643 related articles for article (PubMed ID: 21048783)
21. Moyamoya disease patient mutations in the RING domain of RNF213 reduce its ubiquitin ligase activity and enhance NFκB activation and apoptosis in an AAA+ domain-dependent manner.
Takeda M; Tezuka T; Kim M; Choi J; Oichi Y; Kobayashi H; Harada KH; Mizushima T; Taketani S; Koizumi A; Youssefian S
Biochem Biophys Res Commun; 2020 May; 525(3):668-674. PubMed ID: 32139119
[TBL] [Abstract][Full Text] [Related]
22. MMD-associated
Bhardwaj A; Banh RS; Zhang W; Sidhu SS; Neel BG
Life Sci Alliance; 2022 May; 5(5):. PubMed ID: 35135845
[TBL] [Abstract][Full Text] [Related]
23. Moyamoya vasculopathy shows a genetic mutational gradient decreasing from East to West.
Raso A; Biassoni R; Mascelli S; Nozza P; Ugolotti E; Di Marco E; De Marco P; Merello E; Cama A; Pavanello M; Capra V
J Neurosurg Sci; 2020 Apr; 64(2):165-172. PubMed ID: 27787485
[TBL] [Abstract][Full Text] [Related]
24. Transient middle cerebral artery occlusion in mice induces neuronal expression of RNF213, a susceptibility gene for moyamoya disease.
Sato-Maeda M; Fujimura M; Kanoke A; Morita-Fujimura Y; Niizuma K; Tominaga T
Brain Res; 2016 Jan; 1630():50-5. PubMed ID: 26556774
[TBL] [Abstract][Full Text] [Related]
25. Association between the rs112735431 polymorphism of the RNF213 gene and moyamoya disease: A case-control study and meta-analysis.
Huang Y; Cheng D; Zhang J; Zhao W
J Clin Neurosci; 2016 Oct; 32():14-8. PubMed ID: 27515544
[TBL] [Abstract][Full Text] [Related]
26. Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing.
Shoemaker LD; Clark MJ; Patwardhan A; Chandratillake G; Garcia S; Chen R; Morgan AA; Leng N; Kirk S; Chen R; Cook DJ; Snyder M; Steinberg GK
G3 (Bethesda); 2015 Nov; 6(1):41-9. PubMed ID: 26530418
[TBL] [Abstract][Full Text] [Related]
27. Meta-analysis of the association between RNF213 polymorphisms and clinical features of moyamoya disease in Asian population.
Jiang X; Liu L; Ai S; Xie X; Deng J; Jiang Z; Teng B; Liu C; Huang H
Clin Neurol Neurosurg; 2023 Aug; 231():107801. PubMed ID: 37267801
[TBL] [Abstract][Full Text] [Related]
28. The Clinical and Vascular Characteristics of RNF213 c.14576G>A Variant-Related Intracranial Major Artery Disease in China.
Cheng W; Xue S; Wu F; Song X; Huang Q; Song H; Wu J
Behav Neurol; 2019; 2019():7908392. PubMed ID: 30992731
[TBL] [Abstract][Full Text] [Related]
29. RNF213-Related Vasculopathy: Various Systemic Vascular Diseases Involving RNF213 Gene Mutations: Review.
Murai Y; Matano F; Kubota A; Nounaka Y; Ishisaka E; Shirokane K; Koketsu K; Nakae R; Tamaki T
J Nippon Med Sch; 2024; 91(2):140-145. PubMed ID: 38777780
[TBL] [Abstract][Full Text] [Related]
30. [Precision Medicine for Moyamoya Disease].
Fujimura M
No Shinkei Geka; 2022 Jan; 50(1):216-221. PubMed ID: 35169101
[TBL] [Abstract][Full Text] [Related]
31. Temporal profile of magnetic resonance angiography and decreased ratio of regulatory T cells after immunological adjuvant administration to mice lacking RNF213, a susceptibility gene for moyamoya disease.
Kanoke A; Fujimura M; Niizuma K; Fujimura T; Kakizaki A; Ito A; Sakata H; Sato-Maeda M; Kure S; Tominaga T
Brain Res; 2016 Jul; 1642():1-9. PubMed ID: 26972532
[TBL] [Abstract][Full Text] [Related]
32. The Genetic Basis of Moyamoya Disease.
Mertens R; Graupera M; Gerhardt H; Bersano A; Tournier-Lasserve E; Mensah MA; Mundlos S; Vajkoczy P
Transl Stroke Res; 2022 Feb; 13(1):25-45. PubMed ID: 34529262
[TBL] [Abstract][Full Text] [Related]
33. Role of Ring Finger Protein 213 in Moyamoya Disease.
Ma YG; Zhang Q; Yu LB; Zhao JZ
Chin Med J (Engl); 2016 Oct; 129(20):2497-2501. PubMed ID: 27748344
[TBL] [Abstract][Full Text] [Related]
34. Rare and Low-Frequency Variants in RNF213 Confer Susceptibility to Moyamoya Syndrome Associated with Hyperthyroidism.
Nomura S; Akagawa H; Yamaguchi K; Ishikawa T; Kawashima A; Kasuya H; Mukawa M; Nariai T; Maehara T; Okada Y; Kawamata T
World Neurosurg; 2019 Jul; 127():e460-e466. PubMed ID: 30922903
[TBL] [Abstract][Full Text] [Related]
35. Systematic Validation of RNF213 Coding Variants in Japanese Patients With Moyamoya Disease.
Moteki Y; Onda H; Kasuya H; Yoneyama T; Okada Y; Hirota K; Mukawa M; Nariai T; Mitani S; Akagawa H
J Am Heart Assoc; 2015 May; 4(5):. PubMed ID: 25964206
[TBL] [Abstract][Full Text] [Related]
36. Association between RNF213 c.14576G>A Variant (rs112735431) and Peripheral Pulmonary Artery Stenosis in Moyamoya Disease.
Ozaki D; Endo H; Tashiro R; Sugimura K; Tatebe S; Yasuda S; Tomata Y; Endo T; Tominaga K; Niizuma K; Fujimura M; Tominaga T
Cerebrovasc Dis; 2022; 51(3):282-287. PubMed ID: 34710878
[TBL] [Abstract][Full Text] [Related]
37. Genetic variant RNF213 c.14576G>A in various phenotypes of intracranial major artery stenosis/occlusion.
Miyawaki S; Imai H; Shimizu M; Yagi S; Ono H; Mukasa A; Nakatomi H; Shimizu T; Saito N
Stroke; 2013 Oct; 44(10):2894-7. PubMed ID: 23970789
[TBL] [Abstract][Full Text] [Related]
38. RNF213 rare variants in an ethnically diverse population with Moyamoya disease.
Cecchi AC; Guo D; Ren Z; Flynn K; Santos-Cortez RL; Leal SM; Wang GT; Regalado ES; Steinberg GK; Shendure J; Bamshad MJ; ; Grotta JC; Nickerson DA; Pannu H; Milewicz DM
Stroke; 2014 Nov; 45(11):3200-7. PubMed ID: 25278557
[TBL] [Abstract][Full Text] [Related]
39. The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.
Zhang Q; Liu Y; Yu L; Duan R; Ma Y; Ge P; Zhang D; Zhang Y; Wang R; Wang S; Zhao Y; Cao Y; Liu X; Deng X; Zhao J; Zhang X
World Neurosurg; 2017 Mar; 99():701-708.e1. PubMed ID: 28063898
[TBL] [Abstract][Full Text] [Related]
40. Temporal profile of the vascular anatomy evaluated by 9.4-T magnetic resonance angiography and histopathological analysis in mice lacking RNF213: a susceptibility gene for moyamoya disease.
Sonobe S; Fujimura M; Niizuma K; Nishijima Y; Ito A; Shimizu H; Kikuchi A; Arai-Ichinoi N; Kure S; Tominaga T
Brain Res; 2014 Mar; 1552():64-71. PubMed ID: 24440776
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]