All Stories

  1. MicroRNAs Play Key Roles in Progenitor Maintenance, Proliferation, and Osteogenic Differentiation of Osteogenic Progenitor Cells in Syndromic and Nonsyndromic Craniosynostosis
  2. Identification of Genes and microRNAs Associated with Midfacial Hypoplasia in Mice
  3. Overexpression of miR-320-3p, miR-381-3p, and miR-27a-3p Suppresses Genes Related to Midline Facial Cleft in Mouse Cranial Neural Crest Cells
  4. miR-302a/b/d-3p Differentially Expressed During Frontonasal Development Is Sensitive to Retinoic Acid Exposure
  5. Associations between metabolic disorders and Sjögren's disease
  6. Genes Related to Frontonasal Malformations Are Regulated by miR-338-5p, miR-653-5p, and miR-374-5p in O9-1 Cells
  7. Craniofacial bone anomalies related to cholesterol synthesis defects
  8. Response to Letter, “Autophagy Plays a Crucial Role in Ameloblast Differentiation”
  9. Single-cell multiomics decodes regulatory programs for mouse secondary palate development
  10. Loss of Sc5d results in micrognathia due to a failure in osteoblast differentiation
  11. Editorial: Animal models and transgenic technology in Craniofacial biology
  12. Editorial: Deep learning for disease prediction in next-generation sequencing and biomedical imaging data
  13. Autophagy Plays a Crucial Role in Ameloblast Differentiation
  14. MicroRNAs and Gene Regulatory Networks Related to Cleft Lip and Palate
  15. FaceBase: A Community-Driven Hub for Data-Intensive Research
  16. Hematopoietic–Mesenchymal Signals Regulate the Properties of Mesenchymal Stem Cells
  17. Spatiotemporal MicroRNA-Gene Expression Network Related to Orofacial Clefts
  18. Impaired GATE16-mediated exocytosis in exocrine tissues causes Sjögren’s syndrome-like exocrinopathy
  19. Micro-computed tomography assessment of bone structure in aging mice
  20. Suppression of microRNA 124-3p and microRNA 340-5p ameliorates retinoic acid-induced cleft palate in mice
  21. Crucial Roles of microRNA-16-5p and microRNA-27b-3p in Ameloblast Differentiation Through Regulation of Genes Associated With Amelogenesis Imperfecta
  22. CleftGeneDB: a resource for annotating genes associated with cleft lip and cleft palate
  23. Dexamethasone Suppresses Palatal Cell Proliferation through miR-130a-3p
  24. Mesenchymal stromal cells in the bone marrow niche consist of multi-populations with distinct transcriptional and epigenetic properties
  25. MicroRNA-124-3p Plays a Crucial Role in Cleft Palate Induced by Retinoic Acid
  26. Identification of microRNAs and gene regulatory networks in cleft lip common in humans and mice
  27. Amino acid metabolism and autophagy in skeletal development and homeostasis
  28. Overexpression of miR-1306-5p, miR-3195, and miR-3914 Inhibits Ameloblast Differentiation through Suppression of Genes Associated with Human Amelogenesis Imperfecta
  29. Phenytoin Inhibits Cell Proliferation through microRNA-196a-5p in Mouse Lip Mesenchymal Cells
  30. Excessive All-Trans Retinoic Acid Inhibits Cell Proliferation Through Upregulated MicroRNA-4680-3p in Cultured Human Palate Cells
  31. Cell signaling regulation in salivary gland development
  32. Role of Metabolism in Bone Development and Homeostasis
  33. Secondary Genome-Wide Association Study Using Novel Analytical Strategies Disentangle Genetic Components of Cleft Lip and/or Cleft Palate in 1q32.2
  34. Gene–environment interplay and MicroRNAs in cleft lip and cleft palate
  35. An integrative, genomic, transcriptomic and network-assisted study to identify genes associated with human cleft lip with or without cleft palate
  36. Disruption of Dhcr7 and Insig1/2 in cholesterol metabolism causes defects in bone formation and homeostasis through primary cilium formation
  37. A developmental stage specific network approach for studying dynamic transcription factor-microRNA co-regulation during craniofacial development
  38. MicroRNA-124-3p suppresses mouse lip mesenchymal cell proliferation through the regulation of genes associated with cleft lip in the mouse
  39. Critical microRNAs and regulatory motifs in cleft palate identified by a conserved miRNA–TF–gene network approach in humans and mice
  40. MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells
  41. MicroRNA-655-3p and microRNA-497-5p inhibit cell proliferation in cultured human lip cells through the regulation of genes related to human cleft lip
  42. Cholesterol metabolism plays a crucial role in the regulation of autophagy for cell differentiation of granular convoluted tubules in male mouse submandibular glands
  43. Network-based identification of critical regulators as putative drivers of human cleft lip
  44. WNT/β-catenin signaling plays a crucial role in myoblast fusion through regulation of nephrin expression during development
  45. Molecular Regulatory Mechanism of Exocytosis in the Salivary Glands
  46. The role of acetyltransferases for the temporal-specific accessibility of β-catenin to the myogenic gene locus
  47. Gene datasets associated with mouse cleft palate
  48. Genes and microRNAs associated with mouse cleft palate: A systematic review and bioinformatics analysis
  49. Molecular mechanisms of midfacial developmental defects
  50. Mouse genetic models for temporomandibular joint development and disorders
  51. Integration of comprehensive 3D microCT and signaling analysis reveals differential regulatory mechanisms of craniofacial bone development
  52. WNT/β-Catenin Signaling Regulates Multiple Steps of Myogenesis by Regulating Step-Specific Targets
  53. TGF  regulates epithelial-mesenchymal interactions through WNT signaling activity to control muscle development in the soft palate
  54. Modulation of lipid metabolic defects rescues cleft palate in Tgfbr2 mutant mice
  55. Noncanonical Transforming Growth Factor   (TGF ) Signaling in Cranial Neural Crest Cells Causes Tongue Muscle Developmental Defects
  56. CTGF Mediates Smad-Dependent Transforming Growth Factor β Signaling To Regulate Mesenchymal Cell Proliferation during Palate Development
  57. Enrichment of GABARAP Relative to LC3 in the Axonal Initial Segments of Neurons
  58. Abstract 76
  59. Abstract 75
  60. Mice with Tak1 Deficiency in Neural Crest Lineage Exhibit Cleft Palate Associated with Abnormal Tongue Development
  61. Identification of candidate downstream targets of TGFβ signaling during palate development by genome‐wide transcript profiling
  62. Smad4-Irf6 genetic interaction and TGF -mediated IRF6 signaling cascade are crucial for palatal fusion in mice
  63. Modulation of noncanonical TGF-β signaling prevents cleft palate in Tgfbr2 mutant mice
  64. Role of the transcription factor Sp1 in regulating the expression of the murine cathepsin E gene
  65. Fibroblast Growth Factor 9 (FGF9)-Pituitary Homeobox 2 (PITX2) Pathway Mediates Transforming Growth Factor   (TGF ) Signaling to Regulate Cell Proliferation in Palatal Mesenchyme during Mouse Palatogenesis
  66. The FaceBase Consortium: A comprehensive program to facilitate craniofacial research
  67. Liver autophagy contributes to the maintenance of blood glucose and amino acid levels
  68. Tgf-β-mediated FasL-Fas-Caspase Pathway Is Crucial during Palatogenesis
  69. 154: TGF-BETA-MEDIATED FGF9-PITX2 SIGNALING REGULATES CELL PROLIFERATION DURING PALATE FORMATION
  70. The mechanism of TGF-β signaling during palate development
  71. Msx1 and Dlx5 function synergistically to regulate frontal bone development
  72. 137A: TGF-BETA MEDIATED FGF9 SIGNALING REGULATES CELL PROLIFERATION IN PALATAL MESENCHYMAL CELLS
  73. TGF-β mediated FGF10 signaling in cranial neural crest cells controls development of myogenic progenitor cells through tissue–tissue interactions during tongue morphogenesis
  74. TGF-²-induced Shc Signaling Persists In The Absence Of The Type II Receptor
  75. Transforming Growth Factor-  Regulates Basal Transcriptional Regulatory Machinery to Control Cell Proliferation and Differentiation in Cranial Neural Crest-derived Osteoprogenitor Cells
  76. The Atg8 Conjugation System Is Indispensable for Proper Development of Autophagic Isolation Membranes in Mice
  77. Homeostatic Levels of p62 Control Cytoplasmic Inclusion Body Formation in Autophagy-Deficient Mice
  78. Cathepsin E Prevents Tumor Growth and Metastasis by Catalyzing the Proteolytic Release of Soluble TRAIL from Tumor Cell Surface
  79. Association of cathepsin E with tumor growth arrest through angiogenesis inhibition and enhanced immune responses
  80. Essential role for autophagy protein Atg7 in the maintenance of axonal homeostasis and the prevention of axonal degeneration
  81. Loss of autophagy in the central nervous system causes neurodegeneration in mice
  82. Excess Peroxisomes Are Degraded by Autophagic Machinery in Mammals
  83. Impairment of starvation-induced and constitutive autophagy in Atg7 -deficient mice