Research Perspectives in Inherited Lymphatic Disease
Identifieur interne : 006D53 ( Main/Exploration ); précédent : 006D52; suivant : 006D54Research Perspectives in Inherited Lymphatic Disease
Auteurs : Robert E. Ferrell [États-Unis] ; David N. Finegold [États-Unis]Source :
- Annals of the New York Academy of Sciences [ 0077-8923 ] ; 2008-05.
Descripteurs français
- KwdFr :
- MESH :
- génétique : Facteurs de transcription Forkhead, Lymphoedème, Maladies lymphatiques, Syndrome de Noonan.
- tendances : Recherche.
- Animaux, Humains, Lymphangiogenèse.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Forkhead Transcription Factors.
- genetics : Lymphatic Diseases, Lymphedema, Noonan Syndrome.
- trends : Research.
- Animals, Humans, Lymphangiogenesis.
Abstract
Genetic studies of inherited lymphedema have provided the starting point for the molecular dissection of lymphatic development and disease. Here, we update the recent contribution of the study of inherited lymphedema and discuss the parallels between mouse models of lymphedema and inherited lymphedema. That the known mutations leading to lymphatic phenotypes explain fewer than half the cases of lymphedema means that the continued study of these disorders may reveal new pathways in lymphatic biology.
Url:
DOI: 10.1196/annals.1413.012
Affiliations:
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Le document en format XML
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Finegold</name><affiliation wicri:level="4"><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania</wicri:regionArea><placeName><region type="state">Pennsylvanie</region><settlement type="city">Pittsburgh</settlement></placeName><orgName type="university">Université de Pittsburgh</orgName></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Annals of the New York Academy of Sciences</title><title level="j" type="alt">ANNALS OF NEW YORK ACADEMY SCIENCES</title><idno type="ISSN">0077-8923</idno><idno type="eISSN">1749-6632</idno><imprint><biblScope unit="vol">1131</biblScope><biblScope unit="issue">1</biblScope><biblScope unit="page" from="134">134</biblScope><biblScope unit="page" to="139">139</biblScope><biblScope unit="page-count">5</biblScope><publisher>Blackwell Publishing Inc</publisher><pubPlace>Malden, USA</pubPlace><date type="published" when="2008-05">2008-05</date></imprint><idno type="ISSN">0077-8923</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">0077-8923</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Animals</term><term>Forkhead Transcription Factors (genetics)</term><term>Humans</term><term>Lymphangiogenesis</term><term>Lymphatic Diseases (genetics)</term><term>Lymphedema (genetics)</term><term>Noonan Syndrome (genetics)</term><term>Research (trends)</term></keywords><keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term><term>Facteurs de transcription Forkhead (génétique)</term><term>Humains</term><term>Lymphangiogenèse</term><term>Lymphoedème (génétique)</term><term>Maladies lymphatiques (génétique)</term><term>Recherche (tendances)</term><term>Syndrome de Noonan (génétique)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Forkhead Transcription Factors</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Lymphatic Diseases</term><term>Lymphedema</term><term>Noonan Syndrome</term></keywords><keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Facteurs de transcription Forkhead</term><term>Lymphoedème</term><term>Maladies lymphatiques</term><term>Syndrome de Noonan</term></keywords><keywords scheme="MESH" qualifier="tendances" xml:lang="fr"><term>Recherche</term></keywords><keywords scheme="MESH" qualifier="trends" xml:lang="en"><term>Research</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Animals</term><term>Humans</term><term>Lymphangiogenesis</term></keywords><keywords scheme="MESH" xml:lang="fr"><term>Animaux</term><term>Humains</term><term>Lymphangiogenèse</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Genetic studies of inherited lymphedema have provided the starting point for the molecular dissection of lymphatic development and disease. Here, we update the recent contribution of the study of inherited lymphedema and discuss the parallels between mouse models of lymphedema and inherited lymphedema. That the known mutations leading to lymphatic phenotypes explain fewer than half the cases of lymphedema means that the continued study of these disorders may reveal new pathways in lymphatic biology.</div></front></TEI><affiliations><list><country><li>États-Unis</li></country><region><li>Pennsylvanie</li></region><settlement><li>Pittsburgh</li></settlement><orgName><li>Université de Pittsburgh</li></orgName></list><tree><country name="États-Unis"><region name="Pennsylvanie"><name sortKey="Ferrell, Robert E" sort="Ferrell, Robert E" uniqKey="Ferrell R" first="Robert E." last="Ferrell">Robert E. Ferrell</name></region><name sortKey="Finegold, David N" sort="Finegold, David N" uniqKey="Finegold D" first="David N." last="Finegold">David N. Finegold</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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