Frataxin Deficit Leads to Reduced Dynamics of Growth Cones in Dorsal Root Ganglia Neurons of Friedreich's Ataxia YG8sR Model: A Multilinear Algebra Approach

Autor: Muñoz-Lasso DC, Mollá B, Sáenz-Gamboa JJ, Insuasty E, de la Iglesia-Vaya M, Pook MA, Pallardó FV, Palau F, Gonzalez-Cabo P

Publikováno v: FRONTIERS IN MOLECULAR NEUROSCIENCE
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Frontiers in Molecular Neuroscience
r-FISABIO. Repositorio Institucional de Producción Científica

Computational techniques for analyzing biological images offer a great potential to enhance our knowledge of the biological processes underlying disorders of the nervous system. Friedreich's Ataxia (FRDA) is a rare progressive neurodegenerative inher

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6454bf5840368c9c19247bdc02302b3f
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=21824

Interruptions of the FXN GAA Repeat Tract Delay the Age at Onset of Friedreich's Ataxia in a Location Dependent Manner.

Autor: Nethisinghe S; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, Queen Square, London WC1N 3BG, UK., Kesavan M; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, Queen Square, London WC1N 3BG, UK., Ging H; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, Queen Square, London WC1N 3BG, UK., Labrum R; Neurogenetics Service, Rare and Inherited Disease Laboratory, London North Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3BH, UK., Polke JM; Neurogenetics Service, Rare and Inherited Disease Laboratory, London North Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3BH, UK., Islam S; UCL Queen Square Institute of Neurology, London WC1N 3BG, UK., Garcia-Moreno H; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, Queen Square, London WC1N 3BG, UK., Callaghan MF; Wellcome Centre for Human Neuroimaging, UCL Queen Square Institute of Neurology, University College London, London WC1N 3AR, UK., Cavalcanti F; Institute for Biomedical Research and Innovation (IRIB), Italian National Research Council (CNR), 87050 Mangone, Italy., Pook MA; Ataxia Research Group, Division of Biosciences, Department of Life Sciences, College of Health and Life Sciences, Brunel University London, Uxbridge UB8 3PH, UK.; Synthetic Biology Theme, Institute of Environment, Health and Societies, Brunel University London, Uxbridge UB8 3PH, UK., Giunti P; Ataxia Centre, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, Queen Square, London WC1N 3BG, UK.

Publikováno v: International journal of molecular sciences [Int J Mol Sci] 2021 Jul 13; Vol. 22 (14). Date of Electronic Publication: 2021 Jul 13.

Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11p13-11q13, and exclusion of mu-calpain as the multiple endocrine neoplasia type 1 gene

Autor: Pang, JT, Lloyd, SE, Wooding, C, Farren, B, Pottinger, B, Harding, B, Leigh, SE, Pook, MA, Benham, FJ, Gillett, GT, Taggart, RT, Thakker, RV

Forty loci (16 polymorphic and 24 non-polymorphic) together with 23 cosmids isolated from a chromosome 11-specific library were used to construct a detailed genetic map of 11p13-11q13. The map was constructed by using a panel of 13 somatic cell hybri

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2ec7ce12f26d79201da2915df0f1fc80
https://ora.ox.ac.uk/objects/uuid:5a80438b-00b8-4bd4-8e9c-27e30a700ad2

Mitochondria and the reactive species interactome: shaping the future of mitoredox medicine.

Autor: Chatre, Laurent¹ (AUTHOR) chatre@cyceron.fr

Publikováno v: Journal of Mitochondria, Plastids & Endosymbiosis. Dec2024, Vol. 2 Issue 1, p1-38. 38p.

Uromodulin and progression of IgA nephropathy.

Autor: Chen, Zijin¹ (AUTHOR), Xu, Lin-lin² (AUTHOR), Du, Wen¹ (AUTHOR), Ouyang, Yan¹ (AUTHOR), Gu, Xiangchen¹ (AUTHOR), Fang, Zhengying¹ (AUTHOR), Yu, Xialian¹ (AUTHOR), Li, Junru¹ (AUTHOR), Xie, Lin¹ (AUTHOR), Jin, Yuanmeng¹ (AUTHOR), Ma, Jun¹ (AUTHOR), Wang, Zhaohui¹ (AUTHOR), Pan, Xiaoxia¹ (AUTHOR), Zhang, Wen¹ (AUTHOR), Ren, Hong¹ (AUTHOR), Wang, Weiming¹ (AUTHOR), Chen, Xiaonong¹ (AUTHOR), Zhou, Xu-jie² (AUTHOR) zhouxujie@bjmu.edu.cn, Zhang, Hong² (AUTHOR), Chen, Nan¹ (AUTHOR)

Publikováno v: Clinical Kidney Journal. Aug2024, Vol. 17 Issue 8, p1-11. 11p.