Found: 85
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The human c- abl oncogene in the philadelphia translocation.
- Published in:
- Journal of Cellular Physiology, 1984, v. 121, p. 179, doi. 10.1002/jcp.1041210421
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- Publication type:
- Article
Prevalence of pathogenic BRCA1/2 germline mutations among 802 women with unilateral triple-negative breast cancer without family cancer history.
- Published in:
- 2018
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- Publication type:
- journal article
Spectrum of transforming sequences detected by tumorigenicity assay in a large series of human neoplasms.
- Published in:
- International Journal of Cancer, 1999, v. 80, n. 6, p. 857, doi. 10.1002/(SICI)1097-0215(19990315)80:6<857::AID-IJC10>3.0.CO;2-B
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- Publication type:
- Article
High frequency of Ki- ras codon 12 mutations in pancreatic adenocarcinomas.
- Published in:
- International Journal of Cancer, 1989, v. 43, n. 6, p. 1037, doi. 10.1002/ijc.2910430614
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- Publication type:
- Article
Epstein-barr virus-positive recipient type B-cells survive in a 'complete chimera' after allogeneic bone-marrow transplantation.
- Published in:
- International Journal of Cancer, 1988, v. 42, n. 5, p. 672, doi. 10.1002/ijc.2910420506
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- Publication type:
- Article
Diagnosis of CoPAN by whole exome sequencing: Waking up a sleeping tiger's eye.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 7, p. 1878, doi. 10.1002/ajmg.a.38252
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- Publication type:
- Article
DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2017, v. 173, n. 5, p. 1369, doi. 10.1002/ajmg.a.38164
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- Publication type:
- Article
Exome sequencing reveals a novel CWF19L1 mutation associated with intellectual disability and cerebellar atrophy.
- Published in:
- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 6, p. 1502, doi. 10.1002/ajmg.a.37632
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- Publication type:
- Article
Ethical framework for previously collected biobank samples.
- Published in:
- 2007
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- Publication type:
- Letter
Implications of delayed bone marrow aspirations at the end of treatment induction for risk stratification and outcome in children with acute lymphoblastic leukaemia.
- Published in:
- British Journal of Haematology, 2016, v. 173, n. 5, p. 742, doi. 10.1111/bjh.13989
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- Publication type:
- Article
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk.
- Published in:
- Nature Genetics, 2010, v. 42, n. 6, p. 492, doi. 10.1038/ng.585
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- Publication type:
- Article
Acute Lymphoblastic Leukemia in Children.
- Published in:
- Deutsches Ärzteblatt International, 2012, v. 109, n. 40, p. 652, doi. 10.3238/arztebl.2012.0652
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- Publication type:
- Article
Association of Prolactin and Its Receptor Gene Regions with Familial Breast Cancer.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 4, p. 1513, doi. 10.1210/jc.2005-1899
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- Publication type:
- Article
Ph-positive chronic myeloid leukemia with loss of the segment distal to M-bcr.
- Published in:
- Genes, Chromosomes & Cancer, 1992, v. 4, n. 1, p. 92, doi. 10.1002/gcc.2870040115
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- Publication type:
- Article
Validation of Minimal Residual Disease as Surrogate Endpoint for Event-Free Survival in Childhood Acute Lymphoblastic Leukemia.
- Published in:
- JNCI Cancer Spectrum, 2018, v. 2, n. 4, p. N.PAG, doi. 10.1093/jncics/pky069
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- Publication type:
- Article
Friedrich Vogel 1925–2006.
- Published in:
- 2007
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- Publication type:
- Obituary
Genetic Variation in ABCC4 and CFTR and Acute Pancreatitis during Treatment of Pediatric Acute Lymphoblastic Leukemia.
- Published in:
- Journal of Clinical Medicine, 2021, v. 10, n. 21, p. 4815, doi. 10.3390/jcm10214815
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- Publication type:
- Article
Association of a Common AKAP9 Variant With Breast Cancer Risk: A Collaborative Analysis.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2008, v. 100, n. 6, p. 437, doi. 10.1093/jnci/djn037
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- Publication type:
- Article
Allelotype analysis in relapsed childhood acute lymphoblastic leukemia.
- Published in:
- Oncogene, 2003, v. 22, n. 44, p. 6970, doi. 10.1038/sj.onc.1206974
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- Publication type:
- Article
Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-13069-6
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- Publication type:
- Article
Molecular analysis of the cyclin-dependent kinase inhibitor family: p16(CDKN2/MTS1/INK4A), p18(INK4C) and p27(Kip1) genes in neuroblastomas.
- Published in:
- Cancer (0008543X), 1996, v. 77, n. 3, p. 570, doi. 10.1002/(SICI)1097-0142(19960201)77:3<570::AID-CNCR21>3.0.CO;2-0
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- Publication type:
- Article
Clinical and molecular characterization of the BRCA2 p.Asn3124Ile variant reveals substantial evidence for pathogenic significance.
- Published in:
- Breast Cancer Research & Treatment, 2014, v. 145, n. 2, p. 451, doi. 10.1007/s10549-014-2943-5
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- Publication type:
- Article
Molecular and clinical characterization of an in frame deletion of uncertain clinical significance in the BRCA2 gene.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 133, n. 2, p. 725, doi. 10.1007/s10549-011-1917-0
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- Publication type:
- Article
A variant affecting miRNAs binding in the circadian gene Neuronal PAS domain protein 2 ( NPAS2) is not associated with breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 127, n. 3, p. 769, doi. 10.1007/s10549-010-1157-8
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- Publication type:
- Article
Genetic variants within miR-126 and miR-335 are not associated with breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 127, n. 2, p. 549, doi. 10.1007/s10549-010-1244-x
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- Publication type:
- Article
A genetic variant in the pre-miR-27a oncogene is associated with a reduced familial breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 121, n. 3, p. 693, doi. 10.1007/s10549-009-0633-5
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- Publication type:
- Article
Polymorphisms in BRCA2 resulting in aberrant codon-usage and their analysis on familial breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 118, n. 2, p. 407, doi. 10.1007/s10549-009-0348-7
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- Publication type:
- Article
The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study.
- Published in:
- Breast Cancer Research & Treatment, 2008, v. 111, n. 1, p. 139
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- Publication type:
- Article
Genetic variation in the major mitotic checkpoint genes does not affect familial breast cancer risk.
- Published in:
- Breast Cancer Research & Treatment, 2007, v. 106, n. 2, p. 205, doi. 10.1007/s10549-007-9496-9
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- Publication type:
- Article
Identification of three distinct regions of deletion on the long arm of chromosome 11 in childhood acute lymphoblastic leukemia.
- Published in:
- Oncogene, 1999, v. 18, n. 51, p. 7387, doi. 10.1038/sj.onc.1203145
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- Publication type:
- Article
An oncogenic fusion product of the phosphatidylinositol 3-kinase p85β subunit and HUMORF8, a putative deubiquitinating enzyme.
- Published in:
- Oncogene, 1998, v. 16, n. 13, p. 1767, doi. 10.1038/sj.onc.1201695
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- Publication type:
- Article
Intracellular signaling of the Ufo/Axl receptor tyrosine kinase is mediated mainly by a multi-substrate docking-site.
- Published in:
- Oncogene, 1997, v. 14, n. 22, p. 2619, doi. 10.1038/sj.onc.1201123
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- Publication type:
- Article
Thiopurine Methyltransferase (TPMT) Genotype and Early Treatment Response to Mercaptopurine in Childhood Acute Lymphoblastic Leukemia.
- Published in:
- JAMA: Journal of the American Medical Association, 2005, v. 293, n. 12, p. 1485, doi. 10.1001/jama.293.12.1485
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- Publication type:
- Article
Autoimmune-thrombocytopenia and sle in a patient with 5q-anomaly and deletion of the c-fms oncogene.
- Published in:
- American Journal of Hematology, 1994, v. 45, n. 1, p. 79, doi. 10.1002/ajh.2830450112
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- Publication type:
- Article
The association between breast cancer and S100P methylation in peripheral blood by multicenter case-control studies.
- Published in:
- Carcinogenesis, 2017, v. 38, n. 3, p. 312, doi. 10.1093/carcin/bgx004
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- Publication type:
- Article
A variant affecting a putative miRNA target site in estrogen receptor (ESR) 1 is associated with breast cancer risk in premenopausal women.
- Published in:
- Carcinogenesis, 2009, v. 30, n. 1, p. 59, doi. 10.1093/carcin/bgn253
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- Publication type:
- Article
SNPs in ultraconserved elements and familial breast cancer risk.
- Published in:
- Carcinogenesis, 2008, v. 29, n. 2, p. 351, doi. 10.1093/carcin/bgm290
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- Publication type:
- Article
Copy number variant in the candidate tumor suppressor gene MTUS1 and familial breast cancer risk.
- Published in:
- Carcinogenesis, 2007, v. 28, n. 7, p. 1442, doi. 10.1093/carcin/bgm033
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- Publication type:
- Article
Associations of genetic variants in the estrogen receptor coactivators PPARGC1A, PPARGC1B and EP300 with familial breast cancer.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 11, p. 2201, doi. 10.1093/carcin/bgl067
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- Publication type:
- Article
Association of the CASP10 V410I variant with reduced familial breast cancer risk and interaction with the CASP8 D302H variant.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 3, p. 606, doi. 10.1093/carcin/bgi248
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- Publication type:
- Article
Association of genetic variants in the Rho guanine nucleotide exchange factor AKAP13 with familial breast cancer.
- Published in:
- Carcinogenesis, 2006, v. 27, n. 3, p. 593, doi. 10.1093/carcin/bgi245
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- Publication type:
- Article
Association of death receptor 4 haplotype 626C–683C with an increased breast cancer risk.
- Published in:
- Carcinogenesis, 2005, v. 26, n. 11, p. 1975, doi. 10.1093/carcin/bgi164
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- Publication type:
- Article
The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk.
- Published in:
- Carcinogenesis, 2005, v. 26, n. 3, p. 643
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- Publication type:
- Article
Gain of 1q21 and distinct adverse cytogenetic abnormalities correlate with increased microcirculation in multiple myeloma.
- Published in:
- International Journal of Cancer, 2008, v. 122, n. 12, p. 2871, doi. 10.1002/ijc.23455
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- Publication type:
- Article
Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 11, p. 2917, doi. 10.1002/ijc.21696
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- Publication type:
- Article
Association of the ARLTS1 Cys148Arg variant with familial breast cancer risk.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 10, p. 2505, doi. 10.1002/ijc.21687
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- Publication type:
- Article
c-MYC Asn11Ser is associated with increased risk for familial breast cancer.
- Published in:
- International Journal of Cancer, 2005, v. 117, n. 4, p. 638, doi. 10.1002/ijc.21225
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- Publication type:
- Article
Activation of gef-h1, a guanine nucleotide exchange factor for RhoA, by DNA transfection.
- Published in:
- International Journal of Cancer, 2005, v. 113, n. 4, p. 533, doi. 10.1002/ijc.20626
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- Publication type:
- Article
Identifying progression-associated genes in adult T-cell leukemia/lymphoma by using oligonucleotide microarrays.
- Published in:
- International Journal of Cancer, 2004, v. 109, n. 6, p. 875, doi. 10.1002/ijc.20028
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- Publication type:
- Article
Breast cancer in young women (≤35 years): Genomic aberrations detected by comparative genomic hybridization.
- Published in:
- International Journal of Cancer, 2003, v. 107, n. 4, p. 583, doi. 10.1002/ijc.11460
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- Publication type:
- Article