206 related articles for article (PubMed ID: 19336738)
1. Codanin-1, the protein encoded by the gene mutated in congenital dyserythropoietic anemia type I (CDAN1), is cell cycle-regulated.
Noy-Lotan S; Dgany O; Lahmi R; Marcoux N; Krasnov T; Yissachar N; Ginsberg D; Motro B; Resnitzky P; Yaniv I; Kupfer GM; Tamary H
Haematologica; 2009 May; 94(5):629-37. PubMed ID: 19336738
[TBL] [Abstract][Full Text] [Related]
2. Characterization of the interactions between Codanin-1 and C15Orf41, two proteins implicated in congenital dyserythropoietic anemia type I disease.
Swickley G; Bloch Y; Malka L; Meiri A; Noy-Lotan S; Yanai A; Tamary H; Motro B
BMC Mol Cell Biol; 2020 Mar; 21(1):18. PubMed ID: 32293259
[TBL] [Abstract][Full Text] [Related]
3. Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Dgany O; Avidan N; Delaunay J; Krasnov T; Shalmon L; Shalev H; Eidelitz-Markus T; Kapelushnik J; Cattan D; Pariente A; Tulliez M; Crétien A; Schischmanoff PO; Iolascon A; Fibach E; Koren A; Rössler J; Le Merrer M; Yaniv I; Zaizov R; Ben-Asher E; Olender T; Lancet D; Beckmann JS; Tamary H
Am J Hum Genet; 2002 Dec; 71(6):1467-74. PubMed ID: 12434312
[TBL] [Abstract][Full Text] [Related]
4. Codanin-1 mutations in congenital dyserythropoietic anemia type 1 affect HP1{alpha} localization in erythroblasts.
Renella R; Roberts NA; Brown JM; De Gobbi M; Bird LE; Hassanali T; Sharpe JA; Sloane-Stanley J; Ferguson DJ; Cordell J; Buckle VJ; Higgs DR; Wood WG
Blood; 2011 Jun; 117(25):6928-38. PubMed ID: 21364188
[TBL] [Abstract][Full Text] [Related]
5. A complex comprising C15ORF41 and Codanin-1: the products of two genes mutated in congenital dyserythropoietic anaemia type I (CDA-I).
Shroff M; Knebel A; Toth R; Rouse J
Biochem J; 2020 May; 477(10):1893-1905. PubMed ID: 32239177
[TBL] [Abstract][Full Text] [Related]
6. Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II.
Iolascon A; Delaunay J
Haematologica; 2009 May; 94(5):599-602. PubMed ID: 19407313
[TBL] [Abstract][Full Text] [Related]
7. Codanin-1, mutated in the anaemic disease CDAI, regulates Asf1 function in S-phase histone supply.
Ask K; Jasencakova Z; Menard P; Feng Y; Almouzni G; Groth A
EMBO J; 2012 Apr; 31(8):2013-23. PubMed ID: 22407294
[TBL] [Abstract][Full Text] [Related]
8. Codanin-1 mutations engineered in human erythroid cells demonstrate role of CDAN1 in terminal erythroid maturation.
Murphy ZC; Getman MR; Myers JA; Burgos Villar KN; Leshen E; Kurita R; Nakamura Y; Steiner LA
Exp Hematol; 2020 Nov; 91():32-38.e6. PubMed ID: 33075436
[TBL] [Abstract][Full Text] [Related]
9.
Noy-Lotan S; Dgany O; Marcoux N; Atkins A; Kupfer GM; Bosques L; Gottschalk C; Steinberg-Shemer O; Motro B; Tamary H
Front Physiol; 2021; 12():685242. PubMed ID: 34234691
[TBL] [Abstract][Full Text] [Related]
10. Clinical and molecular variability in congenital dyserythropoietic anaemia type I.
Tamary H; Dgany O; Proust A; Krasnov T; Avidan N; Eidelitz-Markus T; Tchernia G; Geneviève D; Cormier-Daire V; Bader-Meunier B; Ferrero-Vacher C; Munzer M; Gruppo R; Fibach E; Konen O; Yaniv I; Delaunay J
Br J Haematol; 2005 Aug; 130(4):628-34. PubMed ID: 16098079
[TBL] [Abstract][Full Text] [Related]
11. New Codanin-1 Gene Mutations in a Italian Patient with Congenital Dyserythropoietic Anemia Type I and Heterozygous Beta-Thalassemia.
D'Alcamo E; Agrigento V; Pitrolo L; Sclafani S; Barone R; Calvaruso G; Buffa V; Maggio A
Indian J Hematol Blood Transfus; 2016 Jun; 32(Suppl 1):278-81. PubMed ID: 27408412
[TBL] [Abstract][Full Text] [Related]
12. Transcriptional regulation of the mouse PNRC2 promoter by the nuclear factor Y (NFY) and E2F1.
Zhou D; Masri S; Ye JJ; Chen S
Gene; 2005 Nov; 361():89-100. PubMed ID: 16181749
[TBL] [Abstract][Full Text] [Related]
13. Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis.
Resnitzky P; Shaft D; Shalev H; Kapelushnik J; Dgany O; Krasnov T; Tamary H
Eur J Haematol; 2017 Oct; 99(4):366-371. PubMed ID: 28755517
[TBL] [Abstract][Full Text] [Related]
14. Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I.
Babbs C; Roberts NA; Sanchez-Pulido L; McGowan SJ; Ahmed MR; Brown JM; Sabry MA; ; Bentley DR; McVean GA; Donnelly P; Gileadi O; Ponting CP; Higgs DR; Buckle VJ
Haematologica; 2013 Sep; 98(9):1383-7. PubMed ID: 23716552
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetic and functional insights into CDA-I prevalence and pathogenesis.
Olijnik AA; Roy NBA; Scott C; Marsh JA; Brown J; Lauschke K; Ask K; Roberts N; Downes DJ; Brolih S; Johnson E; Xella B; Proven M; Hipkiss R; Ryan K; Frisk P; Mäkk J; Stattin EM; Sadasivam N; McIlwaine L; Hill QA; Renella R; Hughes JR; Gibbons RJ; Groth A; McHugh PJ; Higgs DR; Buckle VJ; Babbs C
J Med Genet; 2021 Mar; 58(3):185-195. PubMed ID: 32518175
[TBL] [Abstract][Full Text] [Related]
17. Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy.
Goede JS; Benz R; Fehr J; Schwarz K; Heimpel H
Ann Hematol; 2006 Sep; 85(9):591-5. PubMed ID: 16767397
[TBL] [Abstract][Full Text] [Related]
18. Recapitulation of erythropoiesis in congenital dyserythropoietic anaemia type I (CDA-I) identifies defects in differentiation and nucleolar abnormalities.
Scott C; Downes DJ; Brown JM; Beagrie R; Olijnik AA; Gosden M; Schwessinger R; Fisher CA; Rose A; Ferguson DJP; Johnson E; Hill QA; Okoli S; Renella R; Ryan K; Brand M; Hughes J; Roy NBA; Higgs DR; Babbs C; Buckle VJ
Haematologica; 2021 Nov; 106(11):2960-2970. PubMed ID: 33121234
[TBL] [Abstract][Full Text] [Related]
19. Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene.
Ru YX; Zhu XF; Yan WW; Gao JT; Schwarz K; Heimpel H
Ann Hematol; 2008 Sep; 87(9):751-4. PubMed ID: 18575862
[TBL] [Abstract][Full Text] [Related]
20. Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach.
Iolascon A; Esposito MR; Russo R
Haematologica; 2012 Dec; 97(12):1786-94. PubMed ID: 23065504
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
