• A clinical and experimental overview of sirenomelia: insight into the mechanisms of congenital limb malformations
• Aberrant bone marrow vascularization patterns in untreated patients with Gaucher disease type 1
• Aberrant transcriptional networks in step-wise neurogenesis of paroxysmal kinesigenic dyskinesia-induced pluripotent stem cells
• Absence of canonical Smad signaling in ureteral and bladder mesenchyme causes ureteropelvic junction obstruction
• Alpha Fetoprotein
• Alpha Fetoprotein
• Alpha-Fetoprotein Analysis
• Altered gene expression in human placentas after IVF/ICSI
• An Early Function of Polycystin-2 for Left-Right Organizer Induction in Xenopus
• Angiogenic potential in periodontal stem cells from upper and lower jaw: A pilot study
• Ascorbate and Iron Are Required for the Specification and Long-Term Self-Renewal of Human Skeletal Mesenchymal Stromal Cells
• Barx1-mediated inhibition of Wnt signaling in the mouse thoracic foregut controls tracheo-esophageal septation and epithelial differentiation
• Bone marrow pericyte dysfunction in individuals with type 2 diabetes
• Brain mural cell loss in the parietal cortex in Alzheimer's disease correlates with cognitive decline and TDP-43 pathology
• Cloacal exstrophy: an epidemiologic study from the International Clearinghouse for Birth Defects Surveillance and Research
• Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
• Comparative Craniofacial Bone Regeneration Capacities of Mesenchymal Stem Cells Derived from Human Neural Crest Stem Cells and Bone Marrow
• Conditioned Medium from Periodontal Ligament Stem Cells Enhances Periodontal Regeneration
• Congenital agenesis of pubis and bilateral cryptorchidism: A case report
• Congenital hairy polyp of the oropharynx presenting as an esophageal mass in a neonate, a case report and literature review
• Congenital Midline Spinal Hamartoma in a 5-Month-Old Infant
• Cutaneous Manifestations of Tuberous Sclerosis
• Data on cardiac lncRNA <em>STX18-AS1</em> expression in developing human hearts and function during <em>in vitro</em> hESC-cardiomyocyte differentiation
• Defective pericyte recruitment of villous stromal vessels as the possible etiologic cause of hydropic change in complete hydatidiform mole
• Deletion of neural tube defect-associated gene Mthfd1l causes reduced cranial mesenchyme density
• Distinct functions of alternatively spliced isoforms encoded by zebrafish mef2ca and mef2cb
• Distinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathway
• DNA methylation levels of imprinted and nonimprinted genes DMRs associated with defective human spermatozoa
• Does the mesodermal derangement in Chiari Type I malformation extend to the cervical spine? Evidence from an analytical morphometric study on cervical paraspinal muscles
• Ectodermal-derived Endothelin1 is required for patterning the distal and intermediate domains of the mouse mandibular arch
• Ectopia Cordis Associated with Pentalogy of Cantrell-A Case Report
• Ellis van Creveld syndrome--a report of two siblings
• Embryology, Branchial Arches
• Embryology, Branchial Arches
• Encephalocele development from a congenital meningocele: case report
• Focal Dermal Hypoplasia with Osteopathia Striata
• Gene-environment interaction demonstrates the vulnerability of the embryonic heart
• Genetics of clubfoot; recent progress and future perspectives
• Ibuprofen slows migration and inhibits bowel colonization by enteric nervous system precursors in zebrafish, chick and mouse
• Infection and upregulation of proinflammatory cytokines in human brain vascular pericytes by human cytomegalovirus
• Interruption of Wnt signaling in Müller cells ameliorates ischemia-induced retinal neovascularization
• iPSC-derived progenitor stromal cells provide new insights into aberrant musculoskeletal development and resistance to cancer in down syndrome
• Klippel-Trenaunay syndrome presenting with acanthocytosis and splenic and retroperitoneal lymphangioma: a case report
• Latent TGF-β binding protein 3 identifies a second heart field in zebrafish
• Loss of abdominal muscle in Pitx2 mutants associated with altered axial specification of lateral plate mesoderm
• Loss of Neogenin alters branchial arch development and leads to craniofacial skeletal defects
• Low Osteogenic Yield in Human Pluripotent Stem Cells Associates with Differential Neural Crest Promoter Methylation
• Magnetic resonance evaluation of Müllerian remnants in Mayer-Rokitansky-Küster-Hauser 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
• MBTPS1/SKI-1/S1P proprotein convertase is required for ECM signaling and axial elongation during somitogenesis and vertebral development†
• Mesenchymal activin-A overcomes defective human trisomy 21 trophoblast fusion
• Mesenchymal fibroblast growth factor receptor signaling regulates palatal shelf elevation during secondary palate formation
• Mesenchymal stem cells: A therapeutic update
• 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
• Modified horizontal muscle transposition without tenotomy and splitting for a case of inferior rectus and inferior oblique muscles aplasia with hemifacial microsomia
• Murine model indicates 22q11.2 signaling adaptor <em>CRKL</em> is a dosage-sensitive regulator of genitourinary development
• Ndrg2 regulates vertebral specification in differentiating somites
• Nephric duct insertion requires EphA4/EphA7 signaling from the pericloacal mesenchyme
• Noggin is required for early development of murine upper incisors
• Novel mechanisms of early upper and lower urinary tract patterning regulated by RetY1015 docking tyrosine in mice
• Orofacial Muscles: Embryonic Development and Regeneration after Injury
• Papp-a2 modulates development of cranial cartilage and angiogenesis in zebrafish embryos
• Peli1b governs the brain patterning via ERK signaling pathways in zebrafish embryos
• Pentalogy of Cantrell Associated with Ectopia Cordis: A Case Report
• Pentalogy of Cantrell: Case Report With Review of the Literature
• Perivascular Stem Cells at the Tip of Mouse Incisors Regulate Tissue Regeneration
• Possible effects of EXT2 on mesenchymal differentiation--lessons from the zebrafish
• Prenatal diagnosis of Cantrell pentalogy in first trimester screening: case report and review of literature
• Prenatal diagnosis of meningomyelocele resolves as a mature cystic teratoma in the thoracolumbar region
• Renal and urological abnormalities occurring with Mullerian anomalies
• Renal development: a complex process dependent on inductive interaction
• Rhabdomyomatous mesenchymal hamartoma presenting as a sacral skin tag in two neonates with spinal dysraphism
• Role of OVCA1/DPH1 in craniofacial abnormalities of Miller-Dieker syndrome
• Sacral agenesis: a pilot whole exome sequencing and copy number study
• SCAP knockout in SM22alpha-Cre mice induces defective angiogenesis in the placental labyrinth
• SCAP knockout in SM22α-Cre mice induces defective angiogenesis in the placental labyrinth
• Sirenomelia phenotype in bmp7;shh compound mutants: a novel experimental model for studies of caudal body malformations
• Sirenomelia: An anatomical assessment and genetic sex determination of two cases
• Six1 and Eya1 are critical regulators of peri-cloacal mesenchymal progenitors during genitourinary tract development
• Small heat shock proteins are necessary for heart migration and laterality determination in zebrafish
• Spinal extradural meningeal cyst in klippel-trenaunay syndrome
• Stochastic gene expression and environmental stressors trigger variable somite segmentation phenotypes
• Supt20 is required for development of the axial skeleton
• Symptomatic, unilateral, isolated, complete persistent sciatic vein
• T-box genes and retinoic acid signaling regulate the segregation of arterial and venous pole progenitor cells in the murine second heart field
• Tbx5 Buffers Inherent Left/Right Asymmetry Ensuring Symmetric Forelimb Formation
• The aetiology behind torticollis and variable spine defects in patients with Mullerian duct/renal aplasia-cervicothoracic somite dysplasia syndrome: 3D CT scan analysis
• 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
• Torsion of a hydrosalpinx in a virgin patient with Mayer-Rokitansky-Küster-Hauser syndrome: report of a rare condition and its possible etiology
• Trisomy 12 compromises the mesendodermal differentiation propensity of human pluripotent stem cells
• Unusual cortical bone features in a patient with gorlin-goltz syndrome: a case report
• Ureteral Polyp Managed by Endoscopic Techniques
• Ursodeoxycholic Acid Attenuates the Retinal Vascular Abnormalities in Anti-PDGFR-beta Antibody-Induced Pericyte Depletion Mouse Models
• Ursodeoxycholic Acid Attenuates the Retinal Vascular Abnormalities in Anti-PDGFR-β Antibody-Induced Pericyte Depletion Mouse Models
• Uterine rudiments in patients with Mayer-Rokitansky-Küster-Hauser syndrome consist of typical uterine tissue types with predominantly basalis-like endometrium
• Vaginal reconstruction with the Abbè-McIndoe technique: from dermal grafts to autologous in vitro cultured vaginal tissue transplant
• Wdr68 Mediates Dorsal and Ventral Patterning Events for Craniofacial Development
• Wnt Signaling Induces Asymmetric Dynamics in the Actomyosin Cortex of the <em>C. elegans</em> Endomesodermal Precursor Cell
• Wnt8a and Wnt3a cooperate in the axial stem cell niche to promote mammalian body axis extension