Normal myofibrillar development followed by progressive sarcomeric disruption with actin accumulations in a mouse Cfl2 knockout demonstrates requirement of cofilin-2 for muscle maintenance

Author： Agrawal Pankaj B.   Joshi Mugdha   Savic Talia   Chen Zoe   Beggs Alan H.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.21, Iss.10, 2012-05, pp. : 2341-2356

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development

By Uda Manuela   Ottolenghi Chris   Deiana Manila   Kimber Wendy   Forabosco Antonino   Cao Antonio   Schlessinger David   Pilia Giuseppe  

Human Molecular Genetics, Vol. 13, Iss. 11, 2004-06 ,pp. : 1171-1181

Oxford University Press

Access to resources Recommend Favorite

Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development

By Tachikawa M.  

Human Molecular Genetics, Vol. 12, Iss. 12, 2003-06 ,pp. : 1449-1459

Oxford University Press

Access to resources Recommend Favorite

Knockout mouse model for Fxr2 : a model for mental retardation

By McAninch R.  

Human Molecular Genetics, Vol. 11, Iss. 5, 2002-03 ,pp. : 487-498

Oxford University Press

Access to resources Recommend Favorite

Clorgyline-mediated reversal of neurological deficits in a Complexin 2 knockout mouse

By Glynn Dervila   Gibson Helen E.   Harte Michael K.   Reim Kerstin   Jones Susan   Reynolds Gavin P.   Morton A. Jennifer  

Human Molecular Genetics, Vol. 19, Iss. 17, 2010-09 ,pp. : 3402-3412

Oxford University Press

Access to resources Recommend Favorite

Functional muscle analysis of the Tcap knockout mouse

By Markert C.D.   Meaney M.P.   Voelker K.A.   Grange R.W.   Dalley H.W.   Cann J.K.   Ahmed M.   Bishwokarma B.   Walker S.J.   Yu S.X.   Brown M.   Lawlor M.W.   Beggs A.H.   Childers M.K.  

Human Molecular Genetics, Vol. 19, Iss. 11, 2010-06 ,pp. : 2268-2283

Oxford University Press

Access to resources Recommend Favorite