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Regulating p73 isoforms in human tumours
P. J. Coates
Research output
:
Contribution to journal
›
Editorial
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peer-review
30
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Citations (Scopus)
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Keyphrases
Human Tumors
100%
P73 Isoforms
100%
TP73
100%
TP73 Gene
75%
Tumor
50%
TAp73
50%
Colorectal Cancer
25%
Overexpression
25%
Tumourigenesis
25%
Tumor Suppressor
25%
P300
25%
Tumor Subtype
25%
Regulatory Pathways
25%
P53 Isoforms
25%
Altered Expression
25%
Lymphoma
25%
Prognostic Information
25%
Future Therapeutics
25%
Therapeutic Decision-making
25%
Oncogenic Function
25%
Isoform Expression
25%
Oncogenic Transformation
25%
Leukemia
25%
Chemosensitivity
25%
Zinc Finger E-box Binding Homeobox 1 (ZEB1)
25%
Anti-p53
25%
Pathological Characteristics
25%
Medicine and Dentistry
Neoplasm
100%
P73
100%
Carcinogenesis
60%
Protein P53
40%
Intron
20%
Colorectal Carcinoma
20%
Leukemia
20%
Chemosensitivity
20%
Tumor Suppressor Protein
20%
Biochemistry, Genetics and Molecular Biology
Isoform
100%
P73
100%
Carcinogenesis
50%
P53
33%
Tumor Suppressor Protein
16%
Intron
16%
Chemosensitivity
16%
ZEB1
16%