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- Publisher Website: 10.1016/S0304-3940(03)00927-3
- Scopus: eid_2-s2.0-0141560307
- PMID: 14550911
- WOS: WOS:000185863900013
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Article: Enhanced expression of transforming growth factor-beta isoforms in the neural tube of embryos derived from diabetic mice exposed to cyclophosphamide
Title | Enhanced expression of transforming growth factor-beta isoforms in the neural tube of embryos derived from diabetic mice exposed to cyclophosphamide |
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Authors | |
Keywords | Amoeboid microglia Cyclophosphamide Diabetic embryos Neural tube defects Transforming growth factor-β isoforms |
Issue Date | 2003 |
Publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/neulet |
Citation | Neuroscience Letters, 2003, v. 351 n. 1, p. 51-55 How to Cite? |
Abstract | We analyzed the expression pattern of transforming growth factor-β isoforms (TGF-β1, TGF-β2 and TGF-β3) in the developing brain of embryos derived from the normal and diabetic mice exposed to cyclophosphamide (CP), a cytotoxic teratogen. The CP-treated diabetic embryos showed significantly more TGF-β1 and TGF-β2 immunoreactive cells in the regions of telencephalon and diencephalon in comparison to that of CP-treated non-diabetic embryos. Moreover, no cells expressing TGF-β isoforms were detectable in the developing brain of normal and diabetic embryos. The mRNA expression levels of TGF-β isoforms were found to be significantly increased in the developing brain of CP-treated diabetic embryos compared to that of CP-treated non-diabetic embryos as measured by quantitative real time reverse transcription-polymerase chain reaction. The enhanced expression levels of TGF-β isoforms appear to be associated with the increased frequency of neural tube defects observed in the diabetic embryos exposed to CP. © 2003 Elsevier Ireland Ltd. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/162720 |
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.745 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Lian, Q | en_US |
dc.contributor.author | Samuel, TSW | en_US |
dc.contributor.author | Dheen, ST | en_US |
dc.date.accessioned | 2012-09-05T05:22:47Z | - |
dc.date.available | 2012-09-05T05:22:47Z | - |
dc.date.issued | 2003 | en_US |
dc.identifier.citation | Neuroscience Letters, 2003, v. 351 n. 1, p. 51-55 | en_US |
dc.identifier.issn | 0304-3940 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162720 | - |
dc.description.abstract | We analyzed the expression pattern of transforming growth factor-β isoforms (TGF-β1, TGF-β2 and TGF-β3) in the developing brain of embryos derived from the normal and diabetic mice exposed to cyclophosphamide (CP), a cytotoxic teratogen. The CP-treated diabetic embryos showed significantly more TGF-β1 and TGF-β2 immunoreactive cells in the regions of telencephalon and diencephalon in comparison to that of CP-treated non-diabetic embryos. Moreover, no cells expressing TGF-β isoforms were detectable in the developing brain of normal and diabetic embryos. The mRNA expression levels of TGF-β isoforms were found to be significantly increased in the developing brain of CP-treated diabetic embryos compared to that of CP-treated non-diabetic embryos as measured by quantitative real time reverse transcription-polymerase chain reaction. The enhanced expression levels of TGF-β isoforms appear to be associated with the increased frequency of neural tube defects observed in the diabetic embryos exposed to CP. © 2003 Elsevier Ireland Ltd. All rights reserved. | en_US |
dc.language | eng | en_US |
dc.publisher | Elsevier Ireland Ltd. The Journal's web site is located at http://www.elsevier.com/locate/neulet | en_US |
dc.relation.ispartof | Neuroscience Letters | en_US |
dc.subject | Amoeboid microglia | - |
dc.subject | Cyclophosphamide | - |
dc.subject | Diabetic embryos | - |
dc.subject | Neural tube defects | - |
dc.subject | Transforming growth factor-β isoforms | - |
dc.subject.mesh | Animals | en_US |
dc.subject.mesh | Central Nervous System - Embryology - Metabolism | en_US |
dc.subject.mesh | Cyclophosphamide - Toxicity | en_US |
dc.subject.mesh | Diabetes Mellitus, Experimental - Metabolism | en_US |
dc.subject.mesh | Embryo, Mammalian - Drug Effects - Metabolism | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Mice | en_US |
dc.subject.mesh | Pregnancy | en_US |
dc.subject.mesh | Pregnancy In Diabetics - Metabolism | en_US |
dc.subject.mesh | Protein Isoforms - Metabolism | en_US |
dc.subject.mesh | Reverse Transcriptase Polymerase Chain Reaction | en_US |
dc.subject.mesh | Teratogens - Toxicity | en_US |
dc.subject.mesh | Transforming Growth Factor Beta - Biosynthesis | en_US |
dc.subject.mesh | Transforming Growth Factor Beta1 | en_US |
dc.subject.mesh | Transforming Growth Factor Beta2 | en_US |
dc.subject.mesh | Transforming Growth Factor Beta3 | en_US |
dc.title | Enhanced expression of transforming growth factor-beta isoforms in the neural tube of embryos derived from diabetic mice exposed to cyclophosphamide | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lian, Q:qzlian@hkucc.hku.hk | en_US |
dc.identifier.authority | Lian, Q=rp00267 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/S0304-3940(03)00927-3 | en_US |
dc.identifier.pmid | 14550911 | - |
dc.identifier.scopus | eid_2-s2.0-0141560307 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0141560307&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 351 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 51 | en_US |
dc.identifier.epage | 55 | en_US |
dc.identifier.isi | WOS:000185863900013 | - |
dc.publisher.place | Ireland | en_US |
dc.identifier.scopusauthorid | Lian, Q=7003399023 | en_US |
dc.identifier.scopusauthorid | Samuel, TSW=7005025166 | en_US |
dc.identifier.scopusauthorid | Dheen, ST=6701666815 | en_US |
dc.identifier.issnl | 0304-3940 | - |