Generation and characterization of neuregulin-2-deficient mice
Molecular and Cellular Biology, ISSN: 0270-7306, Vol: 24, Issue: 18, Page: 8221-8226
2004
- 37Citations
- 55Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations37
- Citation Indexes37
- 37
- CrossRef34
- Captures55
- Readers55
- 55
Article Description
The neuregulins (NRGs) are a family of four structurally related growth factors that are expressed in the developing and adult brain. NRG-1 is essential for normal heart formation and has been implicated in the development and maintenance of both neurons and glia. NRG-2 was identified on the basis of its homology to NRG-1 and, like NRG-1, is expressed predominantly by neurons in the central nervous system. We have generated mice with the active domain of NRG-2 deleted in an effort to characterize the biological function of NRG-2 in vivo. In contrast to the NRG-1 knockout animals, NRG-2 knockouts have no apparent heart defects and survive embryogenesis. Mutant mice display early growth retardation and reduced reproductive capacity. No obvious histological differences were observed in the major sites of NRG-2 expression. Our results indicate that in vivo NRG-2 activity differs substantially from that of NRG-1 and that it is not essential for normal development in utero.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=4444346330&origin=inward; http://dx.doi.org/10.1128/mcb.24.18.8221-8226.2004; http://www.ncbi.nlm.nih.gov/pubmed/15340081; http://mcb.asm.org/cgi/doi/10.1128/MCB.24.18.8221-8226.2004; https://syndication.highwire.org/content/doi/10.1128/MCB.24.18.8221-8226.2004; https://www.tandfonline.com/doi/full/10.1128/MCB.24.18.8221-8226.2004; https://dx.doi.org/10.1128/mcb.24.18.8221-8226.2004; https://journals.asm.org/doi/10.1128/MCB.24.18.8221-8226.2004; https://mcb.asm.org/content/24/18/8221; https://mcb.asm.org/content/24/18/8221.abstract; https://mcb.asm.org/content/mcb/24/18/8221.full.pdf; https://research-repository.uwa.edu.au/en/publications/86899e46-1942-4b22-914b-2ce189223adb; https://research-repository.uwa.edu.au/en/publications/generation-and-characterization-of-neuregulin-2-deficient-mice; https://research-repository.uwa.edu.au/en/publications/generation-and-characterization-of-neuregulin2deficient-mice(86899e46-1942-4b22-914b-2ce189223adb).html; http://mcb.asm.org/content/24/18/8221; https://journals.asm.org/doi/abs/10.1128/MCB.24.18.8221-8226.2004; http://research-repository.uwa.edu.au/en/publications/generation-and-characterization-of-neuregulin2deficient-mice(86899e46-1942-4b22-914b-2ce189223adb).html
American Society for Microbiology
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