BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

227 related articles for article (PubMed ID: 32369445)

  • 1. Impaired angiogenesis and extracellular matrix metabolism in autosomal-dominant hyper-IgE syndrome.
    Dmitrieva NI; Walts AD; Nguyen DP; Grubb A; Zhang X; Wang X; Ping X; Jin H; Yu Z; Yu ZX; Yang D; Schwartzbeck R; Dalgard CL; Kozel BA; Levin MD; Knutsen RH; Liu D; Milner JD; López DB; O'Connell MP; Lee CR; Myles IA; Hsu AP; Freeman AF; Holland SM; Chen G; Boehm M
    J Clin Invest; 2020 Aug; 130(8):4167-4181. PubMed ID: 32369445
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Hyper-IgE syndromes].
    He YY; Liu B; Xiao XP
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 Jun; 31(11):892-896. PubMed ID: 29775011
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evaluation of the Role of
    Moffitt K; Cheung E; Manis J; Malley R
    Infect Immun; 2018 May; 86(5):. PubMed ID: 29463618
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Pathogenesis of hyper IgE syndrome.
    Heimall J; Freeman A; Holland SM
    Clin Rev Allergy Immunol; 2010 Feb; 38(1):32-8. PubMed ID: 19452285
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An update on the hyper-IgE syndromes.
    Yong PF; Freeman AF; Engelhardt KR; Holland S; Puck JM; Grimbacher B
    Arthritis Res Ther; 2012 Nov; 14(6):228. PubMed ID: 23210525
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Hyper-IgE syndrome with mutation in STAT3 gene - case report and literature review].
    Heropolitańska-Pliszka E; Pietrucha B; Mikołuć B; Bernatowska E
    Med Wieku Rozwoj; 2009; 13(1):19-25. PubMed ID: 19648655
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical manifestations, etiology, and pathogenesis of the hyper-IgE syndromes.
    Freeman AF; Holland SM
    Pediatr Res; 2009 May; 65(5 Pt 2):32R-37R. PubMed ID: 19190525
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Protein stabilization improves STAT3 function in autosomal dominant hyper-IgE syndrome.
    Bocchini CE; Nahmod K; Katsonis P; Kim S; Kasembeli MM; Freeman A; Lichtarge O; Makedonas G; Tweardy DJ
    Blood; 2016 Dec; 128(26):3061-3072. PubMed ID: 27799162
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hyper-IgE syndrome update.
    Sowerwine KJ; Holland SM; Freeman AF
    Ann N Y Acad Sci; 2012 Feb; 1250():25-32. PubMed ID: 22268731
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome.
    Milner JD; Brenchley JM; Laurence A; Freeman AF; Hill BJ; Elias KM; Kanno Y; Spalding C; Elloumi HZ; Paulson ML; Davis J; Hsu A; Asher AI; O'Shea J; Holland SM; Paul WE; Douek DC
    Nature; 2008 Apr; 452(7188):773-6. PubMed ID: 18337720
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical Manifestations and Genetic Analysis of 17 Patients with Autosomal Dominant Hyper-IgE Syndrome in Mainland China: New Reports and a Literature Review.
    Wu J; Chen J; Tian ZQ; Zhang H; Gong RL; Chen TX; Hong L
    J Clin Immunol; 2017 Feb; 37(2):166-179. PubMed ID: 28197791
    [TBL] [Abstract][Full Text] [Related]  

  • 12. TNF overproduction impairs epithelial staphylococcal response in hyper IgE syndrome.
    Myles IA; Anderson ED; Earland NJ; Zarember KA; Sastalla I; Williams KW; Gough P; Moore IN; Ganesan S; Fowler CJ; Laurence A; Garofalo M; Kuhns DB; Kieh MD; Saleem A; Welch PA; Darnell DA; Gallin JI; Freeman AF; Holland SM; Datta SK
    J Clin Invest; 2018 Aug; 128(8):3595-3604. PubMed ID: 30035749
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced T(H)17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome.
    Renner ED; Rylaarsdam S; Anover-Sombke S; Rack AL; Reichenbach J; Carey JC; Zhu Q; Jansson AF; Barboza J; Schimke LF; Leppert MF; Getz MM; Seger RA; Hill HR; Belohradsky BH; Torgerson TR; Ochs HD
    J Allergy Clin Immunol; 2008 Jul; 122(1):181-7. PubMed ID: 18602572
    [TBL] [Abstract][Full Text] [Related]  

  • 14. STAT3 modulates reprogramming efficiency of human somatic cells; insights from autosomal dominant Hyper IgE syndrome caused by STAT3 mutations.
    Yu Z; Dmitrieva NI; Walts AD; Jin H; Liu Y; Ping X; Ferrante EA; Qiu L; Holland SM; Freeman AF; Chen G; Boehm M
    Biol Open; 2020 Sep; 9(9):. PubMed ID: 32580970
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Human hyper-IgE syndrome: singular or plural?
    Zhang Q; Boisson B; Béziat V; Puel A; Casanova JL
    Mamm Genome; 2018 Aug; 29(7-8):603-617. PubMed ID: 30094507
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Generation of human induced pluripotent stem cell lines (NIHTVBi011-A, NIHTVBi012-A, NIHTVBi013-A) from autosomal dominant Hyper IgE syndrome (AD-HIES) patients carrying STAT3 mutation.
    Jin H; Yu Z; Navarengom K; Liu Y; Dmitrieva N; Hsu AP; Schwartzbeck R; Cudrici C; Ferrante EA; Yang D; Holland SM; Freeman AF; Boehm M; Chen G
    Stem Cell Res; 2019 Dec; 41():101586. PubMed ID: 31707214
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The Potential and Limits of Hematopoietic Stem Cell Transplantation for the Treatment of Autosomal Dominant Hyper-IgE Syndrome.
    Yanagimachi M; Ohya T; Yokosuka T; Kajiwara R; Tanaka F; Goto H; Takashima T; Morio T; Yokota S
    J Clin Immunol; 2016 Jul; 36(5):511-6. PubMed ID: 27091139
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Atopic dermatitis, STAT3- and DOCK8-hyper-IgE syndromes differ in IgE-based sensitization pattern.
    Boos AC; Hagl B; Schlesinger A; Halm BE; Ballenberger N; Pinarci M; Heinz V; Kreilinger D; Spielberger BD; Schimke-Marques LF; Sawalle-Belohradsky J; Belohradsky BH; Przybilla B; Schaub B; Wollenberg A; Renner ED
    Allergy; 2014 Jul; 69(7):943-53. PubMed ID: 24898675
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Paucity of genotype-phenotype correlations in STAT3 mutation positive Hyper IgE Syndrome (HIES).
    Heimall J; Davis J; Shaw PA; Hsu AP; Gu W; Welch P; Holland SM; Freeman AF
    Clin Immunol; 2011 Apr; 139(1):75-84. PubMed ID: 21288777
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A deep intronic splice mutation of
    Khourieh J; Rao G; Habib T; Avery DT; Lefèvre-Utile A; Chandesris MO; Belkadi A; Chrabieh M; Alwaseem H; Grandin V; Sarrot-Reynauld F; Sénéchal A; Lortholary O; Kong XF; Boisson-Dupuis S; Picard C; Puel A; Béziat V; Zhang Q; Abel L; Molina H; Marr N; Tangye SG; Casanova JL; Boisson B
    Proc Natl Acad Sci U S A; 2019 Aug; 116(33):16463-16472. PubMed ID: 31346092
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.