Inositol-and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3

SB Ting, T Wilanowski, A Auden, M Hall, AK Voss… - Nature medicine, 2003 - nature.com
The neural tube defects (NTDs) spina bifida and anencephaly are widely prevalent severe
birth defects. The mouse mutant curly tail (ct/ct) has served as a model of NTDs for 50 years …

Grainyhead‐like 3 (Grhl3) deficiency in brain leads to altered locomotor activity and decreased anxiety‐like behaviors in aged mice

S Dworkin, A Auden, DD Partridge… - Developmental …, 2017 - Wiley Online Library
The highly conserved Grainyhead‐like (Grhl) family of transcription factors, comprising three
members in vertebrates (Grhl1‐3), play critical regulatory roles during embryonic …

Grainyhead-like 2 downstream targets act to suppress epithelial-to-mesenchymal transition during neural tube closure

HJ Ray, LA Niswander - Development, 2016 - journals.biologists.com
The transcription factor grainyhead-like 2 (GRHL2) is expressed in non-neural ectoderm
(NNE) and Grhl2 loss results in fully penetrant cranial neural tube defects (NTDs) in mice …

Grainyhead genes and mammalian neural tube closure

P Gustavsson, AJ Copp… - Birth Defects Research …, 2008 - Wiley Online Library
BACKGROUND: Grainyhead genes encode a family of transcription factors that are well
conserved from fly to human. The three mammalian homologues, Grainyhead‐like‐1,‐2, and …

Copy number variation analysis implicates the cell polarity gene glypican 5 as a human spina bifida candidate gene

AG Bassuk, LB Muthuswamy, R Boland… - Human molecular …, 2013 - academic.oup.com
Neural tube defects (NTDs) are common birth defects of complex etiology. Family and
population-based studies have confirmed a genetic component to NTDs. However, despite …

Spatial and temporal expression of the Grainyhead-like transcription factor family during murine development

A Auden, J Caddy, T Wilanowski, SB Ting… - Gene expression …, 2006 - Elsevier
The Drosophila transcription factor Grainyhead (grh) is expressed in ectoderm-derived
tissues where it regulates several key developmental events including cuticle formation …

[HTML][HTML] Groucho homologue Grg5 interacts with the transcription factor Runx2–Cbfa1 and modulates its activity during postnatal growth in mice

WF Wang, YG Wang, AM Reginato, DJ Glotzer… - Developmental …, 2004 - Elsevier
Runx2–Cbfa1, a Runt transcription factor, plays important roles during skeletal development.
It is required for differentiation and function of osteoblasts. In its absence, chondrocyte …

Meta-Analysis of Grainyhead-Like Dependent Transcriptional Networks: A Roadmap for Identifying Novel Conserved Genetic Pathways

N Mathiyalagan, LB Miles, PJ Anderson, T Wilanowski… - Genes, 2019 - mdpi.com
The Drosophila grainyhead (grh) and vertebrate Grainyhead-like (Grhl) transcription factors
are among the most critical genes for epithelial development, maintenance and …

Vangl2 disruption alters the biomechanics of late spinal neurulation leading to spina bifida in mouse embryos

GL Galea, O Nychyk, MA Mole… - Disease models & …, 2018 - journals.biologists.com
Human mutations in the planar cell polarity component VANGL2 are associated with the
neural tube defect spina bifida. Homozygous Vangl2 mutation in mice prevents initiation of …

Growth defect in Grg5 null mice is associated with reduced Ihh signaling in growth plates

WF Wang, YG Wang, AM Reginato… - … dynamics: an official …, 2002 - Wiley Online Library
Gene‐targeted disruption of Grg5, a mouse homologue of Drosophila groucho (gro), results
in postnatal growth retardation in mice. The growth defect, most striking in approximately half …