These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
241 related articles for article (PubMed ID: 36417528)
1. Expression of expanded GGC repeats within Liu Q; Zhang K; Kang Y; Li Y; Deng P; Li Y; Tian Y; Sun Q; Tang Y; Xu K; Zhou Y; Wang JL; Guo J; Li JD; Xia K; Meng Q; Allen EG; Wen Z; Li Z; Jiang H; Shen L; Duan R; Yao B; Tang B; Jin P; Pan Y Sci Adv; 2022 Nov; 8(47):eadd6391. PubMed ID: 36417528 [TBL] [Abstract][Full Text] [Related]
2. Translation of GGC repeat expansions into a toxic polyglycine protein in NIID defines a novel class of human genetic disorders: The polyG diseases. Boivin M; Deng J; Pfister V; Grandgirard E; Oulad-Abdelghani M; Morlet B; Ruffenach F; Negroni L; Koebel P; Jacob H; Riet F; Dijkstra AA; McFadden K; Clayton WA; Hong D; Miyahara H; Iwasaki Y; Sone J; Wang Z; Charlet-Berguerand N Neuron; 2021 Jun; 109(11):1825-1835.e5. PubMed ID: 33887199 [TBL] [Abstract][Full Text] [Related]
3. Microglia contribute to polyG-dependent neurodegeneration in neuronal intranuclear inclusion disease. Zhong S; Lian Y; Zhou B; Ren R; Duan L; Pan Y; Gong Y; Wu X; Cheng D; Zhang P; Lu B; Wang X; Ding J Acta Neuropathol; 2024 Aug; 148(1):21. PubMed ID: 39150562 [TBL] [Abstract][Full Text] [Related]
4. Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders. Tian Y; Wang JL; Huang W; Zeng S; Jiao B; Liu Z; Chen Z; Li Y; Wang Y; Min HX; Wang XJ; You Y; Zhang RX; Chen XY; Yi F; Zhou YF; Long HY; Zhou CJ; Hou X; Wang JP; Xie B; Liang F; Yang ZY; Sun QY; Allen EG; Shafik AM; Kong HE; Guo JF; Yan XX; Hu ZM; Xia K; Jiang H; Xu HW; Duan RH; Jin P; Tang BS; Shen L Am J Hum Genet; 2019 Jul; 105(1):166-176. PubMed ID: 31178126 [TBL] [Abstract][Full Text] [Related]
5. Upstream open reading frame with NOTCH2NLC GGC expansion generates polyglycine aggregates and disrupts nucleocytoplasmic transport: implications for polyglycine diseases. Zhong S; Lian Y; Luo W; Luo R; Wu X; Ji J; Ji Y; Ding J; Wang X Acta Neuropathol; 2021 Dec; 142(6):1003-1023. PubMed ID: 34694469 [TBL] [Abstract][Full Text] [Related]
6. GGC expansions in NOTCH2NLC contribute to Parkinson disease and dopaminergic neuron degeneration. Liu Q; Chen J; Xue J; Zhou X; Tian Y; Xiao Q; Huang W; Pan Y; Zhou X; Li J; Zhao Y; Pan H; Wang Y; He R; Xiang Y; Tu T; Xu Q; Sun Q; Tan J; Yan X; Li J; Guo J; Shen L; Duan R; Tang B; Liu Z Eur J Neurol; 2024 Feb; 31(2):e16145. PubMed ID: 37975799 [TBL] [Abstract][Full Text] [Related]
7. GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation. Fan Y; Li MJ; Yang J; Li SJ; Hao XY; Li JD; Wang YC; Tang MB; Zhang C; Shi JJ; Ma DR; Guo MN; Liu F; Shen S; Yao DB; Zuo CY; Mao CY; Hu ZW; Zhang S; Yang ZH; Guo GY; Yang JH; Xia ZP; Xu YM; Shi CH Brain; 2023 Aug; 146(8):3373-3391. PubMed ID: 36825461 [TBL] [Abstract][Full Text] [Related]
8. A comprehensive study of clinicopathological and genetic features of neuronal intranuclear inclusion disease. Liu M; Gao Y; Yuan Y; Liu X; Wang Y; Li L; Zhang X; Jiang C; Wang Q; Wang Y; Shi C; Xu Y; Yang J Neurol Sci; 2023 Oct; 44(10):3545-3556. PubMed ID: 37184590 [TBL] [Abstract][Full Text] [Related]
9. Long-read sequencing identified repeat expansions in the 5'UTR of the Deng J; Gu M; Miao Y; Yao S; Zhu M; Fang P; Yu X; Li P; Su Y; Huang J; Zhang J; Yu J; Li F; Bai J; Sun W; Huang Y; Yuan Y; Hong D; Wang Z J Med Genet; 2019 Nov; 56(11):758-764. PubMed ID: 31413119 [TBL] [Abstract][Full Text] [Related]
10. Expression of expanded GGC repeats within NOTCH2NLC causes cardiac dysfunction in mouse models. Pan Y; Jiang Y; Wan J; Hu Z; Jiang H; Shen L; Tang B; Tian Y; Liu Q Cell Biosci; 2023 Aug; 13(1):157. PubMed ID: 37644522 [TBL] [Abstract][Full Text] [Related]
11. NOTCH2NLC GGC repeat expansion causes retinal pathology with intranuclear inclusions throughout the retina and causes visual impairment. Sone J; Ueno S; Akagi A; Miyahara H; Tamai C; Riku Y; Yabata H; Koizumi R; Hattori T; Hirose H; Koyanagi Y; Kobayashi R; Okada H; Kishimoto Y; Hashizume Y; Sobue G; Yoshida M; Iwasaki Y Acta Neuropathol Commun; 2023 May; 11(1):71. PubMed ID: 37131242 [TBL] [Abstract][Full Text] [Related]
13. Current advances in neuronal intranuclear inclusion disease. Bao L; Zuo D; Li Q; Chen H; Cui G Neurol Sci; 2023 Jun; 44(6):1881-1889. PubMed ID: 36795299 [TBL] [Abstract][Full Text] [Related]
14. Patients with biallelic GGC repeat expansions in NOTCH2NLC exhibiting a typical neuronal intranuclear inclusion disease phenotype. Kameyama S; Mizuguchi T; Doi H; Koyano S; Okubo M; Tada M; Shimizu H; Fukuda H; Tsuchida N; Uchiyama Y; Koshimizu E; Hamanaka K; Fujita A; Misawa K; Miyatake S; Kanai K; Tanaka F; Matsumoto N Genomics; 2022 Sep; 114(5):110469. PubMed ID: 36041634 [TBL] [Abstract][Full Text] [Related]
15. Wang YC; Fan Y; Yu WK; Shen S; Li JD; Gao Y; Ji Y; Li YS; Yu LL; Zhao ZC; Li SS; Ding Y; Shi CH; Xu YM Stroke Vasc Neurol; 2023 Apr; 8(2):161-168. PubMed ID: 36207023 [TBL] [Abstract][Full Text] [Related]
16. Clinical, radiological, and molecular analyses of neuronal intranuclear inclusion disease with polyglycine inclusions. Furuta M; Sato M; Kasahara H; Tsukagoshi S; Hirayanagi K; Fujita Y; Takai E; Aihara Y; Okamoto K; Ikeda Y J Neurol Sci; 2023 May; 448():120618. PubMed ID: 37001413 [TBL] [Abstract][Full Text] [Related]
17. Association of NOTCH2NLC Repeat Expansions With Parkinson Disease. Ma D; Tan YJ; Ng ASL; Ong HL; Sim W; Lim WK; Teo JX; Ng EYL; Lim EC; Lim EW; Chan LL; Tan LCS; Yi Z; Tan EK JAMA Neurol; 2020 Dec; 77(12):1559-1563. PubMed ID: 32852534 [TBL] [Abstract][Full Text] [Related]
18. Fan Y; Xu Y; Shi C J Med Genet; 2022 Jan; 59(1):1-9. PubMed ID: 34675123 [TBL] [Abstract][Full Text] [Related]
19. Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease. Deng J; Zhou B; Yu J; Han X; Fu J; Li X; Xie X; Zhu M; Zheng Y; Guo X; Li P; Wang Q; Liu J; Zhang W; Yuan Y; Yao S; Wang Z; Hong D J Med Genet; 2022 May; 59(5):462-469. PubMed ID: 33766934 [TBL] [Abstract][Full Text] [Related]
20. First detailed case report of a pediatric patient with neuronal intranuclear inclusion disease diagnosed by NOTCH2NLC genetic testing. Miyamoto Y; Okazaki T; Watanabe K; Togawa M; Adachi T; Kato A; Ochiai R; Tamai C; Sone J; Maegaki Y Brain Dev; 2023 Jan; 45(1):70-76. PubMed ID: 36150977 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]