All Relations between fgf14 and cerebellum

Publication Sentence Publish Date Extraction Date Species
Tiyasha De, Pooja Sharma, Bharathram Upilli, A Vivekanand, Shreya Bari, Akhilesh Kumar Sonakar, Achal Kumar Srivastava, Mohammed Faru. Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient origin. Neurogenetics. 2024-07-08. PMID:38976084. spinocerebellar ataxia type 27b (sca27b), a recently identified dominantly inherited cerebellar disorder is caused by gaa-repeat expansions in intron 1 of fibroblast growth factor 14 (fgf14). 2024-07-08 2024-07-11 Not clear
Marie K Bosch, Jeanne M Nerbonne, R Reid Townsend, Haruko Miyazaki, Nobuyuki Nukina, David M Ornitz, Céline Marionnea. Proteomic analysis of native cerebellar iFGF14 complexes. Channels (Austin, Tex.). vol 10. issue 4. 2017-07-24. PMID:26889602. additional experiments were completed using an anti-pannav antibody to immunoprecipitate nav channel complexes from wild type and fgf14(-/-) mouse cerebellum. 2017-07-24 2023-08-13 mouse
Marie K Bosch, Jeanne M Nerbonne, R Reid Townsend, Haruko Miyazaki, Nobuyuki Nukina, David M Ornitz, Céline Marionnea. Proteomic analysis of native cerebellar iFGF14 complexes. Channels (Austin, Tex.). vol 10. issue 4. 2017-07-24. PMID:26889602. parallel control experiments were performed on cerebellar proteins isolated from mice (fgf14(-/-)) harboring a targeted disruption of the fgf14 locus. 2017-07-24 2023-08-13 mouse
Filippo Tempia, Eriola Hoxha, Giulia Negro, Musaad A Alshammari, Tahani K Alshammari, Neli Panova-Elektronova, Fernanda Laezz. Parallel fiber to Purkinje cell synaptic impairment in a mouse model of spinocerebellar ataxia type 27. Frontiers in cellular neuroscience. vol 9. 2015-06-19. PMID:26089778. to gain insights in the cerebellar deficits in the animal model of the human disease, we applied whole-cell voltage-clamp in the acute cerebellar slice preparation to examine the properties of parallel fibers (pf) to purkinje neuron synapses in fgf14 (-/-) mice and wild type littermates. 2015-06-19 2023-08-13 mouse
J A Coebergh, D E Fransen van de Putte, I N Snoeck, C Ruivenkamp, A van Haeringen, L M Smi. A new variable phenotype in spinocerebellar ataxia 27 (SCA 27) caused by a deletion in the FGF14 gene. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. vol 18. issue 3. 2015-02-12. PMID:24252256. fgf14 regulates brain sodium channels, especially in the cerebellum. 2015-02-12 2023-08-12 Not clear
Vikram G Shakkottai, Maolei Xiao, Lin Xu, Michael Wong, Jeanne M Nerbonne, David M Ornitz, Kelvin A Yamad. FGF14 regulates the intrinsic excitability of cerebellar Purkinje neurons. Neurobiology of disease. vol 33. issue 1. 2009-02-17. PMID:18930825. current clamp recordings from purkinje neurons in cerebellar slices revealed attenuated spontaneous firing in fgf14(-/-) neurons. 2009-02-17 2023-08-12 mouse
Hidehiro Mizusaw. [Autosomal dominant spinocerebellar degeneration--new forms and pathomechanisms]. Rinsho shinkeigaku = Clinical neurology. vol 44. issue 11. 2005-03-04. PMID:15651290. the outlines of some new members, namely autosomal dominant cortical cerebellar atrophy linked to chromosome 16 (16q-adcca), sca14, an ataxia caused by fgf14 mutation and a form of neuroferritinopathy were described. 2005-03-04 2023-08-12 Not clear
Alfredo Brusco, Cinzia Gellera, Claudia Cagnoli, Alessandro Saluto, Alessia Castucci, Chiara Michielotto, Vincenza Fetoni, Caterina Mariotti, Nicola Migone, Stefano Di Donato, Franco Taron. Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families. Archives of neurology. vol 61. issue 5. 2004-06-17. PMID:15148151. autosomal dominant cerebellar ataxias are a clinical and genetically heterogeneous group of progressive neurodegenerative diseases, at present associated with 22 loci (spinocerebellar ataxia [sca] 1-sca8, sca10-sca19, sca21, sca22, fibroblast growth factor 14 [fgf14]-sca, and dentatorubral-pallidoluysian atrophy [drpla]). 2004-06-17 2023-08-12 Not clear
John C van Swieten, Esther Brusse, Bianca M de Graaf, Elmar Krieger, Raoul van de Graaf, Inge de Koning, Anneke Maat-Kievit, Peter Leegwater, Dennis Dooijes, Ben A Oostra, Peter Heutin. A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]. American journal of human genetics. vol 72. issue 1. 2003-02-21. PMID:12489043. the present fgf14 mutation represents a novel gene defect involved in the neurodegeneration of cerebellum and basal ganglia. 2003-02-21 2023-08-12 mouse
Q Wang, D G McEwen, D M Ornit. Subcellular and developmental expression of alternatively spliced forms of fibroblast growth factor 14. Mechanisms of development. vol 90. issue 2. 2000-04-27. PMID:10640713. we also show that during cerebellar development, fgf14 is first observed at postnatal day 1 in post mitotic granule cells, and later in development, in migrating and post migratory granule cells. 2000-04-27 2023-08-12 mouse
Q Wang, D G McEwen, D M Ornit. Subcellular and developmental expression of alternatively spliced forms of fibroblast growth factor 14. Mechanisms of development. vol 90. issue 2. 2000-04-27. PMID:10640713. the developmental expression pattern of fgf14 in the cerebellum is complementary to that of math1, a marker for proliferating granule cells in the external germinal layer. 2000-04-27 2023-08-12 mouse