BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 34680863)

  • 1.
    Murai Y; Ishisaka E; Watanabe A; Sekine T; Shirokane K; Matano F; Nakae R; Tamaki T; Koketsu K; Morita A
    Genes (Basel); 2021 Sep; 12(10):. PubMed ID: 34680863
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic analysis of
    Tashiro R; Fujimura M; Sakata H; Endo H; Tomata Y; Sato-Maeda M; Niizuma K; Tominaga T
    Neurol Res; 2019 Sep; 41(9):811-816. PubMed ID: 31064275
    [No Abstract]   [Full Text] [Related]  

  • 3. Genetic Analysis of Ring Finger Protein 213 (RNF213) c.14576G>A in Intracranial Atherosclerosis of the Anterior and Posterior Circulations.
    Shinya Y; Miyawaki S; Imai H; Hongo H; Ono H; Takenobu A; Nakatomi H; Teraoka A; Saito N
    J Stroke Cerebrovasc Dis; 2017 Nov; 26(11):2638-2644. PubMed ID: 28797616
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ring finger protein 213 c.14576G>A mutation is not involved in internal carotid artery and middle cerebral artery dysplasia.
    Murai Y; Ishisaka E; Watanabe A; Sekine T; Shirokane K; Matano F; Nakae R; Tamaki T; Koketsu K; Morita A
    Sci Rep; 2021 Nov; 11(1):22163. PubMed ID: 34773068
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetic Analysis of RNF213 c.14576G>A Variant in Nonatherosclerotic Quasi-Moyamoya Disease.
    Miyawaki S; Imai H; Shimizu M; Yagi S; Ono H; Nakatomi H; Shimizu T; Saito N
    J Stroke Cerebrovasc Dis; 2015 May; 24(5):1075-9. PubMed ID: 25817623
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Association between moyamoya syndrome and the RNF213 c.14576G>A variant in patients with neurofibromatosis Type 1.
    Phi JH; Choi JW; Seong MW; Kim T; Moon YJ; Lee J; Koh EJ; Ryu SK; Kang TH; Bang JS; Oh CW; Park SS; Lee JY; Wang KC; Kim SK
    J Neurosurg Pediatr; 2016 Jun; 17(6):717-22. PubMed ID: 26849809
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease.
    Kim EH; Yum MS; Ra YS; Park JB; Ahn JS; Kim GH; Goo HW; Ko TS; Yoo HW
    J Neurosurg; 2016 May; 124(5):1221-7. PubMed ID: 26430847
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Hemorrhagic Onset Intracranial Artery Dissection of Middle Cerebral Artery Followed by Progressive Arterial Stenosis with Genetic Variant RNF213 p.Arg4810Lys (rs112735431).
    Shinya Y; Miyawaki S; Nakatomi H; Shin M; Teraoka A; Saito N
    World Neurosurg; 2020 Sep; 141():192-195. PubMed ID: 32438004
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Vascular tortuosity of the internal carotid artery is related to the RNF213 c.14429G > A variant in moyamoya disease.
    An S; Kim T; Oh CW; Bang JS; Lee SU; Heo J
    Sci Rep; 2019 Jun; 9(1):8614. PubMed ID: 31197213
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Role of RNF213 polymorphism in defining quasi-moyamoya disease and definitive moyamoya disease.
    Ishisaka E; Watanabe A; Murai Y; Shirokane K; Matano F; Tsukiyama A; Baba E; Nakagawa S; Tamaki T; Mizunari T; Tanikawa R; Morita A
    Neurosurg Focus; 2021 Sep; 51(3):E2. PubMed ID: 34469872
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Differing phenotypes of Moyamoya disease in a familial case involving heterozygous c.14429G > A variant in RNF213.
    Inoue T; Murakami N; Sakadume S; Kido Y; Kikuchi A; Ichinoi N; Suzuki K; Kure S; Sakuta R
    Pediatr Int; 2015 Aug; 57(4):798-801. PubMed ID: 26315205
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease.
    Miyatake S; Miyake N; Touho H; Nishimura-Tadaki A; Kondo Y; Okada I; Tsurusaki Y; Doi H; Sakai H; Saitsu H; Shimojima K; Yamamoto T; Higurashi M; Kawahara N; Kawauchi H; Nagasaka K; Okamoto N; Mori T; Koyano S; Kuroiwa Y; Taguri M; Morita S; Matsubara Y; Kure S; Matsumoto N
    Neurology; 2012 Mar; 78(11):803-10. PubMed ID: 22377813
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial moyamoya disease in two Turkish siblings with same polymorphism in RNF213 gene but different clinical features.
    Bayram AK; Yilmaz E; Per H; Ito M; Uchino H; Doganay S; Houkin K; Unal E
    Childs Nerv Syst; 2016 Mar; 32(3):569-73. PubMed ID: 26277359
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Development of atherosclerotic-moyamoya syndrome with genetic variant of RNF213 p.R4810K and p.T1727M: A case report.
    Liu Y; Wu X; Fan Z; Cheng J; Zhong L; Lin Y; Qu X
    Clin Neurol Neurosurg; 2018 May; 168():163-166. PubMed ID: 29567577
    [TBL] [Abstract][Full Text] [Related]  

  • 19. RNF213 p.R4810K Polymorphism and the Risk of Moyamoya Disease, Intracranial Major Artery Stenosis/Occlusion, and Quasi-Moyamoya Disease: A Meta-Analysis.
    Wang Y; Mambiya M; Li Q; Yang L; Jia H; Han Y; Liu W
    J Stroke Cerebrovasc Dis; 2018 Aug; 27(8):2259-2270. PubMed ID: 29752070
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Precision Medicine for Moyamoya Disease].
    Fujimura M
    No Shinkei Geka; 2022 Jan; 50(1):216-221. PubMed ID: 35169101
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.