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180万美元的基金会中心批准转到领先的荷兰研究所

被誉为世界最重要的遗传性视网膜退化疾病,在荷兰Radboud大学Nijmegen遗传,实验室和临床研究机构之一,在未来五年180万美元的基金会作为一个FFB研究中心。在这个职位上,奈梅亨将进行协作实验室和临床研究,旨在推进潜力和治疗方案和相关的人类研究。

“奈梅亨已成为不仅在欧洲领先的视网膜研究中心,但在视网膜科学以及国际先驱,说:”斯蒂芬玫瑰,博士,首席研究人员,基金会战斗失明。 “其研究人员已经负责18视网膜疾病的致病基因的发现,他们确定为什么在纤毛的缺陷,在感光器的小筒状结构,广泛的视觉抢劫视网膜疾病是一种常见的链接。奈梅亨还设立了启动如基因疗法治疗人类研究一个优秀的临床操作。“

博士弗兰斯Cremers,奈梅亨中心授予协调员,说他的球队的目标之一是识别和表征在荷兰的所有遗传性视网膜疾病影响的人。 “该中心的补助资金,”他补充说,“也将加强整个欧洲的合作遗传研究的努力,以及我们的努力,以便为在巴基斯坦和印度尼西亚的视网膜疾病的遗传研究。”

在欧洲和亚洲人群中寻找致病基因,可以提供一个大的推动作用,使许多美国人有那些祖先在美国的研究人员和患者。博士解释说:“美国是一种遗传性的大熔炉,”玫瑰“,所以它必须寻找新的基因时,我们蒙上了广泛的国际净。”

奈梅亨的中心批准,将包括以下支持:
•确定新的视网膜疾病的基因 - 包括引起,如视网膜色素变性和老年性黄斑变性的条件 - 通过使用下一代的基因发现技术。

•开发一个更好地了解视网膜ciliopathies - 包括如视网膜色素变性,Usher综合征和Bardet - Biedl综合征的条件 - ,视力的关键蛋白质运输和感光健康受到损害。

•提高视网膜成像技术的选择,并按照未来莱伯先天性黑朦(CEP290突变)和Stargardt病基因治疗临床试验的患者。

新的基金会中心津贴支持什么是视网膜变性疾病,其主要研究者的研究作为Radboud大学Nijmegen研究中心正式称为:博士。弗朗斯Cremers,Anneke巢穴霍兰德,Hannie克雷默,罗纳德Roepman和托马斯Theelen。联合调查:DRS。罗布科林,CAREL Hoyng,吉荣Klevering和欧文范Wijk。

奈梅亨是在欧洲的第三个工厂收到基金会中心批准,在伦敦参加摩菲眼科医院和研究所德拉在巴黎的视觉。
生命不息,战斗不止。
1# 凤凰涅盘
Recognized as one of the world’s foremost institutions for genetic, laboratory and clinical research for inherited retinal degenerative diseases, Radboud University Nijmegen in the Netherlands is receiving $1.8 million over the next five years from the Foundation to serve as an FFB Research Center. In that role, Nijmegen will conduct collaborative laboratory and clinical research intended to advance potential treatments and cures and related human studies.

“Nijmegen has become not only a leading retinal research center in Europe, but an international pioneer in retinal science as well,” says Stephen Rose, Ph.D., chief research officer, Foundation Fighting Blindness. “Its researchers have been responsible for the discovery of 18 retinal-disease-causing genes, and they determined why defects in cilia, tiny tube-like structures in photoreceptors, are a common link to a broad range of vision-robbing retinal diseases. Nijmegen has also established an outstanding clinical operation for launching human studies for treatments like gene therapy.”

Dr. Frans Cremers, the Nijmegen Center Grant coordinator, says that one of his team’s goals is to identify and characterize all people in the Netherlands who are affected by an inherited retinal disease. “The Center Grant funding,” he adds, “will also strengthen our collaborative genetic research efforts across Europe as well as our endeavor to facilitate genetic research for retinal diseases in Pakistan and Indonesia.”

Finding disease-causing genes in European and Asian populations can provide a big boost to researchers and patients in the United States, where so many Americans have those ancestries. “The U.S. is a genetic melting pot,” explains Dr. Rose, “so it is imperative that we cast a wide, international net when searching for new genes.”

Nijmegen’s Center Grant will include support for:
•Identifying new retinal-disease genes — including those causing conditions such as retinitis pigmentosa and age-related macular degeneration — through the use of next-generation genetic discovery technologies.

•Developing a better understanding of retinal ciliopathies — including conditions such as retinitis pigmentosa, Usher syndrome and Bardet-Biedl syndrome — in which the transport of proteins critical to vision and photoreceptor health is compromised.

•Enhancing retinal imaging technologies to select and follow patients for future Leber congenital amaurosis (CEP290 mutations) and Stargardt disease gene therapy clinical trials.

The new Foundation Center Grant supports what is officially known as the Radboud University Nijmegen Research Center for Studying Retinal Degenerative Diseases and its principal investigators: Drs. Frans Cremers, Anneke den Hollander, Hannie Kremer, Ronald Roepman and Thomas Theelen. Co-investigators are: Drs. Rob Collin, Carel Hoyng, Jeroen Klevering and Erwin van Wijk.

Nijmegen is the third facility in Europe to receive a Foundation Center Grant, joining Moorfields Eye Hospital in London and the Institut de la Vision in Paris.
生命不息,战斗不止。
谢谢楼主的分享,FFB对视网膜疾病的研究作出了巨大贡献,他的地位是其他组织不能替代的。
谢谢楼主的分享
谢谢楼主的分享,希望治疗能早点到来!
谢谢楼主的分享.
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