发明名称 |
IDENTIFICATION OF NEURAL DEFECTS ASSOCIATED WITH THE NUCLEOSOMAL ASSEMBLY PROTEIN 1L2 GENE |
摘要 |
A method for screening neural system defects in a human comprises: (A) providing chromosomal material from the human; (B) detecting a modification of the NAP1L2 gene in the chromosomal material, wherein the modification is selected from a) substitution, b) deletion, c) frame-shift, or d) insertion that causes a loss of biological function in the NAP1L2 gene; and (C) correlating the modification of the gene with a potential for a neural system defect. The method can also be practiced with the mouse Nap1l2 gene. |
申请公布号 |
EP1373559(A2) |
申请公布日期 |
2004.01.02 |
申请号 |
EP20010934234 |
申请日期 |
2001.05.04 |
申请人 |
PASTEUR INSTITUT;CENTRE NAT RECH SCIENT |
发明人 |
AVNER PHILIP;ROGNER UTE CHRISTINE;SPYROPOULOS DEMETRI;ROUGEULLE CLAIRE |
分类号 |
G01N33/48;A61K45/00;A61P25/00;A61P35/00;C12N5/10;C12N15/09;C12Q1/68;G01N33/15;G01N33/50;G01N33/53;(IPC1-7):C12Q1/68;C07K14/47;C12N15/63 |
主分类号 |
G01N33/48 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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