Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,035,249 papers from all fields of science
Search
Sign In
Create Free Account
sp100 antigen
Known as:
sp100
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
3 relations
SP100 gene
sp100 Ab:PrThr:Pt:Ser:Ord
sp100 Ab:PrThr:Pt:Ser:Ord:IB
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2013
Review
2013
Retraction: Sp100 as a potent tumor suppressor: accelerated senescence and rapid malignant transformation of human fibroblasts through modulation of an embryonic stem cell program.
D. Negorev
,
O. Vladimirova
,
+6 authors
A. Capobianco
Cancer Research
2013
Corpus ID: 207619043
The authors wish to retract the article entitled "Sp100 as a Potent Tumor Suppressor: Accelerated Senescence and Rapid Malignant…
Expand
Highly Cited
2013
Highly Cited
2013
Sp100 Provides Intrinsic Immunity against Human Papillomavirus Infection
Wesley H. Stepp
,
Jordan M Meyers
,
A. McBride
mBio
2013
Corpus ID: 17418886
ABSTRACT Most DNA viruses associate with, and reorganize, nuclear domain 10 (ND10) bodies upon entry into the host nucleus. In…
Expand
2012
2012
Epitope‐specific anti‐nuclear antibodies are expressed in a mouse model of primary biliary cirrhosis and are cytokine‐dependent
C‐Y. Yang
,
P. Leung
,
+8 authors
M. Gershwin
Clinical and Experimental Immunology
2012
Corpus ID: 9579935
Although the hallmark of primary biliary cirrhosis (PBC) is the presence of anti‐mitochondrial antibodies (AMA), a significant…
Expand
2011
2011
Cdc20 mediates D-box-dependent degradation of Sp100.
Ran Wang
,
Ke Li
,
Cai-hong Zhou
,
J. Xue
,
C. Ji
,
Jin-zhong Chen
Biochemical and Biophysical Research…
2011
Corpus ID: 24623409
Highly Cited
2011
Highly Cited
2011
SUMO Pathway Dependent Recruitment of Cellular Repressors to Herpes Simplex Virus Type 1 Genomes
Delphine Cuchet-Lourenço
,
Chris Boutell
,
+5 authors
R. Everett
PLoS Pathogens
2011
Corpus ID: 22663435
Components of promyelocytic leukaemia (PML) nuclear bodies (ND10) are recruited to sites associated with herpes simplex virus…
Expand
Highly Cited
2007
Highly Cited
2007
Noncovalent interaction between Ubc9 and SUMO promotes SUMO chain formation
P. Knipscheer
,
W. J. van Dijk
,
J. Olsen
,
M. Mann
,
T. Sixma
EMBO Journal
2007
Corpus ID: 8921484
The ubiquitin‐related modifier SUMO regulates a wide range of cellular processes by post‐translational modification with one, or…
Expand
2001
2001
Evidence for separate ND10-binding and homo-oligomerization domains of Sp100.
D. Negorev
,
A. M. Ishov
,
G. Maul
Journal of Cell Science
2001
Corpus ID: 46223550
Nuclear domains called ND10 or PML nuclear bodies consist of an aggregation of several proteins, most notably PML and Sp100. PML…
Expand
Highly Cited
1999
Highly Cited
1999
Viral Immediate-Early Proteins Abrogate the Modification by SUMO-1 of PML and Sp100 Proteins, Correlating with Nuclear Body Disruption
S. Müller
,
A. Dejean
Journal of Virology
1999
Corpus ID: 42755626
ABSTRACT PML nuclear bodies (NBs) are subnuclear structures whose integrity is compromised in certain human diseases, including…
Expand
Highly Cited
1997
Highly Cited
1997
Evidence for Covalent Modification of the Nuclear Dot–associated Proteins PML and Sp100 by PIC1/SUMO-1
T. Sternsdorf
,
K. Jensen
,
H. Will
Journal of Cell Biology
1997
Corpus ID: 16437727
PML and Sp100 proteins are associated with nuclear domains, known as nuclear dots (NDs). They were discovered in the context of…
Expand
Highly Cited
1992
Highly Cited
1992
IFN enhance expression of Sp100, an autoantigen in primary biliary cirrhosis.
H. Guldner
,
C. Szostecki
,
T. Grötzinger
,
H. Will
Journal of Immunology
1992
Corpus ID: 20921655
About 30% of patients suffering from the chronic autoimmune liver disease primary biliary cirrhosis produce autoantibodies…
Expand
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
or Only Accept Required