Found: 21
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Common gene expression signatures in Parkinson's disease are driven by changes in cell composition.
- Published in:
- Acta Neuropathologica Communications, 2020, v. 8, n. 1, p. 1, doi. 10.1186/s40478-020-00932-7
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- Article
Staging listening ecologies.
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- Design Ecologies, 2011, v. 1, n. 2, p. 229, doi. 10.1386/des.1.2.229_1
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- Article
Pharmacokinetics and transcriptional effects of the anti-salmon lice drug emamectin benzoate in Atlantic salmon (Salmo salar L.).
- Published in:
- BMC Pharmacology, 2008, v. 8, p. 1, doi. 10.1186/1471-2210-8-16
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- Article
Switch in FOXA1 Status Associates with Endometrial Cancer Progression.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0098069
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- Article
Somatic Maintenance Resources in the Honeybee Worker Fat Body Are Distributed to Withstand the Most Life-Threatening Challenges at Each Life Stage.
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- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0069870
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- Article
Gene Set Based Integrated Data Analysis Reveals Phenotypic Differences in a Brain Cancer Model.
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- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068288
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- Article
High-Throughput Mutation Profiling of Primary and Metastatic Endometrial Cancers Identifies KRAS, FGFR2 and PIK3CA to Be Frequently Mutated.
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- PLoS ONE, 2012, v. 7, n. 12, p. 1, doi. 10.1371/journal.pone.0052795
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- Article
Genome-Wide Profiling of Histone H3 Lysine 4 and Lysine 27 Trimethylation Reveals an Epigenetic Signature in Prostate Carcinogenesis.
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- PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004687
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- Article
Tumour-associated glial host cells display a stem-like phenotype with a distinct gene expression profile and promote growth of GBM xenografts.
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- 2017
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- Publication type:
- journal article
Inhibition of mitochondrial respiration prevents BRAF-mutant melanoma brain metastasis.
- Published in:
- Acta Neuropathologica Communications, 2019, v. 7, n. 1, p. N.PAG, doi. 10.1186/s40478-019-0712-8
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- Publication type:
- Article
Syndromic X-linked intellectual disability segregating with a missense variant in RLIM.
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- European Journal of Human Genetics, 2015, v. 23, n. 12, p. 1652, doi. 10.1038/ejhg.2015.30
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- Article
Gene expression profiles in rat brain disclose CNS signature genes and regional patterns of functional specialisation.
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- BMC Genomics, 2007, v. 8, p. 94, doi. 10.1186/1471-2164-8-94
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- Publication type:
- Article
A simple spreadsheet-based, MIAME-supportive format for microarray data: MAGE-TAB.
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- BMC Bioinformatics, 2006, v. 7, p. 489, doi. 10.1186/1471-2105-7-489
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- Article
Transcriptome-wide analyses of early immune responses in lumpfish leukocytes upon stimulation with poly(I:C).
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- Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1198211
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- Publication type:
- Article
EPHB4 kinase-inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis.
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- 2016
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- Publication type:
- journal article
Expression profile of heat shock proteins in acute myeloid leukaemia patients reveals a distinct signature strongly associated with FLT3 mutation status - consequences and potentials for pharmacological intervention.
- Published in:
- British Journal of Haematology, 2012, v. 156, n. 4, p. 468, doi. 10.1111/j.1365-2141.2011.08960.x
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- Article
Extended theatre – composition in telematized environments.
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- Technoetic Arts: A Journal of Speculative Research, 2007, v. 5, n. 3, p. 151, doi. 10.1386/tear.5.3.151_1
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- Article
Using performers as tools in the creation of telematic artwork.
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- Technoetic Arts: A Journal of Speculative Research, 2004, v. 2, n. 3, p. 147, doi. 10.1386/tear.2.3.147/0
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- Publication type:
- Article
Transcriptome-wide analyses of early immune responses in lumpfish leukocytes upon stimulation with poly(I:C).
- Published in:
- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2023.1198211
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- Publication type:
- Article
Identification of highly connected and differentially expressed gene subnetworks in metastasizing endometrial cancer.
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- PLoS ONE, 2018, v. 13, n. 11, p. 1, doi. 10.1371/journal.pone.0206665
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- Article
RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.
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- Bioinformatics, 2016, v. 32, n. 19, p. 3018, doi. 10.1093/bioinformatics/btw359
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- Article