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For: Paciotti S, Albi E, Parnetti L, Beccari T. Lysosomal Ceramide Metabolism Disorders: Implications in Parkinson's Disease. J Clin Med 2020;9:E594. [PMID: 32098196 DOI: 10.3390/jcm9020594] [Cited by in Crossref: 11] [Cited by in F6Publishing: 9] [Article Influence: 5.5] [Reference Citation Analysis]
Number Citing Articles
1 Xu YN, Wang Z, Zhang SK, Xu JR, Pan ZX, Wei X, Wen HH, Luo YS, Guo MJ, Zhu Q. Low-grade elevation of palmitate and lipopolysaccharide synergistically induced β-cell damage via inhibition of neutral ceramidase. Mol Cell Endocrinol 2022;539:111473. [PMID: 34610358 DOI: 10.1016/j.mce.2021.111473] [Reference Citation Analysis]
2 Angelopoulou E, Paudel YN, Villa C, Piperi C. Arylsulfatase A (ASA) in Parkinson's Disease: From Pathogenesis to Biomarker Potential. Brain Sci 2020;10:E713. [PMID: 33036336 DOI: 10.3390/brainsci10100713] [Reference Citation Analysis]
3 Alessenko AV, Albi E. Exploring Sphingolipid Implications in Neurodegeneration. Front Neurol 2020;11:437. [PMID: 32528400 DOI: 10.3389/fneur.2020.00437] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 10.0] [Reference Citation Analysis]
4 Zhao YW, Pan HX, Liu Z, Wang Y, Zeng Q, Fang ZH, Luo TF, Xu K, Wang Z, Zhou X, He R, Li B, Zhao G, Xu Q, Sun QY, Yan XX, Tan JQ, Li JC, Guo JF, Tang BS. The Association Between Lysosomal Storage Disorder Genes and Parkinson's Disease: A Large Cohort Study in Chinese Mainland Population. Front Aging Neurosci 2021;13:749109. [PMID: 34867278 DOI: 10.3389/fnagi.2021.749109] [Reference Citation Analysis]
5 Patel T, Carnwath TP, Wang X, Allen M, Lincoln SJ, Lewis-Tuffin LJ, Quicksall ZS, Lin S, Tutor-New FQ, Ho CCG, Min Y, Malphrus KG, Nguyen TT, Martin E, Garcia CA, Alkharboosh RM, Grewal S, Chaichana K, Wharen R, Guerrero-Cazares H, Quinones-Hinojosa A, Ertekin-Taner N. Transcriptional landscape of human microglia implicates age, sex, and APOE-related immunometabolic pathway perturbations. Aging Cell 2022;21:e13606. [PMID: 35388616 DOI: 10.1111/acel.13606] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Ancien F, Pucci F, Rooman M. In Silico Analysis of the Molecular-Level Impact of SMPD1 Variants on Niemann-Pick Disease Severity. Int J Mol Sci 2021;22:4516. [PMID: 33925997 DOI: 10.3390/ijms22094516] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Custodia A, Aramburu-Núñez M, Correa-Paz C, Posado-Fernández A, Gómez-Larrauri A, Castillo J, Gómez-Muñoz A, Sobrino T, Ouro A. Ceramide Metabolism and Parkinson's Disease-Therapeutic Targets. Biomolecules 2021;11:945. [PMID: 34202192 DOI: 10.3390/biom11070945] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
8 Fais M, Dore A, Galioto M, Galleri G, Crosio C, Iaccarino C. Parkinson's Disease-Related Genes and Lipid Alteration. Int J Mol Sci 2021;22:7630. [PMID: 34299248 DOI: 10.3390/ijms22147630] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
9 Tegeder I, Kögel D. When lipid homeostasis runs havoc: Lipotoxicity links lysosomal dysfunction to autophagy. Matrix Biology 2021;100-101:99-117. [DOI: 10.1016/j.matbio.2020.11.005] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
10 Lepe-Balsalobre E, Santotoribio JD, Nuñez-Vazquez R, García-Morillo S, Jiménez-Arriscado P, Hernández-Arévalo P, Delarosa-Rodríguez R, Guerrero JM, Macher HC. Genotype/phenotype relationship in Gaucher disease patients. Novel mutation in glucocerebrosidase gene. Clin Chem Lab Med 2020;58:2017-24. [PMID: 32589593 DOI: 10.1515/cclm-2020-0306] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Coutinho MF, Santos JI, S Mendonça L, Matos L, Prata MJ, S Jurado A, Pedroso de Lima MC, Alves S. Lysosomal Storage Disease-Associated Neuropathy: Targeting Stable Nucleic Acid Lipid Particle (SNALP)-Formulated siRNAs to the Brain as a Therapeutic Approach. Int J Mol Sci 2020;21:E5732. [PMID: 32785133 DOI: 10.3390/ijms21165732] [Reference Citation Analysis]
12 Nasir G, Chopra R, Elwood F, Ahmed SS. Krabbe Disease: Prospects of Finding a Cure Using AAV Gene Therapy. Front Med (Lausanne) 2021;8:760236. [PMID: 34869463 DOI: 10.3389/fmed.2021.760236] [Reference Citation Analysis]
13 Di Lazzaro G, Magrinelli F, Estevez-Fraga C, Valente EM, Pisani A, Bhatia KP. X-Linked Parkinsonism: Phenotypic and Genetic Heterogeneity. Mov Disord 2021;36:1511-25. [PMID: 33960519 DOI: 10.1002/mds.28565] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]