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1. Full Text Complex malformations involving the fetal body wall – definition and classification issues
by Bijok, Julia and Massalska, Diana and Kucińska‐Chahwan, Anna and Posiewka, Anna and Ilnicka, Alicja and Jakiel, Grzegorz and Roszkowski, Tomasz
Prenatal Diagnosis, ISSN 0197-3851, 10/2017, Volume 37, Issue 10, pp. 1033 - 1039
What's already known about this topic? Complex malformations of the fetal body wall constitute a heterogenous group of anomalies encompassing craniofacial... 
PATHOGENESIS | DISCORDANT | SONOGRAPHIC DIAGNOSIS | DEFECTS | MANAGEMENT | ANOMALIES | GENETICS & HEREDITY | FEATURES | OBSTETRICS & GYNECOLOGY | Neural Tube Defects - diagnostic imaging | Encephalocele - embryology | Heart Defects, Congenital - embryology | Humans | Neural Tube Defects - embryology | Intestines - embryology | Umbilical Cord - diagnostic imaging | Limb Deformities, Congenital - embryology | Liver - embryology | Chromosome Aberrations - embryology | Heart Defects, Congenital - diagnostic imaging | Liver - diagnostic imaging | Female | Retrospective Studies | Intestines - abnormalities | Congenital Abnormalities - embryology | Congenital Abnormalities - diagnostic imaging | Gestational Age | Urinary Bladder - abnormalities | Urinary Bladder - embryology | Pregnancy | Ultrasonography, Prenatal | Limb Deformities, Congenital - diagnostic imaging | Liver - abnormalities | Intestines - diagnostic imaging | Encephalocele - diagnostic imaging | Umbilical Cord - abnormalities | Pregnancy Outcome | Liver | Analysis | Limbs | Body wall | Vibration | Spine | Fetuses | Bladder | Defects | Urinary bladder | Animal behavior | Intestine | Classification | Arthropods | Umbilical cord | Aberration | Chromosome aberrations | Anomalies | Index Medicus
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2. Full Text Efficient Endoderm Induction from Human Pluripotent Stem Cells by Logically Directing Signals Controlling Lineage Bifurcations
by Loh, Kyle M and Ang, Jasmin and Ang, Lay Teng and Zhang, Jingyao and Kumar, Vibhor and Auyeong, Jun Qiang and Lee, Kian Leong and Choo, Siew Hua and Lim, Christina Y.Y and Lim, Bing and Nichane, Massimo and Tan, Junru and Noghabi, Monireh Soroush and Azzola, Lisa and Ng, Elizabeth S and Durruthy-Durruthy, Jens and Sebastiano, Vittorio and Poellinger, Lorenz and Elefanty, Andrew G and Stanley, Edouard G and Chen, Qingfeng and Prabhakar, Shyam and Weissman, Irving L
Cell Stem Cell, ISSN 1934-5909, 02/2014, Volume 14, Issue 2, pp. 237 - 252
Human pluripotent stem cell (hPSC) differentiation typically yields heterogeneous populations. Knowledge of signals controlling embryonic lineage bifurcations... 
GASTRULATION | PANCREATIC DIFFERENTIATION | WNT/BETA-CATENIN | DEFINITIVE ENDODERM | SPECIFICATION | LIVER DEVELOPMENT | REGULATORY REGIONS | EMBRYOGENESIS | MOUSE EMBRYO | CLONAL ANALYSIS | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Body Patterning - drug effects | Chromatin - metabolism | Embryonic Stem Cells - metabolism | Transcription, Genetic - drug effects | Embryonic Stem Cells - cytology | Humans | Molecular Sequence Data | Endoderm - embryology | Wnt Proteins - metabolism | Cell Lineage - drug effects | Liver - embryology | Fibroblast Growth Factors - metabolism | Bone Morphogenetic Proteins - metabolism | Endoderm - cytology | Base Sequence | Protein Binding - drug effects | Epigenesis, Genetic - drug effects | Culture Media, Serum-Free - pharmacology | Pluripotent Stem Cells - cytology | Primitive Streak - embryology | Primitive Streak - cytology | Digestive System - embryology | Pancreas - embryology | Animals | MAP Kinase Signaling System - drug effects | Signal Transduction - drug effects | Endoderm - drug effects | Pluripotent Stem Cells - drug effects | Enhancer Elements, Genetic - genetics | Mice | Transforming Growth Factor beta - metabolism | Index Medicus
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3. Full Text Genetic lineage tracing identifies endocardial origin of liver vasculature
by Zhang, Hui and Pu, Wenjuan and Tian, Xueying and Huang, Xiuzhen and He, Lingjuan and Liu, Qiaozhen and Li, Yan and Zhang, Libo and He, Liang and Liu, Kuo and Gillich, Astrid and Zhou, Bin
Nature Genetics, ISSN 1061-4036, 05/2016, Volume 48, Issue 5, pp. 537 - 543
The hepatic vasculature is essential for liver development, homeostasis and regeneration, yet the developmental program of hepatic vessel formation and the... 
Liver Circulation | Endocardium - embryology | Heart Atria - embryology | NFATC Transcription Factors - metabolism | Heart Ventricles - embryology | Coronary Vessels - embryology | Liver - embryology | Endocardium - metabolism | Heart Atria - metabolism | Morphogenesis | Cell Lineage | Liver - blood supply | Animals | Heart Ventricles - metabolism | Mice | Endocardium - cytology | Neovascularization, Physiologic | Genotype | Genetic aspects | Properties | Liver | Coronary arteries | Studies | Heart | Rodents | Coronary vessels | Stem cells | Homeostasis | Veins & arteries | Index Medicus
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4. Full Text MicroRNAs Are Necessary for Vascular Smooth Muscle Growth, Differentiation, and Function
by Albinsson, Sebastian and Suarez, Yajaira and Skoura, Athanasia and Offermanns, Stefan and Miano, Joseph M and Sessa, William C
Arteriosclerosis, Thrombosis, and Vascular Biology, ISSN 1079-5642, 06/2010, Volume 30, Issue 6, pp. 1118 - 1126
OBJECTIVE—Regulation of vascular smooth muscle (VSM) proliferation and contractile differentiation is an important factor in vascular development and... 
Molecular biology | Contractile proteins | Vascular biology | Vascular muscle | molecular biology | ACTIVATION | PHENOTYPE | vascular biology | ACTIN DYNAMICS | PROLIFERATION | DICER | vascular muscle | MOUSE DEVELOPMENT | NEOINTIMAL LESION FORMATION | EMBRYONIC STEM-CELLS | SERUM RESPONSE FACTOR | GENE-EXPRESSION | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | contractile proteins | Endoribonucleases - genetics | Cell Proliferation | Muscle, Smooth, Vascular - metabolism | Transcriptional Activation | Actins - metabolism | Male | MicroRNAs - metabolism | Aorta - metabolism | Muscle, Smooth, Vascular - physiopathology | Muscle, Smooth, Vascular - embryology | Cell Differentiation - genetics | Vasodilation - genetics | Transfection | Gene Expression Regulation, Developmental | DEAD-box RNA Helicases - deficiency | Trans-Activators - genetics | Hemorrhage - embryology | Endoribonucleases - deficiency | Nuclear Proteins - genetics | Microfilament Proteins - genetics | Vasoconstriction - genetics | Liver Diseases - embryology | Hemorrhage - genetics | Liver Diseases - genetics | Umbilical Arteries - pathology | Muscle, Smooth, Vascular - ultrastructure | Cells, Cultured | Umbilical Arteries - embryology | Aorta - embryology | Genotype | Nuclear Proteins - metabolism | Hemorrhage - metabolism | Gestational Age | Mice, Knockout | Aorta - pathology | Muscle Proteins - genetics | DEAD-box RNA Helicases - genetics | Embryo Loss | Phenotype | Stress Fibers - metabolism | Animals | Ribonuclease III | Muscle Development - genetics | Trans-Activators - metabolism | Mice | Liver Diseases - metabolism | Integrases - genetics | Umbilical Arteries - metabolism | Index Medicus
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5. Full Text Immunohistochemical assessment of Pax8 expression during pancreatic islet development and in human neuroendocrine tumors
by Lorenzo, Petra I and Jimenez Moreno, Carmen M and Delgado, Irene and Cobo-Vuilleumier, Nadia and Meier, Raphael and Gomez-Izquierdo, Lourdes and Berney, Thierry and Garcia-Carbonero, Rocio and Rojas, Anabel and Gauthier, Benoit R
Histochemistry and Cell Biology, ISSN 0948-6143, 11/2011, Volume 136, Issue 5, pp. 595 - 607
The paired box transcription factor Pax8 is critical for development of the eye, thyroid gland as well as the urinary and reproductive organs. In adult, Pax8... 
Pax genes | Medicine & Public Health | Antibody cross-reactivity | Anatomy | Transcription factor | Medicine/Public Health, general | Pancreatic islet | Neuroendocrine tumors | SURVIVAL | MICROSCOPY | CANCER | CELL BIOLOGY | TRANSCRIPTION FACTOR PAX4 | GENE | IN-VIVO | BETA-CELL | DIFFERENTIATION | TISSUES | Paired Box Transcription Factors - genetics | Pancreatic Neoplasms - metabolism | Kidney - embryology | Humans | RNA, Messenger - metabolism | Liver - embryology | Embryo, Mammalian - metabolism | Kidney - metabolism | Cell Nucleus - metabolism | Gene Expression Regulation, Developmental | Islets of Langerhans - metabolism | Biomarkers, Tumor - metabolism | Animals, Newborn | Neuroendocrine Tumors - pathology | Neuroendocrine Tumors - metabolism | Liver - metabolism | Pancreatic Neoplasms - pathology | Islets of Langerhans - embryology | Pancreas - metabolism | Pancreas - embryology | Cross Reactions | Animals | Mice | PAX8 Transcription Factor | Paired Box Transcription Factors - metabolism | Immunohistochemistry | Messenger RNA | Analysis | Genes | Stem cells | Thyroid diseases | Monoclonal antibodies | Tumors | Gene expression | Pancreas | Endocrinology | Cancer | Index Medicus | Original Paper
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6. Full Text Parasympathetic Innervation Maintains Epithelial Progenitor Cells During Salivary Organogenesis
by S. M. Knox and I. M. A. Lombaert and X. Reed and L. Vitale-Cross and J. S. Gutkind and M. P. Hoffman
Science, ISSN 0036-8075, 9/2010, Volume 329, Issue 5999, pp. 1645 - 1647
The maintenance of a progenitor cell population as a reservoir of undifferentiated cells is required for organ development and regeneration. However, the... 
Morphogenesis | Cell growth | Receptors | Salivary glands | Innervation | REPORTS | Epithelium | Cholinergic receptors | Progenitor cells | Prostate | Organogenesis | GLAND BRANCHING MORPHOGENESIS | STEM-CELLS | SUBMANDIBULAR-GLAND | K-RAS | NERVES | MULTIDISCIPLINARY SCIENCES | LIVER | CONDITIONAL EXPRESSION | MECHANISMS | DIFFERENTIATION | SKIN | Epithelium - innervation | Male | Neurons - cytology | Acetylcholine - metabolism | Stem Cells - cytology | Prostate - embryology | Epithelial Cells - physiology | Intercellular Signaling Peptides and Proteins - metabolism | Epithelium - embryology | Receptor, Epidermal Growth Factor - metabolism | Neurons - physiology | Prostate - innervation | Cell Differentiation | Epithelial Cells - cytology | Organ Culture Techniques | Signal Transduction | Ganglia, Parasympathetic - physiology | Keratin-5 - genetics | Submandibular Gland - innervation | Carbachol - pharmacology | Heparin-binding EGF-like Growth Factor | Keratin-5 - analysis | Regeneration | Ganglia, Parasympathetic - cytology | Animals | Carbachol - metabolism | Intercellular Signaling Peptides and Proteins - pharmacology | Ganglia, Parasympathetic - embryology | Prostate - cytology | Submandibular Gland - cytology | Morphogenesis - drug effects | Stem Cells - physiology | Mice | Quinazolines - pharmacology | Submandibular Gland - embryology | Receptor, Muscarinic M1 - metabolism | Cell proliferation | Physiological aspects | Research | Developmental biology | Exocrine glands | Nervous system | Embryology | Cellular biology | Morphology | Rodents | Index Medicus
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7. Full Text Mutations affecting the cardiovascular system and other internal organs in zebrafish
by J.N. Chen and P. Haffter and J. Odenthal and E. Vogelsang and M. Brand and F.J. van Eeden and M. Furutani-Seiki and M. Granato and M. Hammerschmidt and C.P. Heisenberg and Y.J. Jiang and D.A. Kane and R.N. Kelsh and M.C. Mullins and C. Nusslein-Volhard
Development, ISSN 0950-1991, 12/1996, Volume 123, Issue 1, pp. 293 - 302
In a screen for early developmental mutants of the zebrafish, we have identified mutations specifically affecting the internal organs. We identified 53... 
Cardiovascular system | Heart | Intestine | Liver | Zebrafish | Circulation | Kidney | cardiovascular system | DEFECTS | intestine | liver | VASCULOGENESIS | MOUSE EMBRYOS | K HY DEVELOPMENTAL BIOLOGY | DEVELOPMENTAL BIOLOGY | heart | DROSOPHILA | kidney | TARGETED DISRUPTION | GENE | circulation | EMBRYONIC LETHALITY | HEART TUBES | zebrafish | DIFFERENTIATION | RECEPTOR TYROSINE KINASE | Heart Defects, Congenital - embryology | Intestines - abnormalities | Kidney - embryology | Cardiomegaly - embryology | Heart Atria - embryology | Heart Rate - genetics | Heart Ventricles - embryology | Intestines - embryology | Embryonic Development | Zebrafish - embryology | Liver - embryology | Zebrafish - genetics | Heart Atria - abnormalities | Heart Defects, Congenital - genetics | Heart Ventricles - abnormalities | Myocardial Contraction - genetics | Phenotype | Animals | Kidney - abnormalities | Liver - abnormalities | Mutation | Cardiomegaly - genetics | Body Patterning - genetics | Cardiovascular System - embryology | Index Medicus
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8. Full Text Jagged1 in the portal vein mesenchyme regulates intrahepatic bile duct development: Insights into Alagille syndrome
by Hofmann, Jennifer J and Zovein, Ann C and Koh, Huilin and Radtke, Freddy and Weinmaster, Gerry and Iruela-Arispe, M. Luisa
Development, ISSN 0950-1991, 12/2010, Volume 137, Issue 23, pp. 4061 - 4072
Mutations in the human Notch ligand jagged 1 (JAG1) result in a multi-system disorder called Alagille syndrome (AGS). AGS is chiefly characterized by a paucity... 
Vascular smooth muscle | Mouse | Liver development | Notch | Endothelium | Vasculature | VASCULAR DEVELOPMENT | LIGAND JAGGED1 | BILIARY-TRACT | DEVELOPMENTAL BIOLOGY | GENE | ENDOTHELIAL-CELLS | NOTCH RECEPTOR EXPRESSION | MICE | DIFFERENTIATION | Liver - pathology | Epithelial Cells - metabolism | Blood Chemical Analysis | Muscle, Smooth, Vascular - metabolism | Humans | Alagille Syndrome - pathology | Liver - embryology | Alagille Syndrome - embryology | Morphogenesis | Intercellular Signaling Peptides and Proteins - metabolism | Bile Ducts, Intrahepatic - metabolism | Serrate-Jagged Proteins | Gene Deletion | Portal Vein - pathology | Cell Differentiation | Membrane Proteins - metabolism | Jagged-1 Protein | Calcium-Binding Proteins - metabolism | SOX9 Transcription Factor - metabolism | Bile Ducts, Intrahepatic - pathology | Portal Vein - metabolism | Mesoderm - embryology | Signal Transduction | Liver - metabolism | Epithelial Cells - pathology | Portal Vein - embryology | Muscle, Smooth, Vascular - pathology | Phenotype | Animals | Cell Aggregation | Mesoderm - metabolism | Mice | Bile Ducts, Intrahepatic - embryology | Mesoderm - pathology | Neovascularization, Physiologic | Index Medicus
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9. Full Text Organ-specific expression of IGF-I during early development of bony fish as revealed in the tilapia, Oreochromis niloticus, by in situ hybridization and immunohistochemistry: indication for the particular importance of local IGF-I
by Berishvili, Giorgi and Shved, Natallia and Eppler, Elisabeth and Clota, Frederic and Baroiller, Jean-François and Reinecke, Manfred
Cell and Tissue Research, ISSN 0302-766X, 8/2006, Volume 325, Issue 2, pp. 287 - 301
The cellular sites of insulin-like growth factor I (IGF-I) synthesis in the early developing tilapia (0-140 days post fertilization, DPF) were investigated.... 
Human Genetics | Heart | Brain | Liver | Gills | Epidermis | Tilapia | Gastro-intestinal tract | Kidney | Biomedicine | Pituitary | Proteomics | Molecular Medicine | Muscle | Pancreas | gastro-intestinal tract | pituitary | tilapia | RAINBOW-TROUT | SEABREAM SPARUS-AURATA | liver | ONCORHYNCHUS-MYKISS | FACTOR MESSENGER-RNA | brain | gills | heart | BROWN TROUT | NA+-K+-ATPASE | CELL BIOLOGY | kidney | pancreas | muscle | TROUT SALMO-TRUTTA | COHO SALMON | HORMONE GH | epidermis | GROWTH-FACTOR-I | Immunohistochemistry | Brain - embryology | Animal Structures - embryology | Kidney - embryology | Skin - metabolism | Heart - embryology | Insulin-Like Growth Factor I - genetics | Gills - embryology | Brain - metabolism | Gastrointestinal Tract - embryology | RNA, Messenger - biosynthesis | Kidney - metabolism | In Situ Hybridization | Gene Expression Regulation, Developmental | Larva - growth & development | Myocardium - metabolism | Muscles - metabolism | Tilapia - metabolism | Skin - embryology | Cartilage - embryology | Insulin-Like Growth Factor I - biosynthesis | Larva - metabolism | Muscles - embryology | Gills - metabolism | Pancreas - metabolism | Cartilage - metabolism | Organ Specificity | Pancreas - embryology | Gastrointestinal Tract - metabolism | Animals | Tilapia - embryology | Animal Structures - metabolism | Index Medicus
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10. Full Text Immunohistochemical evidence of Muc1 expression during rat embryonic development
by Lacunza, E and Ferretti, V and Barbeito, C and Segal-Eiras, A and Croce, M.V
European Journal of Histochemistry, ISSN 1121-760X, 2010, Volume 54, Issue 4, pp. 223 - 228
During embryonic development, studies on mouse and human embryos have established that Muc1/MUC1 expression coincides with the onset of epithelial sheet and... 
Immunohistochemistry | Muc1/MUC1 | Embryonic development | Rat | TUMOR-ASSOCIATED ANTIGENS | rat | embryonic development | TISSUE | EPITHELIAL MUCIN | CELL BIOLOGY | BREAST-CANCER | TEMPORAL EXPRESSION | BENIGN | LIVER | immunohistochemistry | DIFFERENTIATION | MONOCLONAL-ANTIBODIES | MAMMARY-GLAND | Mucin-1 - metabolism | Salivary Glands - embryology | Intestine, Small | Kidney - embryology | Rats - embryology | Stomach - embryology | Embryonic Development - physiology | Trachea - embryology | Liver - embryology | Pancreas - embryology | Immunoenzyme Techniques | Pregnancy | Epithelium - embryology | Animals | Fetus - embryology | Female | Lung - embryology | Esophagus - embryology | Index Medicus
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11. Larval organogenesis of Pagrus pagrus L., 1758 with special attention to the digestive system development
by Darias, Maria Jose and Ortiz-Delgado, J.B and Sarasquete, C and Martínez-Rodríguez, G and Yúfera, M
Histology and Histopathology, ISSN 0213-3911, 07/2007, Volume 22, Issue 7-9, pp. 753 - 768
Organogenesis of the red porgy (Pagrus pagrus L., 1758) was examined from hatching until 63 days post-hatching (dph) using histological and histochemical... 
Fish larvae | Histology | Red porgy | Gut development | Pagrus pagrus | Histochemistry | WINTER FLOUNDER | PLEURONECTES-AMERICANUS | HALIBUT HIPPOGLOSSUS-HIPPOGLOSSUS | PATHOLOGY | PROTON PUMP GENES | red porgy | CELL BIOLOGY | gut development | fish larvae | histology | histochemistry | SPARUS-AURATA L | GILTHEAD SEA BREAM | YELLOWTAIL FLOUNDER | SOLEA-SENEGALENSIS KAUP | ATLANTIC HALIBUT | Branchial Region | Kidney - embryology | Stomach - embryology | Heart - embryology | Mouth - embryology | Fisheries | Intestines - embryology | Digestive System - embryology | Gills - embryology | Liver - embryology | Pancreas - embryology | Organogenesis | Perciformes - growth & development | Animals | Animal Nutritional Physiological Phenomena | Time Factors | Air Sacs - embryology | Larva - growth & development | Yolk Sac - embryology | Esophagus - embryology
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12. Full Text Severe left diaphragmatic hernia limits size of fetal left heart more than does right diaphragmatic hernia
by Byrne, F. A and Keller, R. L and Meadows, J and Miniati, D and Brook, M. M and Silverman, N. H and Moon‐Grady, A. J
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 12/2015, Volume 46, Issue 6, pp. 688 - 694
Objectives To assess whether severity of congenital diaphragmatic hernia (CDH) correlates with the degree of left heart hypoplasia and left ventricle (LV)... 
left heart hypoplasia | congenital diaphragmatic hernia | cardiac development | fetal cardiac output | congenital heart defects | CARDIAC-OUTPUT | SURVIVAL | Z-SCORES | CHILDREN | OBSTETRICS & GYNECOLOGY | ACOUSTICS | DUCTUS VENOSUS | INFANTS | HYPOPLASIA | ECHOCARDIOGRAPHY | FETUSES | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | Hernias, Diaphragmatic, Congenital - embryology | Humans | Echocardiography - methods | Hypoplastic Left Heart Syndrome - diagnostic imaging | Heart Ventricles - embryology | Lung - diagnostic imaging | Fetal Heart - diagnostic imaging | Fetal Heart - anatomy & histology | Heart Ventricles - diagnostic imaging | Liver - embryology | Hypoplastic Left Heart Syndrome - embryology | Liver - diagnostic imaging | Hernias, Diaphragmatic, Congenital - diagnostic imaging | Head - diagnostic imaging | Female | Ultrasonography, Prenatal - methods | Retrospective Studies | Head - embryology | Cross-Sectional Studies | Fetal Development | Organ Size | Fetal Diseases - diagnostic imaging | Gestational Age | Pregnancy | Hernias, Diaphragmatic, Congenital - complications | Lung - embryology | Hernia | Heart | Genetic disorders | Diaphragm | Liver | Index Medicus
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13. Full Text Developmental expression of prion protein and its ligands stress-inducible protein 1 and vitronectin
by Hajj, Glaucia N.M and Santos, Tiago G and Cook, Zanith S.P and Martins, Vilma R
Journal of Comparative Neurology, ISSN 0021-9967, 11/2009, Volume 517, Issue 3, pp. 371 - 384
Prion protein (PrPC) is the normal isoform of PrPSc, a protein involved in neurodegenerative disorders. PrPC participates in neuritogenesis, neuroprotection,... 
Development | Protein expression | Vitronectin | Prion protein | STI1 | CELLS | development | RECEPTOR | CNS | DILATED CARDIOMYOPATHY | NEUROSCIENCES | vitronectin | ZOOLOGY | NEURITE OUTGROWTH | CELLULAR PRION | CREUTZFELDT-JAKOB-DISEASE | DIFFERENTIATION | protein expression | prion protein | SONIC-HEDGEHOG | TRANSGENIC MICE | Brain - embryology | Spinal Cord - metabolism | Kidney - embryology | Heart - embryology | Liver - embryology | Brain - metabolism | Kidney - metabolism | Notochord - metabolism | Time Factors | Myocardium - metabolism | Lung - metabolism | PrPC Proteins - metabolism | PrPC Proteins - genetics | Ganglia, Spinal - embryology | Heat-Shock Proteins - metabolism | Liver - metabolism | Mice, Inbred C57BL | Axons - metabolism | Vitronectin - metabolism | Notochord - embryology | Mice, Knockout | Spinal Cord - embryology | Animals | Lung - embryology | Mice | Ganglia, Spinal - metabolism | Index Medicus
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14. Full Text Case Report: Fetal Bilateral Diaphragmatic Agenesis, Ectopic Liver and Abnormal Pancreas
by Loo, Christine K. C and Pereira, Tamara N and Ramm, Grant A
Fetal and Pediatric Pathology, ISSN 1551-3815, 07/2015, Volume 34, Issue 4, pp. 216 - 222
Congenital bilateral diaphragm agenesis is a very rare condition. We describe limited (abdomen only) autopsy findings of a case of bilateral diaphragm agenesis... 
human fetus | hepatic stellate cell | diaphragm agenesis | PATHOGENESIS | ORIGIN | SUBMESOTHELIAL CELLS | STELLATE CELLS | PEDIATRICS | PATHOLOGY | HERNIA | Abnormalities, Multiple - pathology | Liver - pathology | Diaphragm - pathology | Hernia, Diaphragmatic - pathology | Humans | Male | Liver - embryology | Abnormalities, Multiple - embryology | Fatal Outcome | Adult | Female | Hepatic Stellate Cells - pathology | Diaphragm - abnormalities | Abdominal Cavity - embryology | Hernia, Diaphragmatic - embryology | Pancreas - pathology