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UBQLN2 gene
Known as:
N4BP4
, PLIC2, MOUSE, HOMOLOG OF
, CHAP1/DSK2
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This gene may play a role in protein turnover.
National Institutes of Health
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Related topics
Related topics
4 relations
Protein Degradation Inhibition
UBQLN1 gene
Ubiquilin-2
Narrower (1)
UBQLN2 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
p62/Sequestosome 1 levels increase and phosphorylation is altered in Cx50D47A lenses, but deletion of p62/sequestosome 1 does not improve transparency
Oscar Jara
,
Hubert Mysliwiec
,
P. Minogue
,
V. M. Berthoud
,
E. Beyer
Molecular Vision
2020
Corpus ID: 214680494
Purpose p62/Sequestosome 1 (p62) is a stress-induced protein that is involved in several different intracellular pathways…
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2017
2017
No Evidence for Pathogenic Role of UBQLN2 Mutations in Sporadic Amyotrophic Lateral Sclerosis in the Mainland Chinese Population
Xiao Huang
,
Shen Shen
,
D. Fan
PLoS ONE
2017
Corpus ID: 17424624
Mutations in the UBQLN2 gene, which encodes a member of the ubiquitin-like protein family (ubiquilin-2), have been identified in…
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2016
2016
Ubiquilin2 as a novel marker for detection of urothelial carcinoma cells in urine
K. Shimada
,
Tomomi Fujii
,
Y. Tatsumi
,
S. Anai
,
K. Fujimoto
,
N. Konishi
Diagnostic Cytopathology
2016
Corpus ID: 26773691
Ubiquilin 2 (UBQLN2), an ubiquitin‐related protein, is strongly expressed in urothelial carcinoma cells, in contrast to no or…
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2014
2014
Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis
Hee‐Jung Kim
,
Min-Jung Kwon
,
+4 authors
S. H. Kim
Neurobiology of Aging
2014
Corpus ID: 207161307
2013
2013
Ubiquilin 2 Is Not Associated with Tau Pathology
Anna Nölle
,
E. S. van Haastert
,
R. Zwart
,
J. Hoozemans
,
W. Scheper
PLoS ONE
2013
Corpus ID: 16591639
Accumulation of aberrant proteins in inclusion bodies is a hallmark of many neurodegenerative diseases. Impairment of proteolytic…
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2012
2012
Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis
S. Millecamps
,
P. Corcia
,
+13 authors
F. Salachas
Neurobiology of Aging
2012
Corpus ID: 43766655
Review
2012
Review
2012
Recent Advances in the Genetics of the ALS-FTLD Complex
H. Morris
,
A. Waite
,
N. Williams
,
J. Neal
,
D. Blake
Current Neurology and Neuroscience Reports
2012
Corpus ID: 39026554
There is a clinical and pathological overlap between amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration…
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2012
2012
UBQLN2 in familial amyotrophic lateral sclerosis in the Netherlands
P. V. Doormaal
,
W. V. Rheenen
,
+6 authors
L. Berg
Neurobiology of Aging
2012
Corpus ID: 22059855
2012
2012
Amyotrophic lateral sclerosis, frontotemporal lobar dementia, and p62
S. Appel
,
L. Rowland
Neurology
2012
Corpus ID: 18046584
Amyotrophic lateral sclerosis (ALS) is a familial disease in 10% of cases and is sporadic in 90%; investigations prior to the…
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Highly Cited
1995
Highly Cited
1995
Molecular analysis of a cytoplasmic dynein light intermediate chain reveals homology to a family of ATPases.
Sharon M. Hughes
,
K. Vaughan
,
J. S. Herskovits
,
R. Vallee
Journal of Cell Science
1995
Corpus ID: 25930597
Cytoplasmic dynein is a multi-subunit complex involved in retrograde organelle transport and some aspects of mitosis. In previous…
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