Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter (2012)
- Authors:
- USP affiliated authors: SHINOHARA, ELVIRA MARIA GUERRA - FCF ; ZUGAIB, MARCELO - FM ; CARVALHO, MÁRIO HENRIQUE BURLACCHINI DE - FM
- Unidades: FCF; FM
- Subjects: ABORTO ESPONTÂNEO; VITAMINAS
- Language: Inglês
- Imprenta:
- Publisher: International Society of Nutrigenetics/Nutrigenomics (ISNN)
- Publisher place: Chieti
- Date published: 2012
- Source:
- Título do periódico: Abstracts
- Conference titles: Congress of the International Society of Nutrigenetics/Nutrigenomics
-
ABNT
MONTEIRO, Nathalia Sierra et al. Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. 2012, Anais.. Chieti: International Society of Nutrigenetics/Nutrigenomics (ISNN), 2012. . Acesso em: 19 abr. 2024. -
APA
Monteiro, N. S., Britto, J. C., Giusti, K. C. da S., Carvalho, M. H. B. de, Amorim Filho, A., Zugaib, M., & Guerra-Shinohara, E. M. (2012). Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. In Abstracts. Chieti: International Society of Nutrigenetics/Nutrigenomics (ISNN). -
NLM
Monteiro NS, Britto JC, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. Abstracts. 2012 ;[citado 2024 abr. 19 ] -
Vancouver
Monteiro NS, Britto JC, Giusti KC da S, Carvalho MHB de, Amorim Filho A, Zugaib M, Guerra-Shinohara EM. Vitamins levels in women with recurrent miscarriages and dna methylation in ifng gene promoter. Abstracts. 2012 ;[citado 2024 abr. 19 ] - Association between polymorphisms in the transcobalamin II gene (TC2 C. 776C> G and C. TC267C>G) and methylenetetrahydrofolate reductase gene (MTHFR 677C>T) and risk of having recurrent miscarriages
- Frequencies of autoantibodies in women with recurrent pregnancy losses
- The variant of C. 776C>G polymorphism in transcobalamin gene is associatedwith recurrent pregnancy loss
- Polymorphisms in thrombin-activatable fibrinolysis inhibitor and plasminogen activator inhibitor type 1 in women with primary recurrent pregnancy loss
- Association between the polymorphisms MTHFR c. 677C>T and MTHFR c. 1298A>C and haplotypes with recurrent miscarriages
- Frequency of autoantibodies in women with recurrent miscarriage history
- Polymorphisms in antithrombin and protein c genes and their associationwith recurrent pregnancy loss
- Association between polymorphisms in the transcobalamin II gene (TC2 C. 776C> G and C.TC2 67C>G) and methylenetetrahydrofolate reductase gene (MTHFR C. MTHFR 677C>T) and risk of having recurrent miscarriages
- Association between the polymorphisms MTHFR C677T, MTR A2756G and MTRR A66G with recurrent miscarriages
- Association betweem polymorfisms related to hemostasis and the occurence of recurrent miscarriages
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