MOLECULAR GENETICS OF FACIO AUDIO SYMPHALANGISM
MOLECULAR GENETICS OF FACIO AUDIO SYMPHALANGISM
批准号:
2550555
负责人:
Deborah Krakow
金额:
$8.2万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-09-01 至 2000-08-31
中文摘要
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英文摘要
DESCRIPTION (taken from application)
Facio-audio-symphalangism (FAS) is an autosomal dominant disorder
characterized by a triad of findings including distinct facies, early onset
deafness and progressive joint fusions. We have identified a large Hawaiian
family with this disorder. The goal of this project is to define the
phenotype and natural history of the disease, determine the chromosomal
location of the defective gene and identify the defective gene. To this
end, the specific aims of the proposal are: 1) To define the clinical
phenotype and natural history of facio-audio-symphalangism. We will
delineate the clinical and radiographic findings as well as the natural
history of the disorder in this large, multigeneration family. 2) To
determine the chromosomal location of the defective gene. Employing markers
in both candidate genes and genome wide markers, I will use linkage studies
to determine the chromosomal region containing the disease gene. 3) To
determine if there is locus heterogeneity in facio-audio-symphalangism and
if other phenotypically similar dominantly inherited disorders map to the
same chromosomal location. By performing linkage analysis on other
facio-audio-symphalangism families I will determine if there is more than
one FAS disease gene. I will also carry out linkage studies in families
with related disorders, including multiple synostoses syndrome and proximal
symphalangism, to determine if the disease genes co-localize with FAS. 4)
To identify the disease gene in facio-audio-symphalangism. By a positional
strategy, candidate genes from the FAS interval will be isolated. Mutation
analysis will be used to identify the defective gene in FAS. This project
represents a genetic approach to dissecting the poorly understood process of
the development and maintenance of joint integrity. Identification of a
gene involved in this process will provide the means to identify other genes
involved in this complex pathway and stimulate biologic research in this
area.
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Patient-Centered Outcomes Research Training in Urologic and Gynecologic Cancers (PCORT UroGynCan)
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批准号:10689207
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项目类别:
-
资助金额:$37.53万
-
财政年份:2020
-
负责人:Deborah Krakow
-
依托单位:
Patient-Centered Outcomes Research Training in Urologic and Gynecologic Cancers (PCORT UroGynCan)
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批准号:10024967
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项目类别:
-
资助金额:$39.6万
-
财政年份:2020
-
负责人:Deborah Krakow
-
依托单位:
Patient-Centered Outcomes Research Training in Urologic and Gynecologic Cancers (PCORT UroGynCan)
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批准号:10246498
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项目类别:
-
资助金额:$40.16万
-
财政年份:2020
-
负责人:Deborah Krakow
-
依托单位:
Unraveling the mechanisms of prenatal-onset disorders affecting the skeleton
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批准号:9242561
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项目类别:
-
资助金额:$33.34万
-
财政年份:2014
-
负责人:Deborah Krakow
-
依托单位:
Unraveling the mechanisms of prenatal-onset disorders affecting the skeleton
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批准号:8675030
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项目类别:
-
资助金额:$34.61万
-
财政年份:2014
-
负责人:Deborah Krakow
-
依托单位:
Unraveling the mechanisms of prenatal-onset disorders affecting the skeleton
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批准号:9061402
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项目类别:
-
资助金额:$33.37万
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财政年份:2014
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负责人:Deborah Krakow
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依托单位:
THE SKELETAL DYSPLASIAS (PROJECT 2)
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批准号:7952190
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项目类别:
-
资助金额:$0.47万
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财政年份:2008
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负责人:Deborah Krakow
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依托单位:
ASPERGILLLUS ANGIONVASION AND DISSEMINATION
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批准号:7606110
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项目类别:
-
资助金额:$0.69万
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财政年份:2007
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负责人:Deborah Krakow
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依托单位:
ASPERGILLLUS ANGIONVASION AND DISSEMINATION
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批准号:7376009
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项目类别:
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资助金额:$1.96万
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财政年份:2005
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负责人:Deborah Krakow
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依托单位:
MOLECULAR GENETICS OF FACIO AUDIO SYMPHALANGISM
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批准号:2888729
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项目类别:
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资助金额:$6.73万
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财政年份:1997
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负责人:Deborah Krakow
-
依托单位:
MOLECULAR GENETICS OF FACIO AUDIO SYMPHALANGISM
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批准号:2673356
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项目类别:
-
资助金额:$8.2万
-
财政年份:1997
-
负责人:Deborah Krakow
-
依托单位:
Project 2: The role of the HSP47/FKBP65 chaperone complex in osteogenesis imperfecta
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批准号:9974354
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项目类别:
-
资助金额:$41.74万
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财政年份:--
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负责人:Deborah Krakow
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依托单位:
海外基金