review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0959-437X(98)80092-0 |
P698 | PubMed publication ID | 9690999 |
P2093 | author name string | H H Kazazian | |
P2860 | cites work | Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements | Q24558897 |
The viruses in all of us: characteristics and biological significance of human endogenous retrovirus sequences | Q24606140 | ||
Structure and function of the multifunctional DNA-repair enzyme exonuclease III | Q27730409 | ||
Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition | Q28114795 | ||
LINEs and Alus--the polyA connection | Q28116220 | ||
Cloning of the T gene required in mesoderm formation in the mouse | Q28236865 | ||
A de novo Alu insertion results in neurofibromatosis type 1 | Q28281046 | ||
Reverse transcription of R2Bm RNA is primed by a nick at the chromosomal target site: A mechanism for non-LTR retrotransposition | Q28297748 | ||
Telomerase catalytic subunit homologs from fission yeast and human | Q29615387 | ||
Molecular reconstruction of Sleeping Beauty, a Tc1-like transposon from fish, and its transposition in human cells | Q29617246 | ||
Reverse Transcriptase Encoded by a Human Transposable Element | Q29618213 | ||
High frequency retrotransposition in cultured mammalian cells | Q29618259 | ||
Sequence patterns indicate an enzymatic involvement in integration of mammalian retroposons | Q30004188 | ||
Inactivation of the cholinesterase gene by Alu insertion: possible mechanism for human gene transposition | Q33240323 | ||
Translation of LINE-1 DNA elements in vitro and in human cells | Q33785234 | ||
Sequence-specific single-strand RNA binding protein encoded by the human LINE-1 retrotransposon | Q33887614 | ||
Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy | Q33897836 | ||
Differential expression of a new dominant agouti allele (Aiapy) is correlated with methylation state and is influenced by parental lineage | Q34323420 | ||
The impact of L1 retrotransposons on the human genome | Q34468340 | ||
Inactivation of muscle chloride channel by transposon insertion in myotonic mice | Q34510849 | ||
Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. | Q34553577 | ||
Identification, characterization, and cell specificity of a human LINE-1 promoter | Q34570051 | ||
Cytoplasmic ribonucleoprotein complexes containing human LINE-1 protein and RNA | Q35844482 | ||
Aberrant transcription caused by the insertion of an early transposable element in an intron of the Fas antigen gene of lpr mice | Q36129002 | ||
RNA template requirements for target DNA-primed reverse transcription by the R2 retrotransposable element | Q36552964 | ||
The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome | Q36560640 | ||
Germ line-specific expression of intracisternal A-particle retrotransposons in transgenic mice | Q36561660 | ||
The decline in human Alu retroposition was accompanied by an asymmetric decrease in SRP9/14 binding to dimeric Alu RNA and increased expression of small cytoplasmic Alu RNA. | Q36565648 | ||
Developmental and cell type specificity of LINE-1 expression in mouse testis: implications for transposition | Q36650559 | ||
Translation of the human LINE-1 element, L1Hs | Q36712171 | ||
Ribonucleoprotein particles with LINE-1 RNA in mouse embryonal carcinoma cells | Q36733242 | ||
Unit-length line-1 transcripts in human teratocarcinoma cells | Q36785924 | ||
Many human L1 elements are capable of retrotransposition | Q36859141 | ||
The molecular basis of the obese mutation in ob2J mice | Q38345903 | ||
Functional differences between the human LINE retrotransposon and retroviral reverse transcriptases for in vivo mRNA reverse transcription | Q41082589 | ||
Inactivation of the mouse HPRT locus by a 203-bp retroposon insertion and a 55-kb gene-targeted deletion: establishment of new HPRT-deficient mouse embryonic stem cell lines | Q41104505 | ||
Retrotransposition of a mouse IAP sequence tagged with an indicator gene | Q41699882 | ||
IAP insertion in the murine LamB3 gene results in junctional epidermolysis bullosa | Q42443360 | ||
Isolation of an active human transposable element | Q42614185 | ||
An actively retrotransposing, novel subfamily of mouse L1 elements | Q42637048 | ||
Dysfunction of the Orleans reeler gene arising from exon skipping due to transposition of a full-length copy of an active L1 sequence into the skipped exon | Q42638958 | ||
Characterization of a nondeleterious L1 insertion in an intron of the human factor VIII gene and further evidence of open reading frames in functional L1 elements | Q42640219 | ||
The vibrator mutation causes neurodegeneration via reduced expression of PITP alpha: positional complementation cloning and extragenic suppression | Q42658082 | ||
Origin of the human L1 elements: proposed progenitor genes deduced from a consensus DNA sequence | Q42660978 | ||
A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion | Q42693461 | ||
Identification of an Alu retrotransposition event in close proximity to a strong candidate gene for Huntington's disease | Q45290792 | ||
Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX gene | Q45872014 | ||
Neomorphic agouti mutations in obese yellow mice | Q46156066 | ||
Ancestral, mammalian-wide subfamilies of LINE-1 repetitive sequences | Q47207133 | ||
A human endogenous retroviral superantigen as candidate autoimmune gene in type I diabetes | Q48047077 | ||
Murine Model of Niemann-Pick C Disease: Mutation in a Cholesterol Homeostasis Gene | Q48047362 | ||
The bg allele mutation is due to a LINE1 element retrotransposition | Q48049232 | ||
Mutation detection in the med and medJ alleles of the sodium channel Scn8a. Unusual splicing due to a minor class AT-AC intron | Q48062096 | ||
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element. | Q48066076 | ||
Mutations in the founder of the MIP gene family underlie cataract development in the mouse. | Q48066771 | ||
The spastic mouse: aberrant splicing of glycine receptor beta subunit mRNA caused by intronic insertion of L1 element | Q48078656 | ||
Glycine receptor beta-subunit gene mutation in spastic mouse associated with LINE-1 element insertion. | Q48082303 | ||
Telomerase and retrotransposons: which came first? | Q56902974 | ||
P433 | issue | 3 | |
P304 | page(s) | 343-350 | |
P577 | publication date | 1998-06-01 | |
P1433 | published in | Current Opinion in Genetics & Development | Q13505684 |
P1476 | title | Mobile elements and disease | |
P478 | volume | 8 |
Q40237611 | 6-alkylthio-4-[1-(2,6-difluorophenyl)alkyl]-1H-[1,3,5]triazin-2-ones (ADATs): novel regulators of cell differentiation and proliferation |
Q37218123 | A comprehensive analysis of recently integrated human Ta L1 elements |
Q28512070 | A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant |
Q36263207 | A role for endogenous reverse transcriptase in tumorigenesis and as a target in differentiating cancer therapy. |
Q24656941 | Aberrant caspase-activated DNase (CAD) transcripts in human hepatoma cells |
Q36729306 | Active transposition in genomes |
Q34141813 | Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosome |
Q24675735 | All APOBEC3 family proteins differentially inhibit LINE-1 retrotransposition |
Q35549613 | Alu pair exclusions in the human genome |
Q24555185 | Alu-mediated inactivation of the human CMP- N-acetylneuraminic acid hydroxylase gene |
Q77883168 | An estimated frequency of endogenous insertional mutations in humans |
Q24550997 | Antisense promoter of human L1 retrotransposon drives transcription of adjacent cellular genes |
Q35650901 | Ataxia telangiectasia mutated (ATM) modulates long interspersed element-1 (L1) retrotransposition in human neural stem cells |
Q84782218 | Bioinformatic analysis of TE-spliced new exons within human, mouse and zebrafish genomes |
Q37293212 | Characterization and distribution of retrotransposons and simple sequence repeats in the bovine genome |
Q34092186 | Comparative genomics of the human and mouse T cell receptor loci |
Q23067954 | Demystified. Human endogenous retroviruses |
Q39586006 | Determination of L1 retrotransposition kinetics in cultured cells |
Q42618146 | Different rates of LINE-1 (L1) retrotransposon amplification and evolution in New World monkeys. |
Q39072419 | Differential L1 regulation in pluripotent stem cells of humans and apes. |
Q36331117 | Distribution of a marker of germline methylation differs between major families of transposon-derived repeats in the human genome |
Q37379454 | Environmental influence on L1 retrotransposons in the adult hippocampus |
Q36163349 | Epigenetic control of mammalian LINE-1 retrotransposon by retinoblastoma proteins. |
Q40662096 | Functional reverse transcriptase encoded by the human LINE-1 from baculovirus-infected insect cells |
Q25255521 | Gamma radiation increases endonuclease-dependent L1 retrotransposition in a cultured cell assay |
Q22122336 | Genetics: Junk DNA as an evolutionary force |
Q30650874 | Genomic scrap yard: how genomes utilize all that junk |
Q33266809 | Global mapping of transposon location |
Q52940179 | Growth and decline of introns. |
Q33259824 | Heat-shock promoters: targets for evolution by P transposable elements in Drosophila |
Q37271908 | Heavy metals stimulate human LINE-1 retrotransposition |
Q34363582 | Hierarchical assembly of the Alu domain of the mammalian signal recognition particle |
Q35751107 | Host RNAs, including transposons, are encapsidated by a eukaryotic single-stranded RNA virus |
Q42095539 | How do mammalian transposons induce genetic variation? A conceptual framework: the age, structure, allele frequency, and genome context of transposable elements may define their wide-ranging biological impacts |
Q73134117 | Human endogenous retroviruses and pathogenicity: genomic considerations |
Q56589628 | Hypomethylation of L1 retrotransposons in colorectal cancer and adjacent normal tissue |
Q37415872 | Identification of Cryptic Novel α-Galactosidase A Gene Mutations: Abnormal mRNA Splicing and Large Deletions |
Q42990988 | Identification, characterization and comparative genomics of chimpanzee endogenous retroviruses |
Q37738649 | Insertion Polymorphisms of Mobile Genetic Elements in Sexual and Asexual Populations of Daphnia pulex |
Q29615764 | Interspersed repeats and other mementos of transposable elements in mammalian genomes |
Q33703747 | Ionizing radiation and genetic risks. X. The potential "disease phenotypes" of radiation-induced genetic damage in humans: perspectives from human molecular biology and radiation genetics |
Q37139954 | L1 mobile element expression causes multiple types of toxicity. |
Q34686579 | L1 retrotransposition in neurons is modulated by MeCP2 |
Q33245909 | LINE FUSION GENES: a database of LINE expression in human genes |
Q33211669 | LINE-1 amplification accompanies explosive genome repatterning in rodents |
Q40520772 | LINE-1 distribution in Afrotheria and Xenarthra: implications for understanding the evolution of LINE-1 in eutherian genomes. |
Q40670348 | LINE-1 preTa elements in the human genome. |
Q28584519 | LINEs between Species: Evolutionary Dynamics of LINE-1 Retrotransposons across the Eukaryotic Tree of Life |
Q61658996 | Local Mutagenic Impact of Insertions of LTR Retrotransposons on the Mouse Genome |
Q36181065 | Long terminal repeat retrotransposons jump between species |
Q28469078 | Mammalian small nucleolar RNAs are mobile genetic elements |
Q36224644 | MeCP2 as a genome-wide modulator: the renewal of an old story |
Q35047364 | Mobile genetic elements in protozoan parasites |
Q30428528 | Mobilomics in Saccharomyces cerevisiae strains |
Q24817207 | Modeling the amplification dynamics of human Alu retrotransposons |
Q44119468 | Molecular characterization of a 2.7-kb, 12q13-specific, retroviral-related sequence isolated by RDA from monozygotic twin pairs discordant for schizophrenia |
Q28748621 | Nickel stimulates L1 retrotransposition by a post-transcriptional mechanism |
Q41110305 | PoPoolationTE2: Comparative Population Genomics of Transposable Elements Using Pool-Seq. |
Q42610891 | Quantitative variation of LINE-1 sequences in five species and three subspecies of the subgenus Mus and in five Robertsonian races of Mus musculus domesticus. |
Q33780174 | RISCI--Repeat Induced Sequence Changes Identifier: a comprehensive, comparative genomics-based, in silico subtractive hybridization pipeline to identify repeat induced sequence changes in closely related genomes |
Q42597900 | Redox Regulation of a Novel L1Md-A2 Retrotransposon in Vascular Smooth Muscle Cells |
Q92150005 | Restricted and non-essential redundancy of RNAi and piRNA pathways in mouse oocytes |
Q24805857 | Retrotransposition-Competent Human LINE-1 Induces Apoptosis in Cancer Cells With Intactp53 |
Q34007948 | Retrotransposon-centered analysis of piRNA targeting shows a shift from active to passive retrotransposon transcription in developing mouse testes |
Q34042729 | Retrotransposon-induced heterochromatin spreading in the mouse revealed by insertional polymorphisms |
Q73695300 | Retrotransposons as epigenetic mediators of phenotypic variation in mammals |
Q25255710 | Retroviral elements and their hosts: insertional mutagenesis in the mouse germ line |
Q33963329 | SINE retroposons can be used in vivo as nucleation centers for de novo methylation |
Q31008741 | Specific localization of transcription factors in the chromatin of mouse mature spermatozoa. |
Q27628611 | Structure and assembly of the Alu domain of the mammalian signal recognition particle |
Q36541045 | Structure and expression of mobile ETnII retroelements and their coding-competent MusD relatives in the mouse |
Q42271884 | Structure of the complete bacterial SRP Alu domain |
Q30821572 | TE-Locate: A Tool to Locate and Group Transposable Element Occurrences Using Paired-End Next-Generation Sequencing Data |
Q33851829 | The biological properties and evolutionary dynamics of mammalian LINE-1 retrotransposons |
Q44404819 | The endonuclease NL1Tc encoded by the LINE L1Tc from Trypanosoma cruzi protects parasites from daunorubicin DNA damage. |
Q34570688 | The first steps of transposable elements invasion: parasitic strategy vs. genetic drift |
Q34526958 | The genetics of the target tissue in rheumatoid arthritis |
Q44012138 | The non-LTR (long terminal repeat) retrotransposon L1Tc from Trypanosoma cruzi codes for a protein with RNase H activity. |
Q33724325 | The pathogenic potential of endogenous retroviruses: facts and fantasies |
Q35016886 | The potential regulation of L1 mobility by RNA interference. |
Q33204795 | The repetitive landscape of the chicken genome |
Q34762192 | Tracking an embryonic L1 retrotransposition event |
Q39611509 | Transcriptional regulation of early transposon elements, an active family of mouse long terminal repeat retrotransposons |
Q36901962 | Transcriptomics analysis of iPSC-derived neurons and modeling of neuropsychiatric disorders. |
Q44019080 | Transfer RNA gene-targeted retrotransposition of Dictyostelium TRE5-A into a chromosomal UMP synthase gene trap |
Q28710587 | Transposable elements and viruses as factors in adaptation and evolution: an expansion and strengthening of the TE-Thrust hypothesis |
Q53867468 | Unusual expression of LINE-1 transposable element in the MRL autoimmune lymphoproliferative syndrome-prone strain. |
Q52596587 | Utilization of the IR hybrid dysgenesis system in Drosophila to test in vivo mobilization of synthetic SINEs sharing 3' homology with the I factor. |
Q27013917 | Viral quasispecies evolution |
Q48396756 | Yayoi era mutation disrupts brain and muscle |
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