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ZFYVE26 gene

Known as: zinc finger FYVE-type containing 26, ZINC FINGER FYVE DOMAIN-CONTAINING PROTEIN 26, ZFYVE26 
National Institutes of Health

Related topics

Related topics

6 relations

Broader (1)

Genes
RBSN geneZFYVE16 geneZFYVE19 geneZFYVE21 gene

Narrower (1)

Spastic paraplegia 15, autosomal recessive

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2018
Highly Cited
2018
Role of the AP-5 adaptor protein complex in late endosome-to-Golgi retrieval
The AP-5 adaptor protein complex is presumed to function in membrane traffic, but so far nothing is known about its pathway or… 
2018
2018
ZFYVE26/SPASTIZIN and SPG11/SPATACSIN mutations in hereditary spastic paraplegia types AR-SPG15 and AR-SPG11 have different effects on autophagy and endocytosis
ABSTRACT ZFYVE26/Spastizin and SPG11/Spatacsin encode 2 large proteins that are mutated in hereditary autosomal-recessive spastic… 
2016
2016
Beclin-1 knockdown shows abscission failure but not autophagy defect during oocyte meiotic maturation
ABSTRACT Cytokinesis is the final step in cell division that results in the separation of a parent cell into daughter cells… 
Highly Cited
2013
Highly Cited
2013
Interaction between AP-5 and the hereditary spastic paraplegia proteins SPG11 and SPG15
The adaptor protein complex AP-5 is stably associated with the hereditary spastic paraplegia proteins SPG11 and SPG15 in an… 
Highly Cited
2012
Highly Cited
2012
Spatacsin and spastizin act in the same pathway required for proper spinal motor neuron axon outgrowth in zebrafish
Highly Cited
2009
Highly Cited
2009
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
Background: Hereditary spastic paraplegias (HSP) are clinically and genetically highly heterogeneous. Recently, two novel genes… 
Highly Cited
2009
Highly Cited
2009
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity
Hereditary spastic paraplegias (HSP) constitute a clinically and genetically heterogeneous group of neurodegenerative disorders… 
Highly Cited
2009
Highly Cited
2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
Objective: Hereditary spastic paraplegias (HSPs) are very heterogeneous inherited neurodegenerative disorders. Our group recently… 
Highly Cited
2008
Highly Cited
2008
Hereditary spastic paraplegia with mental impairment and thin corpus callosum in Tunisia: SPG11, SPG15, and further genetic heterogeneity.
OBJECTIVE To perform a clinical and genetic study of Tunisian families with autosomal recessive (AR) hereditary spastic… 
Highly Cited
2001
Highly Cited
2001
SPG15, a new locus for autosomal recessive complicated HSP on chromosome 14q
The authors studied two families with autosomal recessive hereditary spastic paraplegia (HSP) complicated by the presence of… 
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