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For: Moll T, Marshall JNG, Soni N, Zhang S, Cooper-Knock J, Shaw PJ. Membrane lipid raft homeostasis is directly linked to neurodegeneration. Essays Biochem 2021:EBC20210026. [PMID: 34623437 DOI: 10.1042/EBC20210026] [Cited by in Crossref: 3] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Yi S, Wang L, Wang H, Ho MS, Zhang S. Pathogenesis of α-Synuclein in Parkinson’s Disease: From a Neuron-Glia Crosstalk Perspective. IJMS 2022;23:14753. [DOI: 10.3390/ijms232314753] [Reference Citation Analysis]
2 Dehghan A, Pinto RC, Karaman I, Huang J, Durainayagam BR, Ghanbari M, Nazeer A, Zhong Q, Liggi S, Whiley L, Mustafa R, Kivipelto M, Solomon A, Ngandu T, Kanekiyo T, Aikawa T, Radulescu CI, Barnes SJ, Graça G, Chekmeneva E, Camuzeaux S, Lewis MR, Kaluarachchi MR, Ikram MA, Holmes E, Tzoulaki I, Matthews PM, Griffin JL, Elliott P. Metabolome-wide association study on ABCA7 indicates a role of ceramide metabolism in Alzheimer's disease. Proc Natl Acad Sci U S A 2022;119:e2206083119. [PMID: 36269859 DOI: 10.1073/pnas.2206083119] [Reference Citation Analysis]
3 Campos-peña V, Pichardo-rojas P, Sánchez-barbosa T, Ortíz-islas E, Rodríguez-pérez CE, Montes P, Ramos-palacios G, Silva-adaya D, Valencia-quintana R, Cerna-cortes JF, Toral-rios D. Amyloid β, Lipid Metabolism, Basal Cholinergic System, and Therapeutics in Alzheimer’s Disease. IJMS 2022;23:12092. [DOI: 10.3390/ijms232012092] [Reference Citation Analysis]
4 Mccluskey G, Donaghy C, Morrison KE, Mcconville J, Duddy W, Duguez S. The Role of Sphingomyelin and Ceramide in Motor Neuron Diseases. JPM 2022;12:1418. [DOI: 10.3390/jpm12091418] [Reference Citation Analysis]
5 Li L, Ji J, Song F, Hu J. Intercellular Receptor-ligand Binding: Effect of Protein-membrane Interaction. J Mol Biol 2022;:167787. [PMID: 35952805 DOI: 10.1016/j.jmb.2022.167787] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Moll T, Graves E, Urbanek A, Soni N, Ranganathan R, Higginbottom A, Wang S, Head BP, Cooper-knock J, Shaw PJ. GLT8D1 mutations cause amyotrophic lateral sclerosis via disruption of neurotrophin signalling within membrane lipid rafts.. [DOI: 10.1101/2022.06.28.497990] [Reference Citation Analysis]