Loading…

Basic Stereology

Many us who use microscopes are interested in the internal structure or components of three-dimensional objects. Often we must section these objects to observe these internal components. For many years, microtomes have been used to make physical sections, but in recent years confocal microscopes, MR...

Full description

Saved in:
Bibliographic Details
Published in:Microscopy today 2003-02, Vol.11 (1), p.12-17
Main Author: Basgen, John M.
Format: Magazinearticle
Language:English
Citations: 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-c1775-8db5acc1a73792a63be8950a206da545eb34572bfe2bb3ea861a80f8aa20a2cc3
cites
container_end_page 17
container_issue 1
container_start_page 12
container_title Microscopy today
container_volume 11
creator Basgen, John M.
description Many us who use microscopes are interested in the internal structure or components of three-dimensional objects. Often we must section these objects to observe these internal components. For many years, microtomes have been used to make physical sections, but in recent years confocal microscopes, MR imaging, CT scanners, and even standard optical microscopes have been used to obtain “optical” sections. Two-dimensional images of these different types of sections can be used to extract three-dimensional quantitative information about the objects and their internal components, The sectioning process reduces the observed dimensions of the object and components. With apologies to Rene Magritte, the structure portrayed in Figure 1 is not a three-dimensional glomerulus but a two-dimensional profile of a glomerulus. In most cases, interest is on the structure of the three-dimensional object and not the structure in the two-dimensional image. Thus, care must be taken when obtaining and interpreting data from two-dimensional images.
doi_str_mv 10.1017/S1551929500052275
format magazinearticle
fullrecord <record><control><sourceid>cambridge_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1017_S1551929500052275</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cupid>10_1017_S1551929500052275</cupid><sourcerecordid>10_1017_S1551929500052275</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1775-8db5acc1a73792a63be8950a206da545eb34572bfe2bb3ea861a80f8aa20a2cc3</originalsourceid><addsrcrecordid>eNp9j81qwzAQhEVooSYJ9NpbX0DtruS15GMb-geBHJKcxUqWg0MSF6k95O1r09wKPc1h5tudEeIO4QEBzeMaibBWNQEAKWVoIgqFBFKT1VeiGG05-jdinvMexlhpbFUW4vaZcxfu118xxf7Q784zcd3yIcf5Radi-_qyWbzL5ertY_G0lAGNIWkbTxwCstGmVlxpH-3wnxVUDVNJ0euSjPJtVN7ryLZCttBaHhKsQtBTgb93Q-pzTrF1n6k7cjo7BDeucn9WDYy-MHz0qWt20e3773Qaev5D_QCW80yP</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>magazinearticle</recordtype></control><display><type>magazinearticle</type><title>Basic Stereology</title><source>EZB Free E-Journals</source><source>Oxford Journals Online</source><creator>Basgen, John M.</creator><creatorcontrib>Basgen, John M.</creatorcontrib><description>Many us who use microscopes are interested in the internal structure or components of three-dimensional objects. Often we must section these objects to observe these internal components. For many years, microtomes have been used to make physical sections, but in recent years confocal microscopes, MR imaging, CT scanners, and even standard optical microscopes have been used to obtain “optical” sections. Two-dimensional images of these different types of sections can be used to extract three-dimensional quantitative information about the objects and their internal components, The sectioning process reduces the observed dimensions of the object and components. With apologies to Rene Magritte, the structure portrayed in Figure 1 is not a three-dimensional glomerulus but a two-dimensional profile of a glomerulus. In most cases, interest is on the structure of the three-dimensional object and not the structure in the two-dimensional image. Thus, care must be taken when obtaining and interpreting data from two-dimensional images.</description><identifier>ISSN: 1551-9295</identifier><identifier>EISSN: 2150-3583</identifier><identifier>DOI: 10.1017/S1551929500052275</identifier><language>eng</language><publisher>New York, USA: Cambridge University Press</publisher><ispartof>Microscopy today, 2003-02, Vol.11 (1), p.12-17</ispartof><rights>Copyright © Microscopy Society of America 2003</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1775-8db5acc1a73792a63be8950a206da545eb34572bfe2bb3ea861a80f8aa20a2cc3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,27925</link.rule.ids></links><search><creatorcontrib>Basgen, John M.</creatorcontrib><title>Basic Stereology</title><title>Microscopy today</title><addtitle>Micros. Today</addtitle><description>Many us who use microscopes are interested in the internal structure or components of three-dimensional objects. Often we must section these objects to observe these internal components. For many years, microtomes have been used to make physical sections, but in recent years confocal microscopes, MR imaging, CT scanners, and even standard optical microscopes have been used to obtain “optical” sections. Two-dimensional images of these different types of sections can be used to extract three-dimensional quantitative information about the objects and their internal components, The sectioning process reduces the observed dimensions of the object and components. With apologies to Rene Magritte, the structure portrayed in Figure 1 is not a three-dimensional glomerulus but a two-dimensional profile of a glomerulus. In most cases, interest is on the structure of the three-dimensional object and not the structure in the two-dimensional image. Thus, care must be taken when obtaining and interpreting data from two-dimensional images.</description><issn>1551-9295</issn><issn>2150-3583</issn><fulltext>true</fulltext><rsrctype>magazinearticle</rsrctype><creationdate>2003</creationdate><recordtype>magazinearticle</recordtype><recordid>eNp9j81qwzAQhEVooSYJ9NpbX0DtruS15GMb-geBHJKcxUqWg0MSF6k95O1r09wKPc1h5tudEeIO4QEBzeMaibBWNQEAKWVoIgqFBFKT1VeiGG05-jdinvMexlhpbFUW4vaZcxfu118xxf7Q784zcd3yIcf5Radi-_qyWbzL5ertY_G0lAGNIWkbTxwCstGmVlxpH-3wnxVUDVNJ0euSjPJtVN7ryLZCttBaHhKsQtBTgb93Q-pzTrF1n6k7cjo7BDeucn9WDYy-MHz0qWt20e3773Qaev5D_QCW80yP</recordid><startdate>200302</startdate><enddate>200302</enddate><creator>Basgen, John M.</creator><general>Cambridge University Press</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200302</creationdate><title>Basic Stereology</title><author>Basgen, John M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1775-8db5acc1a73792a63be8950a206da545eb34572bfe2bb3ea861a80f8aa20a2cc3</frbrgroupid><rsrctype>magazinearticle</rsrctype><prefilter>magazinearticle</prefilter><language>eng</language><creationdate>2003</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Basgen, John M.</creatorcontrib><collection>CrossRef</collection><jtitle>Microscopy today</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Basgen, John M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Basic Stereology</atitle><jtitle>Microscopy today</jtitle><addtitle>Micros. Today</addtitle><date>2003-02</date><risdate>2003</risdate><volume>11</volume><issue>1</issue><spage>12</spage><epage>17</epage><pages>12-17</pages><issn>1551-9295</issn><eissn>2150-3583</eissn><abstract>Many us who use microscopes are interested in the internal structure or components of three-dimensional objects. Often we must section these objects to observe these internal components. For many years, microtomes have been used to make physical sections, but in recent years confocal microscopes, MR imaging, CT scanners, and even standard optical microscopes have been used to obtain “optical” sections. Two-dimensional images of these different types of sections can be used to extract three-dimensional quantitative information about the objects and their internal components, The sectioning process reduces the observed dimensions of the object and components. With apologies to Rene Magritte, the structure portrayed in Figure 1 is not a three-dimensional glomerulus but a two-dimensional profile of a glomerulus. In most cases, interest is on the structure of the three-dimensional object and not the structure in the two-dimensional image. Thus, care must be taken when obtaining and interpreting data from two-dimensional images.</abstract><cop>New York, USA</cop><pub>Cambridge University Press</pub><doi>10.1017/S1551929500052275</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1551-9295
ispartof Microscopy today, 2003-02, Vol.11 (1), p.12-17
issn 1551-9295
2150-3583
language eng
recordid cdi_crossref_primary_10_1017_S1551929500052275
source EZB Free E-Journals; Oxford Journals Online
title Basic Stereology
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T03%3A17%3A13IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-cambridge_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Basic%20Stereology&rft.jtitle=Microscopy%20today&rft.au=Basgen,%20John%20M.&rft.date=2003-02&rft.volume=11&rft.issue=1&rft.spage=12&rft.epage=17&rft.pages=12-17&rft.issn=1551-9295&rft.eissn=2150-3583&rft_id=info:doi/10.1017/S1551929500052275&rft_dat=%3Ccambridge_cross%3E10_1017_S1551929500052275%3C/cambridge_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c1775-8db5acc1a73792a63be8950a206da545eb34572bfe2bb3ea861a80f8aa20a2cc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rft_cupid=10_1017_S1551929500052275&rfr_iscdi=true