BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

146 related articles for article (PubMed ID: 27723093)

  • 1. Impaired platelet activation in patients with hereditary deficiency of p47
    Carnevale R; Loffredo L; Nocella C; Bartimoccia S; Sanguigni V; Soresina A; Plebani A; Azzari C; Martire B; Pignata C; Violi F
    Br J Haematol; 2018 Feb; 180(3):454-456. PubMed ID: 27723093
    [No Abstract]   [Full Text] [Related]  

  • 2. NADPH Oxidase-2 and Atherothrombosis: Insight From Chronic Granulomatous Disease.
    Violi F; Carnevale R; Loffredo L; Pignatelli P; Gallin JI
    Arterioscler Thromb Vasc Biol; 2017 Feb; 37(2):218-225. PubMed ID: 27932349
    [TBL] [Abstract][Full Text] [Related]  

  • 3.
    Kuhns DB; Hsu AP; Sun D; Lau K; Fink D; Griffith P; Huang DW; Priel DAL; Mendez L; Kreuzburg S; Zerbe CS; De Ravin SS; Malech HL; Holland SM; Wu X; Gallin JI
    Blood Adv; 2019 Jan; 3(2):136-147. PubMed ID: 30651282
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A Novel CYBB Variant Causing X-Linked Chronic Granulomatous Disease in a Patient with Empyema.
    Kitcharoensakkul M; Song Z; Bednarski JJ; Dinauer M
    J Clin Immunol; 2021 Jan; 41(1):266-269. PubMed ID: 33090293
    [No Abstract]   [Full Text] [Related]  

  • 5. Different degrees of NADPH oxidase 2 regulation and in vivo platelet activation: lesson from chronic granulomatous disease.
    Carnevale R; Loffredo L; Sanguigni V; Plebani A; Rossi P; Pignata C; Martire B; Finocchi A; Pietrogrande MC; Azzari C; Soresina AR; Martino S; Cirillo E; Martino F; Pignatelli P; Violi F
    J Am Heart Assoc; 2014 Jun; 3(3):e000920. PubMed ID: 24973227
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Similar percentages in most abundant chronic granulomatous disease autosomal recessive forms in a Spanish cohort.
    Pérez de Diego R; López-Lera A; Ferreira A
    Clin Immunol; 2015 May; 158(1):100-2. PubMed ID: 25805656
    [No Abstract]   [Full Text] [Related]  

  • 7. Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiency.
    Winkler S; van Leeuwen K; Deboer M; Rösen-Wolff A; Roos D; Roesler J
    Ann Hematol; 2013 Jul; 92(7):1003-4. PubMed ID: 23274354
    [No Abstract]   [Full Text] [Related]  

  • 8. Late diagnosis and advances in genetics of chronic granulomatous disease.
    Di Matteo G; Finocchi A
    Clin Exp Immunol; 2021 Feb; 203(2):244-246. PubMed ID: 33314034
    [No Abstract]   [Full Text] [Related]  

  • 9. Structural basis for EROS binding to human phagocyte NADPH oxidase NOX2.
    Liang S; Liu A; Liu Y; Wang F; Zhou Y; Long Y; Wang T; Liu Z; Ren R; Ye RD
    Proc Natl Acad Sci U S A; 2024 Jun; 121(23):e2320388121. PubMed ID: 38805284
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The three CYBA variants (rs4673, rs1049254 and rs1049255) are benign: new evidence from a patient with CGD.
    Sun J; Wen M; Wang Y; Liu D; Ying W; Wang X
    BMC Med Genet; 2017 Nov; 18(1):127. PubMed ID: 29132304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. p47
    Hule GP; Kanvinde PR; Kulkarni MA; van Leeuwen K; de Boer M; Bargir UA; Taur PD; Desai MM; Madkaikar MR
    J Clin Immunol; 2018 Aug; 38(6):638-641. PubMed ID: 30091057
    [No Abstract]   [Full Text] [Related]  

  • 12. LDL oxidation by platelets propagates platelet activation via an oxidative stress-mediated mechanism.
    Carnevale R; Bartimoccia S; Nocella C; Di Santo S; Loffredo L; Illuminati G; Lombardi E; Boz V; Del Ben M; De Marco L; Pignatelli P; Violi F
    Atherosclerosis; 2014 Nov; 237(1):108-16. PubMed ID: 25238217
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Myriad Faces of Chronic Granulomatous Disease: All in an Indian Family with Novel CYBB Defect.
    Vignesh P; Sharma M; Pilania RK; Shandilya JK; Kaur A; Goel S; Kaur A; Suri D; Rawat A; Dalal A; Sarma AS; Singh S
    J Clin Immunol; 2019 Aug; 39(6):611-615. PubMed ID: 31338742
    [No Abstract]   [Full Text] [Related]  

  • 14. Does NADPH oxidase deficiency cause artery dilatation in humans?
    Loffredo L; Carnevale R; Sanguigni V; Plebani A; Rossi P; Pignata C; De Mattia D; Finocchi A; Martire B; Pietrogrande MC; Martino S; Gambineri E; Giardino G; Soresina AR; Martino F; Pignatelli P; Violi F
    Antioxid Redox Signal; 2013 Apr; 18(12):1491-6. PubMed ID: 23216310
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unusual late onset of X-linked chronic granulomatous disease in an adult woman after unsuspicious childhood.
    Lun A; Roesler J; Renz H
    Clin Chem; 2002 May; 48(5):780-1. PubMed ID: 11978610
    [No Abstract]   [Full Text] [Related]  

  • 16. Chronic Granulomatous Disease Due to Neutrophil Cytosolic Factor (NCF2) Gene Mutations in Three Unrelated Families.
    Vignesh P; Rawat A; Kumar A; Suri D; Gupta A; Lau YL; Chan KW; Singh S
    J Clin Immunol; 2017 Feb; 37(2):109-112. PubMed ID: 28035544
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expanding the Clinical Phenotype of Chronic Granulomatous Disease: a Female Patient with a De Novo Mutation in CYBB.
    Wu EY; Kuehn HS; Rosenzweig SD; Aksentijevich I; McShane DB
    J Clin Immunol; 2021 Jan; 41(1):224-226. PubMed ID: 33006108
    [No Abstract]   [Full Text] [Related]  

  • 18. Nox2 NADPH oxidase is dispensable for platelet activation or arterial thrombosis in mice.
    Sonkar VK; Kumar R; Jensen M; Wagner BA; Sharathkumar AA; Miller FJ; Fasano M; Lentz SR; Buettner GR; Dayal S
    Blood Adv; 2019 Apr; 3(8):1272-1284. PubMed ID: 30995985
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Chronic granulomatous disease: Single-center Spanish experience.
    Robles-Marhuenda A; Álvarez-Troncoso J; Rodríguez-Pena R; Busca-Arenzana C; López-Granados E; Arnalich-Fernández F
    Clin Immunol; 2020 Feb; 211():108323. PubMed ID: 31830531
    [No Abstract]   [Full Text] [Related]  

  • 20. Functional and genetic characterization of two extremely rare cases of Williams-Beuren syndrome associated with chronic granulomatous disease.
    Stasia MJ; Mollin M; Martel C; Satre V; Coutton C; Amblard F; Vieville G; van Montfrans JM; Boelens JJ; Veenstra-Knol HE; van Leeuwen K; de Boer M; Brion JP; Roos D
    Eur J Hum Genet; 2013 Oct; 21(10):1079-84. PubMed ID: 23340515
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.