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Do local government sustainability initiatives impact corporate social sustainability practices?
- Published in:
- Business Strategy & the Environment (John Wiley & Sons, Inc), 2024, v. 33, n. 6, p. 5839, doi. 10.1002/bse.3780
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- Publication type:
- Article
Acute loss of DP1, but not DP2, induces p53 mRNA and augments p21Waf1/Cip1 and senescence.
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- Cell Biochemistry & Function, 2012, v. 30, n. 1, p. 54, doi. 10.1002/cbf.1818
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- Publication type:
- Article
Use of near-infrared imaging using indocyanine green associates with the lower incidence of postoperative complications for intestinal and mesenteric injury.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-03361-1
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- Publication type:
- Article
Multi-omics analysis defines highly refractory RAS burdened immature subgroup of infant acute lymphoblastic leukemia.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-32266-4
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- Publication type:
- Article
Dendritic Cells Pre-Pulsed with Wilms' Tumor 1 in Optimized Culture for Cancer Vaccination.
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- Pharmaceutics, 2020, v. 12, n. 4, p. 305, doi. 10.3390/pharmaceutics12040305
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- Publication type:
- Article
Prediction of Soil Adsorption Coefficient in Pesticides Using Physicochemical Properties and Molecular Descriptors by Machine Learning Models.
- Published in:
- Environmental Toxicology & Chemistry, 2020, v. 39, n. 7, p. 1451, doi. 10.1002/etc.4724
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- Publication type:
- Article
Diagnostic challenge of Diamond-Blackfan anemia in mothers and children by whole-exome sequencing.
- Published in:
- 2017
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- Publication type:
- journal article
BCL6 locus is hypermethylated in angioimmunoblastic T-cell lymphoma.
- Published in:
- 2017
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- Publication type:
- journal article
PIEZO1 gene mutation in a Japanese family with hereditary high phosphatidylcholine hemolytic anemia and hemochromatosis-induced diabetes mellitus.
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- 2016
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- Publication type:
- journal article
ALDH2 polymorphism in patients with Diamond-Blackfan anemia in Japan.
- Published in:
- 2016
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- Publication type:
- commentary
Clinical and genetic features of dyskeratosis congenita, cryptic dyskeratosis congenita, and Hoyeraal-Hreidarsson syndrome in Japan.
- Published in:
- 2015
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- Publication type:
- journal article
Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient.
- Published in:
- 2015
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- Publication type:
- Report
Aggressive transformation of anaplastic large cell lymphoma with increased number of ALK-translocated chromosomes.
- Published in:
- 2015
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- Publication type:
- Report
Bullous exudative retinal detachment due to infiltration of leukemic cells in a child with acute lymphoblastic leukemia.
- Published in:
- 2010
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- Publication type:
- journal article
The ex vivo production of ammonia predicts L-asparaginase biological activity in children with acute lymphoblastic leukemia.
- Published in:
- 2009
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- Publication type:
- journal article
The Detection of Immunity against WT1 and SMAD4 P130L of EpCAM + Cancer Cells in Malignant Pleural Effusion.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 20, p. 12177, doi. 10.3390/ijms232012177
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- Publication type:
- Article
Different In Vitro-Generated MUTZ-3-Derived Dendritic Cell Types Secrete Dexosomes with Distinct Phenotypes and Antigen Presentation Potencies.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 15, p. 8362, doi. 10.3390/ijms23158362
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- Publication type:
- Article
Deep sequencing reveals stepwise mutation acquisition in paroxysmal nocturnal hemoglobinuria.
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- Journal of Clinical Investigation, 2014, v. 124, n. 10, p. 4529, doi. 10.1172/JCI74747
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- Publication type:
- Article
Quality Verification with a Cluster−Controlled Manufacturing System to Generate Monocyte−Derived Dendritic Cells.
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- Vaccines, 2021, v. 9, n. 5, p. 533, doi. 10.3390/vaccines9050533
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- Publication type:
- Article
Atypical dyskeratosis congenita diagnosed using whole-exome sequencing.
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- Pediatrics International, 2017, v. 59, n. 8, p. 933, doi. 10.1111/ped.13314
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- Publication type:
- Article
Characterization of six base pair deletion in the putative HNF1-binding site of human PXR promoter.
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- Journal of Human Genetics, 2003, v. 48, n. 11, p. 594, doi. 10.1007/s10038-003-0076-5
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- Publication type:
- Article
An empirical Bayesian framework for somatic mutation detection from cancer genome sequencing data.
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- Nucleic Acids Research, 2013, v. 41, n. 7, p. e89, doi. 10.1093/nar/gkt126
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- Publication type:
- Article
Acute megakaryoblastic leukemia with acquired trisomy 21 and GATA1 mutations in phenotypically normal children.
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- European Journal of Pediatrics, 2015, v. 174, n. 4, p. 525, doi. 10.1007/s00431-014-2430-3
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- Publication type:
- Article
Clonal evolution and clinical implications of genetic abnormalities in blastic transformation of chronic myeloid leukaemia.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23097-w
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- Publication type:
- Article
A giant adrenal pseudocyst presenting with right hypochondralgia and fever: a case report.
- Published in:
- 2011
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- Publication type:
- journal article
COLLECTIVE MODES OF EXCITATION IN DEFORMED NEUTRON-RICH Mg ISOTOPES.
- Published in:
- Modern Physics Letters A, 2010, v. 25, n. 21-23, p. 1783, doi. 10.1142/S0217732310000320
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- Publication type:
- Article
Transmembrane-Domain Trapping: A Novel Method for Isolation of cDNAs Encoding Putative Membrane Proteins.
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- DNA Research, 1998, v. 5, n. 3, p. 187, doi. 10.1093/dnares/5.3.187
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- Publication type:
- Article
Droplet digital polymerase chain reaction assay for the detection of the minor clone of KIT D816V in paediatric acute myeloid leukaemia especially showing RUNX1‐RUNX1T1 transcripts.
- Published in:
- British Journal of Haematology, 2021, v. 194, n. 2, p. 414, doi. 10.1111/bjh.17569
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- Publication type:
- Article
Genomic analysis of multiple myeloma using targeted capture sequencing in the Japanese cohort.
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- British Journal of Haematology, 2020, v. 191, n. 5, p. 755, doi. 10.1111/bjh.16720
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- Publication type:
- Article
The phenotype and clinical course of Japanese Fanconi Anaemia infants is influenced by patient, but not maternal ALDH2 genotype.
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- British Journal of Haematology, 2016, v. 175, n. 3, p. 457, doi. 10.1111/bjh.14243
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- Publication type:
- Article
Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.
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- British Journal of Haematology, 2016, v. 175, n. 3, p. 476, doi. 10.1111/bjh.14247
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- Publication type:
- Article
Genomic analysis of clonal origin of Langerhans cell histiocytosis following acute lymphoblastic leukaemia.
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- British Journal of Haematology, 2016, v. 175, n. 1, p. 169, doi. 10.1111/bjh.13841
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- Publication type:
- Article
Loss of function mutations in RPL27 and RPS27 identified by whole-exome sequencing in Diamond-Blackfan anaemia.
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- British Journal of Haematology, 2015, v. 168, n. 6, p. 854, doi. 10.1111/bjh.13229
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- Publication type:
- Article
Integrated molecular analysis of adult T cell leukemia/lymphoma.
- Published in:
- Nature Genetics, 2015, v. 47, n. 11, p. 1304, doi. 10.1038/ng.3415
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- Publication type:
- Article
Mutational landscape and clonal architecture in grade II and III gliomas.
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- Nature Genetics, 2015, v. 47, n. 5, p. 458, doi. 10.1038/ng.3273
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- Publication type:
- Article
Somatic RHOA mutation in angioimmunoblastic T cell lymphoma.
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- Nature Genetics, 2014, v. 46, n. 2, p. 171, doi. 10.1038/ng.2872
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- Publication type:
- Article
Corrigendum: The landscape of somatic mutations in Down syndrome-related myeloid disorders.
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- Nature Genetics, 2013, v. 45, n. 12, p. 1516, doi. 10.1038/ng1213-1516
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- Publication type:
- Article
The landscape of somatic mutations in Down syndrome-related myeloid disorders.
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- Nature Genetics, 2013, v. 45, n. 11, p. 1293, doi. 10.1038/ng.2759
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- Publication type:
- Article
Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.
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- Nature Genetics, 2013, v. 45, n. 10, p. 1232, doi. 10.1038/ng.2731
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- Publication type:
- Article
Integrated molecular analysis of clear-cell renal cell carcinoma.
- Published in:
- Nature Genetics, 2013, v. 45, n. 8, p. 860, doi. 10.1038/ng.2699
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- Publication type:
- Article
Exome sequencing identifies secondary mutations of SETBP1 and JAK3 in juvenile myelomonocytic leukemia.
- Published in:
- Nature Genetics, 2013, v. 45, n. 8, p. 937, doi. 10.1038/ng.2698
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- Publication type:
- Article
Somatic SETBP1 mutations in myeloid malignancies.
- Published in:
- Nature Genetics, 2013, v. 45, n. 8, p. 942, doi. 10.1038/ng.2696
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- Publication type:
- Article
Transcriptional Regulation of Human Chromatin Assembly Factor ASF1.
- Published in:
- DNA & Cell Biology, 2007, v. 26, n. 2, p. 91, doi. 10.1089/dna.2006.0515
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- Publication type:
- Article
Correction: Integrated Multiregional Analysis Proposing a New Model of Colorectal Cancer Evolution.
- Published in:
- 2017
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- Publication type:
- Correction Notice
TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2023, v. 62, n. 7, p. 412, doi. 10.1002/gcc.23147
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- Publication type:
- Article
UBTF‐internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2023, v. 62, n. 4, p. 202, doi. 10.1002/gcc.23110
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- Publication type:
- Article
Two siblings with familial neuroblastoma with distinct clinical phenotypes harboring an ALK germline mutation.
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- Genes, Chromosomes & Cancer, 2018, v. 57, n. 12, p. 665, doi. 10.1002/gcc.22676
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- Publication type:
- Article
Delphinidin Induces Autolysosome as well as Autophagosome Formation and Delphinidin-Induced Autophagy Exerts a Cell Protective Role.
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- Journal of Biochemical & Molecular Toxicology, 2012, v. 26, n. 11, p. 445, doi. 10.1002/jbt.21443
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- Publication type:
- Article
Accuracy evaluation of mainstream and sidestream end-tidal carbon dioxide monitoring during noninvasive ventilation: a randomized crossover trial (MASCAT-NIV trial).
- Published in:
- Journal of Intensive Care, 2022, v. 10, n. 1, p. 1, doi. 10.1186/s40560-022-00603-w
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- Publication type:
- Article
A novel thymoma-associated autoimmune disease: Anti-PIT-1 antibody syndrome.
- Published in:
- Scientific Reports, 2017, p. 43060, doi. 10.1038/srep43060
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- Publication type:
- Article