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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

197 related articles for article (PubMed ID: 39150562)

  • 1. 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]  

  • 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. CGG repeat expansion in
    Yu J; Liufu T; Zheng Y; Xu J; Meng L; Zhang W; Yuan Y; Hong D; Charlet-Berguerand N; Wang Z; Deng J
    Proc Natl Acad Sci U S A; 2022 Oct; 119(41):e2208649119. PubMed ID: 36191230
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. GGC repeat expansions in NOTCH2NLC cause uN2CpolyG cerebral amyloid angiopathy.
    Bao L; Li X; Tian J; Wang L; Ji Y; Cui Y; Sun W; Zhang J; Xia M; Zhu P; Cui G; Chen H
    Brain; 2024 Aug; ():. PubMed ID: 39167540
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Clinical characteristics of two patients with neuronal intranuclear inclusion disease and literature review.
    Zhao B; Yang M; Wang Z; Yang Q; Zhang Y; Qi X; Pan S; Yu Y
    Front Neurosci; 2022; 16():1056261. PubMed ID: 36545534
    [TBL] [Abstract][Full Text] [Related]  

  • 12.
    Fan Y; Xu Y; Shi C
    J Med Genet; 2022 Jan; 59(1):1-9. PubMed ID: 34675123
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The clinical and neuropathological picture of adult neuronal intranuclear inclusion disease with no radiological abnormality.
    Miki Y; Kamata K; Goto S; Sakuraba H; Mori F; Yamagata K; Kijima H; Fukuda S; Wakabayashi K
    Neuropathology; 2022 Jun; 42(3):204-211. PubMed ID: 35274390
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Neuronal intranuclear inclusion disease: Polyglycine protein is the culprit.
    Ehrlich ME; Ellerby LM
    Neuron; 2021 Jun; 109(11):1757-1760. PubMed ID: 34081916
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Phenotypic bases of NOTCH2NLC GGC expansion positive neuronal intranuclear inclusion disease in a Southeast Asian cohort.
    Chen Z; Xu Z; Cheng Q; Tan YJ; Ong HL; Zhao Y; Lim WK; Teo JX; Foo JN; Lee HY; Tan JMM; Hang L; Yu WY; Ting SKS; Tan EK; Lim TCC; Ng ASL
    Clin Genet; 2020 Sep; 98(3):274-281. PubMed ID: 32602554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Pathologic changes in neuronal intranuclear inclusion disease are linked to aberrant FUS interaction under hyperosmotic stress.
    Wang H; Zheng Y; Yu J; Meng L; Zhang W; Hong D; Wang Z; Yuan Y; Deng J
    Neurobiol Dis; 2024 Jan; 190():106391. PubMed ID: 38145851
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion disease.
    Sone J; Mitsuhashi S; Fujita A; Mizuguchi T; Hamanaka K; Mori K; Koike H; Hashiguchi A; Takashima H; Sugiyama H; Kohno Y; Takiyama Y; Maeda K; Doi H; Koyano S; Takeuchi H; Kawamoto M; Kohara N; Ando T; Ieda T; Kita Y; Kokubun N; Tsuboi Y; Katoh K; Kino Y; Katsuno M; Iwasaki Y; Yoshida M; Tanaka F; Suzuki IK; Frith MC; Matsumoto N; Sobue G
    Nat Genet; 2019 Aug; 51(8):1215-1221. PubMed ID: 31332381
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.