An Overview of Hutchinson Gilford Progeria Syndrome (HGPS)
British Journal of Medicine and Medical Research, 2015 Hutchinson Gilford Progeria Syndrome (HGPS) is a rare genetic disorder. The disorder is characterized by premature aging, generally leading to death. The purpose of this article is to review Hutchinson Gilford Progeria Syndrome and its characteristics.
Maria Tsiligiri +3 more
openaire +1 more source
A Population of Teraelectronvolt Pulsar Wind Nebulae in the H.E.S.S. Galactic Plane Survey
, 2013 The most numerous source class that emerged from the H.E.S.S. Galactic Plane Survey are Pulsar Wind Nebulae (PWNe). The 2013 reanalysis of this survey, undertaken after almost 10 years of observations, provides us with the most sensitive and most ...
Carrigan, S. +9 more
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Enhancement of height system for Malaysia using space technology: the study of the datum bias inconsistencies in Peninsular Malaysia [PDF]
, 2003 The algorithm for orthometric height transfer using GPS has been widely presented. Its practical limitations are mostly due to datum bias inconsistencies and lack of precise geoid.
Mohamed, Azhari +2 more
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Free-standing hybrid films based on graphene and porous carbon particles for flexible supercapacitors [PDF]
, 2017 Free-standing flexible solid-state supercapacitors are attracting attention as a power supply for electronic equipment. Here we report a novel strategy to fabricate free-standing flexible hybrid papers made up of porous carbon particles combined with ...
Fuertes Arias, Antonio Benito +2 more
core +1 more source
Progerin reduces LAP2α-telomere association in Hutchinson-Gilford progeria
eLife, 2015 Hutchinson-Gilford progeria (HGPS) is a premature ageing syndrome caused by a mutation in LMNA, resulting in a truncated form of lamin A called progerin.
Alexandre Chojnowski +15 more
doaj +1 more source
Cells, 2019 Hutchinson-Gilford progeria syndrome (HGPS), a rare premature aging disorder that leads to death at an average age of 14.7 years due to myocardial infarction or stroke, is caused by mutations in the LMNA gene.
Chang Liu +3 more
doaj +1 more source
Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome
Protein & Cell, 2018 Hutchinson-Gilford progeria syndrome (HGPS) and Werner syndrome (WS) are two of the best characterized human progeroid syndromes. HGPS is caused by a point mutation in lamin A (LMNA) gene, resulting in the production of a truncated protein product ...
Zeming Wu +14 more
doaj +1 more source
Fluidez social y política: hacia un diálogonecesario [PDF]
, 2017 Background of INCASI Project H2020-MSCA-RISE-2015 GA 691004. WP1: CompilationLa relació de la mobilitat social amb la política és d'una naturalesa enormement complexa. En aquest article, tractarem de llançar una mica de llum sobre aquesta confusa relació.
Gil Hernández, Carlos +2 more
core +3 more sources
Pluripotent stem cells for pathological modelling of Hutchinson-Gilford Progeria Syndrome (HGPS) and drug discovery [PDF]
, 2015 Xavier Nissan
openalex +1 more source
On the Succinctness of Query Rewriting over OWL 2 QL Ontologies with Shallow Chases [PDF]
, 2014 We investigate the size of first-order rewritings of conjunctive queries over OWL 2 QL ontologies of depth 1 and 2 by means of hypergraph programs computing Boolean functions. Both positive and negative results are obtained.
Kikot, Stanislav +3 more
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