Corrigendum: Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?

IF 3.5 3区医学 Q2 NEUROSCIENCES

Frontiers in Molecular Neuroscience Pub Date : 2024-04-26 eCollection Date: 2024-01-01 DOI:10.3389/fnmol.2024.1411360

Antonio d'Amati, Lavinia Bargiacchi, Sabrina Rossi, Andrea Carai, Luca Bertero, Valeria Barresi, Maria Elena Errico, Anna Maria Buccoliero, Sofia Asioli, Gianluca Marucci, Giada Del Baldo, Angela Mastronuzzi, Evelina Miele, Federica D'Antonio, Elisabetta Schiavello, Veronica Biassoni, Maura Massimino, Marco Gessi, Manila Antonelli, Francesca Gianno

引用次数: 0

Abstract

[This corrects the article DOI: 10.3389/fnmol.2024.1268038.].

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更正：小儿中枢神经系统肿瘤和 2021 年世界卫生组织分类：肿瘤学家需要病理学家做些什么？

[This corrects the article DOI: 10.3389/fnmol.2024.1268038.].

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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来源期刊

Frontiers in Molecular Neuroscience NEUROSCIENCES-

CiteScore

5.70

自引率

2.10%

发文量

669

审稿时长

14 weeks

期刊介绍： Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.

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