Detalhe da pesquisa
1.
The chromatin remodelling factor ATRX suppresses R-loops in transcribed telomeric repeats.
EMBO Rep;
18(6): 914-928, 2017 06.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28487353
2.
Hepcidin is suppressed by erythropoiesis in hemoglobin E ß-thalassemia and ß-thalassemia trait.
Blood;
125(5): 873-80, 2015 Jan 29.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25519750
3.
A large deletion in the human alpha-globin cluster caused by a replication error is associated with an unexpectedly mild phenotype.
Hum Mol Genet;
17(19): 3084-93, 2008 Oct 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18632685
4.
Phenotypic and molecular characterization of a serum-free miniature erythroid differentiation system suitable for high-throughput screening and single-cell assays.
Exp Hematol;
60: 10-20, 2018 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29329925
5.
Editing an α-globin enhancer in primary human hematopoietic stem cells as a treatment for ß-thalassemia.
Nat Commun;
8(1): 424, 2017 09 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28871148
6.
Hb Bart's in cord blood: an accurate indicator of alpha-thalassemia.
Hemoglobin;
30(1): 57-62, 2006.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16540417
7.
Acquired somatic ATRX mutations in myelodysplastic syndrome associated with alpha thalassemia (ATMDS) convey a more severe hematologic phenotype than germline ATRX mutations.
Blood;
103(6): 2019-26, 2004 Mar 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-14592816