Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP 20
Results: 23
Ablation of P2X7 receptor exacerbates gliosis and motoneuron death in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4102, doi. 10.1093/hmg/ddt259
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 20, p. NP, doi. 10.1093/hmg/ddt475
- Publication type:
- Article
Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4206, doi. 10.1093/hmg/ddt272
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- Article
Contents Page.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. NP, doi. 10.1093/hmg/ddt469
- Publication type:
- Article
Differentiation of epidermal keratinocytes is dependent on glucosylceramide:ceramide processing.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4164, doi. 10.1093/hmg/ddt264
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A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4233, doi. 10.1093/hmg/ddt266
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- Article
A mutation in Tubb2b, a human polymicrogyria gene, leads to lethality and abnormal cortical development in the mouse.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4053, doi. 10.1093/hmg/ddt255
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- Article
PLEKHG5 deficiency leads to an intermediate form of autosomal-recessive Charcot–Marie–Tooth disease.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4224, doi. 10.1093/hmg/ddt274
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- Article
New evidence for positive selection helps explain the paternal age effect observed in achondroplasia.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4117, doi. 10.1093/hmg/ddt260
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- Article
The DcpS inhibitor RG3039 improves survival, function and motor unit pathologies in two SMA mouse models.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4084, doi. 10.1093/hmg/ddt258
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- Article
The Bardet–Biedl syndrome-related protein CCDC28B modulates mTORC2 function and interacts with SIN1 to control cilia length independently of the mTOR complex.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4031, doi. 10.1093/hmg/ddt253
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- Article
Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4239, doi. 10.1093/hmg/ddt334
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- Article
Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4194, doi. 10.1093/hmg/ddt267
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- Article
The DcpS inhibitor RG3039 improves motor function in SMA mice.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4074, doi. 10.1093/hmg/ddt257
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- Publication type:
- Article
Dilysine motifs in exon 2b of SMN protein mediate binding to the COPI vesicle protein α-COP and neurite outgrowth in a cell culture model of spinal muscular atrophy.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4043, doi. 10.1093/hmg/ddt254
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- Article
Coronary heart disease is associated with a mutation in mitochondrial tRNA.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4064, doi. 10.1093/hmg/ddt256
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- Article
Linear and extended: a common polyglutamine conformation recognized by the three antibodies MW1, 1C2 and 3B5H10.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4215, doi. 10.1093/hmg/ddt273
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- Article
Decreased number of Gemini of coiled bodies and U12 snRNA level in amyotrophic lateral sclerosis.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4136, doi. 10.1093/hmg/ddt262
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- Article
Type of uromodulin mutation and allelic status influence onset and severity of uromodulin-associated kidney disease in mice.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4148, doi. 10.1093/hmg/ddt263
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- Article
Method for widespread microRNA-155 inhibition prolongs survival in ALS-model mice.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4127, doi. 10.1093/hmg/ddt261
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- Article
Regional chromatin decompaction in Cornelia de Lange syndrome associated with NIPBL disruption can be uncoupled from cohesin and CTCF.
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- Human Molecular Genetics, 2013, v. 22, n. 20, p. 4180, doi. 10.1093/hmg/ddt265
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 20, p. NP, doi. 10.1093/hmg/ddt473
- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 20, p. NP, doi. 10.1093/hmg/ddt471
- Publication type:
- Article