Astrid M Alsema1,2, Marion H C Wijering1,2, Anneke Miedema1,2

  • 1Department of Biomedical Sciences, Section Molecular Neurobiology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Nature neuroscience
|November 5, 2024
PubMed
概括

研究人员绘制了多发性硬化症 (MS) 病变中的基因表达,以了解疾病的进展. 他们在活跃的病变和预测正常白质如何发展为MS病变的途径中确定了不同的基因特征.

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Pleiotropy01:33

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...