Found: 21
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IRF2BP2 Mutation Is Associated with Increased STAT1 and STAT5 Activation in Two Family Members with Inflammatory Conditions and Lymphopenia.
- Published in:
- Pharmaceuticals (14248247), 2021, v. 14, n. 8, p. 797, doi. 10.3390/ph14080797
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- Publication type:
- Article
Heterozygous premature termination in zinc-finger domain of Krüppel-like factor 2 gene associates with dysregulated immunity.
- Published in:
- Frontiers in Immunology, 2022, v. 13, p. 1, doi. 10.3389/fimmu.2022.819929
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- Publication type:
- Article
Reciprocal modulation of Aβ42 aggregation by copper and homocysteine.
- Published in:
- Frontiers in Aging Neuroscience, 2014, v. 6, p. 1, doi. 10.3389/fnagi.2014.00237
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- Publication type:
- Article
Navigating through metaproteomics data: A logbook of database searching.
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- Proteomics, 2015, v. 15, n. 20, p. 3439, doi. 10.1002/pmic.201400560
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- Publication type:
- Article
Colonic metaproteomic signatures of active bacteria and the host in obesity.
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- Proteomics, 2015, v. 15, n. 20, p. 3544, doi. 10.1002/pmic.201500049
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- Publication type:
- Article
Reduced binding of apoE4 to complement factor H promotes amyloid‐β oligomerization and neuroinflammation.
- Published in:
- EMBO Reports, 2023, v. 24, n. 7, p. 1, doi. 10.15252/embr.202256467
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- Publication type:
- Article
Physical and functional interactome atlas of human receptor tyrosine kinases.
- Published in:
- EMBO Reports, 2022, v. 23, n. 6, p. 1, doi. 10.15252/embr.202154041
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- Publication type:
- Article
Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease.
- Published in:
- NPJ Genomic Medicine, 2019, v. 4, n. 1, p. N.PAG, doi. 10.1038/s41525-019-0088-5
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- Publication type:
- Article
Rapid genome editing by CRISPR-Cas9-POLD3 fusion.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.75415
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- Publication type:
- Article
Rapid genome editing by CRISPR-Cas9-POLD3 fusion.
- Published in:
- eLife, 2022, p. 1, doi. 10.7554/eLife.75415
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- Publication type:
- Article
Novel TMEM173 Mutation and the Role of Disease Modifying Alleles.
- Published in:
- Frontiers in Immunology, 2019, v. 10, p. 1, doi. 10.3389/fimmu.2019.02770
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- Publication type:
- Article
The Impact of ETV6-NTRK3 Oncogenic Gene Fusions on Molecular and Signaling Pathway Alterations.
- Published in:
- Cancers, 2023, v. 15, n. 17, p. 4246, doi. 10.3390/cancers15174246
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- Publication type:
- Article
CMGC Kinases in Health and Cancer.
- Published in:
- Cancers, 2023, v. 15, n. 15, p. 3838, doi. 10.3390/cancers15153838
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- Publication type:
- Article
SARS‐CoV‐2–host proteome interactions for antiviral drug discovery.
- Published in:
- Molecular Systems Biology, 2021, v. 17, n. 11, p. 1, doi. 10.15252/msb.202110396
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- Publication type:
- Article
Loss-of-function mutation in IKZF2 leads to immunodeficiency with dysregulated germinal center reactions and reduction of MAIT cells.
- Published in:
- Science Immunology, 2021, v. 6, n. 65, p. 1, doi. 10.1126/sciimmunol.abe3454
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- Publication type:
- Article
Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling.
- Published in:
- Journal of Clinical Immunology, 2023, v. 43, n. 2, p. 358, doi. 10.1007/s10875-022-01375-6
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- Publication type:
- Article
Functional Analysis of FLT4 Mutations Associated with Nonne–Milroy Lymphedema.
- Published in:
- 2009
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- Publication type:
- Letter
Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/SpermineN<sup>1</sup>-Acetyltransferase Overexpression.
- Published in:
- Journal of Investigative Dermatology, 2005, v. 124, n. 3, p. 596, doi. 10.1111/j.0022-202X.2005.23636.x
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- Publication type:
- Article
Functional interaction of VEGF-C and VEGF-D with neuropilin receptors.
- Published in:
- FASEB Journal, 2006, v. 20, n. 9, p. 1462, doi. 10.1096/fj.05-5646com
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- Publication type:
- Article
Somatic MED12 Mutations in Prostate Cancer and Uterine Leiomyomas Promote Tumorigenesis Through Distinct Mechanisms.
- Published in:
- Prostate, 2016, v. 76, n. 1, p. 22, doi. 10.1002/pros.23092
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- Publication type:
- Article
Somatic MED12 Nonsense Mutation Escapes mRNA Decay and Reveals a Motif Required for Nuclear Entry.
- Published in:
- Human Mutation, 2017, v. 38, n. 3, p. 269, doi. 10.1002/humu.23157
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- Publication type:
- Article