Found: 22
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Candidate tumour suppressor genes at 11q23–q24 in breast cancer: evidence of alterations in PIG8, a gene involved in p53-induced apoptosis.
- Published in:
- Oncogene, 2001, v. 20, n. 53, p. 7753, doi. 10.1038/sj.onc.1204993
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- Publication type:
- Article
p53 Mutations are present in colorectal cancer with cytoplasmic p53 accumulation.
- Published in:
- International Journal of Cancer, 2001, v. 92, n. 3, p. 338, doi. 10.1002/ijc.1189
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- Publication type:
- Article
Association between CYP17 gene polymorphism and risk of breast cancer in young women.
- Published in:
- International Journal of Cancer, 1999, v. 84, n. 4, p. 350, doi. 10.1002/(SICI)1097-0215(19990820)84:4<350::AID-IJC3>3.0.CO;2-L
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- Publication type:
- Article
Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 3, p. 377, doi. 10.1093/hmg/ddi448
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- Publication type:
- Article
USF1 and dyslipidemias: converging evidence for a functional intronic variant.
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- Human Molecular Genetics, 2005, v. 14, n. 17, p. 2595, doi. 10.1093/hmg/ddi294
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- Publication type:
- Article
Batten disease (JNCL) is linked to disturbances in mitochondrial, cytoskeletal, and synaptic compartments.
- Published in:
- Journal of Neuroscience Research, 2006, v. 84, n. 5, p. 1124, doi. 10.1002/jnr.21015
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- Publication type:
- Article
Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases.
- Published in:
- BMC Genomics, 2008, v. 9, p. 1, doi. 10.1186/1471-2164-9-146
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- Publication type:
- Article
Neural precursor cells from a fatal human motoneuron disease differentiate despite aberrant gene expression.
- Published in:
- Developmental Neurobiology (19328451), 2007, v. 67, n. 3, p. 270, doi. 10.1002/dneu.20350
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- Publication type:
- Article
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).
- Published in:
- Nature Genetics, 2004, v. 36, n. 4, p. 371, doi. 10.1038/ng1320
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- Publication type:
- Article
Do DNA copy number changes differentiate uterine from non-uterine leiomyosarcomas and predict metastasis?
- Published in:
- Modern Pathology, 2006, v. 19, n. 8, p. 1068, doi. 10.1038/modpathol.3800617
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- Publication type:
- Article
Abstracts of Theses from the Nordic Countries.
- Published in:
- 2002
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- Publication type:
- Abstract
Protein Accumulation and Gene Mutation of p53 in Bilateral Breast Cancer.
- Published in:
- Acta Oncologica, 2001, v. 40, n. 1, p. 56, doi. 10.1080/028418601750071064
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- Publication type:
- Article
Gene Expression Profiling of Gliadin Effects on Intestinal Epithelial Cells Suggests Novel Non-Enzymatic Functions of Pepsin and Trypsin.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066307
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- Publication type:
- Article
GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.786705
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- Publication type:
- Article
High-resolution targeted bisulfite sequencing reveals blood cell type-specific DNA methylation patterns in IL13 and ORMDL3.
- Published in:
- Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01093-7
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- Publication type:
- Article
High-resolution targeted bisulfite sequencing reveals blood cell type-specific DNA methylation patterns in IL13 and ORMDL3.
- Published in:
- Clinical Epigenetics, 2021, v. 13, n. 1, p. 1, doi. 10.1186/s13148-021-01093-7
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- Publication type:
- Article
Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy.
- Published in:
- PLoS ONE, 2021, v. 16, n. 2, p. 1, doi. 10.1371/journal.pone.0245681
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- Publication type:
- Article
Cell cycle arrest and apoptosis provoked by UV radiation‐induced DNA damage are transcriptionally highly divergent responses.
- Published in:
- Nucleic Acids Research, 2003, v. 31, n. 16, p. 4779, doi. 10.1093/nar/gkg675
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- Publication type:
- Article
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients.
- Published in:
- 2021
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- Publication type:
- journal article
Transcript profiles of dendritic cells of PLOSL patients link demyelinating CNS disorders with abnormalities in pathways of actin bundling and immune response.
- Published in:
- Journal of Molecular Medicine, 2007, v. 85, n. 9, p. 971, doi. 10.1007/s00109-007-0191-4
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- Publication type:
- Article
Accurate genetic diagnosis of Finnish pulmonary arterial hypertension patients using oligonucleotide-selective sequencing.
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- Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 4, p. 354, doi. 10.1002/mgg3.147
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- Publication type:
- Article
Genetics and genotype-phenotype correlations in Finnish patients with dilated cardiomyopathy.
- Published in:
- European Heart Journal, 2015, v. 36, n. 34, p. 2327, doi. 10.1093/eurheartj/ehv253
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- Publication type:
- Article