BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

230 related articles for article (PubMed ID: 23686134)

  • 1. Survival and differentiation defects contribute to neutropenia in glucose-6-phosphatase-β (G6PC3) deficiency in a model of mouse neutrophil granulocyte differentiation.
    Gautam S; Kirschnek S; Gentle IE; Kopiniok C; Henneke P; Häcker H; Malleret L; Belaaouaj A; Häcker G
    Cell Death Differ; 2013 Aug; 20(8):1068-79. PubMed ID: 23686134
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-beta-deficient neutrophils in a congenital neutropenia syndrome.
    Jun HS; Lee YM; Cheung YY; McDermott DH; Murphy PM; De Ravin SS; Mansfield BC; Chou JY
    Blood; 2010 Oct; 116(15):2783-92. PubMed ID: 20498302
    [TBL] [Abstract][Full Text] [Related]  

  • 3. G-CSF improves murine G6PC3-deficient neutrophil function by modulating apoptosis and energy homeostasis.
    Jun HS; Lee YM; Song KD; Mansfield BC; Chou JY
    Blood; 2011 Apr; 117(14):3881-92. PubMed ID: 21292774
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Failure to eliminate a phosphorylated glucose analog leads to neutropenia in patients with G6PT and G6PC3 deficiency.
    Veiga-da-Cunha M; Chevalier N; Stephenne X; Defour JP; Paczia N; Ferster A; Achouri Y; Dewulf JP; Linster CL; Bommer GT; Van Schaftingen E
    Proc Natl Acad Sci U S A; 2019 Jan; 116(4):1241-1250. PubMed ID: 30626647
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis.
    McDermott DH; De Ravin SS; Jun HS; Liu Q; Priel DA; Noel P; Takemoto CM; Ojode T; Paul SM; Dunsmore KP; Hilligoss D; Marquesen M; Ulrick J; Kuhns DB; Chou JY; Malech HL; Murphy PM
    Blood; 2010 Oct; 116(15):2793-802. PubMed ID: 20616219
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterisation of Neutropenia-Associated Neutrophil Elastase Mutations in a Murine Differentiation Model In Vitro and In Vivo.
    Wiesmeier M; Gautam S; Kirschnek S; Häcker G
    PLoS One; 2016; 11(12):e0168055. PubMed ID: 27942017
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Glucose-6-phosphatase-β, implicated in a congenital neutropenia syndrome, is essential for macrophage energy homeostasis and functionality.
    Jun HS; Cheung YY; Lee YM; Mansfield BC; Chou JY
    Blood; 2012 Apr; 119(17):4047-55. PubMed ID: 22246029
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A clinical and molecular review of ubiquitous glucose-6-phosphatase deficiency caused by G6PC3 mutations.
    Banka S; Newman WG
    Orphanet J Rare Dis; 2013 Jun; 8():84. PubMed ID: 23758768
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A syndrome with congenital neutropenia and mutations in G6PC3.
    Boztug K; Appaswamy G; Ashikov A; Schäffer AA; Salzer U; Diestelhorst J; Germeshausen M; Brandes G; Lee-Gossler J; Noyan F; Gatzke AK; Minkov M; Greil J; Kratz C; Petropoulou T; Pellier I; Bellanné-Chantelot C; Rezaei N; Mönkemöller K; Irani-Hakimeh N; Bakker H; Gerardy-Schahn R; Zeidler C; Grimbacher B; Welte K; Klein C
    N Engl J Med; 2009 Jan; 360(1):32-43. PubMed ID: 19118303
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathogenic mechanisms and clinical implications of congenital neutropenia syndromes.
    Hauck F; Klein C
    Curr Opin Allergy Clin Immunol; 2013 Dec; 13(6):596-606. PubMed ID: 24145314
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel G6PC3 gene mutation in severe congenital neutropenia: pancytopenia and variable bone marrow phenotype can also be part of this syndrome.
    Arikoglu T; Kuyucu N; Germeshausen M; Kuyucu S
    Eur J Haematol; 2015 Jan; 94(1):79-82. PubMed ID: 24750412
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Impaired neutrophil activity and increased susceptibility to bacterial infection in mice lacking glucose-6-phosphatase-beta.
    Cheung YY; Kim SY; Yiu WH; Pan CJ; Jun HS; Ruef RA; Lee EJ; Westphal H; Mansfield BC; Chou JY
    J Clin Invest; 2007 Mar; 117(3):784-93. PubMed ID: 17318259
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel G6PC3 gene mutation in a patient with severe congenital neutropenia.
    Aytekin C; Germeshausen M; Tuygun N; Dogu F; Ikinciogullari A
    J Pediatr Hematol Oncol; 2013 Mar; 35(2):e81-3. PubMed ID: 23018568
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neutrophil dysfunction triggers inflammatory bowel disease in G6PC3 deficiency.
    Goenka A; Doherty JA; Al-Farsi T; Jagger C; Banka S; Cheesman E; Fagbemi A; Hughes SM; Wynn RF; Hussell T; Arkwright PD
    J Leukoc Biol; 2021 Jun; 109(6):1147-1154. PubMed ID: 32930428
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Survival, but not maturation, is affected in neutrophil progenitors from GSD-1b patients.
    Visser G; de Jager W; Verhagen LP; Smit GP; Wijburg FA; Prakken BJ; Coffer PJ; Buitenhuis M
    J Inherit Metab Dis; 2012 Mar; 35(2):287-300. PubMed ID: 21863279
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Metabolic abnormalities in G6PC3-deficient human neutrophils result in severe functional defects.
    McKinney C; Ellison M; Briones NJ; Baroffio A; Murphy J; Tran AD; Reisz JA; D'Alessandro A; Ambruso DR
    Blood Adv; 2020 Dec; 4(23):5888-5901. PubMed ID: 33259599
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Altered Functions of Neutrophils in Two Chinese Patients With Severe Congenital Neutropenia Type 4 Caused by
    Dai R; Lv G; Li W; Tang W; Chen J; Liu Q; Yang L; Zhang M; Tian Z; Zhou L; Yan X; Wang Y; Ding Y; An Y; Zhang Z; Tang X; Zhao X
    Front Immunol; 2021; 12():699743. PubMed ID: 34305938
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Successful use of empagliflozin to treat neutropenia in two G6PC3-deficient children: Impact of a mutation in SGLT5.
    Boulanger C; Stephenne X; Diederich J; Mounkoro P; Chevalier N; Ferster A; Van Schaftingen E; Veiga-da-Cunha M
    J Inherit Metab Dis; 2022 Jul; 45(4):759-768. PubMed ID: 35506446
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel phenotype variant of severe congenital neutropenia caused by G6PC3 deficiency.
    Estévez OA; Ortega C; Tejero Á; Fernández S; Aguado R; Aróstegui JI; González-Roca E; Peña J; Santamaría M
    Pediatr Blood Cancer; 2013 Jul; 60(7):E29-31. PubMed ID: 23441086
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SLGT2 Inhibitor Rescues Myelopoiesis in G6PC3 Deficiency.
    Hiwarkar P; Bargir U; Pandrowala A; Bodhanwala M; Thakker N; Taur P; Madkaikar M; Desai M
    J Clin Immunol; 2022 Nov; 42(8):1653-1659. PubMed ID: 35838821
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.