GENE OVERVIEW OF KEY PUBLISHED STUDIES FOR ALS


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FALSSALSMaleFemaleBulbarLimbNo dataMean age onsetN
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ANIMAL MODELS

                               

KEY PUBLICATIONS (43)

First_AuthorYearTitlePaper
Bäumer2010Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutationsFull_Paper
Belzil2009Mutations in FUS cause FALS and SALS in French and French Canadian populationsFull_Paper
Belzil2010Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosisFull_Paper
Belzil2011Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosisFull_Paper
Belzil2012Novel FUS Deletion in a Patient With Juvenile Amyotrophic Lateral SclerosisFull_Paper
Bertolin2014Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variantsFull_Paper
Blair2010FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysisFull_Paper
Bosco2010Mutant FUS proteins that cause amyotrophic lateral sclerosis incorporate into stress granulesFull_Paper
Broustal2010FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosisFull_Paper
Brown2012SOD1, ANG, TARDBP and FUS mutations in Amyotrophic Lateral Sclerosis: a United States clinical testing lab experienceFull_Paper
Chio2009Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutationFull_Paper
Conte2011P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosisFull_Paper
Conte2012P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosisFull_Paper
Corrado2010Mutations of FUS Gene in Sporadic Amyotrophic Lateral Sclerosis Full_Paper
Damme2010The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALSFull_Paper
Groen2010FUS mutations in familial amyotrophic lateral sclerosis in the NetherlandsFull_Paper
Groen2010FUS mutations in familial amyotrophic lateral sclerosis in the NetherlandsFull_Paper
Hewitt2010Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosisFull_Paper
Huang2010Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusionsFull_Paper
Huang2010Extensive FUS-immunoreactive pathology in juvenile amyotrophic lateral sclerosis with basophilic inclusionsFull_Paper
Ito2011Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body diseaseFull_Paper
Kwiatkowski2009Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisFull_Paper
Kwon2012Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALSFull_Paper
Lagier-Tourenne2009Rethinking ALS: the FUS about TDP-43Full_Paper
Millecamps2010SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlationsFull_Paper
Mochizuki2012Familial ALS with FUS P525L mutation: two Japanese sisters with multiple systems involvementFull_Paper
Nagayama2012Novel FUS mutation in patients with sporadic amyotrophic lateral sclerosis and corticobasal degenerationFull_Paper
Özoguz2015The distinct genetic pattern of ALS in Turkey and novel mutationsFull_Paper
Rademakers2010Fus gene mutations in familial and sporadic amyotrophic lateral sclerosisFull_Paper
Seleen  Full_Paper
Sproviero2012FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysisFull_Paper
Suzuki2012FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutationFull_Paper
Syriani2011FUS/TLS gene mutations are the second most frequent cause of familial ALS in the Spanish populationFull_Paper
Ticozzi2009Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohortFull_Paper
Tsai2010FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALSFull_Paper
van Blitterswijk2012Evidence for an oligogenic basis of amyotrophic lateral sclerosisFull_Paper
van Blitterswijk2012Genetic overlap between apparently sporadic motor neuron diseasesFull_Paper
van Blitterswijk2012Genetic overlap between apparently sporadic motor neuron diseasesFull_Paper
Van Langenhove2010Genetic contribution of FUS to frontotemporal lobar degenerationFull_Paper
Vance2009Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6Full_Paper
Waibel2010Novel missense and truncating mutations in FUS/TLS in familial ALSFull_Paper
Yan2010Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementiaFull_Paper
Zou2012Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese originFull_Paper