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Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1.
- Published in:
- 2008
- By:
- Publication type:
- journal article
New insights into the human 5-HT;<sub>4</sub> receptor binding site: exploration of a hydrophobic pocket.
- Published in:
- British Journal of Pharmacology, 2004, v. 143, n. 3, p. 361, doi. 10.1038/sj.bjp.0705950
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- Publication type:
- Article
Synthesis and properties of some polyamides and polysulfonamides.
- Published in:
- Journal of Applied Polymer Science, 1974, v. 18, n. 8, p. 2435, doi. 10.1002/app.1974.070180821
- By:
- Publication type:
- Article
Recovery of Female Fertility After Chemotherapy, Irradiation, and Bone Marrow Allograft: Further Evidence Against Massive Oocyte Regeneration by Bone Marrow-Derived Germline Stem Cells.
- Published in:
- 2007
- By:
- Publication type:
- Letter
A NOTCH1-driven MYC enhancer promotes T cell development, transformation and acute lymphoblastic leukemia.
- Published in:
- Nature Medicine, 2014, v. 20, n. 10, p. 1130, doi. 10.1038/nm.3665
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- Publication type:
- Article
Distinctive genotypes in infants with T-cell acute lymphoblastic leukaemia.
- Published in:
- British Journal of Haematology, 2015, v. 171, n. 4, p. 574, doi. 10.1111/bjh.13613
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- Publication type:
- Article
Deletion of the protein tyrosine phosphatase gene PTPN2 in T-cell acute lymphoblastic leukemia.
- Published in:
- Nature Genetics, 2010, v. 42, n. 6, p. 530, doi. 10.1038/ng.587
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- Publication type:
- Article
A recurrent clonally distinct Burkitt lymphoma case highlights genetic key events contributing to oncogenesis.
- Published in:
- Genes, Chromosomes & Cancer, 2019, v. 58, n. 8, p. 595, doi. 10.1002/gcc.22743
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- Publication type:
- Article
Aggressive lymphoma, hemophagocytic lymphohistiocytosis, and G6PD crisis: a lytic cocktail.
- Published in:
- 2022
- By:
- Publication type:
- Letter
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 2, p. 227, doi. 10.1038/ejhg.2009.162
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- Publication type:
- Article
Alternative origin of p13<sup>MTCP1</sup>-encoding transcripts in mature T-cell proliferations with t(X;14) translocations.
- Published in:
- Oncogene, 1997, v. 15, n. 11, p. 1329, doi. 10.1038/sj.onc.1201303
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- Publication type:
- Article
Diseases Transmissible by Blood Transfusion.
- Published in:
- Vox Sanguinis, 1984, v. 47, n. 1, p. 1, doi. 10.1111/j.1423-0410.1984.tb01555.x
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- Publication type:
- Article
The History of PPSB.
- Published in:
- Vox Sanguinis, 1984, v. 46, n. 1, p. 58, doi. 10.1111/j.1423-0410.1984.tb00049.x
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- Publication type:
- Article
Posttransfusional Immunologic Thrombocytopenia.
- Published in:
- Vox Sanguinis, 1979, v. 37, n. 1, p. 21, doi. 10.1111/j.1423-0410.1979.tb02264.x
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- Publication type:
- Article
Biallelic inactivation of REV7 is associated with Fanconi anemia.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Biallelic inactivation of REV7 is associated with Fanconi anemia.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Novel precision medicine approaches and treatment strategies in hematological malignancies.
- Published in:
- Journal of Internal Medicine, 2023, v. 294, n. 4, p. 413, doi. 10.1111/joim.13697
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- Publication type:
- Article
Human parvovirus and aplastic crisis in chronic hemolytic anemias: A study of 24 observations.
- Published in:
- American Journal of Hematology, 1986, v. 23, n. 3, p. 271, doi. 10.1002/ajh.2830230311
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- Publication type:
- Article
A new case of high-molecular-weight kininogen inherited deficiency.
- Published in:
- American Journal of Hematology, 1986, v. 22, n. 4, p. 415, doi. 10.1002/ajh.2830220411
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- Publication type:
- Article
A novel cancer risk prediction score for the natural course of FA patients with biallelic BRCA2/FANCD1 mutations.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 11, p. 1836, doi. 10.1093/hmg/ddad017
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- Publication type:
- Article
Intra-Tumor Heterogeneity (ITH) in Acute Myeloid Leukemia (AML).
- Published in:
- Clinical Lymphoma, Myeloma & Leukemia, 2019, v. 19, p. S237, doi. 10.1016/j.clml.2019.07.128
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- Publication type:
- Article
Human RTEL1 deficiency causes Hoyeraal–Hreidarsson syndrome with short telomeres and genome instability.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 16, p. 3239, doi. 10.1093/hmg/ddt178
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- Publication type:
- Article
A new step in understanding stem cell mobilization in patients with Fanconi anemia: A bridge to gene therapy.
- Published in:
- Transfusion, 2022, v. 62, n. 1, p. 165, doi. 10.1111/trf.16721
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- Publication type:
- Article
A paediatric myelodysplastic syndrome with 5q deletion associated with Fanconi anaemia.
- Published in:
- 2020
- By:
- Publication type:
- Case Study
Fanconi anemia and solid malignancies in childhood: A national retrospective study.
- Published in:
- Pediatric Blood & Cancer, 2015, v. 62, n. 3, p. 463, doi. 10.1002/pbc.25303
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- Publication type:
- Article
Transforming potential of the T‐cell acute lymphoblastic leukemia‐associated homeobox genes HOXA13, TLX1, and TLX3.
- Published in:
- Genes, Chromosomes & Cancer, 2006, v. 45, n. 9, p. 846, doi. 10.1002/gcc.20348
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- Publication type:
- Article
Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases.
- Published in:
- Genes, Chromosomes & Cancer, 2003, v. 38, n. 3, p. 234, doi. 10.1002/gcc.10275
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- Publication type:
- Article
A complex pattern of recurrent chromosomal losses and gains in T-cell prolymphocytic leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 31, n. 3, p. 248, doi. 10.1002/gcc.1141
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- Publication type:
- Article
Immunological profile of Fanconi anemia: A multicentric retrospective analysis of 61 patients.
- Published in:
- American Journal of Hematology, 2013, v. 88, n. 6, p. 472, doi. 10.1002/ajh.23435
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- Publication type:
- Article
Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia.
- Published in:
- American Journal of Hematology, 2013, v. 88, n. 4, p. 306, doi. 10.1002/ajh.23403
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- Publication type:
- Article
Incidence of liver abnormalities in Fanconi anemia patients.
- Published in:
- American Journal of Hematology, 2012, v. 87, n. 5, p. 547, doi. 10.1002/ajh.23153
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- Publication type:
- Article
Castleman's disease and lymphoma: Report of eight cases in HIV-negative patients and literature review.
- Published in:
- American Journal of Hematology, 2002, v. 69, n. 2, p. 119, doi. 10.1002/ajh.10022
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- Publication type:
- Article
A clickable melphalan for monitoring DNA interstrand crosslink accumulation and detecting ICL repair defects in Fanconi anemia patient cells.
- Published in:
- Nucleic Acids Research, 2023, v. 51, n. 15, p. 7988, doi. 10.1093/nar/gkad559
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- Publication type:
- Article
Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in Non- Hodgkin's Lymphoma.
- Published in:
- Journal of Hematology & Oncology, 2014, v. 7, n. 1, p. 1, doi. 10.1186/s13045-014-0082-4
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- Publication type:
- Article
Head and Neck Squamous Cell Carcinoma in 13 Patients With Fanconi Anemia After Hematopoietic Stem Cell Transplantation.
- Published in:
- Cancer (0008543X), 2008, v. 113, n. 12, p. 3315, doi. 10.1002/cncr.23954
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- Publication type:
- Article
Composition and Conformation of Hetero‐ versus Homo‐Fluorinated Triazolamers Influence their Activity on Islet Amyloid Polypeptide Aggregation.
- Published in:
- Chemistry - A European Journal, 2024, v. 30, n. 28, p. 1, doi. 10.1002/chem.202303887
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- Publication type:
- Article
Mutations of the RTEL1 Helicase in a Hoyeraal-Hreidarsson Syndrome Patient Highlight the Importance of the ARCH Domain.
- Published in:
- Human Mutation, 2016, v. 37, n. 5, p. 469, doi. 10.1002/humu.22966
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- Publication type:
- Article
Primary Microcephaly, Impaired DNA Replication, and Genomic Instability Caused by Compound Heterozygous ATR Mutations.
- Published in:
- Human Mutation, 2013, v. 34, n. 2, p. 374, doi. 10.1002/humu.22245
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- Publication type:
- Article
NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype.
- Published in:
- Human Mutation, 2010, v. 31, n. 6, p. E1506, doi. 10.1002/humu.21271
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- Publication type:
- Article
Toward the First Nonpeptidic Molecular Tong Inhibitor of Wild-Type and Mutated HIV-1 Protease Dimerization.
- Published in:
- ChemMedChem, 2010, v. 5, n. 11, p. 1899, doi. 10.1002/cmdc.201000308
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- Publication type:
- Article
Cancer stem cell definitions and terminology: the devil is in the details.
- Published in:
- Nature Reviews Cancer, 2012, v. 12, n. 11, p. 767, doi. 10.1038/nrc3368
- By:
- Publication type:
- Article
Clinical and Molecular Characteristics of Squamous Cell Carcinomas From Fanconi Anemia Patients.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 22, p. 1649, doi. 10.1093/jnci/djn366
- By:
- Publication type:
- Article
XPC deficiency increases risk of hematologic malignancies through mutator phenotype and characteristic mutational signature.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-19633-9
- By:
- Publication type:
- Article
Six cases of hereditary spherocytosis revealed by human parvovirus infection.
- Published in:
- British Journal of Haematology, 1986, v. 62, n. 4, p. 653, doi. 10.1111/j.1365-2141.1986.tb04088.x
- By:
- Publication type:
- Article
dUTPase ( ) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure.
- Published in:
- 2017
- By:
- Publication type:
- journal article