Works matching IS 09646906 AND DT 2013 AND VI 22 AND IP R1

Results: 17

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

By:

Cleary, John D.;
Ranum, Laura P.W.

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

By:

Cooke Bailey, Jessica N.;
Sobrin, Lucia;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.;
Hammond, Christopher J.;
Wiggs, Janey L.

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

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

By:

Janssens, Jonathan;
Van Broeckhoven, Christine

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

By:

Cox, Michael J.;
Cookson, William O.C.M.;
Moffatt, Miriam F.

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

By:

Panoutsopoulou, Kalliope;
Tachmazidou, Ioanna;
Zeggini, Eleftheria

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

By:

Zameel Cader, M.

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

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

By:

Pulido, Rafael;
Stoker, Andrew W.;
Hendriks, Wiljan J.A.J.

Publication type:

Article

The evolving epigenome.

Published in:

Human Molecular Genetics, 2013, v. 22, n. R1, p. R1, doi. 10.1093/hmg/ddt348

By:

Weichenhan, Dieter;
Plass, Christoph

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

By:

Teschendorff, Andrew E.;
West, James;
Beck, Stephan

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

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

By:

Johnston, Jennifer J.;
Biesecker, Leslie G.

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

By:

Svendsen, Clive N.

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

By:

Lovett, Michael

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

By:

Griesenbach, Uta;
Alton, Eric W.F.W.

Publication type:

Article