Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,592,561 papers from all fields of science
Search
Sign In
Create Free Account
ZFYVE26 gene
Known as:
zinc finger FYVE-type containing 26
, ZINC FINGER FYVE DOMAIN-CONTAINING PROTEIN 26
, ZFYVE26
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
6 relations
Broader (1)
Genes
RBSN gene
ZFYVE16 gene
ZFYVE19 gene
ZFYVE21 gene
Narrower (1)
Spastic paraplegia 15, autosomal recessive
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Frequency and phenotype of SPG11 and SPG15 in complicated spastic paraplegia (HSP)
R. Schüle
,
N. Schlipf
,
+11 authors
P. Bauer
2019
Corpus ID: 92988709
Background: Hereditary spastic paraplegias (HSP) are clinically and genetically highly heterogeneous. Recently two novel genes…
Expand
2018
2018
Novel c.C2254T (p.Q752*) mutation in ZFYVE26 (SPG15) gene in a patient with hereditary spastic paraparesis
M. Vinci
,
M. Fichera
,
S. Musumeci
,
F. Calì
,
G. Vitello
Journal Genetika
2018
Corpus ID: 53858803
Hereditary spastic paraplegias are clinically and genetically heterogeneous degenerative disorders, and pathological variants in…
Expand
2018
2018
Identification of novel SPG11 mutations in a cohort of Chinese families with hereditary spastic paraplegia
J. Du
,
Yacen Hu
,
B. Tang
,
Hong Jiang
,
Lu Shen
International Journal of Neuroscience
2018
Corpus ID: 1454671
ABSTRACT Aim of the study: To investigate the mutation frequency of SPG11, SPG15, SPG5 and SPG7 in China. Materials and methods…
Expand
2018
2018
Chapter 2 Lysosomal Dysfunctions in Hereditary Spastic
H. Shimazaki
2018
Corpus ID: 5011991
Hereditary spastic paraplegias (HSPs) comprise a heterogeneous group of inherited neurodegenerative diseases with the cardinal…
Expand
2017
2017
Neuropathology of spastic paraplegia-15 (SPG15) mimics that of Parkinson’s disease
H. Kowa
,
T. Miyawaki
,
+4 authors
T. Toda
Journal of Neurological Sciences
2017
Corpus ID: 54349137
2017
2017
Lysosomal Dysfunctions in Hereditary Spastic Paraplegias
H. Shimazaki
2017
Corpus ID: 80310196
Hereditary spastic paraplegias (HSPs) comprise a heterogeneous group of inherited neu- rodegenerative diseases with the cardinal…
Expand
2016
2016
Beclin-1 knockdown shows abscission failure but not autophagy defect during oocyte meiotic maturation
Seung Yeop You
,
Yong Seok Park
,
+6 authors
J. Oh
Cell Cycle
2016
Corpus ID: 23066534
ABSTRACT Cytokinesis is the final step in cell division that results in the separation of a parent cell into daughter cells…
Expand
2016
2016
Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum
Sanjiban Chakrabarty
,
N. Vijayakumar
,
K. Radhakrishnan
,
K. Satyamoorthy
Journal of Neurology
2016
Corpus ID: 26457441
Hereditary spastic paraplegias (HSPs) are a group of clinically and genetically diverse neurological disorders characterized by…
Expand
2012
2012
Regulation of cytokinesis and its consequences for human health
Antonia P. Sagona
2012
Corpus ID: 145819734
The tumor suppressor activity of Beclin 1 (BECN1), a subunit of class III phosphatidylinositol 3-kinase complex, has been…
Expand
2009
2009
Spastic paraplegia with thinning of the corpus callosum and white matter abnormalities: Further mutations and relative frequency in ZFYVE26/SPG15 in the Italian population
P. Denora
,
M. Muglia
,
+21 authors
F. Santorelli
Journal of Neurological Sciences
2009
Corpus ID: 206280944
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE