224 related articles for article (PubMed ID: 36413407)
1. An RPS19-edited model for Diamond-Blackfan anemia reveals TP53-dependent impairment of hematopoietic stem cell activity.
Bhoopalan SV; Yen JS; Mayuranathan T; Mayberry KD; Yao Y; Lillo Osuna MA; Jang Y; Liyanage JS; Blanc L; Ellis SR; Wlodarski MW; Weiss MJ
JCI Insight; 2023 Jan; 8(1):. PubMed ID: 36413407
[TBL] [Abstract][Full Text] [Related]
2. Successful gene therapy of Diamond-Blackfan anemia in a mouse model and human CD34
Liu Y; Dahl M; Debnath S; Rothe M; Smith EM; Grahn THM; Warsi S; Chen J; Flygare J; Schambach A; Karlsson S
Haematologica; 2022 Feb; 107(2):446-456. PubMed ID: 33440921
[TBL] [Abstract][Full Text] [Related]
3. Proliferation deficiency of multipotent hematopoietic progenitors in ribosomal protein S19 (RPS19)-deficient diamond-Blackfan anemia improves following RPS19 gene transfer.
Hamaguchi I; Flygare J; Nishiura H; Brun AC; Ooka A; Kiefer T; Ma Z; Dahl N; Richter J; Karlsson S
Mol Ther; 2003 May; 7(5 Pt 1):613-22. PubMed ID: 12718904
[TBL] [Abstract][Full Text] [Related]
4. p53-Independent cell cycle and erythroid differentiation defects in murine embryonic stem cells haploinsufficient for Diamond Blackfan anemia-proteins: RPS19 versus RPL5.
Singh SA; Goldberg TA; Henson AL; Husain-Krautter S; Nihrane A; Blanc L; Ellis SR; Lipton JM; Liu JM
PLoS One; 2014; 9(2):e89098. PubMed ID: 24558476
[TBL] [Abstract][Full Text] [Related]
5. Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro.
Moniz H; Gastou M; Leblanc T; Hurtaud C; Crétien A; Lécluse Y; Raslova H; Larghero J; Croisille L; Faubladier M; Bluteau O; Lordier L; Tchernia G; Vainchenker W; Mohandas N; Da Costa L;
Cell Death Dis; 2012 Jul; 3(7):e356. PubMed ID: 22833095
[TBL] [Abstract][Full Text] [Related]
6. Gene therapy of Diamond Blackfan anemia CD34(+) cells leads to improved erythroid development and engraftment following transplantation.
Flygare J; Olsson K; Richter J; Karlsson S
Exp Hematol; 2008 Nov; 36(11):1428-35. PubMed ID: 18715690
[TBL] [Abstract][Full Text] [Related]
7. Lentiviral Vectors with Cellular Promoters Correct Anemia and Lethal Bone Marrow Failure in a Mouse Model for Diamond-Blackfan Anemia.
Debnath S; Jaako P; Siva K; Rothe M; Chen J; Dahl M; Gaspar HB; Flygare J; Schambach A; Karlsson S
Mol Ther; 2017 Aug; 25(8):1805-1814. PubMed ID: 28434866
[TBL] [Abstract][Full Text] [Related]
8. Mice with ribosomal protein S19 deficiency develop bone marrow failure and symptoms like patients with Diamond-Blackfan anemia.
Jaako P; Flygare J; Olsson K; Quere R; Ehinger M; Henson A; Ellis S; Schambach A; Baum C; Richter J; Larsson J; Bryder D; Karlsson S
Blood; 2011 Dec; 118(23):6087-96. PubMed ID: 21989989
[TBL] [Abstract][Full Text] [Related]
9. Ribosomal protein mutations in Korean patients with Diamond-Blackfan anemia.
Chae H; Park J; Lee S; Kim M; Kim Y; Lee JW; Chung NG; Cho B; Jeong DC; Kim J; Kim JR; Park G
Exp Mol Med; 2014 Mar; 46(3):e88. PubMed ID: 24675553
[TBL] [Abstract][Full Text] [Related]
10. Defects of protein production in erythroid cells revealed in a zebrafish Diamond-Blackfan anemia model for mutation in RPS19.
Zhang Y; Ear J; Yang Z; Morimoto K; Zhang B; Lin S
Cell Death Dis; 2014 Jul; 5(7):e1352. PubMed ID: 25058426
[TBL] [Abstract][Full Text] [Related]
11. Erythropoiesis failure due to RPS19 deficiency is independent of an activated Tp53 response in a zebrafish model of Diamond-Blackfan anaemia.
Torihara H; Uechi T; Chakraborty A; Shinya M; Sakai N; Kenmochi N
Br J Haematol; 2011 Mar; 152(5):648-54. PubMed ID: 21223253
[TBL] [Abstract][Full Text] [Related]
12. Eltrombopag Improves Erythroid Differentiation in a Human Induced Pluripotent Stem Cell Model of Diamond Blackfan Anemia.
Qanash H; Li Y; Smith RH; Linask K; Young-Baird S; Hakami W; Keyvanfar K; Choy JS; Zou J; Larochelle A
Cells; 2021 Mar; 10(4):. PubMed ID: 33810313
[TBL] [Abstract][Full Text] [Related]
13. Gene transfer improves erythroid development in ribosomal protein S19-deficient Diamond-Blackfan anemia.
Hamaguchi I; Ooka A; Brun A; Richter J; Dahl N; Karlsson S
Blood; 2002 Oct; 100(8):2724-31. PubMed ID: 12351378
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Ribosomal protein S19 deficiency leads to reduced proliferation and increased apoptosis but does not affect terminal erythroid differentiation in a cell line model of Diamond-Blackfan anemia.
Miyake K; Utsugisawa T; Flygare J; Kiefer T; Hamaguchi I; Richter J; Karlsson S
Stem Cells; 2008 Feb; 26(2):323-9. PubMed ID: 17962699
[TBL] [Abstract][Full Text] [Related]
16. Toward RNA Repair of Diamond Blackfan Anemia Hematopoietic Stem Cells.
D'Allard DL; Liu JM
Hum Gene Ther; 2016 Oct; 27(10):792-801. PubMed ID: 27550323
[TBL] [Abstract][Full Text] [Related]
17. Engineered human Diamond-Blackfan anemia disease model confirms therapeutic effects of clinically applicable lentiviral vector at single-cell resolution.
Liu Y; Schmiderer L; Hjort M; Lang S; Bremborg T; Rydström A; Schambach A; Larsson J; Karlsson S
Haematologica; 2023 Nov; 108(11):3095-3109. PubMed ID: 37199130
[TBL] [Abstract][Full Text] [Related]
18. Bone marrow transplantation without myeloablative conditioning in a mouse model for Diamond-Blackfan anemia corrects the disease phenotype.
Dahl M; Warsi S; Liu Y; Debnath S; Billing M; Siva K; Flygare J; Karlsson S
Exp Hematol; 2021 Jul; 99():44-53.e2. PubMed ID: 34126174
[TBL] [Abstract][Full Text] [Related]
19. Cells depleted for RPS19, a protein associated with Diamond Blackfan Anemia, show defects in 18S ribosomal RNA synthesis and small ribosomal subunit production.
Idol RA; Robledo S; Du HY; Crimmins DL; Wilson DB; Ladenson JH; Bessler M; Mason PJ
Blood Cells Mol Dis; 2007; 39(1):35-43. PubMed ID: 17376718
[TBL] [Abstract][Full Text] [Related]
20. Lentivirus-mediated gene therapy corrects ribosomal biogenesis and shows promise for Diamond Blackfan anemia.
Giménez Y; Palacios M; Sánchez-Domínguez R; Zorbas C; Peral J; Puzik A; Ugalde L; Alberquilla O; Villanueva M; Río P; Gálvez E; Da Costa L; Strullu M; Catala A; Ruiz-Llobet A; Segovia JC; Sevilla J; Strahm B; Niemeyer CM; Beléndez C; Leblanc T; Lafontaine DL; Bueren J; Navarro S
JCI Insight; 2024 May; 9(10):. PubMed ID: 38775150
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
