Found: 12
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Genome sequencing in persistently unsolved white matter disorders.
- Published in:
- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 1, p. 144, doi. 10.1002/acn3.50957
- By:
- Publication type:
- Article
Aberrant pregnancy-associated plasma protein-A expression in breast cancers prognosticates clinical outcomes.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-70774-9
- By:
- Publication type:
- Article
The Role of Cancer-Testis Antigens as Predictive and Prognostic Markers in Non-Small Cell Lung Cancer.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0067876
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- Publication type:
- Article
Correction: BCL-XL is an actionable target for treatment of malignant pleural mesothelioma.
- Published in:
- 2021
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- Publication type:
- Correction Notice
A novel BH3-mimetic, AZD0466, targeting BCL-XL and BCL-2 is effective in pre-clinical models of malignant pleural mesothelioma.
- Published in:
- Cell Death Discovery, 2021, v. 7, n. 1, p. 1, doi. 10.1038/s41420-021-00505-0
- By:
- Publication type:
- Article
BCL-XL is an actionable target for treatment of malignant pleural mesothelioma.
- Published in:
- Cell Death Discovery, 2020, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41420-020-00348-1
- By:
- Publication type:
- Article
Transketolase-like 1 ectopic expression is associated with DNA hypomethylation and induces the Warburg effect in melanoma cells.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform.
- Published in:
- Human Mutation, 2022, v. 43, n. 9, p. 1344, doi. 10.1002/humu.24400
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- Publication type:
- Article
Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10.
- Published in:
- Human Mutation, 2021, v. 42, n. 1, p. 19, doi. 10.1002/humu.24135
- By:
- Publication type:
- Article
Type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform.
- Published in:
- Human Mutation, 2020, v. 41, n. 6, p. 1131, doi. 10.1002/humu.24008
- By:
- Publication type:
- Article
Pathogenic variants in nucleoporin TPR (translocated promoter region, nuclear basket protein) cause severe intellectual disability in humans.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 3, p. 362, doi. 10.1093/hmg/ddab248
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- Publication type:
- Article
PD-L1 and Tumor Infiltrating Lymphocytes as Prognostic Markers in Resected NSCLC.
- Published in:
- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0153954
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- Publication type:
- Article