Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Alyssa Paganoni"'
Autor:
Roberto Oleari, Antonella Lettieri, Stefano Manzini, Alyssa Paganoni, Valentina André, Paolo Grazioli, Marco Busnelli, Paolo Duminuco, Antonio Vitobello, Christophe Philippe, Varoona Bizaoui, Helen L. Storr, Federica Amoruso, Fani Memi, Valeria Vezzoli, Valentina Massa, Peter Scheiffele, Sasha R. Howard, Anna Cariboni
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 3 (2023)
Externí odkaz:
https://doaj.org/article/d4dd80c652134f65ad526bbbecb0b59b
Autor:
Read Jordan E, Canton Ana Pinheiro-Machado, Flavia Tinano, Leonardo Guasti, Montenegro Luciana Ribeiro, Fiona Ryan, Deborah Shears, Alyssa Paganoni, Marta Korbonits, Alexander Jorge, Alessia David, Mendonca Berenice Bilharinho, Brito Vinicius Nahime, Latronico Ana Claudia, Sasha R Howard
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78ea5bb7ef94e6aea5150d9afaf2abd6
https://doi.org/10.1530/endoabs.86.p343
https://doi.org/10.1530/endoabs.86.p343
Autor:
Ana Canton, Flavia Tinano, Leonardo Guasti, Luciana Montenegro, Jesús Argente, Fiona Ryan, Deborah Shears, Maria Edna Melo, Larissa Gomes, Mariana Piana, Raja Brauner, Rafael Spino, Arancha Escribano-Muñoz, Alyssa Paganoni, Marta Korbonits, Ana Krepischi, Silvia Costa, Carlos Eduardo Seraphim, Aline Faria, Berenice Mendonca, Vinicius Brito, Sasha Howard, Ana Claudia Latronico
Publikováno v:
Journal of the Endocrine Society. 6:A643-A644
Methyl-CpG-binding protein 2 (MECP2) is a chromatin-associated protein that can both activate and repress transcription, playing an essential role in neuronal maturation. MECP2 is encoded by an X-linked gene (chromosome Xq28) with high expression in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3ec09ffa22c21d3c528e98c12407320
https://doi.org/10.1210/jendso/bvac150.1331
https://doi.org/10.1210/jendso/bvac150.1331
Autor:
Roberto Oleari, Antonella Lettieri, Stefano Manzini, Alyssa Paganoni, Valentina André, Paolo Grazioli, Marco Busnelli, Paolo Duminuco, Antonio Vitobello, Christophe Philippe, Varoona Bizaoui, Helen L. Storr, Federica Amoruso, Fani Memi, Valeria Vezzoli, Valentina Massa, Peter Scheiffele, Sasha R. Howard, Anna Cariboni
Gonadotropin releasing hormone (GnRH) deficiency is a disorder characterized by absent or delayed puberty, with largely unknown genetic causes. The purpose of this study was to obtain and exploit gene expression profiles of GnRH neurons during develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d24c7b2d3d3cae7b7992982081e3f340
https://doi.org/10.1101/2022.05.24.22275221
https://doi.org/10.1101/2022.05.24.22275221
Autor:
Maria Vittoria Corridori, Roberto Oleari, Valentina Andre, Ludovica Cotellessa, Carles Gaston-Massuet, Anna Cariboni, Hellmut G. Augustin, Khalid Hussain, Lise Roth, Sophia Tahir, Valeria Scagliotti, Lisa Benedetta De Martini, Ivano Eberini, Simona Gulli, Antonella Lettieri, Chiara Parravicini, Francesco Bedogni, Alyssa Paganoni
Publikováno v:
Neuroendocrinology. 111:421-441
Introduction: Gonadotropin-releasing hormone (GnRH) deficiency causes hypogonadotropic hypogonadism (HH), a rare genetic disorder that impairs sexual reproduction. HH can be due to defective GnRH-secreting neuron development or function and may be as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e8e685f3245edc175c9262dc190af1d1
https://doi.org/10.1159/000508375
https://doi.org/10.1159/000508375
Autor:
Iain C.A.F. Robinson, Roberto Oleari, Sakina Rajabali, Hywel Williams, Takahisa Furukawa, Mario J. Cachia, Kimberley L. H. Riegman, Mehul T. Dattani, Daniel Field, Alyssa Paganoni, Louise C. Gregory, M. Albert Basson, Lisa Benedetta De Martini, Anna Cariboni, Antonella Lettieri, Polona Le Quesne Stabej, John Torpiano, Taro Chaya, Nancy Formosa, Danielle E. Whittaker, Louise Ocaka
Publikováno v:
The Journal of Clinical Investigation
The positive regulatory (PR) domain containing 13 (PRDM13) putative chromatin modifier and transcriptional regulator functions downstream of the transcription factor PTF1A, which controls GABAergic fate in the spinal cord and neurogenesis in the hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::970d0170320a2e6e4d7c50418ff635ef
https://doi.org/10.1172/jci141587
https://doi.org/10.1172/jci141587
Autor:
Roberto Oleari, Nancy Formosa, Alyssa Paganoni, Polona Le Quesne-Stabej, GOSgene, Hywel Williams, Anna Cariboni, Iain C.A.F. Robinson, Takahisa Furukawa, Mario J. Cachia, Taro Chaya, M. Albert Basson, Louise Ocaka, Daniel Field, Danielle E. Whittaker, Louise C. Gregory, Kimberley L. H. Riegman, John Torpiano, Lisa Benedetta De Martini, Antonella Lettieri, Sakina Rajabali, Mehul T. Dattani
PRDM13 (PR Domain containing 13) is a putative chromatin modifier and transcriptional regulator that functions downstream of the transcription factor PTF1A, which in turn controls GABAergic fate in the spinal cord and neuronal development in the hypo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00d535062d7dfccc6fad2c0166248ce0
https://doi.org/10.1101/2021.07.28.21260126
https://doi.org/10.1101/2021.07.28.21260126
Publikováno v:
Neuroendocrinology. 109:193-199
In mammals, fertility critically depends on the pulsatile secretion of gonadotropin-releasing hormone (GnRH) by scattered hypothalamic neurons (GnRH neurons). During development, GnRH neurons originate in the nasal placode and migrate first into the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb59f5c8a14904df5943cbf60912a9a1
https://doi.org/10.1159/000495916
https://doi.org/10.1159/000495916
Autor:
Magni, Rossella Cannarella, Alyssa Paganoni, Stefania Cicolari, Roberto Oleari, Rosita Condorelli, Sandro La Vignera, Anna Cariboni, Aldo Calogero, Paolo
Publikováno v:
International Journal of Molecular Sciences; Volume 22; Issue 5; Pages: 2445
Anti-Müllerian hormone (AMH) is secreted by Sertoli or granulosa cells. Recent evidence suggests that AMH may play a role in the pathogenesis of hypogonadotropic hypogonadism (HH) and that its serum levels could help to discriminate HH from delayed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::bba7cfa600f8800f45cc8a86fe8848f0
Autor:
Roberto Oleari, Alyssa Paganoni, Lorenzo A. Pinna, Mauro Salvi, Anna Cariboni, Luca Zanieri, Claudio D'Amore, Christian Borgo, Antonella Lettieri
Publikováno v:
International Journal of Molecular Sciences
Volume 20
Issue 23
Volume 20
Issue 23
Protein kinase CK2 (CK2) is a highly conserved and ubiquitous kinase is involved in crucial biological processes, including proliferation, migration, and differentiation. CK2 holoenzyme is a tetramer composed by two catalytically active (&alpha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::413243aed0b8f6cf80fb0b11d2432522
https://pubmed.ncbi.nlm.nih.gov/31779225
https://pubmed.ncbi.nlm.nih.gov/31779225