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Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0
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- Article
Author Correction: Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
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- 2023
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- Correction Notice
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0
- By:
- Publication type:
- Article
Germline de novo mutations in families with Mendelian cancer syndromes caused by defects in DNA repair.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39248-0
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- Publication type:
- Article
Small non‐coding RNA sequencing reveals global dysregulation of piwi‐interacting RNA (piRNA) expression in gonadal malignant germ cell tumours.
- Published in:
- Andrology, 2023, v. 11, n. 4, p. 738, doi. 10.1111/andr.13312
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- Article
Similarities and differences in patterns of germline mutation between mice and humans.
- Published in:
- Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12023-w
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- Article
IAP Display: A Simple Method to Identify Mouse Strain Specific IAP Insertions.
- Published in:
- Molecular Biotechnology, 2011, v. 47, n. 3, p. 243, doi. 10.1007/s12033-010-9338-6
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- Article
Meiosis and beyond – understanding the mechanistic and evolutionary processes shaping the germline genome.
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- Biological Reviews, 2021, v. 96, n. 3, p. 822, doi. 10.1111/brv.12680
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- Article
De novo detection of somatic mutations in high-throughput single-cell profiling data sets.
- Published in:
- Nature Biotechnology, 2024, v. 42, n. 5, p. 758, doi. 10.1038/s41587-023-01863-z
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- Article
Somatic Mutations Detected in Parkinson Disease Could Affect Genes With a Role in Synaptic and Neuronal Processes.
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- Frontiers in Aging, 2022, p. 1, doi. 10.3389/fragi.2022.851039
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- Article
Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00323-y
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- Article
Understanding the Genomic Structure of Copy-Number Variation of the Low-Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid Arthritis.
- Published in:
- Human Mutation, 2017, v. 38, n. 4, p. 390, doi. 10.1002/humu.23159
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- Publication type:
- Article
Transduction-Specific ATLAS Reveals a Cohort of Highly Active L1 Retrotransposons in Human Populations.
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- Human Mutation, 2013, v. 34, n. 7, p. 974, doi. 10.1002/humu.22327
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- Article
Common clonal origin of conventional T cells and induced regulatory T cells in breast cancer patients.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-21297-y
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- Article