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Marcin Wlodarski
Marcin Wlodarski
Faculty, St. Jude Hospital
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα stjude.org - Αρχική σελίδα
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Frequency and prognostic impact of mutations in SRSF2, U2AF1, and ZRSR2 in patients with myelodysplastic syndromes
F Thol, S Kade, C Schlarmann, P Löffeld, M Morgan, J Krauter, ...
Blood, The Journal of the American Society of Hematology 119 (15), 3578-3584, 2012
5462012
STAT3 mutations unify the pathogenesis of chronic lymphoproliferative disorders of NK cells and T-cell large granular lymphocyte leukemia
A Jerez, MJ Clemente, H Makishima, H Koskela, F LeBlanc, K Peng Ng, ...
Blood, The Journal of the American Society of Hematology 120 (15), 3048-3057, 2012
4682012
Prevalence, clinical characteristics, and prognosis of GATA2-related myelodysplastic syndromes in children and adolescents
MW Wlodarski, S Hirabayashi, V Pastor, J Starý, H Hasle, R Masetti, ...
Blood, The Journal of the American Society of Hematology 127 (11), 1387-1397, 2016
4492016
Mutations in CBL occur frequently in juvenile myelomonocytic leukemia
ML Loh, DS Sakai, C Flotho, M Kang, M Fliegauf, S Archambeault, ...
Blood, The Journal of the American Society of Hematology 114 (9), 1859-1863, 2009
3542009
Childhood cancer predisposition syndromes—a concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and Hematology
T Ripperger, SS Bielack, A Borkhardt, IB Brecht, B Burkhardt, ...
American journal of medical genetics Part A 173 (4), 1017-1037, 2017
3242017
CD4+CD25high Foxp3+ regulatory T cells in myelodysplastic syndrome (MDS)
SY Kordasti, W Ingram, J Hayden, D Darling, L Barber, B Afzali, ...
Blood, The Journal of the American Society of Hematology 110 (3), 847-850, 2007
3212007
Somatic mutations and progressive monosomy modify SAMD9-related phenotypes in humans
F Buonocore, P Kühnen, JP Suntharalingham, I Del Valle, M Digweed, ...
The Journal of clinical investigation 127 (5), 1700-1713, 2017
1802017
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia
A Stray-Pedersen, PH Backe, HS Sorte, L Mørkrid, NY Chokshi, ...
The American Journal of Human Genetics 95 (1), 96-107, 2014
1802014
GATA2 deficiency and related myeloid neoplasms
MW Wlodarski, M Collin, MS Horwitz
Seminars in hematology 54 (2), 81-86, 2017
1712017
Clinical spectrum of pyruvate kinase deficiency: data from the Pyruvate Kinase Deficiency Natural History Study
RF Grace, P Bianchi, EJ van Beers, SW Eber, B Glader, HM Yaish, ...
Blood, The Journal of the American Society of Hematology 131 (20), 2183-2192, 2018
1612018
Pathologic clonal cytotoxic T-cell responses: nonrandom nature of the T-cell–receptor restriction in large granular lymphocyte leukemia
MW Wlodarski, C O'Keefe, EC Howe, AM Risitano, A Rodriguez, ...
Blood 106 (8), 2769-2780, 2005
1502005
SNP array–based karyotyping: differences and similarities between aplastic anemia and hypocellular myelodysplastic syndromes
MG Afable, M Wlodarski, H Makishima, M Shaik, MA Sekeres, RV Tiu, ...
Blood, The Journal of the American Society of Hematology 117 (25), 6876-6884, 2011
1442011
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes
SS Sahoo, VB Pastor, C Goodings, RK Voss, EJ Kozyra, A Szvetnik, ...
Nature medicine 27 (10), 1806-1817, 2021
1402021
Phenotypic differences between healthy effector CTL and leukemic LGL cells support the notion of antigen-triggered clonal transformation in T-LGL leukemia
MW Wlodarski, Z Nearman, A Jankowska, N Babel, J Powers, P Leahy, ...
Journal of Leucocyte Biology 83 (3), 589-601, 2008
1402008
Molecular strategies for detection and quantitation of clonal cytotoxic T-cell responses in aplastic anemia and myelodysplastic syndrome
MW Wlodarski, LP Gondek, ZP Nearman, M Plasilova, M Kalaycio, ED Hsi, ...
Blood 108 (8), 2632-2641, 2006
1352006
RAS-pathway mutation patterns define epigenetic subclasses in juvenile myelomonocytic leukemia
DB Lipka, T Witte, R Toth, J Yang, M Wiesenfarth, P Nöllke, A Fischer, ...
Nature communications 8 (1), 2126, 2017
1252017
Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7
VB Pastor, SS Sahoo, J Boklan, GC Schwabe, E Saribeyoglu, B Strahm, ...
haematologica 103 (3), 427, 2017
1152017
Phosphatidylinositol-3-phosphate kinase pathway activation protects leukemic large granular lymphocytes from undergoing homeostatic apoptosis
AE Schade, JJ Powers, MW Wlodarski, JP Maciejewski
Blood 107 (12), 4834-4840, 2006
1032006
Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes
SS Sahoo, EJ Kozyra, MW Wlodarski
Best Practice & Research Clinical Haematology 33 (3), 101197, 2020
972020
Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants
V Pastor, S Hirabayashi, A Karow, J Wehrle, EJ Kozyra, R Nienhold, ...
Leukemia 31 (3), 759-762, 2017
962017
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