Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Pauline Bourgeois"'
Autor:
Bruno Wacogne, Marine Belinger Podevin, Naïs Vaccari, Claudia Koubevi, Céline Codjiová, Emilie Gutierrez, Pauline Bourgeois, Lucie Davoine, Marjorie Robert-Nicoud, Alain Rouleau, Annie Frelet-Barrand
Publikováno v:
Sensors, Vol 23, Iss 9, p 4325 (2023)
Despite numerous innovations, measuring bacteria concentrations on a routine basis is still time consuming and ensuring accurate measurements requires careful handling. Furthermore, it often requires sampling small volumes of bacteria suspensions whi
Externí odkaz:
https://doaj.org/article/d4bb1e2c1f0c48cba8e79f763678b7b1
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Congenital Central Hypoventilation Syndrome (CCHS) is characterized by central hypoventilation due to abnormal autonomic control of breathing and global dysautonomia. Patients harbour heterozygous PHOX-2B gene mutations which are
Externí odkaz:
https://doaj.org/article/2f1253473d0048dba154b22d6d404e76
Autor:
Baptiste Dumétier, Aymeric Zadoroznyj, Jean Berthelet, Sébastien Causse, Jennifer Allègre, Pauline Bourgeois, Florine Cattin, Cindy Racoeur, Catherine Paul, Carmen Garrido, Laurence Dubrez
Publikováno v:
Oncogene. 42:198-208
Cellular inhibitor of apoptosis-1 (cIAP1) is a signaling regulator with oncogenic properties. It is involved in the regulation of signaling pathways controlling inflammation, cell survival, proliferation, differentiation and motility. It is recruited
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bd90f4707f46001959b7ffe26ac0272
https://doi.org/10.1038/s41388-022-02544-y
https://doi.org/10.1038/s41388-022-02544-y
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
BackgroundCongenital Central Hypoventilation Syndrome (CCHS) is characterized by central hypoventilation due to abnormal autonomic control of breathing and global dysautonomia. Patients harbour heterozygousPHOX-2Bgene mutations which are polyalanine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43bf67b9862a3080fb7f3b399bee63f0
http://link.springer.com/article/10.1186/s13023-020-01601-7
http://link.springer.com/article/10.1186/s13023-020-01601-7
Autor:
Pauline Bourgeois, Teri A. Garstka, Tamara L. Smith, Steve Huck, Ronald W. Toseland, Philip McCallion
Publikováno v:
Journal of clinical psychology. 57(4)
The short-term effectiveness of a Health Education Group (HEP) intervention program for spouses of frail older adults was compared to the usual care (UC) offered to the spouses of frail older persons in a staff model health maintenance organization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c89654edb8afa5a1cbc9eb68f258f08
https://pubmed.ncbi.nlm.nih.gov/11255206
https://pubmed.ncbi.nlm.nih.gov/11255206