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Genome wide DNA methylation analysis of alveolar capillary dysplasia lung tissue reveals aberrant methylation of genes involved in development including the FOXF1 locus.
Slot, Evelien; Boers, Ruben; Boers, Joachim; van IJcken, Wilfred F J; Tibboel, Dick; Gribnau, Joost; Rottier, Robbert; de Klein, Annelies.
Afiliação
  • Slot E; Department of Paediatric Surgery, Erasmus MC - Sophia Children's Hospital Rotterdam, Rotterdam, Netherlands.
  • Boers R; Department of Clinical Genetics, Rm Ee2089, Erasmus MC Rotterdam, Wytemaweg 80, 3015 CN, Rotterdam, Netherlands.
  • Boers J; Department of Developmental Biology, Oncode Institute, Erasmus MC Rotterdam, Rotterdam, Netherlands.
  • van IJcken WFJ; Department of Developmental Biology, Oncode Institute, Erasmus MC Rotterdam, Rotterdam, Netherlands.
  • Tibboel D; Center for Biomics, Erasmus University Medical Center, Erasmus MC, Rotterdam, Netherlands.
  • Gribnau J; Department of Cell Biology, Erasmus University Medical Center, Erasmus MC, Rotterdam, Netherlands.
  • Rottier R; Department of Paediatric Surgery, Erasmus MC - Sophia Children's Hospital Rotterdam, Rotterdam, Netherlands.
  • de Klein A; Department of Developmental Biology, Oncode Institute, Erasmus MC Rotterdam, Rotterdam, Netherlands.
Clin Epigenetics ; 13(1): 148, 2021 07 29.
Article em En | MEDLINE | ID: mdl-34325731
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome da Persistência do Padrão de Circulação Fetal / Alvéolos Pulmonares / Fatores de Transcrição Forkhead / Pulmão Tipo de estudo: Prognostic_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Clin Epigenetics Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome da Persistência do Padrão de Circulação Fetal / Alvéolos Pulmonares / Fatores de Transcrição Forkhead / Pulmão Tipo de estudo: Prognostic_studies Limite: Female / Humans / Infant / Male / Newborn Idioma: En Revista: Clin Epigenetics Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda