Found: 23
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Motif discovery in promoters of genes co-localized and co-expressed during myeloid cells differentiation.
- Published in:
- Nucleic Acids Research, 2009, v. 37, n. 2, p. 533, doi. 10.1093/nar/gkn948
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- Article
Computational reconstruction of the human skeletal muscle secretome.
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- Proteins, 2006, v. 62, n. 3, p. 776, doi. 10.1002/prot.20803
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- Article
Analysis of 22 deletion breakpoints in dystrophin intron 49.
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- Human Genetics, 2002, v. 110, n. 5, p. 418, doi. 10.1007/s00439-002-0721-7
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- Article
The p.A897KfsX4 frameshift variation in desmocollin-2 is not a causative mutation in arrhythmogenic right ventricular cardiomyopathy.
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- European Journal of Human Genetics, 2010, v. 18, n. 7, p. 776, doi. 10.1038/ejhg.2010.19
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- Article
Arrhythmogenic right ventricular cardiomyopathy type 1 (ARVD1): confirmation of locus assignment and mutation screening of four candidate genes.
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- European Journal of Human Genetics, 2003, v. 11, n. 1, p. 69, doi. 10.1038/sj.ejhg.5200914
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- Article
Ultrastructural evidence of intercalated disc remodelling in arrhythmogenic right ventricular cardiomyopathy: an electron microscopy investigation on endomyocardial biopsies.
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- European Heart Journal, 2006, v. 27, n. 15, p. 1847, doi. 10.1093/eurheartj/ehl095
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- Article
Regulatory mutations in transforming growth factor-β3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1
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- Cardiovascular Research, 2005, v. 65, n. 2, p. 366, doi. 10.1016/j.cardiores.2004.10.005
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- Article
Genomic expression during human myelopoiesis.
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- BMC Genomics, 2007, v. 8, p. 264, doi. 10.1186/1471-2164-8-264
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- Article
Novel definition files for human GeneChips based on GeneAnnot.
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- BMC Bioinformatics, 2007, v. 8, p. 446, doi. 10.1186/1471-2105-8-446
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- Article
A multistep bioinformatic approach detects putative regulatory elements in gene promoters.
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- BMC Bioinformatics, 2005, v. 6, p. 121, doi. 10.1186/1471-2105-6-121
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- Article
Detection of chromosomal regions showing differential gene expression in human skeletal muscle and in alveolar rhabdomyosarcoma.
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- BMC Bioinformatics, 2004, v. 5, p. 68, doi. 10.1186/1471-2105-5-68
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- Article
Detecting seeded motifs in DNA sequences.
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- Nucleic Acids Research, 2005, v. 33, n. 15, p. e135, doi. 10.1093/nar/gni131
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- Article
Larval Moulting Cycle and DNA Synthesis in Drosophila hydei Salivary Glands.
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- Nature, 1967, v. 213, n. 5074, p. 424, doi. 10.1038/213424a0
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- Article
Functional analysis reveals splicing mutations of the CASQ2 gene in patients with CPVT: implication for genetic counselling and clinical management.
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- Human Mutation, 2011, v. 32, n. 9, p. 995, doi. 10.1002/humu.21537
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- Article
TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources.
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- BMC Genomics, 2011, v. 12, p. 1, doi. 10.1186/1471-2164-12-121
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- Publication type:
- Article
TRAM (Transcriptome Mapper): database-driven creation and analysis of transcriptome maps from multiple sources.
- Published in:
- BMC Genomics, 2011, v. 12, n. 1, p. 121, doi. 10.1186/1471-2164-12-121
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- Publication type:
- Article
Large majority of single-nucleotide mutations along the dystrophin gene can be explained by more than one mechanism of mutagenesis.
- Published in:
- Human Mutation, 1997, v. 9, n. 6, p. 537, doi. 10.1002/(SICI)1098-1004(1997)9:6<537::AID-HUMU7>3.0.CO;2-Z
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- Article
Novel mutations and polymorphisms in the human dystrophin gene detected by double-strand conformation analysis.
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- Human Mutation, 1997, v. 9, n. 2, p. 188, doi. 10.1002/(SICI)1098-1004(1997)9:2<188::AID-HUMU15>3.0.CO;2-Z
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- Publication type:
- Article
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities.
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- 2007
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- Publication type:
- journal article
A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42–q43.
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- Human Molecular Genetics, 1995, v. 4, n. 11, p. 2151
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- Article
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
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- 1996
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- Publication type:
- journal article
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course.
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- 1995
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- Publication type:
- journal article
Missense mutations in Desmocollin-2 N-terminus, associated with arrhythmogenic right ventricular cardiomyopathy, affect intracellular localization of desmocollin-2 in vitro.
- Published in:
- BMC Medical Genetics, 2007, v. 8, p. 65, doi. 10.1186/1471-2350-8-65
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- Article