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Hemoglobin Lepore Trait: Globin Synthesis in Bone Marrow and Peripheral Blood
There was decreased synthesis of the β-globin chain in the peripheral blood, and equal synthesis of α- and non-α-chains in the bone marrow of three patients with hemoglobin Lepore trait, similar to the findings in patients with heterozygous β-thalassemia. There is a relative instability of the synth...
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Published in: | Science (American Association for the Advancement of Science) 1972-11, Vol.178 (4061), p.623-625 |
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container_end_page | 625 |
container_issue | 4061 |
container_start_page | 623 |
container_title | Science (American Association for the Advancement of Science) |
container_volume | 178 |
creator | Gill, Frances Atwater, Jean Schwartz, Elias |
description | There was decreased synthesis of the β-globin chain in the peripheral blood, and equal synthesis of α- and non-α-chains in the bone marrow of three patients with hemoglobin Lepore trait, similar to the findings in patients with heterozygous β-thalassemia. There is a relative instability of the synthetic mechanism for normal β-chain in these patients. |
doi_str_mv | 10.1126/science.178.4061.623 |
format | article |
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There is a relative instability of the synthetic mechanism for normal β-chain in these patients.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.178.4061.623</identifier><identifier>PMID: 5086396</identifier><language>eng</language><publisher>United States: American Association for the Advancement of Science</publisher><subject>Animal cells ; Bacteria ; Bacterial RNA ; Blood ; Bone marrow ; Bone Marrow - metabolism ; Carbon Isotopes ; Chromatography ; Fleas ; Globins - analysis ; Globins - biosynthesis ; Hemoglobinopathies - blood ; Hemoglobinopathies - metabolism ; Hemoglobins ; Humans ; Leucine - metabolism ; Neurons ; Radioactive decay ; RNA ; Thalassemia - metabolism</subject><ispartof>Science (American Association for the Advancement of Science), 1972-11, Vol.178 (4061), p.623-625</ispartof><rights>Copyright 1972 American Association for the Advancement of Science</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c353t-9f7f559b132327205bfeb56e6e51b48319acd72025d510aa937dd2ff74ecb78a3</citedby><cites>FETCH-LOGICAL-c353t-9f7f559b132327205bfeb56e6e51b48319acd72025d510aa937dd2ff74ecb78a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1735149$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1735149$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,777,781,2871,2872,27905,27906,58219,58452</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/5086396$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gill, Frances</creatorcontrib><creatorcontrib>Atwater, Jean</creatorcontrib><creatorcontrib>Schwartz, Elias</creatorcontrib><title>Hemoglobin Lepore Trait: Globin Synthesis in Bone Marrow and Peripheral Blood</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>There was decreased synthesis of the β-globin chain in the peripheral blood, and equal synthesis of α- and non-α-chains in the bone marrow of three patients with hemoglobin Lepore trait, similar to the findings in patients with heterozygous β-thalassemia. There is a relative instability of the synthetic mechanism for normal β-chain in these patients.</description><subject>Animal cells</subject><subject>Bacteria</subject><subject>Bacterial RNA</subject><subject>Blood</subject><subject>Bone marrow</subject><subject>Bone Marrow - metabolism</subject><subject>Carbon Isotopes</subject><subject>Chromatography</subject><subject>Fleas</subject><subject>Globins - analysis</subject><subject>Globins - biosynthesis</subject><subject>Hemoglobinopathies - blood</subject><subject>Hemoglobinopathies - metabolism</subject><subject>Hemoglobins</subject><subject>Humans</subject><subject>Leucine - metabolism</subject><subject>Neurons</subject><subject>Radioactive decay</subject><subject>RNA</subject><subject>Thalassemia - metabolism</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1972</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LwzAYx4Moc06_wYScvLXmpUkbb27oFDYUnOeQtk9dR9vUpEP27e1o0dPD8387_BCaUxJSyuS9z0poMghpnIQRkTSUjJ-hKSVKBIoRfo6mhHAZJCQWl-jK-z0hvaf4BE0ESSRXcoo2L1Dbr8qmZYPX0FoHeOtM2T3g1SB-HJtuB770uH8WtgG8Mc7ZH2yaHL-DK9sdOFPhRWVtfo0uClN5uBnvDH0-P22XL8H6bfW6fFwHGRe8C1QRF0KolHLGWcyISAtIhQQJgqZRwqkyWd7rTOSCEmMUj_OcFUUcQZbGieEzdDfsts5-H8B3ui59BlVlGrAHrxMqI6YS1QejIZg5672DQreurI07akr0iaIeKeqeoj5R1D3FvnY77h_SGvK_0oit9-eDv_eddf-bMRc0UvwXj1t4kQ</recordid><startdate>19721110</startdate><enddate>19721110</enddate><creator>Gill, Frances</creator><creator>Atwater, Jean</creator><creator>Schwartz, Elias</creator><general>American Association for the Advancement of Science</general><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>7X8</scope></search><sort><creationdate>19721110</creationdate><title>Hemoglobin Lepore Trait: Globin Synthesis in Bone Marrow and Peripheral Blood</title><author>Gill, Frances ; Atwater, Jean ; Schwartz, Elias</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c353t-9f7f559b132327205bfeb56e6e51b48319acd72025d510aa937dd2ff74ecb78a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1972</creationdate><topic>Animal cells</topic><topic>Bacteria</topic><topic>Bacterial RNA</topic><topic>Blood</topic><topic>Bone marrow</topic><topic>Bone Marrow - metabolism</topic><topic>Carbon Isotopes</topic><topic>Chromatography</topic><topic>Fleas</topic><topic>Globins - analysis</topic><topic>Globins - biosynthesis</topic><topic>Hemoglobinopathies - blood</topic><topic>Hemoglobinopathies - metabolism</topic><topic>Hemoglobins</topic><topic>Humans</topic><topic>Leucine - metabolism</topic><topic>Neurons</topic><topic>Radioactive decay</topic><topic>RNA</topic><topic>Thalassemia - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gill, Frances</creatorcontrib><creatorcontrib>Atwater, Jean</creatorcontrib><creatorcontrib>Schwartz, Elias</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Science (American Association for the Advancement of Science)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gill, Frances</au><au>Atwater, Jean</au><au>Schwartz, Elias</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hemoglobin Lepore Trait: Globin Synthesis in Bone Marrow and Peripheral Blood</atitle><jtitle>Science (American Association for the Advancement of Science)</jtitle><addtitle>Science</addtitle><date>1972-11-10</date><risdate>1972</risdate><volume>178</volume><issue>4061</issue><spage>623</spage><epage>625</epage><pages>623-625</pages><issn>0036-8075</issn><eissn>1095-9203</eissn><abstract>There was decreased synthesis of the β-globin chain in the peripheral blood, and equal synthesis of α- and non-α-chains in the bone marrow of three patients with hemoglobin Lepore trait, similar to the findings in patients with heterozygous β-thalassemia. There is a relative instability of the synthetic mechanism for normal β-chain in these patients.</abstract><cop>United States</cop><pub>American Association for the Advancement of Science</pub><pmid>5086396</pmid><doi>10.1126/science.178.4061.623</doi><tpages>3</tpages></addata></record> |
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source | American Association for the Advancement of Science; JSTOR Archival Journals and Primary Sources Collection |
subjects | Animal cells Bacteria Bacterial RNA Blood Bone marrow Bone Marrow - metabolism Carbon Isotopes Chromatography Fleas Globins - analysis Globins - biosynthesis Hemoglobinopathies - blood Hemoglobinopathies - metabolism Hemoglobins Humans Leucine - metabolism Neurons Radioactive decay RNA Thalassemia - metabolism |
title | Hemoglobin Lepore Trait: Globin Synthesis in Bone Marrow and Peripheral Blood |
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