Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations.
about
Tubulin Beta-3 Chain as a New Candidate Protein Biomarker of Human Skin Aging: A Preliminary Study.A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome.Disruption of PCNA-lamins A/C interactions by prelamin A induces DNA replication fork stalling.Relocalization of DNA lesions to the nuclear pore complex.Genetics of Short Stature.Identification of novel RNA isoforms of LMNA.A Tissue Engineered Blood Vessel Model of Hutchinson-Gilford Progeria Syndrome Using Human iPSC-derived Smooth Muscle CellsVitamin D deficiency accelerates ageing and age-related diseases: a novel hypothesis.Computational Exploration for Lead Compounds That Can Reverse the Nuclear Morphology in Progeria.Expression of lamina proteins Lamin and Kugelkern suppresses stem cell proliferation.Smurf2 regulates stability and the autophagic-lysosomal turnover of lamin A and its disease-associated form progerin.A Cell-Intrinsic Interferon-like Response Links Replication Stress to Cellular Aging Caused by Progerin.Targeting of NAT10 enhances healthspan in a mouse model of human accelerated aging syndrome.Causes and consequences of genomic instability in laminopathies: replication stress and interferon response.Progerin phosphorylation in interphase is lower and less mechanosensitive than lamin-A,C in iPS-derived mesenchymal stem cells.Inactivation of hepatic ATRX in Atrx Foxg1cre mice prevents reversal of aging-like phenotypes by thyroxine.Actin Dynamics Couples Extracellular Signals to the Mobility and Molecular Stability of TelomeresPhenotypic heterogeneity of ZMPSTE24 deficiency
P2860
Q33775713-34B064FB-6823-4CCB-972E-1D0809A580B0Q37741619-5E501478-0928-424A-B742-80DCA9411003Q38743495-EC44870A-7B83-407D-8022-7787A0CF984DQ38995558-24572E88-0FB7-4808-B0A6-918277E8C3E0Q39286284-E6F6E409-9E5A-4442-8D9E-18DD35E90326Q40501007-1114B32A-0CF2-4DBB-AEB0-ED80CD329476Q41422120-2546D649-6090-4847-95ED-CCA071DDA5CBQ46300548-2CC35562-2554-41B7-A391-A620624118B2Q46902686-43524CB0-A7B9-4C17-A97E-A3328785C29BQ47324874-9E89679A-643E-45A3-AE4A-39A2E756B689Q50188862-1D3B7F97-08E3-4359-A436-C2EA9EB81369Q50422448-E16240EE-4D67-40D2-B7C0-4F7C90D29907Q52691990-0D87F0DC-2B6C-44F5-94B9-D34E5525B492Q52720096-1EB0824B-4C8F-4E90-ACCD-AF987EAC7728Q55111725-831E814B-9045-499F-BDA7-640C0653562CQ55691576-A069A9FE-270A-454A-B2A7-A03F07AF0C6FQ57044278-CF459F99-887A-4610-95C2-3A8CC5615A2AQ57761604-0538D5B8-DE59-40FD-A35E-587B4C870914
P2860
Hutchinson-Gilford Progeria Syndrome: A premature aging disease caused by LMNA gene mutations.
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
Hutchinson-Gilford Progeria Sy ...... caused by LMNA gene mutations.
@en
type
label
Hutchinson-Gilford Progeria Sy ...... caused by LMNA gene mutations.
@en
prefLabel
Hutchinson-Gilford Progeria Sy ...... caused by LMNA gene mutations.
@en
P2093
P2860
P50
P1476
Hutchinson-Gilford Progeria Sy ...... caused by LMNA gene mutations
@en
P2093
Peter Askjaer
Ray Kreienkamp
Susana Gonzalo
P2860
P356
10.1016/J.ARR.2016.06.007
P577
2016-06-29T00:00:00Z