Zobrazeno 1 - 10
of 141
pro vyhledávání: '"Lysosome-associated membrane glycoprotein"'
Autor:
Yongxiang Wang, Ming Bai, Piyi Zhang, Yu Peng, Zixian Chen, Zhiyu He, Jin Xu, Youqi Zhu, Dongdong Yan, Runqing Wang, Zheng Zhang
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 9, Pp n/a-n/a (2023)
Abstract Background Danon disease is characterized by the failure of lysosomal biogenesis, maturation, and function due to a deficiency of lysosomal membrane structural protein (LAMP2). Methods The current report describes a female patient with a sud
Externí odkaz:
https://doaj.org/article/6ea9c0f46ca8443094fe71a8a3cecf13
Akademický článek
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Autor:
Irene Lopez-Fabuel, Marina Garcia-Macia, Costantina Buondelmonte, Olga Burmistrova, Nicolo Bonora, Paula Alonso-Batan, Brenda Morant-Ferrando, Carlos Vicente-Gutierrez, Daniel Jimenez-Blasco, Ruben Quintana-Cabrera, Emilio Fernandez, Jordi Llop, Pedro Ramos-Cabrer, Aseel Sharaireh, Marta Guevara-Ferrer, Lorna Fitzpatrick, Christopher D. Thompton, Tristan R. McKay, Stephan Storch, Diego L. Medina, Sara E. Mole, Peter O. Fedichev, Angeles Almeida, Juan P. Bolaños
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications
Digital.CSIC. Repositorio Institucional del CSIC
instname
Nature Communications
CLN7 neuronal ceroid lipofuscinosis is an inherited lysosomal storage neurodegenerative disease highly prevalent in children. CLN7/MFSD8 gene encodes a lysosomal membrane glycoprotein, but the biochemical processes affected by CLN7-loss of function a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c646c3f91c4f2ae3f22b4ced9e7be27
https://doaj.org/article/3a651b3190b84e729467d309cc661713
https://doaj.org/article/3a651b3190b84e729467d309cc661713
Akademický článek
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Autor:
Yihui Yang, Xiangjin Zheng, Sha Li, Jinyi Liu, Wan Li, Jie Yi, Weiqi Fu, Jinhua Wang, Guanhua Du, Liwen Ren
Publikováno v:
Acta Pharmaceutica Sinica B, Vol 11, Iss 9, Pp 2783-2797 (2021)
Acta Pharmaceutica Sinica. B
Acta Pharmaceutica Sinica. B
Exosomes are cell-derived nanovesicles with diameters from 30 to 150 nm, released upon fusion of multivesicular bodies with the cell surface. They can transport nucleic acids, proteins, and lipids for intercellular communication and activate signalin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dfeee0d62636797c4da5264a84ca925
https://doi.org/10.1016/j.apsb.2021.01.001
https://doi.org/10.1016/j.apsb.2021.01.001
Autor:
Hiroaki Kajiyama, Yukari Oda, Kimihiro Nishino, Yuki Nishiko, Eiko Yamamoto, Eri Watanabe, Kaoru Niimi, Mayu Shibata
Publikováno v:
Placenta. 117
Lysosome-associated membrane glycoprotein 2 (LAMP-2) is a target protein for glycosylation by N-acetylglucosaminyltransferase IV (GnT-IV), which catalyzes the formation of β1,4GlcNAc branches on the mannose core of N-glycans in choriocarcinoma cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b4bdb530dba974524c57693ff8d362f
https://pubmed.ncbi.nlm.nih.gov/34875536
https://pubmed.ncbi.nlm.nih.gov/34875536
Autor:
Nadine, Zimmann, Petr, Rada, Vojtěch, Žárský, Tamara, Smutná, Kristína, Záhonová, Joel, Dacks, Karel, Harant, Ivan, Hrdý, Jan, Tachezy
Publikováno v:
Molecular & Cellular Proteomics : MCP
The lysosome represents a central degradative compartment of eukaryote cells, yet little is known about the biogenesis and function of this organelle in parasitic protists. Whereas the mannose 6-phosphate (M6P)-dependent system is dominant for lysoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d8b7a8dffd0ed0f52289b27ed2884830
https://pubmed.ncbi.nlm.nih.gov/34763061
https://pubmed.ncbi.nlm.nih.gov/34763061
Publikováno v:
Molecular Medicine Reports
Liver fibrosis is a serious threat to human life and health. Activated hepatic stellate cells (HSCs) play a key role in the occurrence and development of liver fibrosis. Studies have reported that microRNAs (miRNAs/miRs) are involved in the pathologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee1c0b9737aaabe82d7f7d7126062e4b
https://pubmed.ncbi.nlm.nih.gov/34498712
https://pubmed.ncbi.nlm.nih.gov/34498712
Autor:
Yanchun, Ji, Zhipeng, Nie, Feilong, Meng, Cuifang, Hu, Hui, Chen, Lihao, Jin, Mengquan, Chen, Minglian, Zhang, Juanjuan, Zhang, Min, Liang, Meng, Wang, Min-Xin, Guan
Publikováno v:
The Journal of Biological Chemistry
Mitochondrial tRNA 3’-end metabolism is critical for the formation of functional tRNAs. Deficient mitochondrial tRNA 3’-end metabolism is linked to an array of human diseases, including optic neuropathy, but their pathophysiology remains poorly u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::513910878a65d58108a6af53b8e3a784
https://pubmed.ncbi.nlm.nih.gov/34023389
https://pubmed.ncbi.nlm.nih.gov/34023389
Akademický článek
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