245 related articles for article (PubMed ID: 32413188)
1. Genotype-phenotype analysis of LMNA-related diseases predicts phenotype-selective alterations in lamin phosphorylation.
Lin EW; Brady GF; Kwan R; Nesvizhskii AI; Omary MB
FASEB J; 2020 Jul; 34(7):9051-9073. PubMed ID: 32413188
[TBL] [Abstract][Full Text] [Related]
2. In Silico and In Vivo Analysis of Amino Acid Substitutions That Cause Laminopathies.
Hinz BE; Walker SG; Xiong A; Gogal RA; Schnieders MJ; Wallrath LL
Int J Mol Sci; 2021 Oct; 22(20):. PubMed ID: 34681887
[TBL] [Abstract][Full Text] [Related]
3. Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies.
Nicolas HA; Bertrand AT; Labib S; Mohamed-Uvaize M; Bolongo PM; Wu WY; Bilińska ZT; Bonne G; Akimenko MA; Tesson F
Cells; 2020 Oct; 9(11):. PubMed ID: 33142761
[TBL] [Abstract][Full Text] [Related]
4. Novel clinical features and pleiotropic effect in three unrelated patients with LMNA variant.
Turkyilmaz A; Geçkinli BB; Alavanda C; Ates EA; Arman A
Clin Dysmorphol; 2021 Jan; 30(1):10-16. PubMed ID: 33038109
[TBL] [Abstract][Full Text] [Related]
5. Lamin A/C Mechanotransduction in Laminopathies.
Donnaloja F; Carnevali F; Jacchetti E; Raimondi MT
Cells; 2020 May; 9(5):. PubMed ID: 32456328
[TBL] [Abstract][Full Text] [Related]
6. Protein structural and mechanistic basis of progeroid laminopathies.
Marcelot A; Worman HJ; Zinn-Justin S
FEBS J; 2021 May; 288(9):2757-2772. PubMed ID: 32799420
[TBL] [Abstract][Full Text] [Related]
7. The laminopathies: a clinical review.
Rankin J; Ellard S
Clin Genet; 2006 Oct; 70(4):261-74. PubMed ID: 16965317
[TBL] [Abstract][Full Text] [Related]
8. Cardiometabolic assessment of lamin A/C gene mutation carriers: a phenotype-genotype correlation.
Kwapich M; Lacroix D; Espiard S; Ninni S; Brigadeau F; Kouakam C; Degroote P; Laurent JM; Tiffreau V; Jannin A; Humbert L; Ben Hamou A; Tard C; Ben Yaou R; Lamblin N; Klug D; Richard P; Vigouroux C; Bonne G; Vantyghem MC;
Diabetes Metab; 2019 Sep; 45(4):382-389. PubMed ID: 30287275
[TBL] [Abstract][Full Text] [Related]
9. Clinical and functional characterization of a novel mutation in lamin a/c gene in a multigenerational family with arrhythmogenic cardiac laminopathy.
Forleo C; Carmosino M; Resta N; Rampazzo A; Valecce R; Sorrentino S; Iacoviello M; Pisani F; Procino G; Gerbino A; Scardapane A; Simone C; Calore M; Torretta S; Svelto M; Favale S
PLoS One; 2015; 10(4):e0121723. PubMed ID: 25837155
[TBL] [Abstract][Full Text] [Related]
10. Systematic identification of pathological lamin A interactors.
Dittmer TA; Sahni N; Kubben N; Hill DE; Vidal M; Burgess RC; Roukos V; Misteli T
Mol Biol Cell; 2014 May; 25(9):1493-510. PubMed ID: 24623722
[TBL] [Abstract][Full Text] [Related]
11. Gene expression profiling of fibroblasts in a family with LMNA-related cardiomyopathy reveals molecular pathways implicated in disease pathogenesis.
Widyastuti HP; Norden-Krichmar TM; Grosberg A; Zaragoza MV
BMC Med Genet; 2020 Jul; 21(1):152. PubMed ID: 32698886
[TBL] [Abstract][Full Text] [Related]
12. Identification of Genes and Pathways Regulated by Lamin A in Heart.
Coste Pradas J; Auguste G; Matkovich SJ; Lombardi R; Chen SN; Garnett T; Chamberlain K; Riyad JM; Weber T; Singh SK; Robertson MJ; Coarfa C; Marian AJ; Gurha P
J Am Heart Assoc; 2020 Aug; 9(16):e015690. PubMed ID: 32805188
[TBL] [Abstract][Full Text] [Related]
13. The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins.
Al-Saaidi R; Rasmussen TB; Palmfeldt J; Nissen PH; Beqqali A; Hansen J; Pinto YM; Boesen T; Mogensen J; Bross P
Exp Cell Res; 2013 Nov; 319(19):3010-9. PubMed ID: 24001739
[TBL] [Abstract][Full Text] [Related]
14. A CRISPR/Cas9 zebrafish lamin A/C mutant model of muscular laminopathy.
Nicolas HA; Hua K; Quigley H; Ivare J; Tesson F; Akimenko MA
Dev Dyn; 2022 Apr; 251(4):645-661. PubMed ID: 34599606
[TBL] [Abstract][Full Text] [Related]
15. A Novel Lamin A Mutant Responsible for Congenital Muscular Dystrophy Causes Distinct Abnormalities of the Cell Nucleus.
Barateau A; Vadrot N; Vicart P; Ferreiro A; Mayer M; Héron D; Vigouroux C; Buendia B
PLoS One; 2017; 12(1):e0169189. PubMed ID: 28125586
[TBL] [Abstract][Full Text] [Related]
16. Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers.
Magagnotti C; Bachi A; Zerbini G; Fattore E; Fermo I; Riba M; Previtali SC; Ferrari M; Andolfo A; Benedetti S
Biochim Biophys Acta; 2012 Jun; 1822(6):970-9. PubMed ID: 22326558
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Genotype-phenotype correlations in laminopathies: how does fate translate?
Scharner J; Gnocchi VF; Ellis JA; Zammit PS
Biochem Soc Trans; 2010 Feb; 38(Pt 1):257-62. PubMed ID: 20074070
[TBL] [Abstract][Full Text] [Related]
19. Embryonic senescence and laminopathies in a progeroid zebrafish model.
Koshimizu E; Imamura S; Qi J; Toure J; Valdez DM; Carr CE; Hanai J; Kishi S
PLoS One; 2011 Mar; 6(3):e17688. PubMed ID: 21479207
[TBL] [Abstract][Full Text] [Related]
20. Clinical spectrum and genetic variations of
Fan Y; Tan D; Song D; Zhang X; Chang X; Wang Z; Zhang C; Chan SH; Wu Q; Wu L; Wang S; Yan H; Ge L; Yang H; Mao B; Bönnemann C; Liu J; Wang S; Yuan Y; Wu X; Zhang H; Xiong H
J Med Genet; 2021 May; 58(5):326-333. PubMed ID: 32571898
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
