Cumulative inactivation of Nell-1 in Wnt1 expressing cell lineages results in craniofacial skeletal hypoplasia and postnatal hydrocephalus

[1]  Soonchul Lee,et al.  Peroxisome Proliferator-Activated Receptor-γ Knockdown Impairs Bone Morphogenetic Protein-2-Induced Critical-Size Bone Defect Repair. , 2019, The American journal of pathology.

[2]  H. Pan,et al.  Inactivation of Nell‐1 in Chondrocytes Significantly Impedes Appendicular Skeletogenesis , 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[3]  Feng Chen,et al.  Neurexin Superfamily Cell Membrane Receptor Contactin‐Associated Protein Like‐4 (Cntnap4) Is Involved in Neural EGFL‐Like 1 (Nell‐1)‐Responsive Osteogenesis , 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[4]  T. He,et al.  Neural EGF-like protein 1 (NELL-1): Signaling crosstalk in mesenchymal stem cells and applications in regenerative medicine , 2017, Genes & diseases.

[5]  J. An,et al.  Discovery of small molecule inhibitors of the Wnt/β-catenin signaling pathway by targeting β-catenin/Tcf4 interactions , 2017, Experimental biology and medicine.

[6]  Jia Jun Chia,et al.  SLC20A2 Deficiency in Mice Leads to Elevated Phosphate Levels in Cerbrospinal Fluid and Glymphatic Pathway‐Associated Arteriolar Calcification, and Recapitulates Human Idiopathic Basal Ganglia Calcification , 2017, Brain pathology.

[7]  S. Conway,et al.  Restricted Pax3 Deletion within the Neural Tube Results in Congenital Hydrocephalus , 2016, Journal of developmental biology.

[8]  Min Lee,et al.  Novel Wnt Regulator NEL-Like Molecule-1 Antagonizes Adipogenesis and Augments Osteogenesis Induced by Bone Morphogenetic Protein 2. , 2016, The American journal of pathology.

[9]  K. Ting,et al.  Accelerated Chondrogenic Differentiation of Human Perivascular Stem Cells with NELL-1. , 2016, Tissue engineering. Part A.

[10]  L. Pedersen,et al.  Slc20a2 is critical for maintaining a physiologic inorganic phosphate level in cerebrospinal fluid , 2015, neurogenetics.

[11]  M. de Castro,et al.  Inhibition of the Tcf/beta-catenin complex increases apoptosis and impairs adrenocortical tumor cell proliferation and adrenal steroidogenesis , 2015, Oncotarget.

[12]  Benjamin M. Wu,et al.  NELL-1 in the treatment of osteoporotic bone loss , 2015, Nature Communications.

[13]  K. Itoh,et al.  The role of L1cam in murine corticogenesis, and the pathogenesis of hydrocephalus , 2015, Pathology international.

[14]  W. Dobyns,et al.  Infantile hydrocephalus: a review of epidemiology, classification and causes. , 2014, European journal of medical genetics.

[15]  Yoshiyuki Yamazaki,et al.  Targeted gene transfer into ependymal cells through intraventricular injection of AAV1 vector and long-term enzyme replacement via the CSF , 2014, Scientific Reports.

[16]  Philippe Soriano,et al.  The widely used Wnt1-Cre transgene causes developmental phenotypes by ectopic activation of Wnt signaling. , 2013, Developmental biology.

[17]  N. Drouot,et al.  Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases , 2013, Acta Neuropathologica.

[18]  B. Jenny,et al.  Chiari I malformation associated with premature unilateral closure of the posterior intraoccipital synchondrosis in a preterm infant. , 2013, Journal of neurosurgery. Pediatrics.

[19]  A. James,et al.  NELL‐1 promotes cell adhesion and differentiation via integrinβ1 , 2012, Journal of cellular biochemistry.

[20]  S. Kuroda,et al.  The C‐terminal region of NELL1 mediates osteoblastic cell adhesion through integrin α3β1 , 2012, FEBS letters.

[21]  M. García-Castro,et al.  Pax7 Lineage Contributions to the Mammalian Neural Crest , 2012, PloS one.

[22]  A. James,et al.  NELL-1-dependent mineralisation of Saos-2 human osteosarcoma cells is mediated via c-Jun N-terminal kinase pathway activation , 2012, International Orthopaedics.

[23]  A. James,et al.  NELL-1 increases pre-osteoblast mineralization using both phosphate transporter Pit1 and Pit2. , 2012, Biochemical and biophysical research communications.

[24]  A. James,et al.  Calvarial Cleidocraniodysplasia-Like Defects With ENU-Induced Nell-1 Deficiency , 2012, The Journal of craniofacial surgery.

[25]  E. Durward,et al.  Structure-Function Analysis of Nel, a Thrombospondin-1-like Glycoprotein Involved in Neural Development and Functions* , 2011, The Journal of Biological Chemistry.

[26]  Angel Pan,et al.  A new function of Nell-1 protein in repressing adipogenic differentiation. , 2011, Biochemical and biophysical research communications.

[27]  Chen-Yuan Tseng,et al.  Zebrafish calcium/calmodulin‐dependent protein kinase II (cam‐kii) inhibitors: Expression patterns and their roles in zebrafish brain development , 2010, Developmental dynamics : an official publication of the American Association of Anatomists.

[28]  S. Kuroda,et al.  Nell-1, a key Functional Mediator of Runx2, Partially Rescues Calvarial Defects in Runx2+/− Mice , 2010, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[29]  K. Ting,et al.  The Role of NELL-1, a Growth Factor Associated with Craniosynostosis, in Promoting Bone Regeneration , 2010, Journal of dental research.

[30]  L. Smithers,et al.  New directions in craniofacial morphogenesis. , 2010, Developmental biology.

[31]  D. Leroith,et al.  High-Efficient FLPo Deleter Mice in C57BL/6J Background , 2009, PloS one.

[32]  W. Hsu,et al.  Manipulating gene activity in Wnt1‐expressing precursors of neural epithelial and neural crest cells , 2009, Developmental dynamics : an official publication of the American Association of Anatomists.

[33]  P. Dietrich,et al.  Congenital hydrocephalus associated with abnormal subcommissural organ in mice lacking huntingtin in Wnt1 cell lineages. , 2008, Human molecular genetics.

[34]  J. Epstein,et al.  Cre reporter mouse expressing a nuclear localized fusion of GFP and β‐galactosidase reveals new derivatives of Pax3‐expressing precursors , 2008, Genesis.

[35]  M. Seno,et al.  Involvement of MAPK signaling molecules and Runx2 in the NELL1‐induced osteoblastic differentiation , 2008, FEBS letters.

[36]  K. Rajewsky,et al.  Vagaries of conditional gene targeting , 2007, Nature Immunology.

[37]  S. Nishikawa,et al.  Neuroepithelial Cells Supply an Initial Transient Wave of MSC Differentiation , 2007, Cell.

[38]  M. Patel,et al.  The New Field of Neuroskeletal Biology , 2007, Calcified Tissue International.

[39]  G. Fricker,et al.  Choroid plexus epithelial monolayers – a cell culture model from porcine brain , 2006, Cerebrospinal Fluid Research.

[40]  K. Ting,et al.  Craniosynostosis‐Associated Gene Nell‐1 Is Regulated by Runx2 , 2006, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[41]  P. Kostenuik,et al.  Dkk1-mediated inhibition of Wnt signaling in bone results in osteopenia. , 2006, Bone.

[42]  B. Durand,et al.  A deficiency in RFX3 causes hydrocephalus associated with abnormal differentiation of ependymal cells , 2006, The European journal of neuroscience.

[43]  Benjamin Wu,et al.  Nell-1 induces acrania-like cranioskeletal deformities during mouse embryonic development , 2006, Laboratory Investigation.

[44]  Mahlon D. Johnson,et al.  Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects. , 2006, Human molecular genetics.

[45]  M. López-Aranda,et al.  Msx1‐Deficient Mice Fail to Form Prosomere 1 Derivatives, Subcommissural Organ, and Posterior Commissure and Develop Hydrocephalus , 2004, Journal of neuropathology and experimental neurology.

[46]  P. Genever,et al.  Emerging neuroskeletal signalling pathways: a review , 2004, FEBS letters.

[47]  Philippe Soriano,et al.  Cryptic boundaries in roof plate and choroid plexus identified by intersectional gene activation , 2003, Nature Genetics.

[48]  M. Longaker,et al.  Craniosynostosis in transgenic mice overexpressing Nell-1. , 2002, The Journal of clinical investigation.

[49]  A. McMahon,et al.  Inactivation of the beta-catenin gene by Wnt1-Cre-mediated deletion results in dramatic brain malformation and failure of craniofacial development. , 2001, Development.

[50]  M. Wassef,et al.  Ectopic engrailed 1 expression in the dorsal midline causes cell death, abnormal differentiation of circumventricular organs and errors in axonal pathfinding. , 2000, Development.

[51]  A. McMahon,et al.  Fate of the mammalian cranial neural crest during tooth and mandibular morphogenesis. , 2000, Development.

[52]  Chaya Kalcheim,et al.  The Neural Crest: Author Index , 1999 .

[53]  K. Abe,et al.  A novel transgenic technique that allows specific marking of the neural crest cell lineage in mice. , 1999, Developmental biology.

[54]  M. Longaker,et al.  Human NELL‐1 Expressed in Unilateral Coronal Synostosis , 1999, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[55]  V. Sandig,et al.  Reactivation of the Previously Silenced Cytomegalovirus Major Immediate-Early Promoter in the Mouse Liver: Involvement of NFκB , 1998, Journal of Virology.

[56]  F. Brunelle,et al.  Hydrocephalus and craniosynostosis. , 1997, Journal of neurosurgery.

[57]  A. McMahon,et al.  Wnt signalling required for expansion of neural crest and CNS progenitors , 1997, Nature.

[58]  T. Katagiri,et al.  Cloning and characterization of two novel human cDNAs (NELL1 and NELL2) encoding proteins with six EGF-like repeats. , 1996, Genomics.

[59]  H. Aberle,et al.  Cadherin‐catenin complex: Protein interactions and their implications for cadherin function , 1996, Journal of cellular biochemistry.

[60]  J. Jacobberger,et al.  Multiparameter cell cycle analysis , 1996 .

[61]  M. Bronner‐Fraser Origins and developmental potential of the neural crest. , 1995, Experimental cell research.

[62]  K. Hori,et al.  New gene, nel, encoding a Mr 93 K protein with EGF‐like repeats is strongly expressed in neural tissues of early stage chick embryos , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[63]  A. McMahon,et al.  Cis-acting regulatory sequences governing Wnt-1 expression in the developing mouse CNS. , 1994, Development.

[64]  K. Rajewsky,et al.  Deletion of a DNA polymerase beta gene segment in T cells using cell type-specific gene targeting. , 1994, Science.

[65]  R. Nusse,et al.  Expression of two members of the Wnt family during mouse development--restricted temporal and spatial patterns in the developing neural tube. , 1991, Genes & development.

[66]  Andrew P. McMahon,et al.  The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain , 1990, Cell.

[67]  D. V. Cohn,et al.  Target cells in bone for parathormone and calcitonin are different: enrichment for each cell type by sequential digestion of mouse calvaria and selective adhesion to polymeric surfaces. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[68]  Wei Chen,et al.  Wnt and the Wnt signaling pathway in bone development and disease. , 2014, Frontiers in bioscience.

[69]  S. Iseki,et al.  Tissue origins and interactions in the mammalian skull vault. , 2002, Developmental biology.

[70]  Philippe Soriano Generalized lacZ expression with the ROSA26 Cre reporter strain , 1999, Nature Genetics.

[71]  K. Hori,et al.  Erratum: New gene, nel, encoding a Mr 91 K protein with EGF-like repeats is strongly expressed in neural tissues of early stage chick embryos (Developmental Dynamics (1995) 203 (202-213)) , 1996 .

[72]  K. Rajewsky,et al.  A cre-transgenic mouse strain for the ubiquitous deletion of loxP-flanked gene segments including deletion in germ cells. , 1995, Nucleic acids research.