLOS1) interacts with sorting nexin 2 and the endosomal sorting complex required for transport-I (ESCRT-I) component TSG101 to mediate the sorting of epidermal growth factor receptor into endosomal compartments.

Zhang A, He X, Zhang L, Yang L, Woodman P, Li W. Zhang A, et al. Among authors: yang l. J Biol Chem. 2014 Oct 17;289(42):29180-94. doi: 10.1074/jbc.M114.576561. Epub 2014 Sep 2. J Biol Chem. 2014. PMID: 25183008 Free PMC article.

6

Genetic variants and mutational spectrum of Chinese Hermansky-Pudlak syndrome patients.

Liu T, Yuan Y, Bai D, Qi Z, Yang L, Zhang T, Yang X, Li W, Wei A. Liu T, et al. Among authors: yang l, yang x. Pigment Cell Melanoma Res. 2021 Jan;34(1):111-121. doi: 10.1111/pcmr.12916. Epub 2020 Aug 17. Pigment Cell Melanoma Res. 2021. PMID: 32725903

7

NGS-based 100-gene panel of hypopigmentation identifies mutations in Chinese Hermansky-Pudlak syndrome patients.

Wei A, Yuan Y, Bai D, Ma J, Hao Z, Zhang Y, Yu J, Zhou Z, Yang L, Yang X, Li L, Li W. Wei A, et al. Among authors: yang l, yang x. Pigment Cell Melanoma Res. 2016 Nov;29(6):702-706. doi: 10.1111/pcmr.12534. Epub 2016 Oct 19. Pigment Cell Melanoma Res. 2016. PMID: 27593200

8

BLOC-2 subunit HPS6 deficiency affects the tubulation and secretion of von Willebrand factor from mouse endothelial cells.

Ma J, Zhang Z, Yang L, Kriston-Vizi J, Cutler DF, Li W. Ma J, et al. Among authors: yang l. J Genet Genomics. 2016 Dec 20;43(12):686-693. doi: 10.1016/j.jgg.2016.09.007. Epub 2016 Oct 21. J Genet Genomics. 2016. PMID: 27889498 Free PMC article.

9

Instability of BLOC-2 and BLOC-3 in Chinese patients with Hermansky-Pudlak syndrome.

Wei A, Yuan Y, Qi Z, Liu T, Bai D, Zhang Y, Yu J, Yang L, Yang X, Li W. Wei A, et al. Among authors: yang l, yang x. Pigment Cell Melanoma Res. 2019 May;32(3):373-380. doi: 10.1111/pcmr.12748. Epub 2018 Nov 22. Pigment Cell Melanoma Res. 2019. PMID: 30387913

10

A zinc transporter, transmembrane protein 163, is critical for the biogenesis of platelet dense granules.

Yuan Y, Liu T, Huang X, Chen Y, Zhang W, Li T, Yang L, Chen Q, Wang Y, Wei A, Li W. Yuan Y, et al. Among authors: yang l. Blood. 2021 Apr 1;137(13):1804-1817. doi: 10.1182/blood.2020007389. Blood. 2021. PMID: 33513603 Free PMC article.

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