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TRIM21 gene
Known as:
SSA
, TRIM21
, RNF81
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This gene is involved in the modulation of protein ubiquitination.
National Institutes of Health
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Related topics
Related topics
6 relations
Cell Cycle Control
Lupus Erythematosus, Systemic
TRIM21 protein, human
TRIM34 gene
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Narrower (1)
TRIM21 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Map-based estimates of present carbon stocks of grazing lands in Sub-Sahara Africa
N. Batjes
,
E. Milne
,
S. Williams
2015
Corpus ID: 133270181
This report is a detailed review, synthesis, and analysis of the current “state of the science” concerning the potential for…
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2015
2015
Effects of Trade Facilitation on Inequality: A Case Study of Sub-Sahara Africa
E. Olubiyi
2015
Corpus ID: 67762959
Inequality in the sub-Saharan Africa has been on the high side compared to other regions of the world. The policy makers in the…
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2015
2015
Tyrosine phosphorylation of the E 3 ubiquitin ligase TRIM 21 positively regulates interaction with IRF 3 and hence TRIM 21 activity
K. Stacey
,
E. Breen
,
C. Jefferies
2015
Corpus ID: 15361846
Patients suffering from Systemic Lupus Erythematous (SLE) have elevated type I interferon (IFN) levels which correlate with…
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2006
2006
La représentation SSA : sémantique, analyses et implémentation dans GCC
S. Pop
2006
Corpus ID: 177890064
Le langage d'assignation statique unique, SSA, est l'une des representations intermediaires les plus communement utilisees dans…
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2006
2006
Presence of serum TRIM21 antibodies in patients with esophageal squamous cell carcinoma
麻里 久保嶋
2006
Corpus ID: 76809097
2001
2001
Functional topography as a guideline for differential diagnosis of vertical eye movement disorders and oblique muscle surgery
S. Priglinger
,
H. Hametner
,
T. Haslwanter
Spektrum der Augenheilkunde
2001
Corpus ID: 8328993
SummaryAimsThe differential diagnosis of congenital superior oblique paresis (strabismus sursoadductorius), acquired superior…
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Review
2000
Review
2000
[Heredity and immunology in Sjogren's syndrome].
R. Jonsson
,
B. Nakken
,
A. Halse
,
K. Skarstein
,
K. Brokstad
,
Haga Hj
Tidsskrift for Den Norske Laegeforening
2000
Corpus ID: 26006537
BACKGROUND Over the next 3-5 years, the rapid progress in genomic research will enable the discovery of many genes associated…
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1993
1993
A calreticulin‐like protein co‐purifies with a ‘60 kD’ component of Ro/SSA, but is not recognized by antibodies in Sjögren's syndrome sera
J. Lu
,
A. Willis
,
Robert B Sim
Clinical and Experimental Immunology
1993
Corpus ID: 44884090
In this study, we used human tonsils for the isolation of the 60 kD component of the Ro/SSA autoantigen. following the method…
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1987
1987
Prevalence of anti-SSA (Ro) antibodies in a Mexican population of patients with various systemic rheumatic diseases.
I. García-De La Torre
,
Á. Sánchez-Guerrero
,
G. Salmón-de la Torre
,
L. Hernández-Vázquez
Journal of Rheumatology
1987
Corpus ID: 21797792
The prevalence of anti-SSA (Ro) antibodies was investigated in 126 patients with various systemic rheumatic diseases and in 77…
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1985
1985
Congenital complete heart block with maternal primary Sjögren's syndrome.
G. McCormack
,
W. Barth
Southern medical journal (Birmingham, Ala. Print)
1985
Corpus ID: 8496916
We have described a case of congenital complete heart block associated with maternal primary Sjögren's syndrome. This diagnosis…
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