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Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity

Detalles Bibliográficos
Autores principales: Lee, Ho Jin, Pham, Phuong Chi, Hyun, Seung Yeob, Baek, Byungyeob, Kim, Byungjin, Kim, Yunha, Min, Hye-Young, Lee, Jeeyeon, Lee, Ho-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018920/
https://www.ncbi.nlm.nih.gov/pubmed/36927387
http://dx.doi.org/10.1186/s12943-023-01754-6
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author Lee, Ho Jin
Pham, Phuong Chi
Hyun, Seung Yeob
Baek, Byungyeob
Kim, Byungjin
Kim, Yunha
Min, Hye-Young
Lee, Jeeyeon
Lee, Ho-Young
author_facet Lee, Ho Jin
Pham, Phuong Chi
Hyun, Seung Yeob
Baek, Byungyeob
Kim, Byungjin
Kim, Yunha
Min, Hye-Young
Lee, Jeeyeon
Lee, Ho-Young
author_sort Lee, Ho Jin
collection PubMed
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spelling pubmed-100189202023-03-17 Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity Lee, Ho Jin Pham, Phuong Chi Hyun, Seung Yeob Baek, Byungyeob Kim, Byungjin Kim, Yunha Min, Hye-Young Lee, Jeeyeon Lee, Ho-Young Mol Cancer Correction BioMed Central 2023-03-08 /pmc/articles/PMC10018920/ /pubmed/36927387 http://dx.doi.org/10.1186/s12943-023-01754-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Correction
Lee, Ho Jin
Pham, Phuong Chi
Hyun, Seung Yeob
Baek, Byungyeob
Kim, Byungjin
Kim, Yunha
Min, Hye-Young
Lee, Jeeyeon
Lee, Ho-Young
Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity
title Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity
title_full Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity
title_fullStr Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity
title_full_unstemmed Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity
title_short Correction: Development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual IGF1R/Src inhibitor as a novel anticancer agent with minimal toxicity
title_sort correction: development of a 4-aminopyrazolo[3,4-d]pyrimidine-based dual igf1r/src inhibitor as a novel anticancer agent with minimal toxicity
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10018920/
https://www.ncbi.nlm.nih.gov/pubmed/36927387
http://dx.doi.org/10.1186/s12943-023-01754-6
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