Kontaridis, MI;
Roberts, AE;
Schill, L;
Schoyer, L;
Stronach, B;
Andelfinger, G;
Aoki, Y;
Axelrad, ME;
Bakker, A;
Bennett, AM;
et al.
Kontaridis, MI; Roberts, AE; Schill, L; Schoyer, L; Stronach, B; Andelfinger, G; Aoki, Y; Axelrad, ME; Bakker, A; Bennett, AM; Broniscer, A; Castel, P; Chang, CA; Cyganek, L; Das, TK; den Hertog, J; Galperin, E; Garg, S; Gelb, BD; Gordon, K; Green, T; Gripp, KW; Itkin, M; Kiuru, M; Korf, BR; Livingstone, JR; López-Juárez, A; Magoulas, PL; Mansour, S; Milner, T; Parker, E; Pierpont, EI; Plouffe, K; Rauen, KA; Shankar, SP; Smith, SB; Stevenson, DA; Tartaglia, M; Van, R; Wagner, ME; Ware, SM; Zenker, M
(2022)
The seventh international RASopathies symposium: Pathways to a cure-expanding knowledge, enhancing research, and therapeutic discovery.
Am J Med Genet A, 188 (6).
pp. 1915-1927.
ISSN 1552-4833
https://doi.org/10.1002/ajmg.a.62716
SGUL Authors: Mansour, Sahar
Abstract
RASopathies are a group of genetic disorders that are caused by genes that affect the canonical Ras/mitogen-activated protein kinase (MAPK) signaling pathway. Despite tremendous progress in understanding the molecular consequences of these genetic anomalies, little movement has been made in translating these findings to the clinic. This year, the seventh International RASopathies Symposium focused on expanding the research knowledge that we have gained over the years to enhance new discoveries in the field, ones that we hope can lead to effective therapeutic treatments. Indeed, for the first time, research efforts are finally being translated to the clinic, with compassionate use of Ras/MAPK pathway inhibitors for the treatment of RASopathies. This biannual meeting, organized by the RASopathies Network, brought together basic scientists, clinicians, clinician scientists, patients, advocates, and their families, as well as representatives from pharmaceutical companies and the National Institutes of Health. A history of RASopathy gene discovery, identification of new disease genes, and the latest research, both at the bench and in the clinic, were discussed.
Item Type: |
Article
|
Additional Information: |
© 2022 The Authors. American Journal of Medical Genetics Part A published by Wiley Periodicals LLC.
This is an open access article under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
Keywords: |
Costello syndrome, Noonan syndrome, RASopathy, cardiofaciocutaneus syndrome, neurofibromatosis, signaling, cardiofaciocutaneus syndrome, Costello syndrome, neurofibromatosis, Noonan syndrome, RASopathy, signaling, 1103 Clinical Sciences, 0604 Genetics |
SGUL Research Institute / Research Centre: |
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) |
Journal or Publication Title: |
Am J Med Genet A |
ISSN: |
1552-4833 |
Language: |
eng |
Dates: |
Date | Event |
---|
16 May 2022 | Published | 9 March 2022 | Published Online | 5 February 2022 | Accepted |
|
Publisher License: |
Creative Commons: Attribution 4.0 |
Projects: |
Project ID | Funder | Funder ID |
---|
UNSPECIFIED | CFC International | UNSPECIFIED | UNSPECIFIED | Children's Tumor Foundation | http://dx.doi.org/10.13039/100001545 | UNSPECIFIED | Costello Syndrome Family Network | UNSPECIFIED | UNSPECIFIED | International Costello Syndrome Support Group | UNSPECIFIED | UNSPECIFIED | National Center For Advancing Translational Sciences and the National Institute for Child Health and Human Development of the National Institutes of Health | UNSPECIFIED | UNSPECIFIED | Neurofibromatosis Network | UNSPECIFIED | UNSPECIFIED | NIH-R01-HL102368 | UNSPECIFIED | UNSPECIFIED | NIH-R35 HL125742 | UNSPECIFIED | UNSPECIFIED | Noonan Syndrome Association | UNSPECIFIED | UNSPECIFIED | Noonan Syndrome Foundation | UNSPECIFIED | UNSPECIFIED | Noonan UK | UNSPECIFIED | UNSPECIFIED | Masonic Medical Research Institute | UNSPECIFIED | UNSPECIFIED | Revolution Medicines | UNSPECIFIED | UNSPECIFIED | Onconova Therapeutics | UNSPECIFIED | UNSPECIFIED | Day One Biopharmaceuticals | UNSPECIFIED | UNSPECIFIED | Boehringer Ingelheim Fonds | http://dx.doi.org/10.13039/501100001645 | UNSPECIFIED | Igia Pharmaceuticals | UNSPECIFIED | R13TR003727 | Human Development of the National Institutes of Health | UNSPECIFIED | UNSPECIFIED | National Institute for Child Health | UNSPECIFIED | UNSPECIFIED | National Center for Advancing Translational Sciences | http://dx.doi.org/10.13039/100006108 | NIH-R35 HL125742 | National Institutes of Health | http://dx.doi.org/10.13039/100000002 | NIH-R01-HL102368 | National Institutes of Health | http://dx.doi.org/10.13039/100000002 |
|
PubMed ID: |
35266292 |
Web of Science ID: |
WOS:000766395600001 |
|
Go to PubMed abstract |
URI: |
https://openaccess.sgul.ac.uk/id/eprint/114220 |
Publisher's version: |
https://doi.org/10.1002/ajmg.a.62716 |
Statistics
Item downloaded times since 29 Mar 2022.
Actions (login required)
|
Edit Item |