THE GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
THE GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
批准号:
7633234
负责人:
JOANNA C JEN
金额:
$37.51万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-09-01 至 2012-06-30
关键词:
11q23AccountingAffectBirthBrainBrain StemCandidate Disease GeneCell NucleusCephalicChildChildhoodClinicalCranial NervesDefectDevelopmentDiffusionDiffusion Magnetic Resonance ImagingDiseaseEmbryoEmbryonic DevelopmentEye MovementsFamilyFunctional ImagingFunctional Magnetic Resonance ImagingFunctional disorderGenesGeneticGenetic ProgrammingGenetic RecombinationGenotypeGoalsGreekHumanImpairmentIn Situ HybridizationIndividualMagnetic Resonance ImagingMapsMediatingMicrosatellite RepeatsModelingMolecularMusMutant Strains MiceNerveNeuronsOnline Mendelian Inheritance In ManOrganismOrthologous GenePathway interactionsPatientsPatternPhenotypeRecruitment ActivityRelative (related person)ResolutionRoleScanningSignal PathwayStructureSyndromeTechniquesTestingWeightabducens nucleusbasebrain tissuegaze palsygenetic pedigreehorizontal gazehuman tissueinfancyinnovationinsightmutantneural patterningneurodevelopmentneurogenesisneuroimagingnoveloculomotorpositional cloningprogramsscoliosistoolwhite matter
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this proposal is to understand the genetic and functional anatomical basis underlying autosomal recessive horizontal gaze palsy with progressive scoliosis (HGPPS; OMIM 607313), the disease locus of which we recently mapped to 11q23-25. This condition is characterized by a complete absence of conjugate horizontal eye movement at birth, with a delayed development of progressive scoliosis during infancy and childhood. Absent horizontal gaze likely results from maldevelopment of the abducens nuclei, involving both abducens moto- and inter-neurons. The recruitment of additional HGPPS patients has enabled the confirmation as well as narrowing of the candidate region in six ethnically diverse inbred families. Continuing effort to identify new patients may further narrow the region. The specific aims for this proposal are: 1) To test the hypothesis that the HGPPS gene is a novel patterning gene. Already underway, candidate gene sequencing will be prioritized based on neuronal expression pattern, putative function in neurodevelopment, and orthologous genes in mice and other organisms. 2) To test the hypothesis that maldevelopment of the abducens nucleus is the anatomical basis of HGPPS. Innovative high-resolution conventional, diffusion tensor, and functional MRI studies will be performed in normal and genetically characterized patients to define the functional anatomical basis of horizontal gaze dysfunction localizing to the brainstem, which has not been well visualized. 3) To test the hypothesis that the HGPPS gene is important in the normal development of the abducens nucleus and other brainstem structures. We will examine expression of the HGPPS gene in embryonic brain tissue from human and mouse (wildtype and developmental mutants) to study its role in the cascade of genetically programmed signaling pathways mediating neurogenesis. Neuroimaging techniques that we develop will be applicable to the study of other brainstem structures important in oculomotor control. Understanding the anatomical and molecular basis of HGPPS will provide insight into the genetically programmed neurodevelopment of the conjugate horizontal gaze center and other cranial nuclei in the brainstem.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
Effects of failure of development of crossing brainstem pathways on ocular motor control.
穿过脑干通路发育失败对眼部运动控制的影响。
DOI:
10.1016/s0079-6123(08)00618-3
发表时间:
2008
期刊:
Progress in brain research
影响因子:
--
作者:
[Jen,JoannaC]
通讯作者:
Jen,JoannaC
Functional neuroanatomy of the human premotor oculomotor brainstem nuclei: insights from postmortem and advanced in vivo imaging studies.
人类运动前动眼神经脑干核的功能神经解剖学:来自尸检和先进体内成像研究的见解。
DOI:
10.1007/s00221-008-1342-8
发表时间:
2008
期刊:
Experimental brain research
影响因子:
2
作者:
[Rüb,Udo, Jen,JoannaC, Braak,Heiko, Deller,Thomas]
通讯作者:
Deller,Thomas
DOI:
10.1038/ng.2254
发表时间:
2012-04-29
期刊:
NATURE GENETICS
影响因子:
30.8
作者:
[Wan, Jijun, Yourshaw, Michael, Mamsa, Hafsa, Rudnik-Schoeneborn, Sabine, Menezes, Manoj P., Hong, Ji Eun, Leong, Derek W., Senderek, Jan, Salman, Michael S., Chitayat, David, Seeman, Pavel, von Moers, Arpad, Graul-Neumann, Luitgard, Kornberg, Andrew J., Castro-Gago, Manuel, Sobrido, Maria-Jesus, Sanefuji, Masafumi, Shieh, Perry B., Salamon, Noriko, Kim, Ronald C., Vinters, Harry V., Chen, Zugen, Zerres, Klaus, Ryan, Monique M., Nelson, Stanley F., Jen, Joanna C.]
通讯作者:
Jen, Joanna C.
Phase 2 Study of 4-Aminopyridine for the Treatment of Episodic Ataxia Type 2
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批准号:8022784
-
项目类别:
-
资助金额:$19.99万
-
财政年份:2011
-
负责人:JOANNA C JEN
-
依托单位:
Genetics of Familial Episodic Ataxia
-
批准号:7783885
-
项目类别:
-
资助金额:$49.74万
-
财政年份:2009
-
负责人:JOANNA C JEN
-
依托单位:
Pathobiology of Retinal Vasculopathy with Cerebal Leukodystrophy (RVCL)
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批准号:7737340
-
项目类别:
-
资助金额:$56.95万
-
财政年份:2009
-
负责人:JOANNA C JEN
-
依托单位:
International Conference on Episodic Ataxia Syndromes
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批准号:7059049
-
项目类别:
-
资助金额:$3.52万
-
财政年份:2005
-
负责人:JOANNA C JEN
-
依托单位:
THE GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
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批准号:7238562
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项目类别:
-
资助金额:$37.51万
-
财政年份:2004
-
负责人:JOANNA C JEN
-
依托单位:
GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
-
批准号:6735950
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项目类别:
-
资助金额:$38.38万
-
财政年份:2004
-
负责人:JOANNA C JEN
-
依托单位:
THE GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
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批准号:7091119
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项目类别:
-
资助金额:$0.39万
-
财政年份:2004
-
负责人:JOANNA C JEN
-
依托单位:
THE GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
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批准号:7460879
-
项目类别:
-
资助金额:$36.76万
-
财政年份:2004
-
负责人:JOANNA C JEN
-
依托单位:
THE GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
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批准号:7076864
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项目类别:
-
资助金额:$37.72万
-
财政年份:2004
-
负责人:JOANNA C JEN
-
依托单位:
THE GENETIC & FUNCTIONAL ANATOMICAL BASIS OF HGPPS
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批准号:6932303
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项目类别:
-
资助金额:$38.63万
-
财政年份:2004
-
负责人:JOANNA C JEN
-
依托单位:
MUTATIONS IN CALCIUM CHANNELS CAUSING VERTIGO AND ATAXIA
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批准号:2909872
-
项目类别:
-
资助金额:$8.8万
-
财政年份:1998
-
负责人:JOANNA C JEN
-
依托单位:
MUTATIONS IN CALCIUM CHANNELS CAUSING VERTIGO AND ATAXIA
-
批准号:6379189
-
项目类别:
-
资助金额:$7.72万
-
财政年份:1998
-
负责人:JOANNA C JEN
-
依托单位:
MUTATIONS IN CALCIUM CHANNELS CAUSING VERTIGO AND ATAXIA
-
批准号:2598875
-
项目类别:
-
资助金额:$8.8万
-
财政年份:1998
-
负责人:JOANNA C JEN
-
依托单位:
MUTATIONS IN CALCIUM CHANNELS CAUSING VERTIGO AND ATAXIA
-
批准号:6516024
-
项目类别:
-
资助金额:$18.67万
-
财政年份:1998
-
负责人:JOANNA C JEN
-
依托单位:
MUTATIONS IN CALCIUM CHANNELS CAUSING VERTIGO AND ATAXIA
-
批准号:6175716
-
项目类别:
-
资助金额:$8.8万
-
财政年份:1998
-
负责人:JOANNA C JEN
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依托单位:
海外基金