Found: 13
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Discovery of Potential New Gene Variants and Inflammatory Cytokine Associations with Fibromyalgia Syndrome by Whole Exome Sequencing.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065033
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- Article
Missense Mutations in the MEFV Gene Are Associated with Fibromyalgia Syndrome and Correlate with Elevated IL-1β Plasma Levels.
- Published in:
- PLoS ONE, 2009, v. 4, n. 12, p. 1, doi. 10.1371/journal.pone.0008480
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- Article
Analysis of Cancer Mutation Signatures in Blood by a Novel Ultra-Sensitive Assay: Monitoring of Therapy or Recurrence in Non-Metastatic Breast Cancer.
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- PLoS ONE, 2009, v. 4, n. 9, p. 1, doi. 10.1371/journal.pone.0007220
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- Article
Evidence for X-Chromosomal Schizophrenia Associated with microRNA Alterations.
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- PLoS ONE, 2009, v. 4, n. 7, p. 1, doi. 10.1371/journal.pone.0006121
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- Article
Epidemiology of Doublet/Multiplet Mutations in Lung Cancers: Evidence that a Subset Arises by Chronocoordinate Events.
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- PLoS ONE, 2008, v. 3, n. 11, p. 1, doi. 10.1371/journal.pone.0003714
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- Article
Increased risk of idiopathic chronic pancreatitis in cystic fibrosis carriers.
- Published in:
- Human Mutation, 2005, v. 26, n. 4, p. 303, doi. 10.1002/humu.20232
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- Article
Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).
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- Human Mutation, 2005, v. 25, n. 5, p. 505, doi. 10.1002/humu.9338
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- Article
Mutation rates in the dystrophin gene: A hotspot of mutation at a CpG dinucleotide.
- Published in:
- Human Mutation, 2005, v. 25, n. 2, p. 177, doi. 10.1002/humu.20132
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- Article
SNPs in inflammatory genes CCL11, CCL4 and MEFV in a fibromyalgia family study.
- Published in:
- PLoS ONE, 2018, v. 13, n. 6, p. 1, doi. 10.1371/journal.pone.0198625
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- Article
Mutations in the factor IX gene (F9) during the past 150 years have relative rates similar to ancient mutations.
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- Human Mutation, 2002, v. 19, n. 1, p. 49, doi. 10.1002/humu.10018
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- Article
Deep intronic mutations are rarely a cause of hemophilia B.
- Published in:
- Human Mutation, 1999, v. 14, n. 3, p. 267, doi. 10.1002/(SICI)1098-1004(1999)14:3<267::AID-HUMU11>3.0.CO;2-I
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- Article
Highly sensitive mutation screening by REF with low concentrations of urea: A blinded analysis of a 2-kb region of the p53 gene reveals two common haplotypes.
- Published in:
- Human Mutation, 1999, v. 14, n. 2, p. 175, doi. 10.1002/(SICI)1098-1004(1999)14:2<175::AID-HUMU9>3.0.CO;2-3
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- Article
Bi-directional Dideoxy Fingerprinting (Bi-ddF): A Rapid Method for Quantitative Detection of Mutations in Genomic Regions of 300–600 bp.
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- Human Molecular Genetics, 1996, v. 5, n. 1, p. 107, doi. 10.1093/hmg/5.1.107
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- Article