Joe Rainger

Distinct fibroblast lineages determine dermal architecture in skin development and repair

Sox2-positive dermal papilla cells specify hair follicle type in mammalian epidermis

Sox9 Modulates Proliferation and Expression of Osteogenic Markers of Adipose-Derived Stem Cells (ASC)

ANE syndrome caused by mutated RBM28 gene: a novel etiology of combined pituitary hormone deficiency

Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia

Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2

Hippo Pathway in Organ Size Control, Tissue Homeostasis, and Cancer

Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factors

Hypoxia-inducible factors promote breast cancer stem cell specification and maintenance in response to hypoxia or cytotoxic chemotherapy

MicroRNAs and developmental timing

Multiple dose-dependent roles for Sox2 in the patterning and differentiation of anterior foregut endoderm

The Fibroblast Growth Factor signaling pathway

A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome

Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects

Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome

Mutations in SOX2 cause anophthalmia–esophageal–genital (AEG) syndrome