Detalhe da pesquisa
1.
Sites of regulated phosphorylation that control K-Cl cotransporter activity.
Cell
; 138(3): 525-36, 2009 Aug 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-19665974
2.
Rapid degradation of protein tyrosine phosphatase 1B in sickle cells: Possible contribution to sickle cell membrane weakening.
FASEB J
; 36(6): e22360, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35593742
3.
Red cell membrane disorders: structure meets function.
Blood
; 136(11): 1250-1261, 2020 09 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32702754
4.
Inhibition of Band 3 tyrosine phosphorylation: a new mechanism for treatment of sickle cell disease.
Br J Haematol
; 190(4): 599-609, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32346864
5.
RGL2 Deficiency Impairs Human Erythropoiesis By Altering Terminal Erythroid Differentiation and Apoptosis.
Blood
; 130(Suppl_1): 8, 2017 Dec 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31940662
6.
Hereditary elliptocytosis-associated alpha-spectrin mutation p.L155dup as a modifier of sickle cell disease severity.
Pediatr Blood Cancer
; 66(2): e27531, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30393954
7.
Hemolytic anemia and macrothrombocytopenia: A lipid problem?
Am J Hematol
; 98(8): 1335-1340, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-36974979
8.
Cytokinesis failure in RhoA-deficient mouse erythroblasts involves actomyosin and midbody dysregulation and triggers p53 activation.
Blood
; 126(12): 1473-82, 2015 Sep 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-26228485
9.
Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.
Blood Cells Mol Dis
; 61: 4-9, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27667160
10.
Hereditary xerocytosis: Diagnostic considerations.
Am J Hematol
; 93(3): E67-E69, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29210095
11.
K-Cl cotransporter gene expression during human and murine erythroid differentiation.
J Biol Chem
; 286(35): 30492-30503, 2011 Sep 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-21733850
12.
Crosslinks and crosstalk: human cancer syndromes and DNA repair defects.
Cancer Cell
; 6(6): 539-45, 2004 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-15607958
13.
Volume regulation and KCl cotransport in reticulocyte populations of sickle and normal red blood cells.
Blood Cells Mol Dis
; 47(2): 95-9, 2011 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21576026
14.
Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management.
Hematol Oncol Clin North Am
; 33(3): 373-392, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31030808
15.
Corrigendum: The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Front Physiol
; 10: 1331, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31736770
16.
The Spectrum of SPTA1-Associated Hereditary Spherocytosis.
Front Physiol
; 10: 815, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31333484
17.
Compound heterozygosity for two novel mutations in the erythrocyte protein 4.2 gene causing spherocytosis in a Caucasian patient.
Br J Haematol
; 152(6): 780-3, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21275958
18.
Urea stimulation of KCl cotransport induces abnormal volume reduction in sickle reticulocytes.
Blood
; 109(4): 1728-35, 2007 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17023583
19.
Enhanced tumor formation in mice heterozygous for Blm mutation.
Science
; 297(5589): 2051-3, 2002 Sep 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-12242442