| pubmed-article:8497267 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8497267 | lifeskim:mentions | umls-concept:C1336596 | lld:lifeskim |
| pubmed-article:8497267 | lifeskim:mentions | umls-concept:C0012940 | lld:lifeskim |
| pubmed-article:8497267 | lifeskim:mentions | umls-concept:C1420639 | lld:lifeskim |
| pubmed-article:8497267 | lifeskim:mentions | umls-concept:C1711351 | lld:lifeskim |
| pubmed-article:8497267 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:8497267 | pubmed:dateCreated | 1993-6-23 | lld:pubmed |
| pubmed-article:8497267 | pubmed:abstractText | A class of helix-loop-helix (HLH) proteins, including E2A (E12 and E47), E2-2, and HEB, that bind in vitro to DNA sequences present in the immunoglobulin (Ig) enhancers has recently been identified. E12, E47, E2-2, and HEB are each present in B cells. The presence of many different HLH proteins raises the question of which of the HLH proteins actually binds the Ig enhancer elements in B cells. Using monoclonal antibodies specific for both E2A and E2-2, we show that both E2-2 and E2A polypeptides are present in B-cell-specific Ig enhancer-binding complexes. E2-box-binding complexes in pre-B cells contain both E2-2 and E2A HLH subunits, whereas in mature B cells only E2A gene products are present. We show that the difference in E2-box-binding complexes in pre-B and mature B cells may be caused by differential expression of E2A and E2-2. | lld:pubmed |
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| pubmed-article:8497267 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8497267 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8497267 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:8497267 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8497267 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:8497267 | pubmed:issn | 0270-7306 | lld:pubmed |
| pubmed-article:8497267 | pubmed:author | pubmed-author:BainGG | lld:pubmed |
| pubmed-article:8497267 | pubmed:author | pubmed-author:GruenwaldSS | lld:pubmed |
| pubmed-article:8497267 | pubmed:author | pubmed-author:MurreCC | lld:pubmed |
| pubmed-article:8497267 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8497267 | pubmed:volume | 13 | lld:pubmed |
| pubmed-article:8497267 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8497267 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8497267 | pubmed:pagination | 3522-9 | lld:pubmed |
| pubmed-article:8497267 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:8497267 | pubmed:year | 1993 | lld:pubmed |
| pubmed-article:8497267 | pubmed:articleTitle | E2A and E2-2 are subunits of B-cell-specific E2-box DNA-binding proteins. | lld:pubmed |
| pubmed-article:8497267 | pubmed:affiliation | Department of Biology, University of California, San Diego, La Jolla 92130. | lld:pubmed |
| pubmed-article:8497267 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8497267 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8497267 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:8497267 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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