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Mutant Proteins
Known as:
Proteins, Mutant
, Mutant Protein
, Protein, Mutant
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Proteins produced from GENES that have acquired MUTATIONS.
National Institutes of Health
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Related topics
Related topics
8 relations
In Blood
Process of secretion
agonists
antagonists & inhibitors
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2016
Highly Cited
2016
Mutant Calreticulin Requires Both Its Mutant C-terminus and the Thrombopoietin Receptor for Oncogenic Transformation.
Shannon E Elf
,
Nouran S. Abdelfattah
,
+13 authors
A. Mullally
Cancer Discovery
2016
Corpus ID: 207672865
UNLABELLED Somatic mutations in calreticulin (CALR) are present in approximately 40% of patients with myeloproliferative…
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Highly Cited
2010
Highly Cited
2010
Nonsense Mediated Decay Resistant Mutations Are a Source of Expressed Mutant Proteins in Colon Cancer Cell Lines with Microsatellite Instability
David S. Williams
,
M. Bird
,
+5 authors
A. Burgess
PLoS ONE
2010
Corpus ID: 3095842
Background Frameshift mutations in microsatellite instability high (MSI-High) colorectal cancers are a potential source of…
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Highly Cited
1998
Highly Cited
1998
Neuropathy target esterase and a homologous Drosophila neurodegeneration-associated mutant protein contain a novel domain conserved from bacteria to man.
Michael J. Lush
,
Yong Li
,
D. Read
,
A. Willis
,
P. Glynn
Biochemical Journal
1998
Corpus ID: 22070538
The N-terminal amino acid sequences of proteolytic fragments of neuropathy target esterase (NTE), covalently labelled on its…
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Highly Cited
1997
Highly Cited
1997
Characterization of a polymorphism in NAD(P)H: quinone oxidoreductase (DT-diaphorase).
RD Traver
,
D. Siegel
,
+4 authors
D. Ross
British Journal of Cancer
1997
Corpus ID: 12930571
NAD(P)H:quinone oxidoreductase (NQO1, EC 1.6.99.2) is an obligate two-electron reductase that can either bioactivate or detoxify…
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Highly Cited
1996
Highly Cited
1996
Expression of Normal and Mutant Huntingtin in the Developing Brain
P. Bhide
,
Michelle Day
,
+8 authors
M. Difiglia
Journal of Neuroscience
1996
Corpus ID: 16426953
Huntington’s disease (HD) is caused by a genetic mutation that results in a polyglutamine expansion in huntingtin. The time…
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Highly Cited
1995
Highly Cited
1995
Proline‐rich (PxxP) motifs in HIV‐1 Nef bind to SH3 domains of a subset of Src kinases and are required for the enhanced growth of Nef+ viruses but not for down‐regulation of CD4.
K. Saksela
,
Genhong Cheng
,
David Baltimore
EMBO Journal
1995
Corpus ID: 32913142
Human immunodeficiency virus (HIV) and simian immunodeficiency virus Nef proteins contain a conserved motif with the minimal…
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Highly Cited
1995
Highly Cited
1995
CAG expansion affects the expression of mutant huntingtin in the Huntington's disease brain
N. Aronin
,
K. Chase
,
+14 authors
M. Difiglia
Neuron
1995
Corpus ID: 16666584
Highly Cited
1993
Highly Cited
1993
An interleukin 4 (IL-4) mutant protein inhibits both IL-4 or IL-13- induced human immunoglobulin G4 (IgG4) and IgE synthesis and B cell proliferation: support for a common component shared by IL-4…
G. Aversa
,
J. Punnonen
,
+6 authors
Jan E. de Vries
Journal of Experimental Medicine
1993
Corpus ID: 11542163
Interleukin 4 (IL-4) and IL-13 share many biological functions. Both cytokines promote growth of activated human B cells and…
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Highly Cited
1992
Highly Cited
1992
Involvement of the chaperonin dnaK in the rapid degradation of a mutant protein in Escherichia coli.
Sherman MYu
,
A. Goldberg
EMBO Journal
1992
Corpus ID: 9510275
The ability of Escherichia coli rapidly to degrade abnormal proteins is inhibited by mutations affecting any of several heat…
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Highly Cited
1990
Highly Cited
1990
A mutant T4 lysozyme displays five different crystal conformations
H. R. Faber
,
Brian W. Matthews
Nature
1990
Corpus ID: 4266149
PHAGE T4 lysozyme consists of two domains between which is formed the active-site cleft of the enzyme1,2. The…
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