Zobrazeno 1 - 10
of 13
pro vyhledávání: '"ANTONIETTA PORCO"'
Publikováno v:
Biological Research, Vol 45, Iss 2, Pp 117-130 (2012)
A sample of 58 familial breast cancer patients from Venezuela were screened for germline mutations in the coding sequences and exon-intron boundaries of BRCA1 (MIM no. 113705) and BRCA2 (MIM no. 600185) genes by using conformation-sensitive gel elect
Externí odkaz:
https://doaj.org/article/2719322dec7d4727bdc65e4959c4ca25
Publikováno v:
Biological Research, Vol 41, Iss 3, Pp 349-358 (2008)
Corynebacterium glutamicum is widely used in the industrial production of amino acids. We have found that this bacterium grows exponentially on a mineral médium supplemented with gluconate. Gluconate permease and Gluconokinase are expressed in an in
Externí odkaz:
https://doaj.org/article/7769a532fc664280a5aef7dba94558ab
Autor:
Claret Mata, Carolina Pestana, Mary Lares, Antonietta Porco, María Isabel Giacopini, Sara Brito, Jorge Castro
Publikováno v:
Archivos Latinoamericanos de Nutrición, Vol 66, Iss 3, Pp 201-210
El estrés oxidativo constituye un factor importante en el desarrollo de Enfermedades Cardiovasculares (ECVs) debido a los daños graves que provocan las especies reactivas de oxígeno en las biomoléculas, por lo que el consumo adecuado de vitaminas
Externí odkaz:
https://doaj.org/article/70673de05c7543ff9d2ae630a494b930
Autor:
Carlos Alvarez, Andrea Bullones, María Angélica Medina, Anna Vargas, Antonietta Porco, Juan Carlos Méndez, Carolina Pestana
Aging is an irreversible process that produces the progressive decline of physiological functions favoring the development of cardiovascular complications associated with genetic Risk Alleles (RA). A case-control study using a sample of 90 Venezuelan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2af2508c7d89bfc9ad19d82b6bc83a8
https://doi.org/10.21203/rs.3.rs-2288834/v1
https://doi.org/10.21203/rs.3.rs-2288834/v1
Publikováno v:
Investigacion clinica. 57(4)
The molecular diagnosis of haemophilia A (HA) patients has many benefits including diagnosis confirmation and inhibitor risk development prediction. In female carries of a mutation, the molecular diagnosis allows for genetic counseling and prenatal d
Autor:
Claret, Mata, Carolina, Pestana, Mary, Lares, Antonietta, Porco, Maria Isabel, Giacopini, Sara, Brito, Jorge, Castro
Publikováno v:
Archivos latinoamericanos de nutricion. 66(3)
Oxidative stress is an important risk factor for the development of cardiovascular ciseases (CVD) due to the serious damage caused by reactive oxygen species to biomolecules, thus, adequate intake of vitamins with antioxidant properties could prevent
Publikováno v:
Journal of Basic Microbiology. 41:75-83
The initial steps of gluconate metabolism in E. coli, transport and phosphorylation, occur through duplicate activities. These activities have been included in two systems designated as GntI (main) and GntII (subsidiary), encoded by differently regul
Publikováno v:
Journal of Basic Microbiology. 38:395-404
Within the main system for gluconate utilization in E. coli, the gntT gene (located at the minute 76.4) that encodes a permease, is currently the only element involved in the high affinity transport. In this paper, the nucleotide sequence of the upst
Publikováno v:
Biological Research, Volume: 45, Issue: 2, Pages: 117-130, Published: 2012
Biological Research v.45 n.2 2012
SciELO Chile
CONICYT Chile
instacron:CONICYT
Biological Research, Vol 45, Iss 2, Pp 117-130 (2012)
Biological Research v.45 n.2 2012
SciELO Chile
CONICYT Chile
instacron:CONICYT
Biological Research, Vol 45, Iss 2, Pp 117-130 (2012)
A sample of 58 familial breast cancer patients from Venezuela were screened for germline mutations in the coding sequences and exon-intron boundaries of BRCA1 (MIM no. 113705) and BRCA2 (MIM no. 600185) genes by using conformation-sensitive gel elect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e4666d0b8e4a1b75a6591052a0844e6
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602012000200003&lng=en&tlng=en
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0716-97602012000200003&lng=en&tlng=en
Publikováno v:
Haemophilia.
Haemophilia A is caused by mutations in the gene encoding coagulation factor VIII (FVIII). In severe Haemophilia A (sHA), two inversions are responsible for approximately 50% of the genetic alterations (intron 22 and intron 1 inversions). The other m