Concepedia

Mislocalization of prelamin A Tyr646Phe mutant to the nuclear pore complex in human embryonic kidney 293 cells

Yong Hua Pan, Abhimanyu Garg, Anil K. Agarwal

Biochemical and Biophysical Research Communications · 2007 · 20 citations · 17 references

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17

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

Maria Eriksson, W. Ted Brown, Leslie B. Gordon et al. · Nature · 2003 · 2.2K citations · Full text

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Lamin A Truncation in Hutchinson-Gilford Progeria

Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, Pierre Cau et al. · Science · 2003 · 1.5K citations

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Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

Fan Lin, Howard J. Worman · Journal of Biological Chemistry · 1993 · 624 citations · Full text

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Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome

Brian C. Capell, Michael R. Erdos, James P. Madigan et al. · Proceedings of the National Academy of Sciences · 2005 · 388 citations · Full text

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Ras CAAX Peptidomimetic FTI-277 Selectively Blocks Oncogenic Ras Signaling by Inducing Cytoplasmic Accumulation of Inactive Ras-Raf Complexes

Edwina C. Lerner, Yimin Qian, Michelle A. Blaskovich et al. · Journal of Biological Chemistry · 1995 · 360 citations · Full text

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