نتایج جستجو برای: werner syndrome

تعداد نتایج: 624484  

Journal: :Journal of Evolution of Medical and Dental Sciences 2015

2017
Daisuke Kinoshita Ayako Nagasawa Ippei Shimizu Takashi K. Ito Yohko Yoshida Masanori Tsuchida Atsushi Iwama Toshiya Hayano Tohru Minamino

Mutations of the lamin A gene cause various premature aging syndromes, including Hutchinson-Gilford progeria syndrome (HGPS) and atypical Werner syndrome. In HGPS (but not atypical Werner syndrome), extensive loss of vascular smooth muscle cells leads to myocardial infarction with premature death. The underlying mechanisms how single gene mutations can cause various phenotypes are largely unkno...

Journal: :The Journal of biological chemistry 2001
R M Brosh A Majumdar S Desai I D Hickson V A Bohr M M Seidman

Bloom syndrome and Werner syndrome are genome instability disorders, which result from mutations in two different genes encoding helicases. Both enzymes are members of the RecQ family of helicases, have a 3' --> 5' polarity, and require a 3' single strand tail. In addition to their activity in unwinding duplex substrates, recent studies show that the two enzymes are able to unwind G2 and G4 tet...

Journal: :Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 2014

Journal: :Stroke 2009
Dimitri Renard Genevieve Fourcade Didier Milhaud Didier Bessis Vera Esteves-Vieira Amandine Boyer Patrice Roll Patrice Bourgeois Nicolas Levy Annachiara De Sandre-Giovannoli

BACKGROUND AND PURPOSE Laminopathies arise through mutations in genes encoding Lamin A/C (LMNA) or associated proteins. They cause 4 different groups of disorders with diverse severity and often overlapping features: diseases of striated muscle (leading to muscular or cardiac involvement), peripheral neuropathy, lipodystrophy syndromes, and accelerated aging disorders. SUMMARY OF CASE We repo...

Journal: :Clinical, Cosmetic and Investigational Dermatology 2018

Journal: :European Journal of Human Genetics 2012

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