63 related articles for article (PubMed ID: 19591272)
1. Early-onset diabetes mellitus as a presenting feature of Werner's syndrome in an Indian family.
Hoff FW; Xing C; Simha V; Agarwal AK; Zhang X; Lekkala L; Vaishnav MS; Vuitch F; Garg A
Mol Genet Genomic Med; 2024 Jan; 12(1):e2299. PubMed ID: 37815015
[TBL] [Abstract][Full Text] [Related]
2. From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.
Cox LS; Faragher RG
Cell Mol Life Sci; 2007 Oct; 64(19-20):2620-41. PubMed ID: 17660942
[TBL] [Abstract][Full Text] [Related]
3. A Case Report of Werner's Syndrome With a Novel Mutation From India.
Singh A; Ganguly S; Chhabra N; Yadav H; Oshima J
Cureus; 2020 May; 12(5):e8025. PubMed ID: 32528764
[TBL] [Abstract][Full Text] [Related]
4. Human progeroid syndromes, aging and cancer: new genetic and epigenetic insights into old questions.
Ramírez CL; Cadiñanos J; Varela I; Freije JM; López-Otín C
Cell Mol Life Sci; 2007 Jan; 64(2):155-70. PubMed ID: 17131053
[TBL] [Abstract][Full Text] [Related]
5. Review of How Genetic Research on Segmental Progeroid Syndromes Has Documented Genomic Instability as a Hallmark of Aging But Let Us Now Pursue Antigeroid Syndromes!
Martin GM; Hisama FM; Oshima J
J Gerontol A Biol Sci Med Sci; 2021 Jan; 76(2):253-259. PubMed ID: 33295962
[TBL] [Abstract][Full Text] [Related]
6. Looking for disease being a model of human aging.
Hausmanowa-Petrusewicz I; Madej-Pilarczyk A
Acta Myol; 2007 Oct; 26(2):101-4. PubMed ID: 18421896
[TBL] [Abstract][Full Text] [Related]
7. The Legacy of George M. Martin: From Segmental Progeroid Syndromes to Antigeroid Syndromes.
Poot M
Cytogenet Genome Res; 2023; 163(5-6):231-235. PubMed ID: 38522422
[No Abstract] [Full Text] [Related]
8. Werner syndrome (WRN) gene variants and their association with altered function and age-associated diseases.
Lebel M; Monnat RJ
Ageing Res Rev; 2018 Jan; 41():82-97. PubMed ID: 29146545
[TBL] [Abstract][Full Text] [Related]
9. Targeted inhibition of WRN helicase, replication stress and cancer.
Orlovetskie N; Serruya R; Abboud-Jarrous G; Jarrous N
Biochim Biophys Acta Rev Cancer; 2017 Jan; 1867(1):42-48. PubMed ID: 27902925
[TBL] [Abstract][Full Text] [Related]
10. Werner syndrome: Clinical features, pathogenesis and potential therapeutic interventions.
Oshima J; Sidorova JM; Monnat RJ
Ageing Res Rev; 2017 Jan; 33():105-114. PubMed ID: 26993153
[TBL] [Abstract][Full Text] [Related]
11. LMNA mutations in progeroid syndromes.
Huang S; Kennedy BK; Oshima J
Novartis Found Symp; 2005; 264():197-202; discussion 202-7, 227-30. PubMed ID: 15773755
[TBL] [Abstract][Full Text] [Related]
12. LMNA mutations in atypical Werner's syndrome.
Chen L; Lee L; Kudlow BA; Dos Santos HG; Sletvold O; Shafeghati Y; Botha EG; Garg A; Hanson NB; Martin GM; Mian IS; Kennedy BK; Oshima J
Lancet; 2003 Aug; 362(9382):440-5. PubMed ID: 12927431
[TBL] [Abstract][Full Text] [Related]
13. Werner's syndrome helicase participates in transcription of phenobarbital-inducible CYP2B genes in rat and mouse liver.
Lachaud AA; Auclair-Vincent S; Massip L; Audet-Walsh E; Lebel M; Anderson A
Biochem Pharmacol; 2010 Feb; 79(3):463-70. PubMed ID: 19737542
[TBL] [Abstract][Full Text] [Related]
14. [WRN gene].
Katsuya T; Morishita R
Nihon Rinsho; 2009 Jul; 67(7):1277-82. PubMed ID: 19591272
[TBL] [Abstract][Full Text] [Related]
15. Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.
Kihara K; Nakura J; Ye L; Mitsuda N; Kamino K; Zhao Y; Fujioka Y; Miki T; Ogihara T
Jpn J Hum Genet; 1994 Dec; 39(4):403-9. PubMed ID: 7873752
[TBL] [Abstract][Full Text] [Related]
16. The Werner's Syndrome RecQ helicase/exonuclease at the nexus of cancer and aging.
Chun SG; Shaeffer DS; Bryant-Greenwood PK
Hawaii Med J; 2011 Mar; 70(3):52-5. PubMed ID: 21365542
[TBL] [Abstract][Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
