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Artigo de periodico
Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients (2011)
Mitne Neto, Miguel; Costa, Marcela Machado; Marchetto, Maria C. N; Bengtson, Mário Henrique; Joazeiro, Claudio A; Tsuda, Hiroshi; Bellen, Hugo J.; Silva, Helga A. C.; Oliveira, Acary Souza Bulle; Lazar, Monize; Muotri, Alysson Renato; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: IB
Subjects: DOENÇAS NEUROMUSCULARES, CÉLULAS-TRONCO
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ABNT
MITNE NETO, Miguel et al. Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients. Human Molecular Genetics, v. 20, n. 18, p. 3642-3652, 2011Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddr284. Acesso em: 07 set. 2024.
APA
Mitne Neto, M., Costa, M. M., Marchetto, M. C. N., Bengtson, M. H., Joazeiro, C. A., Tsuda, H., et al. (2011). Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients. Human Molecular Genetics, 20( 18), 3642-3652. doi:10.1093/hmg/ddr284
NLM
Mitne Neto M, Costa MM, Marchetto MCN, Bengtson MH, Joazeiro CA, Tsuda H, Bellen HJ, Silva HAC, Oliveira ASB, Lazar M, Muotri AR, Zatz M. Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients [Internet]. Human Molecular Genetics. 2011 ; 20( 18): 3642-3652.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/ddr284
Vancouver
Mitne Neto M, Costa MM, Marchetto MCN, Bengtson MH, Joazeiro CA, Tsuda H, Bellen HJ, Silva HAC, Oliveira ASB, Lazar M, Muotri AR, Zatz M. Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients [Internet]. Human Molecular Genetics. 2011 ; 20( 18): 3642-3652.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/ddr284
Artigo de periodico
Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching (2009)
Carvalho, Cláudia M. B.; Zhang, Feng; Liu, Pengfei; Patel, Ankita; Sahoo, Trilochan; Bacino, Carlos A.; Shaw, Chad; Peacock, Sandra; Pursley, Amber; Tavyev, Y. Jane; Ramocki, Melissa B.; Nawara, Magdalena; Obersztyn, Ewa; Vianna-Morgante, Angela M ; Stankiewicz, Pawel; Zoghbi, Huda Y.; Cheung, Sau Wai; Lupski, James R.
Source: Human Molecular Genetics. Unidade: IB
Subjects: RETARDO MENTAL, GENOMAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Cláudia M. B. et al. Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching. Human Molecular Genetics, v. 18, n. 12, p. 2188-2203, 2009Tradução . . Disponível em: https://doi.org/10.1093/hmg/ddp151. Acesso em: 07 set. 2024.
APA
Carvalho, C. M. B., Zhang, F., Liu, P., Patel, A., Sahoo, T., Bacino, C. A., et al. (2009). Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching. Human Molecular Genetics, 18( 12), 2188-2203. doi:10.1093/hmg/ddp151
NLM
Carvalho CMB, Zhang F, Liu P, Patel A, Sahoo T, Bacino CA, Shaw C, Peacock S, Pursley A, Tavyev YJ, Ramocki MB, Nawara M, Obersztyn E, Vianna-Morgante AM, Stankiewicz P, Zoghbi HY, Cheung SW, Lupski JR. Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching [Internet]. Human Molecular Genetics. 2009 ; 18( 12): 2188-2203.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/ddp151
Vancouver
Carvalho CMB, Zhang F, Liu P, Patel A, Sahoo T, Bacino CA, Shaw C, Peacock S, Pursley A, Tavyev YJ, Ramocki MB, Nawara M, Obersztyn E, Vianna-Morgante AM, Stankiewicz P, Zoghbi HY, Cheung SW, Lupski JR. Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching [Internet]. Human Molecular Genetics. 2009 ; 18( 12): 2188-2203.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/ddp151
Artigo de periodico
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome) (2000)
Sertié, Andréa Laurato; Sossi, Vittorio; Camargo, Ana Maria A; Zatz, Mayana ; Brahe, Christina; Passos-Bueno, Maria Rita
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERTIÉ, Andréa Laurato et al. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics, v. 9, n. 13, p. 2051-2058, 2000Tradução . . Acesso em: 07 set. 2024.
APA
Sertié, A. L., Sossi, V., Camargo, A. M. A., Zatz, M., Brahe, C., & Passos-Bueno, M. R. (2000). Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics, 9( 13), 2051-2058.
NLM
Sertié AL, Sossi V, Camargo AMA, Zatz M, Brahe C, Passos-Bueno MR. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics. 2000 ; 9( 13): 2051-2058.[citado 2024 set. 07 ]
Vancouver
Sertié AL, Sossi V, Camargo AMA, Zatz M, Brahe C, Passos-Bueno MR. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Human Molecular Genetics. 2000 ; 9( 13): 2051-2058.[citado 2024 set. 07 ]
Artigo de periodico
Caveolin-3 in muscular dystrophy (1998)
McNally, Elizabeth M; Moreira, Eloísa de Sá; Duggan, David J; Bönnemann, Carsten G; Lisanti, Michael P; Lidov, Hart G W; Vainzof, Mariz ; Passos-Bueno, Maria Rita ; Hoffman, Eric P; Zatz, Mayana ; Kunkel, Louis M
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MCNALLY, Elizabeth M et al. Caveolin-3 in muscular dystrophy. Human Molecular Genetics, v. 7, n. 5, p. 871-877, 1998Tradução . . Disponível em: https://doi.org/10.1093/hmg/7.5.871. Acesso em: 07 set. 2024.
APA
McNally, E. M., Moreira, E. de S., Duggan, D. J., Bönnemann, C. G., Lisanti, M. P., Lidov, H. G. W., et al. (1998). Caveolin-3 in muscular dystrophy. Human Molecular Genetics, 7( 5), 871-877. doi:10.1093/hmg/7.5.871
NLM
McNally EM, Moreira E de S, Duggan DJ, Bönnemann CG, Lisanti MP, Lidov HGW, Vainzof M, Passos-Bueno MR, Hoffman EP, Zatz M, Kunkel LM. Caveolin-3 in muscular dystrophy [Internet]. Human Molecular Genetics. 1998 ; 7( 5): 871-877.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/7.5.871
Vancouver
McNally EM, Moreira E de S, Duggan DJ, Bönnemann CG, Lisanti MP, Lidov HGW, Vainzof M, Passos-Bueno MR, Hoffman EP, Zatz M, Kunkel LM. Caveolin-3 in muscular dystrophy [Internet]. Human Molecular Genetics. 1998 ; 7( 5): 871-877.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/7.5.871
Artigo de periodico
Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD (1996)
Passos-Bueno, Maria Rita ; Moreira, E S; Vainzof, Mariz ; Marie, Suely Kazue Nagahashi; Zatz, Mayana
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD. Human Molecular Genetics, v. 5, n. 6, p. 815-820, 1996Tradução . . Disponível em: https://doi.org/10.1093/hmg/5.6.815. Acesso em: 07 set. 2024.
APA
Passos-Bueno, M. R., Moreira, E. S., Vainzof, M., Marie, S. K. N., & Zatz, M. (1996). Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD. Human Molecular Genetics, 5( 6), 815-820. doi:10.1093/hmg/5.6.815
NLM
Passos-Bueno MR, Moreira ES, Vainzof M, Marie SKN, Zatz M. Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD [Internet]. Human Molecular Genetics. 1996 ; 5( 6): 815-820.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/5.6.815
Vancouver
Passos-Bueno MR, Moreira ES, Vainzof M, Marie SKN, Zatz M. Linkage analysis in autosomal recessive limb-girdle muscular dystrophy (AR LGMD) maps a sixth form to 5q33-34 (LGMD2F) and indicates that there is at least one more subtype of AR LGMD [Internet]. Human Molecular Genetics. 1996 ; 5( 6): 815-820.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/5.6.815
Artigo de periodico
A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 (1996)
Sertié, A L; Quimby, M; Moreira, E S; Murray, J; Zatz, Mayana ; Antonarakis, S E; Passos-Bueno, Maria Rita
Source: Human Molecular Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SERTIÉ, A L et al. A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. Human Molecular Genetics, v. 5, n. 6, p. 843-847, 1996Tradução . . Disponível em: https://doi.org/10.1093/hmg/5.6.843. Acesso em: 07 set. 2024.
APA
Sertié, A. L., Quimby, M., Moreira, E. S., Murray, J., Zatz, M., Antonarakis, S. E., & Passos-Bueno, M. R. (1996). A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3. Human Molecular Genetics, 5( 6), 843-847. doi:10.1093/hmg/5.6.843
NLM
Sertié AL, Quimby M, Moreira ES, Murray J, Zatz M, Antonarakis SE, Passos-Bueno MR. A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 [Internet]. Human Molecular Genetics. 1996 ; 5( 6): 843-847.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/5.6.843
Vancouver
Sertié AL, Quimby M, Moreira ES, Murray J, Zatz M, Antonarakis SE, Passos-Bueno MR. A gene wich causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 [Internet]. Human Molecular Genetics. 1996 ; 5( 6): 843-847.[citado 2024 set. 07 ] Available from: https://doi.org/10.1093/hmg/5.6.843

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