{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,2]],"date-time":"2025-11-02T16:10:08Z","timestamp":1762099808918},"reference-count":26,"publisher":"Proceedings of the National Academy of Sciences","issue":"6","content-domain":{"domain":["www.pnas.org"],"crossmark-restriction":true},"short-container-title":["Proc. Natl. Acad. Sci. U.S.A."],"published-print":{"date-parts":[[2001,3,13]]},"abstract":"<jats:p>We performed a genome-wide analysis of gene expression in primary human CD15<jats:sup>+<\/jats:sup>myeloid progenitor cells. By using the serial analysis of gene expression (SAGE) technique, we obtained quantitative information for the expression of 37,519 unique SAGE-tag sequences. Of these unique tags, (<jats:italic>i<\/jats:italic>) 25% were detected at high and intermediate levels, whereas 75% were present as single copies, (<jats:italic>ii<\/jats:italic>) 53% of the tags matched known expressed sequences, 34% of which were matched to more than one known expressed sequence, and (<jats:italic>iii<\/jats:italic>) 47% of the tags had no matches and represent potentially novel genes. The correct genes were confirmed by application of the generation of longer cDNA fragments from SAGE tags for gene identification (GLGI) technique for high-copy tags with multiple matches. A set of genes known to be important in myeloid differentiation were expressed at various levels and used different spliced forms. This study provides a normal baseline for comparison of gene expression in myeloid diseases. The strategy of using SAGE and GLGI techniques in this study has broad applications to the genome-wide identification of expressed genes.<\/jats:p>","DOI":"10.1073\/pnas.051013798","type":"journal-article","created":{"date-parts":[[2002,7,26]],"date-time":"2002-07-26T14:41:48Z","timestamp":1027694508000},"page":"3340-3345","update-policy":"http:\/\/dx.doi.org\/10.1073\/pnas.cm10313","source":"Crossref","is-referenced-by-count":32,"title":["The pattern of gene expression in human CD15<sup>+<\/sup>myeloid progenitor cells"],"prefix":"10.1073","volume":"98","author":[{"given":"Sanggyu","family":"Lee","sequence":"first","affiliation":[{"name":"Departments of Medicine and Computer Science, University of Chicago Medical Center, 5841 South Maryland, MC2115, Chicago, IL 60637"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Guolin","family":"Zhou","sequence":"additional","affiliation":[{"name":"Departments of Medicine and Computer Science, University of Chicago Medical Center, 5841 South Maryland, MC2115, Chicago, IL 60637"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Terry","family":"Clark","sequence":"additional","affiliation":[{"name":"Departments of Medicine and Computer Science, University of Chicago Medical Center, 5841 South Maryland, MC2115, Chicago, IL 60637"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jianjun","family":"Chen","sequence":"additional","affiliation":[{"name":"Departments of Medicine and Computer Science, University of Chicago Medical Center, 5841 South Maryland, MC2115, Chicago, IL 60637"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Janet D.","family":"Rowley","sequence":"additional","affiliation":[{"name":"Departments of Medicine and Computer Science, University of Chicago Medical Center, 5841 South Maryland, MC2115, Chicago, IL 60637"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"San Ming","family":"Wang","sequence":"additional","affiliation":[{"name":"Departments of Medicine and Computer Science, University of Chicago Medical Center, 5841 South Maryland, MC2115, Chicago, IL 60637"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"341","published-online":{"date-parts":[[2001,3,13]]},"reference":[{"key":"e_1_3_3_1_2","volume-title":"Principles and Practice of Hematology","author":"Robert I","year":"1995","unstructured":", eds I Robert, S E Handin, P S Thomas (Lippincott, Philadephia Principles and Practice of Hematology, 1995)."},{"key":"e_1_3_3_2_2","first-page":"59","volume":"36","author":"Rowley J D","year":"1999","unstructured":"J D Rowley Semin Hematol 36, 59\u201372 (1999).","journal-title":"Semin Hematol"},{"key":"e_1_3_3_3_2","doi-asserted-by":"publisher","DOI":"10.1126\/science.270.5235.484"},{"key":"e_1_3_3_4_2","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.97.1.349"},{"key":"e_1_3_3_5_2","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.97.8.4162"},{"key":"e_1_3_3_6_2","doi-asserted-by":"publisher","DOI":"10.1038\/70487"},{"key":"e_1_3_3_7_2","doi-asserted-by":"publisher","DOI":"10.1006\/excr.1993.1030"},{"key":"e_1_3_3_8_2","doi-asserted-by":"crossref","first-page":"3840","DOI":"10.4049\/jimmunol.139.11.3840","volume":"139","author":"Gondo H","year":"1987","unstructured":"H Gondo, J Kudo, J W White, C Barr, P Selvanayagam, G F Saunders J Immunol 139, 3840\u20133848 (1987).","journal-title":"J Immunol"},{"key":"e_1_3_3_9_2","doi-asserted-by":"publisher","DOI":"10.1038\/359644a0"},{"key":"e_1_3_3_10_2","first-page":"389","volume":"1","author":"Woodgett J R","year":"1990","unstructured":"J R Woodgett Semin Cancer Biol 1, 389\u2013397 (1990).","journal-title":"Semin Cancer Biol"},{"key":"e_1_3_3_11_2","first-page":"19","volume":"1","author":"Abate C","year":"1990","unstructured":"C Abate, T Curran Semin Cancer Biol 1, 19\u201326 (1990).","journal-title":"Semin Cancer Biol"},{"key":"e_1_3_3_12_2","doi-asserted-by":"publisher","DOI":"10.1002\/jlb.63.2.153"},{"key":"e_1_3_3_13_2","first-page":"798","volume-title":"Leukocyte Typing IV","author":"Bettelheim P","year":"1989","unstructured":"P Bettelheim Leukocyte Typing IV, ed W Knapp (Oxford Univ. 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