Cited by 131Protein Degradation and InhibitorsMultiple Myeloma Research and TreatmentsAcute Myeloid Leukemia Research

The DOI matches its Crossref record; 62 of the 62 references it cites were found in a registry or an index.

Crbn I391V is sufficient to confer in vivo sensitivity to thalidomide and its derivatives in mice

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Abstract

Key Points: Crbn I391V mice degrade known thalidomide derivative targets and recapitulate thalidomide-induced cytopenias and teratogenicity. Degradation of Ck1α is sufficient to explain the in vivo therapeutic window of lenalidomide in del(5q) myelodysplastic syndrome.

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Crossref · 10.1182/blood-2018-05-852798

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Metadata

Authors
Fink, E. C., McConkey, M., Adams, D. N., Haldar, S. D., Kennedy, J. A., Guirguis, A. A., Udeshi, N. D., Mani, D. R., Chen, M., Liddicoat, B., Svinkina, T., Nguyen, A. T., Carr, S. A., & Ebert, B. L.
Affiliations
Broad Institute (US)
Venue
Blood
Published
2018-10-04
Volume
132
Issue
14
Pages
1535-1544
ISSN
  • 0006-4971 (ISSN-L)
  • 1528-0020
OpenAlex
W2886628870
Cited by
131
References
62
Citations by year
2026: 19 · 2025: 22 · 2024: 20 · 2023: 13 · 2022: 14 · 2021: 16 · 2020: 16 · 2019: 7 · 2018: 3
FWCI
3.73
Type
journal article
Language
en
Open access
Locations
  • Blood (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Howard Hughes Medical Institute
  • Edward P. Evans Foundation
  • Henry and Marilyn Taub Foundation
  • National Institutes of Health
  • National Heart, Lung, and Blood Institute (R01HL082945)
  • National Cancer Institute (F30CA199988, P01CA108631, P50CA206963, P01CA066996)
  • National Institute of General Medical Sciences (T32GM007753)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Degradation and Inhibitors
  • Health Sciences › Medicine › Hematology › Multiple Myeloma Research and Treatments
  • Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
Keywords
thalidomide, lenalidomide, thalidomide derivatives, del(5q) myelodysplastic syndrome, teratogenicity, therapeutic window, E3 ubiquitin ligase
MeSH terms
Lenalidomide, Animals, Antineoplastic Agents, Disease Models, Animal, Female, Hematopoiesis, Male, Mice, Inbred C57BL, Myelodysplastic Syndromes, Nerve Tissue Proteins, Thalidomide, Point Mutation, Casein Kinase I, Adaptor Proteins, Signal Transducing, Mice

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