Found: 11
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Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes.
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- Genes, Chromosomes & Cancer, 2016, v. 55, n. 4, p. 322, doi. 10.1002/gcc.22333
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- Article
Transfusion intensity, not the cumulative red blood cell transfusion burden, determines the prognosis of patients with myelodysplastic syndrome on chronic transfusion support.
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- American Journal of Hematology, 2011, v. 86, n. 3, p. 245, doi. 10.1002/ajh.21959
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- Article
Discovery of genomic alterations through coregulation analysis of closely linked genes: a frequent gain in 17q25.3 in prostate cancer Bermudo et al. Genomics in prostate cancer: gain in 17q25.3.
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- Annals of the New York Academy of Sciences, 2010, v. 1210, n. 1, p. 17, doi. 10.1111/j.1749-6632.2010.05780.x
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- Article
Chronic lymphocytic leukaemia with 17p deletion: a retrospective analysis of prognostic factors and therapy results.
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- British Journal of Haematology, 2012, v. 157, n. 1, p. 67, doi. 10.1111/j.1365-2141.2011.09000.x
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- Article
Recurrent mutations of NOTCH genes in follicular lymphoma identify a distinctive subset of tumours.
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- Journal of Pathology, 2014, v. 234, n. 3, p. 423, doi. 10.1002/path.4428
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- Article
CD49d (ITGA4) expression is a predictor of time to first treatment in patients with chronic lymphocytic leukaemia and mutated IGHV status.
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- British Journal of Haematology, 2016, v. 172, n. 1, p. 48, doi. 10.1111/bjh.13788
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- Article
Non-coding recurrent mutations in chronic lymphocytic leukaemia.
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- Nature, 2015, v. 526, n. 7574, p. 519, doi. 10.1038/nature14666
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- Article
Inhibition of 5-lipoxygenase induces cell growth arrest and apoptosis in rat Kupffer cells: implications for liver fibrosis.
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- FASEB Journal, 2003, v. 17, n. 12, p. 1745, doi. 10.1096/fj.02-1157fje
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- Article
Factores terapéuticos en psicoterapia grupal: un estudio desde la perspectiva de los participantes.
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- Revista de la Asociación Española de Neuropsiquiatría, 2018, v. 38, n. 134, p. 473, doi. 10.4321/S0211-57352018000200007
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- Article
A Novel Recurrent Breakpoint Responsible for Rearrangements in the Williams-Beuren Region.
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- Cytogenetic & Genome Research, 2015, v. 146, n. 3, p. 181, doi. 10.1159/000439463
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- Article
Pericentric X chromosome in a family.
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- Clinical Genetics, 1981, v. 20, n. 3, p. 234, doi. 10.1111/j.1399-0004.1981.tb01836.x
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- Article