Familial Dysautonomia: Mechanisms and Models
Author:
Affiliation:
1. The University of Tennessee, USA
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v39n4/1415-4757-gmb-1678-4685-GMB-2015-0335.pdf
Reference114 articles.
1. Involvment of IKAP in peripheral target innervation and in specific JNK and NGF signaling in developing PNS neurons;Abashidze A;PLoS One,2014
2. Peripheral nerve abnormalities in the Riley-Day syndrome. Findings in a sural nerve biopsy;Aguayo AJ;Arch Neurol,1971
3. Familial dysautonomia is caused by mutations of the IKAP gene;Anderson SL;Am J Hum Genet,2001
4. Tocotrienols reverse IKAP and monoamine oxidase deficiencies in familial dysautonomia;Anderson SL;Biochem Biophys Res Commun,2005
5. Hypothalamic attacks with thalamic lesions: II anatomic considerations;Aring CD;Arch Neurol Psychiat,1945
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3. Metabolic Deficits in the Retina of a Familial Dysautonomia Mouse Model;Metabolites;2024-07-31
4. Age-dependent regulation of ELP1 exon 20 splicing in Familial Dysautonomia by RNA Polymerase II kinetics and chromatin structure;PLOS ONE;2024-06-03
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