Literatura académica sobre el tema "GGGGCC repeats"
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Artículos de revistas sobre el tema "GGGGCC repeats"
Jiao, Bin, Mengli Wang, Hao Feng, Han Bao, Feiran Zhang, Hao Wu, Junling Wang, Beisha Tang, Peng Jin y Lu Shen. "Downregulation of TOP2 modulates neurodegeneration caused by GGGGCC expanded repeats". Human Molecular Genetics 30, n.º 10 (22 de marzo de 2021): 893–901. http://dx.doi.org/10.1093/hmg/ddab079.
Texto completoLiu, Xiaole, Xinyue Zhao, Jinhan He, Sishi Wang, Xinfei Shen, Qingfeng Liu y Shenlin Wang. "Advances in the Structure of GGGGCC Repeat RNA Sequence and Its Interaction with Small Molecules and Protein Partners". Molecules 28, n.º 15 (1 de agosto de 2023): 5801. http://dx.doi.org/10.3390/molecules28155801.
Texto completovan ‘t Spijker, Heleen M., Emily E. Stackpole, Sandra Almeida, Olga Katsara, Botao Liu, Kuang Shen, Robert J. Schneider, Fen-Biao Gao y Joel D. Richter. "Ribosome profiling reveals novel regulation of C9ORF72 GGGGCC repeat-containing RNA translation". RNA 28, n.º 2 (30 de noviembre de 2021): 123–38. http://dx.doi.org/10.1261/rna.078963.121.
Texto completoBabić Leko, Mirjana, Vera Župunski, Jason Kirincich, Dinko Smilović, Tibor Hortobágyi, Patrick R. Hof y Goran Šimić. "Molecular Mechanisms of Neurodegeneration Related to C9orf72 Hexanucleotide Repeat Expansion". Behavioural Neurology 2019 (15 de enero de 2019): 1–18. http://dx.doi.org/10.1155/2019/2909168.
Texto completoHatanaka, Yukari, Tomohiro Umeda, Keiko Shigemori, Toshihide Takeuchi, Yoshitaka Nagai y Takami Tomiyama. "C9orf72 Hexanucleotide Repeat Expansion-Related Neuropathology Is Attenuated by Nasal Rifampicin in Mice". Biomedicines 10, n.º 5 (6 de mayo de 2022): 1080. http://dx.doi.org/10.3390/biomedicines10051080.
Texto completoZhang, Yong-Jie, Lin Guo, Patrick K. Gonzales, Tania F. Gendron, Yanwei Wu, Karen Jansen-West, Aliesha D. O’Raw et al. "Heterochromatin anomalies and double-stranded RNA accumulation underlie C9orf72 poly(PR) toxicity". Science 363, n.º 6428 (14 de febrero de 2019): eaav2606. http://dx.doi.org/10.1126/science.aav2606.
Texto completoHaeusler, Aaron R. "Nucleotide Structural Polymorphisms Formed by GGGGCC Repeats Cause C9orf72 Abortive Transcription and Nucleolar Stress". Biophysical Journal 106, n.º 2 (enero de 2014): 488a. http://dx.doi.org/10.1016/j.bpj.2013.11.4477.
Texto completoTeng, Ye, Ming Zhu y Zhidong Qiu. "G-quadruplexes in Repeat Expansion Disorders". International Journal of Molecular Sciences 24, n.º 3 (25 de enero de 2023): 2375. http://dx.doi.org/10.3390/ijms24032375.
Texto completoBalendra, Rubika, Igor Ruiz de los Mozos, Hana M. Odeh, Idoia Glaria, Carmelo Milioto, Katherine M. Wilson, Agnieszka M. Ule et al. "Transcriptome-wide RNA binding analysis of C9orf72 poly(PR) dipeptides". Life Science Alliance 6, n.º 9 (12 de julio de 2023): e202201824. http://dx.doi.org/10.26508/lsa.202201824.
Texto completoReddy, Kaalak, Monika H. M. Schmidt, Jaimie M. Geist, Neha P. Thakkar, Gagan B. Panigrahi, Yuh-Hwa Wang y Christopher E. Pearson. "Processing of double-R-loops in (CAG)·(CTG) and C9orf72 (GGGGCC)·(GGCCCC) repeats causes instability". Nucleic Acids Research 42, n.º 16 (21 de agosto de 2014): 10473–87. http://dx.doi.org/10.1093/nar/gku658.
Texto completoTesis sobre el tema "GGGGCC repeats"
taki, motahareh. "DEVELOPING PROBES FOR LABEL-FREE DETECTION OF HEXANUCLEOTIDE GGGGCC REPEATS BY ELECTROCHEMICAL IMPEDANCE SPECTROSCOPY". OpenSIUC, 2019. https://opensiuc.lib.siu.edu/theses/2634.
Texto completoPietri, David. "Structure and function of the C9ORF72-SMCR8-WDR41 complex and its implication for Amyotrophic Lateral Sclerosis (ALS)". Electronic Thesis or Diss., Strasbourg, 2023. http://www.theses.fr/2023STRAJ087.
Texto completoAmyotrophic lateral sclerosis (ALS or Charcot disease) is the third most common neurodegenerative disease. The main genetic cause of ALS is an expansion of GGGGCC repeats in the C9ORF72 gene which protein forms a complex with the SMCR8 and WDR41 proteins. To better understand its molecular functions, solving its structure was a main goal of my thesis. In parallel, we discovered that C9ORF72 regulates a newly described mechanism of biogenesis of newly-formed lysosomes, called autophagic lysosome reformation (ALR). This process has been extensively investigated during my thesis, in order to better understand its regulation, particularly for the regeneration of lysosomes in basal conditions and amino acid deprivation. My work reveals a new partner of the C9ORF72 complex as a novel function in lysosome biogenesis. These results could thus explain the dysfunction of lysosomes and neurodegeneration observed in ALS, which open new therapeutic ways for this devastating disease
Workinger, Paul M. y Paul M. Workinger. "Familial Amyotrophic Lateral Sclerosis with a focus on C9orf72 Hexanucleotide GGGGCC Repeat Expansion Associated ALS with Frontotemporal Dementia". Thesis, The University of Arizona, 2017. http://hdl.handle.net/10150/625350.
Texto completoActas de conferencias sobre el tema "GGGGCC repeats"
Brčić, Jasna y Janez Plavec. "NMR study of DNA oligonucleotides containing ALS/FTD associated GGGGCC repeat". En XVIth Symposium on Chemistry of Nucleic Acid Components. Prague: Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, 2014. http://dx.doi.org/10.1135/css201414236.
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