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- Publisher Website: 10.1007/978-1-4939-7142-8_13
- Scopus: eid_2-s2.0-85029395026
- PMID: 28735489
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Article: A Zebrafish Model for Evaluating the Function of Human Leukemic Gene IDH1 and Its Mutation
Title | A Zebrafish Model for Evaluating the Function of Human Leukemic Gene IDH1 and Its Mutation |
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Authors | |
Keywords | Hematopoiesis Mutation Myeloid malignancy Myelopoiesis Transient expression Zebrafish |
Issue Date | 2017 |
Publisher | Humana Press, Inc. The Journal's web site is located at http://link.springer.com/bookseries/7651 |
Citation | Methods in Molecular Biology, 2017, v. 1633, p. 193-218 How to Cite? |
Abstract | The recent advent of next-generation sequencing (NGS) has greatly accelerated identification of gene mutations in myeloid malignancies at unprecedented speed that will soon outpace their functional validation by conventional laboratory techniques and animal models. A high-throughput whole-organism model is useful for the functional validation of new mutations. We recently reported the use of zebrafish to evaluate the hematopoietic function of isocitrate dehydrogenase 1 (IDH1) and the effects of expressing human IDH1-R132H that is frequently identified in human acute myeloid leukemia (AML), in myelopoiesis, with a view to develop zebrafish as a model of AML. Here, we use IDH1 as an example to describe a comprehensive approach to evaluate hematopoietic gene function and the effects of mutations using zebrafish as a model. |
Persistent Identifier | http://hdl.handle.net/10722/245108 |
ISSN | 2023 SCImago Journal Rankings: 0.399 |
DC Field | Value | Language |
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dc.contributor.author | Ma, ACH | - |
dc.contributor.author | Shi, X | - |
dc.contributor.author | He, BA | - |
dc.contributor.author | Guo, Y | - |
dc.contributor.author | Leung, AYH | - |
dc.date.accessioned | 2017-09-18T02:04:45Z | - |
dc.date.available | 2017-09-18T02:04:45Z | - |
dc.date.issued | 2017 | - |
dc.identifier.citation | Methods in Molecular Biology, 2017, v. 1633, p. 193-218 | - |
dc.identifier.issn | 1064-3745 | - |
dc.identifier.uri | http://hdl.handle.net/10722/245108 | - |
dc.description.abstract | The recent advent of next-generation sequencing (NGS) has greatly accelerated identification of gene mutations in myeloid malignancies at unprecedented speed that will soon outpace their functional validation by conventional laboratory techniques and animal models. A high-throughput whole-organism model is useful for the functional validation of new mutations. We recently reported the use of zebrafish to evaluate the hematopoietic function of isocitrate dehydrogenase 1 (IDH1) and the effects of expressing human IDH1-R132H that is frequently identified in human acute myeloid leukemia (AML), in myelopoiesis, with a view to develop zebrafish as a model of AML. Here, we use IDH1 as an example to describe a comprehensive approach to evaluate hematopoietic gene function and the effects of mutations using zebrafish as a model. | - |
dc.language | eng | - |
dc.publisher | Humana Press, Inc. The Journal's web site is located at http://link.springer.com/bookseries/7651 | - |
dc.relation.ispartof | Methods in Molecular Biology | - |
dc.rights | The final publication is available at Springer via http://dx.doi.org/[insert DOI] | - |
dc.subject | Hematopoiesis | - |
dc.subject | Mutation | - |
dc.subject | Myeloid malignancy | - |
dc.subject | Myelopoiesis | - |
dc.subject | Transient expression | - |
dc.subject | Zebrafish | - |
dc.title | A Zebrafish Model for Evaluating the Function of Human Leukemic Gene IDH1 and Its Mutation | - |
dc.type | Article | - |
dc.identifier.email | He, BA: alexhe@hku.hk | - |
dc.identifier.email | Leung, AYH: ayhleung@hku.hk | - |
dc.identifier.authority | Leung, AYH=rp00265 | - |
dc.identifier.doi | 10.1007/978-1-4939-7142-8_13 | - |
dc.identifier.pmid | 28735489 | - |
dc.identifier.scopus | eid_2-s2.0-85029395026 | - |
dc.identifier.hkuros | 275924 | - |
dc.identifier.volume | 1633 | - |
dc.identifier.spage | 193 | - |
dc.identifier.epage | 218 | - |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1064-3745 | - |