Detalhe da pesquisa
1.
Patient-derived xenograft mouse models to investigate tropism to the central nervous system and retina of primary and secondary central nervous system lymphoma.
Neuropathol Appl Neurobiol
; 49(2): e12899, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36879456
2.
Novel mutation in two brothers with Hermansky Pudlak syndrome type 3.
Blood Cells Mol Dis
; 67: 75-80, 2017 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28284561
3.
Novel mutation in Hermansky-Pudlak syndrome type 2 with mild immunological phenotype.
Platelets
; 24(7): 538-43, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23215637
4.
Cellular and Humoral SARS-CoV-2 Vaccination Responses in 192 Adult Recipients of Allogeneic Hematopoietic Cell Transplantation.
Vaccines (Basel)
; 10(11)2022 Oct 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-36366291
5.
Characterization of human septin interactions.
Biol Chem
; 392(8-9): 751-61, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21767235
6.
Lethal phenotype of mice carrying a Sept11 null mutation.
Biol Chem
; 392(8-9): 779-81, 2011 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21824005
7.
Septin expression in proliferative retinal membranes.
J Histochem Cytochem
; 55(11): 1089-94, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17625225
8.
Establishment of a long-term culture system for rat colon epithelial cells.
In Vitro Cell Dev Biol Anim
; 40(8-9): 278-84, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15723563
9.
BRAF inhibitor-associated ERK activation drives development of chronic lymphocytic leukemia.
J Clin Invest
; 124(11): 5074-84, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25329694
10.
Deletion of human GP1BB and SEPT5 is associated with Bernard-Soulier syndrome, platelet secretion defect, polymicrogyria, and developmental delay.
Thromb Haemost
; 106(3): 475-83, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21800012
11.
Human endothelial and platelet septin SEPT11: cloning of novel variants and characterisation of interaction partners.
Thromb Haemost
; 104(6): 1201-10, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20978712