Anita Becker-Heck
Publications by Year
Research Areas
Cystic Fibrosis Research Advances, Genetic and Kidney Cyst Diseases, Protist diversity and phylogeny, Genetic Syndromes and Imprinting, Prenatal Screening and Diagnostics
Most-Cited Works
- → CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs(2010)340 cited
- → The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formation(2010)332 cited
- → CCDC103 mutations cause primary ciliary dyskinesia by disrupting assembly of ciliary dynein arms(2012)249 cited
- → Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure(2011)227 cited
- → Deletions and Point Mutations of LRRC50 Cause Primary Ciliary Dyskinesia Due to Dynein Arm Defects(2009)215 cited
- → Mutations inCCDC39andCCDC40are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms(2012)190 cited
- → Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization(2015)102 cited
- → Mutations in CCDC 39 and CCDC 40 are the Major Cause of Primary Ciliary Dyskinesia with Axonemal Disorganization and Absent Inner Dynein Arms(2020)20 cited
- → Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure(2021)17 cited
- → Dynein Dysfunction as a Cause of Primary Ciliary Dyskinesia and Other Ciliopathies(2011)11 cited