198 related articles for article (PubMed ID: 19270485)
21. Novel LMNA mutation in atypical Werner syndrome presenting with ischemic disease.
Renard D; Fourcade G; Milhaud D; Bessis D; Esteves-Vieira V; Boyer A; Roll P; Bourgeois P; Levy N; De Sandre-Giovannoli A
Stroke; 2009 Feb; 40(2):e11-4. PubMed ID: 19095983
[TBL] [Abstract][Full Text] [Related]
22. Elevation of urinary hyaluronic acid in Werner's syndrome and progeria.
Kieras FJ; Brown WT; Houck GE; Zebrower M
Biochem Med Metab Biol; 1986 Dec; 36(3):276-82. PubMed ID: 3801210
[TBL] [Abstract][Full Text] [Related]
23. A progeroid syndrome in mice is caused by defects in A-type lamins.
Mounkes LC; Kozlov S; Hernandez L; Sullivan T; Stewart CL
Nature; 2003 May; 423(6937):298-301. PubMed ID: 12748643
[TBL] [Abstract][Full Text] [Related]
24. Cytogenetics of Werner's syndrome cultured skin fibroblasts: variegated translocation mosaicism.
Salk D; Au K; Hoehn H; Martin GM
Cytogenet Cell Genet; 1981; 30(2):92-107. PubMed ID: 7273860
[TBL] [Abstract][Full Text] [Related]
25. DNA methylation signatures in Blood DNA of Hutchinson-Gilford Progeria syndrome.
Bejaoui Y; Razzaq A; Yousri NA; Oshima J; Megarbane A; Qannan A; Potabattula R; Alam T; Martin GM; Horn HF; Haaf T; Horvath S; El Hajj N
Aging Cell; 2022 Feb; 21(2):e13555. PubMed ID: 35045206
[TBL] [Abstract][Full Text] [Related]
26. Aging and nuclear organization: lamins and progeria.
Mounkes LC; Stewart CL
Curr Opin Cell Biol; 2004 Jun; 16(3):322-7. PubMed ID: 15145358
[TBL] [Abstract][Full Text] [Related]
27. Progeroid syndrome with scleroderma-like skin changes associated with homozygous R435C LMNA mutation.
Madej-Pilarczyk A; Rosińska-Borkowska D; Rekawek J; Marchel M; Szaluś E; Jabłońska S; Hausmanowa-Petrusewicz I
Am J Med Genet A; 2009 Nov; 149A(11):2387-92. PubMed ID: 19842191
[TBL] [Abstract][Full Text] [Related]
28. Diabetes mellitus coexisted with progeria: a case report of atypical Werner syndrome with novel LMNA mutations and literature review.
He G; Yan Z; Sun L; Lv Y; Guo W; Gang X; Wang G
Endocr J; 2019 Nov; 66(11):961-969. PubMed ID: 31270292
[TBL] [Abstract][Full Text] [Related]
29. Hyaluronate synthesized by cultured skin fibroblasts derived from patients with Werner's syndrome.
Nakamura T; Takagaki K; Kubo K; Saito T; Endo M; Mori S; Morisaki N; Saito Y; Yoshida S
Biochim Biophys Acta; 1992 Jun; 1139(1-2):84-90. PubMed ID: 1610921
[TBL] [Abstract][Full Text] [Related]
30. Differential stem cell aging kinetics in Hutchinson-Gilford progeria syndrome and Werner syndrome.
Wu Z; Zhang W; Song M; Wang W; Wei G; Li W; Lei J; Huang Y; Sang Y; Chan P; Chen C; Qu J; Suzuki K; Belmonte JCI; Liu GH
Protein Cell; 2018 Apr; 9(4):333-350. PubMed ID: 29476423
[TBL] [Abstract][Full Text] [Related]
31. A novel mutation in a patient with Werner's syndrome.
Nakayama T; Ochiai T; Takahashi Y; Ohkubo K; Hironaga T; Kokubun S
Gerontology; 2002; 48(4):215-9. PubMed ID: 12053110
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. A Case of Novel Lamin A/C Mutation Manifesting as Atypical Progeroid Syndrome and Cardiomyopathy.
Guo X; Ling C; Liu Y; Zhang X; Zhang S
Can J Cardiol; 2016 Sep; 32(9):1166.e29-31. PubMed ID: 27265359
[TBL] [Abstract][Full Text] [Related]
34. [Werner's syndrome and endocrine disorders].
Zantour B; Messaoud R; Zouali M; Ladjimi A; Braham H; Hamza H; Zebidi A; Sfar MH
Ann Endocrinol (Paris); 2003 Jun; 64(3):205-9. PubMed ID: 12910063
[TBL] [Abstract][Full Text] [Related]
35. Juvenile-onset generalized lipodystrophy due to a novel heterozygous missense LMNA mutation affecting lamin C.
Patni N; Xing C; Agarwal AK; Garg A
Am J Med Genet A; 2017 Sep; 173(9):2517-2521. PubMed ID: 28686329
[TBL] [Abstract][Full Text] [Related]
36. A subtype of laminopathies: Generalized lipodystrophy-associated progeroid syndrome caused by LMNA gene c.29C>T mutation.
Huang S; Zhang Y; Zhan Z; Gong S
J Diabetes Investig; 2023 Oct; 14(10):1221-1225. PubMed ID: 37448194
[TBL] [Abstract][Full Text] [Related]
37. Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance.
Liang L; Zhang H; Gu X
Acta Paediatr; 2009 Aug; 98(8):1365-8. PubMed ID: 19432833
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. [Werner syndrome-like disease in 3 brothers. Differential diagnosis of progeria syndrome].
Mensing H; Schaeg G; Burck U; Meigel W
Hautarzt; 1982 Oct; 33(10):542-7. PubMed ID: 7152896
[TBL] [Abstract][Full Text] [Related]
40. Dermal fibroblasts in Hutchinson-Gilford progeria syndrome with the lamin A G608G mutation have dysmorphic nuclei and are hypersensitive to heat stress.
Paradisi M; McClintock D; Boguslavsky RL; Pedicelli C; Worman HJ; Djabali K
BMC Cell Biol; 2005 Jun; 6():27. PubMed ID: 15982412
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]