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Details on Person Classical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein function

Class:IdLiteratureReference:2514804
_displayNameClassical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein function
_timestamp2012-10-10 13:03:26
author[Person:2514805] Kirschner, Ryan
[Person:2327821] Hubmacher, Dirk
[Person:2514767] Iyengar, Garud
[Person:2514796] Kaur, Jasvir
[Person:2327833] Fagotto-Kaufmann, Christine
[Person:2514809] Brömme, Dieter
[Person:2514786] Bartels, Rainer
[Person:2327731] Reinhardt, Dieter P
created[InstanceEdit:2514810] Jupe, S, 2012-10-10
journalJ. Biol. Chem.
pages32810-23
pubMedIdentifier21784848
titleClassical and neonatal Marfan syndrome mutations in fibrillin-1 cause differential protease susceptibilities and protein function
volume286
year2011
(literatureReference)[Summation:2485097] All mammals have three fibrillin genes (Davis & Summers 2012...
[Summation:2514780] Fibrillin-1 can be degraded by MMP3 (Ashworth et al. 1999) a...
[Reaction:2514772] Fibrillin-1 degradation by MMP3, CTSK, CTSL2 [Homo sapiens]
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