Phox2b mutation mediated by Atoh1 expression impaired respiratory rhythm and ventilatory responses to hypoxia and hypercapnia (2022)
- Authors:
- USP affiliated authors: MOREIRA, ANA CAROLINA TAKAKURA - ICB ; MOREIRA, THIAGO DOS SANTOS - ICB ; SILVA, TALITA DE MELO E - ICB ; SILVA, PHELIPE EDUARDO - ICB ; FERREIRA, CAROLINE BORGES - ICB ; Castro, Claudio Lucio de - ICB
- Unidade: ICB
- DOI: 10.7554/eLife.73130
- Subjects: FISIOLOGIA; FARMACOLOGIA; TRANSCRIÇÃO GÊNICA; MUTAÇÃO GENÉTICA; RESPIRAÇÃO ANIMAL; MODELOS ANIMAIS DE DOENÇAS; CAMUNDONGOS; ANÓXIA; APNEIA DO SONO TIPO CENTRAL
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
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- Este artigo é de acesso aberto
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- Cor do Acesso Aberto: gold
- Licença: cc-by
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ABNT
FERREIRA, Caroline Borges et al. Phox2b mutation mediated by Atoh1 expression impaired respiratory rhythm and ventilatory responses to hypoxia and hypercapnia. eLife, v. 11, p. 1-23, 2022Tradução . . Disponível em: https://doi.org/10.7554/eLife.73130. Acesso em: 05 jun. 2024. -
APA
Ferreira, C. B., Silva, T. de M. e, Silva, P. E., Castro, C. L. de, Czeisler, C., Otero, J. J., et al. (2022). Phox2b mutation mediated by Atoh1 expression impaired respiratory rhythm and ventilatory responses to hypoxia and hypercapnia. eLife, 11, 1-23. doi:10.7554/eLife.73130 -
NLM
Ferreira CB, Silva T de M e, Silva PE, Castro CL de, Czeisler C, Otero JJ, Moreira ACT, Moreira T dos S. Phox2b mutation mediated by Atoh1 expression impaired respiratory rhythm and ventilatory responses to hypoxia and hypercapnia [Internet]. eLife. 2022 ; 11 1-23.[citado 2024 jun. 05 ] Available from: https://doi.org/10.7554/eLife.73130 -
Vancouver
Ferreira CB, Silva T de M e, Silva PE, Castro CL de, Czeisler C, Otero JJ, Moreira ACT, Moreira T dos S. Phox2b mutation mediated by Atoh1 expression impaired respiratory rhythm and ventilatory responses to hypoxia and hypercapnia [Internet]. eLife. 2022 ; 11 1-23.[citado 2024 jun. 05 ] Available from: https://doi.org/10.7554/eLife.73130 - Respiratory deficits in a female rat model of Parkinson's disease
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Informações sobre o DOI: 10.7554/eLife.73130 (Fonte: oaDOI API)
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