Found: 16
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Integrated microRNA–mRNA Expression Profiling Identifies Novel Targets and Networks Associated with Autism.
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- Journal of Personalized Medicine, 2022, v. 12, n. 6, p. 920, doi. 10.3390/jpm12060920
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- Article
Identification of DCAF1 by Clinical Exome Sequencing and Methylation Analysis as a Candidate Gene for Autism and Intellectual Disability: A Case Report.
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- Journal of Personalized Medicine, 2022, v. 12, n. 6, p. 886, doi. 10.3390/jpm12060886
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- Article
Multidisciplinary Consulting Team for Complicated Cases of Neurodevelopmental and Neurobehavioral Disorders: Assessing the Opportunities and Challenges of Integrating Pharmacogenomics into a Team Setting.
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- Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 599, doi. 10.3390/jpm12040599
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- Article
MicroRNA Expression Profiles in Autism Spectrum Disorder: Role for miR-181 in Immunomodulation.
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- Journal of Personalized Medicine, 2021, v. 11, n. 9, p. 922, doi. 10.3390/jpm11090922
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- Article
Molecular Dysregulation in Autism Spectrum Disorder.
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- Journal of Personalized Medicine, 2021, v. 11, n. 9, p. 848, doi. 10.3390/jpm11090848
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- Article
Implementing Pharmacogenomics Testing: Single Center Experience at Arkansas Children's Hospital.
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- Journal of Personalized Medicine, 2021, v. 11, n. 5, p. 394, doi. 10.3390/jpm11050394
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- Article
A variant upstream of IFNL3 (IL28B) creating a new interferon gene IFNL4 is associated with impaired clearance of hepatitis C virus.
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- Nature Genetics, 2013, v. 45, n. 2, p. 164, doi. 10.1038/ng.2521
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- Article
Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma.
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- Nature Genetics, 2009, v. 41, n. 5, p. 518, doi. 10.1038/ng.340
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- Article
NOTCH2 in breast cancer: association of SNPrs11249433 with gene expression in ER-positivebreast tumors without TP53 mutations.
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- Molecular Cancer, 2010, v. 9, p. 113, doi. 10.1186/1476-4598-9-113
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- Article
Differential Analysis of Ovarian and Endometrial Cancers Identifies a Methylator Phenotype.
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- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0032941
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- Article
Longitudinal Assessment of the Nevus Phenotype in a Melanoma Kindred.
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- Journal of Investigative Dermatology, 2004, v. 123, n. 3, p. 576, doi. 10.1111/j.0022-202X.2004.23312.x
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- Article
Identification and Sequencing of a Putative Variant of Proopiomelanocortin in Human Epidermis and Epidermal Cells in Culture.
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- Journal of Investigative Dermatology, 1998, v. 111, n. 3, p. 485, doi. 10.1046/j.1523-1747.1998.00315.x
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- Article
Mapping of the UGT1A locus identifies an uncommon coding variant that affects mRNA expression and protects from bladder cancer.
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- Human Molecular Genetics, 2012, v. 21, n. 8, p. 1918, doi. 10.1093/hmg/ddr619
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- Article
A Functional Variant at a Prostate Cancer Predisposition Locus at 8q24 Is Associated with PVT1 Expression.
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- PLoS Genetics, 2011, v. 7, n. 7, p. 1, doi. 10.1371/journal.pgen.1002165
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- Article
Genetic Variant as a Selection Marker for Anti-Prostate Stem Cell Antigen Immunotherapy of Bladder Cancer.
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- JNCI: Journal of the National Cancer Institute, 2013, v. 105, n. 1, p. 69, doi. 10.1093/jnci/djs458
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- Article
A Pilot Comparison of High- Versus Low-Tech Palatability Assessment Tools in Young Children.
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- Pediatric Drugs, 2021, v. 23, n. 1, p. 95, doi. 10.1007/s40272-020-00430-2
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- Article