Sandbox Reserved 705: Difference between revisions

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Patients develop tumors of the nervous system : meningiomas, schwannomas, neurofibromas.<ref>PMID:3125435</ref>
Patients develop tumors of the nervous system : meningiomas, schwannomas, neurofibromas.<ref>PMID:3125435</ref>
Mutations in the Nf2 gene lead to tumor proliferation as well in humans as in mice. Therefore Merlin-1 is a tumor suppressor protein. To know more about the type of Nf2 mutations and the related deseases you can follow the link that leads you to the Portal to Swiss-Prot diseases and variants [http://swissvar.expasy.org/cgi-bin/swissvar/result?global_textfield=merlin the Portal to Swiss-Prot diseases and variants ]
Mutations in the Nf2 gene lead to tumor proliferation as well in humans as in mice. Therefore Merlin-1 is a tumor suppressor protein. To know more about the type of Nf2 mutations and the related deseases you can follow the link that leads you to the Portal to Swiss-Prot diseases and variants [http://swissvar.expasy.org/cgi-bin/swissvar/result?global_textfield=merlin the Portal to Swiss-Prot diseases and variants ]
<Structure load='1NI2' size='300' frame='true' align='right' caption='Ezrin' scene='Insert optional scene name here' />
<Structure load='1GC7' size='300' frame='true' align='right' caption='Radixin' scene='Insert optional scene name here' />
<Structure load='1EF1' size='300' frame='true' align='right' caption='Moesin' scene='Insert optional scene name here' />
<Structure load='1E5W' size='500' frame='true' align='right' caption='Moesin' scene='Insert optional scene name here' />
<Structure load='3u8z' size='500' frame='true' align='right' caption='Merlin' scene='Insert optional scene name here' />


==ERM Proteins==
==ERM Proteins==
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