Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 3
Results: 21
Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3).
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. 508, doi. 10.1093/hmg/dds449
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- Article
Expression of DUX4 in zebrafish development recapitulates facioscapulohumeral muscular dystrophy.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 568, doi. 10.1093/hmg/dds467
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. NP, doi. 10.1093/hmg/dds550
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- Article
MicroRNA-205 regulates the expression of Parkinson's disease-related leucine-rich repeat kinase 2 protein.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 608, doi. 10.1093/hmg/dds470
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- Article
Cover Page.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. NP, doi. 10.1093/hmg/dds548
- Publication type:
- Article
Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 433, doi. 10.1093/hmg/dds439
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- Article
Genome-wide copy number variation study in anorectal malformations.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 621, doi. 10.1093/hmg/dds451
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- Article
p63 control of desmosome gene expression and adhesion is compromised in AEC syndrome.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 531, doi. 10.1093/hmg/dds464
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- Article
Somatic gain-of-function mutations in PIK3CA in patients with macrodactyly.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 444, doi. 10.1093/hmg/dds440
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- Publication type:
- Article
The molecular function and clinical phenotype of partial deletions of the IGF2/H19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 544, doi. 10.1093/hmg/dds465
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- Article
Bone marrow transplantation improves the outcome of Atm-deficient mice through the migration of ATM-competent cells.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 493, doi. 10.1093/hmg/dds448
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- Article
Gene therapy provides long-term visual function in a pre-clinical model of retinitis pigmentosa.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 558, doi. 10.1093/hmg/dds466
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. NP, doi. 10.1093/hmg/dds549
- Publication type:
- Article
Trans-chromosomic mice containing a human CYP3A cluster for prediction of xenobiotic metabolism in humans.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. 578, doi. 10.1093/hmg/dds468
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- Publication type:
- Article
iPS cell modeling of Best disease: insights into the pathophysiology of an inherited macular degeneration.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 593, doi. 10.1093/hmg/dds469
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- Publication type:
- Article
ORMDL3 modulates store-operated calcium entry and lymphocyte activation.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 519, doi. 10.1093/hmg/dds450
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. NP, doi. 10.1093/hmg/dds547
- Publication type:
- Article
Seven functional classes of Barth syndrome mutation.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. 483, doi. 10.1093/hmg/dds447
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- Article
Abnormal cerebellar development and ataxia in CARP VIII morphant zebrafish.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 417, doi. 10.1093/hmg/dds438
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- Publication type:
- Article
Kidins220 accumulates with tau in human Alzheimer's disease and related models: modulation of its calpain-processing by GSK3β/PP1 imbalance.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 3, p. 466
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- Publication type:
- Article
Hip14l-deficient mice develop neuropathological and behavioural features of Huntington disease.
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- Human Molecular Genetics, 2013, v. 22, n. 3, p. 452, doi. 10.1093/hmg/dds441
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- Publication type:
- Article