Gigaxonin, human

Known as: GAN, Kelch-Like Family Member 16, Gigaxonin 
Gigaxonin (597 aa, ~68 kDa) is encoded by the human GAN gene. This protein plays a role in the modulation of both protein ubiquitination and… (More)

Topic mentions per year

Topic mentions per year

1993-2018
051019932018

Papers overview

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2013
2013
Giant axonal neuropathy (GAN) is an early-onset neurological disorder caused by mutations in the GAN gene (encoding for gigaxonin… (More)
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2011
2011
Giant Axonal Neuropathy (GAN) is a fatal neurodegenerative disorder with early onset characterized by a severe deterioration of… (More)
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2009
2009
Gigaxonin mutations cause the fatal human neurodegenerative disorder giant axonal neuropathy (GAN). Broad deterioration of the… (More)
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2009
2009
The so-called General Adaptive Neighborhood Image Processing (GANIP) approach is presented in a two parts paper dealing… (More)
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2007
2007
The recent development of microarray technology provided unprecedented opportunities to understand the genetic basis of aging. So… (More)
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2005
2005
Giant axonal neuropathy (GAN) is a devastating sensory and motor neuropathy caused by mutations in the GAN gene, which encodes… (More)
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2005
2005
Gigaxonin is mutated in human giant axonal neuropathy (GAN), an autosomal recessive neurodegenerative disorder. The presence of… (More)
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2004
2004
Mutations in the gigaxonin gene cause giant axonal neuropathy. The amino-terminus of gigaxonin contains a BTB domain but no… (More)
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2004
2004
Giant axonal neuropathy (GAN) is a rare autosomal recessive neurodegenerative disorder of early onset, clinically characterized… (More)
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1993
1993
The gastrointestinal autonomic nerve tumor (GAN tumor) is an uncommon stromal tumor of the intestinal tract and retroperitoneum… (More)
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