PMC Links for Gene (Select 6310) - PMC

Seppe Leysen, Rebecca Jane Burnley, Elizabeth Rodriguez, Lech-Gustav Milroy, Lorenzo Soini, Carolyn J. Adamski, Larissa Nitschke, Rachel Davis, Tomas Obsil, Lucas Brunsveld, Tom Crabbe, Huda Yahya Zoghbi, Christian Ottmann, Jeremy Martin Davis

J Mol Biol. 2021 Sep 17; 433(19): 167174. doi: 10.1016/j.jmb.2021.167174

PMCID:: PMC8505757

Article

Select item 67304125.

Disease Progression Despite Early Loss of Polyglutamine Protein Expression in SCA7 Mouse Model

Dominique Helmlinger, Gretta Abou-Sleymane, Gaël Yvert, Stéphane Rousseau, Chantal Weber, Yvon Trottier, Jean-Louis Mandel, Didier Devys

J Neurosci. 2004 Feb 25; 24(8): 1881–1887. doi: 10.1523/JNEUROSCI.4407-03.2004

PMCID:: PMC6730412

Article PDF–466K

Select item 53923246.

Ataxin-1 regulates epithelial–mesenchymal transition of cervical cancer cells

A-Ram Kang, Hyoung-Tae An, Jesang Ko, Seongman Kang

Oncotarget. 2017 Mar 14; 8(11): 18248–18259. Published online 2017 Feb 14. doi: 10.18632/oncotarget.15319

PMCID:: PMC5392324

Article PDF–5.5M

Select item 51159607.

RNAi prevents and reverses phenotypes induced by mutant human ataxin‐1

Megan S. Keiser, Alejandro Mas Monteys, Romuald Corbau, Pedro Gonzalez‐Alegre, Beverly L. Davidson

Ann Neurol. 2016 Nov; 80(5): 754–765. Published online 2016 Nov 2. doi: 10.1002/ana.24789

PMCID:: PMC5115960

Article PDF–989K

Select item 49567198.

High relative frequency of SCA1 in Poland reflecting a potential founder effect

Wioletta Krysa, Anna Sulek, Maria Rakowicz, Walentyna Szirkowiec, Jacek Zaremba

Neurol Sci. 2016; 37: 1319–1325. Published online 2016 May 19. doi: 10.1007/s10072-016-2594-x

PMCID:: PMC4956719

Article PDF–544K

Select item 44117589.

Genetic characterization of Spinocerebellar ataxia 1 in a South Indian cohort

Dhanya Kumaran, Krishnan Balagopal, Reginald George Alex Tharmaraj, Sanjith Aaron, Kuryan George, Jayaprakash Muliyil, Ajith Sivadasan, Sumita Danda, Mathew Alexander, Gaiti Hasan

BMC Med Genet. 2014; 15: 114. Published online 2014 Oct 25. doi: 10.1186/s12881-014-0114-5

PMCID:: PMC4411758

Article PDF–1.1M

Select item 409437210.

Non-invasive detection of neurochemical changes prior to overt pathology in a mouse model of spinocerebellar ataxia type 1

Uzay E. Emir, Howard Brent Clark, Manda L. Vollmers, Lynn E. Eberly, Gülin Ӧz

J Neurochem. Author manuscript; available in PMC 2014 Dec 1.

Published in final edited form as: J Neurochem. 2013 Dec; 127(5): 660–668. Published online 2013 Sep 17. doi: 10.1111/jnc.12435

PMCID:: PMC4094372

Article PDF–2.0M

Select item 379654511.

Protein-Protein Interactions as a Strategy towards Protein-Specific Drug Design: The Example of Ataxin-1

Cesira de Chiara, Rajesh P. Menon, Geoff Kelly, Annalisa Pastore

PLoS One. 2013; 8(10): e76456. Published online 2013 Oct 14. doi: 10.1371/journal.pone.0076456

PMCID:: PMC3796545

Article PDF–924K

Select item 372463912.

An Out-of-frame Overlapping Reading Frame in the Ataxin-1 Coding Sequence Encodes a Novel Ataxin-1 Interacting Protein

Danny Bergeron, Catherine Lapointe, Cyntia Bissonnette, Guillaume Tremblay, Julie Motard, Xavier Roucou

J Biol Chem. 2013 Jul 26; 288(30): 21824–21835. Published online 2013 Jun 12. doi: 10.1074/jbc.M113.472654

PMCID:: PMC3724639

Article PDF–3.1M

Select item 366710313.

Autosomal dominant hereditary ataxia in Sri Lanka

Dulika S Sumathipala, Gayan S Abeysekera, Rohan W Jayasekara, Chantal ME Tallaksen, Vajira HW Dissanayake

BMC Neurol. 2013; 13: 39. Published online 2013 May 1. doi: 10.1186/1471-2377-13-39

PMCID:: PMC3667103

Article PDF–345K

Select item 360276114.

Self-Assembly and Conformational Heterogeneity of the AXH Domain of Ataxin-1: An Unusual Example of a Chameleon Fold

Cesira de Chiara, Martin Rees, Raj P. Menon, Kris Pauwels, Ceri Lawrence, Petr V. Konarev, Dmitri I. Svergun, Stephen R. Martin, Yu Wai Chen, Annalisa Pastore

Biophys J. 2013 Mar 19; 104(6): 1304–1313. doi: 10.1016/j.bpj.2013.01.048

PMCID:: PMC3602761

Article PDF–1.3M

Select item 339064715.

Ataxin-1 Poly(Q)-induced Proteotoxic Stress and Apoptosis Are Attenuated in Neural Cells by Docosahexaenoic Acid-derived Neuroprotectin D1

Jorgelina M. Calandria, Pranab K. Mukherjee, Juan Carlos de Rivero Vaccari, Min Zhu, Nicos A. Petasis, Nicolas G. Bazan

J Biol Chem. 2012 Jul 6; 287(28): 23726–23739. Published online 2012 Apr 16. doi: 10.1074/jbc.M111.287078

PMCID:: PMC3390647

Article PDF–3.4M

Select item 284677116.

Noninvasive Detection of Presymptomatic and Progressive Neurodegeneration in a Mouse Model of Spinocerebellar Ataxia Type 1

Gülin Öz, Christopher D. Nelson, Dee M. Koski, Pierre-Gilles Henry, Małgorzata Marjańska, Dinesh K. Deelchand, Ryan Shanley, Lynn E. Eberly, Harry T. Orr, H. Brent Clark

J Neurosci. 2010 Mar 10; 30(10): 3831–3838. doi: 10.1523/JNEUROSCI.5612-09.2010

PMCID:: PMC2846771

Article PDF–1.2M

Select item 199576317.

Ataxin-1 Fusion Partners Alter PolyQ Lethality and Aggregation

Tina Rich, Archana Varadaraj

PLoS One. 2007; 2(10): e1014. Published online 2007 Oct 10. doi: 10.1371/journal.pone.0001014

PMCID:: PMC1995763

Article PDF–312K

Select item 746206518.

miR760 regulates ATXN1 levels via interaction with its 5′ untranslated region

Larissa Nitschke, Ambika Tewari, Stephanie L. Coffin, Eder Xhako, Kaifang Pang, Vincenzo A. Gennarino, Jennifer L. Johnson, Francisco A. Blanco, Zhandong Liu, Huda Y. Zoghbi

Genes Dev. 2020 Sep 1; 34(17-18): 1147–1160. doi: 10.1101/gad.339317.120

PMCID:: PMC7462065

Article PDF–2.1M

Select item 629269319.

Molecular pathway analysis towards understanding tissue vulnerability in spinocerebellar ataxia type 1

Terri M Driessen, Paul J Lee, Janghoo Lim

eLife. 2018; 7: e39981. Published online 2018 Dec 3. doi: 10.7554/eLife.39981

PMCID:: PMC6292693

Article PDF–6.2M

Select item 367543820.

Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability

Tuva Barøy, Doriana Misceo, Petter Strømme, Asbjørg Stray-Pedersen, Asbjørn Holmgren, Olaug Kristin Rødningen, Anne Blomhoff, Johan Robert Helle, Alice Stormyr, Bjørn Tvedt, Madeleine Fannemel, Eirik Frengen

Orphanet J Rare Dis. 2013; 8: 3. Published online 2013 Jan 7. doi: 10.1186/1750-1172-8-3