PLP1-lacZ transgenic mice reveal that splice variants containing "human-specific" exons are relatively minor in comparison to the archetypal transcript and that an upstream regulatory element bolsters expression during early postnatal brain development.
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| Title: | PLP1-lacZ transgenic mice reveal that splice variants containing "human-specific" exons are relatively minor in comparison to the archetypal transcript and that an upstream regulatory element bolsters expression during early postnatal brain development. |
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| Authors: | Patyal P; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR, United States., Fil D; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR, United States., Hamdan H; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR, United States., Wight PA; Department of Physiology and Cell Biology, University of Arkansas for Medical Sciences, Little Rock, AR, United States. |
| Source: | Frontiers in cellular neuroscience [Front Cell Neurosci] 2023 Jan 11; Vol. 16, pp. 1087145. Date of Electronic Publication: 2023 Jan 11 (Print Publication: 2022). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Frontiers Research Foundation Country of Publication: Switzerland NLM ID: 101477935 Publication Model: eCollection Cited Medium: Print ISSN: 1662-5102 (Print) Linking ISSN: 16625102 NLM ISO Abbreviation: Front Cell Neurosci Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
| ISSN: | 1662-5102 |
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| DOI: | 10.3389/fncel.2022.1087145 |
