| scholarly article | Q13442814 |
| P2093 | author name string | J B Burch | |
| R Silva | |||
| P2860 | cites work | The abundant LINE-1 family of repeated DNA sequences in mammals: genes and pseudogenes | Q68759955 |
| Isolation of a protein fraction that binds preferentially to chicken middle repetitive DNA | Q70802570 | ||
| Nonviral retroposons: genes, pseudogenes, and transposable elements generated by the reverse flow of genetic information | Q29618191 | ||
| Organization, sequence and nuclease hypersensitivity of repetitive elements flanking the chicken apoVLDLII gene: extended sequence similarity to elements flanking the chicken vitellogenin gene | Q35940010 | ||
| A processed chicken pseudogene (CPS1) related to the ras oncogene superfamily | Q36094112 | ||
| Target sites for the transposition of rat long interspersed repeated DNA elements (LINEs) are not random | Q36098444 | ||
| Tissue-specific expression of a chicken calmodulin pseudogene lacking intervening sequences | Q36615054 | ||
| The major and minor chicken vitellogenin genes are each adjacent to partially deleted pseudogene copies of the other | Q36759463 | ||
| Genomic structure and possible retroviral origin of the chicken CR1 repetitive DNA sequence family | Q37575032 | ||
| Form and Function of Retroviral Proviruses | Q40103422 | ||
| A chicken middle-repetitive DNA sequence which shares homology with mammalian ubiquitous repeats | Q40500227 | ||
| A new repetitive element of the CR1 family downstream of the chicken vitellogenin gene | Q40566964 | ||
| Bombyx mori 28S ribosomal genes contain insertion elements similar to the Type I and II elements of Drosophila melanogaster. | Q41414011 | ||
| Highly preferred targets for retrovirus integration | Q44445802 | ||
| Insertional mutagenesis of the myc locus by a LINE-1 sequence in a human breast carcinoma | Q48324246 | ||
| Deoxyribonuclease I sensitivity of the ovomucoid-ovoinhibitor gene complex in oviduct nuclei and relative location of CR1 repetitive sequences | Q48336736 | ||
| Pseudogenes for human small nuclear RNA U3 appear to arise by integration of self-primed reverse transcripts of the RNA into new chromosomal sites. | Q48400274 | ||
| Characterization of deoxyribonucleic acid sequences at the 5' and 3' borders of the 100-kilobase pair ovalbumin gene domain | Q48400436 | ||
| The LINE-1 family of primates may encode a reverse transcriptase-like protein | Q56905162 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 3563-3566 | |
| P577 | publication date | 1989-08-01 | |
| P1433 | published in | Molecular and Cellular Biology | Q3319478 |
| P1476 | title | Evidence that chicken CR1 elements represent a novel family of retroposons | |
| P478 | volume | 9 |
| Q39131335 | A recent chicken repeat 1 retrotransposition confirms the Coscoroba-Cape Barren goose clade |
| Q42605149 | A sequence with homology to human HPFH-linked enhancer elements and to a family of G-protein linked membrane receptor genes is located downstream of the chicken beta-globin locus. |
| Q42614810 | Association of a Chicken Repetitive Element with the Endogenous Virus-21 Slow-Feathering Locus |
| Q28776647 | CORE-SINEs: eukaryotic short interspersed retroposing elements with common sequence motifs |
| Q33288656 | CR1 clade of non-LTR retrotransposons from Maculinea butterflies (Lepidoptera: Lycaenidae): evidence for recent horizontal transmission |
| Q33200676 | Cell type-specific expression of LINE-1 open reading frames 1 and 2 in fetal and adult human tissues |
| Q42665232 | Chicken repeat 1 (CR1) elements, which define an ancient family of vertebrate non-LTR retrotransposons, contain two closely spaced open reading frames |
| Q36516467 | Chicken repeat 1 elements contain a pol-like open reading frame and belong to the non-long terminal repeat class of retrotransposons |
| Q35850893 | Chromatin studies reveal that an ERE is located far upstream of a vitellogenin gene and that a distal tissue-specific hypersensitive site is conserved for two coordinately regulated vitellogenin genes |
| Q46380738 | Conserved regulatory elements in the promoter region of the N-CAM gene |
| Q42671143 | Cytogenetic repartition of chicken CR1 sequences evidenced by PRINS in Galliformes and some other birds. |
| Q33792470 | DINE-1, the highest copy number repeats in Drosophila melanogaster are non-autonomous endonuclease-encoding rolling-circle transposable elements (Helentrons). |
| Q33491932 | Evolution of serum albumin intron-1 is shaped by a 5' truncated non-long terminal repeat retrotransposon in western Palearctic water frogs (Neobatrachia). |
| Q44145080 | Maque, a family of extremely short interspersed repetitive elements: characterization, possible mechanism of transposition, and evolutionary implications |
| Q93532181 | New nucleotide sequence data on the EMBL File Server |
| Q33277371 | Phylogenomic investigation of CR1 LINE diversity in reptiles |
| Q48088232 | Primary sequence, evolution, and repetitive elements of the Gallus gallus (chicken) beta-globin cluster |
| Q33387687 | Recent CR1 non-LTR retrotransposon activity in coscoroba reveals an insertion site preference |
| Q47848291 | Retrotransposable CR1-like elements in crotalinae snake genomes. |
| Q37541805 | Sequence conservation in avian CR1: an interspersed repetitive DNA family evolving under functional constraints |
| Q33343539 | Specific chicken repeat 1 (CR1) retrotransposon insertion suggests phylogenetic affinity of rockfowls (genus Picathartes) to crows and ravens (Corvidae). |
| Q47957046 | Structure and evolution of the alternatively spliced fast troponin T isoform gene |
| Q42645272 | Subfamilies of CR1 non-LTR retrotransposons have different 5'UTR sequences but are otherwise conserved |
| Q28776785 | The 3' ends of tRNA-derived short interspersed repetitive elements are derived from the 3' ends of long interspersed repetitive elements |
| Q53600497 | The Specific Requirements for CR1 Retrotransposition Explain the Scarcity of Retrogenes in Birds. |
| Q48198041 | The alpha A-crystallin gene: conserved features of the 5'-flanking regions in human, mouse, and chicken |
| Q37380306 | The role of LINEs and CpG islands in dosage compensation on the chicken Z chromosome |
| Q33279847 | Transposable elements are enriched within or in close proximity to xenobiotic-metabolizing cytochrome P450 genes |
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