Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP R1
Results: 17
Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD–ALS spectrum disorders.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R77, doi. 10.1093/hmg/ddt349
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- Publication type:
- Article
Subscription Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. NP, doi. 10.1093/hmg/ddt483
- Publication type:
- Article
Contents Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. NP, doi. 10.1093/hmg/ddt480
- Publication type:
- Article
Repeat-associated non-ATG (RAN) translation in neurological disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R45, doi. 10.1093/hmg/ddt371
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- Publication type:
- Article
Sequencing the human microbiome in health and disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R88, doi. 10.1093/hmg/ddt398
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- Publication type:
- Article
In search of low-frequency and rare variants affecting complex traits.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R16, doi. 10.1093/hmg/ddt376
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- Publication type:
- Article
Cover Page.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. NP, doi. 10.1093/hmg/ddt481
- Publication type:
- Article
Advances in the genomics of common eye diseases.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R59, doi. 10.1093/hmg/ddt396
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- Publication type:
- Article
PTPs emerge as PIPs: protein tyrosine phosphatases with lipid-phosphatase activities in human disease.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R66, doi. 10.1093/hmg/ddt347
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- Publication type:
- Article
The evolving epigenome.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R1, doi. 10.1093/hmg/ddt348
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- Publication type:
- Article
Age-associated epigenetic drift: implications, and a case of epigenetic thrift?
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R7, doi. 10.1093/hmg/ddt375
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- Publication type:
- Article
The molecular pathogenesis of migraine: new developments and opportunities.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R39, doi. 10.1093/hmg/ddt364
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- Publication type:
- Article
Databases of genomic variation and phenotypes: existing resources and future needs.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R27, doi. 10.1093/hmg/ddt384
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- Publication type:
- Article
Editorial Board.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. NP, doi. 10.1093/hmg/ddt482
- Publication type:
- Article
Back to the future: how human induced pluripotent stem cells will transform regenerative medicine.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R32, doi. 10.1093/hmg/ddt379
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- Publication type:
- Article
The applications of single-cell genomics.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R22, doi. 10.1093/hmg/ddt377
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- Publication type:
- Article
Moving forward: cystic fibrosis gene therapy.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. R1, p. R52, doi. 10.1093/hmg/ddt372
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- Publication type:
- Article