Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.
Identifieur interne : 004483 ( Main/Exploration ); précédent : 004482; suivant : 004484Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.
Auteurs : R. Bordet [France] ; F. Broly ; A. Destée ; C. LibersaSource :
- Advances in neurology [ 0091-3952 ] ; 1996.
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
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 001596
- to stream PubMed, to step Curation: 001555
- to stream PubMed, to step Checkpoint: 001555
- to stream Ncbi, to step Merge: 001D96
- to stream Ncbi, to step Curation: 001D96
- to stream Ncbi, to step Checkpoint: 001D96
- to stream Main, to step Merge: 004D46
- to stream Main, to step Curation: 004483
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><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 wicri:level="3"><nlm:affiliation>Department of Neurology A, Hôpital B, CHRU, Lille, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Department of Neurology A, Hôpital B, CHRU, Lille</wicri:regionArea><placeName><region type="region">Hauts-de-France</region><region type="old region">Nord-Pas-de-Calais</region><settlement type="city">Lille</settlement></placeName></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></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="1996">1996</date><idno type="RBID">pubmed:8615190</idno><idno type="pmid">8615190</idno><idno type="wicri:Area/PubMed/Corpus">001596</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">001596</idno><idno type="wicri:Area/PubMed/Curation">001555</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">001555</idno><idno type="wicri:Area/PubMed/Checkpoint">001555</idno><idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">001555</idno><idno type="wicri:Area/Ncbi/Merge">001D96</idno><idno type="wicri:Area/Ncbi/Curation">001D96</idno><idno type="wicri:Area/Ncbi/Checkpoint">001D96</idno><idno type="wicri:doubleKey">0091-3952:1996:Bordet R:debrisoquine:hydroxylation:genotype</idno><idno type="wicri:Area/Main/Merge">004D46</idno><idno type="wicri:Area/Main/Curation">004483</idno><idno type="wicri:Area/Main/Exploration">004483</idno></publicationStmt><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 wicri:level="3"><nlm:affiliation>Department of Neurology A, Hôpital B, CHRU, Lille, France.</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Department of Neurology A, Hôpital B, CHRU, Lille</wicri:regionArea><placeName><region type="region">Hauts-de-France</region><region type="old region">Nord-Pas-de-Calais</region><settlement type="city">Lille</settlement></placeName></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></analytic><series><title level="j">Advances in neurology</title><idno type="ISSN">0091-3952</idno><imprint><date when="1996" type="published">1996</date></imprint></series></biblStruct></sourceDesc></fileDesc><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></keywords><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></keywords></textClass></profileDesc></teiHeader></TEI><affiliations><list><country><li>France</li></country><region><li>Hauts-de-France</li><li>Nord-Pas-de-Calais</li></region><settlement><li>Lille</li></settlement></list><tree><noCountry><name sortKey="Broly, F" sort="Broly, F" uniqKey="Broly F" first="F" last="Broly">F. Broly</name><name sortKey="Destee, A" sort="Destee, A" uniqKey="Destee A" first="A" last="Destée">A. Destée</name><name sortKey="Libersa, C" sort="Libersa, C" uniqKey="Libersa C" first="C" last="Libersa">C. Libersa</name></noCountry><country name="France"><region name="Hauts-de-France"><name sortKey="Bordet, R" sort="Bordet, R" uniqKey="Bordet R" first="R" last="Bordet">R. Bordet</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/ParkinsonFranceV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 004483 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 004483 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Sante
|area= ParkinsonFranceV1
|flux= Main
|étape= Exploration
|type= RBID
|clé= pubmed:8615190
|texte= Debrisoquine hydroxylation genotype in familial forms of idiopathic Parkinson's disease.
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/RBID.i -Sk "pubmed:8615190" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd \
| NlmPubMed2Wicri -a ParkinsonFranceV1
| This area was generated with Dilib version V0.6.29. |  |