342 related articles for article (PubMed ID: 28377399)
21. Diamond-Blackfan anemia, ribosome and erythropoiesis.
Da Costa L; Moniz H; Simansour M; Tchernia G; Mohandas N; Leblanc T
Transfus Clin Biol; 2010 Sep; 17(3):112-9. PubMed ID: 20655265
[TBL] [Abstract][Full Text] [Related]
22. Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia.
Sankaran VG; Ghazvinian R; Do R; Thiru P; Vergilio JA; Beggs AH; Sieff CA; Orkin SH; Nathan DG; Lander ES; Gazda HT
J Clin Invest; 2012 Jul; 122(7):2439-43. PubMed ID: 22706301
[TBL] [Abstract][Full Text] [Related]
23. Loss of GATA-1 full length as a cause of Diamond-Blackfan anemia phenotype.
Parrella S; Aspesi A; Quarello P; Garelli E; Pavesi E; Carando A; Nardi M; Ellis SR; Ramenghi U; Dianzani I
Pediatr Blood Cancer; 2014 Jul; 61(7):1319-21. PubMed ID: 24453067
[TBL] [Abstract][Full Text] [Related]
24. TNF-mediated inflammation represses GATA1 and activates p38 MAP kinase in RPS19-deficient hematopoietic progenitors.
Bibikova E; Youn MY; Danilova N; Ono-Uruga Y; Konto-Ghiorghi Y; Ochoa R; Narla A; Glader B; Lin S; Sakamoto KM
Blood; 2014 Dec; 124(25):3791-8. PubMed ID: 25270909
[TBL] [Abstract][Full Text] [Related]
25. Elucidation of the EP defect in Diamond-Blackfan anemia by characterization and prospective isolation of human EPs.
Iskander D; Psaila B; Gerrard G; Chaidos A; En Foong H; Harrington Y; Karnik LC; Roberts I; de la Fuente J; Karadimitris A
Blood; 2015 Apr; 125(16):2553-7. PubMed ID: 25755292
[TBL] [Abstract][Full Text] [Related]
26. Novel and known ribosomal causes of Diamond-Blackfan anaemia identified through comprehensive genomic characterisation.
Mirabello L; Khincha PP; Ellis SR; Giri N; Brodie S; Chandrasekharappa SC; Donovan FX; Zhou W; Hicks BD; Boland JF; Yeager M; Jones K; Zhu B; Wang M; Alter BP; Savage SA
J Med Genet; 2017 Jun; 54(6):417-425. PubMed ID: 28280134
[TBL] [Abstract][Full Text] [Related]
27. An RNA interference model of RPS19 deficiency in Diamond-Blackfan anemia recapitulates defective hematopoiesis and rescue by dexamethasone: identification of dexamethasone-responsive genes by microarray.
Ebert BL; Lee MM; Pretz JL; Subramanian A; Mak R; Golub TR; Sieff CA
Blood; 2005 Jun; 105(12):4620-6. PubMed ID: 15755903
[TBL] [Abstract][Full Text] [Related]
28. Transcription factors Fli1 and EKLF in the differentiation of megakaryocytic and erythroid progenitor in 5q- syndrome and in Diamond-Blackfan anemia.
Neuwirtova R; Fuchs O; Holicka M; Vostry M; Kostecka A; Hajkova H; Jonasova A; Cermak J; Cmejla R; Pospisilova D; Belickova M; Siskova M; Hochova I; Vondrakova J; Sponerova D; Kadlckova E; Novakova L; Brezinova J; Michalova K
Ann Hematol; 2013 Jan; 92(1):11-8. PubMed ID: 22965552
[TBL] [Abstract][Full Text] [Related]
29. Defective ribosomal protein gene expression alters transcription, translation, apoptosis, and oncogenic pathways in Diamond-Blackfan anemia.
Gazda HT; Kho AT; Sanoudou D; Zaucha JM; Kohane IS; Sieff CA; Beggs AH
Stem Cells; 2006 Sep; 24(9):2034-44. PubMed ID: 16741228
[TBL] [Abstract][Full Text] [Related]
30. [Molecular mechanisms underlying the pathology of Diamond-Blackfan anemia].
Toki T; Ito E
Rinsho Ketsueki; 2015 Jul; 56(7):867-76. PubMed ID: 26251151
[TBL] [Abstract][Full Text] [Related]
31. Diamond-Blackfan anaemia caused by a de novo initiation codon mutation resulting in a shorter isoform of GATA1.
Chen T; Zhang Q; Shang X; Zou S; Qin J; Li K; Lin B; Tao Z; Long X; Xu X
Clin Genet; 2022 Dec; 102(6):548-554. PubMed ID: 36029112
[TBL] [Abstract][Full Text] [Related]
32. Glucocorticoids improve erythroid progenitor maintenance and dampen Trp53 response in a mouse model of Diamond-Blackfan anaemia.
Sjögren SE; Siva K; Soneji S; George AJ; Winkler M; Jaako P; Wlodarski M; Karlsson S; Hannan RD; Flygare J
Br J Haematol; 2015 Nov; 171(4):517-29. PubMed ID: 26305041
[TBL] [Abstract][Full Text] [Related]
33. Enhanced alternative splicing of the FLVCR1 gene in Diamond Blackfan anemia disrupts FLVCR1 expression and function that are critical for erythropoiesis.
Rey MA; Duffy SP; Brown JK; Kennedy JA; Dick JE; Dror Y; Tailor CS
Haematologica; 2008 Nov; 93(11):1617-26. PubMed ID: 18815190
[TBL] [Abstract][Full Text] [Related]
34. Global transcriptome and chromatin occupancy analysis reveal the short isoform of GATA1 is deficient for erythroid specification and gene expression.
Chlon TM; McNulty M; Goldenson B; Rosinski A; Crispino JD
Haematologica; 2015 May; 100(5):575-84. PubMed ID: 25682601
[TBL] [Abstract][Full Text] [Related]
35. Lymphoblastoid cell lines from Diamond Blackfan anaemia patients exhibit a full ribosomal stress phenotype that is rescued by gene therapy.
Aspesi A; Monteleone V; Betti M; Actis C; Morleo G; Sculco M; Guarrera S; Wlodarski MW; Ramenghi U; Santoro C; Ellis SR; Loreni F; Follenzi A; Dianzani I
Sci Rep; 2017 Sep; 7(1):12010. PubMed ID: 28931864
[TBL] [Abstract][Full Text] [Related]
36. SATB1 Chromatin Loops Regulate Megakaryocyte/Erythroid Progenitor Expansion by Facilitating HSP70 and GATA1 Induction.
Wilkes MC; Chae HD; Scanlon V; Cepika AM; Wentworth EP; Saxena M; Eskin A; Chen Z; Glader B; Grazia Roncarolo M; Nelson SF; Sakamoto KM
Stem Cells; 2023 Jun; 41(6):560-569. PubMed ID: 36987811
[TBL] [Abstract][Full Text] [Related]
37. [Diagnostic targets and exosome sequence analysis of Diamond-Blackfan anemia in Japan].
Toki T; Ito E
Rinsho Ketsueki; 2018; 59(7):945-952. PubMed ID: 30078807
[TBL] [Abstract][Full Text] [Related]
38. RPS19 mutations in patients with Diamond-Blackfan anemia.
Campagnoli MF; Ramenghi U; Armiraglio M; Quarello P; Garelli E; Carando A; Avondo F; Pavesi E; Fribourg S; Gleizes PE; Loreni F; Dianzani I
Hum Mutat; 2008 Jul; 29(7):911-20. PubMed ID: 18412286
[TBL] [Abstract][Full Text] [Related]
39. Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
Wang R; Yoshida K; Toki T; Sawada T; Uechi T; Okuno Y; Sato-Otsubo A; Kudo K; Kamimaki I; Kanezaki R; Shiraishi Y; Chiba K; Tanaka H; Terui K; Sato T; Iribe Y; Ohga S; Kuramitsu M; Hamaguchi I; Ohara A; Hara J; Goi K; Matsubara K; Koike K; Ishiguro A; Okamoto Y; Watanabe K; Kanno H; Kojima S; Miyano S; Kenmochi N; Ogawa S; Ito E
Br J Haematol; 2015 Mar; 168(6):854-64. PubMed ID: 25424902
[TBL] [Abstract][Full Text] [Related]
40. Novel deletion of RPL15 identified by array-comparative genomic hybridization in Diamond-Blackfan anemia.
Landowski M; O'Donohue MF; Buros C; Ghazvinian R; Montel-Lehry N; Vlachos A; Sieff CA; Newburger PE; Niewiadomska E; Matysiak M; Glader B; Atsidaftos E; Lipton JM; Beggs AH; Gleizes PE; Gazda HT
Hum Genet; 2013 Nov; 132(11):1265-74. PubMed ID: 23812780
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
