• A definitive role of Shp-2 tyrosine phosphatase in mediating embryonic stem cell differentiation and hematopoiesis
• A genetic screen for modifiers of Drosophila decapentaplegic signaling identifies mutations in punt, Mothers against dpp and the BMP-7 homologue, 60A
• Aberrant bone marrow vascularization patterns in untreated patients with Gaucher disease type 1
• An Early Function of Polycystin-2 for Left-Right Organizer Induction in Xenopus
• BmprIa is required in mesenchymal tissue and has limited redundant function with BmprIb in tooth and palate development
• Bone marrow pericyte dysfunction in individuals with type 2 diabetes
• Clinical and radiological findings in Arnold Chiari malformation
• Congenital Midline Spinal Hamartoma in a 5-Month-Old Infant
• Diminished callus size and cartilage synthesis in alpha 1 beta 1 integrin-deficient mice during bone fracture healing
• Does the mesodermal derangement in Chiari Type I malformation extend to the cervical spine? Evidence from an analytical morphometric study on cervical paraspinal muscles
• Dysmorphogenesis of kidney cortical peritubular capillaries in angiopoietin-2-deficient mice
• FGFR3 is a target of the homeobox transcription factor SHOX in limb development
• Gelatin-based resorbable sponge as a carrier matrix for human mesenchymal stem cells in cartilage regeneration therapy
• Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization
• Human mesenchymal stem cells are not of donor origin in patients with severe aplastic anemia who underwent sex-mismatched allogeneic bone marrow transplant
• Ibuprofen slows migration and inhibits bowel colonization by enteric nervous system precursors in zebrafish, chick and mouse
• In vitro cartilage formation of composites of synovium-derived mesenchymal stem cells with collagen gel
• Latent TGF-β binding protein 3 identifies a second heart field in zebrafish
• Lesser forms of cleft lip associated with the branchio-oculo-facial syndrome
• Mapping cellular processes in the mesenchyme during palatal development in the absence of Tbx1 reveals complex proliferation changes and perturbed cell packing and polarity
• Mesenchymal fibroblast growth factor receptor signaling regulates palatal shelf elevation during secondary palate formation
• Mice doubly deficient in <em>Six4</em> and <em>Six5</em> show ventral body wall defects reproducing human omphalocele
• Mice doubly deficient in Six4 and Six5 show ventral body wall defects reproducing human omphalocele
• Over-expression of the chondroitin sulphate proteoglycan versican is associated with defective neural crest migration in the Pax3 mutant mouse (splotch)
• Prx1 and Prx2 are upstream regulators of sonic hedgehog and control cell proliferation during mandibular arch morphogenesis
• Recombinase-mediated cassette exchange reveals the selective use of Gq/G11-dependent and -independent endothelin 1/endothelin type A receptor signaling in pharyngeal arch development
• Renal and urological abnormalities occurring with Mullerian anomalies
• Role of endoplasmic reticulum stress in epithelial-mesenchymal transition of alveolar epithelial cells: effects of misfolded surfactant protein
• Sacral agenesis: a pilot whole exome sequencing and copy number study
• Stem cell-derived endothelial cells/progenitors migrate and pattern in the embryo using the VEGF signaling pathway
• Structure and function of lamellar bodies, lipid-protein complexes involved in storage and secretion of cellular lipids
• TGF-beta3-induced palatogenesis requires matrix metalloproteinases
• The apical ectodermal ridge of the mouse model of ectrodactyly Dlx5;Dlx6-/- shows altered stratification and cell polarity, which are restored by exogenous Wnt5a ligand
• The Boston-type craniosynostosis mutation MSX2 (P148H) results in enhanced susceptibility of MSX2 to ubiquitin-dependent degradation
• Tissue-specific binding of radiolabeled activin A by activin receptors and follistatin in postimplantation rat and mouse embryos
• Upper beak truncation in chicken embryos with the cleft primary palate mutation is due to an epithelial defect in the frontonasal mass
• Uterine rudiments in patients with Mayer-Rokitansky-Küster-Hauser syndrome consist of typical uterine tissue types with predominantly basalis-like endometrium