419 related articles for article (PubMed ID: 28857661)
21. Truncated prelamin A expression in HGPS-like patients: a transcriptional study.
Barthélémy F; Navarro C; Fayek R; Da Silva N; Roll P; Sigaudy S; Oshima J; Bonne G; Papadopoulou-Legbelou K; Evangeliou AE; Spilioti M; Lemerrer M; Wevers RA; Morava E; Robaglia-Schlupp A; Lévy N; Bartoli M; De Sandre-Giovannoli A
Eur J Hum Genet; 2015 Aug; 23(8):1051-61. PubMed ID: 25649378
[TBL] [Abstract][Full Text] [Related]
22. Hutchinson-Gilford progeria syndrome through the lens of transcription.
Prokocimer M; Barkan R; Gruenbaum Y
Aging Cell; 2013 Aug; 12(4):533-43. PubMed ID: 23496208
[TBL] [Abstract][Full Text] [Related]
23. LMNA-associated cardiocutaneous progeria: an inherited autosomal dominant premature aging syndrome with late onset.
Kane MS; Lindsay ME; Judge DP; Barrowman J; Ap Rhys C; Simonson L; Dietz HC; Michaelis S
Am J Med Genet A; 2013 Jul; 161A(7):1599-611. PubMed ID: 23666920
[TBL] [Abstract][Full Text] [Related]
24. A lamin A protein isoform overexpressed in Hutchinson-Gilford progeria syndrome interferes with mitosis in progeria and normal cells.
Cao K; Capell BC; Erdos MR; Djabali K; Collins FS
Proc Natl Acad Sci U S A; 2007 Mar; 104(12):4949-54. PubMed ID: 17360355
[TBL] [Abstract][Full Text] [Related]
25. Eliminating the synthesis of mature lamin A reduces disease phenotypes in mice carrying a Hutchinson-Gilford progeria syndrome allele.
Yang SH; Qiao X; Farber E; Chang SY; Fong LG; Young SG
J Biol Chem; 2008 Mar; 283(11):7094-9. PubMed ID: 18178963
[TBL] [Abstract][Full Text] [Related]
26. Towards delineating the chain of events that cause premature senescence in the accelerated aging syndrome Hutchinson-Gilford progeria (HGPS).
Dreesen O
Biochem Soc Trans; 2020 Jun; 48(3):981-991. PubMed ID: 32539085
[TBL] [Abstract][Full Text] [Related]
27. [Hutchinson-Gilford progeria in the light of contemporary genetics].
Madej-Pilarczyk A
Med Wieku Rozwoj; 2006; 10(1 Pt 2):355-62. PubMed ID: 17028399
[TBL] [Abstract][Full Text] [Related]
28. Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newborn.
Reunert J; Wentzell R; Walter M; Jakubiczka S; Zenker M; Brune T; Rust S; Marquardt T
Eur J Hum Genet; 2012 Sep; 20(9):933-7. PubMed ID: 22419169
[TBL] [Abstract][Full Text] [Related]
29. Antagonistic functions of LMNA isoforms in energy expenditure and lifespan.
Lopez-Mejia IC; de Toledo M; Chavey C; Lapasset L; Cavelier P; Lopez-Herrera C; Chebli K; Fort P; Beranger G; Fajas L; Amri EZ; Casas F; Tazi J
EMBO Rep; 2014 May; 15(5):529-39. PubMed ID: 24639560
[TBL] [Abstract][Full Text] [Related]
30. Inhibiting farnesylation of progerin prevents the characteristic nuclear blebbing of Hutchinson-Gilford progeria syndrome.
Capell BC; Erdos MR; Madigan JP; Fiordalisi JJ; Varga R; Conneely KN; Gordon LB; Der CJ; Cox AD; Collins FS
Proc Natl Acad Sci U S A; 2005 Sep; 102(36):12879-84. PubMed ID: 16129833
[TBL] [Abstract][Full Text] [Related]
31. Epigenetic involvement in Hutchinson-Gilford progeria syndrome: a mini-review.
Arancio W; Pizzolanti G; Genovese SI; Pitrone M; Giordano C
Gerontology; 2014; 60(3):197-203. PubMed ID: 24603298
[TBL] [Abstract][Full Text] [Related]
32. [The role of lamins and mutations of LMNA gene in physiological and premature aging].
Sliwińska MA
Postepy Biochem; 2007; 53(1):46-52. PubMed ID: 17718387
[TBL] [Abstract][Full Text] [Related]
33. Antisense oligonucleotide induction of progerin in human myogenic cells.
Luo YB; Mitrpant C; Adams AM; Johnsen RD; Fletcher S; Mastaglia FL; Wilton SD
PLoS One; 2014; 9(6):e98306. PubMed ID: 24892300
[TBL] [Abstract][Full Text] [Related]
34. Interplay of primary sequence, position and secondary RNA structure determines alternative splicing of LMNA in a pre-mature aging syndrome.
Shilo A; Tosto FA; Rausch JW; Le Grice SFJ; Misteli T
Nucleic Acids Res; 2019 Jun; 47(11):5922-5935. PubMed ID: 31006814
[TBL] [Abstract][Full Text] [Related]
35. Investigation of splicing changes and post-translational processing of LMNA in sporadic inclusion body myositis.
Luo YB; Mitrpant C; Johnsen R; Fabian V; Needham M; Fletcher S; Wilton SD; Mastaglia FL
Int J Clin Exp Pathol; 2013; 6(9):1723-33. PubMed ID: 24040437
[TBL] [Abstract][Full Text] [Related]
36. In vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice.
Koblan LW; Erdos MR; Wilson C; Cabral WA; Levy JM; Xiong ZM; Tavarez UL; Davison LM; Gete YG; Mao X; Newby GA; Doherty SP; Narisu N; Sheng Q; Krilow C; Lin CY; Gordon LB; Cao K; Collins FS; Brown JD; Liu DR
Nature; 2021 Jan; 589(7843):608-614. PubMed ID: 33408413
[TBL] [Abstract][Full Text] [Related]
37. Discordant gene expression signatures and related phenotypic differences in lamin A- and A/C-related Hutchinson-Gilford progeria syndrome (HGPS).
Plasilova M; Chattopadhyay C; Ghosh A; Wenzel F; Demougin P; Noppen C; Schaub N; Szinnai G; Terracciano L; Heinimann K
PLoS One; 2011; 6(6):e21433. PubMed ID: 21738662
[TBL] [Abstract][Full Text] [Related]
38. Coronary artery disease in a Werner syndrome-like form of progeria characterized by low levels of progerin, a splice variant of lamin A.
Hisama FM; Lessel D; Leistritz D; Friedrich K; McBride KL; Pastore MT; Gottesman GS; Saha B; Martin GM; Kubisch C; Oshima J
Am J Med Genet A; 2011 Dec; 155A(12):3002-6. PubMed ID: 22065502
[TBL] [Abstract][Full Text] [Related]
39. Dysregulated interactions between lamin A and SUN1 induce abnormalities in the nuclear envelope and endoplasmic reticulum in progeric laminopathies.
Chen ZJ; Wang WP; Chen YC; Wang JY; Lin WH; Tai LA; Liou GG; Yang CS; Chi YH
J Cell Sci; 2014 Apr; 127(Pt 8):1792-804. PubMed ID: 24522183
[TBL] [Abstract][Full Text] [Related]
40. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome.
Eriksson M; Brown WT; Gordon LB; Glynn MW; Singer J; Scott L; Erdos MR; Robbins CM; Moses TY; Berglund P; Dutra A; Pak E; Durkin S; Csoka AB; Boehnke M; Glover TW; Collins FS
Nature; 2003 May; 423(6937):293-8. PubMed ID: 12714972
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
