Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules
Genomic imprinting refers to a process that distinguishes paternally derived chromosomes from maternally derived chromosomes. Everman and Cassidy review how imprinting was initially identified, present some hypotheses about the mechanisms of imprinting, and speculate on the evolutionary forces maint...
Gespeichert in:
| Veröffentlicht in: | Journal of the American Academy of Child and Adolescent Psychiatry 2000-03, Vol.39 (3), p.386-389 |
|---|---|
| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 389 |
|---|---|
| container_issue | 3 |
| container_start_page | 386 |
| container_title | Journal of the American Academy of Child and Adolescent Psychiatry |
| container_volume | 39 |
| creator | EVERMAN, DAVID B. CASSIDY, SUZANNE B. |
| description | Genomic imprinting refers to a process that distinguishes paternally derived chromosomes from maternally derived chromosomes. Everman and Cassidy review how imprinting was initially identified, present some hypotheses about the mechanisms of imprinting, and speculate on the evolutionary forces maintaining this phenomenon. They also discuss the molecular bases for two disorders in which imprinting is involved--Prader-Willi and Angelman syndromes. |
| doi_str_mv | 10.1097/00004583-200003000-00022 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_212629798</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0890856709661682</els_id><sourcerecordid>50831925</sourcerecordid><originalsourceid>FETCH-LOGICAL-c445t-73eea9434eb1b87a10d43c93f4f466b3b8041b2d065e7122bd5fc380f1ced4383</originalsourceid><addsrcrecordid>eNqFkF1LwzAUhoMobk7_ggTxtjNfbdLd6dQ5GAii4F1o01OXuTUzaQX_vZmbH3cGDjkXzzl58yCEKRlSkssLEo9IFU_YpuOxkliM7aE-TZlMUkHVPuoTlZNEpZnsoaMQFhGhUqlD1KNEUkEy0kezCTTQWhOwq_F4bpfV3LkKX9vgfAU-jPDzdDrEkXIra_B0tfa2aW3zMsJXHorX2OF2DvihW0I4Rgd1sQxwsrsH6On25nF8l8zuJ9Px5SwxQqRtIjlAkQsuoKSlkgUlleAm57WoRZaVvFRE0JJVJEtBUsbKKq0NV6SmBiKp-ACdbfeuvXvrILR64TrfxCc1oyxjucw3kNpCxrsQPNQ6Rl8V_kNTojcW9bdF_WNRf1mMo6e7_V25gurP4FZbBM53QBFMsax90RgbfjmmslxuIlxtMYgy3i14HYyFJv7CejCtrpz9P8wnBeOLsg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>212629798</pqid></control><display><type>article</type><title>Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><source>Applied Social Sciences Index & Abstracts (ASSIA)</source><source>Access via ScienceDirect (Elsevier)</source><creator>EVERMAN, DAVID B. ; CASSIDY, SUZANNE B.</creator><creatorcontrib>EVERMAN, DAVID B. ; CASSIDY, SUZANNE B.</creatorcontrib><description>Genomic imprinting refers to a process that distinguishes paternally derived chromosomes from maternally derived chromosomes. Everman and Cassidy review how imprinting was initially identified, present some hypotheses about the mechanisms of imprinting, and speculate on the evolutionary forces maintaining this phenomenon. They also discuss the molecular bases for two disorders in which imprinting is involved--Prader-Willi and Angelman syndromes.</description><identifier>ISSN: 0890-8567</identifier><identifier>EISSN: 1527-5418</identifier><identifier>DOI: 10.1097/00004583-200003000-00022</identifier><identifier>PMID: 10714060</identifier><identifier>CODEN: JAAPEE</identifier><language>eng</language><publisher>Hagerstown, MD: Elsevier Inc</publisher><subject>Angelman Syndrome - genetics ; Biological and medical sciences ; Child ; Child development ; Child, Preschool ; Children & youth ; Chromosome Deletion ; Chromosome Mapping ; Chromosomes, Human, Pair 15 ; Complex syndromes ; Female ; Genetics ; Genomic Imprinting - genetics ; Humans ; Ligases - genetics ; Male ; Medical disorders ; Medical genetics ; Medical sciences ; Neurology ; Prader-Willi Syndrome - diagnosis ; Prader-Willi Syndrome - genetics ; Ubiquitin-Protein Ligases</subject><ispartof>Journal of the American Academy of Child and Adolescent Psychiatry, 2000-03, Vol.39 (3), p.386-389</ispartof><rights>2000 The American Academy of Child and Adolescent Psychiatry</rights><rights>2000 INIST-CNRS</rights><rights>Copyright Lippincott Williams & Wilkins Mar 2000</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-73eea9434eb1b87a10d43c93f4f466b3b8041b2d065e7122bd5fc380f1ced4383</citedby><cites>FETCH-LOGICAL-c445t-73eea9434eb1b87a10d43c93f4f466b3b8041b2d065e7122bd5fc380f1ced4383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1097/00004583-200003000-00022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27929,27930,31004,46000</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1286978$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10714060$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>EVERMAN, DAVID B.</creatorcontrib><creatorcontrib>CASSIDY, SUZANNE B.</creatorcontrib><title>Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules</title><title>Journal of the American Academy of Child and Adolescent Psychiatry</title><addtitle>J Am Acad Child Adolesc Psychiatry</addtitle><description>Genomic imprinting refers to a process that distinguishes paternally derived chromosomes from maternally derived chromosomes. Everman and Cassidy review how imprinting was initially identified, present some hypotheses about the mechanisms of imprinting, and speculate on the evolutionary forces maintaining this phenomenon. They also discuss the molecular bases for two disorders in which imprinting is involved--Prader-Willi and Angelman syndromes.</description><subject>Angelman Syndrome - genetics</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child development</subject><subject>Child, Preschool</subject><subject>Children & youth</subject><subject>Chromosome Deletion</subject><subject>Chromosome Mapping</subject><subject>Chromosomes, Human, Pair 15</subject><subject>Complex syndromes</subject><subject>Female</subject><subject>Genetics</subject><subject>Genomic Imprinting - genetics</subject><subject>Humans</subject><subject>Ligases - genetics</subject><subject>Male</subject><subject>Medical disorders</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Neurology</subject><subject>Prader-Willi Syndrome - diagnosis</subject><subject>Prader-Willi Syndrome - genetics</subject><subject>Ubiquitin-Protein Ligases</subject><issn>0890-8567</issn><issn>1527-5418</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqFkF1LwzAUhoMobk7_ggTxtjNfbdLd6dQ5GAii4F1o01OXuTUzaQX_vZmbH3cGDjkXzzl58yCEKRlSkssLEo9IFU_YpuOxkliM7aE-TZlMUkHVPuoTlZNEpZnsoaMQFhGhUqlD1KNEUkEy0kezCTTQWhOwq_F4bpfV3LkKX9vgfAU-jPDzdDrEkXIra_B0tfa2aW3zMsJXHorX2OF2DvihW0I4Rgd1sQxwsrsH6On25nF8l8zuJ9Px5SwxQqRtIjlAkQsuoKSlkgUlleAm57WoRZaVvFRE0JJVJEtBUsbKKq0NV6SmBiKp-ACdbfeuvXvrILR64TrfxCc1oyxjucw3kNpCxrsQPNQ6Rl8V_kNTojcW9bdF_WNRf1mMo6e7_V25gurP4FZbBM53QBFMsax90RgbfjmmslxuIlxtMYgy3i14HYyFJv7CejCtrpz9P8wnBeOLsg</recordid><startdate>20000301</startdate><enddate>20000301</enddate><creator>EVERMAN, DAVID B.</creator><creator>CASSIDY, SUZANNE B.</creator><general>Elsevier Inc</general><general>Lippincott</general><general>Elsevier BV</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>7TK</scope><scope>K9.</scope></search><sort><creationdate>20000301</creationdate><title>Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules</title><author>EVERMAN, DAVID B. ; CASSIDY, SUZANNE B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-73eea9434eb1b87a10d43c93f4f466b3b8041b2d065e7122bd5fc380f1ced4383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Angelman Syndrome - genetics</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child development</topic><topic>Child, Preschool</topic><topic>Children & youth</topic><topic>Chromosome Deletion</topic><topic>Chromosome Mapping</topic><topic>Chromosomes, Human, Pair 15</topic><topic>Complex syndromes</topic><topic>Female</topic><topic>Genetics</topic><topic>Genomic Imprinting - genetics</topic><topic>Humans</topic><topic>Ligases - genetics</topic><topic>Male</topic><topic>Medical disorders</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Neurology</topic><topic>Prader-Willi Syndrome - diagnosis</topic><topic>Prader-Willi Syndrome - genetics</topic><topic>Ubiquitin-Protein Ligases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>EVERMAN, DAVID B.</creatorcontrib><creatorcontrib>CASSIDY, SUZANNE B.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index & Abstracts (ASSIA)</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Journal of the American Academy of Child and Adolescent Psychiatry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>EVERMAN, DAVID B.</au><au>CASSIDY, SUZANNE B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules</atitle><jtitle>Journal of the American Academy of Child and Adolescent Psychiatry</jtitle><addtitle>J Am Acad Child Adolesc Psychiatry</addtitle><date>2000-03-01</date><risdate>2000</risdate><volume>39</volume><issue>3</issue><spage>386</spage><epage>389</epage><pages>386-389</pages><issn>0890-8567</issn><eissn>1527-5418</eissn><coden>JAAPEE</coden><abstract>Genomic imprinting refers to a process that distinguishes paternally derived chromosomes from maternally derived chromosomes. Everman and Cassidy review how imprinting was initially identified, present some hypotheses about the mechanisms of imprinting, and speculate on the evolutionary forces maintaining this phenomenon. They also discuss the molecular bases for two disorders in which imprinting is involved--Prader-Willi and Angelman syndromes.</abstract><cop>Hagerstown, MD</cop><pub>Elsevier Inc</pub><pmid>10714060</pmid><doi>10.1097/00004583-200003000-00022</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0890-8567 |
| ispartof | Journal of the American Academy of Child and Adolescent Psychiatry, 2000-03, Vol.39 (3), p.386-389 |
| issn | 0890-8567 1527-5418 |
| language | eng |
| recordid | cdi_proquest_journals_212629798 |
| source | MEDLINE; Journals@Ovid Complete; Applied Social Sciences Index & Abstracts (ASSIA); Access via ScienceDirect (Elsevier) |
| subjects | Angelman Syndrome - genetics Biological and medical sciences Child Child development Child, Preschool Children & youth Chromosome Deletion Chromosome Mapping Chromosomes, Human, Pair 15 Complex syndromes Female Genetics Genomic Imprinting - genetics Humans Ligases - genetics Male Medical disorders Medical genetics Medical sciences Neurology Prader-Willi Syndrome - diagnosis Prader-Willi Syndrome - genetics Ubiquitin-Protein Ligases |
| title | Genetics of Childhood Disorders: XII. Genomic Imprinting: Breaking the Rules |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-09T20%3A24%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genetics%20of%20Childhood%20Disorders:%20XII.%20Genomic%20Imprinting:%20Breaking%20the%20Rules&rft.jtitle=Journal%20of%20the%20American%20Academy%20of%20Child%20and%20Adolescent%20Psychiatry&rft.au=EVERMAN,%20DAVID%20B.&rft.date=2000-03-01&rft.volume=39&rft.issue=3&rft.spage=386&rft.epage=389&rft.pages=386-389&rft.issn=0890-8567&rft.eissn=1527-5418&rft.coden=JAAPEE&rft_id=info:doi/10.1097/00004583-200003000-00022&rft_dat=%3Cproquest_cross%3E50831925%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=212629798&rft_id=info:pmid/10714060&rft_els_id=S0890856709661682&rfr_iscdi=true |