Movement Disorders (revue)

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Alterations of striatal neurons in benign hereditary chorea

Identifieur interne : 003A27 ( Main/Exploration ); précédent : 003A26; suivant : 003A28

Alterations of striatal neurons in benign hereditary chorea

Auteurs : Galit Kleiner-Fisman [États-Unis] ; Noel Y. Calingasan [États-Unis] ; Mary Putt [États-Unis] ; June Chen [États-Unis] ; M. Flint Beal [États-Unis] ; Anthony E. Lang [Canada]

Source :

RBID : ISTEX:93B807CB7E16134EA05B9026D8B2B230655481A7

English descriptors

Abstract

Benign hereditary chorea (BHC) recently has been associated with mutations in TITF‐1 gene, although a pathological study of an individual with BHC and a TITF‐1 mutation revealed no significant gross or microscopic abnormalities using standard methods. Immunohistochemical staining of striatal tissue from a BHC‐affected postmortem brain was performed using antibodies against neurotransmitters of interneurons whose tangential migration is mediated by TITF‐1. There was a loss of most TITF‐1–mediated striatal interneurons in the BHC specimen compared to four matched control brains. © 2005 Movement Disorder Society

Url:
DOI: 10.1002/mds.20577


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Alterations of striatal neurons in benign hereditary chorea</title>
<author>
<name sortKey="Kleiner Isman, Galit" sort="Kleiner Isman, Galit" uniqKey="Kleiner Isman G" first="Galit" last="Kleiner-Fisman">Galit Kleiner-Fisman</name>
</author>
<author>
<name sortKey="Calingasan, Noel Y" sort="Calingasan, Noel Y" uniqKey="Calingasan N" first="Noel Y." last="Calingasan">Noel Y. Calingasan</name>
</author>
<author>
<name sortKey="Putt, Mary" sort="Putt, Mary" uniqKey="Putt M" first="Mary" last="Putt">Mary Putt</name>
</author>
<author>
<name sortKey="Chen, June" sort="Chen, June" uniqKey="Chen J" first="June" last="Chen">June Chen</name>
</author>
<author>
<name sortKey="Beal, M Flint" sort="Beal, M Flint" uniqKey="Beal M" first="M. Flint" last="Beal">M. Flint Beal</name>
</author>
<author>
<name sortKey="Lang, Anthony E" sort="Lang, Anthony E" uniqKey="Lang A" first="Anthony E." last="Lang">Anthony E. Lang</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:93B807CB7E16134EA05B9026D8B2B230655481A7</idno>
<date when="2005" year="2005">2005</date>
<idno type="doi">10.1002/mds.20577</idno>
<idno type="url">https://api.istex.fr/document/93B807CB7E16134EA05B9026D8B2B230655481A7/fulltext/pdf</idno>
<idno type="wicri:Area/Istex/Corpus">003126</idno>
<idno type="wicri:Area/Istex/Curation">003126</idno>
<idno type="wicri:Area/Istex/Checkpoint">002437</idno>
<idno type="wicri:doubleKey">0885-3185:2005:Kleiner Isman G:alterations:of:striatal</idno>
<idno type="wicri:source">PubMed</idno>
<idno type="RBID">pubmed:15986422</idno>
<idno type="wicri:Area/PubMed/Corpus">003014</idno>
<idno type="wicri:Area/PubMed/Curation">003014</idno>
<idno type="wicri:Area/PubMed/Checkpoint">003238</idno>
<idno type="wicri:Area/Ncbi/Merge">001298</idno>
<idno type="wicri:Area/Ncbi/Curation">001298</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">001298</idno>
<idno type="wicri:doubleKey">0885-3185:2005:Kleiner Fisman G:alterations:of:striatal</idno>
<idno type="wicri:Area/Main/Merge">005114</idno>
<idno type="wicri:Area/Main/Curation">003A27</idno>
<idno type="wicri:Area/Main/Exploration">003A27</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Alterations of striatal neurons in benign hereditary chorea</title>
<author>
<name sortKey="Kleiner Isman, Galit" sort="Kleiner Isman, Galit" uniqKey="Kleiner Isman G" first="Galit" last="Kleiner-Fisman">Galit Kleiner-Fisman</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Parkinson's Disease Research, Education and Clinical Center (PADRECC), Philadelphia VA Hospital, Philadelphia, Pennsylvania</wicri:regionArea>
<placeName>
<region type="state">Pennsylvanie</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Calingasan, Noel Y" sort="Calingasan, Noel Y" uniqKey="Calingasan N" first="Noel Y." last="Calingasan">Noel Y. Calingasan</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York, New York</wicri:regionArea>
<placeName>
<region type="state">État de New York</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Putt, Mary" sort="Putt, Mary" uniqKey="Putt M" first="Mary" last="Putt">Mary Putt</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biostatistics and Epidemiology, University of Pennsylvania, Philadelphia, Pennsylvania</wicri:regionArea>
<placeName>
<region type="state">Pennsylvanie</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Chen, June" sort="Chen, June" uniqKey="Chen J" first="June" last="Chen">June Chen</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York, New York</wicri:regionArea>
<placeName>
<region type="state">État de New York</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Beal, M Flint" sort="Beal, M Flint" uniqKey="Beal M" first="M. Flint" last="Beal">M. Flint Beal</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York, New York</wicri:regionArea>
<placeName>
<region type="state">État de New York</region>
</placeName>
</affiliation>
</author>
<author>
<name sortKey="Lang, Anthony E" sort="Lang, Anthony E" uniqKey="Lang A" first="Anthony E." last="Lang">Anthony E. Lang</name>
<affiliation wicri:level="4">
<country xml:lang="fr">Canada</country>
<wicri:regionArea>The Morton and Gloria Shulman Movement Disorders Center, Toronto Western Hospital, University of Toronto, Toronto, Ontario</wicri:regionArea>
<orgName type="university">Université de Toronto</orgName>
<placeName>
<settlement type="city">Toronto</settlement>
<region type="state">Ontario</region>
</placeName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Movement Disorders</title>
<title level="j" type="sub">Official Journal of the Movement Disorder Society</title>
<title level="j" type="abbrev">Mov. Disord.</title>
<idno type="ISSN">0885-3185</idno>
<idno type="eISSN">1531-8257</idno>
<imprint>
<publisher>Wiley Subscription Services, Inc., A Wiley Company</publisher>
<pubPlace>Hoboken</pubPlace>
<date type="published" when="2005-10">2005-10</date>
<biblScope unit="vol">20</biblScope>
<biblScope unit="issue">10</biblScope>
<biblScope unit="page" from="1353">1353</biblScope>
<biblScope unit="page" to="1357">1357</biblScope>
</imprint>
<idno type="ISSN">0885-3185</idno>
</series>
<idno type="istex">93B807CB7E16134EA05B9026D8B2B230655481A7</idno>
<idno type="DOI">10.1002/mds.20577</idno>
<idno type="ArticleID">MDS20577</idno>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Antibodies (immunology)</term>
<term>Cell Movement</term>
<term>Chorea (genetics)</term>
<term>Chorea (metabolism)</term>
<term>Chorea (pathology)</term>
<term>Chromosomes, Human, Pair 14 (genetics)</term>
<term>Corpus Striatum (metabolism)</term>
<term>Corpus Striatum (pathology)</term>
<term>Fatal Outcome</term>
<term>Humans</term>
<term>Immunohistochemistry</term>
<term>Interneurons (immunology)</term>
<term>Interneurons (metabolism)</term>
<term>Interneurons (pathology)</term>
<term>Middle Aged</term>
<term>Neurons (metabolism)</term>
<term>Neurons (pathology)</term>
<term>Neurotransmitter Agents (immunology)</term>
<term>Nuclear Proteins (genetics)</term>
<term>Nuclear Proteins (metabolism)</term>
<term>Point Mutation (genetics)</term>
<term>TITF‐1</term>
<term>Transcription Factors (genetics)</term>
<term>Transcription Factors (metabolism)</term>
<term>benign hereditary chorea</term>
<term>migration</term>
<term>pathology</term>
<term>projection neurons</term>
<term>striatal interneurons</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Nuclear Proteins</term>
<term>Transcription Factors</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="immunology" xml:lang="en">
<term>Antibodies</term>
<term>Neurotransmitter Agents</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Chorea</term>
<term>Chromosomes, Human, Pair 14</term>
<term>Point Mutation</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en">
<term>Interneurons</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Chorea</term>
<term>Corpus Striatum</term>
<term>Interneurons</term>
<term>Neurons</term>
<term>Nuclear Proteins</term>
<term>Transcription Factors</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en">
<term>Chorea</term>
<term>Corpus Striatum</term>
<term>Interneurons</term>
<term>Neurons</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Cell Movement</term>
<term>Fatal Outcome</term>
<term>Humans</term>
<term>Immunohistochemistry</term>
<term>Middle Aged</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Benign hereditary chorea (BHC) recently has been associated with mutations in TITF‐1 gene, although a pathological study of an individual with BHC and a TITF‐1 mutation revealed no significant gross or microscopic abnormalities using standard methods. Immunohistochemical staining of striatal tissue from a BHC‐affected postmortem brain was performed using antibodies against neurotransmitters of interneurons whose tangential migration is mediated by TITF‐1. There was a loss of most TITF‐1–mediated striatal interneurons in the BHC specimen compared to four matched control brains. © 2005 Movement Disorder Society</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>Canada</li>
<li>États-Unis</li>
</country>
<region>
<li>Ontario</li>
<li>Pennsylvanie</li>
<li>État de New York</li>
</region>
<settlement>
<li>Toronto</li>
</settlement>
<orgName>
<li>Université de Toronto</li>
</orgName>
</list>
<tree>
<country name="États-Unis">
<region name="Pennsylvanie">
<name sortKey="Kleiner Isman, Galit" sort="Kleiner Isman, Galit" uniqKey="Kleiner Isman G" first="Galit" last="Kleiner-Fisman">Galit Kleiner-Fisman</name>
</region>
<name sortKey="Beal, M Flint" sort="Beal, M Flint" uniqKey="Beal M" first="M. Flint" last="Beal">M. Flint Beal</name>
<name sortKey="Calingasan, Noel Y" sort="Calingasan, Noel Y" uniqKey="Calingasan N" first="Noel Y." last="Calingasan">Noel Y. Calingasan</name>
<name sortKey="Chen, June" sort="Chen, June" uniqKey="Chen J" first="June" last="Chen">June Chen</name>
<name sortKey="Putt, Mary" sort="Putt, Mary" uniqKey="Putt M" first="Mary" last="Putt">Mary Putt</name>
</country>
<country name="Canada">
<region name="Ontario">
<name sortKey="Lang, Anthony E" sort="Lang, Anthony E" uniqKey="Lang A" first="Anthony E." last="Lang">Anthony E. Lang</name>
</region>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003A27 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 003A27 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:93B807CB7E16134EA05B9026D8B2B230655481A7
   |texte=   Alterations of striatal neurons in benign hereditary chorea
}}

Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024