MNS1 Is Essential for Spermiogenesis and Motile Ciliary Functions in Mice

Loss of SPEF2 Function in Mice Results in Spermatogenesis Defects and Primary Ciliary Dyskinesia1

(2011) Anu Sironen et al.   BIOLOGY OF REPRODUCTION

Nxf3 is expressed in Sertoli cells, but is dispensable for spermatogenesis

(2011) Jian Zhou et al.   MOLECULAR REPRODUCTION AND DEVELOPMENT

The making of abnormal spermatozoa: cellular and molecular mechanisms underlying pathological spermiogenesis

(2010) Hector E. Chemes et al.   CELL AND TISSUE RESEARCH

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

(2010) Anita Becker-Heck et al.   NATURE GENETICS

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

(2010) Anne-Christine Merveille et al.   NATURE GENETICS

Meig1 deficiency causes a severe defect in mouse spermatogenesis

(2009) Yehuda Salzberg et al.   DEVELOPMENTAL BIOLOGY

MEIG1 is essential for spermiogenesis in mice

(2009) Z. Zhang et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA