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Repetitive disruptions of the nuclear envelope invoke temporary loss of cellular compartmentalization in laminopathies.
Published in:
Human Molecular Genetics, 2011, v. 20, n. 21, p. 4175, doi. 10.1093/hmg/ddr344
By:
- De Vos, Winnok H.;
- Houben, Frederik;
- Kamps, Miriam;
- Malhas, Ashraf;
- Verheyen, Fons;
- Cox, Juliën;
- Manders, Erik M.M.;
- Verstraeten, Valerie L.R.M.;
- van Steensel, Maurice A.M.;
- Marcelis, Carlo L.M.;
- van den Wijngaard, Arthur;
- Vaux, David J.;
- Ramaekers, Frans C.S.;
- Broers, Jos L.V.
Publication type:
Article
Compound heterozygosity for mutations in LMNA causes a progeria syndrome without prelamin A accumulation.
Published in:
Human Molecular Genetics, 2006, v. 15, n. 16, p. 2509, doi. 10.1093/hmg/ddl172
By:
- Verstraeten, Valerie L.R.M.;
- Broers, Jos L.V.;
- van Steensel, Maurice A.M.;
- Zinn-Justin, Sophie;
- Ramaekers, Frans C.S.;
- Steijlen, Peter M.;
- Kamps, Miriam;
- Kuijpers, Helma J.H.;
- Merckx, Diane;
- Smeets, Hubert J.M.;
- Hennekam, Raoul C.M.;
- Marcelis, Carlo L.M.;
- van den Wijngaard, Arthur
Publication type:
Article