Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder (2022)
- Authors:
- USP affiliated authors: ULRICH, ALEXANDER HENNING - IQ ; FERNANDES, ANDREA BALAN - ICB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; CAMPOS, GABRIELE DA SILVA - IB ; GLASER, TALITA - IQ
- Unidades: IQ; ICB; IB
- DOI: 10.1038/s41398-022-01997-9
- Subjects: MICROBIOLOGIA; FÁRMACOS IMUNOSSUPRESSORES; TRANSTORNO DO ESPECTRO AUTISTA; CANAIS DE CÁLCIO; DISTÚRBIOS PSICOLÓGICOS; HERANÇA GENÉTICA; VARIAÇÃO GENÉTICA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Translational Psychiatry
- ISSN: 2158-3188
- Volume/Número/Paginação/Ano: v. 12, art. 234, p. 1-11, 2022
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
SILVA, André Luíz Teles e et al. Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder. Translational Psychiatry, v. 12, p. 1-11, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41398-022-01997-9. Acesso em: 28 out. 2024. -
APA
Silva, A. L. T. e, Glaser, T., Oliveira, K. G., Velloso, J. da C. C., Wang, J. Y. T., Campos, G. da S., et al. (2022). Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder. Translational Psychiatry, 12, 1-11. doi:10.1038/s41398-022-01997-9 -
NLM
Silva ALT e, Glaser T, Oliveira KG, Velloso J da CC, Wang JYT, Campos G da S, Ulrich H, Balan A, Zarrei M, Higginbotham EJ, Scherer SW, Passos-Bueno MR, Sertié AL. Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder [Internet]. Translational Psychiatry. 2022 ; 12 1-11.[citado 2024 out. 28 ] Available from: https://doi.org/10.1038/s41398-022-01997-9 -
Vancouver
Silva ALT e, Glaser T, Oliveira KG, Velloso J da CC, Wang JYT, Campos G da S, Ulrich H, Balan A, Zarrei M, Higginbotham EJ, Scherer SW, Passos-Bueno MR, Sertié AL. Rare CACNA1H and RELN variants interact through mTORC1 pathway in oligogenic autism spectrum disorder [Internet]. Translational Psychiatry. 2022 ; 12 1-11.[citado 2024 out. 28 ] Available from: https://doi.org/10.1038/s41398-022-01997-9 - Purinergic Signaling in Neurodevelopment, Neuroinflammation and Neurodegeneration
- Purinergic receptors in neurogenic processes
- Purinergic signaling: an overview
- Huntingtin protein maintains balanced energetics in mouse cardiomyocytes
- Purinergic signaling in brain physiology
- Therapeutic effects of cannabinoids and their applications in COVID-19 treatment
- P2Y2 receptor activation promotes esophageal cancer cells proliferation via ERK1/2 pathway
- Adenosinergic-dopaminergic signaling in mood disorders: a mini-review
- Ginkgolides and Huperzine A for complementary treatment of Alzheimer's disease
- Purine nucleotides metabolism and signaling in huntington’s disease: search for a target for novel therapies
Informações sobre o DOI: 10.1038/s41398-022-01997-9 (Fonte: oaDOI API)
Download do texto completo
Tipo | Nome | Link | |
---|---|---|---|
Rare CACNA1H and RELN var... | Direct link |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas