Found: 34
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Human metallothionein genes-primary structure of the metallothionein-II gene and a related processed gene.
- Published in:
- Nature, 1982, v. 299, n. 5886, p. 797, doi. 10.1038/299797a0
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- Article
Zebrafish Chromosome 14 Gene Differential Expression in the fmr1 <sup> h u 2787</sup> Model of Fragile X Syndrome.
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- Frontiers in Genetics, 2021, v. 11, p. 1, doi. 10.3389/fgene.2021.625466
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- Article
Dynamic mutations on the move in Banff.
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- Nature Genetics, 2004, v. 36, n. 7, p. 667, doi. 10.1038/ng0704-667
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- Article
Tumor Suppressor WWOX Contributes to the Elimination of Tumorigenic Cells in Drosophila melanogaster.
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- PLoS ONE, 2015, v. 10, n. 8, p. 1, doi. 10.1371/journal.pone.0136356
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- Article
Ubiquitous Expression of CUG or CAG Trinucleotide Repeat RNA Causes Common Morphological Defects in a Drosophila Model of RNA-Mediated Pathology.
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- PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0038516
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- Article
A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum.
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- Journal of Molecular Medicine, 2001, v. 79, n. 9, p. 536, doi. 10.1007/s001090100275
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- Article
FRA16D common chromosomal fragile site oxido-reductase (FOR/WWOX) protects against the effects of ionizing radiation in Drosophila.
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- Oncogene, 2005, v. 24, n. 43, p. 6590, doi. 10.1038/sj.onc.1208806
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- Article
Fragile X syndrome<sup>*</sup>: The most common cause of familial intellectual handicap.
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- Medical Journal of Australia, 1993, v. 158, n. 7, p. 482, doi. 10.5694/j.1326-5377.1993.tb137582.x
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- Article
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene.
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- Nucleic Acids Research, 1997, v. 25, n. 1, p. 147, doi. 10.1093/nar/25.1.147
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- Article
The Enemy within: Innate Surveillance-Mediated Cell Death, the Common Mechanism of Neurodegenerative Disease.
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- Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00193
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- Article
Non-self mutation: double-stranded RNA elicits antiviral pathogenic response in a Drosophila model of expanded CAG repeat neurodegenerative diseases.
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- Human Molecular Genetics, 2019, v. 28, n. 18, p. 3000, doi. 10.1093/hmg/ddz096
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- Article
Neurodegenerative diseases have genetic hallmarks of autoinflammatory disease.
- Published in:
- Human Molecular Genetics, 2018, v. 27, p. R108, doi. 10.1093/hmg/ddy139
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- Article
Distinct roles for Toll and autophagy pathways in double-stranded RNA toxicity in a Drosophila model of expanded repeat neurodegenerative diseases.
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- Human Molecular Genetics, 2013, v. 22, n. 14, p. 2811, doi. 10.1093/hmg/ddt130
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- Article
Comparative toxicity of polyglutamine, polyalanine and polyleucine tracts in Drosophila models of expanded repeat disease.
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- Human Molecular Genetics, 2012, v. 21, n. 3, p. 536, doi. 10.1093/hmg/ddr487
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- Article
Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases.
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- Human Molecular Genetics, 2011, v. 20, n. 19, p. 3757, doi. 10.1093/hmg/ddr292
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- Article
Perturbation of the Akt/Gsk3-β signalling pathway is common to Drosophila expressing expanded untranslated CAG, CUG and AUUCU repeat RNAs.
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- Human Molecular Genetics, 2011, v. 20, n. 14, p. 2783, doi. 10.1093/hmg/ddr177
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- Article
Tumor suppressor WWOX moderates the mitochondrial respiratory complex.
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- Genes, Chromosomes & Cancer, 2015, v. 54, n. 12, p. 745, doi. 10.1002/gcc.22286
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- Article
Common chromosomal fragile site FRA16D tumor suppressor WWOX gene expression and metabolic reprograming in cells.
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- Genes, Chromosomes & Cancer, 2013, v. 52, n. 9, p. 823, doi. 10.1002/gcc.22078
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- Article
Molecular Biology of the WWOX Gene That Spans Chromosomal Fragile Site FRA16D.
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- Cells (2073-4409), 2021, v. 10, n. 7, p. 1637, doi. 10.3390/cells10071637
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- Article
WWOX, the chromosomal fragile site FRA16D spanning gene: Its role in metabolism and contribution to cancer.
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- Experimental Biology & Medicine, 2015, v. 240, n. 3, p. 338, doi. 10.1177/1535370214565990
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- Article
Molecular genetics of pseudoxanthoma elasticum: type and frequency of mutations in ABCC6.
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- Human Mutation, 2005, v. 26, n. 3, p. 235, doi. 10.1002/humu.20206
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- Article
Drosophila orthologue of WWOX, the chromosomal fragile site FRA16D tumour suppressor gene, functions in aerobic metabolism and regulates reactive oxygen species.
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- Human Molecular Genetics, 2011, v. 20, n. 3, p. 497, doi. 10.1093/hmg/ddq495
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- Article
Selective neuronal requirement for huntingtin in the developing zebrafish.
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- Human Molecular Genetics, 2009, v. 18, n. 24, p. 4830, doi. 10.1093/hmg/ddp455
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- Article
Huntingtin-deficient zebrafish exhibit defects in iron utilization and development.
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- Human Molecular Genetics, 2007, v. 16, n. 16, p. 1905, doi. 10.1093/hmg/ddm138
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- Article
Contribution of mGluR and Fmr1 functional pathways to neurite morphogenesis, craniofacial development and fragile X syndrome.
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- Human Molecular Genetics, 2006, v. 15, n. 23, p. 3446, doi. 10.1093/hmg/ddl422
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- Article
Common chromosomal fragile site FRA16D mutation in cancer cells.
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- Human Molecular Genetics, 2005, v. 14, n. 10, p. 1341, doi. 10.1093/hmg/ddi144
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- Article
The pathogenic agent in Drosophila models of ‘polyglutamine’ diseases.
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- Human Molecular Genetics, 2005, v. 14, n. 8, p. 1041, doi. 10.1093/hmg/ddi096
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- Article
Dynamic mutations: a decade ofunstable expanded repeats in human genetic disease.
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- Human Molecular Genetics, 2001, v. 10, n. 20, p. 2187, doi. 10.1093/hmg/10.20.2187
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- Article
Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells.
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- Human Molecular Genetics, 2000, v. 9, n. 11, p. 1651, doi. 10.1093/hmg/9.11.1651
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- Article
RNA pathogenesis viaToll-like receptor-activated inflammation in expanded repeat neurodegenerative diseases.
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- Frontiers in Molecular Neuroscience, 2013, v. 6, p. 1, doi. 10.3389/fnmol.2013.00025
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- Article
Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21‐hydroxylase deficiency.
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- Medical Journal of Australia, 1990, v. 152, n. 2, p. 132, doi. 10.5694/j.1326-5377.1992.tb126428.x
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- Article
Repeat offenders: Simple repeat sequences and complex genetic problems.
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- Human Mutation, 1996, v. 8, n. 1, p. 1, doi. 10.1002/(SICI)1098-1004(1996)8:1<1::AID-HUMU1>3.0.CO;2-G
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- Article
CAG repeat expansion in autosomal dominant familial spastic paraparesis: novel expansion in a subset of patients.
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- Human Molecular Genetics, 1998, v. 7, n. 11, p. 1779, doi. 10.1093/hmg/7.11.1779
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- Article
Physical linkage of the fragile site FRA11B and a Jacobsen Syndrome chromosome deletion breakpoint in 11q23. 3.
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- Human Molecular Genetics, 1994, v. 3, n. 12, p. 2123
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- Article