Found: 37
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Granuloma formation in ANCA-associated vasculitides.
- Published in:
- APMIS, 2009, v. 117, p. 32, doi. 10.1111/j.1600-0463.2009.02474.x
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- Publication type:
- Article
Mutations of the puratrophin-1 ( PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 4, p. 363, doi. 10.1007/s10038-006-0372-y
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- Publication type:
- Article
Thousand-Fold Acceleration of Phase Decomposition in Polymer/Liquid Crystal Blends.
- Published in:
- ChemPhysChem, 2009, v. 10, n. 15, p. 2620, doi. 10.1002/cphc.200900505
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- Publication type:
- Article
Caveolin-1 Single Nucleotide Polymorphism in Antineutrophil Cytoplasmic Antibody Associated Vasculitis.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0069022
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- Publication type:
- Article
Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease.
- Published in:
- Journal of Molecular Medicine, 2010, v. 88, n. 4, p. 431, doi. 10.1007/s00109-010-0589-2
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- Publication type:
- Article
A functionally relevant IRF5 haplotype is associated with reduced risk to Wegener’s granulomatosis.
- Published in:
- Journal of Molecular Medicine, 2010, v. 88, n. 4, p. 413, doi. 10.1007/s00109-009-0580-y
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- Publication type:
- Article
ASK1 and MAP2K6 as modifiers of age at onset in Huntington’s disease.
- Published in:
- Journal of Molecular Medicine, 2008, v. 86, n. 4, p. 485, doi. 10.1007/s00109-007-0299-6
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- Publication type:
- Article
Screening for candidate gene regions in narcolepsy using a microsatellite based approach and pooled DNA.
- Published in:
- Journal of Molecular Medicine, 2004, v. 82, n. 10, p. 696, doi. 10.1007/s00109-004-0569-5
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- Publication type:
- Article
Polymorphisms of the tumor necrosis factor receptors: no association with narcolepsy in German patients.
- Published in:
- Journal of Molecular Medicine, 2003, v. 81, n. 2, p. 87, doi. 10.1007/s00109-002-0405-8
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- Publication type:
- Article
NR2A and NR2B receptor gene variations modify age at onset in Huntington disease in a sex-specific manner.
- Published in:
- Human Genetics, 2007, v. 122, n. 2, p. 175, doi. 10.1007/s00439-007-0393-4
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- Publication type:
- Article
Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease.
- Published in:
- Human Genetics, 2006, v. 120, n. 2, p. 285, doi. 10.1007/s00439-006-0221-2
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- Publication type:
- Article
New genomic region for Wegener’s granulomatosis as revealed by an extended association screen with 202 apoptosis-related genes.
- Published in:
- Human Genetics, 2004, v. 114, n. 5, p. 468, doi. 10.1007/s00439-004-1092-z
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- Publication type:
- Article
Novel NUP98::ASH1L Gene Fusion in Acute Myeloid Leukemia Detected by Optical Genome Mapping.
- Published in:
- Cancers, 2023, v. 15, n. 11, p. 2942, doi. 10.3390/cancers15112942
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- Publication type:
- Article
Genetic Variation of PPARs.
- Published in:
- PPAR Research, 2009, p. 1, doi. 10.1155/2009/189091
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- Publication type:
- Article
Genetic Variability of RXRB, PPARA, and PPARG in Wegener's Granulomatosis.
- Published in:
- PPAR Research, 2009, p. 1, doi. 10.1155/2009/786781
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- Publication type:
- Article
NMDA receptor gene variations as modifiers in Huntington disease: a replication study.
- Published in:
- PLoS Currents, 2011, p. 454, doi. 10.1371/currents.RRN1247
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- Publication type:
- Article
Is the retina affected in Huntington disease?
- Published in:
- Acta Neuropathologica, 2005, v. 110, n. 5, p. 523, doi. 10.1007/s00401-005-1092-7
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- Publication type:
- Article
Eotaxin-3 in Churg–Strauss syndrome: a clinical and immunogenetic study.
- Published in:
- 2011
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- Publication type:
- Journal Article
Eotaxin-3 in Churg–Strauss syndrome: a clinical and immunogenetic study.
- Published in:
- Rheumatology, 2011, v. 50, n. 10, p. 1823, doi. 10.1093/rheumatology/keq445
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- Publication type:
- Article
Contrasting association of a non-synonymous leptin receptor gene polymorphism with Wegener’s granulomatosis and Churg–Strauss syndrome.
- Published in:
- Rheumatology, 2010, v. 49, n. 5, p. 907, doi. 10.1093/rheumatology/kep420
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- Publication type:
- Article
Failure to confirm influence of Methyltetrahydrofolate reductase (MTHFR) polymorphisms on age at onset of Huntington disease.
- Published in:
- Journal of Negative Results in Biomedicine, 2005, v. 4, p. 12, doi. 10.1186/1477-5751-4-12
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- Publication type:
- Article
Association study with Wegener granulomatosis of the human phospholipase C γ2 gene.
- Published in:
- Journal of Negative Results in Biomedicine, 2005, v. 4, p. 1, doi. 10.1186/1477-5751-4-1
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- Publication type:
- Article
Hypoparathyroidism, Sensorineural deafness and renal disease (Barakat syndrome) caused by a reduced gene dosage in GATA3: a case report and review of literature.
- Published in:
- BMC Endocrine Disorders, 2019, v. 19, n. 1, p. N.PAG, doi. 10.1186/s12902-019-0438-4
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- Publication type:
- Article
Genetic variations in the genes encoding receptor activator nuclear factor κ B (RANK), receptor activator nuclear factor κ B ligand (RANKL) and osteoprotegerin (OPG) in patients with psoriasis and psoriatic arthritis: A case-control study.
- Published in:
- Journal of Dermatology, 2011, v. 38, n. 6, p. 519, doi. 10.1111/j.1346-8138.2010.01055.x
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- Publication type:
- Article
HLA-DPB1 as a Risk Factor for Relapse in Antineutrophil Cytoplasmic Antibody-Associated Vasculitis: A Cohort Study.
- Published in:
- Arthritis & Rheumatology, 2016, v. 68, n. 7, p. 1721, doi. 10.1002/art.39620
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- Publication type:
- Article
The SEM6A6 Locus Is Not Associated With Granulomatosis With Polyangiitis or Other Forms of Antineutrophil Cytoplasmic Antibody-Associated Vasculitides in Europeans: Comment on the Article by Xie et al.
- Published in:
- Arthritis & Rheumatology, 2014, v. 66, n. 5, p. 1400, doi. 10.1002/art.38367
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- Publication type:
- Article
PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease.
- Published in:
- Molecular Neurodegeneration, 2011, v. 6, n. 1, p. 32, doi. 10.1186/1750-1326-6-32
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- Publication type:
- Article
PGC-1alpha as modifier of onset age in Huntington disease.
- Published in:
- Molecular Neurodegeneration, 2009, v. 4, p. 1, doi. 10.1186/1750-1326-4-10
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- Publication type:
- Article
Spinocerebellar ataxias: An example of the challenges associated with genetic databases for dynamic mutations.
- Published in:
- Human Mutation, 2012, v. 33, n. 9, p. 1359, doi. 10.1002/humu.22156
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- Publication type:
- Article
Risk factors and myocardial infarction in patients with obstructive sleep apnea: impact of β2-adrenergic receptor polymorphisms.
- Published in:
- BMC Medicine, 2007, v. 5, p. 1, doi. 10.1186/1741-7015-5-1
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- Publication type:
- Article
Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1.
- Published in:
- Neurogenetics, 2010, v. 11, n. 4, p. 435, doi. 10.1007/s10048-010-0248-3
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- Publication type:
- Article
The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease.
- Published in:
- Neurogenetics, 2006, v. 7, n. 1, p. 27, doi. 10.1007/s10048-005-0023-z
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- Publication type:
- Article
Huntington's disease as caused by 34 CAG repeats.
- Published in:
- Movement Disorders, 2008, v. 23, n. 6, p. 879, doi. 10.1002/mds.21958
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- Publication type:
- Article
Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene.
- Published in:
- Movement Disorders, 2007, v. 22, n. 14, p. 2135, doi. 10.1002/mds.21673
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- Publication type:
- Article
No association between polymorphisms in the BDNF gene and age at onset in Huntington disease.
- Published in:
- BMC Medical Genetics, 2006, v. 7, p. 1, doi. 10.1186/1471-2350-7-79
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- Publication type:
- Article
Glutathione S-Transferase ℣ 1 variation does not influence age at onset of Huntington's disease.
- Published in:
- BMC Medical Genetics, 2004, v. 5, p. 7, doi. 10.1186/1471-2350-5-7
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- Publication type:
- Article
ApoE polymorphisms in narcolepsy.
- Published in:
- BMC Medical Genetics, 2001, v. 2, p. 1
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- Publication type:
- Article