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<meta name="keywords" content="C5193213, finding, obesity, variation in, ppargc1b polymorphism, autosomal dominant, autosomal recessive, birth defects, chromosomal disease, chromosome, clinical features, clinical findings, clinical genetics, clinical recommendations, clinvar, congenital chromosomal disease, consumer genetic resources, cytogenetic location, disease characteristics, disease definitions, disease descriptions, disease ontology, disease synonyms, disease vocabulary, dysmorphology, entrez, familial disease, gene, gene-disease relationship, genereviews, genetic disease, genetic disorder, genetic terminology, genetic testing registry, genetics home reference, genomic disease, gtr, hereditary disease, heritable disease, hpo, human phenotype ontology, inherited disease, management guidelines, maternal inheritance, medgen, medical genetics, medical subject headings, mesh, mitochondrial inheritance, mode of inheritance, national center for biotechnology information, national institutes of health, national library of medicine, ncbi, nih, nlm, omim, ordo, orphanet, paternal inheritance, phenome, position statements, professional practice guidelines, rare disease, reference sequence, refseq, snomed ct, syndrome, undiagnosed diseases, x-linked recessive" /><meta name="description" content="" /><meta name="robots" content="index,nofollow,noarchive" />
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<div><div class="rprt full-rprt"><div class="portlet" style="border-top-style: none; margin-top: 0px; padding-top: 0px; margin-bottom: 0px; padding-left: 0.2em;">
|
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<!--
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||
UID=1676181
|
||
ConceptID=C5193213
|
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-->
|
||
<!--imgCountBooks = 0--><h1 class="medgenTitle"><div class="MedGenTitleText">PPARGC1B polymorphism</div></h1><div class="aux"><div class="resc"><dl class="rprtid"><dt>MedGen UID: </dt><dd>1676181</dd><dt><span class="dotprefix"> •</span>Concept ID: </dt><dd><a href="/medgen/docs/help/#sources" target="_blank" title="Concept Unique Identifier from NLM's Unified Medical Language system (UMLS) Click for more information."><span class="highlight" style="background-color:">C5193213</span></a></dd><dt><span class="dotprefix"> •</span></dt><dd>Finding</dd></dl></div></div><table class="medgenTable"><tbody><tr><td>Synonym:</td>
|
||
<td>Obesity, variation in</td></tr>
|
||
<tr><td colspan="2" class="small"> </td></tr><tr><td>OMIM<span class="superscript">®</span>:</td>
|
||
<td><a href="https://omim.org/entry/608886" target="_blank">608886</a></td></tr>
|
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</tbody></table></div><div class="rprt-body jig-ncbiinpagenav" data-jigconfig="smoothScroll: false, gotoTopLink: true, gotoTopLinkText: '', gotoTopLinkAttrs: {'title': 'Go to the top of the page'},allHeadingLevels: ['h1'], topOfPageTOC: true, tocId: 'my-toc'"><div id="rprt-tabs-1" class="rprt-tab"><div id="tb-termsProp-1"><div class="leftCol mgCol"><div>
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<div class="portlet mgSection" id="ID_105">
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<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Professional_guidelines">Professional guidelines</h1><a sid="105" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
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<div class="portlet_content ln"><h3 class="subhead">PubMed<a class="help jig-ncbi-popper" data-jig="ncbipopper" href="#guidelinesHelpPM"><img class="pulldown" src="//static.pubmed.gov/portal/portal3rc.fcgi/4223267/img/4204968" /></a></h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/27752142">Systems genetics analysis of pharmacogenomics variation during antidepressant treatment.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Madsen MB,
|
||
Kogelman LJA,
|
||
Kadarmideen HN,
|
||
Rasmussen HB</span><br />
|
||
<span class="medgenPMjournal">Pharmacogenomics J</span>
|
||
2018 Jan;18(1):144-152.
|
||
Epub 2016 Oct 18
|
||
doi: 10.1038/tpj.2016.68.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27752142" target="_blank">27752142</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=(ppargc1b%20polymorphism)%20AND%20(%22english%20and%20humans%22%5BFilter%5D)%20AND%20(%20(%22practice%20guideline%22%5BFilter%5D)%20OR%20(practice*%5Btitl%5D%20AND%20(guideline%5Btitl%5D%20OR%20parameter%5Btitl%5D%20OR%20resource%5Btitl%5D%20OR%20bulletin%5Btitl%5D%20OR%20best%5Btitl%5D))%20OR%20(genetic*%5Btitl%5D%20AND%20(evaluation%5Btitl%5D%20OR%20counseling%5Btitl%5D%20OR%20screening%5Btitl%5D%20OR%20test*%5Btitl%5D))%20OR%20(clinical%5Btitl%5D%20AND%20((expert%5Btitl%5D%20AND%20consensus%5Btitl%5D)%20OR%20utility%5Btitl%5D%20OR%20guideline*%5Btitl%5D))%20OR%20(management%5Btitl%5D%20AND%20(clinical%5Btitl%5D%20OR%20diagnos*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20pain%5Btitl%5D%20OR%20surveillance%5Btitl%5D%20OR%20emergency%5Btitl%5D%20OR%20guideline*%5Btitl%5D%20OR%20therap*))%20OR%20(treatment%5Btitl%5D%20AND%20((evaluation%5Btitl%5D%20AND%20diagnosis%5Btitl%5D)%20OR%20(assessment%5Btitl%5D%20AND%20prevention%5Btitl%5D)%20OR%20therap*))%20OR%20(Diagnos*%5Btitl%5D%20AND%20(prenatal%5Btitl%5D%20OR%20treatment%5Btitl%5D%20OR%20follow-up%5Btitl%5D%20OR%20statement%5Btitl%5D%20OR%20criteria%5Btitl%5D%20OR%20newborn%5Btitl%5D%20OR%20differential%5Btitl%5D%20OR%20neonatal%5Btitl%5D%20OR%20neonate%5Btitl%5D))%20OR%20(guideline*%5Btitl%5D%20AND%20(pharmacogenetic*%5Btitl%5D%20OR%20recommendation%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20evidence-based%5Btitl%5D%20OR%20consensus%5Btitl%5D%20OR%20(technical%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20(molecular%5Btitl%5D%20AND%20testing%5Btitl%5D)))%20OR%20(risk%5Btitl%5D%20AND%20assessment%5Btitl%5D)%20OR%20(recommendation*%5Btitl%5D%20AND%20(statement%5Btitl%5D%20OR%20Evidence-based%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(care%20AND%20((Patient%5Btitl%5D%20AND%20standard*%5Btitl%5D)%20OR%20primary%5Btitl%5D%20OR%20psychosocial%5Btitl%5D))%20OR%20(Health%5Btitl%5D%20AND%20supervision%5Btitl%5D)%20OR%20(statement%5Btitl%5D%20AND%20(policy%5Btitl%5D%20OR%20position%5Btitl%5D%20OR%20Consensus%5Btitl%5D))%20OR%20(pharmacogenetics%5Btitl%5D%20AND%20(Dosing%5Btitl%5D%20OR%20therap*%5Btitl%5D%20OR%20genotype*%5Btitl%5D%20OR%20drug*%5Btitl%5D))%20OR%20(Chemotherapy%5Btitl%5D%20AND%20decision*%5Btitl%5D)%20OR%20(screening%5Btitl%5D%20AND%20(newborn%5Btitl%5D%20OR%20neonat*%5Btitl%5D%20OR%20detection%5Btitl%5D%20OR%20diagnos*%5Btitl%5D))%20OR%20(criteria%5Btitl%5D%20OR%20genotype*%5Btitl%5D)%20)%20NOT%20(%22Case%20reports%22%5BPublication%20type%5D%20OR%20%22clinical%20study%22%5BPublication%20Type%5D%20OR%20%22randomized%20controlled%20trial%22%5BPublication%20Type%5D)" title="PubMed search">See all (1)</a></div></div>
|
||
</div>
|
||
<div class="display-none help-popup" id="guidelinesHelpPM">These guidelines are articles in PubMed that match specific search criteria developed by MedGen to capture the most relevant practice guidelines. This list may not be comprehensive and may include broader topics as well. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div><div class="display-none help-popup" id="guidelinesHelpCurated">These guidelines are manually curated by the MedGen team
|
||
to supplement articles available in PubMed. See the <a href="/medgen/docs/faq/" title="Frequently asked questions" target="_blank">FAQ</a> for details.</div>
|
||
<div class="portlet mgSection" id="ID_103">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_clinical_studies">Recent clinical studies</h1><a sid="103" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln"><h3 class="subhead">Etiology</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/36745138">Genetic and Epigenetic Regulation of the Innate Immune Response to Gout.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">de Lima JD,
|
||
de Paula AGP,
|
||
Yuasa BS,
|
||
de Souza Smanioto CC,
|
||
da Cruz Silva MC,
|
||
Dos Santos PI,
|
||
Prado KB,
|
||
Winter Boldt AB,
|
||
Braga TT</span><br />
|
||
<span class="medgenPMjournal">Immunol Invest</span>
|
||
2023 Apr;52(3):364-397.
|
||
Epub 2023 Feb 6
|
||
doi: 10.1080/08820139.2023.2168554.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36745138" target="_blank">36745138</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/36587194">Association between PPARγ, PPARGC1A, and PPARGC1B genetic variants and susceptibility of gastric cancer in an Eastern Chinese population.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chen B,
|
||
Wang Y,
|
||
Tang W,
|
||
Chen Y,
|
||
Liu C,
|
||
Kang M,
|
||
Xie J</span><br />
|
||
<span class="medgenPMjournal">BMC Med Genomics</span>
|
||
2022 Dec 31;15(1):274.
|
||
doi: 10.1186/s12920-022-01428-0.
|
||
<span class="bold">PMID: </span><a href="/pubmed/36587194" target="_blank">36587194</a><a href="/pmc/articles/PMC9805199" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/32701715">PPARGC1B Is Associated with Nontraumatic Osteonecrosis of the Femoral Head: A Genomewide Association Study on a Chart-Reviewed Cohort.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang Y,
|
||
Bowen TR,
|
||
Lietman SA,
|
||
Suk M,
|
||
Williams MS,
|
||
Lee MTM</span><br />
|
||
<span class="medgenPMjournal">J Bone Joint Surg Am</span>
|
||
2020 Sep 16;102(18):1628-1636.
|
||
doi: 10.2106/JBJS.19.01335.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32701715" target="_blank">32701715</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/28394398">Genetic variants of PPAR-gamma coactivator 1B augment NLRP3-mediated inflammation in gouty arthritis.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Chang WC,
|
||
Jan Wu YJ,
|
||
Chung WH,
|
||
Lee YS,
|
||
Chin SW,
|
||
Chen TJ,
|
||
Chang YS,
|
||
Chen DY,
|
||
Hung SI</span><br />
|
||
<span class="medgenPMjournal">Rheumatology (Oxford)</span>
|
||
2017 Mar 1;56(3):457-466.
|
||
doi: 10.1093/rheumatology/kew337.
|
||
<span class="bold">PMID: </span><a href="/pubmed/28394398" target="_blank">28394398</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/23866026">PPARγ and PPARGC1B polymorphisms modify the association between phthalate metabolites and breast cancer risk.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Martínez-Nava GA,
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Burguete-García AI,
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López-Carrillo L,
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<span class="bold">PMID: </span><a href="/pubmed/23866026" target="_blank">23866026</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/34390315">The current role of NLRP3 inflammasome polymorphism in gout susceptibility.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/32701715">PPARGC1B Is Associated with Nontraumatic Osteonecrosis of the Femoral Head: A Genomewide Association Study on a Chart-Reviewed Cohort.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/24203067">Top single nucleotide polymorphisms affecting carbohydrate metabolism in metabolic syndrome: from the LIPGENE study.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Delgado-Lista J,
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<span class="bold">PMID: </span><a href="/pubmed/24203067" target="_blank">24203067</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/21692888">Genetic effect of single-nucleotide polymorphisms in the PPARGC1B gene on airway hyperreactivity in asthmatic patients.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Lee SH,
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<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22PPARGC1B%20polymorphism%22%20AND%20Diagnosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (6)</a></div><h3 class="subhead">Therapy</h3>
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<div class="nl"><a target="_blank" href="/pubmed/29895819">Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/29258006">Genetic variants in PPARGC1B and CNTN4 are associated with thromboxane A(2) formation and with cardiovascular event free survival in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT).</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">McCarthy NS,
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Vangjeli C,
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Surendran P,
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Treumann A,
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Rooney C,
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Ho E,
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Sever P,
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Thom S,
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Hughes AD,
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Munroe PB,
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Howard P,
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Johnson T,
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Caulfield M,
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Shields DC,
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O'Brien E,
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<span class="bold">PMID: </span><a href="/pubmed/29258006" target="_blank">29258006</a><a href="/pmc/articles/PMC5813793" target="_blank" class="PubMedFree">Free PMC Article</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/27752142">Systems genetics analysis of pharmacogenomics variation during antidepressant treatment.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Madsen MB,
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Kogelman LJA,
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Kadarmideen HN,
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Rasmussen HB</span><br />
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2018 Jan;18(1):144-152.
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<span class="bold">PMID: </span><a href="/pubmed/27752142" target="_blank">27752142</a></div>
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<div class="nl"><a target="_blank" href="/pubmed/27658772">Estrogen Signals Through Peroxisome Proliferator-Activated Receptor-γ Coactivator 1α to Reduce Oxidative Damage Associated With Diet-Induced Fatty Liver Disease.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Besse-Patin A,
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Léveillé M,
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Oropeza D,
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Nguyen BN,
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Prat A,
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Estall JL</span><br />
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<span class="medgenPMjournal">Gastroenterology</span>
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2017 Jan;152(1):243-256.
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Epub 2016 Sep 20
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doi: 10.1053/j.gastro.2016.09.017.
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<span class="bold">PMID: </span><a href="/pubmed/27658772" target="_blank">27658772</a></div>
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||
|
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<div class="nl"><a target="_blank" href="/pubmed/24317794">Common variation at PPARGC1A/B and change in body composition and metabolic traits following preventive interventions: the Diabetes Prevention Program.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Franks PW,
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Christophi CA,
|
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Jablonski KA,
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Billings LK,
|
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Delahanty LM,
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Horton ES,
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Knowler WC,
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Florez JC;
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Diabetes Prevention Program Research Group</span><br />
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<span class="medgenPMjournal">Diabetologia</span>
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2014 Mar;57(3):485-90.
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Epub 2013 Dec 7
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<span class="bold">PMID: </span><a href="/pubmed/24317794" target="_blank">24317794</a><a href="/pmc/articles/PMC4154629" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22PPARGC1B%20polymorphism%22%20AND%20Therapy%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (5)</a></div><h3 class="subhead">Prognosis</h3>
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<div class="nl"><a target="_blank" href="/pubmed/32701715">PPARGC1B Is Associated with Nontraumatic Osteonecrosis of the Femoral Head: A Genomewide Association Study on a Chart-Reviewed Cohort.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Zhang Y,
|
||
Bowen TR,
|
||
Lietman SA,
|
||
Suk M,
|
||
Williams MS,
|
||
Lee MTM</span><br />
|
||
<span class="medgenPMjournal">J Bone Joint Surg Am</span>
|
||
2020 Sep 16;102(18):1628-1636.
|
||
doi: 10.2106/JBJS.19.01335.
|
||
<span class="bold">PMID: </span><a href="/pubmed/32701715" target="_blank">32701715</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29762540">The Role of Peroxisome Proliferator-Activated Receptors and Their Transcriptional Coactivators Gene Variations in Human Trainability: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Petr M,
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Stastny P,
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Zajac A,
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Tufano JJ,
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Maciejewska-Skrendo A</span><br />
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<span class="medgenPMjournal">Int J Mol Sci</span>
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2018 May 15;19(5)
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doi: 10.3390/ijms19051472.
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<span class="bold">PMID: </span><a href="/pubmed/29762540" target="_blank">29762540</a><a href="/pmc/articles/PMC5983571" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/29258006">Genetic variants in PPARGC1B and CNTN4 are associated with thromboxane A(2) formation and with cardiovascular event free survival in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McCarthy NS,
|
||
Vangjeli C,
|
||
Surendran P,
|
||
Treumann A,
|
||
Rooney C,
|
||
Ho E,
|
||
Sever P,
|
||
Thom S,
|
||
Hughes AD,
|
||
Munroe PB,
|
||
Howard P,
|
||
Johnson T,
|
||
Caulfield M,
|
||
Shields DC,
|
||
O'Brien E,
|
||
Fitzgerald DJ,
|
||
Stanton AV</span><br />
|
||
<span class="medgenPMjournal">Atherosclerosis</span>
|
||
2018 Feb;269:42-49.
|
||
Epub 2017 Dec 8
|
||
doi: 10.1016/j.atherosclerosis.2017.12.013.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29258006" target="_blank">29258006</a><a href="/pmc/articles/PMC5813793" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22PPARGC1B%20polymorphism%22%20AND%20Prognosis%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (3)</a></div><h3 class="subhead">Clinical prediction guides</h3>
|
||
<div class="nl"><a target="_blank" href="/pubmed/29258006">Genetic variants in PPARGC1B and CNTN4 are associated with thromboxane A(2) formation and with cardiovascular event free survival in the Anglo-Scandinavian Cardiac Outcomes Trial (ASCOT).</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">McCarthy NS,
|
||
Vangjeli C,
|
||
Surendran P,
|
||
Treumann A,
|
||
Rooney C,
|
||
Ho E,
|
||
Sever P,
|
||
Thom S,
|
||
Hughes AD,
|
||
Munroe PB,
|
||
Howard P,
|
||
Johnson T,
|
||
Caulfield M,
|
||
Shields DC,
|
||
O'Brien E,
|
||
Fitzgerald DJ,
|
||
Stanton AV</span><br />
|
||
<span class="medgenPMjournal">Atherosclerosis</span>
|
||
2018 Feb;269:42-49.
|
||
Epub 2017 Dec 8
|
||
doi: 10.1016/j.atherosclerosis.2017.12.013.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29258006" target="_blank">29258006</a><a href="/pmc/articles/PMC5813793" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27658772">Estrogen Signals Through Peroxisome Proliferator-Activated Receptor-γ Coactivator 1α to Reduce Oxidative Damage Associated With Diet-Induced Fatty Liver Disease.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Besse-Patin A,
|
||
Léveillé M,
|
||
Oropeza D,
|
||
Nguyen BN,
|
||
Prat A,
|
||
Estall JL</span><br />
|
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<span class="medgenPMjournal">Gastroenterology</span>
|
||
2017 Jan;152(1):243-256.
|
||
Epub 2016 Sep 20
|
||
doi: 10.1053/j.gastro.2016.09.017.
|
||
<span class="bold">PMID: </span><a href="/pubmed/27658772" target="_blank">27658772</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/27108113">PPARGC1B gene is associated with Kashin-Beck disease in Han Chinese.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Wen Y,
|
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Hao J,
|
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Xiao X,
|
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Wang W,
|
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Guo X,
|
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Lin W,
|
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Yang T,
|
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Liu X,
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Shen H,
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Tan L,
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Chen X,
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Tian Q,
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Deng HW,
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Zhang F</span><br />
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<span class="medgenPMjournal">Funct Integr Genomics</span>
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2016 Jul;16(4):459-63.
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Epub 2016 Apr 23
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<span class="bold">PMID: </span><a href="/pubmed/27108113" target="_blank">27108113</a></div>
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||
|
||
<div class="nl"><a target="_blank" href="/pubmed/25494292">Analysis of clinical indexes and RUNX3, TBKBP1, PPARGC1B polymorphisms in Chinese Han patients with ankylosing spondylitis.</a></div>
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<div class="portlet_content ln"><span class="medgenPMauthor">Liu J,
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Lian Z,
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Xiao Y,
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Shi LL,
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Chai W,
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<span class="bold">PMID: </span><a href="/pubmed/25494292" target="_blank">25494292</a></div>
|
||
|
||
<div class="nl"><a target="_blank" href="/pubmed/21269472">Genetic variation of ESR1 and its co-activator PPARGC1B is synergistic in augmenting the risk of estrogen receptor-positive breast cancer.</a></div>
|
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<div class="portlet_content ln"><span class="medgenPMauthor">Li Y,
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Li Y,
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Wedrén S,
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Li G,
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Charn TH,
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Desai KV,
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Bonnard C,
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Czene K,
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Humphreys K,
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Darabi H,
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Einarsdóttir K,
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Heikkinen T,
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Aittomäki K,
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Blomqvist C,
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Chia KS,
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Nevanlinna H,
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Hall P,
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<span class="bold">PMID: </span><a href="/pubmed/21269472" target="_blank">21269472</a><a href="/pmc/articles/PMC3109578" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22PPARGC1B%20polymorphism%22%20AND%20Clinical%20prediction%20guides%2Fbroad%5Bfilter%5D%20%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (10)</a></div></div>
|
||
</div>
|
||
|
||
<div class="portlet mgSection" id="ID_104">
|
||
<div class="portlet_head mgSectionHead ui-widget-header"><h1 class="nl" id="Recent_systematic_reviews">Recent systematic reviews</h1><a sid="104" href="#" class="portlet_shutter" title="Show/hide content"></a></div>
|
||
<div class="portlet_content ln">
|
||
<div class="nl"><a target="_blank" href="/pubmed/29762540">The Role of Peroxisome Proliferator-Activated Receptors and Their Transcriptional Coactivators Gene Variations in Human Trainability: A Systematic Review.</a></div>
|
||
<div class="portlet_content ln"><span class="medgenPMauthor">Petr M,
|
||
Stastny P,
|
||
Zajac A,
|
||
Tufano JJ,
|
||
Maciejewska-Skrendo A</span><br />
|
||
<span class="medgenPMjournal">Int J Mol Sci</span>
|
||
2018 May 15;19(5)
|
||
doi: 10.3390/ijms19051472.
|
||
<span class="bold">PMID: </span><a href="/pubmed/29762540" target="_blank">29762540</a><a href="/pmc/articles/PMC5983571" target="_blank" class="PubMedFree">Free PMC Article</a></div>
|
||
<div><a target="_blank" href="https://pubmed.ncbi.nlm.nih.gov/?term=%22PPARGC1B%20polymorphism%22%20AND%20systematic%5Bsb%5D%20AND%20%22english%20and%20humans%22%5Bfilter%5D%20NOT%20comment%5BPTYP%5D%20NOT%20letter%5BPTYP%5D" title="PubMed search">See all (1)</a></div></div>
|
||
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|
||
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|
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