Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/111759
Título: Fibroblast growth factor signaling in axons: from development to disease
Autor: Tomé, Diogo 
Dias, Marta S.
Correia, Joana
Almeida, Ramiro D. 
Palavras-chave: FGF; Signaling pathways; Axons; Presynaptic terminal; Axonal injury; Neuronal disorders
Data: 16-Out-2023
Editora: Signal Transduction Society
Projeto: LCF/PR/ HP20/52300001 
PTDC/NAN-OPT/7989/2020 
UIDB/04501/2020 
UIDP/04501/2020 
UIDB/04539/2020 
info:eu-repo/grantAgreement/UIDP/04539/2020 
LA/P/0058/2020 
SFRH/BD/139368/2018 
SFRH/BD/141092/2018 
Título da revista, periódico, livro ou evento: Cell Communication and Signaling
Volume: 21
Número: 1
Resumo: The fibroblast growth factor (FGF) family regulates various and important aspects of nervous system development, ranging from the well-established roles in neuronal patterning to more recent and exciting functions in axonal growth and synaptogenesis. In addition, FGFs play a critical role in axonal regeneration, particularly after spinal cord injury, confirming their versatile nature in the nervous system. Due to their widespread involvement in neural development, the FGF system also underlies several human neurological disorders. While particular attention has been given to FGFs in a whole-cell context, their effects at the axonal level are in most cases undervalued. Here we discuss the endeavor of the FGF system in axons, we delve into this neuronal subcompartment to provide an original view of this multipurpose family of growth factors in nervous system (dys)function. Video Abstract.
URI: https://hdl.handle.net/10316/111759
ISSN: 1478-811X
DOI: 10.1186/s12964-023-01284-0
Direitos: openAccess
Aparece nas coleções:I&D CNC - Artigos em Revistas Internacionais

Ficheiros deste registo:
Mostrar registo em formato completo

Visualizações de página

78
Visto em 30/out/2024

Downloads

34
Visto em 30/out/2024

Google ScholarTM

Verificar

Altmetric

Altmetric


Este registo está protegido por Licença Creative Commons Creative Commons