Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Monica, Beltrame"'
Autor:
Silvia Moleri, Sara Mercurio, Alex Pezzotta, Donatella D’Angelo, Alessia Brix, Alice Plebani, Giulia Lini, Marialaura Di Fuorti, Monica Beltrame
Publikováno v:
Cells, Vol 12, Iss 18, p 2309 (2023)
Mutations in the transcription factor-coding gene SOX18, the growth factor-coding gene VEGFC and its receptor-coding gene VEGFR3/FLT4 cause primary lymphedema in humans. In mammals, SOX18, together with COUP-TFII/NR2F2, activates the expression of Pr
Externí odkaz:
https://doaj.org/article/7862bb5dc2164199b67b2fb56c1dd6a3
Autor:
Massimo M. Santoro, Monica Beltrame, Daniela Panáková, Arndt F. Siekmann, Natascia Tiso, Marina Venero Galanternik, Hyun Min Jung, Brant M. Weinstein
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 7 (2019)
Since its introduction, the zebrafish has provided an important reference system to model and study cardiovascular development as well as lymphangiogenesis in vertebrates. A scientific workshop, held at the 2018 European Zebrafish Principal Investiga
Externí odkaz:
https://doaj.org/article/c5bd31a428304e608309d2e7b68f3346
Autor:
Raffaella Fittipaldi, Pamela Floris, Valentina Proserpio, Franco Cotelli, Monica Beltrame, Giuseppina Caretti
Publikováno v:
Cells, Vol 10, Iss 5, p 1233 (2021)
SMYD3 (SET and MYND domain containing protein 3) is a methylase over-expressed in cancer cells and involved in oncogenesis. While several studies uncovered key functions for SMYD3 in cancer models, the SMYD3 role in physiological conditions has not b
Externí odkaz:
https://doaj.org/article/0a4e2083a76d4901a2c4a85caad34d8b
Autor:
Silvia Carra, Efrem Foglia, Solei Cermenati, Erica Bresciani, Costanza Giampietro, Carla Lora Lamia, Elisabetta Dejana, Monica Beltrame, Franco Cotelli
Publikováno v:
PLoS ONE, Vol 7, Iss 12, p e51245 (2012)
BACKGROUND: Endothelial cell junctions control blood vessel permeability. Altered permeability can be associated with vascular fragility that leads to vessel weakness and haemorrhage formation. In vivo studies on the function of genes involved in the
Externí odkaz:
https://doaj.org/article/6431f449ff574ef6a73227714e31aac1
Autor:
Thomas Vaccari, David S. Horner, Elena Morelli, Monica Beltrame, Maria Enrica Pasini, Valeria Mastrodonato
Publikováno v:
Seminars in Cell & Developmental Biology. 74:29-39
ESCRT (Endosomal Sorting Complex Required for Transport) proteins have been shown to control an increasing number of membrane-associated processes. Some of these, and prominently regulation of receptor trafficking, profoundly shape signal transductio
Autor:
Erica Bresciani, Stefano Confalonieri, Solei Cermenati, Simona Cimbro, Efrem Foglia, Monica Beltrame, Pier Paolo Di Fiore, Franco Cotelli
Publikováno v:
PLoS ONE, Vol 5, Iss 12, p e14296 (2010)
BACKGROUND:Notch signaling is an evolutionarily conserved regulatory circuitry implicated in cell fate determination in various developmental processes including hematopoietic stem cell self-renewal and differentiation of blood lineages. Known endoge
Externí odkaz:
https://doaj.org/article/ac56c0ea022048c78118c51f5e4d58b4
Autor:
Franco Cotelli, Rolland Reinbold, Lorenzo Sangiorgio, Gianluca Deflorian, Paride Pelucchi, Alberto Albertini, Antonio Giordano, Ileana Zucchi, James Kehler, Alessandra Mezzelani, Gianfranco Bellipanni, Silvia Carra, Mira Palizban, Solei Cermenati, Martin Götte, Valentina Martino, Monica Beltrame
Publikováno v:
Journal of cellular physiology
(2017): 1455–1467. doi:10.1002/jcp.26032
info:cnr-pdr/source/autori:Carra S.; Sangiorgio L.; Pelucchi P.; Cermenati S.; Mezzelani A.; Martino V.; Palizban M.; Albertini A.; Götte M.; Kehler J.; Deflorian G.; Beltrame M.; Giordano A.; Reinbold R.; Cotelli F.; Bellipanni G.; Zucchi I./titolo:Zebrafish Tmem230a cooperates with the Delta%2FNotch signaling pathway to modulate endothelial cell number in angiogenic vessels/doi:10.1002%2Fjcp.26032/rivista:Journal of cellular physiology (Print)/anno:2017/pagina_da:1455/pagina_a:1467/intervallo_pagine:1455–1467/volume
(2017): 1455–1467. doi:10.1002/jcp.26032
info:cnr-pdr/source/autori:Carra S.; Sangiorgio L.; Pelucchi P.; Cermenati S.; Mezzelani A.; Martino V.; Palizban M.; Albertini A.; Götte M.; Kehler J.; Deflorian G.; Beltrame M.; Giordano A.; Reinbold R.; Cotelli F.; Bellipanni G.; Zucchi I./titolo:Zebrafish Tmem230a cooperates with the Delta%2FNotch signaling pathway to modulate endothelial cell number in angiogenic vessels/doi:10.1002%2Fjcp.26032/rivista:Journal of cellular physiology (Print)/anno:2017/pagina_da:1455/pagina_a:1467/intervallo_pagine:1455–1467/volume
During embryonic development, new arteries and veins form from preexisting vessels in response to specific angiogenic signals. Angiogenic signaling is complex since not all endothelial cells exposed to angiogenic signals respond equally. Some cells w
Autor:
Matea Cortolano, Gerhard Thiel, Sebastian Höler, Anna Moroni, Monica Beltrame, Kerri Kukovetz, Anja J. Engel
Publikováno v:
Biophysical Journal. 118:482a-483a
Autor:
Sarah De Val, Anne K. Lagendijk, Donatella D'Angelo, Tania Radziewic, Stefan Schulte-Merker, Monica Beltrame, Elisabetta Dejana, Mathias Francois, George Bou-Gharios, Jason S. Carroll, Indrika Ratnayaka, Alice Omini, Dorien Hermkens, Ivy Kim-Ni Chiang, Cathy Pichol-Thievend, Jeroen Overman, Ke Liu, Emmanuelle Lesieur, Monica Corada, Benjamin M. Hogan, Kelly A. Holmes, Patrick P.L. Tam, Martin Fritzsche, Nicolas Fossat, Alice Neal
Arterial specification and differentiation are influenced by a number of regulatory pathways. While it is known that the Vegfa-Notch cascade plays a central role, the transcriptional hierarchy controlling arterial specification has not been fully del
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dabd70dd5ee7225f350a98632bcdfe3
Autor:
Franco Salerno, Monica Beltrame, Franco Cotelli, Cinzia Bragato, Marina Mora, Silvia Carra, Flavia Blasevich, Lorenzo Maggi, Alessia Brix, Renato Mantegazza, Andrea Bassi
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866:165662
Pompe disease (PD) is an autosomal recessive muscular disorder caused by deficiency of the glycogen hydrolytic enzyme acid α-glucosidase (GAA). The enzyme replacement therapy, currently the only available therapy for PD patients, is efficacious in i