Related references
Note: Only part of the references are listed.Laminopathies and the long strange trip from basic cell biology to therapy
Howard J. Worman et al.
JOURNAL OF CLINICAL INVESTIGATION (2009)
Progerin elicits disease phenotypes of progeria in mice whether or not it is farnesylated
Shao H. Yang et al.
JOURNAL OF CLINICAL INVESTIGATION (2008)
Specific and conserved sequences in D-melanogaster and C-elegans lamins and histone H2A mediate the attachment of lamins to chromosomes
Anna Mattout et al.
JOURNAL OF CELL SCIENCE (2007)
Lamin B1 duplications cause autosomal dominant leukodystrophy
Quasar S. Padiath et al.
NATURE GENETICS (2006)
A farnesyltransferase inhibitor improves disease phenotypes in mice with a Hutchinson-Gilford progeria syndrome mutation
Shao H. Yang et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy
Robert A. Hegele et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Mutant nuclear lamin A leads to progressive alterations of epigenetic control in premature aging
Dale K. Shumaker et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
The truncated prelamin A in Hutchinson-Gilford progeria syndrome alters segregation of A-type and B-type lamin homopolymers
E Delbarre et al.
HUMAN MOLECULAR GENETICS (2006)
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
M Columbaro et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2005)
Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome
P Scaffidi et al.
NATURE MEDICINE (2005)
Expression and purification of recombinant human histones
Y Tanaka et al.
METHODS (2004)
Conformation, orientation, and adsorption kinetics of dermaseptin B2 onto synthetic supports at aqueous/solid interface
S Noinville et al.
BIOPHYSICAL JOURNAL (2003)
Lamin A truncation in Hutchinson-Gilford progeria
A De Sandre-Giovannoli et al.
SCIENCE (2003)
Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome
M Eriksson et al.
NATURE (2003)
The carboxyl-terminal region common to lamins A and C contains a DNA binding domain
VN Stierlé et al.
BIOCHEMISTRY (2003)