Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Cristina Camprubí"'
Publikováno v:
Advances in experimental medicine and biology. 1166
Epigenetic information refers to heritable changes in gene expression that occur without modifications at the DNA sequence level. These changes are orchestrated by different epigenetic mechanisms such as DNA methylation, posttranslational modificatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::84d3aa6dc6ac566f538085ea71d706fc
https://pubmed.ncbi.nlm.nih.gov/31301046
https://pubmed.ncbi.nlm.nih.gov/31301046
Autor:
Cristina Camprubí, Joan Blanco
Epigenetics is the study of how certain genes are activated without modification at the DNA sequence level, resulting in genetically similar individuals having different clinical outcomes. As contemporary medicine increasingly aims to personalize the
Publikováno v:
Genetic Damage in Human Spermatozoa ISBN: 9783030216634
Epigenetic information refers to heritable changes in gene expression that occur without modifications at the DNA sequence level. These changes are orchestrated by different epigenetic mechanisms such as DNA methylation, posttranslational modificatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bd0076a8ed6714df8380b53d14822d53
https://doi.org/10.1007/978-3-030-21664-1_4
https://doi.org/10.1007/978-3-030-21664-1_4
Autor:
Joan Blanco, Cristina Camprubí
Publikováno v:
Epigenetics and Assisted Reproduction ISBN: 9781315208701
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98b5fadc1f66bb4bc4fc5af230f80465
https://doi.org/10.1201/9781315208701-8
https://doi.org/10.1201/9781315208701-8
Publikováno v:
Epigenetics and Assisted Reproduction ISBN: 9781315208701
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc8622f9022fb55e06ee0121de000fd8
https://doi.org/10.1201/9781315208701-13
https://doi.org/10.1201/9781315208701-13
Autor:
Albert Salas-Huetos, Riccardo Aiese Cigliano, Cristina Camprubí, Nicolás Garrido, Joan Blanco
Publikováno v:
Epigenomics. 9(10)
Aim: To characterize the sperm methylome in semen samples from 19 donors with proven fertility. Materials & methods: Bisulfite-converted sperm DNA was hybridized on the HumanMethylation450 Infinium BeadChip platform. CpG fluorescence intensities were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c69be633d1fc7dae20161da4dd7f659
https://pubmed.ncbi.nlm.nih.gov/28877596
https://pubmed.ncbi.nlm.nih.gov/28877596
Autor:
Joan Blanco, Cristina Camprubí
Publikováno v:
A Practical Guide to Sperm Analysis ISBN: 9781315151632
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a44cd68096fffdd8e7056b9d983156a3
https://doi.org/10.4324/9781315151632-10
https://doi.org/10.4324/9781315151632-10
Autor:
Montserrat Milà, David Monk, Francisco Martínez, Zeynep Tümer, Marta Sánchez Delgado, Cristina Camprubí
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 165:472-478
The phenotype overlap between autism spectrum disorders (ASD) & intellectual disabilities (ID) is mirrored at the genetic level, with common genes being reported mutated in variety of developmental disabilities. However despite widespread genetic scr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::879c0714f537baf6732e9352aa6dafde
https://doi.org/10.1002/ajmg.b.32250
https://doi.org/10.1002/ajmg.b.32250
Autor:
Cristina Camprubí, Maria Carme Pons, Nicolás Garrido, Joan Blanco, Marta Pladevall, Mark Grossmann
Publikováno v:
Journal of Assisted Reproduction and Genetics. 30:1125-1131
To find out whether the MTHFR rs1801133 polymorphism is a risk factor for male infertility in the Spanish population. To determine if a pattern of sperm DNA hypomethylation at the paternally imprinted loci H19-ICR and/or IG-DMR is related to the MTHF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e94e613a6319ca98c008fbd481d23e9
https://doi.org/10.1007/s10815-013-0013-2
https://doi.org/10.1007/s10815-013-0013-2