SPG21: Difference between revisions

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'''Maspardin''' is a [[protein]] that in humans is encoded by the ''SPG21'' [[gene]].<ref name="pmid11113139">{{cite journal | author = Zeitlmann L, Sirim P, Kremmer E, Kolanus W | title = Cloning of ACP33 as a novel intracellular ligand of CD4 | journal = J Biol Chem | volume = 276 | issue = 12 | pages = 9123–32 | year = 2001 | month = Mar | pmid = 11113139 | pmc = | doi = 10.1074/jbc.M009270200 }}</ref><ref name="pmid14564668">{{cite journal | author = Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH | title = Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia | journal = Am J Hum Genet | volume = 73 | issue = 5 | pages = 1147–56 | year = 2003 | month = Oct | pmid = 14564668 | pmc = 1180493 | doi = 10.1086/379522 }}</ref><ref name="entrez"/>
'''Maspardin''' is a [[protein]] that in humans is encoded by the ''SPG21'' [[gene]].<ref name="pmid11113139">{{cite journal | author = Zeitlmann L, Sirim P, Kremmer E, Kolanus W | title = Cloning of ACP33 as a novel intracellular ligand of CD4 | journal = J Biol Chem | volume = 276 | issue = 12 | pages = 9123–32 |date=Mar 2001 | pmid = 11113139 | pmc = | doi = 10.1074/jbc.M009270200 }}</ref><ref name="pmid14564668">{{cite journal | author = Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH | title = Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia | journal = Am J Hum Genet | volume = 73 | issue = 5 | pages = 1147–56 |date=Oct 2003 | pmid = 14564668 | pmc = 1180493 | doi = 10.1086/379522 }}</ref><ref name="entrez"/>


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Revision as of 07:22, 30 January 2014

Template:PBB Maspardin is a protein that in humans is encoded by the SPG21 gene.[1][2][3]

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Interactions

SPG21 has been shown to interact with CD4.[1]

References

  1. ^ a b Zeitlmann L, Sirim P, Kremmer E, Kolanus W (Mar 2001). "Cloning of ACP33 as a novel intracellular ligand of CD4". J Biol Chem. 276 (12): 9123–32. doi:10.1074/jbc.M009270200. PMID 11113139.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link) Cite error: The named reference "pmid11113139" was defined multiple times with different content (see the help page).
  2. ^ Simpson MA, Cross H, Proukakis C, Pryde A, Hershberger R, Chatonnet A, Patton MA, Crosby AH (Oct 2003). "Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia". Am J Hum Genet. 73 (5): 1147–56. doi:10.1086/379522. PMC 1180493. PMID 14564668.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ Cite error: The named reference entrez was invoked but never defined (see the help page).

Further reading

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