Andrea Messina

Publications | Mémoires et thèses

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28 publications

En préparation
 
Transcriptomic profiling of murine GnRH neurons reveals developmental trajectories linked to human reproduction
Zouaghi Yassine, Alpern Daniel, Gardeux Vincent, Russeil Julie, Deplancke Bart, Santoni Federico, Pitteloud Nelly, Messina Andrea.
[DOI][serval:BIB_9467A01746F7]
2024
 
Fasting induces metabolic switches and spatial redistributions of lipid processing and neuronal interactions in tanycytes.
Brunner M., Lopez-Rodriguez D., Estrada-Meza J., Dali R., Rohrbach A., Deglise T., Messina A., Thorens B., Santoni F., Langlet F., 2024/08/04. Nature communications, 15 (1) p. 6604. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_0B3E856627D3]
 
Publisher Correction: Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Kentistou K.A., Kaisinger L.R., Stankovic S., Vaudel M., Mendes de Oliveira E., Messina A., Walters R.G., Liu X., Busch A.S., Helgason H. et al., 2024/08. Nature genetics, 56 (8) pp. 1763-1764. Peer-reviewed.
[DOI][Pmid][serval:BIB_B0CB1995E799]
 
Understanding the genetic complexity of puberty timing across the allele frequency spectrum.
Kentistou K.A., Kaisinger L.R., Stankovic S., Vaudel M., Mendes de Oliveira E., Messina A., Walters R.G., Liu X., Busch A.S., Helgason H. et al., 2024/07. Nature genetics, 56 (7) pp. 1397-1411. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_CFE58C5B5334]
2022
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.
[URN][DOI][WoS][Pmid][serval:BIB_07E5C5166534]
 
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.
[DOI][WoS][Pmid][serval:BIB_58FCF069BC65]
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.
[URN][DOI][WoS][Pmid][serval:BIB_008517AC197F]
2021
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.
[URN][DOI][WoS][Pmid][serval:BIB_5EFE487E7386]
2020
 
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.
[DOI][WoS][Pmid][serval:BIB_DD363A0A5D79]
 
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.
[DOI][WoS][Pmid][serval:BIB_42A6F083D6D2]
 
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.
[DOI][serval:BIB_E8DE040E71EA]
 
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.
[DOI][WoS][Pmid][serval:BIB_3475FDA95309]
2019
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.
[URN][DOI][WoS][Pmid][serval:BIB_8F3CDBBED609]
 
Flipping the GnRH switch with microRNAs
Messina Andrea, 2019/05/01., 21st European Congress of Endocrinology pp. S18.2 dans Endocrine Abstracts, Bioscientifica.
[DOI][serval:BIB_C81AD1BB73F5]
2018
 
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.
[DOI][WoS][Pmid][serval:BIB_4784D51A916B]
2017
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.
[URN][DOI][WoS][Pmid][serval:BIB_569EB14591C9]
 
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.
[DOI][WoS][Pmid][serval:BIB_53B7ED3CE3C2]
Hypothalamic microRNAs flip the switch for fertility.
Messina A., Prevot V., 2017/02/07. Oncotarget, 8 (6) pp. 8993-8994. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_EC094B47D27A]
2016
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.
[URN][DOI][Pmid][serval:BIB_4A7C86DC11B4]
 
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.
[DOI][WoS][Pmid][serval:BIB_DBC93979EAE0]
 
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.
[DOI][WoS][Pmid][serval:BIB_D2DE5F6E4CC3]
2014
 
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.
[DOI][WoS][Pmid][serval:BIB_63FCE3DBD300]
 
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.
[DOI][WoS][Pmid][serval:BIB_A2CB76E9E319]
2013
 
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.
[DOI][Pmid][serval:BIB_5468B9F08445]
 
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.
[DOI][WoS][Pmid][serval:BIB_F9AFF6EBB931]
2011
 
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.
[DOI][WoS][Pmid][serval:BIB_BF173C66A068]
2008
 
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.
[DOI][WoS][Pmid][serval:BIB_2FE44EEAD6C1]
2007
 
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.
[DOI][WoS][Pmid][serval:BIB_286268894D20]
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