Hutchinson-Gilford progeria patient-derived cardiomyocyte model of carrying LMNA gene variant c.1824 C > T

Author:

Perales Selene,Sigamani Vinoth,Rajasingh Sheeja,Czirok Andras,Rajasingh JohnsonORCID

Funder

NHLBI Division of Intramural Research

American Heart Association

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Histology,Pathology and Forensic Medicine

Reference43 articles.

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2. Bishop WR, Doll R, Kirschmeier P (2011) 15 - Farnesyl Transferase inhibitors: from targeted cancer therapeutic to a potential treatment for progeria. In: Tamanoi F, Hrycyna CA, Bergo MO (eds) The Enzymes, vol 29. Academic Press, pp 275–303

3. Bolderson E, Burgess JT, Li J, Gandhi NS, Boucher D, Croft LV, Beard S, Plowman JJ, Suraweera A, Adams MN, Naqi A, Zhang SD, Sinclair DA, O’Byrne KJ, Richard DJ (2019) Barrier-to-autointegration factor 1 (Banf1) regulates poly [ADP-ribose] polymerase 1 (PARP1) activity following oxidative DNA damage. Nat Commun 10(1):5501. https://doi.org/10.1038/s41467-019-13167-5

4. Bonne G, Barletta MRD, Varnous S, Bécane H-M, Hammouda E-H, Merlini L, Muntoni F, Greenberg CR, Gary F, Urtizberea J-A (1999) Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat Genet 21(3):285–288

5. Brodsky GL, Muntoni F, Miocic S, Sinagra G, Sewry C, Mestroni L (2000) Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement. Circulation 101(5):473–476

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