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Bicaudal C, a novel regulator of Dvl signaling abutting RNA-processing bodies, controls cilia orientation and leftward flow

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Bicaudal C, a novel regulator of Dvl signaling abutting RNA-processing bodies, controls cilia orientation and leftward flow

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New roles of Bicc1 in cilia formation, cell adhesion, and in adult kidneys

Relative plus constructions

Sequential and directional insulation by conserved CTCF sites underlies the Hox timer in stembryos

RNA-based nanomedicines and their clinical applications

Differential impact of TGF beta/SMAD signaling activity elicited by Activin A and Nodal on endoderm differentiation of epiblast stem cells

Targeted search for scaling genes reveals matrix metalloproteinase 3 as a scaler of the dorsal-ventral pattern in Xenopus laevis embryos

Tuning SAS-6 architecture with monobodies impairs distinct steps of centriole assembly

Automated Analysis of Cerebrospinal Fluid Flow and Motile Cilia Properties in The Central Canal of Zebrafish Embryos

Highly motile nanoscale magnetic artificial cilia

A helical inner scaffold provides a structural basis for centriole cohesion

Architecture of the centriole cartwheel‐containing region revealed by cryo‐electron tomography

In vitro modeling of early mouse development

Role of the RNA-binding protein Bicaudal-C1 and interacting factors in cystic kidney diseases

90 YEARS OF PROGESTERONE Progesterone receptor signaling in the normal breast and its implications for cancer

Comparative Transcriptomics Analyses across Species, Organs, and Developmental Stages Reveal Functionally Constrained lncRNAs

Multi-color Molecular Visualization of Signaling Proteins Reveals How C-Terminal Src Kinase Nanoclusters Regulate T Cell Receptor Activation

Novel features of centriole polarity and cartwheel stacking revealed by cryo-tomography

Flagellar microtubule doublet assembly in vitro reveals a regulatory role of tubulin C-terminal tails

Tissue- and sex-specific small RNAomes reveal sex differences in response to the environment

Mutations in Bcl9 and Pygo genes cause congenital heart defects by tissue-specific perturbation of Wnt/beta-catenin signaling