Found: 23
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Universal heteroplasmy of human mitochondrial DNA.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 2, p. 384, doi. 10.1093/hmg/dds435
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- Publication type:
- Article
Molecular pathogenesis of polymerase γ-related neurodegeneration.
- Published in:
- 2014
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- Publication type:
- journal article
Molecular pathogenesis of polymerase gamma-related neurodegeneration.
- Published in:
- Annals of Neurology, 2014, v. 76, n. 1, p. 66, doi. 10.1002/ana.24185
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- Publication type:
- Article
Single-cell DNA sequencing identifies risk-associated clonal complexity and evolutionary trajectories in childhood medulloblastoma development.
- Published in:
- Acta Neuropathologica, 2022, v. 144, n. 3, p. 565, doi. 10.1007/s00401-022-02464-x
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- Publication type:
- Article
Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans.
- Published in:
- PLoS Genetics, 2015, v. 11, n. 5, p. 1, doi. 10.1371/journal.pgen.1005040
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- Publication type:
- Article
Regulation of CHK1 inhibitor resistance by a c-Rel and USP1 dependent pathway.
- Published in:
- Biochemical Journal, 2022, v. 479, n. 19, p. 2063, doi. 10.1042/BCJ20220102
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- Publication type:
- Article
Up-regulation of the PI3K/AKT and RHO/RAC/PAK signalling pathways in CHK1 inhibitor resistant Eµ-Myc lymphoma cells.
- Published in:
- Biochemical Journal, 2022, v. 479, n. 19, p. 2131, doi. 10.1042/BCJ20220103
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- Publication type:
- Article
Mutation of the RelA(p65) Thr505 phosphosite disrupts the DNA replication stress response leading to CHK1 inhibitor resistance.
- Published in:
- Biochemical Journal, 2022, v. 479, n. 19, p. 2087, doi. 10.1042/BCJ20220089
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- Publication type:
- Article
Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype.
- Published in:
- BMC Developmental Biology, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12861-021-00245-5
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- Publication type:
- Article
Retinal pigment epithelium extracellular vesicles are potent inducers of age‐related macular degeneration disease phenotype in the outer retina.
- Published in:
- Journal of Extracellular Vesicles, 2022, v. 11, n. 12, p. 1, doi. 10.1002/jev2.12295
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- Publication type:
- Article
HDBR Expression: A Unique Resource for Global and Individual Gene Expression Studies during Early Human Brain Development.
- Published in:
- Frontiers in Neuroanatomy, 2016, v. 10, p. 1, doi. 10.3389/fnana.2016.00086
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- Publication type:
- Article
Anti-cancer effects of butyrate: use of micro-array technology to investigate mechanisms.
- Published in:
- 2003
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- Publication type:
- journal article
Anti-cancer effects of butyrate: use of micro-array technology to investigate mechanisms.
- Published in:
- Proceedings of the Nutrition Society, 2003, v. 62, n. 1, p. 107, doi. 10.1079/PNS2002230
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- Publication type:
- Article
Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-27318-0
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- Publication type:
- Article
Heteroplasmic mitochondrial DNA variants in cardiovascular diseases.
- Published in:
- PLoS Genetics, 2022, v. 18, n. 4, p. 1, doi. 10.1371/journal.pgen.1010068
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- Publication type:
- Article
Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47933-x
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- Publication type:
- Article
Release of Histone H3K4-reading transcription factors from chromosomes in mitosis is independent of adjacent H3 phosphorylation.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-43115-3
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- Publication type:
- Article
Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2.
- Published in:
- Science Immunology, 2019, v. 4, n. 42, p. 1, doi. 10.1126/sciimmunol.aav7501
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- Publication type:
- Article
pRB-Depleted Pluripotent Stem Cell Retinal Organoids Recapitulate Cell State Transitions of Retinoblastoma Development and Suggest an Important Role for pRB in Retinal Cell Differentiation.
- Published in:
- Stem Cells Translational Medicine, 2022, v. 11, n. 4, p. 415, doi. 10.1093/stcltm/szac008
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- Publication type:
- Article
Epigenetic modifiers DNMT3A and BCOR are recurrently mutated in CYLD cutaneous syndrome.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12746-w
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- Publication type:
- Article
The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease.
- Published in:
- Movement Disorders, 2020, v. 35, n. 12, p. 2134, doi. 10.1002/mds.28354
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- Publication type:
- Article
Single-cell RNA sequencing reveals transcriptional changes of human choroidal and retinal pigment epithelium cells during fetal development, in healthy adult and intermediate age-related macular degeneration.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 10, p. 1698, doi. 10.1093/hmg/ddad007
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- Publication type:
- Article
Spatial transcriptomics reveals novel genes during the remodelling of the embryonic human arterial valves.
- Published in:
- PLoS Genetics, 2023, v. 19, n. 11, p. 1, doi. 10.1371/journal.pgen.1010777
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- Publication type:
- Article