BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

180 related articles for article (PubMed ID: 25912935)

  • 21. GATA1 erythroid-specific regulation of SEC23B expression and its implication in the pathogenesis of congenital dyserythropoietic anemia type II.
    Russo R; Andolfo I; Gambale A; De Rosa G; Manna F; Arillo A; Wandroo F; Bisconte MG; Iolascon A
    Haematologica; 2017 Sep; 102(9):e371-e374. PubMed ID: 28550189
    [No Abstract]   [Full Text] [Related]  

  • 22. Identification of a novel splice variant in
    Jang W; Ha DJ; Nahm CH; Park J; Kim SJ; Lee JE; Moon Y
    Hematology; 2024 Dec; 29(1):2343163. PubMed ID: 38655690
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Congenital dyserythropoietic anaemia type I with nails and bone abnormalities.
    García-Zamora E; Naz-Villalba E; Pampín-Franco A; García-Iñigo FJ; López-Estebaranz JL
    Clin Exp Dermatol; 2020 Jun; 45(4):515-517. PubMed ID: 31900952
    [No Abstract]   [Full Text] [Related]  

  • 24. [Analysis of genotype and phenotype of SEC23B gene in a family affected with congenital dyserythropoietic anemia type II].
    Li D; Li B; Qu S; Cao W; Yang Y; Ma Y; Hou T
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Dec; 34(6):874-878. PubMed ID: 29188620
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Successful hematopoietic stem cell transplantation in a patient with congenital dyserythropoietic anemia type II.
    Unal S; Russo R; Gumruk F; Kuskonmaz B; Cetin M; Sayli T; Tavil B; Langella C; Iolascon A; Uckan Cetinkaya D
    Pediatr Transplant; 2014 Jun; 18(4):E130-3. PubMed ID: 24724984
    [TBL] [Abstract][Full Text] [Related]  

  • 26. KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity.
    Ravindranath Y; Johnson RM; Goyette G; Buck S; Gadgeel M; Gallagher PG
    J Pediatr Hematol Oncol; 2018 Aug; 40(6):e405-e409. PubMed ID: 29300242
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Fetal presentation of congenital dyserythropoietic anemia type 1 with novel compound heterozygous CDAN1 mutations.
    Meznarich JA; Draper L; Christensen RD; Yaish HM; Luem ND; Pysher TJ; Jung G; Nemeth E; Ganz T; Ward DM
    Blood Cells Mol Dis; 2018 Jul; 71():63-66. PubMed ID: 29599085
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Congenital dyserythropoietic anemia in China: a case report from two families and a review.
    Ru Y; Liu G; Bai J; Dong S; Nie N; Zhang H; Zhao S; Zheng Y; Zhu X; Nie G; Zhang F; Eyden B
    Ann Hematol; 2014 May; 93(5):773-7. PubMed ID: 24196372
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A Chinese family carrying novel mutations in SEC23B and HFE2, the genes responsible for congenital dyserythropoietic anaemia II (CDA II) and primary iron overload, respectively.
    Liu G; Niu S; Dong A; Cai H; Anderson GJ; Han B; Nie G
    Br J Haematol; 2012 Jul; 158(1):143-5. PubMed ID: 22428539
    [No Abstract]   [Full Text] [Related]  

  • 30. A dyserythropoietic anemia associated with homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), a variant with an unstable α chain.
    Garçon L; Iolascon A; Pissard S; Esposito MR; Russo R; Fenneteau O; Fénéant-Thibault M; Heimpel H; Delaunay J
    Hemoglobin; 2010; 34(6):576-81. PubMed ID: 21077766
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.
    Russo R; Esposito MR; Asci R; Gambale A; Perrotta S; Ramenghi U; Forni GL; Uygun V; Delaunay J; Iolascon A
    Am J Hematol; 2010 Dec; 85(12):915-20. PubMed ID: 20941788
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [New mutation site of SEC23B gene in type Ⅱ congenital erythrocythememia anemia: one case report and literatures review].
    Chang LX; Zhu XF; Wang YW; Dong SX; Zhao SX; Ru YX
    Zhonghua Xue Ye Xue Za Zhi; 2019 Apr; 40(4):317-320. PubMed ID: 31104444
    [No Abstract]   [Full Text] [Related]  

  • 33. Identification of CDAN1, C15ORF41 and SEC23B mutations in Chinese patients affected by congenital dyserythropoietic anemia.
    Wang Y; Ru Y; Liu G; Dong S; Li Y; Zhu X; Zhang F; Chang YZ; Nie G
    Gene; 2018 Jan; 640():73-78. PubMed ID: 29031773
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Erythroblast multinuclearity in bone marrow and spleen. Congenital dyserythropoietic anemia-like abnormalities without functional evidence of dyserythropoiesis.
    Lillicrap DP; Corbett WE; Giles AR; Ginsburg AD
    Arch Pathol Lab Med; 1987 Jun; 111(6):536-9. PubMed ID: 3579510
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Variant analysis of SEC23B gene in 4 families with congenital dyserythropoietic anemia].
    Feng Y; Shi P; Liu N; Kong X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Aug; 38(8):727-730. PubMed ID: 34365611
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.
    Saptarshi AN; Dongerdiye RK; More TA; Kedar PS
    Ital J Pediatr; 2023 Jul; 49(1):84. PubMed ID: 37455305
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.
    Bianchi P; Fermo E; Vercellati C; Boschetti C; Barcellini W; Iurlo A; Marcello AP; Righetti PG; Zanella A
    Hum Mutat; 2009 Sep; 30(9):1292-8. PubMed ID: 19621418
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A common human missense mutation of vesicle coat protein SEC23B leads to growth restriction and chronic pancreatitis in mice.
    Wei W; Liu Z; Zhang C; Khoriaty R; Zhu M; Zhang B
    J Biol Chem; 2022 Jan; 298(1):101536. PubMed ID: 34954140
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Functions of the COPII gene paralogs SEC23A and SEC23B are interchangeable in vivo.
    Khoriaty R; Hesketh GG; Bernard A; Weyand AC; Mellacheruvu D; Zhu G; Hoenerhoff MJ; McGee B; Everett L; Adams EJ; Zhang B; Saunders TL; Nesvizhskii AI; Klionsky DJ; Shavit JA; Gingras AC; Ginsburg D
    Proc Natl Acad Sci U S A; 2018 Aug; 115(33):E7748-E7757. PubMed ID: 30065114
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A comprehensive study of the neonatal manifestations of congenital dyserythropoietic anemia type I.
    Shalev H; Kapelushnik J; Moser A; Dgany O; Krasnov T; Tamary H
    J Pediatr Hematol Oncol; 2004 Nov; 26(11):746-8. PubMed ID: 15543010
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.