Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Beatrice Mandon-Pepin"'
Autor:
Panagiotis Filis, Natasha Walker, Linda Robertson, Emily Eaton-Turner, Lauma Ramona, Michelle Bellingham, Maria R. Amezaga, Zulin Zhang, Beatrice Mandon-Pepin, Neil P. Evans, Richard M. Sharpe, Corinne Cotinot, William D. Rees, Peter O'Shaughnessy, Paul A. Fowler
Publikováno v:
Environment International, Vol 124, Iss , Pp 98-108 (2019)
Background: The increased incidence of diseases, including metabolic syndrome and infertility, may be related to exposure to the mixture of chemicals, which are ubiquitous in the modern environment (environmental chemicals, ECs). Xeno-detoxification
Externí odkaz:
https://doaj.org/article/adc6986ef00a48638d8c496636f10498
Publikováno v:
PLoS ONE, Vol 10, Iss 11, p e0141482 (2015)
The successful achievement of early ovarian folliculogenesis is important for fertility and reproductive life span. This complex biological process requires the appropriate expression of numerous genes at each developmental stage, in each follicular
Externí odkaz:
https://doaj.org/article/248e4b96dad447d5992dc5efd9861471
Autor:
Eloïse Airaud, Aurélie Dewaele, Laurent Boulanger, Nathalie Daniel-Carlier, Frank Giton, Beatrice Mandon-Pepin, Maëlle Pannetier, Geneviève Jolivet, Cloé Pierson, Eric Pailhoux, Erwana Harscoët, Nathalie Daniel
Publikováno v:
Endocrinology
Endocrinology, Endocrine Society, 2021, ⟨10.1210/endocr/bqab210⟩
{date}
Endocrinology, Endocrine Society, 2022, 163 (1), ⟨10.1210/endocr/bqab210⟩
Endocrinology, Endocrine Society, 2021, ⟨10.1210/endocr/bqab210⟩
{date}
Endocrinology, Endocrine Society, 2022, 163 (1), ⟨10.1210/endocr/bqab210⟩
AROMATASE, encoded by the CYP19A1 gene, is the cytochrome enzyme responsible for the synthesis of estrogens in vertebrates. In most mammals a peak of expression of the CYP19A1 gene occurs in the fetal XX gonad when sexual differentiation starts up. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1760ab13fbb6a1ccd6d064555bd50a2e
https://hal.archives-ouvertes.fr/hal-03370216
https://hal.archives-ouvertes.fr/hal-03370216
Autor:
Eli Sellem, Elodie Poumerol, Luc Jouneau, Bruno Passet, Eric Pailhoux, Beatrice Mandon-Pepin, Johan Castille, Manon Chadourne
Publikováno v:
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology, Frontiers media, 2021, 9, ⟨10.3389/fcell.2021.700290⟩
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Frontiers in Cell and Developmental Biology, Frontiers media, 2021, 9, ⟨10.3389/fcell.2021.700290⟩
Frontiers in Cell and Developmental Biology, Vol 9 (2021)
Spermatogenesis involves coordinated processes, including meiosis, to produce functional gametes. We previously reportedTopaz1as a germ cell-specific gene highly conserved in vertebrates.Topaz1knockout males are sterile with testes that lack haploid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d2b003def38bb667238fb11da42becc
https://hal.inrae.fr/hal-03281905
https://hal.inrae.fr/hal-03281905
Autor:
Eli Sellem, Bruno Passet, Manon Chadourne, Elodie Poumerol, Johan Castille, Eric Pailhoux, Beatrice Mandon-Pepin, Luc Jouneau
Spermatogenesis comprises a coordinated process, including meiosis, to produce fertile male gametes. Previous study reported that Topaz1 is a germ cell specific gene highly conserved in vertebrates. Topaz1 knockout male mice are sterile. The mutant t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7a3da79064f93b2c229ec20fea0902b
https://doi.org/10.1101/2021.03.09.434544
https://doi.org/10.1101/2021.03.09.434544
Autor:
François Vialard, Valérie Serazin, François Marcelli, Beatrice Mandon-Pepin, Nelly Swierkowsky-Blanchard, Anne-Laure Barbotin, Farah Ghieh, Clara Leroy
Publikováno v:
Basic and clinical andrology
Basic and clinical andrology, BioMed Central, 2021, 31 (1), ⟨10.1186/s12610-021-00138-4⟩
Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-5 (2021)
Basic and Clinical Andrology
Basic and clinical andrology, BioMed Central, 2021, 31 (1), ⟨10.1186/s12610-021-00138-4⟩
Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-5 (2021)
Basic and Clinical Andrology
International audience; Whereas the initially strategy for the genetic analysis of male infertility was based on a candidate gene approach, the development of next-generation sequencing technologies (such as whole-exome sequencing (WES)) provides an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25ac474fbf34a10e4cc81e18215411ed
https://hal.inrae.fr/hal-03327919
https://hal.inrae.fr/hal-03327919
Publikováno v:
Basic and clinical andrology
Basic and clinical andrology, BioMed Central, 2021, 31 (1), ⟨10.1186/s12610-021-00127-7⟩
Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-15 (2021)
Basic and Clinical Andrology
Basic and clinical andrology, BioMed Central, 2021, 31 (1), ⟨10.1186/s12610-021-00127-7⟩
Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-15 (2021)
Basic and Clinical Andrology
International audience; Abstract Spermatogenesis is a complex process regulated by a multitude of genes. The identification and characterization of male-germ-cell-specific genes is crucial to understanding the mechanisms through which the cells devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9485207908404bd6c72b52fd45389d
https://hal.archives-ouvertes.fr/hal-03216070
https://hal.archives-ouvertes.fr/hal-03216070
Autor:
François Vialard, Anne-Laure Barbotin, Valérie Serazin, François Marcelli, Beatrice Mandon-Pepin, Clara Leroy, Henri-Jean Garchon, Julie Prasivoravong, Joanne Fortemps, Farah Ghieh, Sophie Ferlicot
Publikováno v:
Basic and clinical andrology
Basic and clinical andrology, BioMed Central, 2021, 31 (1), ⟨10.1186/s12610-021-00145-5⟩
Basic and clinical andrology, BioMed Central, 2021, 31 (27), ⟨10.1186/s12610-021-00145-5⟩
Basic and Clinical Andrology
Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-8 (2021)
Basic and clinical andrology, BioMed Central, 2021, 31 (1), ⟨10.1186/s12610-021-00145-5⟩
Basic and clinical andrology, BioMed Central, 2021, 31 (27), ⟨10.1186/s12610-021-00145-5⟩
Basic and Clinical Andrology
Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-8 (2021)
Background Although chromosome rearrangements are responsible for spermatogenesis failure, their impact depends greatly on the chromosomes involved. At present, karyotyping and Y chromosome microdeletion screening are the first-line genetic tests for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6885238ba8a0de6ec32f05e2a32aa661
https://hal.inrae.fr/hal-03455754
https://hal.inrae.fr/hal-03455754
Autor:
Hubert Lepidi, Anne-Laure Pelissier-Alicot, Beatrice Mandon-Pepin, Blandine Courbiere, Magalie Barbier, Elodie Poumerol, Pierre Castel, Olivier J. Manzoni, Virginie Tassistro
Publikováno v:
Archives of Toxicology
Archives of Toxicology, Springer Verlag, 2020, 94 (12), pp.4131-4141. ⟨10.1007/s00204-020-02877-1⟩
Archives of Toxicology, 2020, 94 (12), pp.4131-4141. ⟨10.1007/s00204-020-02877-1⟩
Archives of Toxicology, Springer Verlag, 2020, 94 (12), pp.4131-4141. ⟨10.1007/s00204-020-02877-1⟩
Archives of Toxicology, 2020, 94 (12), pp.4131-4141. ⟨10.1007/s00204-020-02877-1⟩
International audience; In animals, research in the past two decades has demonstrated the strong involvement of the endocannabinoid system (ECS) in numerous steps of the reproductive process, including ovarian physiology. Reproductive lifespan is clo
Publikováno v:
Basic and clinical andrology
Basic and clinical andrology, 2019, 29 (1), pp.4. ⟨10.1186/s12610-019-0086-6⟩
Basic and Clinical Andrology 4 (29), 16p. (2019)
Basic and clinical andrology, BioMed Central, 2019, 29 (1), pp.4. ⟨10.1186/s12610-019-0086-6⟩
Basic and Clinical Andrology
Basic and Clinical Andrology, Vol 29, Iss 1, Pp 1-16 (2019)
Basic and clinical andrology, 2019, 29 (1), pp.4. ⟨10.1186/s12610-019-0086-6⟩
Basic and Clinical Andrology 4 (29), 16p. (2019)
Basic and clinical andrology, BioMed Central, 2019, 29 (1), pp.4. ⟨10.1186/s12610-019-0086-6⟩
Basic and Clinical Andrology
Basic and Clinical Andrology, Vol 29, Iss 1, Pp 1-16 (2019)
Résumé Comme pour beaucoup de maladies humaines, les analyses génétiques en cas d’azoospermie étaient initialement limitées à la réalisation d’un caryotype, conduisant au diagnostic de réarrangements chromosomiques comme pour le syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8209ad1ee287ca3ae4b9df7935ae3374
https://hal.science/hal-02315267/document
https://hal.science/hal-02315267/document