BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

331 related articles for article (PubMed ID: 26821380)

  • 1. Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia.
    Fernández-Murray JP; Prykhozhij SV; Dufay JN; Steele SL; Gaston D; Nasrallah GK; Coombs AJ; Liwski RS; Fernandez CV; Berman JN; McMaster CR
    PLoS Genet; 2016 Jan; 12(1):e1005783. PubMed ID: 26821380
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.
    LeBlanc MA; Bettle A; Berman JN; Price VE; Pambrun C; Yu Z; Tiller M; McMaster CR; Fernandez CV
    Pediatr Blood Cancer; 2016 Jul; 63(7):1307-9. PubMed ID: 27038157
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Characterization of Human and Yeast Mitochondrial Glycine Carriers with Implications for Heme Biosynthesis and Anemia.
    Lunetti P; Damiano F; De Benedetto G; Siculella L; Pennetta A; Muto L; Paradies E; Marobbio CM; Dolce V; Capobianco L
    J Biol Chem; 2016 Sep; 291(38):19746-59. PubMed ID: 27476175
    [TBL] [Abstract][Full Text] [Related]  

  • 4. SLC25 Family Member Genetic Interactions Identify a Role for
    Dufay JN; Fernández-Murray JP; McMaster CR
    G3 (Bethesda); 2017 Jun; 7(6):1861-1873. PubMed ID: 28404662
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia.
    Guernsey DL; Jiang H; Campagna DR; Evans SC; Ferguson M; Kellogg MD; Lachance M; Matsuoka M; Nightingale M; Rideout A; Saint-Amant L; Schmidt PJ; Orr A; Bottomley SS; Fleming MD; Ludman M; Dyack S; Fernandez CV; Samuels ME
    Nat Genet; 2009 Jun; 41(6):651-3. PubMed ID: 19412178
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effect of 5-aminolevulinic acid on erythropoiesis: a preclinical in vitro characterization for the treatment of congenital sideroblastic anemia.
    Fujiwara T; Okamoto K; Niikuni R; Takahashi K; Okitsu Y; Fukuhara N; Onishi Y; Ishizawa K; Ichinohasama R; Nakamura Y; Nakajima M; Tanaka T; Harigae H
    Biochem Biophys Res Commun; 2014 Nov; 454(1):102-8. PubMed ID: 25450364
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular pathophysiology and genetic mutations in congenital sideroblastic anemia.
    Fujiwara T; Harigae H
    Free Radic Biol Med; 2019 Mar; 133():179-185. PubMed ID: 30098397
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38.
    Uminski K; Houston DS; Hartley JN; Liu J; Cuvelier GDE; Israels SJ
    Pediatr Blood Cancer; 2020 Oct; 67(10):e28623. PubMed ID: 32790119
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing.
    Mehri M; Zarin M; Ardalani F; Najmabadi H; Azarkeivan A; Neishabury M
    Blood Cells Mol Dis; 2018 Jul; 71():39-44. PubMed ID: 29499877
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathophysiology and genetic mutations in congenital sideroblastic anemia.
    Fujiwara T; Harigae H
    Pediatr Int; 2013 Dec; 55(6):675-9. PubMed ID: 24003969
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Update on the biology of heme synthesis in erythroid cells].
    Fujiwara T; Harigae H
    Rinsho Ketsueki; 2015 Feb; 56(2):119-27. PubMed ID: 25765790
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Novel frameshift variant (c.409dupG) in
    Ravindra N; Athiyarath R; S E; S S; Kulkarni U; N A F; Korula A; Shaji RV; George B; Edison ES
    J Clin Pathol; 2021 Mar; 74(3):157-162. PubMed ID: 32605921
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Diagnosis and treatment of sideroblastic anemias: from defective heme synthesis to abnormal RNA splicing.
    Cazzola M; Malcovati L
    Hematology Am Soc Hematol Educ Program; 2015; 2015():19-25. PubMed ID: 26637696
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia.
    Kannengiesser C; Sanchez M; Sweeney M; Hetet G; Kerr B; Moran E; Fuster Soler JL; Maloum K; Matthes T; Oudot C; Lascaux A; Pondarré C; Sevilla Navarro J; Vidyatilake S; Beaumont C; Grandchamp B; May A
    Haematologica; 2011 Jun; 96(6):808-13. PubMed ID: 21393332
    [TBL] [Abstract][Full Text] [Related]  

  • 15. GLRX5 mutations impair heme biosynthetic enzymes ALA synthase 2 and ferrochelatase in Human congenital sideroblastic anemia.
    Daher R; Mansouri A; Martelli A; Bayart S; Manceau H; Callebaut I; Moulouel B; Gouya L; Puy H; Kannengiesser C; Karim Z
    Mol Genet Metab; 2019 Nov; 128(3):342-351. PubMed ID: 30660387
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis.
    Pondarre C; Campagna DR; Antiochos B; Sikorski L; Mulhern H; Fleming MD
    Blood; 2007 Apr; 109(8):3567-9. PubMed ID: 17192398
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Congenital sideroblastic anaemia with a novel frameshift mutation in SLC25A38.
    Wong WS; Wong HF; Cheng CK; Chang KO; Chan NP; Ng MH; Wong KF
    J Clin Pathol; 2015 Mar; 68(3):249-51. PubMed ID: 25512395
    [No Abstract]   [Full Text] [Related]  

  • 18. Systematic molecular genetic analysis of congenital sideroblastic anemia: evidence for genetic heterogeneity and identification of novel mutations.
    Bergmann AK; Campagna DR; McLoughlin EM; Agarwal S; Fleming MD; Bottomley SS; Neufeld EJ
    Pediatr Blood Cancer; 2010 Feb; 54(2):273-8. PubMed ID: 19731322
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation.
    Le Rouzic MA; Fouquet C; Leblanc T; Touati M; Fouyssac F; Vermylen C; Jäkel N; Guichard JF; Maloum K; Toutain F; Lutz P; Perel Y; Manceau H; Kannengiesser C; Vannier JP
    Blood Cells Mol Dis; 2017 Jul; 66():11-18. PubMed ID: 28772256
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Regulation and tissue-specific expression of δ-aminolevulinic acid synthases in non-syndromic sideroblastic anemias and porphyrias.
    Peoc'h K; Nicolas G; Schmitt C; Mirmiran A; Daher R; Lefebvre T; Gouya L; Karim Z; Puy H
    Mol Genet Metab; 2019 Nov; 128(3):190-197. PubMed ID: 30737140
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.