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Single-cell transcription profiles in Bloom syndrome patients link BLM deficiency with altered condensin complex expression signatures.
Gönenc, Ipek Ilgin; Wolff, Alexander; Schmidt, Julia; Zibat, Arne; Müller, Christian; Cyganek, Lukas; Argyriou, Loukas; Räschle, Markus; Yigit, Gökhan; Wollnik, Bernd.
Afiliação
  • Gönenc II; Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.
  • Wolff A; Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.
  • Schmidt J; Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.
  • Zibat A; Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.
  • Müller C; Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.
  • Cyganek L; Stem Cell Unit, Clinic for Cardiology and Pneumology, University Medical Center Göttingen, 37075 Göttingen, Germany.
  • Argyriou L; German Center for Cardiovascular Research (DZHK), Partner Site Göttingen, 37075 Göttingen, Germany.
  • Räschle M; Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.
  • Yigit G; Department of Molecular Genetics, Technical University of Kaiserslautern, 67663 Kaiserslautern, Germany.
  • Wollnik B; Institute of Human Genetics, University Medical Center Göttingen, 37073 Göttingen, Germany.
Hum Mol Genet ; 31(13): 2185-2193, 2022 07 07.
Article em En | MEDLINE | ID: mdl-35099000
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Bloom / Microcefalia Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Bloom / Microcefalia Idioma: En Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha