about
sameAs
The cell nucleus and aging: tantalizing clues and hopeful promisesThe nuclear envelopathies and human diseasesThe spectrum of WRN mutations in Werner syndrome patientsTMEM120A and B: Nuclear Envelope Transmembrane Proteins Important for Adipocyte DifferentiationAccumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndromeLamin B1 is required for mouse development and nuclear integrityHuman RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biologyThe epidemiology of premature aging and associated comorbiditiesRoles of Werner syndrome protein in protection of genome integrityTwo faces of p53: aging and tumor suppressionAltered protein dynamics of disease-associated lamin A mutantsMolecular insights into the premature aging disease progeriaSearch and insights into novel genetic alterations leading to classical and atypical Werner syndromeWhen lamins go bad: nuclear structure and diseaseThe role of RecQ helicases in non-homologous end-joiningOverlapping syndromes in laminopathies: a meta-analysis of the reported literatureInherited conduction system abnormalities--one group of diseases, many genesEpigenetic inactivation of the premature aging Werner syndrome gene in human cancerPOLD1 Germline Mutations in Patients Initially Diagnosed with Werner SyndromeWerner syndrome: Clinical features, pathogenesis and potential therapeutic interventionsDefects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient miceHow Research on Human Progeroid and Antigeroid Syndromes Can Contribute to the Longevity Dividend InitiativeOxidative stress and antioxidant response in fibroblasts from Werner and atypical Werner syndromes.Diseases of the nuclear envelope.The posttranslational processing of prelamin A and disease.Blocking protein farnesyltransferase improves nuclear shape in fibroblasts from humans with progeroid syndromesA Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) with Progeroid Features."Laminopathies": a wide spectrum of human diseases.Inner nuclear membrane proteins: impact on human disease.Chromatin remodeling, DNA damage repair and aging.Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation.Prelamin A, Zmpste24, misshapen cell nuclei, and progeria--new evidence suggesting that protein farnesylation could be important for disease pathogenesis.Molecular genetic analysis of the nested Drosophila melanogaster lamin C geneRole of the nuclear envelope in genome organization and gene expression.Generation of induced pluripotent stem cell lines from 3 distinct laminopathies bearing heterogeneous mutations in lamin A/CEmerin-lacking mice show minimal motor and cardiac dysfunctions with nuclear-associated vacuoles.Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid featuresOverlapping syndrome with familial partial lipodystrophy, Dunnigan variety and cardiomyopathy due to amino-terminal heterozygous missense lamin A/C mutationsNanotopography alters nuclear protein expression, proliferation and differentiation of human mesenchymal stem/stromal cellsPhenotype-Genotype Analysis of Chinese Patients with Early-Onset LMNA-Related Muscular Dystrophy.
P2860
Q21090227-E28A5C12-FDB7-4801-B4AA-27BD450E201AQ21284427-4D64ADB3-73C7-4378-B1F7-8E7870A32844Q24324195-B337A550-48E0-49C0-B86A-1E92D32D5E89Q24337875-CFDE5DA1-377C-4BED-8DE7-FAA1CEAA743CQ24562621-9346A01C-6A65-4754-80FE-91078AFE27BBQ24564213-43E6FF18-E61F-4322-A95B-17735C017FADQ24620195-0EC9CA2D-A94F-4D36-B26F-B0B6845270BDQ24628974-FBCC428A-B9DD-42D2-B279-BE64F1AE58FCQ24643050-5B6C992B-005E-4F1F-9081-6D94217677EFQ24681014-CD72ACBF-04D4-45FE-91EF-0CD16DF48B50Q24791233-E962D11C-4762-46DA-B17E-341583B14F7CQ26768972-8300F057-D0D8-48BF-BE3E-B58DB885A9EDQ26825460-4681133E-79A0-4F98-B7C4-30324058EEC9Q26827624-707FEA02-4070-43F9-BD93-7EB84C1018B1Q26829119-C70BEEED-43DE-48D6-A85E-DC7BDE1E04F4Q26851708-AD2EC65A-1835-4C7E-82F8-2956E9A2E8AAQ28236888-A3E7BBC1-C750-4CD9-897A-BABC610585E5Q28242111-836EF5CE-6564-4F2A-A0BC-49B9D8F441D6Q28265079-BDF23480-8597-4E3B-BA5A-00E4F8CE72E3Q28274227-6BEDCF42-DDEF-48E1-B69D-D233E7C8F233Q28591672-43963D95-25F8-48DD-832F-C18D63DE0949Q28601451-B3149E45-3F79-443C-A9C7-0C3EBE094173Q33577727-AA60BB18-82CD-42AA-B72B-614BDE9A4158Q33687043-3F0E5ECC-CF01-4A9A-A56F-E9D648A6631AQ33758494-AE326936-E599-499C-A161-D9355CD34C6DQ33930224-B97AE5AA-E2F2-4892-A95C-E29401208983Q34215118-D682A3D9-20CE-49DA-B3BE-3E1CC0C6F7D3Q34242119-2BD672E4-F957-4F7F-8C79-AA3F972690E5Q34252203-187EAA62-29D5-4768-B5FB-47147C317F54Q34342179-ACBC10EC-E604-4927-BBC5-693C6319C1AAQ34440150-B9BDB7DD-A30E-4184-A4C8-AD7479ED831EQ34457223-56504F14-93E1-4B3A-8B47-93B3CAA77829Q34588990-BCF826EA-6244-4E6E-9F76-DB9C427CDCA9Q34632599-4B2F80E6-ED28-4249-9254-F9704626A45AQ35052074-355A2A83-FBFC-4FC2-8E8D-D5091CE7D2BBQ35088026-6BAEF243-3A71-4716-8CC8-1972CB58A8FAQ35129273-7AB3197D-1679-4BD3-B799-BB02028C190CQ35148933-F7A48ABC-FF47-426A-97A7-FF54E057D90CQ35529662-10921664-3ABE-4C73-BFC7-EE2025B7664BQ35670575-FA4DD368-97D2-4370-8B80-18E5514D1066
P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
LMNA mutations in atypical Werner's syndrome
@ast
LMNA mutations in atypical Werner's syndrome
@en
LMNA mutations in atypical Werner's syndrome
@nl
type
label
LMNA mutations in atypical Werner's syndrome
@ast
LMNA mutations in atypical Werner's syndrome
@en
LMNA mutations in atypical Werner's syndrome
@nl
prefLabel
LMNA mutations in atypical Werner's syndrome
@ast
LMNA mutations in atypical Werner's syndrome
@en
LMNA mutations in atypical Werner's syndrome
@nl
P2093
P1433
P1476
LMNA mutations in atypical Werner's syndrome
@en
P2093
Abhimanyu Garg
Brian A Kudlow
Brian K Kennedy
Eleanor G Botha
George M Martin
Heloisa G Dos Santos
I Saira Mian
Junko Oshima
Lishan Chen
P356
10.1016/S0140-6736(03)14069-X
P407
P577
2003-08-09T00:00:00Z