These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

140 related articles for article (PubMed ID: 30030262)

  • 1. Multi-OMICS analyses unveil
    Carapito R; Carapito C; Morlon A; Paul N; Vaca Jacome AS; Alsaleh G; Rolli V; Tahar O; Aouadi I; Rompais M; Delalande F; Pichot A; Georgel P; Messer L; Sibilia J; Cianferani S; Van Dorsselaer A; Bahram S
    Ann Rheum Dis; 2018 Nov; 77(11):1675-1687. PubMed ID: 30030262
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Putative modifier genes in mevalonate kinase deficiency.
    Marcuzzi A; Vozzi D; Girardelli M; Tricarico PM; Knowles A; Crovella S; Vuch J; Tommasini A; Piscianz E; Bianco AM
    Mol Med Rep; 2016 Apr; 13(4):3181-9. PubMed ID: 26935981
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A20 inhibition of STAT1 expression in myeloid cells: a novel endogenous regulatory mechanism preventing development of enthesitis.
    De Wilde K; Martens A; Lambrecht S; Jacques P; Drennan MB; Debusschere K; Govindarajan S; Coudenys J; Verheugen E; Windels F; Catrysse L; Lories R; McGonagle D; Beyaert R; van Loo G; Elewaut D
    Ann Rheum Dis; 2017 Mar; 76(3):585-592. PubMed ID: 27551052
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Overlap of familial Mediterranean fever and hyper-IgD syndrome in an Arabic kindred.
    Moussa T; Aladbe B; Taha RZ; Remmers EF; El-Shanti H; Fathalla BM
    J Clin Immunol; 2015 Apr; 35(3):249-53. PubMed ID: 25708585
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Analysis of NLRP3, MVK and TNFRSF1A variants in adult Greek patients with autoinflammatory symptoms.
    Karagianni P; Nezos A; Ioakeim F; Tzioufas AG; Moutsopoulos HM
    Clin Exp Rheumatol; 2018; 36(6 Suppl 115):86-89. PubMed ID: 30418111
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotype.
    Santos JA; Aróstegui JI; Brito MJ; Neves C; Conde M
    Gene; 2014 Jun; 542(2):217-20. PubMed ID: 24656624
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Limb girdle myasthenia with digenic RAPSN and a novel disease gene AK9 mutations.
    Lam CW; Wong KS; Leung HW; Law CY
    Eur J Hum Genet; 2017 Feb; 25(2):192-199. PubMed ID: 27966543
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Perinatal onset mevalonate kinase deficiency.
    Steiner LA; Ehrenkranz RA; Peterec SM; Steiner RD; Reyes-Múgica M; Gallagher PG
    Pediatr Dev Pathol; 2011; 14(4):301-6. PubMed ID: 21425920
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Endothelial transcriptomic changes induced by oxidized low density lipoprotein disclose an up-regulation of Jak-Stat pathway.
    Laguna-Fernández A; Novella S; Bueno-Betí C; Marrugat J; Hermenegildo C
    Vascul Pharmacol; 2015 Oct; 73():104-14. PubMed ID: 26028607
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Common variable immunodeficiency, impaired neurological development and reduced numbers of T regulatory cells in a 10-year-old boy with a STAT1 gain-of-function mutation.
    Kobbe R; Kolster M; Fuchs S; Schulze-Sturm U; Jenderny J; Kochhan L; Staab J; Tolosa E; Grimbacher B; Meyer T
    Gene; 2016 Jul; 586(2):234-8. PubMed ID: 27063510
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome sequencing reveals a signal transducer and activator of transcription 1 (STAT1) mutation in a child with recalcitrant cutaneous fusariosis.
    Wang X; Lin Z; Gao L; Wang A; Wan Z; Chen W; Yang Y; Li R
    J Allergy Clin Immunol; 2013 Apr; 131(4):1242-3. PubMed ID: 23245795
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Activation of JAK-STAT1 signal transduction pathway in lesional skin and monocytes from patients with systemic lupus erythematosus.
    Li J; Zhao S; Yi M; Hu X; Li J; Xie H; Zhu W; Chen M
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2011 Feb; 36(2):109-15. PubMed ID: 21368418
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mevalonate kinase deficiency (hyper-IgD syndrome) overlap mutation familial Mediterranean fever.
    Flores Robles BJ; Peiró Callizo ME; Sanabria Sanchinel AA; Fernández Díaz C
    Reumatol Clin; 2017; 13(1):57. PubMed ID: 27079959
    [No Abstract]   [Full Text] [Related]  

  • 17. Canakinumab for the Treatment of Autoinflammatory Recurrent Fever Syndromes.
    De Benedetti F; Gattorno M; Anton J; Ben-Chetrit E; Frenkel J; Hoffman HM; Koné-Paut I; Lachmann HJ; Ozen S; Simon A; Zeft A; Calvo Penades I; Moutschen M; Quartier P; Kasapcopur O; Shcherbina A; Hofer M; Hashkes PJ; Van der Hilst J; Hara R; Bujan-Rivas S; Constantin T; Gul A; Livneh A; Brogan P; Cattalini M; Obici L; Lheritier K; Speziale A; Junge G
    N Engl J Med; 2018 May; 378(20):1908-1919. PubMed ID: 29768139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Mevalonate kinase deficiency in 2016].
    Galeotti C; Georgin-Lavialle S; Sarrabay G; Touitou I; Koné-Paut I
    Rev Med Interne; 2018 Apr; 39(4):265-270. PubMed ID: 27659743
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Inhibition of JAK/STAT signaling pathway prevents high-glucose-induced increase in endothelin-1 synthesis in human endothelial cells.
    Manea SA; Manea A; Heltianu C
    Cell Tissue Res; 2010 Apr; 340(1):71-9. PubMed ID: 20217138
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular insights of two STAT1 variants from rock bream (Oplegnathus fasciatus) and their transcriptional regulation in response to pathogenic stress, interleukin-10, and tissue injury.
    Bathige SDNK; Umasuthan N; Godahewa GI; Thulasitha WS; Jayasinghe JDHE; Wan Q; Lee J
    Fish Shellfish Immunol; 2017 Oct; 69():128-141. PubMed ID: 28818616
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.