Interferon-gamma reduces the proliferation of M. tuberculosis within macrophages from a patient with a novel hypomorphic NEMO mutation (2016)
- Authors:
- USP affiliated authors: LIMA, MARIA REGINA D'IMPERIO - ICB ; CONDINO NETO, ANTONIO - ICB
- Unidade: ICB
- DOI: 10.1002/pbc.26098
- Subjects: DISPLASIA ECTODÉRMICA; IMUNOLOGIA; INTERFERONS; MACRÓFAGOS; MYCOBACTERIUM TUBERCULOSIS; MUTAÇÃO GENÉTICA; LINFÓCITOS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Pediatric Bood & Cancer
- ISSN: 1545-5009
- Volume/Número/Paginação/Ano: v. 63, p. 1863-1866, 2016
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
KHAN, Taj Ali et al. Interferon-gamma reduces the proliferation of M. tuberculosis within macrophages from a patient with a novel hypomorphic NEMO mutation. Pediatric Bood & Cancer, v. 63, p. 1863-1866, 2016Tradução . . Disponível em: https://doi.org/10.1002/pbc.26098. Acesso em: 03 mar. 2026. -
APA
Khan, T. A., Ishfaq, M., Bonfim, C. C. B., Rahman, H., Iqbal, A., Lima, M. R. D. 'I., et al. (2016). Interferon-gamma reduces the proliferation of M. tuberculosis within macrophages from a patient with a novel hypomorphic NEMO mutation. Pediatric Bood & Cancer, 63, 1863-1866. doi:10.1002/pbc.26098 -
NLM
Khan TA, Ishfaq M, Bonfim CCB, Rahman H, Iqbal A, Lima MRD'I, Carvalho BTC, Cabral-Marques O, Condino Neto A. Interferon-gamma reduces the proliferation of M. tuberculosis within macrophages from a patient with a novel hypomorphic NEMO mutation [Internet]. Pediatric Bood & Cancer. 2016 ; 63 1863-1866.[citado 2026 mar. 03 ] Available from: https://doi.org/10.1002/pbc.26098 -
Vancouver
Khan TA, Ishfaq M, Bonfim CCB, Rahman H, Iqbal A, Lima MRD'I, Carvalho BTC, Cabral-Marques O, Condino Neto A. Interferon-gamma reduces the proliferation of M. tuberculosis within macrophages from a patient with a novel hypomorphic NEMO mutation [Internet]. Pediatric Bood & Cancer. 2016 ; 63 1863-1866.[citado 2026 mar. 03 ] Available from: https://doi.org/10.1002/pbc.26098 - Tuberculosis in an autosomal recessive case of chronic granulomatous disease due to mutation of the NCF1 gene
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Informações sobre o DOI: 10.1002/pbc.26098 (Fonte: oaDOI API)
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