TY - JOUR AU - Villalba-Benito, Leticia AU - López-López, Daniel AU - Torroglosa, Ana AU - Casimiro-Soriguer, Carlos S. AU - Luzón-Toro, Berta AU - Fernández, Raquel María AU - Moya-Jiménez, María José AU - Antiñolo, Guillermo AU - Dopazo, Joaquín AU - Borrego, Salud PY - 2021 DO - 10.1186/s13148-021-01040-6 UR - http://hdl.handle.net/10668/4394 T2 - Clinical Epigenetics AB - BackgroundHirschsprung disease (HSCR, OMIM 142623) is a rare congenital disorder that results from a failure to fully colonize the gut by enteric precursor cells (EPCs) derived from the neural crest. Such incomplete gut colonization is due to... LA - en PB - BioMed Central, Springer Nature KW - Hirschsprung disease KW - Whole genome bisulfte sequencing KW - DNA methylation KW - Enteric nervous system development KW - Epigenetic regulation KW - Neural crest KW - CpG islands KW - Genome KW - Enfermedad de hirschsprung KW - Secuenciación completa del genoma KW - Metilación de ADN KW - Sistema nervioso entérico KW - Epigenómica KW - Cresta neural KW - Islas de CpG KW - Genoma KW - Medical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies KW - Medical Subject Headings::Persons::Persons::Age Groups::Child::Child, Preschool KW - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Structures::Base Sequence::GC Rich Sequence::CpG Islands KW - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Processes::DNA Methylation KW - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Processes::Gene Expression Regulation::Epigenesis, Genetic KW - Medical Subject Headings::Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics::Genomics::Epigenomics KW - Medical Subject Headings::Check Tags::Female KW - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease KW - Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome KW - Medical Subject Headings::Diseases::Congenital, Hereditary, and Neonatal Diseases and Abnormalities::Congenital Abnormalities::Digestive System Abnormalities::Hirschsprung Disease KW - Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans KW - Medical Subject Headings::Persons::Persons::Age Groups::Infant KW - Medical Subject Headings::Check Tags::Male KW - Medical Subject Headings::Anatomy::Embryonic Structures::Neural Crest KW - Medical Subject Headings::Phenomena and Processes::Cell Physiological Phenomena::Cell Physiological Processes::Signal Transduction KW - Medical Subject Headings::Psychiatry and Psychology::Behavior and Behavior Mechanisms::Motivation::Goals KW - Medical Subject Headings::Anatomy::Nervous System::Peripheral Nervous System::Autonomic Nervous System::Enteric Nervous System KW - Medical Subject Headings::Phenomena and Processes::Cell Physiological Phenomena::Cell Physiological Processes::Cell Growth Processes::Cell Proliferation KW - Medical Subject Headings::Information Science::Information Science::Information Storage and Retrieval::Databases as Topic::Databases, Factual::Databases, Genetic TI - Genome-wide analysis of DNA methylation in Hirschsprung enteric precursor cells: unraveling the epigenetic landscape of enteric nervous system development TY - research article ER -