Výsledky vyhledávání - "Preimplantation Diagnosis/methods"

Genome-wide haplotyping embryos developing from 0PN and 1PN zygotes increases transferrable embryos in PGT-M

Autor: Masoud Zamani Esteki, Eric Legius, Cindy Melotte, Thomy de Ravel, Karen Peeraer, Joris Vermeesch, Christel Meuleman, Thiery Voet, Eftychia Dimitriadou, Ellen Denayer, Jia Ding, Sophie Debrock, Aspasia Destouni, Heleen Masset, Kris Van Den Bogaert

Publikováno v: Human Reproduction, 33(12), 2302-2311. Oxford University Press
Human Reproduction (Oxford, England)
Human Reproduction

STUDY QUESTION: Can genome-wide haplotyping increase success following preimplantation genetic testing for a monogenic disorder (PGT-M) by including zygotes with absence of pronuclei (0PN) or the presence of only one pronucleus (1PN)? SUMMARY ANSWER:

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::852ee978305a2b6db1dd6979d88de266
https://doi.org/10.1093/humrep/dey325

Zobrazit plný text záznamu

Estimation of age-dependent decrease in blastocyst euploidy by next generation sequencing:development of a novel prediction model

Autor: Sandro C, Esteves, José F, Carvalho, Ciro D, Martinhago, Augusto A, Melo, Fabiola C, Bento, Peter, Humaidan, Carlo, Alviggi

Publikováno v: Esteves, S C, Carvalho, J F, Martinhago, C D, Melo, A A, Bento, F C, Humaidan, P, Alviggi, C & POSEIDON (Patient-Oriented Strategies Encompassing IndividualizeD Oocyte Number) Group 2019, ' Estimation of age-dependent decrease in blastocyst euploidy by next generation sequencing : development of a novel prediction model ', Panminerva medica, vol. 61, no. 1, pp. 3-10 . https://doi.org/10.23736/S0031-0808.18.03507-3

BACKGROUND: We developed a model to estimate the female age-dependent decrease in blastocyst euploidy and the impact of blastocyst cohort size on the likelihood of having at least one euploid blastocyst for transfer.METHODS: Retrospective analysis of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f02f21e475ea79c1160034cac9008d
https://pure.au.dk/portal/da/publications/estimation-of-agedependent-decrease-in-blastocyst-euploidy-by-next-generation-sequencing(ffdf8c07-38f3-4e0c-8b3a-efb328a9d0e9).html

Zobrazit plný text záznamu

Gonadotropin Releasing Hormone Agonists or Antagonists for Preimplantation Genetic Diagnosis (PGD)? A Prospective Randomised Trial

Autor: M. De Vos, Christophe Blockeel, A. De Vos, H. Tournaye, Catherine Staessen, Veerle Vloeberghs, S Parikh, W. Verpoest, M. De Rycke

Publikováno v: Current Pharmaceutical Biotechnology. 18

Background: The use of GnRH analogue medication is essential in reproductive medicine to avoid premature ovulation by pituitary suppression for the duration of ovarian stimulation by gonadotrophins. The type of pituitary suppression by either GnRH ag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::326909dab6fa969dbfd0e2bf3144160c
https://doi.org/10.2174/1389201018666170808130526

Zobrazit plný text záznamu

Introduction en Suisse des analyses sur le patrimoine génétique de l'embryon : progrès ou dérive ?

Autor: Irion Fournet, Nicole, Irion, Olivier

Publikováno v: Revue médicale suisse, Vol. 12, No 500 (2016) pp. 39-43

The Swiss law on Assisted Reproductive Techniques (LPMA) has been modified in order to authorize preimplantation genetic diagnosis (PGD). PGD has been performed for 20 years. Switzerland is one of the last european countries where it is still prohibi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______1400::df10aff0f2cd67825a3563842adae672
https://archive-ouverte.unige.ch/unige:98798

Zobrazit plný text záznamu

Non-invasive pre-implantation genetic diagnosis of X-linked disorders

Autor: Safia El Messaoudi, Ounissa Aït-Ahmed, Alain R. Thierry, Said Assou, Samir Hamamah

Publikováno v: Medical Hypotheses
Medical Hypotheses, Elsevier, 2014, 83, pp.506--8. ⟨10.1016/j.mehy.2014.08.019⟩

Pre-implantation genetic diagnosis (PGD) is a powerful clinical tool to identify embryos with or at risk of specific genetic diseases before implantation in utero after in vitro fertilization (IVF). PGD is performed on embryo biopsies that are obtain

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41b2e99a1844884284c385247dc19c52
https://hal.umontpellier.fr/hal-02181365

Zobrazit plný text záznamu

Novel universal approach for preimplantation genetic diagnosis of beta-thalassaemia in combination with HLA matching of embryos

Autor: Van de Velde, H., Georgiou, I., De Rycke, M., Schots, R., Sermon, K., Lissens, W., Devroey, P., Van Steirteghem, A., Liebaers, I.

BACKGROUND: Beta-Thalassaemia results from co-inheritance of two mutant beta-globin alleles. Allogeneic cord blood cell transplantation (CBT) from an HLA-identical sibling donor is an excellent treatment option for beta-thalassaemia. In families with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10561::b726636e0bcef62e7874b50e5251c6fe
http://olympias.lib.uoi.gr/jspui/handle/123456789/19692

Zobrazit plný text záznamu

Two pregnancies after preimplantation genetic diagnosis for osteogenesis imperfecta type I and type IV

Autor: Hubert Joris, Anne De Paepe, Hilde Van De Velde, Andre Van Steirteghem, Willy Lissens, Inge Liebaers, Anick De Vos, M. Vandervorst, Karen Sermon

Publikováno v: Human genetics. 106(6)

Osteogenesis imperfecta (OI) is an autosomal dominant genetic disorder characterized by the presence of brittle bones and decreased bone mass (osteopenia), as a result of mutations in the genes that encode the chains of type I collagen, the major pro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87993724abbb917d636bcb5d36df0c6a
https://pubmed.ncbi.nlm.nih.gov/10942108

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání