Enteric Nervous System: Development and Developmental Disturbances—Part 1
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[1] B. Pasini,et al. Frequency of RET mutations in long‐ and short‐segment Hirschsprung disease , 1997, Human mutation.
[2] P. Lane,et al. Association of megacolon with a new dominant spotting gene (Dom) in the mouse. , 1984, The Journal of heredity.
[3] P. Corvol,et al. Ontogeny of endothelins-1 and -3, their receptors, and endothelin converting enzyme-1 in the early human embryo. , 1998, The Journal of clinical investigation.
[4] C. Goridis,et al. The mouse homeodomain protein Phox2 regulates Ncam promoter activity in concert with Cux/CDP and is a putative determinant of neurotransmitter phenotype. , 1993, Development.
[5] I. Mason,et al. Expression of ret in the chicken embryo suggests roles in regionalisation of the vagal neural tube and somites and in development of multiple neural crest and placodal lineages , 1995, Mechanisms of Development.
[6] L. Korngut,et al. Characterisation of the human GFRα-3locus and investigation of the gene in Hirschsprung disease , 2000, Journal of medical genetics.
[7] J. Furness,et al. Locations and chemistries of sympathetic nerve cells that project to the gastrointestinal tract and spleen. , 1994, Archives of histology and cytology.
[8] M. Saarma,et al. Retarded Growth and Deficits in the Enteric and Parasympathetic Nervous System in Mice Lacking GFRα2, a Functional Neurturin Receptor , 1999, Neuron.
[9] J. Milbrandt,et al. Neurturin and GDNF promote proliferation and survival of enteric neuron and glial progenitors in vitro. , 1998, Developmental biology.
[10] J. Keast,et al. Projections of pelvic autonomic neurons within the lower bowel of the male rat: an anterograde labelling study , 1998, Neuroscience.
[11] P. Puri,et al. Intestinal neuronal dysplasia in twins. , 1996, Journal of pediatric gastroenterology and nutrition.
[12] R. Hammer,et al. Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice , 1994, Cell.
[13] A. Puliti,et al. HOX11L1, a gene involved in peripheral nervous system development, maps to human chromosome 2p13.1→p12 and mouse chromosome 6C3–D1 , 1999, Cytogenetic and Genome Research.
[14] M. Anvret,et al. A Heterozygous Frameshift Mutation in the Endothelin-3 (EDN-3) Gene in Isolated Hirschsprung's Disease , 1999, Pediatric Research.
[15] J. Weissenbach,et al. A gene for Hirschsprung disease maps to the proximal long arm of chromosome 10 , 1993, Nature Genetics.
[16] J. Milbrandt,et al. Artemin, a Novel Member of the GDNF Ligand Family, Supports Peripheral and Central Neurons and Signals through the GFRα3–RET Receptor Complex , 1998, Neuron.
[17] Geoffrey A. Donnan,et al. Activated Macrophages and Microglia Induce Dopaminergic Sprouting in the Injured Striatum and Express Brain-Derived Neurotrophic Factor and Glial Cell Line-Derived Neurotrophic Factor , 1999, The Journal of Neuroscience.
[18] Y. Ouchi,et al. Elevated blood pressure and craniofaclal abnormalities in mice deficient in endothelin-1 , 1994, Nature.
[19] A. Rosenthal,et al. The GDNF Protein FamilyGene Ablation Studies Reveal What They Really Do and How , 1999, Neuron.
[20] D G Wilkinson,et al. Control of cell behavior during vertebrate development by Slug, a zinc finger gene. , 1994, Science.
[21] D. Reiche,et al. Enteric pathways in the stomach , 2001, The Anatomical record.
[22] B. Ponder,et al. Mutations of the RET proto-oncogene in Hirschsprung's disease , 1994, Nature.
[23] M. Saarma,et al. GDNF Family Neurotrophic Factor Signaling: Four Masters, One Servant? , 1999, Molecular and Cellular Neuroscience.
[24] T. P. Rothman,et al. Promotion of the development of enteric neurons and glia by neuropoietic cytokines: interactions with neurotrophin-3. , 1998, Developmental biology.
[25] J. Furness,et al. The enteric nervous system and regulation of intestinal motility. , 1999, Annual review of physiology.
[26] W. Pavan,et al. Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3 , 2000, Human Genetics.
[27] F. Costantini,et al. Expression of the c-ret proto-oncogene during mouse embryogenesis. , 1993, Development.
[28] G. D. Maxwell,et al. Cell cycle changes during neural crest cell differentiation in vitro. , 1976, Developmental biology.
[29] J. Osinga,et al. Mutations in Hirschsprung Disease: When Does a Mutation Contribute to the Phenotype , 1997, European journal of human genetics : EJHG.
[30] J. Lile,et al. GDNF: a glial cell line-derived neurotrophic factor for midbrain dopaminergic neurons. , 1993, Science.
[31] M. Saarma. GDNF – a stranger in the TGF-β superfamily? , 2000 .
[32] R. Kapur. Contemporary approaches toward understanding the pathogenesis of Hirschsprung disease. , 1993, Pediatric pathology.
[33] N. Nomura,et al. Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease , 2001, Nature Genetics.
[34] R. Palmiter,et al. Goosecoid and the organizer. , 1992 .
[35] A. Chakravarti. Endothelin receptor-mediated signaling in hirschsprung disease. , 1996, Human molecular genetics.
[36] P. Iannaccone,et al. Expression of Human GLI in Mice Results in Failure to Thrive, Early Death, and Patchy Hirschsprung-like Gastrointestinal Dilatation , 1997, Molecular medicine.
[37] T. Powley. Vagal input to the enteric nervous system , 2000, Gut.
[38] B. Hoffer,et al. Glial cell line-derived neurotrophic factor receptor α1 availability regulates glial cell line-derived neurotrophic factor signaling: evidence from mice carrying one or two mutated alleles , 1999, Neuroscience.
[39] D. Newgreen,et al. A single rostrocaudal colonization of the rodent intestine by enteric neuron precursors is revealed by the expression of Phox2b, Ret, and p75 and by explants grown under the kidney capsule or in organ culture. , 1998, Developmental biology.
[40] R. Mirsky,et al. Glial cells in the enteric nervous system contain glial fibrillary acidic protein , 1980, Nature.
[41] K. Robertson,et al. Hirschsprung’s disease: genetic mutations in mice and men , 1997, Gut.
[42] K. Fischbeck,et al. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy , 1991, Nature.
[43] L. S. Palmer. THE PHYSIOLOGICAL RELATION OF PLANT CAROTINOIDS TO THE CAROTINOIDS OF THE COW, HORSE, SHEEP, GOAT, PIG, AND HEN , 1916 .
[44] A. Álvarez-Buylla,et al. The subventricular zone: source of neuronal precursors for brain repair. , 2000, Progress in brain research.
[45] C. Tabin,et al. Epithelial-mesenchymal signaling during the regionalization of the chick gut. , 1998, Development.
[46] M. Sanicola,et al. Developmental regulation of GDNF response and receptor expression in the enteric nervous system. , 2000, Development.
[47] S. Tilghman,et al. The temporal requirement for endothelin receptor-B signalling during neural crest development , 1999, Nature.
[48] R. Thorpe,et al. Molecular identity, distribution and heterogeneity of glial fibrillary acidic protein: an immunoblotting and immunohistochemical study of Schwann cells, satellite cells, enteric glia and astrocytes , 1984, Journal of neurocytology.
[49] Holschneider,et al. Rectal biopsy for diagnosis of intestinal neuronal dysplasia in children: a prospective multicentre study on interobserver variation and clinical outcome , 1999, Gut.
[50] M. Devoto,et al. Exclusion of linkage between RET and neuronal intestinal dysplasia type B. , 1996, American journal of medical genetics.
[51] P. D. Lumb,et al. Back to the drawing board , 1998, Virchows Archiv.
[52] Hideki Enomoto,et al. The GDNF family ligands and receptors — implications for neural development , 2000, Current Opinion in Neurobiology.
[53] N Clerc,et al. Intrinsic primary afferent neuronsof the intestine , 1998, Progress in Neurobiology.
[54] T. Shimotake,et al. Mutational analysis of RET/GDNF/NTN genes in children with total colonic aganglionosis with small bowel involvement. , 2000, American journal of medical genetics.
[55] Masashi Yanagisawa,et al. A missense mutation of the endothelin-B receptor gene in multigenic hirschsprung's disease , 1994, Cell.
[56] D. Anderson,et al. MASH1 activates expression of the paired homeodomain transcription factor Phox2a, and couples pan-neuronal and subtype-specific components of autonomic neuronal identity. , 1998, Development.
[57] L. Mulligan,et al. Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus. , 1994, Journal of medical genetics.
[58] A. Munnich,et al. Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease. , 1998, Human molecular genetics.
[59] E. Quigley,et al. Achalasia of the cardia and multiple endocrine neoplasia 2B. , 1994, The American journal of gastroenterology.
[60] A. Munnich,et al. Expression of the RET proto-oncogene in human embryos. , 1998, American journal of medical genetics.
[61] H. Hirakawa,et al. Is intestinal neuronal dysplasia a disorder of the neuromuscular junction? , 1996, Journal of pediatric surgery.
[62] D. Newgreen,et al. GDNF is a chemoattractant for enteric neural cells. , 2001, Developmental biology.
[63] A. Joyner,et al. Dynamic expression of the murine Achaete-Scute homologue Mash-1 in the developing nervous system , 1993, Mechanisms of Development.
[64] H. Gao,et al. [Neurturin: a relative of glial-cell-line-derived neurotrophic factor]. , 1998, Sheng li ke xue jin zhan [Progress in physiology].
[65] N. Philip,et al. Possible homozygous Waardenburg syndrome in a fetus with exencephaly. , 1995, American journal of medical genetics.
[66] D. Newgreen,et al. GDNF and ET-3 differentially modulate the numbers of avian enteric neural crest cells and enteric neurons in vitro. , 1998, Developmental biology.
[67] J. Hutson,et al. Rectal mucosal biopsy compared with laparoscopic seromuscular biopsy in the diagnosis of intestinal neuronal dysplasia in children with slow-transit constipation. , 2000, Journal of pediatric surgery.
[68] J. Turtle,et al. Colonic and oesophageal disturbance in a patient with multiple endocrine neoplasia, type 2b. , 1978, Australian and New Zealand journal of medicine.
[69] M. Barbacid,et al. Neurotrophin-3 induces neural crest-derived cells from fetal rat gut to develop in vitro as neurons or glia , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.
[70] T. P. Rothman,et al. Neurotrophin-3 Is Required for the Survival–Differentiation of Subsets of Developing Enteric Neurons , 2001, The Journal of Neuroscience.
[71] J. Galligan,et al. Multiple mechanisms of fast excitatory synaptic transmission in the enteric nervous system. , 2000, Journal of the autonomic nervous system.
[72] Chaya Kalcheim,et al. The Neural Crest: General Introduction , 1999 .
[73] J. Furness. Types of neurons in the enteric nervous system. , 2000, Journal of the autonomic nervous system.
[74] J. Hutson,et al. Intractable constipation with a decrease in substance P-immunoreactive fibres: is it a variant of intestinal neuronal dysplasia? , 1996, Journal of pediatric surgery.
[75] A. von Deimling,et al. Investigation of germline GFRα-1 mutations in Hirschsprung disease , 1999 .
[76] J. Bowles,et al. Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators. , 2000, Developmental biology.
[77] R I Richards,et al. Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n , 1991, Science.
[78] R. Hofstra,et al. A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma , 1994, Nature.
[79] S. Baylin,et al. An achaete-scute homologue essential for neuroendocrine differentiation in the lung , 1997, Nature.
[80] R. Mirsky,et al. Endothelins control the timing of Schwann cell generation in vitro and in vivo. , 2000, Developmental biology.
[81] F. Ponti,et al. Plasticity in the enteric nervous system. , 1999, Gastroenterology.
[82] D. Newgreen,et al. Origin of interstitial cells of Cajal in the mouse intestine. , 1996, Developmental biology.
[83] E. McCabe,et al. Overo lethal white foal syndrome: equine model of aganglionic megacolon (Hirschsprung disease). , 1990, American journal of medical genetics.
[84] D. Tibboel,et al. Ablation of various regions within the avian vagal neural crest has differential effects on ganglion formation in the fore‐, mid‐ and hindgut , 1993, Developmental dynamics : an official publication of the American Association of Anatomists.
[85] C. Tabin,et al. Sonic hedgehog differentially regulates expression of GLI and GLI3 during limb development. , 1996, Developmental biology.
[86] R. Oppenheim,et al. Expression pattern of GDNF, c-ret, and GFRalphas suggests novel roles for GDNF ligands during early organogenesis in the chick embryo. , 2000, Developmental biology.
[87] J. Massagué. TGFβ Signaling: Receptors, Transducers, and Mad Proteins , 1996, Cell.
[88] S. Korsmeyer,et al. Enx (Hox11L1)-deficient mice develop myenteric neuronal hyperplasia and megacolon , 1997, Nature Medicine.
[89] Frank Costantini,et al. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret , 1994, Nature.
[90] R. Agarwala,et al. The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome. , 1999, Genome research.
[91] D. Newgreen,et al. Migration of enteric neural crest cells in relation to growth of the gut in avian embryos. , 1996, Acta anatomica.
[92] G. Yancopoulos,et al. GDNF in a Bind with Known Orphan: Accessory Implicated in New Twist , 1996, Neuron.
[93] G. Donnan,et al. Inhibition of brain‐derived neurotrophic factor and glial cell line‐derived neurotrophic factor expression reduces dopaminergic sprouting in the injured striatum , 2000, The European journal of neuroscience.
[94] P. Lumb,et al. Are giant ganglia a reliable marker of intestinal neuronal dysplasia type B (IND B)? , 1998, Virchows Archiv.
[95] M. Adachi,et al. Paired-like homeodomain proteins Phox2a/Arix and Phox2b/NBPhox have similar genetic organization and independently regulate dopamine beta-hydroxylase gene transcription. , 2000, DNA and cell biology.
[96] A. McMahon,et al. Hedgehog and Bmp genes are coexpressed at many diverse sites of cell-cell interaction in the mouse embryo. , 1995, Developmental biology.
[97] D. Lloyd,et al. Expression of endothelin 3 by mesenchymal cells of embryonic mouse caecum , 1999, Gut.
[98] T. Tsuzuki,et al. Spatial and temporal expression of the ret proto-oncogene product in embryonic, infant and adult rat tissues. , 1995, Oncogene.
[99] C. L. Yntema,et al. The origin of intrinsic ganglia of trunk viscera from vagal neural crest in the chick embryo , 1954, The Journal of comparative neurology.
[100] David J. Anderson,et al. Two rat homologues of Drosophila achaete-scute specifically expressed in neuronal precursors , 1990, Nature.
[101] J. Daisley,et al. Trophic actions of neurotrophin-3 on postnatal rat myenteric neurons in vitro , 2000, Neuroscience Letters.
[102] Gudrun Valdimarsdottir. TGFβ signal transduction in endothelial cells. , 2004 .
[103] T. Kameda,et al. The concentric structure of the developing gut is regulated by Sonic hedgehog derived from endodermal epithelium. , 2000, Development.
[104] M. Wegner,et al. Expression of the SOX10 gene during human development , 1998, FEBS letters.
[105] V. Heyningen. One gene—four syndromes , 1994, Nature.
[106] A. Ghysen,et al. From DNA to form: the achaete-scute complex. , 1988, Genes & development.
[107] J. Milbrandt,et al. GFRα-Mediated Localization of RET to Lipid Rafts Is Required for Effective Downstream Signaling, Differentiation, and Neuronal Survival , 2000, Neuron.
[108] F. Costantini,et al. Common origin and developmental dependence on c-ret of subsets of enteric and sympathetic neuroblasts. , 1996, Development.
[109] G. Sobue,et al. Biological properties of Ret with cysteine mutations correlate with multiple endocrine neoplasia type 2A, familial medullary thyroid carcinoma, and Hirschsprung's disease phenotype. , 1997, Cancer research.
[110] P. Lumb,et al. Back to the drawing board. Intestinal neuronal dysplasia type B: not a histological entity yet. , 1998, Virchows Archiv : an international journal of pathology.
[111] Giovanni Romeo,et al. SOX10 mutations in patients with Waardenburg-Hirschsprung disease , 1998, Nature Genetics.
[112] A. Eichmann,et al. Endothelin-B receptor is expressed by neural crest cells in the avian embryo. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[113] C. Eng. RET proto-oncogene in the development of human cancer. , 1999, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.
[114] L. Olson,et al. Cellular and developmental patterns of expression of Ret and glial cell line-derived neurotrophic factor receptor alpha mRNAs , 1997, Experimental Brain Research.
[115] U. Greferath,et al. Innervation of the esophagus in mice that lack MASH1 , 1999, The Journal of comparative neurology.
[116] B. Ure,et al. Hirschsprung's disease and intestinal neuronal dysplasia – a frequent association with implications for the postoperative course , 1999, Pediatric Surgery International.
[117] Y. Watanabe,et al. ret Proto-oncogene product is a useful marker of lineage determination in the development of the enteric nervous system in rats. , 1997, Journal of pediatric surgery.
[118] P. Puri. Intestinal neuronal dysplasia. , 2003, Seminars in pediatric surgery.
[119] X. Morin,et al. Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis. , 1997, Development.
[120] H. Hellmich,et al. Embryonic expression of glial cell-line derived neurotrophic factor (GDNF) suggests multiple developmental roles in neural differentiation and epithelial-mesenchymal interactions , 1996, Mechanisms of Development.
[121] V. Smith,et al. Coordinated expression of 3' hox genes during murine embryonal gut development: an enteric Hox code. , 1999, Gastroenterology.
[122] C. Baldwin,et al. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome , 1992, Nature.
[123] A. Chakravarti,et al. Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease. , 1995, Human molecular genetics.
[124] I. Fariñas,et al. Renal and neuronal abnormalities in mice lacking GDNF , 1996, Nature.
[125] J. Hoehner,et al. Alterations in neurotrophin and neurotrophin-receptor localization in Hirschsprung's disease. , 1996, Journal of pediatric surgery.
[126] P. Tam,et al. Incidence of RET mutations in patients with Hirschsprung's disease. , 2000, Journal of pediatric surgery.
[127] M. Wegner,et al. Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome. , 2000, Human molecular genetics.
[128] R. Bolande. Neurocristopathy: its growth and development in 20 years. , 1997, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.
[129] Jonas Frisén,et al. Renal agenesis and the absence of enteric neurons in mice lacking GDNF , 1996, Nature.
[130] T. Saito,et al. Mammalian achaete-scute homolog 1 is transiently expressed by spatially restricted subsets of early neuroepithelial and neural crest cells. , 1991, Genes & development.
[131] J. Louis,et al. GDNF–Induced Activation of the Ret Protein Tyrosine Kinase Is Mediated by GDNFR-α, a Novel Receptor for GDNF , 1996, Cell.
[132] P. Tam,et al. Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease. , 1996, Human molecular genetics.
[133] S. Baylin,et al. Tissue-specific expression of human achaete-scute homologue-1 in neuroendocrine tumors: transcriptional regulation by dual inhibitory regions. , 1997, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.
[134] S J Brookes,et al. Classes of enteric nerve cells in the guinea‐pig small intestine , 2001, The Anatomical record.
[135] T. P. Rothman,et al. Inhibition of in vitro enteric neuronal development by endothelin-3: mediation by endothelin B receptors. , 1999, Development.
[136] S. Korsmeyer,et al. Development expression of Hox11 and specification of splenic cell fate. , 1995, The American journal of pathology.
[137] D. Newgreen,et al. Enteric Nervous System: Development and Developmental Disturbances—Part 2 , 2002, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
[138] X. Morin,et al. Defects in Sensory and Autonomic Ganglia and Absence of Locus Coeruleus in Mice Deficient for the Homeobox Gene Phox2a , 1997, Neuron.
[139] David J. Anderson,et al. The cellular function of MASH1 in autonomic neurogenesis , 1995, Neuron.
[140] R. Balling,et al. Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene , 1992, Nature.
[141] M. Wegner,et al. The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences. , 2000, Nucleic acids research.
[142] T. Matise,et al. A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10 , 1993, Nature Genetics.
[143] M. Epstein,et al. Expression of the GDNF receptors Ret and GFRα1 in the developing avian enteric nervous system , 1999, The Journal of comparative neurology.
[144] D. Tibboel,et al. A model for aganglionosis in the chicken embryo. , 1989, Journal of pediatric surgery.
[145] D. Cass. Hirschsprung's disease: an historical review. , 1986, Progress in pediatric surgery.
[146] W. Meier-Ruge,et al. Histopathological criteria for intestinal neuronal dysplasia of the submucosal plexus (type B) , 2004, Virchows Archiv.
[147] J. Milbrandt,et al. Gene Targeting Reveals a Critical Role for Neurturin in the Development and Maintenance of Enteric, Sensory, and Parasympathetic Neurons , 1999, Neuron.
[148] D. Bocangel,et al. Glial cell line-derived neurotrophic factor (GDNF) is a neurotrophic factor for sensory neurons: comparison with the effects of the neurotrophins. , 1997, Journal of neurobiology.
[149] W. Webster. Embryogenesis of the enteric ganglia in normal mice and in mice that develop congenital aganglionic megacolon. , 1973, Journal of embryology and experimental morphology.
[150] G. Burnstock,et al. Adrenergic Innervation of Bowel in Hirschsprung's Disease , 1969, British medical journal.
[151] M. Goossens,et al. Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease. , 2001, Human molecular genetics.
[152] L. Olson,et al. Glial cell line‐derived neurotrophic factor stimulates fiber formation and survival in cultured neurons from peripheral autonomic ganglia , 1995, Journal of neuroscience research.
[153] Marcello Costa,et al. Distribution of peptide‐containing nerve fibres in achalasia of the oesophagus , 1996, Journal of gastroenterology and hepatology.
[154] R. Hammer,et al. Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene. , 1998, Development.
[155] M. Parisi,et al. Genetics of Hirschsprung disease , 2000, Current opinion in pediatrics.
[156] M. Fukuzawa,et al. Mutational analysis of the endothelin-B receptor gene in Japanese Hirschsprung's disease. , 1998, Journal of pediatric surgery.
[157] D. O’Briain,et al. Intestinal neuronal dysplasia is a possible cause of persistent bowel symptoms after pull-through operation for Hirschsprung's disease. , 1995, Journal of pediatric surgery.
[158] W. Snider,et al. IB4-Binding DRG Neurons Switch from NGF to GDNF Dependence in Early Postnatal Life , 1997, Neuron.
[159] D. Lloyd,et al. Time-dependent effects of endothelin-3 on enteric nervous system development in an organ culture model of Hirschsprung's disease. , 2000, Journal of pediatric surgery.
[160] V. Tennyson,et al. Distinct subpopulations of enteric neuronal progenitors defined by time of development, sympathoadrenal lineage markers and Mash-1-dependence. , 1996, Development.
[161] C. Henderson,et al. GDNF: a potent survival factor for motoneurons present in peripheral nerve and muscle. , 1994, Science.
[162] B. Smith. Myenteric plexus in Hirschsprung's disease. , 1967, Gut.
[163] J. Milbrandt,et al. GFRα1-Deficient Mice Have Deficits in the Enteric Nervous System and Kidneys , 1998, Neuron.
[164] M. Goulding,et al. Pax‐3, a novel murine DNA binding protein expressed during early neurogenesis. , 1991, The EMBO journal.
[165] A. Munnich,et al. Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease , 1996, Nature Genetics.
[166] W. Pavan,et al. SOX10 mutation disrupts neural crest development in Dom Hirschsprung mouse model , 1998, Nature Genetics.
[167] A. Chakravarti,et al. Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient , 1996, Nature Genetics.
[168] R. Kapur. Hirschsprung disease and other enteric dysganglionoses. , 1999, Critical reviews in clinical laboratory sciences.
[169] P. Puri,et al. Novel mutations of the endothelin-B receptor gene in isolated patients with Hirschsprung's disease. , 1996, Human molecular genetics.
[170] S. Baylin,et al. Identification of a human achaete-scute homolog highly expressed in neuroendocrine tumors. , 1993, Proceedings of the National Academy of Sciences of the United States of America.
[171] R. Cusano,et al. Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation , 2000, Journal of medical genetics.
[172] B. Ponder,et al. Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A , 1993, Nature.
[173] M. Abu-Elmagd,et al. Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system. , 2000, Brain research. Developmental brain research.
[174] M. Hirsch,et al. Control of noradrenergic differentiation and Phox2a expression by MASH1 in the central and peripheral nervous system. , 1998, Development.
[175] H. Young,et al. Expression of Ret‐, p75NTR‐, Phox2a‐, Phox2b‐, and tyrosine hydroxylase‐immunoreactivity by undifferentiated neural crest‐derived cells and different classes of enteric neurons in the embryonic mouse gut , 1999, Developmental dynamics : an official publication of the American Association of Anatomists.
[176] D. Melton,et al. Hedgehog signals regulate multiple aspects of gastrointestinal development. , 2000, Development.
[177] G. Raisman,et al. Signalling by the RET receptor tyrosine kinase and its role in the development of the mammalian enteric nervous system. , 1999, Development.
[178] D. O’Briain,et al. Notable postnatal alterations in the myenteric plexus of normal human bowel , 1999, Gut.
[179] R. Nagai,et al. Aortic arch malformations and ventricular septal defect in mice deficient in endothelin-1. , 1995, The Journal of clinical investigation.
[180] C. Atkins,et al. Multipotential progenitors of the mammalian enteric nervous system capable of colonising aganglionic bowel in organ culture. , 1999, Development.
[181] A. Buj-Bello,et al. Characterization of a multicomponent receptor for GDNF , 1996, Nature.
[182] H. Ehrenreich,et al. Phenotype, intestinal morphology, and survival of homozygous and heterozygous endothelin B receptor--deficient (spotting lethal) rats. , 2000, Journal of pediatric surgery.
[183] E. Olson,et al. The basic helix-loop-helix transcription factor dHAND, a marker gene for the developing human sympathetic nervous system, is expressed in both high- and low-stage neuroblastomas. , 1999, Laboratory investigation; a journal of technical methods and pathology.
[184] C. Cortesini,et al. The muscle coat of the lower esophageal sphincter in patients with achalasia and hypertensive sphincter. An electron microscopic study. , 1985, Journal of submicroscopic cytology.
[185] I. Fariñas,et al. GFRα1 Is an Essential Receptor Component for GDNF in the Developing Nervous System and Kidney , 1998, Neuron.
[186] F. Luyten,et al. Smad-interacting Protein 1 Is a Repressor of Liver/Bone/Kidney Alkaline Phosphatase Transcription in Bone Morphogenetic Protein-induced Osteogenic Differentiation of C2C12 Cells* , 2001, The Journal of Biological Chemistry.
[187] J. N. Schullinger,et al. Peripherin: a novel marker for the immunohistochemical study of malformations of the enteric nervous system. , 1996, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.
[188] M. Tiveron,et al. The Expression Pattern of the Transcription Factor Phox2 Delineates Synaptic Pathways of the Autonomic Nervous System , 1996, The Journal of Neuroscience.
[189] S. Banani,et al. Intestinal neuronal dysplasia as a cause of surgical failure in Hirschsprung's disease: a new modality for surgical management. , 1996, Journal of pediatric surgery.
[190] V. Nataf,et al. Effect of the Steel gene product on melanogenesis in avian neural crest cell cultures. , 1994, Differentiation; research in biological diversity.
[191] T. P. Rothman,et al. Age-Dependent Differences in the Effects of GDNF and NT-3 on the Development of Neurons and Glia from Neural Crest-Derived Precursors Immunoselected from the Fetal Rat Gut: Expression of GFRα-1in Vitroandin Vivo , 1998 .
[192] Mart Saarma,et al. Defects in enteric innervation and kidney development in mice lacking GDNF , 1996, Nature.
[193] J. Osinga,et al. A loss-of-function mutation in the endothelin-converting enzyme 1 (ECE-1) associated with Hirschsprung disease, cardiac defects, and autonomic dysfunction. , 1999, American journal of human genetics.
[194] M. Yanagisawa,et al. The expression patterns of endothelin-A receptor and endothelin 1 in the avian embryo , 1998, Mechanisms of Development.
[195] S. Sekiya,et al. An Enhancer Element for Expression of the Ncx(Enx, Hox11L1) Gene in Neural Crest-derived Cells* , 1999, The Journal of Biological Chemistry.
[196] I. Mason. The GDNF Receptor: Recent Progress and Unanswered Questions , 1996, Molecular and Cellular Neuroscience.
[197] M. Hatano,et al. A novel pathogenesis of megacolon in Ncx/Hox11L.1 deficient mice. , 1997, The Journal of clinical investigation.
[198] S J H Brookes,et al. The Enteric Nervous System , 2016, Advances in Experimental Medicine and Biology.
[199] M. Yanagisawa,et al. The expression pattern of endothelin 3 in the avian embryo , 1998, Mechanisms of Development.
[200] E. Dupin,et al. Endothelin 3 promotes neural crest cell proliferation and mediates a vast increase in melanocyte number in culture. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[201] A. Lalwani,et al. Point mutation in the MITF gene causing Waardenburg syndrome type II in a three-generation Indian family. , 1998, American journal of medical genetics.
[202] M. Wegner,et al. Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[203] A. Chakravarti,et al. A genetic study of Hirschsprung disease. , 1990, American journal of human genetics.
[204] X. Morin,et al. The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives , 1999, Nature.
[205] M. Şenocak,et al. Diagnostic difficulties in neuronal intestinal dysplasia and segmental colitis. , 2000, Journal of pediatric surgery.
[206] G. Di Cairano,et al. Unilateral renal agenesis in a family with medullary thyroid carcinoma. , 2000, The New England journal of medicine.
[207] J. Epstein,et al. Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret. , 2000, The Journal of clinical investigation.
[208] J. Bornstein,et al. Evidence that enteric motility reflexes can be initiated through entirely intrinsic mechanisms in the guinea‐pig small intestine , 1995, Neurogastroenterology and motility : the official journal of the European Gastrointestinal Motility Society.
[209] S. Brookes,et al. Neurochemical classification of myenteric neurons in the guinea-pig ileum , 1996, Neuroscience.
[210] V. Pachnis,et al. Development of the mammalian enteric nervous system. , 1999, Current opinion in genetics & development.
[211] R. Kapur. Early Death of Neural Crest Cells Is Responsible for Total Enteric Aganglionosis in Sox10Dom/Sox10Dom Mouse Embryos , 1999, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
[212] R. Hammer,et al. Transgenic expression of the endothelin-B receptor prevents congenital intestinal aganglionosis in a rat model of Hirschsprung disease. , 1998, The Journal of clinical investigation.
[213] C. Lacroix,et al. Peripheral neuropathy with hypomyelination, chronic intestinal pseudo‐obstruction and deafness: A developmental “neural crest syndrome” related to a SOX10 mutation , 2000, Annals of neurology.
[214] P. Puri,et al. Abnormal internal anal sphincter innervation in patients with Hirschsprung's disease and allied disorders. , 1996, Journal of pediatric surgery.
[215] P. Lane. Association of megacolon with two recessive spotting genes in the mouse. , 1966, The Journal of heredity.
[216] David J. Anderson,et al. Mammalian achaete-scute homolog 1 is required for the early development of olfactory and autonomic neurons , 1993, Cell.
[217] T. P. Rothman,et al. From neural crest to bowel: development of the enteric nervous system. , 1993, Journal of neurobiology.
[218] A. Schärli. Neuronal intestinal dysplasia , 2004, Pediatric Surgery International.
[219] R. Vejsada,et al. Persephin, a Novel Neurotrophic Factor Related to GDNF and Neurturin , 1998, Neuron.
[220] R. Hofstra,et al. Oncological implications of RET gene mutations in Hirschsprung’s disease , 1998, Gut.
[221] K. Arnos,et al. Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations , 1998, Human Genetics.
[222] D. Champeval,et al. Sacral neural crest cells colonise aganglionic hindgut in vivo but fail to compensate for lack of enteric ganglia. , 2000, Developmental biology.
[223] Andrew P. McMahon,et al. Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity , 1993, Cell.
[224] B. Pasini,et al. Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease , 1994, Nature.
[225] J. Rothstein,et al. Glutamatergic Enteric Neurons , 1997, The Journal of Neuroscience.
[226] R. Palmiter,et al. A transgenic model for studying development of the enteric nervous system in normal and aganglionic mice. , 1992, Development.
[227] Y. Jeng,et al. Congenital Interstitial Cell of Cajal Hyperplasia With Neuronal Intestinal Dysplasia , 2000, The American journal of surgical pathology.
[228] S. Brookes,et al. The neurochemical coding and projections of circular muscle motor neurons in the human colon. , 1997, Gastroenterology.
[229] J. Massagué. TGF-beta signal transduction. , 1998, Annual review of biochemistry.
[230] L. Nelles,et al. SIP1, a Novel Zinc Finger/Homeodomain Repressor, Interacts with Smad Proteins and Binds to 5′-CACCT Sequences in Candidate Target Genes* , 1999, The Journal of Biological Chemistry.
[231] S. Vanner,et al. Neural reflexes controlling intestinal microcirculation. , 1996, The American journal of physiology.