Loading…
Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation
How tissues generate and maintain the correct number of cells is a fundamental problem in biology. In principle, tissue turnover can occur by the differentiation of stem cells, as is well documented for blood, skin and intestine, or by the duplication of existing differentiated cells. Recent work on...
Saved in:
Published in: | Nature 2004-05, Vol.429 (6987), p.41-46 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c679t-8f24739b41899637bea7999e3d253ca2968caa038a61e022828e94a8fac1892d3 |
---|---|
cites | cdi_FETCH-LOGICAL-c679t-8f24739b41899637bea7999e3d253ca2968caa038a61e022828e94a8fac1892d3 |
container_end_page | 46 |
container_issue | 6987 |
container_start_page | 41 |
container_title | Nature |
container_volume | 429 |
creator | Melton, Douglas A Dor, Yuval Brown, Juliana Martinez, Olga I |
description | How tissues generate and maintain the correct number of cells is a fundamental problem in biology. In principle, tissue turnover can occur by the differentiation of stem cells, as is well documented for blood, skin and intestine, or by the duplication of existing differentiated cells. Recent work on adult stem cells has highlighted their potential contribution to organ maintenance and repair. However, the extent to which stem cells actually participate in these processes
in vivo
is not clear. Here we introduce a method for genetic lineage tracing to determine the contribution of stem cells to a tissue of interest. We focus on pancreatic β-cells, whose postnatal origins remain controversial. Our analysis shows that pre-existing β-cells, rather than pluripotent stem cells, are the major source of new β-cells during adult life and after pancreatectomy in mice. These results suggest that terminally differentiated β-cells retain a significant proliferative capacity
in vivo
and cast doubt on the idea that adult stem cells have a significant role in β-cell replenishment. |
doi_str_mv | 10.1038/nature02520 |
format | article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_743164716</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A186370835</galeid><sourcerecordid>A186370835</sourcerecordid><originalsourceid>FETCH-LOGICAL-c679t-8f24739b41899637bea7999e3d253ca2968caa038a61e022828e94a8fac1892d3</originalsourceid><addsrcrecordid>eNqF0luLEzEUAOBBFLeuPvkuo6AiOmtuM0keS_GysCjoim8Op5mTbpa5dJMMuH_LH-JvMt0W20pV8hDIfOdkzsnJsoeUnFDC1ese4uiRsJKRW9mEClkVolLydjYhhKmCKF4dZfdCuCSElFSKu9kRLSnTTPJJ9m3ajG3Ml9AbjxCdyX_-KAy2bcjBY24H32GTz6_zgK0tmnHZOpPY0Oce4gX6PF5An4eI3U1U3jhr0WMf3Y26n92x0AZ8sNmPsy9v35zP3hdnH9-dzqZnhamkjoWyTEiu54IqrSsu5whSa428YSU3wHSlDEAqFiqaKmWKKdQClAWTIljDj7Pn67xLP1yNGGLdubD6IehxGEMtBaeVkLRK8tm_JdUkdU_8F1KpZUUVSfDJH_ByGH2fyq0ZESUvhWAJFWu0gBZr19shejAL7NFDO_RoXTqeUpWKTw9WbpPuebN0V_UuOjmA0mqwc-Zg1hd7AclE_B4XMIZQn37-tG9f_t1Oz7_OPhzUxg8heLT10rsO_HVNSb0a03pnTJN-tGnZOE_ztbWbuUzg6QZAMNBan-bThR0nORPl6jVfrV1In_oF-m3vD9_7eM3Xh7_z7ZpfGn8HHA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>204535442</pqid></control><display><type>article</type><title>Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation</title><source>Nature_系列刊</source><creator>Melton, Douglas A ; Dor, Yuval ; Brown, Juliana ; Martinez, Olga I</creator><creatorcontrib>Melton, Douglas A ; Dor, Yuval ; Brown, Juliana ; Martinez, Olga I</creatorcontrib><description>How tissues generate and maintain the correct number of cells is a fundamental problem in biology. In principle, tissue turnover can occur by the differentiation of stem cells, as is well documented for blood, skin and intestine, or by the duplication of existing differentiated cells. Recent work on adult stem cells has highlighted their potential contribution to organ maintenance and repair. However, the extent to which stem cells actually participate in these processes
in vivo
is not clear. Here we introduce a method for genetic lineage tracing to determine the contribution of stem cells to a tissue of interest. We focus on pancreatic β-cells, whose postnatal origins remain controversial. Our analysis shows that pre-existing β-cells, rather than pluripotent stem cells, are the major source of new β-cells during adult life and after pancreatectomy in mice. These results suggest that terminally differentiated β-cells retain a significant proliferative capacity
in vivo
and cast doubt on the idea that adult stem cells have a significant role in β-cell replenishment.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature02520</identifier><identifier>PMID: 15129273</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Aging - physiology ; Animals ; Biological and medical sciences ; Cell Count ; Cell Differentiation ; Cell differentiation, maturation, development, hematopoiesis ; Cell Division ; Cell Lineage - physiology ; Cell physiology ; Cellular biology ; Fundamental and applied biological sciences. Psychology ; Humanities and Social Sciences ; Islets of Langerhans - cytology ; Islets of Langerhans - metabolism ; Mice ; Mice, Transgenic ; Molecular and cellular biology ; multidisciplinary ; Pancreas ; Pancreatectomy ; Pluripotent Stem Cells - cytology ; Recombination, Genetic ; Regeneration - physiology ; Science ; Science (multidisciplinary) ; Stem cells</subject><ispartof>Nature, 2004-05, Vol.429 (6987), p.41-46</ispartof><rights>Macmillan Magazines Ltd. 2004</rights><rights>2004 INIST-CNRS</rights><rights>COPYRIGHT 2004 Nature Publishing Group</rights><rights>Copyright Macmillan Journals Ltd. May 6, 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c679t-8f24739b41899637bea7999e3d253ca2968caa038a61e022828e94a8fac1892d3</citedby><cites>FETCH-LOGICAL-c679t-8f24739b41899637bea7999e3d253ca2968caa038a61e022828e94a8fac1892d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2725,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15732456$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15129273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Melton, Douglas A</creatorcontrib><creatorcontrib>Dor, Yuval</creatorcontrib><creatorcontrib>Brown, Juliana</creatorcontrib><creatorcontrib>Martinez, Olga I</creatorcontrib><title>Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation</title><title>Nature</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>How tissues generate and maintain the correct number of cells is a fundamental problem in biology. In principle, tissue turnover can occur by the differentiation of stem cells, as is well documented for blood, skin and intestine, or by the duplication of existing differentiated cells. Recent work on adult stem cells has highlighted their potential contribution to organ maintenance and repair. However, the extent to which stem cells actually participate in these processes
in vivo
is not clear. Here we introduce a method for genetic lineage tracing to determine the contribution of stem cells to a tissue of interest. We focus on pancreatic β-cells, whose postnatal origins remain controversial. Our analysis shows that pre-existing β-cells, rather than pluripotent stem cells, are the major source of new β-cells during adult life and after pancreatectomy in mice. These results suggest that terminally differentiated β-cells retain a significant proliferative capacity
in vivo
and cast doubt on the idea that adult stem cells have a significant role in β-cell replenishment.</description><subject>Aging - physiology</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Count</subject><subject>Cell Differentiation</subject><subject>Cell differentiation, maturation, development, hematopoiesis</subject><subject>Cell Division</subject><subject>Cell Lineage - physiology</subject><subject>Cell physiology</subject><subject>Cellular biology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humanities and Social Sciences</subject><subject>Islets of Langerhans - cytology</subject><subject>Islets of Langerhans - metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Molecular and cellular biology</subject><subject>multidisciplinary</subject><subject>Pancreas</subject><subject>Pancreatectomy</subject><subject>Pluripotent Stem Cells - cytology</subject><subject>Recombination, Genetic</subject><subject>Regeneration - physiology</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Stem cells</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqF0luLEzEUAOBBFLeuPvkuo6AiOmtuM0keS_GysCjoim8Op5mTbpa5dJMMuH_LH-JvMt0W20pV8hDIfOdkzsnJsoeUnFDC1ese4uiRsJKRW9mEClkVolLydjYhhKmCKF4dZfdCuCSElFSKu9kRLSnTTPJJ9m3ajG3Ml9AbjxCdyX_-KAy2bcjBY24H32GTz6_zgK0tmnHZOpPY0Oce4gX6PF5An4eI3U1U3jhr0WMf3Y26n92x0AZ8sNmPsy9v35zP3hdnH9-dzqZnhamkjoWyTEiu54IqrSsu5whSa428YSU3wHSlDEAqFiqaKmWKKdQClAWTIljDj7Pn67xLP1yNGGLdubD6IehxGEMtBaeVkLRK8tm_JdUkdU_8F1KpZUUVSfDJH_ByGH2fyq0ZESUvhWAJFWu0gBZr19shejAL7NFDO_RoXTqeUpWKTw9WbpPuebN0V_UuOjmA0mqwc-Zg1hd7AclE_B4XMIZQn37-tG9f_t1Oz7_OPhzUxg8heLT10rsO_HVNSb0a03pnTJN-tGnZOE_ztbWbuUzg6QZAMNBan-bThR0nORPl6jVfrV1In_oF-m3vD9_7eM3Xh7_z7ZpfGn8HHA</recordid><startdate>20040506</startdate><enddate>20040506</enddate><creator>Melton, Douglas A</creator><creator>Dor, Yuval</creator><creator>Brown, Juliana</creator><creator>Martinez, Olga I</creator><general>Nature Publishing Group UK</general><general>Nature Publishing</general><general>Nature Publishing Group</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>ATWCN</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7TG</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>S0X</scope><scope>SOI</scope><scope>7X8</scope><scope>7SC</scope><scope>7SP</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>JQ2</scope><scope>KR7</scope><scope>L7M</scope><scope>L~C</scope><scope>L~D</scope></search><sort><creationdate>20040506</creationdate><title>Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation</title><author>Melton, Douglas A ; Dor, Yuval ; Brown, Juliana ; Martinez, Olga I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c679t-8f24739b41899637bea7999e3d253ca2968caa038a61e022828e94a8fac1892d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Aging - physiology</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Count</topic><topic>Cell Differentiation</topic><topic>Cell differentiation, maturation, development, hematopoiesis</topic><topic>Cell Division</topic><topic>Cell Lineage - physiology</topic><topic>Cell physiology</topic><topic>Cellular biology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humanities and Social Sciences</topic><topic>Islets of Langerhans - cytology</topic><topic>Islets of Langerhans - metabolism</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Molecular and cellular biology</topic><topic>multidisciplinary</topic><topic>Pancreas</topic><topic>Pancreatectomy</topic><topic>Pluripotent Stem Cells - cytology</topic><topic>Recombination, Genetic</topic><topic>Regeneration - physiology</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Stem cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Melton, Douglas A</creatorcontrib><creatorcontrib>Dor, Yuval</creatorcontrib><creatorcontrib>Brown, Juliana</creatorcontrib><creatorcontrib>Martinez, Olga I</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>Gale In Context: Middle School</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Database (1962 - current)</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>Biological Sciences</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>ProQuest_Research Library</collection><collection>Science Database (ProQuest)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>University of Michigan</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Computer and Information Systems Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>ProQuest Computer Science Collection</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><jtitle>Nature</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Melton, Douglas A</au><au>Dor, Yuval</au><au>Brown, Juliana</au><au>Martinez, Olga I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation</atitle><jtitle>Nature</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2004-05-06</date><risdate>2004</risdate><volume>429</volume><issue>6987</issue><spage>41</spage><epage>46</epage><pages>41-46</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>How tissues generate and maintain the correct number of cells is a fundamental problem in biology. In principle, tissue turnover can occur by the differentiation of stem cells, as is well documented for blood, skin and intestine, or by the duplication of existing differentiated cells. Recent work on adult stem cells has highlighted their potential contribution to organ maintenance and repair. However, the extent to which stem cells actually participate in these processes
in vivo
is not clear. Here we introduce a method for genetic lineage tracing to determine the contribution of stem cells to a tissue of interest. We focus on pancreatic β-cells, whose postnatal origins remain controversial. Our analysis shows that pre-existing β-cells, rather than pluripotent stem cells, are the major source of new β-cells during adult life and after pancreatectomy in mice. These results suggest that terminally differentiated β-cells retain a significant proliferative capacity
in vivo
and cast doubt on the idea that adult stem cells have a significant role in β-cell replenishment.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>15129273</pmid><doi>10.1038/nature02520</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature, 2004-05, Vol.429 (6987), p.41-46 |
issn | 0028-0836 1476-4687 |
language | eng |
recordid | cdi_proquest_miscellaneous_743164716 |
source | Nature_系列刊 |
subjects | Aging - physiology Animals Biological and medical sciences Cell Count Cell Differentiation Cell differentiation, maturation, development, hematopoiesis Cell Division Cell Lineage - physiology Cell physiology Cellular biology Fundamental and applied biological sciences. Psychology Humanities and Social Sciences Islets of Langerhans - cytology Islets of Langerhans - metabolism Mice Mice, Transgenic Molecular and cellular biology multidisciplinary Pancreas Pancreatectomy Pluripotent Stem Cells - cytology Recombination, Genetic Regeneration - physiology Science Science (multidisciplinary) Stem cells |
title | Adult pancreatic β-cells are formed by self-duplication rather than stem-cell differentiation |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T13%3A04%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Adult%20pancreatic%20%CE%B2-cells%20are%20formed%20by%20self-duplication%20rather%20than%20stem-cell%20differentiation&rft.jtitle=Nature&rft.au=Melton,%20Douglas%20A&rft.date=2004-05-06&rft.volume=429&rft.issue=6987&rft.spage=41&rft.epage=46&rft.pages=41-46&rft.issn=0028-0836&rft.eissn=1476-4687&rft.coden=NATUAS&rft_id=info:doi/10.1038/nature02520&rft_dat=%3Cgale_proqu%3EA186370835%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c679t-8f24739b41899637bea7999e3d253ca2968caa038a61e022828e94a8fac1892d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=204535442&rft_id=info:pmid/15129273&rft_galeid=A186370835&rfr_iscdi=true |