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Lamin A/C deficiency is 'unnerving'

Mutations in the nuclear intermediate filament lamin A/C (LMNA) gene are associated with Emery-Dreifuss muscular dystrophy, but cause the disease by unknown mechanisms. Méjat et al. show that one mechanism ...

Biology /

created Jan 05, 2009 | popularity 3 / 5 (1) | comments 0




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Scientists develop novel technique to map protein interactions leading to better understanding of disease mechanisms

Scientists have developed a powerful new technique, named BioID, to screen for both interacting and neighboring proteins in their native cellular environment. Elucidating protein interactions is key to better understanding ...

Biology / Cell & Microbiology

created Mar 15, 2012 | popularity 3 / 5 (1) | comments 0

Researchers ID traits of people with rare accelerated aging syndrome

UT Southwestern Medical Center researchers have provided the most extensive account to date of the unique observable characteristics seen in patients with an extremely rare premature aging syndrome.

Medicine & Health / Diseases, Conditions, Syndromes

created Dec 15, 2009 | popularity not rated yet | comments 0


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