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Artigo de periodico
A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster (2014)
Gao, Ge; Vibranovski, Maria ; Zhang, Li; Zheng, Li; Liu, Ming; Zhang, Young E; Li, Xinmin; Zhang, Wenxia; Fan, Qichang; VanKuren, Nicholas W; Long, Manyuan; Wei, Liping
Source: Genome Research. Unidade: IB
Subjects: CROMOSSOMOS SEXUAIS (EVOLUÇÃO), DROSOPHILA, RNA, EXPRESSÃO GÊNICA, GENOMAS
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ABNT
GAO, Ge et al. A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster. Genome Research, v. 24, n. 4, p. 629-638, 2014Tradução . . Disponível em: https://doi.org/10.1101/gr.165837.113. Acesso em: 13 nov. 2024.
APA
Gao, G., Vibranovski, M., Zhang, L., Zheng, L., Liu, M., Zhang, Y. E., et al. (2014). A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster. Genome Research, 24( 4), 629-638. doi:10.1101/gr.165837.113
NLM
Gao G, Vibranovski M, Zhang L, Zheng L, Liu M, Zhang YE, Li X, Zhang W, Fan Q, VanKuren NW, Long M, Wei L. A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster [Internet]. Genome Research. 2014 ; 24( 4): 629-638.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1101/gr.165837.113
Vancouver
Gao G, Vibranovski M, Zhang L, Zheng L, Liu M, Zhang YE, Li X, Zhang W, Fan Q, VanKuren NW, Long M, Wei L. A long-term demasculinization of X-linked intergenic noncoding RNAs in Drosophila melanogaster [Internet]. Genome Research. 2014 ; 24( 4): 629-638.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1101/gr.165837.113
Artigo de periodico
A novel dataset for identifying sex-biased genes in Drosophila (2014)
VanKuren, Nicholas W; Vibranovski, Maria
Source: Journal of Genomics. Unidade: IB
Subjects: EXPRESSÃO GÊNICA, FENÓTIPOS, TESTÍCULO, OVÁRIO, DROSOPHILA
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ABNT
VANKUREN, Nicholas W e VIBRANOVSKI, Maria. A novel dataset for identifying sex-biased genes in Drosophila. Journal of Genomics, v. 2, p. 64-67, 2014Tradução . . Disponível em: https://doi.org/10.7150/jgen.7955. Acesso em: 13 nov. 2024.
APA
VanKuren, N. W., & Vibranovski, M. (2014). A novel dataset for identifying sex-biased genes in Drosophila. Journal of Genomics, 2, 64-67. doi:10.7150/jgen.7955
NLM
VanKuren NW, Vibranovski M. A novel dataset for identifying sex-biased genes in Drosophila [Internet]. Journal of Genomics. 2014 ; 2 64-67.[citado 2024 nov. 13 ] Available from: https://doi.org/10.7150/jgen.7955
Vancouver
VanKuren NW, Vibranovski M. A novel dataset for identifying sex-biased genes in Drosophila [Internet]. Journal of Genomics. 2014 ; 2 64-67.[citado 2024 nov. 13 ] Available from: https://doi.org/10.7150/jgen.7955
Artigo de periodico
New gene evolution: little did we know (2013)
Long, Manyuan; VanKuren, Nicholas W; Chen, Sidi; Vibranovski, Maria
Source: Annual Review of Genetics. Unidade: IB
Subjects: GENÉTICA, POLIMORFISMO, EVOLUÇÃO, GENES
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ABNT
LONG, Manyuan et al. New gene evolution: little did we know. Annual Review of Genetics, v. 47, p. 325-351, 2013Tradução . . Disponível em: https://doi.org/10.1146/annurev-genet-111212-133301. Acesso em: 13 nov. 2024.
APA
Long, M., VanKuren, N. W., Chen, S., & Vibranovski, M. (2013). New gene evolution: little did we know. Annual Review of Genetics, 47, 325-351. doi:10.1146/annurev-genet-111212-133301
NLM
Long M, VanKuren NW, Chen S, Vibranovski M. New gene evolution: little did we know [Internet]. Annual Review of Genetics. 2013 ; 47 325-351.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1146/annurev-genet-111212-133301
Vancouver
Long M, VanKuren NW, Chen S, Vibranovski M. New gene evolution: little did we know [Internet]. Annual Review of Genetics. 2013 ; 47 325-351.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1146/annurev-genet-111212-133301
Artigo de periodico
New genes expressed in human brains: implications for annotating evolving genomes (2012)
Zhang, Yong E; Landback, Patrick; Vibranovski, Maria ; Long, Manyuan
Source: BioEssays. Unidade: IB
Subjects: GENES, CÉREBRO (EVOLUÇÃO), COGNIÇÃO
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ABNT
ZHANG, Yong E et al. New genes expressed in human brains: implications for annotating evolving genomes. BioEssays, v. No 2012, n. 11, p. 982-991, 2012Tradução . . Disponível em: https://doi.org/10.1002/bies.201200008. Acesso em: 13 nov. 2024.
APA
Zhang, Y. E., Landback, P., Vibranovski, M., & Long, M. (2012). New genes expressed in human brains: implications for annotating evolving genomes. BioEssays, No 2012( 11), 982-991. doi:10.1002/bies.201200008
NLM
Zhang YE, Landback P, Vibranovski M, Long M. New genes expressed in human brains: implications for annotating evolving genomes [Internet]. BioEssays. 2012 ; No 2012( 11): 982-991.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/bies.201200008
Vancouver
Zhang YE, Landback P, Vibranovski M, Long M. New genes expressed in human brains: implications for annotating evolving genomes [Internet]. BioEssays. 2012 ; No 2012( 11): 982-991.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/bies.201200008
Artigo de periodico
Segmental dataset and whole body expression data do not support the hypothesis that non-random movement is an intrinsic property of Drosophila retrogenes (2012)
Vibranovski, Maria ; Zhang, Yong E; Kemkemer, Claus; VanKuren, Nicholas W; Lopes, Hedibert F; Karr, Timothy L; Long, Manyuan
Source: BMC Evolutionary Biology. Unidade: IB
Subjects: CROMOSSOMOS SEXUAIS, DROSOPHILA, GENÉTICA
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ABNT
VIBRANOVSKI, Maria et al. Segmental dataset and whole body expression data do not support the hypothesis that non-random movement is an intrinsic property of Drosophila retrogenes. BMC Evolutionary Biology, v. 12, n. 1, p. 169-178, 2012Tradução . . Disponível em: https://doi.org/10.1186/1471-2148-12-169. Acesso em: 13 nov. 2024.
APA
Vibranovski, M., Zhang, Y. E., Kemkemer, C., VanKuren, N. W., Lopes, H. F., Karr, T. L., & Long, M. (2012). Segmental dataset and whole body expression data do not support the hypothesis that non-random movement is an intrinsic property of Drosophila retrogenes. BMC Evolutionary Biology, 12( 1), 169-178. doi:10.1186/1471-2148-12-169
NLM
Vibranovski M, Zhang YE, Kemkemer C, VanKuren NW, Lopes HF, Karr TL, Long M. Segmental dataset and whole body expression data do not support the hypothesis that non-random movement is an intrinsic property of Drosophila retrogenes [Internet]. BMC Evolutionary Biology. 2012 ; 12( 1): 169-178.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1186/1471-2148-12-169
Vancouver
Vibranovski M, Zhang YE, Kemkemer C, VanKuren NW, Lopes HF, Karr TL, Long M. Segmental dataset and whole body expression data do not support the hypothesis that non-random movement is an intrinsic property of Drosophila retrogenes [Internet]. BMC Evolutionary Biology. 2012 ; 12( 1): 169-178.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1186/1471-2148-12-169
Artigo de periodico
Re-analysis of the larval testis data on meiotic sex chromosome inactivation revealed evidence for tissue-specific gene expression related to the drosophila X chromosome (2012)
Vibranovski, Maria ; Zhang, Yong E; Kemkemer, Claus; Lopes, Hedibert F.; Karr, Timothy L.; Long, Manyuan; Lopes, Hedibert F; Timothy L Karr; Manyuan Long
Source: BMC Biology. Unidade: IB
Subjects: CROMOSSOMO X, DROSOPHILA, LARVA
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ABNT
VIBRANOVSKI, Maria et al. Re-analysis of the larval testis data on meiotic sex chromosome inactivation revealed evidence for tissue-specific gene expression related to the drosophila X chromosome. BMC Biology, v. 10, n. Ju 2012, p. 01-13, 2012Tradução . . Disponível em: https://doi.org/10.1186/1741-7007-10-49. Acesso em: 13 nov. 2024.
APA
Vibranovski, M., Zhang, Y. E., Kemkemer, C., Lopes, H. F., Karr, T. L., Long, M., et al. (2012). Re-analysis of the larval testis data on meiotic sex chromosome inactivation revealed evidence for tissue-specific gene expression related to the drosophila X chromosome. BMC Biology, 10( Ju 2012), 01-13. doi:10.1186/1741-7007-10-49
NLM
Vibranovski M, Zhang YE, Kemkemer C, Lopes HF, Karr TL, Long M, Lopes HF, Timothy L Karr, Manyuan Long. Re-analysis of the larval testis data on meiotic sex chromosome inactivation revealed evidence for tissue-specific gene expression related to the drosophila X chromosome [Internet]. BMC Biology. 2012 ;10( Ju 2012): 01-13.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1186/1741-7007-10-49
Vancouver
Vibranovski M, Zhang YE, Kemkemer C, Lopes HF, Karr TL, Long M, Lopes HF, Timothy L Karr, Manyuan Long. Re-analysis of the larval testis data on meiotic sex chromosome inactivation revealed evidence for tissue-specific gene expression related to the drosophila X chromosome [Internet]. BMC Biology. 2012 ;10( Ju 2012): 01-13.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1186/1741-7007-10-49
Artigo de periodico
Reshaping of global gene expression networks and sex-biased gene expression by integration of a young gene (2012)
Chen, Sidi; Ni, Xiaochun; Krinsky, Benjamin H; Zhang, Young E; Vibranovski, Maria ; White, Kevin P; Long, Manyuan
Source: The EMBO Journal. Unidade: IB
Subjects: EXPRESSÃO GÊNICA, GAMETAS, EVOLUÇÃO (GENÉTICA), DROSOPHILA
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ABNT
CHEN, Sidi et al. Reshaping of global gene expression networks and sex-biased gene expression by integration of a young gene. The EMBO Journal, v. 31, n. 12, p. 2798-2809, 2012Tradução . . Disponível em: https://doi.org/10.1038/emboj.2012.108. Acesso em: 13 nov. 2024.
APA
Chen, S., Ni, X., Krinsky, B. H., Zhang, Y. E., Vibranovski, M., White, K. P., & Long, M. (2012). Reshaping of global gene expression networks and sex-biased gene expression by integration of a young gene. The EMBO Journal, 31( 12), 2798-2809. doi:10.1038/emboj.2012.108
NLM
Chen S, Ni X, Krinsky BH, Zhang YE, Vibranovski M, White KP, Long M. Reshaping of global gene expression networks and sex-biased gene expression by integration of a young gene [Internet]. The EMBO Journal. 2012 ; 31( 12): 2798-2809.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/emboj.2012.108
Vancouver
Chen S, Ni X, Krinsky BH, Zhang YE, Vibranovski M, White KP, Long M. Reshaping of global gene expression networks and sex-biased gene expression by integration of a young gene [Internet]. The EMBO Journal. 2012 ; 31( 12): 2798-2809.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1038/emboj.2012.108
Artigo de periodico
Retrogenes moved out of the Z chromosome in the cilkworm (2012)
Wang, Jun; Long, Manyuan; Vibranovski, Maria
Source: Journal of Molecular Evolution. Unidades: FMRP, IB
Subjects: CROMOSSOMOS, EXPRESSÃO GÊNICA, GENÉTICA
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ABNT
WANG, Jun e LONG, Manyuan e VIBRANOVSKI, Maria. Retrogenes moved out of the Z chromosome in the cilkworm. Journal of Molecular Evolution, v. 74, n. 3-4, p. 113-126, 2012Tradução . . Disponível em: https://doi.org/10.1007/s00239-012-9499-y. Acesso em: 13 nov. 2024.
APA
Wang, J., Long, M., & Vibranovski, M. (2012). Retrogenes moved out of the Z chromosome in the cilkworm. Journal of Molecular Evolution, 74( 3-4), 113-126. doi:10.1007/s00239-012-9499-y
NLM
Wang J, Long M, Vibranovski M. Retrogenes moved out of the Z chromosome in the cilkworm [Internet]. Journal of Molecular Evolution. 2012 ; 74( 3-4): 113-126.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s00239-012-9499-y
Vancouver
Wang J, Long M, Vibranovski M. Retrogenes moved out of the Z chromosome in the cilkworm [Internet]. Journal of Molecular Evolution. 2012 ; 74( 3-4): 113-126.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1007/s00239-012-9499-y
Artigo de periodico
Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies (2010)
Miller, David T.; Adam, Margaret P.; Aradhya, Swaroop; Biesecker, Leslie G.; Brothman, Arthur R.; Carter, Nigel P; Church, Deanna M.; Crolla, John, A; Eichler, E.; Epstein, Charles J; Faucett, W. Andrew; Feuk, Lars; Friedman, Jan M; Hamosh, Ada; Jackson, Laird; Kaminsky, Erin B.; Kok, Klaas; Krantz, Ian D.; Kuhn, Robert H; Lee, Charles; Ostell, James M.; Rosenberg, Carla ; Scherer, Stephen W; Spinner, Nancy B.; Stavropoulos, Dimitri J.; Tepperberg, James H.; Thorland, Erik C.; Vermeesch, Joris R; Waggoner, Darrel J.; Watson, Michael S.; Martin, Christa Lese; Ledbetter, David H.
Source: The American Journal of Human Genetics. Unidade: IB
Subjects: DOENÇAS GENÉTICAS, DIAGNÓSTICO CLÍNICO
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ABNT
MILLER, David T. et al. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, v. 86 n. 5, p. 749-764, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2010.04.006. Acesso em: 13 nov. 2024.
APA
Miller, D. T., Adam, M. P., Aradhya, S., Biesecker, L. G., Brothman, A. R., Carter, N. P., et al. (2010). Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. The American Journal of Human Genetics, 86 n. 5, 749-764. doi:10.1016/j.ajhg.2010.04.006
NLM
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006
Vancouver
Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla J, Eichler E, Epstein CJ, Faucett WA, Feuk L, Friedman JM, Hamosh A, Jackson L, Kaminsky EB, Kok K, Krantz ID, Kuhn RH, Lee C, Ostell JM, Rosenberg C, Scherer SW, Spinner NB, Stavropoulos DJ, Tepperberg JH, Thorland EC, Vermeesch JR, Waggoner DJ, Watson MS, Martin CL, Ledbetter DH. Consensus Statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies [Internet]. The American Journal of Human Genetics. 2010 ; 86 n. 5 749-764.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1016/j.ajhg.2010.04.006
Artigo de periodico
Mutations in the Caveolin-3 gene: when are they pathogenic? (2001)
Paula, Flavia de; Vainzof, Mariz ; Bernardino, Andréa L. F.; McNally, Elizabeth; Kunkel, Louis M; Zatz, Mayana
Source: American Journal of Medical Genetics. Unidade: IB
Subjects: GENÉTICA MÉDICA, DISTROFIA MUSCULAR
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ABNT
PAULA, Flavia de et al. Mutations in the Caveolin-3 gene: when are they pathogenic?. American Journal of Medical Genetics, v. 99, p. 303-307, 2001Tradução . . Disponível em: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o. Acesso em: 13 nov. 2024.
APA
Paula, F. de, Vainzof, M., Bernardino, A. L. F., McNally, E., Kunkel, L. M., & Zatz, M. (2001). Mutations in the Caveolin-3 gene: when are they pathogenic? American Journal of Medical Genetics, 99, 303-307. doi:10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
NLM
Paula F de, Vainzof M, Bernardino ALF, McNally E, Kunkel LM, Zatz M. Mutations in the Caveolin-3 gene: when are they pathogenic? [Internet]. American Journal of Medical Genetics. 2001 ; 99 303-307.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
Vancouver
Paula F de, Vainzof M, Bernardino ALF, McNally E, Kunkel LM, Zatz M. Mutations in the Caveolin-3 gene: when are they pathogenic? [Internet]. American Journal of Medical Genetics. 2001 ; 99 303-307.[citado 2024 nov. 13 ] Available from: https://doi.org/10.1002/1096-8628(2001)9999:9999%3C::aid-ajmg1168%3E3.0.co;2-o
Trabalho de evento-resumo periodico
Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients (1999)
Paula, F de; Vainzof, Mariz ; McNally, E E; Kunkel, L M; Zatz, Mayana
Source: American Journal of Human Genetics. Conference titles: American Society of Human Genetics. Unidade: IB
Assunto: GENÉTICA MÉDICA
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ABNT
PAULA, F de et al. Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo. . Acesso em: 13 nov. 2024. , 1999
APA
Paula, F. de, Vainzof, M., McNally, E. E., Kunkel, L. M., & Zatz, M. (1999). Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. San Francisco: Instituto de Biociências, Universidade de São Paulo.
NLM
Paula F de, Vainzof M, McNally EE, Kunkel LM, Zatz M. Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 nov. 13 ]
Vancouver
Paula F de, Vainzof M, McNally EE, Kunkel LM, Zatz M. Screening of mutations in the Caveolin-3 gene in brazilian limb-girdle muscular dystrophy patients. American Journal of Human Genetics. 1999 ; 65( 4):[citado 2024 nov. 13 ]

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