Found: 15
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Universal False Discovery Rate Estimation Methodology for Genome-Wide Association Studies.
- Published in:
- Human Heredity, 2008, v. 65, n. 4, p. 183, doi. 10.1159/000112365
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- Publication type:
- Article
Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study.
- Published in:
- 2019
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- Publication type:
- journal article
Network-based repurposing identifies anti-alarmins as drug candidates to control severe lung inflammation in COVID-19.
- Published in:
- PLoS ONE, 2021, v. 16, n. 7, p. 1, doi. 10.1371/journal.pone.0254374
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- Publication type:
- Article
Gaussian Mixture Models in R.
- Published in:
- R Journal, 2023, v. 15, n. 2, p. 56, doi. 10.32614/rj-2023-043
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- Publication type:
- Article
A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysis.
- Published in:
- Briefings in Bioinformatics, 2013, v. 14, n. 6, p. 671
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- Publication type:
- Article
P1‐061: DOUBLE‐BLIND ARGUMENT FOR A SYNERGISTIC THERAPEUTIC EFFECT OF A FIXED LOW‐DOSE COMBINATION OF ACAMPROSATE AND BACLOFEN IN ALZHEIMER'S DISEASE.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2018, v. 14, p. P292, doi. 10.1016/j.jalz.2018.06.063
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- Publication type:
- Article
Polytherapy with a combination of three repurposed drugs (PXT3003) down-regulates Pmp22 overexpression and improves myelination, axonal and functional parameters in models of CMT1A neuropathy.
- Published in:
- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 282, doi. 10.1186/s13023-014-0201-x
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- Publication type:
- Article
Polytherapy with a combination of three repurposed drugs (PXT3003) down-regulates Pmp22 over-expression and improves myelination, axonal and functional parameters in models of CMT1A neuropathy.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
A Rasch Analysis of the Charcot-Marie-Tooth Neuropathy Score (CMTNS) in a Cohort of Charcot-Marie-Tooth Type 1A Patients.
- Published in:
- PLoS ONE, 2017, v. 12, n. 1, p. 1, doi. 10.1371/journal.pone.0169878
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- Publication type:
- Article
Variants of the MATP/ SLC45A2 gene are protective for melanoma in the French population.
- Published in:
- Human Mutation, 2008, v. 29, n. 9, p. 1154, doi. 10.1002/humu.20823
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- Publication type:
- Article
ChEBI: a database and ontology for chemical entities of biological interest.
- Published in:
- Nucleic Acids Research, 2008, v. 36, p. D344
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- Publication type:
- Article
Syndrome de Gougerot-Sjögren: Vers une médecine de précision.
- Published in:
- Médecine Sciences, 2022, v. 38, n. 2, p. 148, doi. 10.1051/medsci/2021258
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- Publication type:
- Article
An Association Study of 22 Candidate Genes in Psoriasis Families Reveals Shared Genetic Factors with Other Autoimmune and Skin Disorders.
- Published in:
- Journal of Investigative Dermatology, 2009, v. 129, n. 11, p. 2637, doi. 10.1038/jid.2009.157
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- Publication type:
- Article
The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma.
- Published in:
- International Journal of Cancer, 2014, v. 134, n. 9, p. 2098, doi. 10.1002/ijc.28543
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- Publication type:
- Article
A Multi-Marker Genetic Association Test Based on the Rasch Model Applied to Alzheimer’s Disease.
- Published in:
- PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138223
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- Publication type:
- Article