Andrea Messina

Publications | Mémoires et thèses

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24 publications

2022 | 2021 | 2020 | 2019 | 2018 | 2017 | 2016 | 2014 | 2013 | 2011 | 2008 | 2007 |
NOS1 mutations cause hypogonadotropic hypogonadism with sensory and cognitive deficits that can be reversed in infantile mice.
Chachlaki K., Messina A., Delli V., Leysen V., Maurnyi C., Huber C., Ternier G., Skrapits K., Papadakis G., Shruti S. et al., 2022/10/05. Science translational medicine, 14 (665) pp. eabh2369. Peer-reviewed.
 
GnRH replacement rescues cognition in Down syndrome.
Manfredi-Lozano M., Leysen V., Adamo M., Paiva I., Rovera R., Pignat J.M., Timzoura F.E., Candlish M., Eddarkaoui S., Malone S.A. et al., 2022/09/02. Science, 377 (6610) pp. eabq4515. Peer-reviewed.
Transcriptome profiling of kisspeptin neurons from the mouse arcuate nucleus reveals new mechanisms in estrogenic control of fertility.
Göcz B., Rumpler É., Sárvári M., Skrapits K., Takács S., Farkas I., Csillag V., Trinh S.H., Bardóczi Z., Ruska Y. et al., 2022/07/05. Proceedings of the National Academy of Sciences of the United States of America, 119 (27) pp. e2113749119. Peer-reviewed.
Testosterone-induced increase in libido in a patient with a loss-of-function mutation in the AR gene.
Marino L., Messina A., S Acierno J., Phan-Hug F., J Niederländer N., Santoni F., La Rosa S., Pitteloud N., 2021/06/01. Endocrinology, diabetes & metabolism case reports, 2021 (1). Peer-reviewed.
 
Pathogenic mosaic variants in congenital hypogonadotropic hypogonadism.
Acierno J.S., Xu C., Papadakis G.E., Niederländer N.J., Rademaker J.D., Meylan J., Messina A., Kolesinska Z., Quinton R., Lang-Muritano M. et al., 2020/11. Genetics in medicine, 22 (11) pp. 1759-1767. Peer-reviewed.
 
Neuropilin-1 expression in GnRH neurons regulates prepubertal weight gain and sexual attraction.
Vanacker C., Trova S., Shruti S., Casoni F., Messina A., Croizier S., Malone S., Ternier G., Hanchate N.K., Rasika S. et al., 2020/10/01. The EMBO journal, 39 (19) pp. e104633. Peer-reviewed.
 
Clinical and genetic overlap between congenital hypogonadotropic hypogonadism and cornelia de lange syndrome
Xu Cheng, Messina Andrea, Acierno James, Niederlander Nicolas, Santoni Federico, Papadakis Georgios, Pignatelli Duarte, Avbelj Stefanija Magdalena, Keefe Kimberly, Balasubramanian Ravikumar et al., 2020/08/21. dans Endocrine Abstracts, Bioscientifica.
 
Neuron-Derived Neurotrophic Factor Is Mutated in Congenital Hypogonadotropic Hypogonadism
Messina Andrea, Pulli Kristiina, Santini Sara, Acierno James, Känsäkoski Johanna, Cassatella Daniele, Xu Cheng, Casoni Filippo, Conte Daniele, Malone Samuel A. et al., 2020/01. The American Journal of Human Genetics, 106 (1) pp. 58-70. Peer-reviewed.
Defective AMH signaling disrupts GnRH neuron development and function and contributes to hypogonadotropic hypogonadism.
Malone S.A., Papadakis G.E., Messina A., Mimouni NEH, Trova S., Imbernon M., Allet C., Cimino I., Acierno J., Cassatella D. et al., 2019/07/10. eLife, 8. Peer-reviewed.
 
Flipping the GnRH switch with microRNAs
Messina Andrea, 2019/05/01., 21st European Congress of Endocrinology pp. S18.2 dans Endocrine Abstracts, Bioscientifica.
 
β-Klotho deficiency shifts the gut-liver bile acid axis and induces hepatic alterations in mice.
Somm E., Henry H., Bruce S.J., Bonnet N., Montandon S.A., Niederländer N.J., Messina A., Aeby S., Rosikiewicz M., Fajas L. et al., 2018/11/01. American journal of physiology. Endocrinology and metabolism, 315 (5) pp. E833-E847. Peer-reviewed.
KLB, encoding β-Klotho, is mutated in patients with congenital hypogonadotropic hypogonadism.
Xu C., Messina A., Somm E., Miraoui H., Kinnunen T., Acierno J., Niederländer N.J., Bouilly J., Dwyer A.A., Sidis Y. et al., 2017/10. EMBO molecular medicine, 9 (10) pp. 1379-1397. Peer-reviewed.
 
Les micro-ARN - Nouveaux acteurs du contrôle hypothalamique de la fertilité [MicroRNAs: new players in the hypothalamic control of fertility]
Messina A., Langlet F., Prevot V., 2017/05. Medecine sciences, 33 (5) pp. 506-511. Peer-reviewed.
Hypothalamic microRNAs flip the switch for fertility.
Messina A., Prevot V., 2017/02/07. Oncotarget, 8 (6) pp. 8993-8994. Peer-reviewed.
Mutations in CEP78 Cause Cone-Rod Dystrophy and Hearing Loss Associated with Primary-Cilia Defects.
Nikopoulos K., Farinelli P., Giangreco B., Tsika C., Royer-Bertrand B., Mbefo M.K., Bedoni N., Kjellström U., El Zaoui I., Di Gioia S.A. et al., 2016/09/01. American journal of human genetics, 99 (3) pp. 770-776. Peer-reviewed.
 
Novel role for anti-Müllerian hormone in the regulation of GnRH neuron excitability and hormone secretion.
Cimino I., Casoni F., Liu X., Messina A., Parkash J., Jamin S.P., Catteau-Jonard S., Collier F., Baroncini M., Dewailly D. et al., 2016/01/12. Nature communications, 7 p. 10055. Peer-reviewed.
 
A microRNA switch regulates the rise in hypothalamic GnRH production before puberty.
Messina A., Langlet F., Chachlaki K., Roa J., Rasika S., Jouy N., Gallet S., Gaytan F., Parkash J., Tena-Sempere M. et al., 2016. Nature Neuroscience, 19 (6) pp. 835-844. Peer-reviewed.
 
Brain endothelial cells control fertility through ovarian-steroid-dependent release of semaphorin 3A.
Giacobini P., Parkash J., Campagne C., Messina A., Casoni F., Vanacker C., Langlet F., Hobo B., Cagnoni G., Gallet S. et al., 2014/03. PLoS biology, 12 (3) pp. e1001808. Peer-reviewed.
 
Hypothalamic tanycytes are an ERK-gated conduit for leptin into the brain.
Balland E., Dam J., Langlet F., Caron E., Steculorum S., Messina A., Rasika S., Falluel-Morel A., Anouar Y., Dehouck B. et al., 2014/02/04. Cell metabolism, 19 (2) pp. 293-301. Peer-reviewed.
 
Semaphorin signaling in the development and function of the gonadotropin hormone-releasing hormone system.
Messina A., Giacobini P., 2013/09/23. Frontiers in endocrinology, 4 p. 133. Peer-reviewed.
 
Tanycytic VEGF-A boosts blood-hypothalamus barrier plasticity and access of metabolic signals to the arcuate nucleus in response to fasting.
Langlet F., Levin B.E., Luquet S., Mazzone M., Messina A., Dunn-Meynell A.A., Balland E., Lacombe A., Mazur D., Carmeliet P. et al., 2013/04/02. Cell metabolism, 17 (4) pp. 607-617. Peer-reviewed.
 
Dysregulation of Semaphorin7A/β1-integrin signaling leads to defective GnRH-1 cell migration, abnormal gonadal development and altered fertility.
Messina A., Ferraris N., Wray S., Cagnoni G., Donohue D.E., Casoni F., Kramer P.R., Derijck A.A., Adolfs Y., Fasolo A. et al., 2011/12/15. Human molecular genetics, 20 (24) pp. 4759-4774. Peer-reviewed.
 
Semaphorin 4D regulates gonadotropin hormone-releasing hormone-1 neuronal migration through PlexinB1-Met complex.
Giacobini P., Messina A., Morello F., Ferraris N., Corso S., Penachioni J., Giordano S., Tamagnone L., Fasolo A., 2008/11/03. The Journal of cell biology, 183 (3) pp. 555-566. Peer-reviewed.
 
Hepatocyte growth factor acts as a motogen and guidance signal for gonadotropin hormone-releasing hormone-1 neuronal migration.
Giacobini P., Messina A., Wray S., Giampietro C., Crepaldi T., Carmeliet P., Fasolo A., 2007/01/10. The Journal of neuroscience, 27 (2) pp. 431-445. Peer-reviewed.
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