Related references
Note: Only part of the references are listed.Knockdown of Homeobox B5 (HOXB5) Inhibits Cell Proliferation, Migration, and Invasion in Non-Small Cell Lung Cancer Cells Through Inactivation of the Wnt/β-Catenin Pathway
Bin Zhang et al.
ONCOLOGY RESEARCH (2018)
HOXA5 localization in postnatal and adult mouse brain is suggestive of regulatory roles in postmitotic neurons
Benoit Lizen et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2017)
Homeobox, Wnt, and Fibroblast Growth Factor Signaling is Augmented During Alveogenesis in Mice Lacking Superoxide Dismutase 3, Extracellular
Tania A. Thimraj et al.
LUNG (2017)
Genes and molecular pathways underpinning ciliopathies
Jeremy F. Reiter et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2017)
The Cilium: Cellular Antenna and Central Processing Unit
Jarema J. Malicki et al.
TRENDS IN CELL BIOLOGY (2017)
HOXA5 plays tissue-specific roles in the developing respiratory system
Kim Landry-Truchon et al.
DEVELOPMENT (2017)
Systematic expression analysis of Hox genes at adulthood reveals novel patterns in the central nervous system
Bertrand Hutlet et al.
BRAIN STRUCTURE & FUNCTION (2016)
HOXB5 induces invasion and migration through direct transcriptional up-regulation of β-catenin in human gastric carcinoma
Chang-Soo Hong et al.
BIOCHEMICAL JOURNAL (2015)
The Meckel-Gruber syndrome protein TMEM67 controls basal body positioning and epithelial branching morphogenesis in mice via the non-canonical Wnt pathway
Zakia A. Abdelhamed et al.
DISEASE MODELS & MECHANISMS (2015)
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
Gabrielle Wheway et al.
NATURE CELL BIOLOGY (2015)
HTSeq-a Python framework to work with high-throughput sequencing data
Simon Anders et al.
BIOINFORMATICS (2015)
featureCounts: an efficient general purpose program for assigning sequence reads to genomic features
Yang Liao et al.
BIOINFORMATICS (2014)
Otx2 cell-autonomously determines dorsal mesencephalon versus cerebellum fate independently of isthmic organizing activity
Luca G. Di Giovannantonio et al.
DEVELOPMENT (2014)
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Michael I. Love et al.
GENOME BIOLOGY (2014)
Variable expressivity of ciliopathy neurological phenotypes that encompass MeckelGruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects
Zakia A. Abdelhamed et al.
HUMAN MOLECULAR GENETICS (2013)
The interfascicular trigeminal nucleus: A precerebellar nucleus in the mouse defined by retrograde neuronal tracing and genetic fate mapping
Yuhong Fu et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2013)
WNT3 Inhibits Cerebellar Granule Neuron Progenitor Proliferation and Medulloblastoma Formation via MAPK Activation
Sandrine L. Anne et al.
PLOS ONE (2013)
WNT signaling increases proliferation and impairs differentiation of stem cells in the developing cerebellum
Yanxin Pei et al.
DEVELOPMENT (2012)
Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome
Andrea Aguilar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
Wnt ligands signal in a cooperative manner to promote foregut organogenesis
Mayumi F. Miller et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition
Francesc R. Garcia-Gonzalo et al.
NATURE GENETICS (2011)
Defective Wnt-dependent cerebellar midline fusion in a mouse model of Joubert syndrome
Madeline A. Lancaster et al.
NATURE MEDICINE (2011)
Mechanisms of Disease: Ciliopathies
Friedhelm Hildebrandt et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Wnt/β-catenin Signalling Is Active in a Highly Dynamic Pattern during Development of the Mouse Cerebellum
Hayden J. Selvadurai et al.
PLOS ONE (2011)
The primary cilium at a glance
Peter Satir et al.
JOURNAL OF CELL SCIENCE (2010)
The primary cilium: a signalling centre during vertebrate development
Sarah C. Goetz et al.
NATURE REVIEWS GENETICS (2010)
The Primary Cilium as a Complex Signaling Center
Nicolas F. Berbari et al.
CURRENT BIOLOGY (2009)
The primary cilium as a cellular signaling center: lessons from disease
Madeline A. Lancaster et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2009)
A Mouse Model for Meckel Syndrome Type 3
Susan A. Cook et al.
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY (2009)
Primary cilia are required for cerebellar development and Shh-dependent expansion of progenitor pool
N. Spassky et al.
DEVELOPMENTAL BIOLOGY (2008)
Cerebellum morphogenesis: the foliation pattern is orchestrated by multi-cellular anchoring centers
Anamaria Sudarov et al.
NEURAL DEVELOPMENT (2007)
Cilia proteins control cerebellar morphogenesis by promoting expansion of the granule progenitor pool
Victor V. Chizhikov et al.
JOURNAL OF NEUROSCIENCE (2007)
The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome
Lekbir Baala et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome
Enza Maria Valente et al.
NATURE GENETICS (2006)
Sonic hedgehog regulates Gli activator and repressor functions with spatial and temporal precision in the mid/hindbrain region
S Blaess et al.
DEVELOPMENT (2006)
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
UM Smith et al.
NATURE GENETICS (2006)
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome
M Kyttälä et al.
NATURE GENETICS (2006)
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative study
C Thauvin-Robinet et al.
JOURNAL OF MEDICAL GENETICS (2006)
NPHP1 gene deletion is a rare cause of Joubert syndrome related disorders
M Castori et al.
JOURNAL OF MEDICAL GENETICS (2005)
Development of multiorgan pathology in the wpk rat model of polycystic kidney disease
VH Gattone et al.
ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY (2004)
The NPHP1 gene deletion associated with juvenile nephronophthisis is present in a subset of individuals with Joubert syndrome
MA Parisi et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Sonic hedgehog signaling is required for expansion of granule neuron precursors and patterning of the mouse cerebellum
PM Lewis et al.
DEVELOPMENTAL BIOLOGY (2004)
Spatial pattern of sonic hedgehog signaling through Gli genes during cerebellum development
JMD Corrales et al.
DEVELOPMENT (2004)
Cerebellar vermis hypoplasia in a patient with Bardet-Biedl syndrome
E Baskin et al.
JOURNAL OF CHILD NEUROLOGY (2002)
Identification of the gene for oral-facial-digital type I syndrome
MI Ferrante et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Share Paper
