Lethal phenotype of mice carrying a Sept11 null mutation
Biological Chemistry, ISSN: 1431-6730, Vol: 392, Issue: 8-9, Page: 779-781
2011
- 22Citations
- 24Captures
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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
- Citations22
- Citation Indexes22
- CrossRef22
- 18
- Captures24
- Readers24
- 24
Conference Paper Description
Septins are cytoskeletal GTP-binding proteins involved in processes characterized by active membrane movement, such as cytokinesis, vesicle trafficking and exocytosis. Most septins are expressed ubiquitously, however, some septins accumulate in particular tissues. The ubiquitous SEPT11 also shows high expression levels in the central nervous system and in platelets. Here, SEPT11 is involved in vesicle trafficking and may play a role in synaptic connectivity. Interestingly, mice that harbor a homozygous Sept11 null mutation, die in utero. From day 11.5 post coitum onwards, development of homozygous embryos seems to be retarded and the embryos from day 13.5 onwards were dead. © 2011 by Walter de Gruyter Berlin Boston.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=80052697945&origin=inward; http://dx.doi.org/10.1515/bc.2011.093; http://www.ncbi.nlm.nih.gov/pubmed/21824005; https://www.degruyter.com/view/j/bchm.2011.392.issue-8-9/bc.2011.093/bc.2011.093.xml; https://www.degruyter.com/view/j/bchm.2011.392.issue-8-9/bc.2011.093/bc.2011.093.pdf; https://www.degruyter.com/document/doi/10.1515/BC.2011.093/html
Walter de Gruyter GmbH
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