156 related articles for article (PubMed ID: 30919159)
1. Rs10230207 genotype confers changes in HDAC9 and TWIST1, but not FERD3L in lymphoblasts from patients with intracranial aneurysm.
Lansdell TA; Fisher C; Simmonds K; Reeves MJ; Woo D; Dorrance AM; Demel SL
Neurogenetics; 2019 May; 20(2):83-89. PubMed ID: 30919159
[TBL] [Abstract][Full Text] [Related]
2. HDAC9, TWIST1 and FERD3L gene expression in asymptomatic stable and unstable carotid plaques.
Ferronato S; Gelati M; Scuro A; Olivato S; Malerba G; Romanelli MG; Gomez-Lira M; Setacci C
Inflamm Res; 2016 Apr; 65(4):261-3. PubMed ID: 26621503
[TBL] [Abstract][Full Text] [Related]
3. Deficiency of the stroke relevant HDAC9 gene attenuates atherosclerosis in accord with allele-specific effects at 7p21.1.
Azghandi S; Prell C; van der Laan SW; Schneider M; Malik R; Berer K; Gerdes N; Pasterkamp G; Weber C; Haffner C; Dichgans M
Stroke; 2015 Jan; 46(1):197-202. PubMed ID: 25388417
[TBL] [Abstract][Full Text] [Related]
4. Histone deacetylase 9 inhibition upregulates microRNA-92a to repress the progression of intracranial aneurysm via silencing Bcl-2-like protein 11.
Cai Y; Huang D; Ma W; Wang M; Qin Q; Jiang Z; Liu M
J Drug Target; 2021 Aug; 29(7):761-770. PubMed ID: 33480300
[TBL] [Abstract][Full Text] [Related]
5.
Hirsch N; Dahan I; D'haene E; Avni M; Vergult S; Vidal-García M; Magini P; Graziano C; Severi G; Bonora E; Nardone AM; Brancati F; Fernández-Jaén A; Rory OJ; Hallgrímsson B; Birnbaum RY
Genome Res; 2022 Jul; 32(7):1242-1253. PubMed ID: 35710300
[TBL] [Abstract][Full Text] [Related]
6. Contiguous gene deletion neighboring TWIST1 identified in a patient with Saethre-Chotzen syndrome associated with neurodevelopmental delay: Possible contribution of HDAC9.
Shimbo H; Oyoshi T; Kurosawa K
Congenit Anom (Kyoto); 2018 Jan; 58(1):33-35. PubMed ID: 28220539
[TBL] [Abstract][Full Text] [Related]
7. Association between rs2107595 HDAC9 gene polymorphism and advanced carotid atherosclerosis in the Slovenian cohort.
Grbić E; Gorkič N; Pleskovič A; Zorc M; Ljuca F; Gasparini M; Mrđa B; Cilenšek I; Mankoč S; Banach M; Petrovič D; Fras Z
Lipids Health Dis; 2020 Apr; 19(1):71. PubMed ID: 32284067
[TBL] [Abstract][Full Text] [Related]
8. Evidence HDAC9 genetic variant associated with ischemic stroke increases risk via promoting carotid atherosclerosis.
Markus HS; Mäkelä KM; Bevan S; Raitoharju E; Oksala N; Bis JC; O'Donnell C; Hainsworth A; Lehtimäki T
Stroke; 2013 May; 44(5):1220-5. PubMed ID: 23449258
[TBL] [Abstract][Full Text] [Related]
9. Synergistic Expression of Histone Deacetylase 9 and Matrix Metalloproteinase 12 in M4 Macrophages in Advanced Carotid Plaques.
Oksala NKJ; Seppälä I; Rahikainen R; Mäkelä KM; Raitoharju E; Illig T; Klopp N; Kholova I; Laaksonen R; Karhunen PJ; Hytönen VP; Lehtimäki T
Eur J Vasc Endovasc Surg; 2017 May; 53(5):632-640. PubMed ID: 28343758
[TBL] [Abstract][Full Text] [Related]
10. Variants in an Hdac9 intronic enhancer plasmid impact Twist1 expression in vitro.
Siekmann TE; Gerber MM; Toland AE
Mamm Genome; 2016 Apr; 27(3-4):99-110. PubMed ID: 26721262
[TBL] [Abstract][Full Text] [Related]
11. Expression of Circulating miR-17-92 Cluster and HDAC9 Gene in Atherosclerotic Patients with Unstable and Stable Carotid Plaques.
Ferronato S; Mombello A; Posenato I; Candiani P; Scuro A; Setacci C; Gomez-Lira M
Genet Test Mol Biomarkers; 2017 Jun; 21(6):402-405. PubMed ID: 28436693
[TBL] [Abstract][Full Text] [Related]
12. Aberrant expression and regulatory role of histone deacetylase 9 in vascular endothelial cell injury in intracranial aneurysm.
Sun J; Zhang L; Cheng Q; Wu Y
Biomol Biomed; 2024 Jan; 24(1):61-72. PubMed ID: 37573538
[TBL] [Abstract][Full Text] [Related]
13. The Atherosclerosis Risk Variant rs2107595 Mediates Allele-Specific Transcriptional Regulation of
Prestel M; Prell-Schicker C; Webb T; Malik R; Lindner B; Ziesch N; Rex-Haffner M; Röh S; Viturawong T; Lehm M; Mokry M; den Ruijter H; Haitjema S; Asare Y; Söllner F; Najafabadi MG; Aherrahrou R; Civelek M; Samani NJ; Mann M; Haffner C; Dichgans M
Stroke; 2019 Oct; 50(10):2651-2660. PubMed ID: 31500558
[TBL] [Abstract][Full Text] [Related]
14. Association Between the Gene Polymorphisms of HDAC9 and the Risk of Atherosclerosis and Ischemic Stroke.
Qingxu G; Yan Z; Jiannan X; Yunlong L
Pathol Oncol Res; 2016 Jan; 22(1):103-7. PubMed ID: 26347468
[TBL] [Abstract][Full Text] [Related]
15. Unraveling the transcriptional regulation of TWIST1 in limb development.
Hirsch N; Eshel R; Bar Yaacov R; Shahar T; Shmulevich F; Dahan I; Levaot N; Kaplan T; Lupiáñez DG; Birnbaum RY
PLoS Genet; 2018 Oct; 14(10):e1007738. PubMed ID: 30372441
[TBL] [Abstract][Full Text] [Related]
16. HDAC9 Variant Rs2107595 Modifies Susceptibility to Coronary Artery Disease and the Severity of Coronary Atherosclerosis in a Chinese Han Population.
Wang XB; Han YD; Sabina S; Cui NH; Zhang S; Liu ZJ; Li C; Zheng F
PLoS One; 2016; 11(8):e0160449. PubMed ID: 27494404
[TBL] [Abstract][Full Text] [Related]
17. Associations among Genetic Variants and Intracranial Aneurysm in a Chinese Population.
Li B; Hu C; Liu J; Liao X; Xun J; Xiao M; Yan J
Yonsei Med J; 2019 Jul; 60(7):651-658. PubMed ID: 31250579
[TBL] [Abstract][Full Text] [Related]
18. An HDAC9-MALAT1-BRG1 complex mediates smooth muscle dysfunction in thoracic aortic aneurysm.
Lino Cardenas CL; Kessinger CW; Cheng Y; MacDonald C; MacGillivray T; Ghoshhajra B; Huleihel L; Nuri S; Yeri AS; Jaffer FA; Kaminski N; Ellinor P; Weintraub NL; Malhotra R; Isselbacher EM; Lindsay ME
Nat Commun; 2018 Mar; 9(1):1009. PubMed ID: 29520069
[TBL] [Abstract][Full Text] [Related]
19. HDAC9 Polymorphism Alters Blood Gene Expression in Patients with Large Vessel Atherosclerotic Stroke.
Shroff N; Ander BP; Zhan X; Stamova B; Liu D; Hull H; Hamade FR; Dykstra-Aiello C; Ng K; Sharp FR; Jickling GC
Transl Stroke Res; 2019 Feb; 10(1):19-25. PubMed ID: 29651704
[TBL] [Abstract][Full Text] [Related]
20. HDAC9 rs11984041 polymorphism is associated with diabetic retinopathy in Slovenian patients with type 2 diabetes mellitus.
Cilenšek I; Lapuh V; Globočnik Petrovič M; Petrovič D
Gene; 2021 Sep; 796-797():145802. PubMed ID: 34175397
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
