Found: 16
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Slow repair of bulky DNA adducts along the nontranscribed strand of the human p53 gene may explain the strand bias of transversion mutations in cancers.
- Published in:
- Oncogene, 1998, v. 16, n. 10, p. 1241, doi. 10.1038/sj.onc.1201647
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- Publication type:
- Article
Human chromosome 21 orthologous region on mouse chromosome 17 is a major determinant of Down syndrome-related developmental cognitive deficits.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 3, p. 578, doi. 10.1093/hmg/ddt446
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- Publication type:
- Article
A mouse model of Down syndrome trisomic for all human chromosome 21 syntenic regions.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 14, p. 2780, doi. 10.1093/hmg/ddq179
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- Publication type:
- Article
Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 9, p. 1702, doi. 10.1093/hmg/ddq047
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- Publication type:
- Article
Duplication of the entire 22.9 Mb human chromosome 21 syntenic region on mouse chromosome 16 causes cardiovascular and gastrointestinal abnormalities.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 11, p. 1359, doi. 10.1093/hmg/ddm086
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- Publication type:
- Article
Preferential DNA damage and poor repair determine ras gene mutational hotspot in human cancer.
- Published in:
- 2002
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- Publication type:
- journal article
Preferential DNA Damage and Poor Repair Determine ras Gene Mutational Hotspot in Human Cancer.
- Published in:
- JNCI: Journal of the National Cancer Institute, 2002, v. 94, n. 20, p. 1527, doi. 10.1093/jnci/94.20.1527
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- Publication type:
- Article
Coat Color-Facilitated Efficient Generation and Analysis of a Mouse Model of Down Syndrome Triplicated for All Human Chromosome 21 Orthologous Regions.
- Published in:
- Genes, 2021, v. 12, n. 8, p. 1215, doi. 10.3390/genes12081215
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- Publication type:
- Article
Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice.
- Published in:
- Mammalian Genome, 2010, v. 21, n. 5/6, p. 258, doi. 10.1007/s00335-010-9262-x
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- Publication type:
- Article
Mouse-based genetic modeling and analysis of Down syndrome.
- Published in:
- British Medical Bulletin, 2016, v. 120, n. 1, p. 111, doi. 10.1093/bmb/ldw040
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- Publication type:
- Article
Engineered chromosome-based genetic mapping establishes a 3.7 Mb critical genomic region for Down syndrome-associated heart defects in mice.
- Published in:
- Human Genetics, 2014, v. 133, n. 6, p. 743, doi. 10.1007/s00439-013-1407-z
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- Publication type:
- Article
Genetic analysis of Down syndrome-associated heart defects in mice.
- Published in:
- Human Genetics, 2011, v. 130, n. 5, p. 623, doi. 10.1007/s00439-011-0980-2
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- Publication type:
- Article
Erratum to: Genetic analysis of Down syndrome-associated heart defects in mice.
- Published in:
- 2011
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- Publication type:
- Correction notice
Dissection of a Down syndrome-associated trisomy to separate the gene dosage-dependent and -independent effects of an extra chromosome.
- Published in:
- Human Molecular Genetics, 2023, v. 32, n. 13, p. 2205, doi. 10.1093/hmg/ddad056
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- Publication type:
- Article
Genetic dissection of the Down syndrome critical region.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 22, p. 6540, doi. 10.1093/hmg/ddv364
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- Publication type:
- Article
A Deficiency in the Region Homologous to Human 17q21.33-q23.2 Causes Heart Defects in Mice.
- Published in:
- Genetics, 2006, v. 173, n. 1, p. 297, doi. 10.1534/genetics.105.054833
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- Publication type:
- Article