PB1814: RARE PHENOTYPE WITH CD33 ABSENT IN ACUTE MYELOID LEUKEMIA MIMICKING MRD POSITIVITY: A CASE REPORT

Autor: L. O Marani, A. Costa, F. B Silva, M. I. A Madeira, P. S Scheucher, J. L S Schiavinato, A. S. G Lima, K. B B Pagnano, B. K Duarte, S. Freeman, E. M Rego, F. Traina, L. L Figueiredo-Pontes

Publikováno v: HemaSphere, Vol 6, Pp 1694-1695 (2022)

Externí odkaz: https://doaj.org/article/7165a4fb48984a1f9b28d47bb5554654

S252: M2-POLARIZED MACROPHAGES CONTROL LEUKEMIC STEM CELL FATE BY PROMOTING METABOLIC REPROGRAMMING

Autor: I. Weinhäuser, D. A. Pereira-Martins, J. R. Hilberink, L. Y. Almeida, D. R. A. Silveira, L. Quek, S. M Hogeling, J. M. Mota, E. Ammatuna, A. R. Lucena-Araujo, G. A. Huls, E. M. Rego, J. J. Schuringa

Publikováno v: HemaSphere. 6:153-154

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b14d25ad87295567cee8c5dc80a01526
https://doi.org/10.1097/01.hs9.0000843900.20659.ec

PEDIATRICS LABORATORY RESEARCH

Autor: M. S. Brassesco, E. T. Valera, J. A. Pezuk, A. G. Morales, J. C. Oliveira, K. Umezawa, E. M. Rego, G. C. Carlotti, C. A. Scrideli, L. G. Tone, J.-i. Adachi, T. Suzuki, T. Yanagisawa, K. Fukuoka, K. Mishima, K. Wakiya, M. Matsutani, R. Nishikawa, A. Fernandez-L, M. Squatrito, P. Northcott, E. C. Holland, M. D. Taylor, Z. Nahle, A. M. Kenney, D. M. Ashley, A. Muscat, L. Gordon, L. Rigby, D. Birks, N. Foreman, E. Algar, L. K. Donovan, N. Potter, T. Warr, G. Pilkington, A. Erdreich-Epstein, H. Zhou, X. Ren, T. B. Davidson, M. Schur, L. Ji, R. Sposto, S. Asgharzadeh, L. Hiddingh, V. Caretti, E. Hulleman, G.-J. L. Kaspers, W. P. Vandertop, D. P. Noske, T. Wurdinger, T. Lagerweij, P. W. Koken, G. G. Kaspers, E. E. Bar, K. Schreck, C. G. Eberhart, D. A. Largaespada, J. D. Larson, F. J. Rodriquez, A. M. Demer, A. L. Sarver, A. Dubuc, R. B. Jenkins, A. J. Dupuy, N. G. Copeland, N. A. Jenkins, M. A. Taylor, M. Monje, M. E. Freret, P. A. Beachy, M. H. Jansen, P. W. Vandertop, K. Dorris, M. Sobo, E. Panditharatna, C. Liu, M.-O. Kim, L. Miles, S. Goldman, S. Gardner, C. Stevenson, T. Maugans, M. Fouladi, R. Drissi, D. W. Fults, M. Mumert, C. A. Pedone, X. Wu, P. A. Northcott, A. M. Saratsis, S. Magge, B. Rood, A. Hill, J. Nazarian, D. G. van Vuurden, M. Bugiani, P. Wesseling, G. J. Kaspers, V. Gopalakrishnan, C. Das, M. Gireud, P. Taylor, A. Singh, D. Lee, K. Aldape, G. Fuller, J. Fangusaro, V. Rajaram, C. Eberhart

Publikováno v: Neuro-Oncology. 13:iii102-iii106

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761bd56d684fb9f0b433a153dfd52ca9
https://doi.org/10.1093/neuonc/nor157

Analysis of five polymorphic DNA markers for indirect genetic diagnosis of haemophilia A in the Brazilian population

Autor: J D, Massaro, C E V, Wiezel, Y C N, Muniz, E M, Rego, L C O, de Oliveira, C T, Mendes-Junior, A L, Simões

Publikováno v: Haemophilia : the official journal of the World Federation of Hemophilia. 17(5)

Hemophilia A is an X-linked, inherited, bleeding disorder caused by the partial or total inactivity of the coagulation factor VIII (FVIII). Due to difficulties in the direct recognition of the disease-associated mutation in the F8 gene, indirect diag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fc995d294de8a0aa85cb909e6e7d4a30
https://pubmed.ncbi.nlm.nih.gov/21649803

Retinoic acid (RA) and As2O3 treatment in transgenic models of acute promyelocytic leukemia (APL) unravel the distinct nature of the leukemogenic process induced by the PML-RARalpha and PLZF-RARalpha oncoproteins

Autor: E M, Rego, L Z, He, R P, Warrell, Z G, Wang, P P, Pandolfi

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America. 97(18)

Acute promyelocytic leukemia (APL) is associated with chromosomal translocations always involving the RARalpha gene, which variably fuses to one of several distinct loci, including PML or PLZF (X genes) in t(15;17) or t(11;17), respectively. APL in p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8dac547296b8f62074c1fed0840899a6
https://pubmed.ncbi.nlm.nih.gov/10954752