Detalhe da pesquisa
1.
RUNX1 is required in granulocyte-monocyte progenitors to attenuate inflammatory cytokine production by neutrophils.
Genes Dev
; 37(13-14): 605-620, 2023 07 01.
Artigo
Inglês
| MEDLINE | ID: mdl-37536952
2.
Truncated CSF3 receptors induce pro-inflammatory responses in severe congenital neutropenia.
Br J Haematol
; 200(1): 79-86, 2023 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36168923
3.
A congenital CSF3R mutation in chronic neutropenia reveals a vital role for a cytokine receptor extracellular hinge motif in the response to granulocyte colony-stimulating factor.
Pediatr Blood Cancer
; 70(4): e30039, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36316822
4.
Congenital neutropenia: disease models guiding new treatment strategies.
Curr Opin Hematol
; 29(1): 27-33, 2022 01 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34854832
5.
ICL-induced miR139-3p and miR199a-3p have opposite roles in hematopoietic cell expansion and leukemic transformation.
Blood
; 125(25): 3937-48, 2015 Jun 18.
Artigo
Inglês
| MEDLINE | ID: mdl-25778535
6.
Myeloid conditional deletion and transgenic models reveal a threshold for the neutrophil survival factor Serpinb1.
Biol Chem
; 397(9): 897-905, 2016 09 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27107834
7.
Inherited biallelic CSF3R mutations in severe congenital neutropenia.
Blood
; 123(24): 3811-7, 2014 Jun 12.
Artigo
Inglês
| MEDLINE | ID: mdl-24753537
8.
Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis.
Blood
; 123(14): 2229-37, 2014 Apr 03.
Artigo
Inglês
| MEDLINE | ID: mdl-24523240
9.
The JH2 domain and SH2-JH2 linker regulate JAK2 activity: A detailed kinetic analysis of wild type and V617F mutant kinase domains.
Biochim Biophys Acta
; 1844(10): 1835-41, 2014 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-25107665
10.
Mutant allelic burden in acute myeloid leukaemia: Why bother?
Br J Haematol
; 188(6): 817-818, 2020 03.
Artigo
Inglês
| MEDLINE | ID: mdl-31580476
11.
Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes.
Haematologica
; 100(10): 1285-93, 2015 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-26185170
12.
FcγRIIb on myeloid cells and intrinsic renal cells rather than B cells protects from nephrotoxic nephritis.
J Immunol
; 190(1): 340-8, 2013 Jan 01.
Artigo
Inglês
| MEDLINE | ID: mdl-23203925
13.
IFNγ induces monopoiesis and inhibits neutrophil development during inflammation.
Blood
; 119(6): 1543-54, 2012 Feb 09.
Artigo
Inglês
| MEDLINE | ID: mdl-22117048
14.
Ribosomal deficiencies in Diamond-Blackfan anemia impair translation of transcripts essential for differentiation of murine and human erythroblasts.
Blood
; 119(1): 262-72, 2012 Jan 05.
Artigo
Inglês
| MEDLINE | ID: mdl-22058113
15.
Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia.
Blood
; 119(22): 5071-7, 2012 May 31.
Artigo
Inglês
| MEDLINE | ID: mdl-22371884
16.
Dicer1 deletion in myeloid-committed progenitors causes neutrophil dysplasia and blocks macrophage/dendritic cell development in mice.
Blood
; 119(20): 4723-30, 2012 May 17.
Artigo
Inglês
| MEDLINE | ID: mdl-22353998
17.
Recurrently affected genes in juvenile myelomonocytic leukaemia.
Br J Haematol
; 182(1): 135-138, 2018 07.
Artigo
Inglês
| MEDLINE | ID: mdl-28485469
18.
Peroxiredoxin-controlled G-CSF signalling at the endoplasmic reticulum-early endosome interface.
J Cell Sci
; 124(Pt 21): 3695-705, 2011 Nov 01.
Artigo
Inglês
| MEDLINE | ID: mdl-22045733
19.
MiR-17/20/93/106 promote hematopoietic cell expansion by targeting sequestosome 1-regulated pathways in mice.
Blood
; 118(4): 916-25, 2011 Jul 28.
Artigo
Inglês
| MEDLINE | ID: mdl-21628417
20.
Gata2-regulated Gfi1b expression controls endothelial programming during endothelial-to-hematopoietic transition.
Blood Adv
; 7(10): 2082-2093, 2023 05 23.
Artigo
Inglês
| MEDLINE | ID: mdl-36649572