| pubmed-article:19622385 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19622385 | lifeskim:mentions | umls-concept:C0031939 | lld:lifeskim |
| pubmed-article:19622385 | lifeskim:mentions | umls-concept:C0542341 | lld:lifeskim |
| pubmed-article:19622385 | lifeskim:mentions | umls-concept:C1449575 | lld:lifeskim |
| pubmed-article:19622385 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:19622385 | pubmed:dateCreated | 2010-2-1 | lld:pubmed |
| pubmed-article:19622385 | pubmed:abstractText | Microarray analysis has provided a new understanding of pineal function by identifying genes that are highly expressed in this tissue relative to other tissues and also by identifying over 600 genes that are expressed on a 24-h schedule. This effort has highlighted surprising similarity to the retina and has provided reason to explore new avenues of study including intracellular signaling, signal transduction, transcriptional cascades, thyroid/retinoic acid hormone signaling, metal biology, RNA splicing, and the role the pineal gland plays in the immune/inflammation response. The new foundation that microarray analysis has provided will broadly support future research on pineal function. | lld:pubmed |
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