Found: 20
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Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3807, doi. 10.1093/hmg/ddt231
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- Article
Genome-wide loss of 5-hmC is a novel epigenetic feature of Huntington's disease.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3641, doi. 10.1093/hmg/ddt214
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- Article
Loss of dermatan sulfate epimerase (DSE) function results in musculocontractural Ehlers–Danlos syndrome.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3761, doi. 10.1093/hmg/ddt227
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- Article
Pharmacological chaperones as a potential therapeutic option in methylmalonic aciduria cblB type.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3680, doi. 10.1093/hmg/ddt217
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- Article
GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3609, doi. 10.1093/hmg/ddt212
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- Publication type:
- Article
Silencing of the Drosophila ortholog of SOX5 in heart leads to cardiac dysfunction as detected by optical coherence tomography.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3798
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- Publication type:
- Article
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3654, doi. 10.1093/hmg/ddt215
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- Article
ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3690, doi. 10.1093/hmg/ddt222
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- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. NP, doi. 10.1093/hmg/ddt416
- Publication type:
- Article
Dual AAV therapy ameliorates exercise-induced muscle injury and functional ischemia in murine models of Duchenne muscular dystrophy.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3720, doi. 10.1093/hmg/ddt224
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- Publication type:
- Article
A novel mouse model for genetic variation in 10-formyltetrahydrofolate synthetase exhibits disturbed purine synthesis with impacts on pregnancy and embryonic development.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3705, doi. 10.1093/hmg/ddt223
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- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. NP, doi. 10.1093/hmg/ddt415
- Publication type:
- Article
Enrichment of processed pseudogene transcripts in L1-ribonucleoprotein particles.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3730, doi. 10.1093/hmg/ddt225
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- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. NP, doi. 10.1093/hmg/ddt413
- Publication type:
- Article
The lysosomal inhibitor, chloroquine, increases cell surface BMPR-II levels and restores BMP9 signalling in endothelial cells harbouring BMPR-II mutations.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3667, doi. 10.1093/hmg/ddt216
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- Article
The functional genetic link of NLGN4X knockdown and neurodevelopment in neural stem cells.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3749, doi. 10.1093/hmg/ddt226
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- Article
The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3773, doi. 10.1093/hmg/ddt228
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- Publication type:
- Article
A Y328C missense mutation in spermine synthase causes a mild form of Snyder–Robinson syndrome.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3789, doi. 10.1093/hmg/ddt229
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- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. NP, doi. 10.1093/hmg/ddt414
- Publication type:
- Article
MicroRNA-22 and promoter motif polymorphisms at the Chga locus in genetic hypertension: functional and therapeutic implications for gene expression and the pathogenesis of hypertension.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3624, doi. 10.1093/hmg/ddt213
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- Publication type:
- Article