Activating Point Mutations
Activating Point Mutations is a type of genetic alteration characterized by a single nucleotide change within a receptor tyrosine kinase gene that results in constitutive activation of its kinase domain, thereby promoting oncogenic signaling.
879
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78.6K
Citations
5.6K
Authors
1.4K
Institutions
Publications per year
2017–2026
100
879
Christian Thiede, Christine Steudel, Brigitte Mohr et al. · Blood · 2002 · 1.7K citations · Full text
Medicine, Genetics, Hematology +14
Clinical Effect of Point Mutations in Myelodysplastic Syndromes
Rafael Bejar, Kristen E. Stevenson, Omar Abdel‐Wahab et al. · New England Journal of Medicine · 2011 · 1.6K citations
Medicine, Genetics, Hematology +17
1–5 of 879
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Fondazione IRCCS Istituto Nazionale dei Tumori, Italy
5 publications · 333 citations
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1–5 of 5.6K
1.4K
National Institutes of Health
Bethesda, United States
28 h-index
132 publications
21K citations

Howard Hughes Medical Institute
Chevy Chase, United States
24 h-index
114 publications
36.5K citations
National Cancer Institute
Bethesda, United States
23 h-index
82 publications
14.1K citations
Inserm
Paris, France
20 h-index
156 publications
21.6K citations
Dana-Farber Cancer Institute
Boston, United States
19 h-index
121 publications
21.1K citations
Harvard University
Cambridge, United States
18 h-index
95 publications
17.4K citations
The University of Texas Southwestern Medical Center
Dallas, United States
16 h-index
43 publications
4.1K citations
University of California, San Francisco
San Francisco, United States
16 h-index
65 publications
9.5K citations
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JBC · 60 publications · 4.7K citations
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Repository · 75 publications · 9.5K citations
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MCB · 35 publications · 2.9K citations
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28 publications · 4.3K citations
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PNAS · 26 publications · 4.5K citations
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