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Registro Completo |
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Biblioteca(s): |
Embrapa Café. |
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Data corrente: |
10/01/2018 |
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Data da última atualização: |
10/01/2018 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
KIWUKA, C.; GOUDSMIT, E.; TOURNEBIZE, R.; BELLANGER, L.; CROUZILLAT, D.; KIGGUNDU, A.; ANTEN, N.; ANDRADE, A. C.; KOCHKO, A.; MUSOLI, P.; PONCET, V. |
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Afiliação: |
Catherine Kiwuka; Eva Goudsmit; Rémi Tournebize; Laurence Bellanger; Dominique Crouzillat; Andrew Kiggundu; Niels Anten; ALAN CARVALHO ANDRADE, SAPC; Alexandre Kochko; Pascal Musoli; Valérie Poncet. |
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Título: |
Genetic characterization and relationships of Uganda wild, feral and cultivated Coffea canephora (Robusta) for future sustainable use. |
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Ano de publicação: |
2017 |
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Fonte/Imprenta: |
In: EUCARPIA GENETIC RESOURCES, 2017, Montpellier, France. Abstracts book... Montpellier, France: INRA, 2017. |
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Idioma: |
Inglês |
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Conteúdo: |
The ability of crops to adapt to environmental changes such as the predicted climate change strongly depends on the genetic variation that exists within the crops. |
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Thesagro: |
Coffea Canephora. |
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Thesaurus Nal: |
Climate change; Genetic variation; Genotype. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/170766/1/Genetic-characterization-and-relationships-of-Ugandan-wild.pdf
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Marc: |
LEADER 01039nam a2200277 a 4500
001 2084899
005 2018-01-10
008 2017 bl uuuu u00u1 u #d
100 1 $aKIWUKA, C.
245 $aGenetic characterization and relationships of Uganda wild, feral and cultivated Coffea canephora (Robusta) for future sustainable use.$h[electronic resource]
260 $aIn: EUCARPIA GENETIC RESOURCES, 2017, Montpellier, France. Abstracts book... Montpellier, France: INRA$c2017
520 $aThe ability of crops to adapt to environmental changes such as the predicted climate change strongly depends on the genetic variation that exists within the crops.
650 $aClimate change
650 $aGenetic variation
650 $aGenotype
650 $aCoffea Canephora
700 1 $aGOUDSMIT, E.
700 1 $aTOURNEBIZE, R.
700 1 $aBELLANGER, L.
700 1 $aCROUZILLAT, D.
700 1 $aKIGGUNDU, A.
700 1 $aANTEN, N.
700 1 $aANDRADE, A. C.
700 1 $aKOCHKO, A.
700 1 $aMUSOLI, P.
700 1 $aPONCET, V.
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Registro original: |
Embrapa Café (CNPCa) |
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Registro Completo
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Biblioteca(s): |
Embrapa Gado de Leite. |
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Data corrente: |
18/03/2011 |
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Data da última atualização: |
23/01/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
B - 1 |
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Autoria: |
FURTADO, C. L. M.; SILVA, P. V.; GUIMARAES, M. F. M.; SERÃO, N. V. L.; GUIMARÃES, J. D.; GUIMARÃES, S. E. F. |
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Afiliação: |
CRISTIANA LIBARDI MIRANDA FURTADO, UFV; PRISCILA VENDRAMINI SILVA, UFV; MARTA FONSECA MARTINS GUIMARAES, CNPGL; NICOLA VERGARA LOPES SERÃO, UFV; JOSÉ DOMINGOS GUIMARÃES, UFV; SIMONE ELIZA FACIONI GUIMARÃES, UFV. |
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Título: |
Differential expression of genes in follicular cells of swines. |
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Ano de publicação: |
2010 |
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Fonte/Imprenta: |
Revista Brasileira de Zootecnia, v. 39,n. 5, p. p.1023-1028, 2010. |
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DOI: |
https://doi.org/10.1590/S1516-35982010000500012 |
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Idioma: |
Inglês |
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Conteúdo: |
The main purpose of the present study was to identify for candidate genes related to ovulation in swines. To do so, it was investigated in ovarian follicular cells through quantitative real-time PCR the differential expression of the following genes: steroidogenic acute regulator (STAR), GATA-binding protein 4 (GATA), prostaglandin F2α (PGF2α), progesterone receptor (P4R), follicle-stimulating hormone receptor (FSHR), and cytochrome P450 aromatase (CYP19). These genes encode hormone receptors (FSHR and P4R), hormone (PGF2α), steroidogenic proteins (STAR and CYP19) and transcription factor (GATA). Folicular cells were collected from sows with high and low number of piglets/litters during the follicular phase of the estrus cycle. There was difference in transcript abundance among low and high prolific sows for the STAR, GATA, PGF2α, P4R and CYP19 genes. For the FSHR gene, the fold change was not considered to be significantly different. Because in the present study only the transcript level of the above mentioned genes was analyzed, no inference can be made regarded to protein translation or activity. Therefore, gene sequence trials and other functional studies will be necessary to complement the present results, allowing a better understanding on biological complexity of these genes and their use as markers for prolificity in swines. |
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Palavras-Chave: |
Genes candidatos; PCR quantitativo em tempo real; Produção de suínos; Tamanho de leitegada. |
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Thesagro: |
Ovulação. |
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Categoria do assunto: |
L Ciência Animal e Produtos de Origem Animal |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/881526/1/Differential-expression-of-genes-in-follicular-cells-of-swines.pdf
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Marc: |
LEADER 02174naa a2200253 a 4500
001 1881526
005 2023-01-23
008 2010 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1590/S1516-35982010000500012$2DOI
100 1 $aFURTADO, C. L. M.
245 $aDifferential expression of genes in follicular cells of swines.$h[electronic resource]
260 $c2010
520 $aThe main purpose of the present study was to identify for candidate genes related to ovulation in swines. To do so, it was investigated in ovarian follicular cells through quantitative real-time PCR the differential expression of the following genes: steroidogenic acute regulator (STAR), GATA-binding protein 4 (GATA), prostaglandin F2α (PGF2α), progesterone receptor (P4R), follicle-stimulating hormone receptor (FSHR), and cytochrome P450 aromatase (CYP19). These genes encode hormone receptors (FSHR and P4R), hormone (PGF2α), steroidogenic proteins (STAR and CYP19) and transcription factor (GATA). Folicular cells were collected from sows with high and low number of piglets/litters during the follicular phase of the estrus cycle. There was difference in transcript abundance among low and high prolific sows for the STAR, GATA, PGF2α, P4R and CYP19 genes. For the FSHR gene, the fold change was not considered to be significantly different. Because in the present study only the transcript level of the above mentioned genes was analyzed, no inference can be made regarded to protein translation or activity. Therefore, gene sequence trials and other functional studies will be necessary to complement the present results, allowing a better understanding on biological complexity of these genes and their use as markers for prolificity in swines.
650 $aOvulação
653 $aGenes candidatos
653 $aPCR quantitativo em tempo real
653 $aProdução de suínos
653 $aTamanho de leitegada
700 1 $aSILVA, P. V.
700 1 $aGUIMARAES, M. F. M.
700 1 $aSERÃO, N. V. L.
700 1 $aGUIMARÃES, J. D.
700 1 $aGUIMARÃES, S. E. F.
773 $tRevista Brasileira de Zootecnia$gv. 39,n. 5, p. p.1023-1028, 2010.
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Embrapa Gado de Leite (CNPGL) |
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