A meckelin–filamin A interaction mediates ciliogenesis

By Adams Matthew   Simms Roslyn J.   Abdelhamed Zakia   Dawe Helen R.   Szymanska Katarzyna   Logan Clare V.   Wheway Gabrielle   Pitt Eva   Gull Keith   Knowles Margaret A.   Blair Edward   Cross Sally H.   Sayer John A.   Johnson Colin A.  

Human Molecular Genetics, Vol. 21, Iss. 6, 2012-03 ,pp. : 1272-1286

Oxford University Press

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A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A

By Carabalona Aurelie   Beguin Shirley   Pallesi-Pocachard Emilie   Buhler Emmanuelle   Pellegrino Christophe   Arnaud Karen   Hubert Philippe   Oualha Mehdi   Siffroi Jean Pierre   Khantane Sabrina   Coupry Isabelle   Goizet Cyril   Gelot Antoinette Bernabe   Represa Alfonso   Cardoso Carlos  

Human Molecular Genetics, Vol. 21, Iss. 5, 2012-03 ,pp. : 1004-1017

Oxford University Press

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Cardiac malformations and midline skeletal defects in mice lacking filamin A

By Hart Alan W.   Morgan Joanne E.   Schneider Jürgen   West Katrine   McKie Lisa   Bhattacharya Shoumo   Jackson Ian J.   Cross Sally H.  

Human Molecular Genetics, Vol. 15, Iss. 16, 2006-08 ,pp. : 2457-2467

Oxford University Press

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Filamin C interacts with the muscular dystrophy KY protein and is abnormally distributed in mouse KY deficient muscle fibres

By Beatham Jane  

Human Molecular Genetics, Vol. 13, Iss. 22, 2004-11 ,pp. : 2863-2874

Oxford University Press

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Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females

By Schachter S.C.  

Human Molecular Genetics, Vol. 10, Iss. 17, 2001-08 ,pp. : 1775-1783

Oxford University Press

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