Rapid identification and characterisation of genes involved in skeletal development

快速鉴定和表征参与骨骼发育的基因

• 批准号: nhmrc : 1002658
• 负责人: Dr Peter Farlie
• 金额: $ 36.71万
• 依托单位: Murdoch Childrens Research Institute
• 依托单位国家: 澳大利亚
• 项目类别: NHMRC Project Grants
• 财政年份: 2011
• 资助国家: 澳大利亚
• 起止时间: 2011-01-01 至 2013-12-31
• 项目状态: 已结题
• 来源: https://researchdata.edu.au/rapid-identification-characterisation-skeletal-development/108843
• 关键词: Rapid; identification; characterisation; genes; involved

Birth defects are common and have an enormous impact on both the individual and their family. Birth defects are by definition the products of abnormal development of the embryo. Our research is aimed at identifying the normal mechanisms that usually prevail during development and the disturbances to those mechanisms that result in birth defects. These findings will lead to improved diagnostic, therapeutic and preventative options for families affected by birth defects

出生缺陷是常见的，对个人和家庭都有巨大的影响。出生缺陷的定义是胚胎发育异常的产物。我们的研究旨在确定通常在发育过程中占主导地位的正常机制，以及导致出生缺陷的这些机制的干扰。这些发现将为受出生缺陷影响的家庭提供更好的诊断、治疗和预防选择