Anita Becker-Heck

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

Anne‐Christine Merveille, Erica E. Davis, Anita Becker-Heck et al. · Nature Genetics · 2010 · 339 citations · Full text

Normal Ciliary Motility, Molecular Biology, Cytoskeleton +4

The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation

Anita Becker-Heck, Irene E. Zohn, Noriko Okabe et al. · Nature Genetics · 2010 · 331 citations · Full text

Left-right Axis Formation, Signal Transduction, Coiled-coil Domain +10

CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms

Jennifer R. Panizzi, Anita Becker-Heck, Victoria Castleman et al. · Nature Genetics · 2012 · 249 citations

Medicine, Pathology, Ciliary Dynein Arms +4

Mutations of <i>DNAH11</i> in patients with primary ciliary dyskinesia with normal ciliary ultrastructure

Michael R. Knowles, Margaret W. Leigh, Johnny L. Carson et al. · Thorax · 2011 · 223 citations · Full text

Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects

Niki T. Loges, Heike Olbrich, Anita Becker-Heck et al. · The American Journal of Human Genetics · 2009 · 215 citations · Full text

Point Mutations, Dynein Arm Defects, Pathology +2