Overexpression of Ankyrin Repeat Domain Containing Protein 1 Gene (ANKRD1) in Polymyositis Muscle Biopsies Is Correlated to Hypoxia (2014)
- Authors:
- USP affiliated authors: SHINJO, SAMUEL KATSUYUKI - FM ; SHINJO, SUELI MIEKO OBA - FM ; MARIE, SUELY KAZUE NAGAHASHI - FM
- Unidade: FM
- Subjects: MÚSCULOS (FISIOPATOLOGIA); EXPRESSÃO GENÉTICA; BIÓPSIA; RESUMOS (EVENTOS)
- Language: Inglês
- Imprenta:
- Source:
- Título: Arthritis and rheumatism
- ISSN: 0004-3591
- Volume/Número/Paginação/Ano: v. 66, n. S10, p. S967, res. 2220, 2014
- Conference titles: ACR/ARHP Annual Meeting
-
ABNT
SHINJO, Samuel Katsuyuki et al. Overexpression of Ankyrin Repeat Domain Containing Protein 1 Gene (ANKRD1) in Polymyositis Muscle Biopsies Is Correlated to Hypoxia. Arthritis and rheumatism. Atlanta: Faculdade de Medicina, Universidade de São Paulo. Disponível em: http://onlinelibrary.wiley.com/doi/10.1002/art.v66.S10/issuetoc. Acesso em: 12 fev. 2026. , 2014 -
APA
Shinjo, S. K., Oba-Shinjo, S. M., Uno, M., & Marie, S. K. N. (2014). Overexpression of Ankyrin Repeat Domain Containing Protein 1 Gene (ANKRD1) in Polymyositis Muscle Biopsies Is Correlated to Hypoxia. Arthritis and rheumatism. Atlanta: Faculdade de Medicina, Universidade de São Paulo. Recuperado de http://onlinelibrary.wiley.com/doi/10.1002/art.v66.S10/issuetoc -
NLM
Shinjo SK, Oba-Shinjo SM, Uno M, Marie SKN. Overexpression of Ankyrin Repeat Domain Containing Protein 1 Gene (ANKRD1) in Polymyositis Muscle Biopsies Is Correlated to Hypoxia [Internet]. Arthritis and rheumatism. 2014 ; 66( S10): S967.[citado 2026 fev. 12 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/art.v66.S10/issuetoc -
Vancouver
Shinjo SK, Oba-Shinjo SM, Uno M, Marie SKN. Overexpression of Ankyrin Repeat Domain Containing Protein 1 Gene (ANKRD1) in Polymyositis Muscle Biopsies Is Correlated to Hypoxia [Internet]. Arthritis and rheumatism. 2014 ; 66( S10): S967.[citado 2026 fev. 12 ] Available from: http://onlinelibrary.wiley.com/doi/10.1002/art.v66.S10/issuetoc - A Brazilian family with inclusion body myopathy associated with Paget's disease of bone and frontotemporal dementia linked to the VCP pGly97Glu mutation
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