| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A central role of GPIb-IX in the procoagulant function of platelets that is independent of the 45-kDa GPIbα N-terminal extracellular domain
|
Ravanat, Catherine
|
|
|
116 |
7 |
p. 1157-1164
|
artikel
|
| 2 |
CD99 and CD99L2 act at the same site as, but independently of, PECAM-1 during leukocyte diapedesis
|
Bixel, M. Gabriele
|
|
|
116 |
7 |
p. 1172-1184
|
artikel
|
| 3 |
Diffuse large B-cell lymphomas with CDKN2A deletion have a distinct gene expression signature and a poor prognosis under R-CHOP treatment: a GELA study
|
Jardin, Fabrice
|
|
|
116 |
7 |
p. 1092-1104
|
artikel
|
| 4 |
Down syndrome childhood acute lymphoblastic leukemia has a unique spectrum of sentinel cytogenetic lesions that influences treatment outcome: a report from the Children's Oncology Group
|
Maloney, Kelly W.
|
|
|
116 |
7 |
p. 1045-1050
|
artikel
|
| 5 |
Editorial Board
|
|
|
|
116 |
7 |
p. i
|
artikel
|
| 6 |
Evidence against a protein in plasma that is a product of a factor XI mRNA splice variant missing exons 6 and 7
|
Gailani, David
|
|
|
116 |
7 |
p. 1185-1186
|
artikel
|
| 7 |
Genomewide DNA methylation analysis reveals novel targets for drug development in mantle cell lymphoma
|
Leshchenko, Violetta V.
|
|
|
116 |
7 |
p. 1025-1034
|
artikel
|
| 8 |
High-throughput immunoglobulin repertoire analysis distinguishes between human IgM memory and switched memory B-cell populations
|
Wu, Yu-Chang
|
|
|
116 |
7 |
p. 1070-1078
|
artikel
|
| 9 |
Hydroxyurea in essential thrombocythemia: rate and clinical relevance of responses by European LeukemiaNet criteria
|
Carobbio, Alessandra
|
|
|
116 |
7 |
p. 1051-1055
|
artikel
|
| 10 |
Incidence and prognostic value of TET2 alterations in de novo acute myeloid leukemia achieving complete remission
|
Nibourel, Olivier
|
|
|
116 |
7 |
p. 1132-1135
|
artikel
|
| 11 |
Influence of bone marrow stromal microenvironment on forodesine-induced responses in CLL primary cells
|
Balakrishnan, Kumudha
|
|
|
116 |
7 |
p. 1083-1091
|
artikel
|
| 12 |
Interferon-γ and tumor necrosis factor-α induce an immunoinhibitory molecule, B7-H1, via nuclear factor-κB activation in blasts in myelodysplastic syndromes
|
Kondo, Asaka
|
|
|
116 |
7 |
p. 1124-1131
|
artikel
|
| 13 |
“Micro”-managing the MiRNome in SzS
|
Chng, Wee J.
|
|
|
116 |
7 |
p. 1021-1022
|
artikel
|
| 14 |
MicroRNA expression in Sézary syndrome: identification, function, and diagnostic potential
|
Ballabio, Erica
|
|
|
116 |
7 |
p. 1105-1113
|
artikel
|
| 15 |
Obesity is associated with an increased risk of monoclonal gammopathy of undetermined significance among black and white women
|
Landgren, Ola
|
|
|
116 |
7 |
p. 1056-1059
|
artikel
|
| 16 |
Pediatric mastocytosis–associated KIT extracellular domain mutations exhibit different functional and signaling properties compared with KIT-phosphotransferase domain mutations
|
Yang, Ying
|
|
|
116 |
7 |
p. 1114-1123
|
artikel
|
| 17 |
Redirecting T-cell specificity by introducing a tumor-specific chimeric antigen receptor
|
Jena, Bipulendu
|
|
|
116 |
7 |
p. 1035-1044
|
artikel
|
| 18 |
Repression of Id2 expression by Gfi-1 is required for B-cell and myeloid development
|
Li, Huajie
|
|
|
116 |
7 |
p. 1060-1069
|
artikel
|
| 19 |
Response: Further thoughts on the “phantom” Δ6/7 FXI isoform
|
Asselta, Rosanna
|
|
|
116 |
7 |
p. 1186-1187
|
artikel
|
| 20 |
S100A10: a complex inflammatory role
|
Miles, Lindsey A.
|
|
|
116 |
7 |
p. 1022-1024
|
artikel
|
| 21 |
S100A10 regulates plasminogen-dependent macrophage invasion
|
O'Connell, Paul A.
|
|
|
116 |
7 |
p. 1136-1146
|
artikel
|
| 22 |
Similar yet different
|
Izraeli, Shai
|
|
|
116 |
7 |
p. 1019-1020
|
artikel
|
| 23 |
The platelet interior revisited: electron tomography reveals tubular α-granule subtypes
|
van Nispen tot Pannerden, Hezder
|
|
|
116 |
7 |
p. 1147-1156
|
artikel
|
| 24 |
The White House crusade against … MGUS?
|
Lonial, Sagar
|
|
|
116 |
7 |
p. 1020-1021
|
artikel
|
| 25 |
Th17/Treg ratio in human graft-versus-host disease
|
Ratajczak, Philippe
|
|
|
116 |
7 |
p. 1165-1171
|
artikel
|
| 26 |
XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease
|
Marsh, Rebecca A.
|
|
|
116 |
7 |
p. 1079-1082
|
artikel
|
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