Výsledky vyhledávání

Akademický článek

Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertility

Autor: Hela Bellil, Farah Ghieh, Emeline Hermel, Béatrice Mandon-Pepin, François Vialard

Publikováno v: Basic and Clinical Andrology, Vol 31, Iss 1, Pp 1-15 (2021)

Résumé La spermatogenèse est un processus complexe régulé par une multitude de gènes. L’identification et la caractérisation des gènes spécifiques des cellules germinales mâles sont essentielles pour comprendre les mécanismes par lesquel

Externí odkaz: https://doaj.org/article/6bf1a3f4e6b748bfa5f9dfd53919d2a6

Zobrazit plný text záznamu

A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report

Autor: Bérénice Hervé, François Vialard, Elodie Herzog, Marine Poulain, Hela Bellil, Jean-Marc Ayoubi

Publikováno v: Journal of Assisted Reproduction and Genetics
Journal of Assisted Reproduction and Genetics, Springer Verlag, 2020, 37 (3), pp.573-577. ⟨10.1007/s10815-020-01690-0⟩
J Assist Reprod Genet

International audience; Tetrasomy 9p (ORPHA: 3310) (i(9p)) is a rare chromosomal imbalance. It is characterized by the presence of a supernumerary chromosome incorporating two copies of the short arm of chromosome 9 and is usually present in a mosaic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::149cea5ccf9c3776680c36a591621c6c
https://doi.org/10.1007/s10815-020-01690-0

Zobrazit plný text záznamu

Human testis-expressed (TEX) genes: a review focused on spermatogenesis and male fertility

Autor: Beatrice Mandon-Pepin, Emeline Hermel, Hela Bellil, François Vialard, Farah Ghieh

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

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

Zobrazit plný text záznamu

Prenatal diagnosis of 2q13 duplications: The crucial role of the family survey in genetic counseling on novel copy number variations

Autor: Bérénice Hervé, Thibaud Quibel, Rodolphe Dard, D. Molina-Gomes, F. Vialard, Sophie Roy, Hela Bellil

Publikováno v: European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2020, 63 (8), ⟨10.1016/j.ejmg.2020.103956⟩

International audience; In recent years, the introduction of novel genome analysis technologies (such as array comparative genomic hybridization) has enabled the prenatal diagnosis of various recurrent copy number variations (CNVs). Some of these CNV

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::989f7a57b8e623cb0ef019e27aaedb9e
https://doi.org/10.1016/j.ejmg.2020.103956

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání