Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Sara Cioffi"'
Autor:
Ilaria Favicchia, Gemma Flore, Sara Cioffi, Gabriella Lania, Antonio Baldini, Elizabeth Illingworth
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
ObjectivesTbx1 mutant mice are a widely used model of 22q11.2 deletion syndrome (22q11.2DS) because they manifest a broad spectrum of physical and behavioral abnormalities that is similar to that found in 22q11.2DS patients. In Tbx1 mutants, brain ab
Externí odkaz:
https://doaj.org/article/9e4848ca92734767bed9884a9f28a86e
Autor:
Gioia Mastromoro, Giulio Calcagni, Paolo Versacci, Carolina Putotto, Marcello Chinali, Caterina Lambiase, Marta Unolt, Elena Pelliccione, Silvia Anaclerio, Cinzia Caprio, Sara Cioffi, Marchesa Bilio, Anwar Baban, Fabrizio Drago, Maria Cristina Digilio, Bruno Marino, Antonio Baldini
Publikováno v:
PLoS ONE, Vol 14, Iss 4, p e0211170 (2019)
INTRODUCTION AND HYPOTHESIS:Patients with 22q11 deletion syndrome (22q11.2DS) present, in about 75% of cases, typical patterns of cardiac defects, with a particular involvement on the ventricular outflow tract and great arteries. However, in this gen
Externí odkaz:
https://doaj.org/article/b11194a58e96490993baa88b1b30daeb
Autor:
Sara Cioffi, Gemma Flore, Stefania Martucciello, Marchesa Bilio, Maria Giuseppina Turturo, Elizabeth Illingworth
The loss of a single copy of TBX1 accounts for most of the clinical signs and symptoms of 22q11.2 deletion syndrome (22q11.2DS), a common genetic disorder that is characterized by multiple congenital anomalies and brain-related clinical problems, som
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3018000b62a6090661eb6491c88afd0b
https://doi.org/10.1101/2022.03.16.484566
https://doi.org/10.1101/2022.03.16.484566
Autor:
Friso Heslinga, Thomas Hankemeier, Guido Krenning, Pranitha Kamat, SARA CIOFFI, Jan-Luuk Hillebrands, Paul Van der Leest, Rui Ning Chia, Dinara Faizullina
Publikováno v:
Journal of Vascular Research. 56:1-134
Autor:
Maria Giuseppina Turturo, Stefania Martucciello, Marchesa Bilio, Elizabeth Illingworth, Antonio Baldini, Li Chen, Sara Cioffi
Publikováno v:
The FASEB journal 34 (2020): 15062–15079. doi:10.1096/fj.201902202R
info:cnr-pdr/source/autori:Martucciello S.; Turturo M.G.; Bilio M.; Cioffi S.; Chen L.; Baldini A.; Illingworth E./titolo:A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3/doi:10.1096%2Ffj.201902202R/rivista:The FASEB journal/anno:2020/pagina_da:15062/pagina_a:15079/intervallo_pagine:15062–15079/volume:34
info:cnr-pdr/source/autori:Martucciello S.; Turturo M.G.; Bilio M.; Cioffi S.; Chen L.; Baldini A.; Illingworth E./titolo:A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3/doi:10.1096%2Ffj.201902202R/rivista:The FASEB journal/anno:2020/pagina_da:15062/pagina_a:15079/intervallo_pagine:15062–15079/volume:34
The transcription factor TBX1 is the major gene implicated in 22q11.2 deletion syndrome (22q11.2DS). The complex clinical phenotype includes vascular anomalies and a recent report presented new cases of primary lymphedema in 22q11.2DS patients. We ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f0132a42bb2fe14e6ec084774f4e75b
http://hdl.handle.net/11588/841611
http://hdl.handle.net/11588/841611
Autor:
Liao Y. Chen, Stefania Martucciello, Antonio Baldini, Turturo Mg, Sara Cioffi, Elisabeth Anne Illingworth
The transcription factorTBX1is the major gene implicated in 22q11.2 deletion syndrome. The complex clinical phenotype includes vascular anomalies and a recent report presented new cases of primary lymphedema in 22q11.2DS patients. We have previously
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48a1857b2ec95942c50f1015f53e268e
https://doi.org/10.1101/553578
https://doi.org/10.1101/553578
Autor:
Angela Chambery, Olga Pastorino, Rosita Russo, Federica Barbieri, Elisabeth Anne Illingworth, Michele Grieco, Luca Colucci-D'Amato, Sara Cioffi, Maria Teresa Gentile
Publikováno v:
Experimental cell research 364 (2018): 50–58. doi:10.1016/j.yexcr.2018.01.025
info:cnr-pdr/source/autori:Gentile, Maria Teresa; Russo, Rosita; Pastorino, Olga; Cioffi, Sara; Barbieri, Federica; Illingworth, Elisabeth Anne; Grieco, Michele; Chambery, Angela; Colucci-D'Amato, Luca/titolo:Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1%2F2 pathway/doi:10.1016%2Fj.yexcr.2018.01.025/rivista:Experimental cell research/anno:2018/pagina_da:50/pagina_a:58/intervallo_pagine:50–58/volume:364
info:cnr-pdr/source/autori:Gentile, Maria Teresa; Russo, Rosita; Pastorino, Olga; Cioffi, Sara; Barbieri, Federica; Illingworth, Elisabeth Anne; Grieco, Michele; Chambery, Angela; Colucci-D'Amato, Luca/titolo:Ruta graveolens water extract inhibits cell-cell network formation in human umbilical endothelial cells via MEK-ERK1%2F2 pathway/doi:10.1016%2Fj.yexcr.2018.01.025/rivista:Experimental cell research/anno:2018/pagina_da:50/pagina_a:58/intervallo_pagine:50–58/volume:364
Angiogenesis is a process encompassing several steps such as endothelial cells proliferation, differentiation and migration to form a vascular network, involving different signal transduction pathways. Among these, ERK1/2 signaling mediates VEGF-depe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c31febe588a6bd769b5384bb286f2dba
https://www.sciencedirect.com/science/article/pii/S0014482718300363?via=ihub
https://www.sciencedirect.com/science/article/pii/S0014482718300363?via=ihub
Autor:
Luigi Meccariello, Sara Cioffi, Predrag Grubor, Raffaele Franzese, Raffaele Cioffi, Giacinto di
Publikováno v:
Medicinska istrazivanja. 47:51-56
The term flat-back syndrome has been used to describe symptoms resulting from distraction instrumentation into the lower lumbar spine or sacrum and other factors that may aggravate the loss of lumbar lordosis include thoracolumbar kyphosis, fixed tho
Publikováno v:
Cerebral cortex (N. Y. N. Y., 1991) 27 (2017): 2210–2225. doi:10.1093/cercor/bhw076
info:cnr-pdr/source/autori:Flore, Gemma; Cioffi, Sara; Bilio, Marchesa; Illingworth, Elizabeth/titolo:Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome/doi:10.1093%2Fcercor%2Fbhw076/rivista:Cerebral cortex (N. Y. N. Y., 1991)/anno:2017/pagina_da:2210/pagina_a:2225/intervallo_pagine:2210–2225/volume:27
info:cnr-pdr/source/autori:Flore, Gemma; Cioffi, Sara; Bilio, Marchesa; Illingworth, Elizabeth/titolo:Cortical Development Requires Mesodermal Expression of Tbx1, a Gene Haploinsufficient in 22q11.2 Deletion Syndrome/doi:10.1093%2Fcercor%2Fbhw076/rivista:Cerebral cortex (N. Y. N. Y., 1991)/anno:2017/pagina_da:2210/pagina_a:2225/intervallo_pagine:2210–2225/volume:27
In mammals, proper temporal control of neurogenesis and neural migration during embryonic development ensures correct formation of the cerebral cortex. Changes in the distribution of cortical projection neurons and interneurons are associated with be