| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Adele G Marthaler, Alisa Tubsuwan, Benjamin Schmid, Ulla B Poulsen, Poul Hyttel, Jørgen E Nielsen, Troels T Nielsen, Bjørn Hols. Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H271. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345803. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Alexander F Engelbrecht, Ulrike A Mau-Holzmann, Poul Hyttel, Jørgen E Nielsen, Troels T Nielsen, Bjørn Hols. Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H196. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345804. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Poul Hyttel, Troels T Nielsen, Jørgen E Nielsen, Bjørn Hols. Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H266. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345805. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Alexander F Engelbrecht, Ulrike A Mau-Holzmann, Poul Hyttel, Jørgen E Nielsen, Troels T Nielsen, Bjørn Hols. Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H271. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345809. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Benjamin Schmid, Alisa Tubsuwan, Ulla B Poulsen, Poul Hyttel, Troels T Nielsen, Jørgen E Nielsen, Bjørn Hols. Generation of spinocerebellar ataxia type 2 patient-derived iPSC line H196. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345814. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Adele G Marthaler, Alisa Tubsuwan, Benjamin Schmid, Ulla B Poulsen, Alexander F Engelbrecht, Ulrike A Mau-Holzmann, Poul Hyttel, Troels T Nielsen, Jørgen E Nielsen, Bjørn Hols. Generation of an isogenic, gene-corrected control cell line of the spinocerebellar ataxia type 2 patient-derived iPSC line H266. Stem cell research. vol 16. issue 1. 2016-12-13. PMID:27345815. |
spinocerebellar ataxia type 2 (sca2) is a neurodegenerative disease primarily affecting the cerebellum. |
2016-12-13 |
2023-08-13 |
Not clear |
| Harini Sarva, William Lawrence Severt, Nuri Jacoby, Seth L Pullman, Rachel Saunders-Pullma. Secondary orthostatic tremor in the setting of cerebellar degeneration. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. vol 27. 2016-11-07. PMID:26765757. |
we present two patients with ot and cerebellar degeneration, one of whom had spinocerebellar ataxia type 2 and a good treatment response. |
2016-11-07 |
2023-08-13 |
Not clear |
| Giselle Melo Fontes Silva, José Luiz Pedroso, Diogo Fernandes Dos Santos, Pedro Braga-Neto, Lucila Bizari Fernandes Do Prado, Luciane Bizari Coin De Carvalho, Orlando G P Barsottini, Gilmar Fernandes Do Prad. NREM-related parasomnias in Machado-Joseph disease: clinical and polysomnographic evaluation. Journal of sleep research. vol 25. issue 1. 2016-10-28. PMID:26359123. |
spinocerebellar ataxias (sca) are autosomal dominant neurodegenerative disorders that affect the cerebellum and its connections, and have a marked clinical and genetic variability. |
2016-10-28 |
2023-08-13 |
human |
| Jan Cendeli. Transplantation and Stem Cell Therapy for Cerebellar Degenerations. Cerebellum (London, England). vol 15. issue 1. 2016-10-21. PMID:26155762. |
in purkinje cell degeneration mice, lurcher mutant mice and mouse models of spinocerebellar ataxia type 1 and type 2 and niemann-pick disease type c. despite the lack of direct comparative studies, it appears that there might be differences in graft development and functioning between various types of cerebellar degeneration. |
2016-10-21 |
2023-08-13 |
mouse |
| Sriram Jayabal, Lovisa Ljungberg, Thomas Erwes, Alexander Cormier, Sabrina Quilez, Sara El Jaouhari, Alanna J Wat. Rapid Onset of Motor Deficits in a Mouse Model of Spinocerebellar Ataxia Type 6 Precedes Late Cerebellar Degeneration. eNeuro. vol 2. issue 6. 2016-09-20. PMID:26730403. |
rapid onset of motor deficits in a mouse model of spinocerebellar ataxia type 6 precedes late cerebellar degeneration. |
2016-09-20 |
2023-08-13 |
mouse |
| Nura Hamidu Alkali, Sunday A Bwala, Saeed A Alimi, Shyngle I Oyakhir. Spinocerebellar ataxia type-7: Report of a family in Northwest Nigeria. Annals of African medicine. vol 15. issue 2. 2016-09-16. PMID:27044733. |
spinocerebellar ataxia type-7 (sca7) is a cytosine-adenine-guanine (cag) repeat polyglutamine disorder characterized by progressive degeneration of the cerebellum, brainstem, spinal cord, and retina. |
2016-09-16 |
2023-08-13 |
Not clear |
| Chiharu Isono, Makito Hirano, Hikaru Sakamoto, Shuichi Ueno, Susumu Kusunoki, Yusaku Nakamur. Differential Progression of Dysphagia in Heredity and Sporadic Ataxias Involving Multiple Systems. European neurology. vol 74. issue 5-6. 2016-08-29. PMID:26618669. |
sporadic ataxia affecting multiple systems, such as cerebellar, extrapyramidal, and autonomic systems, is known as multiple system atrophy cerebellar type (msa-c), while similar multisystem involvements are seen in certain types of hereditary ataxia, such as spinocerebellar ataxia type 3 (sca3). |
2016-08-29 |
2023-08-13 |
Not clear |
| Lena Constantin, Brandon J Wainwrigh. MicroRNAs Promote Granule Cell Expansion in the Cerebellum Through Gli2. Cerebellum (London, England). vol 14. issue 6. 2016-08-15. PMID:25910616. |
their deregulation results in cerebellar neuronal degeneration and spinocerebellar ataxia type 1 and contributes to medulloblastoma. |
2016-08-15 |
2023-08-13 |
mouse |
| Sarah Doss, Jan Leo Rinnenthal, Tanja Schmitz-Hübsch, Alexander U Brandt, Sebastian Papazoglou, Silke Lux, Stephan Maul, Jens Würfel, Matthias Endres, Thomas Klockgether, Martina Minnerop, Friedemann Pau. Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency. Journal of neurology. vol 262. issue 8. 2016-06-22. PMID:26041613. |
cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency. |
2016-06-22 |
2023-08-13 |
Not clear |
| Carlos R Hernandez-Castillo, Víctor Galvez, Roberto E Mercadillo, Rosalinda Díaz, Petra Yescas, Leticia Martinez, Adriana Ochoa, Luis Velazquez-Perez, Juan Fernandez-Rui. Functional connectivity changes related to cognitive and motor performance in spinocerebellar ataxia type 2. Movement disorders : official journal of the Movement Disorder Society. vol 30. issue 10. 2016-06-17. PMID:26256273. |
several neuropathological studies in spinocerebellar ataxia type 2 (sca2) have revealed significant atrophy of the cerebellum, brainstem, sensorimotor cortex, and several regions in the frontal lobe. |
2016-06-17 |
2023-08-13 |
Not clear |
| Megan S Keiser, Jeffrey H Kordower, Pedro Gonzalez-Alegre, Beverly L Davidso. Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy. Brain : a journal of neurology. vol 138. issue Pt 12. 2016-05-04. PMID:26490326. |
spinocerebellar ataxia type 1 is one of nine polyglutamine expansion diseases and is characterized by cerebellar ataxia and neuronal degeneration in the cerebellum and brainstem. |
2016-05-04 |
2023-08-13 |
mouse |
| Megan S Keiser, Jeffrey H Kordower, Pedro Gonzalez-Alegre, Beverly L Davidso. Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy. Brain : a journal of neurology. vol 138. issue Pt 12. 2016-05-04. PMID:26490326. |
collectively the data illustrate the biodistribution and tolerability of raav1.mis1egfp administration to the adult rhesus cerebellum and are supportive of clinical application for spinocerebellar ataxia type 1. |
2016-05-04 |
2023-08-13 |
mouse |
| Jian-Wen Chen, Li Zhao, Feng Zhang, Lan Li, Yu-Hang Gu, Jing-Yuan Zhou, Hui Zhang, Ming Meng, Kai-Hua Zhang, Wei-Dong Le, Chun-Bo Don. Clinical Characteristics, Radiological Features and Gene Mutation in 10 Chinese Families with Spinocerebellar Ataxias. Chinese medical journal. vol 128. issue 13. 2016-03-15. PMID:26112709. |
spinocerebellar ataxias (scas) are a group of neurodegenerative disorders that primarily cause the degeneration in the cerebellum, spinal cord, and brainstem. |
2016-03-15 |
2023-08-13 |
Not clear |
| Irene Pulido-Valdeolivas, David Gómez-Andrés, Irene Sanz-Gallego, Estrella Rausell, Javier Arp. Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit. Cerebellum & ataxias. vol 3. 2016-02-24. PMID:26909158. |
spinocerebellar ataxia type 3 (sca3) is a neurodegenerative disorder that affects the cerebellar system and other subcortical regions of the brain. |
2016-02-24 |
2023-08-13 |
Not clear |
| David D Bushart, Geoffrey G Murphy, Vikram G Shakkotta. Precision medicine in spinocerebellar ataxias: treatment based on common mechanisms of disease. Annals of translational medicine. vol 4. issue 2. 2016-02-18. PMID:26889478. |
spinocerebellar ataxias (scas) are a heterogeneous group of dominantly inherited neurodegenerative disorders affecting the cerebellum and its associated pathways. |
2016-02-18 |
2023-08-13 |
Not clear |