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Artigo de periodico
Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance (2021)
Quintas, Carmen Oleaga ; Oliveira Júnior, Edgar Borges de; Rosain, Jérémie ; Rapaport, Franck ; Deswarte, Caroline ; Guérin, Antoine; Sajjath, Sairaj Munavar ; Zhou, Yu Jerry ; Marot, Stéphane; Lozano, Claire ; Branco, Lidia ; Hidalgo, Nuria Fernández ; Lew, Dukhee Betty ; Brunel, Anne Sophiehttps ; Thomas, Caroline; Launay, Elise ; Arias, Andrés Augusto ; Cuffel, Alexis; Monjo, Vanesa Cunill ; Neehus, Anna-Lena ; Marques, Laura; Roynard, Manon; Vélez, Marcela Moncada ; Gerçeker, Bengü; Colobran, Roger ; Vigué, Marie-Gabrielle; Herrera, Gabriela Lopez ; Ruiz, Laura Berron ; Méndez, Nora Hilda Segura ; Romanillos, Patricia O’Farrill ; Voyer, Tom Le; Puel, Anne ; Chantelot, Christine Bellanné ; Ramirez, Kacy A.; Diaz, Lazaro Lorenzo ; Alejo, Noé Ramirez ; Diego, Rebeca Pérez de ; Condino Neto, Antonio ; Mellouli, Fethi ; Gallego, Carlos Rodriguez; Witte, Torsten ; Restrepo, José Franco; Jobim, Mariana ; Dupuis, Stéphanie Boisson ; Jeziorski, Eric ; Fieschi, Claire ; Vogt, Guillaume ; Donadieu, Jean ; Pasquet, Marlène ; Vasconcelos, Julia; Ardeniz, Fatma Omur; Gallo, Mónica Martínez ; Campos, Regis A.; Jobim, Luiz Fernando; Barricarte, Rubén Martínez ; Liu, Kang; Cobat, Aurélie; Abel, Laurent ; Casanova, Jean-Laurent ; Bustamante, Jacinta
Source: Journal of Clinical Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, TUBERCULOSE, INTERLEUCINA 8, POLIMORFISMO, ALELOS, IMUNOGENÉTICA, MUTAÇÃO GENÉTICA, FENÓTIPOS
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ABNT
QUINTAS, Carmen Oleaga et al. Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance. Journal of Clinical Immunology, p. 19 , 2021Tradução . . Disponível em: https://doi.org/10.1007/s10875-020-00930-3. Acesso em: 23 ago. 2024.
APA
Quintas, C. O., Oliveira Júnior, E. B. de, Rosain, J., Rapaport, F., Deswarte, C., Guérin, A., et al. (2021). Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance. Journal of Clinical Immunology, 19 . doi:10.1007/s10875-020-00930-3
NLM
Quintas CO, Oliveira Júnior EB de, Rosain J, Rapaport F, Deswarte C, Guérin A, Sajjath SM, Zhou YJ, Marot S, Lozano C, Branco L, Hidalgo NF, Lew DB, Brunel AS, Thomas C, Launay E, Arias AA, Cuffel A, Monjo VC, Neehus A-L, Marques L, Roynard M, Vélez MM, Gerçeker B, Colobran R, Vigué M-G, Herrera GL, Ruiz LB, Méndez NHS, Romanillos PO’F, Voyer TL, Puel A, Chantelot CB, Ramirez KA, Diaz LL, Alejo NR, Diego RP de, Condino Neto A, Mellouli F, Gallego CR, Witte T, Restrepo JF, Jobim M, Dupuis SB, Jeziorski E, Fieschi C, Vogt G, Donadieu J, Pasquet M, Vasconcelos J, Ardeniz FO, Gallo MM, Campos RA, Jobim LF, Barricarte RM, Liu K, Cobat A, Abel L, Casanova J-L, Bustamante J. Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance [Internet]. Journal of Clinical Immunology. 2021 ;19 .[citado 2024 ago. 23 ] Available from: https://doi.org/10.1007/s10875-020-00930-3
Vancouver
Quintas CO, Oliveira Júnior EB de, Rosain J, Rapaport F, Deswarte C, Guérin A, Sajjath SM, Zhou YJ, Marot S, Lozano C, Branco L, Hidalgo NF, Lew DB, Brunel AS, Thomas C, Launay E, Arias AA, Cuffel A, Monjo VC, Neehus A-L, Marques L, Roynard M, Vélez MM, Gerçeker B, Colobran R, Vigué M-G, Herrera GL, Ruiz LB, Méndez NHS, Romanillos PO’F, Voyer TL, Puel A, Chantelot CB, Ramirez KA, Diaz LL, Alejo NR, Diego RP de, Condino Neto A, Mellouli F, Gallego CR, Witte T, Restrepo JF, Jobim M, Dupuis SB, Jeziorski E, Fieschi C, Vogt G, Donadieu J, Pasquet M, Vasconcelos J, Ardeniz FO, Gallo MM, Campos RA, Jobim LF, Barricarte RM, Liu K, Cobat A, Abel L, Casanova J-L, Bustamante J. Inherited GATA2 deficiency is dominant by haploinsufficiency and displays incomplete clinical penetrance [Internet]. Journal of Clinical Immunology. 2021 ;19 .[citado 2024 ago. 23 ] Available from: https://doi.org/10.1007/s10875-020-00930-3
Artigo de periodico
Hematologically important mutations: X-linked chronic granulomatous disease (fourth update) (2021)
Roos, Dirk; Leeuwen, Karin van; Hsu, Amy P.; Priel, Debra Long ; Begtrup, Amber ; Brandon, Rhonda; Stasia, Marie José ; Bakri, Faris Ghalib ; Köker, Nezihe ; Köker, Mustafa Yavuz ; Madkaika, Manisha; Boer, Martin de ; Morato, Maria Bravo Garcia ; Shephard, Juan Luis Valdivieso; Roesler, Joachim ; Kanegane, Hirokazu ; Kawai, Toshinao ; Matteo, Gigliola Di ; Shahrooei, Mohammad ; Bustamante, Jacinta ; Rawat, Amit ; Vignesh, Pandiarajan ; Mortaz, Esmaeil ; Fayezi, Abbas; Cagdas, Deniz ; Tezcan, Ilhan ; Kitcharoensakkul, Maleewan ; Dinauer, Mary C. ; Meyts, Isabelle; Wolach, Baruch; Condino Neto, Antonio ; Zerbe, Christa S. ; Holland, Steven M.; Malech, Harry L. ; Gallin, John I.; Kuhns, Douglas B.
Source: Blood Cells, Molecules and Diseases. Unidade: ICB
Subjects: IMUNOLOGIA, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, MUTAÇÃO GENÉTICA, DOENÇAS SANGUÍNEAS E LINFÁTICAS, SUPERÓXIDO DISMUTASE, ATIVAÇÃO ENZIMÁTICA, IMUNOGENÉTICA, ENZIMAS
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ABNT
ROOS, Dirk et al. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update). Blood Cells, Molecules and Diseases, v. 90, p. 1-36, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2021.102587. Acesso em: 23 ago. 2024.
APA
Roos, D., Leeuwen, K. van, Hsu, A. P., Priel, D. L., Begtrup, A., Brandon, R., et al. (2021). Hematologically important mutations: X-linked chronic granulomatous disease (fourth update). Blood Cells, Molecules and Diseases, 90, 1-36. doi:10.1016/j.bcmd.2021.102587
NLM
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Stasia MJ, Bakri FG, Köker N, Köker MY, Madkaika M, Boer M de, Morato MBG, Shephard JLV, Roesler J, Kanegane H, Kawai T, Matteo GD, Shahrooei M, Bustamante J, Rawat A, Vignesh P, Mortaz E, Fayezi A, Cagdas D, Tezcan I, Kitcharoensakkul M, Dinauer MC, Meyts I, Wolach B, Condino Neto A, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 90 1-36.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102587
Vancouver
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Stasia MJ, Bakri FG, Köker N, Köker MY, Madkaika M, Boer M de, Morato MBG, Shephard JLV, Roesler J, Kanegane H, Kawai T, Matteo GD, Shahrooei M, Bustamante J, Rawat A, Vignesh P, Mortaz E, Fayezi A, Cagdas D, Tezcan I, Kitcharoensakkul M, Dinauer MC, Meyts I, Wolach B, Condino Neto A, Zerbe CS, Holland SM, Malech HL, Gallin JI, Kuhns DB. Hematologically important mutations: X-linked chronic granulomatous disease (fourth update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 90 1-36.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102587
Artigo de periodico
Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update) (2021)
Roos, Dirk ; Leeuwen, Karin van ; Hsu, Amy P. ; Priel, Debra Long ; Begtrup, Amber ; Brandon, Rhonda; Rawat, Amit ; Vignesh, Pandiarajan ; Madkaikar, Manesha ; Stasia, Marie José ; Bakri, Faris Ghalib ; Boer, Martin de ; Roesler, Joachim ; Köker, Nezihe ; Köker, Mustafa Yavuz ; Jakobsen, Marianne ; Bustamante, Jacinta ; Morato, Maria Bravo Garcia ; Condino Neto, Antonio
Source: Blood Cells, Molecules and Diseases. Unidade: ICB
Subjects: IMUNOLOGIA, DOENÇAS GENÉTICAS, IMUNODEFICIÊNCIA DE VARIÁVEL COMUM, IMUNOGENÉTICA, MUTAÇÃO GENÉTICA, POLIMORFISMO, INIBIDORES DE ENZIMAS, PERÓXIDO DE HIDROGÊNIO, APOPTOSE, HERANÇA GENÉTICA
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ABNT
ROOS, Dirk et al. Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update). Blood Cells, Molecules and Diseases, v. 92, p. 1-16, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2021.102596. Acesso em: 23 ago. 2024.
APA
Roos, D., Leeuwen, K. van, Hsu, A. P., Priel, D. L., Begtrup, A., Brandon, R., et al. (2021). Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update). Blood Cells, Molecules and Diseases, 92, 1-16. doi:10.1016/j.bcmd.2021.102596
NLM
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, Boer M de, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Morato MBG, Condino Neto A. Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 92 1-16.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102596
Vancouver
Roos D, Leeuwen K van, Hsu AP, Priel DL, Begtrup A, Brandon R, Rawat A, Vignesh P, Madkaikar M, Stasia MJ, Bakri FG, Boer M de, Roesler J, Köker N, Köker MY, Jakobsen M, Bustamante J, Morato MBG, Condino Neto A. Hematologically important mutations: the autosomal forms of chronic granulomatous disease (third update) [Internet]. Blood Cells, Molecules and Diseases. 2021 ; 92 1-16.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.bcmd.2021.102596
Artigo de periodico
Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant (2018)
Boisson-Dupuis, Stéphanie; Ramires-Alejo, Noe; Li, Zhi; Patin, Etienne; Rao, Geetha; Kerner, Gaspard; Lim, Che Kang; Krementsov, Dimitry N.; Hernandez, Nicholas; Ma, Cidy S.; Zhang, Qian; Markle, Janet; Martinez-Barricarte, Ruben; Payne, Kathryn; Fisch, Robert; Deswarte, Caroline; Halpern, Joshua; Bouaziz, Matthieu; Mulwa, Jeanette; Sivanesan, Durga; Lazarov, Tomi; Naves, Rodrigo; Garcia, Patricia; Itan, Yuval; Boisson, Bertrand; Checci, Alix; Jabot-Hanin, Fabienne; Cobat, Aurélie; Guennoun, Andrea; Jackson, Carolyn C.; Pekcan, Sevai; Caliskaner, Zafer; Inostroza, Jaime; Costa-Carvalho, Beatriz Tavares; Albuquerque, José Antonio Tavares de; Gacia-Ortiz, Humberto; Orozco, Lorena; Ozcelik, Tayfun; Abid, Ahmed; Rhorfi, Ismail Abderahmani; Souhi, Hicham; Amrani, Hicham Naji; Zegmout, Adil; Geissmann, Frédéric; Michnick, Stephen W.; Muller-Fleckenstein, Ingrid; Fleckenstein, Bernhard; Puel, Anne; Ciancanelli, Michael J.; Marr, Nico; Abolhassani, Hassan; Balcells, Maria Elvira; Strickler, Alexis; Abarca, Katia; Teuscher, Cory; Ochs, Hans D.; Reisli, Ismail; Sayar, Esra H.; El-Baghdadi, Jamila; Bustamante, Jacinta; Hammarströn, Lennart; Tangye, Stuart G.; Pellegrini, Sandra; Quintana-Murci, Lluis; Abel, Laurent; Casanova, Jean-Laurent; Condino-Neto, Antonio
Source: Science Immunology. Unidade: ICB
Subjects: TUBERCULOSE, VARIAÇÃO GENÉTICA, IMUNIDADE, CITOCINAS, DIFERENCIAÇÃO CELULAR, ATIVAÇÃO ENZIMÁTICA, IMUNOGENÉTICA
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ABNT
BOISSON-DUPUIS, Stéphanie et al. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant. Science Immunology, v. 3, 2018Tradução . . Disponível em: https://doi.org/10.1126/sciimmunol.aau8714. Acesso em: 23 ago. 2024.
APA
Boisson-Dupuis, S., Ramires-Alejo, N., Li, Z., Patin, E., Rao, G., Kerner, G., et al. (2018). Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant. Science Immunology, 3. doi:10.1126/sciimmunol.aau8714
NLM
Boisson-Dupuis S, Ramires-Alejo N, Li Z, Patin E, Rao G, Kerner G, Lim CK, Krementsov DN, Hernandez N, Ma CS, Zhang Q, Markle J, Martinez-Barricarte R, Payne K, Fisch R, Deswarte C, Halpern J, Bouaziz M, Mulwa J, Sivanesan D, Lazarov T, Naves R, Garcia P, Itan Y, Boisson B, Checci A, Jabot-Hanin F, Cobat A, Guennoun A, Jackson CC, Pekcan S, Caliskaner Z, Inostroza J, Costa-Carvalho BT, Albuquerque JAT de, Gacia-Ortiz H, Orozco L, Ozcelik T, Abid A, Rhorfi IA, Souhi H, Amrani HN, Zegmout A, Geissmann F, Michnick SW, Muller-Fleckenstein I, Fleckenstein B, Puel A, Ciancanelli MJ, Marr N, Abolhassani H, Balcells ME, Strickler A, Abarca K, Teuscher C, Ochs HD, Reisli I, Sayar EH, El-Baghdadi J, Bustamante J, Hammarströn L, Tangye SG, Pellegrini S, Quintana-Murci L, Abel L, Casanova J-L, Condino-Neto A. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant [Internet]. Science Immunology. 2018 ; 3[citado 2024 ago. 23 ] Available from: https://doi.org/10.1126/sciimmunol.aau8714
Vancouver
Boisson-Dupuis S, Ramires-Alejo N, Li Z, Patin E, Rao G, Kerner G, Lim CK, Krementsov DN, Hernandez N, Ma CS, Zhang Q, Markle J, Martinez-Barricarte R, Payne K, Fisch R, Deswarte C, Halpern J, Bouaziz M, Mulwa J, Sivanesan D, Lazarov T, Naves R, Garcia P, Itan Y, Boisson B, Checci A, Jabot-Hanin F, Cobat A, Guennoun A, Jackson CC, Pekcan S, Caliskaner Z, Inostroza J, Costa-Carvalho BT, Albuquerque JAT de, Gacia-Ortiz H, Orozco L, Ozcelik T, Abid A, Rhorfi IA, Souhi H, Amrani HN, Zegmout A, Geissmann F, Michnick SW, Muller-Fleckenstein I, Fleckenstein B, Puel A, Ciancanelli MJ, Marr N, Abolhassani H, Balcells ME, Strickler A, Abarca K, Teuscher C, Ochs HD, Reisli I, Sayar EH, El-Baghdadi J, Bustamante J, Hammarströn L, Tangye SG, Pellegrini S, Quintana-Murci L, Abel L, Casanova J-L, Condino-Neto A. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant [Internet]. Science Immunology. 2018 ; 3[citado 2024 ago. 23 ] Available from: https://doi.org/10.1126/sciimmunol.aau8714
Artigo de periodico
Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations (2017)
Miot, Charline; Imai, Kohsuke; Imai, Chihaya; Mancini, Anthony J.; Kucuk, Zeynep Yesim; Kawai, Tokomki; Nishikomori, Ryuta; Ito, Etsuro; Pellier, Isabelle; Girod, Sophie Dupuis; Rosain, Jeremie; Sasaki, Shinya; Chandrakasan, Shanmuganathan; Schmid, Jana Pachlopnik; Okano, Tsubasa; Colin, Estelle; Olaya-Vargas, Alberto; Yamazaki-Nakashimada, Marco; Qasim, Waseem; Padilla, Sara Espinosa; Jones, Andrea; Krol, Alfons; Cole, Nyree; Jolles, Stephen; Bleesing, Jack; Vraetz, Thomas; Gennery, Andrew R.; Abinun, Mario; Güngör, Tayfun; Costa-Carvalho, Beatriz; Condino-Neto, Antonio; Veys, Paul; Holland, Steven M.; Uzel, Gulbu; Moshous, Despina; Neven, Benedicte; Blanche, Stéphane; Ehl, Stephan; Döffinger, Rainer; Patel, Smita Y.; Puel, Anne; Bustamante, Jacinta; Gelfand, Erwin W.; Casanova, Jean-Laurent; Orange, Jordan S.; Picard, Capucine
Source: Blood. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
MIOT, Charline et al. Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations. Blood, v. 130, n. 12, p. 1456-1467, 2017Tradução . . Disponível em: https://doi.org/10.1182/blood-2017-03-771600. Acesso em: 23 ago. 2024.
APA
Miot, C., Imai, K., Imai, C., Mancini, A. J., Kucuk, Z. Y., Kawai, T., et al. (2017). Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations. Blood, 130( 12), 1456-1467. doi:10.1182/blood-2017-03-771600
NLM
Miot C, Imai K, Imai C, Mancini AJ, Kucuk ZY, Kawai T, Nishikomori R, Ito E, Pellier I, Girod SD, Rosain J, Sasaki S, Chandrakasan S, Schmid JP, Okano T, Colin E, Olaya-Vargas A, Yamazaki-Nakashimada M, Qasim W, Padilla SE, Jones A, Krol A, Cole N, Jolles S, Bleesing J, Vraetz T, Gennery AR, Abinun M, Güngör T, Costa-Carvalho B, Condino-Neto A, Veys P, Holland SM, Uzel G, Moshous D, Neven B, Blanche S, Ehl S, Döffinger R, Patel SY, Puel A, Bustamante J, Gelfand EW, Casanova J-L, Orange JS, Picard C. Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations [Internet]. Blood. 2017 ; 130( 12): 1456-1467.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1182/blood-2017-03-771600
Vancouver
Miot C, Imai K, Imai C, Mancini AJ, Kucuk ZY, Kawai T, Nishikomori R, Ito E, Pellier I, Girod SD, Rosain J, Sasaki S, Chandrakasan S, Schmid JP, Okano T, Colin E, Olaya-Vargas A, Yamazaki-Nakashimada M, Qasim W, Padilla SE, Jones A, Krol A, Cole N, Jolles S, Bleesing J, Vraetz T, Gennery AR, Abinun M, Güngör T, Costa-Carvalho B, Condino-Neto A, Veys P, Holland SM, Uzel G, Moshous D, Neven B, Blanche S, Ehl S, Döffinger R, Patel SY, Puel A, Bustamante J, Gelfand EW, Casanova J-L, Orange JS, Picard C. Hematopoietic stem cell transplantation in 29 patientshemizygous for hypomorphic IKBKG/NEMO mutations [Internet]. Blood. 2017 ; 130( 12): 1456-1467.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1182/blood-2017-03-771600
Artigo de periodico
Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity (2017)
Schimke, Lena F; Hibbard, James; Martinez-Barricarte, Ruben; Khan, Taj Ali; Cavalcante, Ricardo de Souza; Oliveira-Junior, Edgar Borges de; França, Tábata Takahashi; Iqbal, Asif; Yamamoto, Guilherme; Arslanian, Christina; Feriotti, Claudia; Costa, Tânia Alves; Bustamante, Jacinta; Boisson-Dupuis, Stéphanie; Casanova, Jean-Laurent; Barbuto, José Alexandre Marzagão ; Zatz, Mayana ; Mendes, Rinaldo Poncio; Calich, Vera Lúcia Garcia; Ochs, Hans D; Torgerson, Troy R; Cabral-Marques, Otavio; Condino Neto, Antonio
Source: Journal of Infectious Diseases. Unidades: ICB, IB
Subjects: PARACOCCIDIOIDOMICOSE, IMUNOLOGIA, MUTAÇÃO GENÉTICA, PREDISPOSIÇÃO GENÉTICA PARA DOENÇA, INFECÇÕES BACTERIANAS E MICOSES
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ABNT
SCHIMKE, Lena F et al. Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity. Journal of Infectious Diseases, v. 216, n. 12, p. 1623-1634, 2017Tradução . . Disponível em: https://doi.org/10.1093/infdis/jix522. Acesso em: 23 ago. 2024.
APA
Schimke, L. F., Hibbard, J., Martinez-Barricarte, R., Khan, T. A., Cavalcante, R. de S., Oliveira-Junior, E. B. de, et al. (2017). Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity. Journal of Infectious Diseases, 216( 12), 1623-1634. doi:10.1093/infdis/jix522
NLM
Schimke LF, Hibbard J, Martinez-Barricarte R, Khan TA, Cavalcante R de S, Oliveira-Junior EB de, França TT, Iqbal A, Yamamoto G, Arslanian C, Feriotti C, Costa TA, Bustamante J, Boisson-Dupuis S, Casanova J-L, Barbuto JAM, Zatz M, Mendes RP, Calich VLG, Ochs HD, Torgerson TR, Cabral-Marques O, Condino Neto A. Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity [Internet]. Journal of Infectious Diseases. 2017 ; 216( 12): 1623-1634.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1093/infdis/jix522
Vancouver
Schimke LF, Hibbard J, Martinez-Barricarte R, Khan TA, Cavalcante R de S, Oliveira-Junior EB de, França TT, Iqbal A, Yamamoto G, Arslanian C, Feriotti C, Costa TA, Bustamante J, Boisson-Dupuis S, Casanova J-L, Barbuto JAM, Zatz M, Mendes RP, Calich VLG, Ochs HD, Torgerson TR, Cabral-Marques O, Condino Neto A. Paracoccidioidomycosis Associated With a Heterozygous STAT4 Mutation and Impaired IFN-γ Immunity [Internet]. Journal of Infectious Diseases. 2017 ; 216( 12): 1623-1634.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1093/infdis/jix522
Artigo de periodico-carta/editorial
Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency (2015)
Conti, Francesca; Aragão Filho, Walmir Cutrim; Prando, Carolina; Deswarte, Caroline; Hubeau, Marjorie; Newburger, Peter E.; Casanova, Jean-Laurent; Bustamante, Jacinta; Condino-Neto, Antonio
Source: Journal of Allergy and Clinical Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, MUTAÇÃO, FAGÓCITOS, MACRÓFAGOS
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ABNT
CONTI, Francesca et al. Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency. Journal of Allergy and Clinical Immunology. Philadelphia: Instituto de Ciências Biomédicas, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.jaci.2014.11.004. Acesso em: 23 ago. 2024. , 2015
APA
Conti, F., Aragão Filho, W. C., Prando, C., Deswarte, C., Hubeau, M., Newburger, P. E., et al. (2015). Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency. Journal of Allergy and Clinical Immunology. Philadelphia: Instituto de Ciências Biomédicas, Universidade de São Paulo. doi:10.1016/j.jaci.2014.11.004
NLM
Conti F, Aragão Filho WC, Prando C, Deswarte C, Hubeau M, Newburger PE, Casanova J-L, Bustamante J, Condino-Neto A. Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency [Internet]. Journal of Allergy and Clinical Immunology. 2015 ; 135( 5): 1393-1395.e1.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.jaci.2014.11.004
Vancouver
Conti F, Aragão Filho WC, Prando C, Deswarte C, Hubeau M, Newburger PE, Casanova J-L, Bustamante J, Condino-Neto A. Phagocyte nicotinamide adenine dinucleotide phosphate oxidase activity in patients with inherited IFN-γR1 or IFN-γR2 deficiency [Internet]. Journal of Allergy and Clinical Immunology. 2015 ; 135( 5): 1393-1395.e1.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.jaci.2014.11.004
Artigo de periodico
Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry (2015)
Oliveira-Junior, Edgar Borges de; Zurro, Nuria Bengala; Prando, Carolina; Cabral-Marques, Otavio; Pereira, Paulo Vitor Soeiro; Schimke, Lena-Friederick; Klaver, Stefanie; Buzolin, Marcia; Blancas-Galicia, Lizbeth; Santos-Argumedo, Leopoldo; Pietropaolo-Cienfuegos, Dino Roberto; Espinosa-Rosales, Francisco; King, Alejandra; Sorensen, Ricardo; Porras, Oscar; Roxo Junior, Persio; Forte, Wilma Carvalho Neves; Orellana, Julio Cesar; Lozano, Alejandro; Galicchio, Miguel; Regairaz, Lorena; Grumach, Anete Sevciovic; Costa-Carvalho, Beatriz Tavares; Bustamante, Jacinta; Bezrodnik, Liliana; Oleastro, Matias; Danielian, Silvia; Condino Neto, Antonio
Source: Pediatric Blood & Cancer. Unidades: FMRP, ICB
Subjects: GENÉTICA MÉDICA, MUTAÇÃO, INFECÇÕES BACTERIANAS
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ABNT
OLIVEIRA-JUNIOR, Edgar Borges de et al. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, v. 62, n. 12, p. 2101-2107, 2015Tradução . . Disponível em: https://doi.org/10.1002/pbc.25674. Acesso em: 23 ago. 2024.
APA
Oliveira-Junior, E. B. de, Zurro, N. B., Prando, C., Cabral-Marques, O., Pereira, P. V. S., Schimke, L. -F., et al. (2015). Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry. Pediatric Blood & Cancer, 62( 12), 2101-2107. doi:10.1002/pbc.25674
NLM
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo Junior P, Forte WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/pbc.25674
Vancouver
Oliveira-Junior EB de, Zurro NB, Prando C, Cabral-Marques O, Pereira PVS, Schimke L-F, Klaver S, Buzolin M, Blancas-Galicia L, Santos-Argumedo L, Pietropaolo-Cienfuegos DR, Espinosa-Rosales F, King A, Sorensen R, Porras O, Roxo Junior P, Forte WCN, Orellana JC, Lozano A, Galicchio M, Regairaz L, Grumach AS, Costa-Carvalho BT, Bustamante J, Bezrodnik L, Oleastro M, Danielian S, Condino Neto A. Clinical and genotypic spectrum of chronic granulomatous disease in 71 Latin American patients: first report from the LASID registry [Internet]. Pediatric Blood & Cancer. 2015 ; 62( 12): 2101-2107.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1002/pbc.25674
Artigo de periodico
ICON: the early diagnosis of congenital immunodeficiencies (2014)
Routes, John; Abinun, Mario; Al-Herz, Waleed; Bustamante, Jacinta; Condino-Neto, Antonio; De La Morena, Maria Teresa; Etzioni, Amos; Gambineri, Eleonora; Haddad, Elie; Kobrynski, Lisa; Le Deist, Francoise; Nonoyama, Shigeaki; Oliveira, João Bosco; Perez, Elena; Picard, Capucine; Rezaei, Nima; Sleasman, John; Sullivan, Kathleen E.; Torgerson, Troy
Source: Journal of Clinical Immunology. Unidade: ICB
Subjects: IMUNOLOGIA, DOENÇAS CONGÊNITAS
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ABNT
ROUTES, John et al. ICON: the early diagnosis of congenital immunodeficiencies. Journal of Clinical Immunology, v. 34, n. 4, p. 398-424, 2014Tradução . . Disponível em: https://doi.org/10.1007/s10875-014-0003-x. Acesso em: 23 ago. 2024.
APA
Routes, J., Abinun, M., Al-Herz, W., Bustamante, J., Condino-Neto, A., De La Morena, M. T., et al. (2014). ICON: the early diagnosis of congenital immunodeficiencies. Journal of Clinical Immunology, 34( 4), 398-424. doi:10.1007/s10875-014-0003-x
NLM
Routes J, Abinun M, Al-Herz W, Bustamante J, Condino-Neto A, De La Morena MT, Etzioni A, Gambineri E, Haddad E, Kobrynski L, Le Deist F, Nonoyama S, Oliveira JB, Perez E, Picard C, Rezaei N, Sleasman J, Sullivan KE, Torgerson T. ICON: the early diagnosis of congenital immunodeficiencies [Internet]. Journal of Clinical Immunology. 2014 ; 34( 4): 398-424.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1007/s10875-014-0003-x
Vancouver
Routes J, Abinun M, Al-Herz W, Bustamante J, Condino-Neto A, De La Morena MT, Etzioni A, Gambineri E, Haddad E, Kobrynski L, Le Deist F, Nonoyama S, Oliveira JB, Perez E, Picard C, Rezaei N, Sleasman J, Sullivan KE, Torgerson T. ICON: the early diagnosis of congenital immunodeficiencies [Internet]. Journal of Clinical Immunology. 2014 ; 34( 4): 398-424.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1007/s10875-014-0003-x
Artigo de periodico
High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease (2012)
Oliveira-Junior, Edgar Borges de; Prando, Carolina; López, Juan Alvaro; Arango, Julian Camilo; Buzolin, Marcia; Rehder, Jussara; Pedroza, Luis Alberto; Frazão, Josias Brito; Dantas, Vera Maria; Roxo Junior, Persio; Grumach, Anete Sevciovic; Costa-Carvalho, Beatriz Tavares; Bustamante, Jacinta; Condino-Neto, Antonio
Source: Scandinavian Journal of Immunology. Unidades: FMRP, ICB
Subjects: DOENÇAS GENÉTICAS, GRANULOMA, CROMATOGRAFIA LÍQUIDA, MUTAÇÃO GENÉTICA (ANÁLISE)
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ABNT
OLIVEIRA-JUNIOR, Edgar Borges de et al. High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease. Scandinavian Journal of Immunology, v. 76, n. 2, p. 158-166, 2012Tradução . . Disponível em: https://doi.org/10.1111/j.1365-3083.2012.02714.x. Acesso em: 23 ago. 2024.
APA
Oliveira-Junior, E. B. de, Prando, C., López, J. A., Arango, J. C., Buzolin, M., Rehder, J., et al. (2012). High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease. Scandinavian Journal of Immunology, 76( 2), 158-166. doi:10.1111/j.1365-3083.2012.02714.x
NLM
Oliveira-Junior EB de, Prando C, López JA, Arango JC, Buzolin M, Rehder J, Pedroza LA, Frazão JB, Dantas VM, Roxo Junior P, Grumach AS, Costa-Carvalho BT, Bustamante J, Condino-Neto A. High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease [Internet]. Scandinavian Journal of Immunology. 2012 ; 76( 2): 158-166.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1111/j.1365-3083.2012.02714.x
Vancouver
Oliveira-Junior EB de, Prando C, López JA, Arango JC, Buzolin M, Rehder J, Pedroza LA, Frazão JB, Dantas VM, Roxo Junior P, Grumach AS, Costa-Carvalho BT, Bustamante J, Condino-Neto A. High-performance liquid chromatography under partially denaturing conditions (dHPLC) is a fast and cost effective method for screening molecular defects: four novel mutations found in x-linked chronic granulomatous disease [Internet]. Scandinavian Journal of Immunology. 2012 ; 76( 2): 158-166.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1111/j.1365-3083.2012.02714.x
Artigo de periodico
Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease (2011)
Bustamante, Jacinta; Arias, Andres A.; Vogt, Guillaume; Picard, Capucine; Galicia, Lizbeth Blancas; Prando, Carolina; Grant, Audrey V.; Marchal, Christophe C.; Hubeau, Marjorie; Chapgier, Ariane; Beaucoudrey, Ludovic de; Puel, Anne; Feinberg, Jacqueline; Valinetz, Ethan; Jannière, Lucile; Besse, Céline; Boland, Anne; Brisseau, Jean-Marie; Blanche, Stéphane; Lortholary, Olivier; Fieschi, Claire; Emile, Jean-François; Boisson-Dupuis, Stéphanie; Al-Muhsen, Saleh; Woda, Bruce; Newburger, Peter E.; Condino-Neto, Antonio; Dinauer, Mary C.; Abel, Laurent; Casanova, Jean-Laurent
Source: Nature Immunology. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
BUSTAMANTE, Jacinta et al. Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease. Nature Immunology, v. 12, n. 3, p. 213-221, 2011Tradução . . Disponível em: https://doi.org/10.1038/ni.1992. Acesso em: 23 ago. 2024.
APA
Bustamante, J., Arias, A. A., Vogt, G., Picard, C., Galicia, L. B., Prando, C., et al. (2011). Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease. Nature Immunology, 12( 3), 213-221. doi:10.1038/ni.1992
NLM
Bustamante J, Arias AA, Vogt G, Picard C, Galicia LB, Prando C, Grant AV, Marchal CC, Hubeau M, Chapgier A, Beaucoudrey L de, Puel A, Feinberg J, Valinetz E, Jannière L, Besse C, Boland A, Brisseau J-M, Blanche S, Lortholary O, Fieschi C, Emile J-F, Boisson-Dupuis S, Al-Muhsen S, Woda B, Newburger PE, Condino-Neto A, Dinauer MC, Abel L, Casanova J-L. Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease [Internet]. Nature Immunology. 2011 ; 12( 3): 213-221.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1038/ni.1992
Vancouver
Bustamante J, Arias AA, Vogt G, Picard C, Galicia LB, Prando C, Grant AV, Marchal CC, Hubeau M, Chapgier A, Beaucoudrey L de, Puel A, Feinberg J, Valinetz E, Jannière L, Besse C, Boland A, Brisseau J-M, Blanche S, Lortholary O, Fieschi C, Emile J-F, Boisson-Dupuis S, Al-Muhsen S, Woda B, Newburger PE, Condino-Neto A, Dinauer MC, Abel L, Casanova J-L. Germline CYBB mutations that selectively affect macrophages in kindreds with X-linked predisposition to tuberculous mycobacterial disease [Internet]. Nature Immunology. 2011 ; 12( 3): 213-221.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1038/ni.1992
Artigo de periodico
Hematologically important mutations: X-linked chronic granulomatous disease (third update) (2010)
Roos, Dirk; Kuhns, Douglas B.; Maddalena, Anne; Roesler, Joachim; Lopez, Juan Alvaro; Ariga, Tadashi; Avcin, Tadej; Boer, Martin de; Bustamante, Jacinta; Condino Neto, Antonio; Di Matteo, Gigliola; He, Jianxin; Hill, Harry R.; Holland, Steven M.; Kannengiesser, Caroline; Köker, M. Yavuz; Kondratenko, Irina; Leeuwen, Karin van; Malech, Harry L.; Marodi, Lázló; Nunoi, Hiroyuki; Stasia, Marie-José; Ventura, Anna Maria; Witwer, Carl T.; Wolach, Baruch; Gallin, John I.
Source: Blood Cells, Moleculares and Diseases. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
ROOS, Dirk et al. Hematologically important mutations: X-linked chronic granulomatous disease (third update). Blood Cells, Moleculares and Diseases, v. 45, n. 3, p. 246-265, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.bcmd.2010.07.012. Acesso em: 23 ago. 2024.
APA
Roos, D., Kuhns, D. B., Maddalena, A., Roesler, J., Lopez, J. A., Ariga, T., et al. (2010). Hematologically important mutations: X-linked chronic granulomatous disease (third update). Blood Cells, Moleculares and Diseases, 45( 3), 246-265. doi:10.1016/j.bcmd.2010.07.012
NLM
Roos D, Kuhns DB, Maddalena A, Roesler J, Lopez JA, Ariga T, Avcin T, Boer M de, Bustamante J, Condino Neto A, Di Matteo G, He J, Hill HR, Holland SM, Kannengiesser C, Köker MY, Kondratenko I, Leeuwen K van, Malech HL, Marodi L, Nunoi H, Stasia M-J, Ventura AM, Witwer CT, Wolach B, Gallin JI. Hematologically important mutations: X-linked chronic granulomatous disease (third update) [Internet]. Blood Cells, Moleculares and Diseases. 2010 ; 45( 3): 246-265.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.bcmd.2010.07.012
Vancouver
Roos D, Kuhns DB, Maddalena A, Roesler J, Lopez JA, Ariga T, Avcin T, Boer M de, Bustamante J, Condino Neto A, Di Matteo G, He J, Hill HR, Holland SM, Kannengiesser C, Köker MY, Kondratenko I, Leeuwen K van, Malech HL, Marodi L, Nunoi H, Stasia M-J, Ventura AM, Witwer CT, Wolach B, Gallin JI. Hematologically important mutations: X-linked chronic granulomatous disease (third update) [Internet]. Blood Cells, Moleculares and Diseases. 2010 ; 45( 3): 246-265.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1016/j.bcmd.2010.07.012
Trabalho de evento-resumo periodico
The role of nuclear factor kappa B (NF-'kappa'B) and the IL-12/23-IFN-'gama' axis in the activation of the NADPH oxidase system (2009)
Aragão-Filho, Walmir; Moreira, Juliana; Luengo-Blanco, Marcos; Prando, Carolina; Bustamante, Jacinta; Rehder, Jussara; Padden, Carolyn; Casanova, Jean-Laurent; Newburger, Peter E.; Condino-Neto, Antônio
Source: Clinical Immunology. Conference titles: Annual Meeting of Federation of Clinical Immunology Societies - FOCIS. Unidade: ICB
Assunto: IMUNOLOGIA
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ABNT
ARAGÃO-FILHO, Walmir et al. The role of nuclear factor kappa B (NF-'kappa'B) and the IL-12/23-IFN-'gama' axis in the activation of the NADPH oxidase system. Clinical Immunology. San Francisco: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 23 ago. 2024. , 2009
APA
Aragão-Filho, W., Moreira, J., Luengo-Blanco, M., Prando, C., Bustamante, J., Rehder, J., et al. (2009). The role of nuclear factor kappa B (NF-'kappa'B) and the IL-12/23-IFN-'gama' axis in the activation of the NADPH oxidase system. Clinical Immunology. San Francisco: Instituto de Ciências Biomédicas, Universidade de São Paulo.
NLM
Aragão-Filho W, Moreira J, Luengo-Blanco M, Prando C, Bustamante J, Rehder J, Padden C, Casanova J-L, Newburger PE, Condino-Neto A. The role of nuclear factor kappa B (NF-'kappa'B) and the IL-12/23-IFN-'gama' axis in the activation of the NADPH oxidase system. Clinical Immunology. 2009 ; 131[citado 2024 ago. 23 ]
Vancouver
Aragão-Filho W, Moreira J, Luengo-Blanco M, Prando C, Bustamante J, Rehder J, Padden C, Casanova J-L, Newburger PE, Condino-Neto A. The role of nuclear factor kappa B (NF-'kappa'B) and the IL-12/23-IFN-'gama' axis in the activation of the NADPH oxidase system. Clinical Immunology. 2009 ; 131[citado 2024 ago. 23 ]
Trabalho de evento-resumo periodico
Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes (2008)
Luengo, Marcos; Prado, Carolina; Bustamante, Jacinta; Pereira, Paulo Vitor; Aragão-filho, Walmir; Padden, Carolyn; Casanova, Jean-Laurent; Newburger, Peter; Condino Neto, Antonio
Source: Clinical Immunology. Conference titles: Annual Meeting of Federation of Clinical Immunology Societies - FOCIS. Unidade: ICB
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LUENGO, Marcos et al. Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. Orlando: Instituto de Ciências Biomédicas, Universidade de São Paulo. . Acesso em: 23 ago. 2024. , 2008
APA
Luengo, M., Prado, C., Bustamante, J., Pereira, P. V., Aragão-filho, W., Padden, C., et al. (2008). Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. Orlando: Instituto de Ciências Biomédicas, Universidade de São Paulo.
NLM
Luengo M, Prado C, Bustamante J, Pereira PV, Aragão-filho W, Padden C, Casanova J-L, Newburger P, Condino Neto A. Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. 2008 ; 127[citado 2024 ago. 23 ]
Vancouver
Luengo M, Prado C, Bustamante J, Pereira PV, Aragão-filho W, Padden C, Casanova J-L, Newburger P, Condino Neto A. Essential role of nuclear factor-kappa B for NADPH oxidase activity, CYBB and NCF-1 gene expression in normal and anhidrotic ectodermal dysplasia leukocytes. Clinical Immunology. 2008 ; 127[citado 2024 ago. 23 ]
Artigo de periodico
Essential role of nuclear factor-kB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes (2008)
Luengo-Blanco, Marcos; Prando, Carolina; Bustamante, Jacinta; Aragão-Filho, Walmir Cutrim; Pereira, Paulo Vitor Soeiro; Rehder, Jussara; Padden, Carolyn; Casanova, Jean-Laurent; Newburger, Peter E.; Condino-Neto, Antonio
Source: Blood. Unidade: ICB
Assunto: IMUNOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LUENGO-BLANCO, Marcos et al. Essential role of nuclear factor-kB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes. Blood, v. 112, n. 4, p. 1453-1460, 2008Tradução . . Disponível em: https://doi.org/10.1182/blood-2007-07-099267. Acesso em: 23 ago. 2024.
APA
Luengo-Blanco, M., Prando, C., Bustamante, J., Aragão-Filho, W. C., Pereira, P. V. S., Rehder, J., et al. (2008). Essential role of nuclear factor-kB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes. Blood, 112( 4), 1453-1460. doi:10.1182/blood-2007-07-099267
NLM
Luengo-Blanco M, Prando C, Bustamante J, Aragão-Filho WC, Pereira PVS, Rehder J, Padden C, Casanova J-L, Newburger PE, Condino-Neto A. Essential role of nuclear factor-kB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes [Internet]. Blood. 2008 ; 112( 4): 1453-1460.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1182/blood-2007-07-099267
Vancouver
Luengo-Blanco M, Prando C, Bustamante J, Aragão-Filho WC, Pereira PVS, Rehder J, Padden C, Casanova J-L, Newburger PE, Condino-Neto A. Essential role of nuclear factor-kB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes [Internet]. Blood. 2008 ; 112( 4): 1453-1460.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1182/blood-2007-07-099267

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