195 related articles for article (PubMed ID: 28359055)
1. Lack of Prenylated Proteins, Autophagy Impairment and Apoptosis in SH-SY5Y Neuronal Cell Model of Mevalonate Kinase Deficiency.
Tricarico PM; Romeo A; Gratton R; Crovella S; Celsi F
Cell Physiol Biochem; 2017; 41(4):1649-1660. PubMed ID: 28359055
[TBL] [Abstract][Full Text] [Related]
2. Defective Protein Prenylation in a Spectrum of Patients With Mevalonate Kinase Deficiency.
Munoz MA; Jurczyluk J; Simon A; Hissaria P; Arts RJW; Coman D; Boros C; Mehr S; Rogers MJ
Front Immunol; 2019; 10():1900. PubMed ID: 31474985
[TBL] [Abstract][Full Text] [Related]
3. 25-Hydroxycholesterol and inflammation in Lovastatin-deregulated mevalonate pathway.
Tricarico PM; Gratton R; Braga L; Celsi F; Crovella S
Int J Biochem Cell Biol; 2017 Nov; 92():26-33. PubMed ID: 28918367
[TBL] [Abstract][Full Text] [Related]
4. Molecular and cellular consequences of mevalonate kinase deficiency.
Politiek FA; Turkenburg M; Henneman L; Ofman R; Waterham HR
Biochim Biophys Acta Mol Basis Dis; 2024 Jun; 1870(5):167177. PubMed ID: 38636615
[TBL] [Abstract][Full Text] [Related]
5. Compromized geranylgeranylation of RhoA and Rac1 in mevalonate kinase deficiency.
Henneman L; Schneiders MS; Turkenburg M; Waterham HR
J Inherit Metab Dis; 2010 Oct; 33(5):625-32. PubMed ID: 20814828
[TBL] [Abstract][Full Text] [Related]
6. Respiratory deficiency in yeast mevalonate kinase deficient may explain MKD-associate metabolic disorder in humans.
Santos MMS; Elsztein C; De Souza RB; Paiva SSL; Silva JA; Crovella S; De Morais MA
Curr Genet; 2018 Aug; 64(4):871-881. PubMed ID: 29374778
[TBL] [Abstract][Full Text] [Related]
7. Mevalonate Pathway Blockade, Mitochondrial Dysfunction and Autophagy: A Possible Link.
Tricarico PM; Crovella S; Celsi F
Int J Mol Sci; 2015 Jul; 16(7):16067-84. PubMed ID: 26184189
[TBL] [Abstract][Full Text] [Related]
8. Compromised Protein Prenylation as Pathogenic Mechanism in Mevalonate Kinase Deficiency.
Politiek FA; Waterham HR
Front Immunol; 2021; 12():724991. PubMed ID: 34539662
[TBL] [Abstract][Full Text] [Related]
9. Increased core body temperature exacerbates defective protein prenylation in mouse models of mevalonate kinase deficiency.
Munoz MA; Skinner OP; Masle-Farquhar E; Jurczyluk J; Xiao Y; Fletcher EK; Kristianto E; Hodson MP; O'Donoghue SI; Kaur S; Brink R; Zahra DG; Deenick EK; Perry KA; Robertson AA; Mehr S; Hissaria P; Mulders-Manders CM; Simon A; Rogers MJ
J Clin Invest; 2022 Oct; 132(19):. PubMed ID: 36189795
[TBL] [Abstract][Full Text] [Related]
10. Repositioning of Tak-475 In Mevalonate Kinase Disease: Translating Theory Into Practice.
Marcuzzi A; Loganes C; Celeghini C; Kleiner G
Curr Med Chem; 2018; 25(24):2783-2796. PubMed ID: 28901277
[TBL] [Abstract][Full Text] [Related]
11. MMAB, a novel candidate gene to be screened in the molecular diagnosis of Mevalonate Kinase Deficiency.
Mezzavilla M; Moura RR; Celsi F; Tricarico PM; Crovella S
Rheumatol Int; 2018 Jan; 38(1):121-127. PubMed ID: 29234874
[TBL] [Abstract][Full Text] [Related]
12. Mevalonate kinase deficiency and neuroinflammation: balance between apoptosis and pyroptosis.
Tricarico PM; Marcuzzi A; Piscianz E; Monasta L; Crovella S; Kleiner G
Int J Mol Sci; 2013 Nov; 14(12):23274-88. PubMed ID: 24287904
[TBL] [Abstract][Full Text] [Related]
13. Prolonged treatment with mevalonolactone induces oxidative stress response with reactive oxygen species production, mitochondrial depolarization and inflammation in human glioblastoma U-87 MG cells.
Gratton R; Tricarico PM; Celsi F; Crovella S
Neurochem Int; 2018 Nov; 120():233-237. PubMed ID: 29753116
[TBL] [Abstract][Full Text] [Related]
14. Phenotypic diversity, disease progression, and pathogenicity of MVK missense variants in mevalonic aciduria.
Brennenstuhl H; Nashawi M; Schröter J; Baronio F; Beedgen L; Gleich F; Jeltsch K; von Landenberg C; Martini S; Simon A; Thiel C; Tsiakas K; Opladen T; Kölker S; Hoffmann GF; Haas D;
J Inherit Metab Dis; 2021 Sep; 44(5):1272-1287. PubMed ID: 34145613
[TBL] [Abstract][Full Text] [Related]
15. A novel missense mutation in MVK associated with MK deficiency and dyserythropoietic anemia.
Samkari A; Borzutzky A; Fermo E; Treaba DO; Dedeoglu F; Altura RA
Pediatrics; 2010 Apr; 125(4):e964-8. PubMed ID: 20194276
[TBL] [Abstract][Full Text] [Related]
16. Evolutionary hypothesis of the Mevalonate Kinase Deficiency.
Vuch J; Marcuzzi A; Bianco AM; Tommasini A; Zanin V; Crovella S
Med Hypotheses; 2013 Jan; 80(1):67-9. PubMed ID: 23168296
[TBL] [Abstract][Full Text] [Related]
17. Mevalonate kinase deficiency leads to decreased prenylation of Rab GTPases.
Jurczyluk J; Munoz MA; Skinner OP; Chai RC; Ali N; Palendira U; Quinn JM; Preston A; Tangye SG; Brown AJ; Argent E; Ziegler JB; Mehr S; Rogers MJ
Immunol Cell Biol; 2016 Nov; 94(10):994-999. PubMed ID: 27377765
[TBL] [Abstract][Full Text] [Related]
18. Mutational spectrum and genotype-phenotype correlations in mevalonate kinase deficiency.
Mandey SH; Schneiders MS; Koster J; Waterham HR
Hum Mutat; 2006 Aug; 27(8):796-802. PubMed ID: 16835861
[TBL] [Abstract][Full Text] [Related]
19. Vasculitis in a patient with mevalonate kinase deficiency (MKD): a case report.
Omoyinmi E; Rowczenio D; Sebire N; Brogan PA; Eleftheriou D
Pediatr Rheumatol Online J; 2021 Nov; 19(1):161. PubMed ID: 34809655
[TBL] [Abstract][Full Text] [Related]
20. GRID2 a novel gene possibly associated with mevalonate kinase deficiency.
Moura R; Tricarico PM; Campos Coelho AV; Crovella S
Rheumatol Int; 2015 Apr; 35(4):657-9. PubMed ID: 25146332
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
