Published in Birth Defects Res A Clin Mol Teratol on August 01, 2010
Strange as it may seem: the many links between Wnt signaling, planar cell polarity, and cilia. Genes Dev (2011) 1.94
The continuing challenge of understanding, preventing, and treating neural tube defects. Science (2013) 1.86
Neural tube defects. Annu Rev Neurosci (2014) 1.69
Photoreceptor sensory cilia and ciliopathies: focus on CEP290, RPGR and their interacting proteins. Cilia (2012) 1.27
Molecular mechanisms of inner ear development. Cold Spring Harb Perspect Biol (2012) 1.16
RFX2 is broadly required for ciliogenesis during vertebrate development. Dev Biol (2011) 1.06
Neural tube defects--disorders of neurulation and related embryonic processes. Wiley Interdiscip Rev Dev Biol (2012) 1.05
Meckel-Gruber syndrome and the role of primary cilia in kidney, skeleton, and central nervous system development. Organogenesis (2013) 0.98
Mouse models of ciliopathies: the state of the art. Dis Model Mech (2012) 0.94
Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome. Nat Commun (2015) 0.88
Holoprosencephaly: signaling interactions between the brain and the face, the environment and the genes, and the phenotypic variability in animal models and humans. Wiley Interdiscip Rev Dev Biol (2014) 0.88
Sept6 is required for ciliogenesis in Kupffer's vesicle, the pronephros, and the neural tube during early embryonic development. Mol Cell Biol (2014) 0.84
From Planar Cell Polarity to Ciliogenesis and Back: The Curious Tale of the PPE and CPLANE proteins. Trends Cell Biol (2017) 0.83
Modeling anterior development in mice: diet as modulator of risk for neural tube defects. Am J Med Genet C Semin Med Genet (2013) 0.81
RFX7 is required for the formation of cilia in the neural tube. Mech Dev (2014) 0.81
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis. Mech Dev (2012) 0.81
Evidence for SHH as a candidate gene for encephalocele. Clin Dysmorphol (2012) 0.79
Novel Jbts17 mutant mouse model of Joubert syndrome with cilia transition zone defects and cerebellar and other ciliopathy related anomalies. Hum Mol Genet (2015) 0.79
MiR-302/367 regulate neural progenitor proliferation, differentiation timing, and survival in neurulation. Dev Biol (2015) 0.79
Signaling in cell differentiation and morphogenesis. Cold Spring Harb Perspect Biol (2012) 0.78
Endocytic recycling protein EHD1 regulates primary cilia morphogenesis and SHH signaling during neural tube development. Sci Rep (2016) 0.77
SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delamination. Sci Rep (2016) 0.77
Mutations in the Motile Cilia Gene DNAAF1 Are Associated with Neural Tube Defects in Humans. G3 (Bethesda) (2016) 0.77
Role of the ANKMY2-FKBP38 axis in regulation of the Sonic hedgehog (Shh) signaling pathway. J Biol Chem (2014) 0.77
Arsenic inhibits hedgehog signaling during P19 cell differentiation. Toxicol Appl Pharmacol (2014) 0.77
A critical role of noggin in developing folate-nonresponsive NTD in Fkbp8 -/- embryos. Childs Nerv Syst (2014) 0.76
Dido mutations trigger perinatal death and generate brain abnormalities and behavioral alterations in surviving adult mice. Proc Natl Acad Sci U S A (2015) 0.76
Exome sequencing identifies three novel candidate genes implicated in intellectual disability. PLoS One (2014) 0.75
Cranial nerve development requires co-ordinated Shh and canonical Wnt signaling. PLoS One (2015) 0.75
G-protein-coupled receptor signaling and neural tube closure defects. Birth Defects Res A Clin Mol Teratol (2016) 0.75
Heterotrimeric G protein signaling in polycystic kidney disease. Physiol Genomics (2016) 0.75
The effect of inhibiting glycinamide ribonucleotide formyl transferase on the development of neural tube in mice. Nutr Metab (Lond) (2016) 0.75
La-related protein 6 controls ciliated cell differentiation. Cilia (2017) 0.75
Identification and Validation of Novel Hedgehog-Responsive Enhancers Predicted by Computational Analysis of Ci/Gli Binding Site Density. PLoS One (2015) 0.75
Variants in TNIP1, a regulator of the NF-kB pathway, found in two patients with neural tube defects. Childs Nerv Syst (2016) 0.75
Neuropilin-1 promotes Hedgehog signaling through a novel cytoplasmic motif. J Biol Chem (2017) 0.75
Epigenomic Landscapes of hESC-Derived Neural Rosettes: Modeling Neural Tube Formation and Diseases. Cell Rep (2017) 0.75
Folate-dependent methylation of septins governs ciliogenesis during neural tube closure. FASEB J (2017) 0.75
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function. Nature (1996) 11.46
Altered neural cell fates and medulloblastoma in mouse patched mutants. Science (1997) 11.44
Vertebrate Smoothened functions at the primary cilium. Nature (2005) 9.24
Patched1 regulates hedgehog signaling at the primary cilium. Science (2007) 9.21
Hedgehog signalling in the mouse requires intraflagellar transport proteins. Nature (2003) 8.38
Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity. Cell (1993) 7.41
Hedgehog signaling in development and cancer. Dev Cell (2008) 6.60
An LDL-receptor-related protein mediates Wnt signalling in mice. Nature (2000) 6.34
Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. PLoS Genet (2005) 6.15
The mouse Fused locus encodes Axin, an inhibitor of the Wnt signaling pathway that regulates embryonic axis formation. Cell (1997) 6.10
Cilia and Hedgehog responsiveness in the mouse. Proc Natl Acad Sci U S A (2005) 5.87
Hedgehog: functions and mechanisms. Genes Dev (2008) 5.69
The graded response to Sonic Hedgehog depends on cilia architecture. Dev Cell (2007) 5.35
Cilia and developmental signaling. Annu Rev Cell Dev Biol (2007) 4.88
Gli2, but not Gli1, is required for initial Shh signaling and ectopic activation of the Shh pathway. Development (2002) 4.80
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates. Nat Genet (2005) 4.76
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome. Nat Genet (2007) 4.63
Mouse intraflagellar transport proteins regulate both the activator and repressor functions of Gli transcription factors. Development (2005) 4.32
The genetic basis of mammalian neurulation. Nat Rev Genet (2003) 4.14
A mouse model of greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene. Nat Genet (1993) 3.99
Vertebrate Hedgehog signalling modulated by induction of a Hedgehog-binding protein. Nature (1999) 3.87
Ciliary proteins link basal body polarization to planar cell polarity regulation. Nat Genet (2007) 3.79
The Oak Ridge Polycystic Kidney (orpk) disease gene is required for left-right axis determination. Development (2000) 3.74
The primary cilium as a complex signaling center. Curr Biol (2009) 3.73
Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli. Dev Biol (2005) 3.63
Genetic elimination of Suppressor of fused reveals an essential repressor function in the mammalian Hedgehog signaling pathway. Dev Cell (2006) 3.62
The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells. J Neurosci (2006) 3.36
Mammalian suppressor-of-fused modulates nuclear-cytoplasmic shuttling of Gli-1. Nat Cell Biol (1999) 3.32
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse. Curr Biol (2003) 3.31
Rab23 is an essential negative regulator of the mouse Sonic hedgehog signalling pathway. Nature (2001) 3.23
THM1 negatively modulates mouse sonic hedgehog signal transduction and affects retrograde intraflagellar transport in cilia. Nat Genet (2008) 3.19
Left-right asymmetry and kinesin superfamily protein KIF3A: new insights in determination of laterality and mesoderm induction by kif3A-/- mice analysis. J Cell Biol (1999) 3.14
Beta-arrestin-mediated localization of smoothened to the primary cilium. Science (2008) 3.10
PTK7/CCK-4 is a novel regulator of planar cell polarity in vertebrates. Nature (2004) 3.10
Interpretation of the sonic hedgehog morphogen gradient by a temporal adaptation mechanism. Nature (2007) 2.97
Dishevelled genes mediate a conserved mammalian PCP pathway to regulate convergent extension during neurulation. Development (2006) 2.96
Intraflagellar transport is essential for endochondral bone formation. Development (2006) 2.90
Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure. Development (2002) 2.71
Diminished Sonic hedgehog signaling and lack of floor plate differentiation in Gli2 mutant mice. Development (1998) 2.67
Smoothened mutants reveal redundant roles for Shh and Ihh signaling including regulation of L/R symmetry by the mouse node. Cell (2001) 2.65
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. Am J Hum Genet (2008) 2.65
The mammalian Cos2 homolog Kif7 plays an essential role in modulating Hh signal transduction during development. Curr Biol (2009) 2.63
Holoprosencephaly. Orphanet J Rare Dis (2007) 2.63
The cell surface membrane proteins Cdo and Boc are components and targets of the Hedgehog signaling pathway and feedback network in mice. Dev Cell (2006) 2.62
The output of Hedgehog signaling is controlled by the dynamic association between Suppressor of Fused and the Gli proteins. Genes Dev (2010) 2.60
Cilium-independent regulation of Gli protein function by Sufu in Hedgehog signaling is evolutionarily conserved. Genes Dev (2009) 2.59
Hedgehog signal transduction by Smoothened: pharmacologic evidence for a 2-step activation process. Proc Natl Acad Sci U S A (2009) 2.47
Gli2 trafficking links Hedgehog-dependent activation of Smoothened in the primary cilium to transcriptional activation in the nucleus. Proc Natl Acad Sci U S A (2009) 2.43
The sonic hedgehog-patched-gli pathway in human development and disease. Am J Hum Genet (2000) 2.42
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis. Nat Genet (2002) 2.30
Intraflagellar transport, cilia, and mammalian Hedgehog signaling: analysis in mouse embryonic fibroblasts. Dev Dyn (2008) 2.30
Boc is a receptor for sonic hedgehog in the guidance of commissural axons. Nature (2006) 2.29
Characterization of the physical interaction of Gli proteins with SUFU proteins. J Biol Chem (2002) 2.29
Murine dishevelled 3 functions in redundant pathways with dishevelled 1 and 2 in normal cardiac outflow tract, cochlea, and neural tube development. PLoS Genet (2008) 2.29
Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification. Hum Mol Genet (2001) 2.28
Ftm is a novel basal body protein of cilia involved in Shh signalling. Development (2007) 2.25
Activity-dependent internalization of smoothened mediated by beta-arrestin 2 and GRK2. Science (2004) 2.19
A phenotype-based screen for embryonic lethal mutations in the mouse. Proc Natl Acad Sci U S A (1998) 2.18
Cdo functions at multiple points in the Sonic Hedgehog pathway, and Cdo-deficient mice accurately model human holoprosencephaly. Dev Cell (2006) 2.13
Genetics and development of neural tube defects. J Pathol (2010) 2.10
A direct requirement for Hedgehog signaling for normal specification of all ventral progenitor domains in the presumptive mammalian spinal cord. Genes Dev (2002) 2.09
Essential role of beta-adrenergic receptor kinase 1 in cardiac development and function. Proc Natl Acad Sci U S A (1996) 2.06
The kinesin protein Kif7 is a critical regulator of Gli transcription factors in mammalian hedgehog signaling. Sci Signal (2009) 2.05
Feedback control of mammalian Hedgehog signaling by the Hedgehog-binding protein, Hip1, modulates Fgf signaling during branching morphogenesis of the lung. Genes Dev (2003) 2.00
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features. Proc Natl Acad Sci U S A (2003) 1.98
Mouse Kif7/Costal2 is a cilia-associated protein that regulates Sonic hedgehog signaling. Proc Natl Acad Sci U S A (2009) 1.95
The planar cell polarity effector Fuz is essential for targeted membrane trafficking, ciliogenesis and mouse embryonic development. Nat Cell Biol (2009) 1.90
The Hedgehog-binding proteins Gas1 and Cdo cooperate to positively regulate Shh signaling during mouse development. Genes Dev (2007) 1.87
The SIL gene is required for mouse embryonic axial development and left-right specification. Nature (1999) 1.81
Ciliary biology: understanding the cellular and genetic basis of human ciliopathies. Am J Med Genet C Semin Med Genet (2009) 1.81
Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly. Hum Genet (2002) 1.80
Hedgehog-mediated patterning of the mammalian embryo requires transporter-like function of dispatched. Cell (2002) 1.77
Cardiac and CNS defects in a mouse with targeted disruption of suppressor of fused. Development (2005) 1.75
The primary cilium at the crossroads of mammalian hedgehog signaling. Curr Top Dev Biol (2008) 1.75
Gas1 extends the range of Hedgehog action by facilitating its signaling. Genes Dev (2007) 1.74
Growth and pattern of the mammalian neural tube are governed by partially overlapping feedback activities of the hedgehog antagonists patched 1 and Hhip1. Development (2004) 1.72
RAB23 mutations in Carpenter syndrome imply an unexpected role for hedgehog signaling in cranial-suture development and obesity. Am J Hum Genet (2007) 1.72
A gradient of Gli activity mediates graded Sonic Hedgehog signaling in the neural tube. Genes Dev (2005) 1.68
Interplays of Gli2 and Gli3 and their requirement in mediating Shh-dependent sclerotome induction. Development (2003) 1.68
Negative regulation of Gli1 and Gli2 activator function by Suppressor of fused through multiple mechanisms. Differentiation (2005) 1.68
Mice lacking the ski proto-oncogene have defects in neurulation, craniofacial, patterning, and skeletal muscle development. Genes Dev (1997) 1.68
Tectonic, a novel regulator of the Hedgehog pathway required for both activation and inhibition. Genes Dev (2005) 1.65
A role for the Tubby-like protein 1 in rhodopsin transport. Invest Ophthalmol Vis Sci (2001) 1.64
Morphogens and the control of cell proliferation and patterning in the spinal cord. Cell Cycle (2007) 1.63
Mouse Rab23 regulates hedgehog signaling from smoothened to Gli proteins. Dev Biol (2005) 1.62
Wnt canonical pathway restricts graded Shh/Gli patterning activity through the regulation of Gli3 expression. Development (2007) 1.60
The mechanisms of dorsoventral patterning in the vertebrate neural tube. Dev Biol (2005) 1.58
A mouse model for Meckel syndrome reveals Mks1 is required for ciliogenesis and Hedgehog signaling. Hum Mol Genet (2009) 1.55
Suppressor of Fused inhibits mammalian Hedgehog signaling in the absence of cilia. Dev Biol (2009) 1.52
Mouse Dispatched homolog1 is required for long-range, but not juxtacrine, Hh signaling. Curr Biol (2002) 1.52
Development of the vertebrate central nervous system: formation of the neural tube. Prenat Diagn (2009) 1.49
Phosphorylation of Gli2 by protein kinase A is required for Gli2 processing and degradation and the Sonic Hedgehog-regulated mouse development. Dev Biol (2008) 1.48
Neurulation in the cranial region--normal and abnormal. J Anat (2005) 1.47
Sonic hedgehog and the molecular regulation of mouse neural tube closure. Development (2002) 1.44
Cordon-bleu is a conserved gene involved in neural tube formation. Dev Biol (2003) 1.44
Primary cilia are not required for normal canonical Wnt signaling in the mouse embryo. PLoS One (2009) 1.44
Mouse patched1 controls body size determination and limb patterning. Development (1999) 1.42
Establishing and interpreting graded Sonic Hedgehog signaling during vertebrate neural tube patterning: the role of negative feedback. Cold Spring Harb Perspect Biol (2009) 1.41
The emergent design of the neural tube: prepattern, SHH morphogen and GLI code. Curr Opin Genet Dev (2003) 1.38
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates. Nat Genet (2005) 4.76
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse. Curr Biol (2003) 3.31
The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. Hum Mol Genet (2006) 3.06
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain (2003) 2.55
Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure. Development (2007) 2.45
Genetics of human neural tube defects. Hum Mol Genet (2009) 2.28
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Hum Mol Genet (2006) 2.14
Vangl2 acts via RhoA signaling to regulate polarized cell movements during development of the proximal outflow tract. Circ Res (2005) 2.13
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse. Hum Mol Genet (2003) 2.11
In vivo genetic ablation by Cre-mediated expression of diphtheria toxin fragment A. Genesis (2005) 2.08
Disruption of planar cell polarity signaling results in congenital heart defects and cardiomyopathy attributable to early cardiomyocyte disorganization. Circ Res (2007) 1.85
Neural tube defects. Annu Rev Neurosci (2014) 1.69
Folic acid prevents exencephaly in Cited2 deficient mice. Hum Mol Genet (2002) 1.55
Fetal spina bifida in a mouse model: loss of neural function in utero. J Neurosurg (2007) 1.53
Spatiotemporal analysis of programmed cell death during mouse cardiac septation. Anat Rec A Discov Mol Cell Evol Biol (2004) 1.51
Development of the vertebrate central nervous system: formation of the neural tube. Prenat Diagn (2009) 1.49
Sonic hedgehog and the molecular regulation of mouse neural tube closure. Development (2002) 1.44
Cordon-bleu is a conserved gene involved in neural tube formation. Dev Biol (2003) 1.44
Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening. Dis Model Mech (2013) 1.34
Gene-environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 function. Hum Mol Genet (2008) 1.33
Neural plate morphogenesis during mouse neurulation is regulated by antagonism of Bmp signalling. Development (2007) 1.27
Integrity of the methylation cycle is essential for mammalian neural tube closure. Birth Defects Res A Clin Mol Teratol (2006) 1.26
Deciphering the Mechanisms of Developmental Disorders (DMDD): a new programme for phenotyping embryonic lethal mice. Dis Model Mech (2013) 1.18
Mouse models of neural tube defects: investigating preventive mechanisms. Am J Med Genet C Semin Med Genet (2005) 1.17
Abnormal folate metabolism in foetuses affected by neural tube defects. Brain (2007) 1.16
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model. Hum Mol Genet (2007) 1.15
Apoptosis is not required for mammalian neural tube closure. Proc Natl Acad Sci U S A (2009) 1.11
Expression pattern of glypican-4 suggests multiple roles during mouse development. Dev Dyn (2005) 1.11
Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis. Hum Mutat (2011) 1.06
Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans. Hum Mol Genet (2011) 1.03
Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol. Hum Mol Genet (2003) 1.02
Cardiac neural crest of the mouse embryo: axial level of origin, migratory pathway and cell autonomy of the splotch (Sp2H) mutant effect. Development (2004) 1.00
Excess methionine suppresses the methylation cycle and inhibits neural tube closure in mouse embryos. FEBS Lett (2006) 1.00
Maternal diabetes increases the risk of caudal regression caused by retinoic acid. Diabetes (2002) 1.00
MRC-Wellcome Trust Human Developmental Biology Resource: enabling studies of human developmental gene expression. Trends Genet (2005) 0.99
Homocysteine is embryotoxic but does not cause neural tube defects in mouse embryos. Anat Embryol (Berl) (2003) 0.95
Quantitative analysis of s-adenosylmethionine and s-adenosylhomocysteine in neurulation-stage mouse embryos by liquid chromatography tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci (2006) 0.94
Dorsoventral patterning in oesophageal atresia with tracheo-oesophageal fistula: Evidence from a new mouse model. J Pediatr Surg (2002) 0.94
Foregut separation and tracheo-oesophageal malformations: the role of tracheal outgrowth, dorso-ventral patterning and programmed cell death. Dev Biol (2009) 0.93
The genetic background of the curly tail strain confers susceptibility to folate-deficiency-induced exencephaly. Birth Defects Res A Clin Mol Teratol (2010) 0.93
Role of Sonic hedgehog in the development of the trachea and oesophagus. J Pediatr Surg (2003) 0.92
Grainyhead genes and mammalian neural tube closure. Birth Defects Res A Clin Mol Teratol (2008) 0.90
Understanding the causes and prevention of neural tube defects: Insights from the splotch mouse model. Birth Defects Res A Clin Mol Teratol (2009) 0.90
Lamin b1 polymorphism influences morphology of the nuclear envelope, cell cycle progression, and risk of neural tube defects in mice. PLoS Genet (2012) 0.90
Cloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system. Genomics (2002) 0.88
Tethering of the spinal cord in mouse fetuses and neonates with spina bifida. J Neurosurg (2003) 0.87
EphrinA-EphA receptor interactions in mouse spinal neurulation: implications for neural fold fusion. Int J Dev Biol (2009) 0.87
Epithelial fusion during neural tube morphogenesis. Birth Defects Res A Clin Mol Teratol (2012) 0.86
Over-expression of Grhl2 causes spina bifida in the Axial defects mutant mouse. Hum Mol Genet (2011) 0.86
Syndecan 4 interacts genetically with Vangl2 to regulate neural tube closure and planar cell polarity. Development (2013) 0.86
Differential protein expression at the stage of neural tube closure in the mouse embryo. J Biol Chem (2002) 0.85
Heparan sulphate proteoglycans and spinal neurulation in the mouse embryo. Development (2002) 0.84
Neural tube defects induced by folate deficiency in mutant curly tail (Grhl3) embryos are associated with alteration in folate one-carbon metabolism but are unlikely to result from diminished methylation. Birth Defects Res A Clin Mol Teratol (2010) 0.84
Embryology of oesophageal atresia. Semin Pediatr Surg (2009) 0.83
Zic4, a zinc-finger transcription factor, is expressed in the developing mouse nervous system. Dev Dyn (2005) 0.83
Knowledge and periconceptional use of folic acid for the prevention of neural tube defects in ethnic communities in the United Kingdom: systematic review and meta-analysis. Birth Defects Res A Clin Mol Teratol (2013) 0.83
D-chiro-inositol is more effective than myo-inositol in preventing folate-resistant mouse neural tube defects. Hum Reprod (2002) 0.82
Quantitative analysis of myo-inositol in urine, blood and nutritional supplements by high-performance liquid chromatography tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci (2011) 0.81
Planar cell polarity aligns osteoblast division in response to substrate strain. J Bone Miner Res (2015) 0.81
Multiple developmental roles of Ahnak are suggested by localization to sites of placentation and neural plate fusion in the mouse conceptus. Mech Dev (2002) 0.81
Folate metabolite profiling of different cell types and embryos suggests variation in folate one-carbon metabolism, including developmental changes in human embryonic brain. Mol Cell Biochem (2013) 0.81
Do cells become homeless during neural tube closure? Cell Cycle (2009) 0.81
Lack of motor neuron differentiation is an intrinsic property of the mouse secondary neural tube. Dev Dyn (2010) 0.81
Nucleotide precursors prevent folic acid-resistant neural tube defects in the mouse. Brain (2013) 0.80
Induction of chondrogenesis in neural crest cells by mutant fibroblast growth factor receptors. Dev Dyn (2002) 0.80
Convergent extension analysis in mouse whole embryo culture. Methods Mol Biol (2012) 0.80
Novel exomphalos genetic mouse model: the importance of accurate phenotypic classification. J Pediatr Surg (2013) 0.79
Multiple developmental roles of Ahnak are suggested by localization to sites of placentation and neural plate fusion in the mouse conceptus. Gene Expr Patterns (2002) 0.79
Genomic organization and embryonic expression of Igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia. Mol Cell Neurosci (2003) 0.78
Is LMNB1 a susceptibility gene for neural tube defects in humans? Birth Defects Res A Clin Mol Teratol (2013) 0.78
Diffusion microscopic MRI of the mouse embryo: Protocol and practical implementation in the splotch mouse model. Magn Reson Med (2014) 0.76
Could microRNAs be biomarkers for neural tube defects? J Neurochem (2012) 0.76
Laminin and integrin expression in the ventral ectodermal ridge of the mouse embryo: implications for regulation of BMP signalling. Dev Dyn (2012) 0.75
Inositol for prevention of neural tube defects: a pilot randomised controlled trial - CORRIGENDUM. Br J Nutr (2016) 0.75