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Laminopathy
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1	Title: Spatial regulation of gene activity Instructor: Tokameh Mahmoudi Dept. of Biochemistry, email: Abstract Add to Reading List Source URL: www.erasmusmc.nl Language: English - Date: 2013-09-04 09:27:19 Lamin Nuclear membrane LMNA Progeria Cell nucleus Laminopathy Sankar Ghosh Biology Cell biology Nuclear lamina
2	Progeria Research Foundation Add to Reading List Source URL: www.progeriaresearch.org Language: English - Date: 2015-03-10 09:16:54 Rare diseases Aging Gerontology Progeria Syndromes Farnesyltransferase inhibitor Laminopathy Progerin Medical research Health Medicine Genodermatoses
3	QUICK FACTS as of November 1, 2014 MISSION: To Discover Treatments and the Cure for Hutchinson-Gilford Progeria Syndrome and its Aging-related Disorders PRF BY THE NUMBERS:  Identified children living with Progeria: 1 Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2014-11-20 11:24:49 Rare diseases Aging Gerontology Progeria Syndromes Farnesyltransferase inhibitor Laminopathy Progerin Medical research Health Medicine Genodermatoses
4	c Indian Academy of Sciences RESEARCH NOTE First report of a novel LMNA mutation in a Chinese family Add to Reading List Source URL: www.ias.ac.in Language: English - Date: 2015-01-06 06:22:19 LMNA Laminopathy Emery–Dreifuss muscular dystrophy Progeria Limb-girdle muscular dystrophy Dilated cardiomyopathy Lamin Nuclear lamina Mutation Health Muscular dystrophy Biology
5	The Progeria Handbook A Guide for Families & Health Care Providers of Children with Progeria The mission of The Progeria Research Foundation is to discover the cause, treatment, and cure for Hutchinson-Gilford Progeria S Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:20:00 Gerontology Genodermatoses Progeria LMNA Laminopathy Progerin Jonathan Hutchinson Senescence Health Medicine Aging
6	PDF Document Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:01:00 Aging Gerontology Rare diseases Progeria Syndromes LMNA Progerin Laminopathy Senescence Health Medicine Genodermatoses
7	De Novo LMNA Mutations Cause a New Form of Congenital Muscular Dystrophy Susana Quijano-Roy, MD, PhD,1–3 Blaise Mbieleu, MD,1 Carsten G. Bo¨nnemann, MD, PhD,4 Pierre-Yves Jeannet, MD, PhD,5 Jaume Colomer, MD,6 Nigel F Add to Reading List Source URL: curecmd.org Language: English - Date: 2010-05-05 13:30:48 Emery–Dreifuss muscular dystrophy Limb-girdle muscular dystrophy LMNA Hypotonia Dystrophin Congenital muscular dystrophy Facioscapulohumeral muscular dystrophy Dysferlin Duchenne muscular dystrophy Muscular dystrophy Health Laminopathy
8	QUICK FACTS as of June 30, 2014 MISSION: To Discover Treatments and the Cure for Hutchinson-Gilford Progeria Syndrome and its Aging-related Disorders PRF BY THE NUMBERS:  Identified children living with Progeria: 118* Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2014-07-13 09:40:59 Rare diseases Aging Gerontology Progeria Syndromes Farnesyltransferase inhibitor Laminopathy Progerin Medical research Health Medicine Genodermatoses
9	news W W W. P RO G E R I A R E S E A R C H . O R G • M AY, [removed]THE PRF TEAM MESSAGE FROM THE PRESIDENT Add to Reading List Source URL: progeriaresearch.org Language: English - Date: 2013-08-03 16:02:00 Aging Gerontology Genodermatoses Rare diseases Progeria Syndromes Hayley Okines Farnesyltransferase inhibitor Laminopathy Health Biology Medicine
10	news W W W. P RO G E R I A R E S E A R C H . O R G • M AY, [removed]THE PRF TEAM MESSAGE FROM THE PRESIDENT Add to Reading List Source URL: www.progeriaresearch.org Language: English - Date: 2013-08-03 16:02:00 Aging Gerontology Genodermatoses Rare diseases Progeria Syndromes Hayley Okines Farnesyltransferase inhibitor Laminopathy Health Biology Medicine