You searched for early development

Human macrophages survive and adopt activated genotypes in living zebrafish

Colin D. Paul, Alexus Devine, Kevin Bishop, et al.

Selected by Giuliana Clemente

Presence of midline cilia supersedes the expression of Lefty1 in forming the midline barrier during the establishment of left-right asymmetry

Natalia A Shylo, Dylan A Ramrattan, Scott D Weatherbee

Selected by Hannah Brunsdon

A non-cell autonomous actin redistribution enables isotropic retinal growth

Marija Matejcic, Guillaume Salbreux, Caren Norden

Selected by Yara E. Sánchez Corrales

Rearing temperature and fatty acid supplementation jointly affect membrane fluidity and heat tolerance in Daphnia

Dominik Martin-Creuzburg, Bret L. Coggins, Dieter Ebert, et al.

Selected by Alexander Little

A SoxB gene acts as an anterior gap gene and regulates posterior segment addition in the spider Parasteatoda tepidariorum

Christian L. B. Paese, Anna Schoenauer, Daniel J. Leite, et al.

Selected by Erik Clark

Wnt/β-catenin regulates an ancient signaling network during zebrafish scale development

Andrew J Aman, Alexis N Fulbright, David M Parichy

Selected by Andreas van Impel

Long-term live imaging of the Drosophila adult midgut reveals real-time dynamics of cell division, differentiation, and loss

Judy Martin, Erin Nicole Sanders, Paola Moreno-Roman, et al.

Selected by Natalie Dye

From spiral cleavage to bilateral symmetry: The developmental cell lineage of the annelid brain

Pavel Vopalensky, Maria Antonietta Tosches, Kaia Achim, et al.

Selected by Erik Clark

Lineage tracing axial progenitors using Nkx1.2CreERT2 mice defines their trunk and tail contributions

Aida Rodrigo Albors, Pamela A Halley, Kate G Storey

Selected by Pierre Osteil

An Epiblast Stem Cell derived multipotent progenitor population for axial extension

Shlomit Edri, Penelope Hayward, Peter Baillie-Johnson, et al.

Selected by Pierre Osteil

Inheritance of OCT4 predetermines fate choice in human embryonic stem cells

Samuel C. Wolff, Raluca Dumitru, Kasia M. Kedziora, et al.

Selected by Claire Simon & Sophie Morgani

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

Claudio Cantù, Anastasia Felker, Dario Zimmerli, et al.