Your browser doesn't support javascript.
loading
The HSA21 gene EURL/C21ORF91 controls neurogenesis within the cerebral cortex and is implicated in the pathogenesis of Down Syndrome.
Li, Shan Shan; Qu, Zhengdong; Haas, Matilda; Ngo, Linh; Heo, You Jeong; Kang, Hyo Jung; Britto, Joanne Maria; Cullen, Hayley Daniella; Vanyai, Hannah Kate; Tan, Seong-Seng; Chan-Ling, Tailoi; Gunnersen, Jenny Margaret; Heng, Julian Ik-Tsen.
Afiliación
  • Li SS; EMBL Australia, The Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria 3800, Australia.
  • Qu Z; EMBL Australia, The Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria 3800, Australia.
  • Haas M; EMBL Australia, The Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria 3800, Australia.
  • Ngo L; EMBL Australia, The Australian Regenerative Medicine Institute, Monash University, Clayton, Victoria 3800, Australia.
  • Heo YJ; The Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands and Centre for Medical Research, The University of Western Australia, Crawley, Western Australia, 6009, Australia.
  • Kang HJ; Department of Life Science, Chung-Ang University, Seoul, Korea.
  • Britto JM; Department of Life Science, Chung-Ang University, Seoul, Korea.
  • Cullen HD; Department of Neurobiology, Yale School of Medicine, New Haven, CT 06510, USA.
  • Vanyai HK; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria 3010, Australia.
  • Tan SS; The Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands and Centre for Medical Research, The University of Western Australia, Crawley, Western Australia, 6009, Australia.
  • Chan-Ling T; The Harry Perkins Institute of Medical Research, QEII Medical Centre, Nedlands and Centre for Medical Research, The University of Western Australia, Crawley, Western Australia, 6009, Australia.
  • Gunnersen JM; The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria 3010, Australia.
  • Heng JI; Discipline of Anatomy, School of Medical Sciences, Bosch Institute, The University of Sydney, Sydney, New South Wales, Australia.
Sci Rep ; 6: 29514, 2016 07 11.
Article en En | MEDLINE | ID: mdl-27404227
Asunto(s)
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_doencas_nao_transmissiveis Asunto principal: Cromosomas Humanos Par 21 / Corteza Cerebral / Síndrome de Down / Neurogénesis / Proteínas del Tejido Nervioso Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2016 Tipo del documento: Article País de afiliación: Australia
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 Problema de salud: 1_doencas_nao_transmissiveis Asunto principal: Cromosomas Humanos Par 21 / Corteza Cerebral / Síndrome de Down / Neurogénesis / Proteínas del Tejido Nervioso Tipo de estudio: Etiology_studies / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Sci Rep Año: 2016 Tipo del documento: Article País de afiliación: Australia