ParkinsonFranceV1, PubMed, Corpus, bibRecord, 001596

Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.

Identifieur interne : 001596 ( PubMed/Corpus ); précédent : 001595; suivant : 001597

Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.

Auteurs : R. Bordet ; F. Broly ; A. Destée ; C. Libersa

Source :

Advances in neurology [ 0091-3952 ] ; 1996.

RBID : pubmed:8615190

English descriptors

KwdEn :
- Aged, Base Sequence, Cytochrome P-450 CYP2D6, Cytochrome P-450 Enzyme System (genetics), Cytochrome P-450 Enzyme System (metabolism), DNA (analysis), Debrisoquin (metabolism), Female, Genotype, Heterozygote, Homozygote, Humans, Hydroxylation, Male, Mixed Function Oxygenases (genetics), Mixed Function Oxygenases (metabolism), Molecular Sequence Data, Parkinson Disease (enzymology), Parkinson Disease (genetics), Parkinson Disease (metabolism), Polymorphism, Restriction Fragment Length.
MESH :
- chemical , analysis : DNA.
- chemical , genetics : Cytochrome P-450 Enzyme System, Mixed Function Oxygenases.
- chemical , metabolism : Cytochrome P-450 Enzyme System, Debrisoquin, Mixed Function Oxygenases.
- chemical : Cytochrome P-450 CYP2D6.
- enzymology : Parkinson Disease.
- genetics : Parkinson Disease.
- metabolism : Parkinson Disease.
- Aged, Base Sequence, Female, Genotype, Heterozygote, Homozygote, Humans, Hydroxylation, Male, Molecular Sequence Data, Polymorphism, Restriction Fragment Length.

PubMed: 8615190

Links to Exploration step

pubmed:8615190

Le document en format XML

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<author><name sortKey="Bordet, R" sort="Bordet, R" uniqKey="Bordet R" first="R" last="Bordet">R. Bordet</name>
<affiliation><nlm:affiliation>Department of Neurology A, Hôpital B, CHRU, Lille, France.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Broly, F" sort="Broly, F" uniqKey="Broly F" first="F" last="Broly">F. Broly</name>
</author>
<author><name sortKey="Destee, A" sort="Destee, A" uniqKey="Destee A" first="A" last="Destée">A. Destée</name>
</author>
<author><name sortKey="Libersa, C" sort="Libersa, C" uniqKey="Libersa C" first="C" last="Libersa">C. Libersa</name>
</author>
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<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1996">1996</date>
<idno type="RBID">pubmed:8615190</idno>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.</title>
<author><name sortKey="Bordet, R" sort="Bordet, R" uniqKey="Bordet R" first="R" last="Bordet">R. Bordet</name>
<affiliation><nlm:affiliation>Department of Neurology A, Hôpital B, CHRU, Lille, France.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Broly, F" sort="Broly, F" uniqKey="Broly F" first="F" last="Broly">F. Broly</name>
</author>
<author><name sortKey="Destee, A" sort="Destee, A" uniqKey="Destee A" first="A" last="Destée">A. Destée</name>
</author>
<author><name sortKey="Libersa, C" sort="Libersa, C" uniqKey="Libersa C" first="C" last="Libersa">C. Libersa</name>
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<series><title level="j">Advances in neurology</title>
<idno type="ISSN">0091-3952</idno>
<imprint><date when="1996" type="published">1996</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Base Sequence</term>
<term>Cytochrome P-450 CYP2D6</term>
<term>Cytochrome P-450 Enzyme System (genetics)</term>
<term>Cytochrome P-450 Enzyme System (metabolism)</term>
<term>DNA (analysis)</term>
<term>Debrisoquin (metabolism)</term>
<term>Female</term>
<term>Genotype</term>
<term>Heterozygote</term>
<term>Homozygote</term>
<term>Humans</term>
<term>Hydroxylation</term>
<term>Male</term>
<term>Mixed Function Oxygenases (genetics)</term>
<term>Mixed Function Oxygenases (metabolism)</term>
<term>Molecular Sequence Data</term>
<term>Parkinson Disease (enzymology)</term>
<term>Parkinson Disease (genetics)</term>
<term>Parkinson Disease (metabolism)</term>
<term>Polymorphism, Restriction Fragment Length</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analysis" xml:lang="en"><term>DNA</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Cytochrome P-450 Enzyme System</term>
<term>Mixed Function Oxygenases</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Cytochrome P-450 Enzyme System</term>
<term>Debrisoquin</term>
<term>Mixed Function Oxygenases</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Cytochrome P-450 CYP2D6</term>
</keywords>
<keywords scheme="MESH" qualifier="enzymology" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Base Sequence</term>
<term>Female</term>
<term>Genotype</term>
<term>Heterozygote</term>
<term>Homozygote</term>
<term>Humans</term>
<term>Hydroxylation</term>
<term>Male</term>
<term>Molecular Sequence Data</term>
<term>Polymorphism, Restriction Fragment Length</term>
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<DateCreated><Year>1996</Year>
<Month>05</Month>
<Day>31</Day>
</DateCreated>
<DateCompleted><Year>1996</Year>
<Month>05</Month>
<Day>31</Day>
</DateCompleted>
<DateRevised><Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0091-3952</ISSN>
<JournalIssue CitedMedium="Print"><Volume>69</Volume>
<PubDate><Year>1996</Year>
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<Title>Advances in neurology</Title>
<ISOAbbreviation>Adv Neurol</ISOAbbreviation>
</Journal>
<ArticleTitle>Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.</ArticleTitle>
<Pagination><MedlinePgn>97-100</MedlinePgn>
</Pagination>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Bordet</LastName>
<ForeName>R</ForeName>
<Initials>R</Initials>
<AffiliationInfo><Affiliation>Department of Neurology A, Hôpital B, CHRU, Lille, France.</Affiliation>
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</Author>
<Author ValidYN="Y"><LastName>Broly</LastName>
<ForeName>F</ForeName>
<Initials>F</Initials>
</Author>
<Author ValidYN="Y"><LastName>Destée</LastName>
<ForeName>A</ForeName>
<Initials>A</Initials>
</Author>
<Author ValidYN="Y"><LastName>Libersa</LastName>
<ForeName>C</ForeName>
<Initials>C</Initials>
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<Language>eng</Language>
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<NameOfSubstance UI="D003577">Cytochrome P-450 Enzyme System</NameOfSubstance>
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<Chemical><RegistryNumber>EC 1.-</RegistryNumber>
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<Chemical><RegistryNumber>EC 1.14.14.1</RegistryNumber>
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<MeshHeading><DescriptorName UI="D001483" MajorTopicYN="N">Base Sequence</DescriptorName>
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<MeshHeading><DescriptorName UI="D019389" MajorTopicYN="N">Cytochrome P-450 CYP2D6</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003577" MajorTopicYN="N">Cytochrome P-450 Enzyme System</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004247" MajorTopicYN="N">DNA</DescriptorName>
<QualifierName UI="Q000032" MajorTopicYN="N">analysis</QualifierName>
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<MeshHeading><DescriptorName UI="D003647" MajorTopicYN="N">Debrisoquin</DescriptorName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005260" MajorTopicYN="N">Female</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005838" MajorTopicYN="N">Genotype</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006579" MajorTopicYN="N">Heterozygote</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006720" MajorTopicYN="N">Homozygote</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006900" MajorTopicYN="N">Hydroxylation</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008297" MajorTopicYN="N">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D006899" MajorTopicYN="N">Mixed Function Oxygenases</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D008969" MajorTopicYN="N">Molecular Sequence Data</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010300" MajorTopicYN="N">Parkinson Disease</DescriptorName>
<QualifierName UI="Q000201" MajorTopicYN="N">enzymology</QualifierName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
<QualifierName UI="Q000378" MajorTopicYN="Y">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012150" MajorTopicYN="N">Polymorphism, Restriction Fragment Length</DescriptorName>
</MeshHeading>
</MeshHeadingList>
</MedlineCitation>
<PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>1996</Year>
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	La maladie de Parkinson en France (serveur d'exploration)
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La maladie de Parkinson en France (serveur d'exploration)

Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.

Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.

Source :

English descriptors

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki