Detalhe da pesquisa
1.
Differential effects of RASA3 mutations on hematopoiesis are profoundly influenced by genetic background and molecular variant.
PLoS Genet
; 16(12): e1008857, 2020 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-33370780
2.
Rasa3 regulates stage-specific cell cycle progression in murine erythropoiesis.
Blood Cells Mol Dis
; 87: 102524, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33341069
3.
PPAR-α and glucocorticoid receptor synergize to promote erythroid progenitor self-renewal.
Nature
; 522(7557): 474-7, 2015 Jun 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-25970251
4.
Neomorphic effects of the neonatal anemia (Nan-Eklf) mutation contribute to deficits throughout development.
Development
; 144(3): 430-440, 2017 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28143845
5.
Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability.
Nucleic Acids Res
; 45(3): 1130-1143, 2017 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-28180284
6.
Iron regulatory protein-1 protects against mitoferrin-1-deficient porphyria.
J Biol Chem
; 289(11): 7835-43, 2014 Mar 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-24509859
7.
Critical function for the Ras-GTPase activating protein RASA3 in vertebrate erythropoiesis and megakaryopoiesis.
Proc Natl Acad Sci U S A
; 109(30): 12099-104, 2012 Jul 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-22773809
8.
Strain-specific variations in cation content and transport in mouse erythrocytes.
Physiol Genomics
; 45(9): 343-50, 2013 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23482811
9.
Severe anemia in the Nan mutant mouse caused by sequence-selective disruption of erythroid Kruppel-like factor.
Proc Natl Acad Sci U S A
; 107(34): 15151-6, 2010 Aug 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-20696915
10.
Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes.
Proc Natl Acad Sci U S A
; 107(13): 6022-7, 2010 Mar 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-20231455
11.
Cell-specific mitotic defect and dyserythropoiesis associated with erythroid band 3 deficiency.
Nat Genet
; 34(1): 59-64, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12669066
12.
Strain-specific hyperkyphosis and megaesophagus in Add1 null mice.
Genesis
; 50(12): 882-91, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-22926980
13.
Tropomodulin 1-null mice have a mild spherocytic elliptocytosis with appearance of tropomodulin 3 in red blood cells and disruption of the membrane skeleton.
Blood
; 116(14): 2590-9, 2010 Oct 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20585041
14.
Analysis of novel sph (spherocytosis) alleles in mice reveals allele-specific loss of band 3 and adducin in alpha-spectrin-deficient red cells.
Blood
; 115(9): 1804-14, 2010 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-20056793
15.
Sequence variation at multiple loci influences red cell hemoglobin concentration.
Blood
; 116(25): e139-49, 2010 Dec 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-20833975
16.
Mitoferrin is essential for erythroid iron assimilation.
Nature
; 440(7080): 96-100, 2006 Mar 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-16511496
17.
Comparison of unrestrained plethysmography and forced oscillation for identifying genetic variability of airway responsiveness in inbred mice.
Physiol Genomics
; 43(1): 1-11, 2011 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20823217
18.
Protein 4.2 binds to the carboxyl-terminal EF-hands of erythroid alpha-spectrin in a calcium- and calmodulin-dependent manner.
J Biol Chem
; 285(7): 4757-70, 2010 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20007969
19.
Comparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in ß-adducin null red cells.
Br J Haematol
; 154(4): 492-501, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21689084
20.
Comparative proteomics reveals deficiency of NHE-1 (Slc9a1) in RBCs from the beta-adducin knockout mouse model of hemolytic anemia.
Blood Cells Mol Dis
; 47(2): 85-94, 2011 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21592827