Whole Transcriptome Screening Reveals Myelination Deficits in Dysplastic Human Temporal Neocortex.

Donkels, Catharina; Pfeifer, Dietmar; Janz, Philipp; Huber, Susanne; Nakagawa, Julia; Prinz, Marco; Schulze-Bonhage, Andreas; Weyerbrock, Astrid; Zentner, Josef; Haas, Carola A

Donkels, Catharina; Pfeifer, Dietmar; Janz, Philipp; Huber, Susanne; Nakagawa, Julia; Prinz, Marco; Schulze-Bonhage, Andreas; Weyerbrock, Astrid; Zentner, Josef; Haas, Carola A.

Afiliação

Donkels C; Experimental Epilepsy Research, Department of Neurosurgery.
Pfeifer D; Faculty of Biology.
Janz P; Department of Hematology, Oncology and Stem Cell Transplantation.
Huber S; Experimental Epilepsy Research, Department of Neurosurgery.
Nakagawa J; Faculty of Biology.
Prinz M; Experimental Epilepsy Research, Department of Neurosurgery.
Schulze-Bonhage A; Experimental Epilepsy Research, Department of Neurosurgery.
Weyerbrock A; Department of Neurosurgery.
Zentner J; Institute of Neuropathology.
Haas CA; Center for Biological Signalling Studies.

Cereb Cortex ; 27(2): 1558-1572, 2017 02 01.

Article em En | MEDLINE | ID: mdl-26796214

Assuntos

Epilepsia/fisiopatologia; Neocórtex/metabolismo; Oligodendroglia/metabolismo; Transcriptoma/fisiologia; Adolescente; Adulto; Criança; Pré-Escolar; Feminino; Humanos; Lactente; Masculino; Malformações do Desenvolvimento Cortical/metabolismo; Proteína Básica da Mielina/metabolismo; Adulto Jovem

Palavras-chave

brain malformation; development; epilepsy; microarray; oligodendrocyte

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oligodendroglia / Neocórtex / Epilepsia / Transcriptoma Idioma: En Ano de publicação: 2017 Tipo de documento: Article

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