LRRC23 is a conserved component of the radial spoke that is necessary for sperm motility and male fertility in mice

ARMC12 regulates spatiotemporal mitochondrial dynamics during spermiogenesis and is required for male fertility

(2021) Keisuke Shimada et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse

(2021) Jintao Zhang et al.   HUMAN MOLECULAR GENETICS

TTC12 Loss-of-Function Mutations Cause Primary Ciliary Dyskinesia and Unveil Distinct Dynein Assembly Mechanisms in Motile Cilia Versus Flagella

(2020) Lucie Thomas et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD

(2020) Chaofeng Tu et al.   HUMAN GENETICS

A nonsense variant in NME5 causes human primary ciliary dyskinesia with radial spoke defects

(2020) Eun Hye Cho et al.   CLINICAL GENETICS

The FOXJ1 target Cfap206 is required for sperm motility, mucociliary clearance of the airways and brain development

(2020) Anja Beckers et al.   DEVELOPMENT

Sperm proteins SOF1, TMEM95, and SPACA6 are required for sperm−oocyte fusion in mice

(2020) Taichi Noda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Rsph4a is essential for the triplet radial spoke head assembly of the mouse motile cilia

(2020) Hiroshi Yoke et al.   PLoS Genetics

Structures of radial spokes and associated complexes important for ciliary motility

(2020) Miao Gui et al.   NATURE STRUCTURAL & MOLECULAR BIOLOGY

Radial spoke proteins regulate otolith formation during early zebrafish development

(2018) Xiao Han et al.   FASEB JOURNAL

Radial spoke head 6 homolog A is required for sperm flagellum formation and male fertility in mice

(2018) Ferheen Abbasi et al.   JOURNAL OF CELL SCIENCE

The Mammalian Spermatogenesis Single-Cell Transcriptome, from Spermatogonial Stem Cells to Spermatids

(2018) Brian P. Hermann et al.   Cell Reports

TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa

(2017) Julio M. Castaneda et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Functional anatomy of the mammalian sperm flagellum

(2016) Charles B. Lindemann et al.   Cytoskeleton

Radial Spokes—A Snapshot of the Motility Regulation, Assembly, and Evolution of Cilia and Flagella

(2016) Xiaoyan Zhu et al.   Cold Spring Harbor Perspectives in Biology

Absence of Radial Spokes in Mouse Node Cilia Is Required for Rotational Movement but Confers Ultrastructural Instability as a Trade-Off

(2015) Kyosuke Shinohara et al.   DEVELOPMENTAL CELL

DRC3 connects the N-DRC to dynein g to regulate flagellar waveform

(2015) Junya Awata et al.   MOLECULAR BIOLOGY OF THE CELL

Mutations inRSPH1Cause Primary Ciliary Dyskinesia with a Unique Clinical and Ciliary Phenotype

(2014) Michael R. Knowles et al.   AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE

Diagnosis and management of primary ciliary dyskinesia

(2014) J. S. Lucas et al.   ARCHIVES OF DISEASE IN CHILDHOOD

CRISPRdirect: software for designing CRISPR/Cas guide RNA with reduced off-target sites

(2014) Yuki Naito et al.   BIOINFORMATICS

Reduced pachytene piRNAs and translation underlie spermiogenic arrest in Maelstrom mutant mice

(2014) J. Castaneda et al.   EMBO JOURNAL

SHCBP1L, a conserved protein in mammals, is predominantly expressed in male germ cells and maintains spindle stability during meiosis in testis

(2014) Mingxi Liu et al.   MOLECULAR HUMAN REPRODUCTION

Cryo-electron tomography reveals ciliary defects underlying human RSPH1 primary ciliary dyskinesia

(2014) Jianfeng Lin et al.   Nature Communications

Loss-of-Function Mutations in RSPH1 Cause Primary Ciliary Dyskinesia with Central-Complex and Radial-Spoke Defects

(2013) Esther Kott et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Founder Mutation inRSPH4AIdentified in Patients of Hispanic Descent with Primary Ciliary Dyskinesia

(2013) M. Leigh Anne Daniels et al.   HUMAN MUTATION

A flagellar A-kinase anchoring protein with two amphipathic helices forms a structural scaffold in the radial spoke complex

(2012) Priyanka Sivadas et al.   JOURNAL OF CELL BIOLOGY

Sequential assembly of flagellar radial spokes

(2011) Dennis R. Diener et al.   Cytoskeleton

Building Blocks of the Nexin-Dynein Regulatory Complex inChlamydomonasFlagella

(2011) Jianfeng Lin et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Cryoelectron tomography of radial spokes in cilia and flagella

(2011) Gaia Pigino et al.   JOURNAL OF CELL BIOLOGY

Role of a-kinase anchoring proteins (AKAPs) in reproduction

(2010) Michaela Luconi   Frontiers in Bioscience-Landmark

Proteomic characterization of sperm radial spokes identifies a novel spoke protein with an ubiquitin domain

(2009) Yuhkoh Satouh et al.   FEBS LETTERS

IC138 Defines a Subdomain at the Base of the I1 Dynein That Regulates Microtubule Sliding and Flagellar Motility

(2009) Raqual Bower et al.   MOLECULAR BIOLOGY OF THE CELL

Mutations inHydinimpair ciliary motility in mice

(2008) Karl-Ferdinand Lechtreck et al.   JOURNAL OF CELL BIOLOGY