The Impact of Transposable Elements in Genome Evolution and Genetic Instability and Their Implications in Various Diseases

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' The Impact of Transposable Elements in Genome Evolution and Genetic Instability and Their Implications in Various Diseases' 의 주제별 논문영향력
논문영향력 선정 방법
논문영향력 요약
주제
  • 생물진화
  • cancer
  • evolution
  • gene expression
  • transposableelements
동일주제 총논문수 논문피인용 총횟수 주제별 논문영향력의 평균
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' The Impact of Transposable Elements in Genome Evolution and Genetic Instability and Their Implications in Various Diseases' 의 참고문헌

  • Which transposable elements are active in the human genome?
    Mills RE Trends Genet 23 : 183 ~ 191 [2007]
  • Transposable elements and psychiatric disorders
    Guffanti G Am J Med Genet B Neuropsychiatr Genet 165B : 201 ~ 216 [2014]
  • Transposable element insertions have strongly affected human evolution
    Britten RJ Proc Natl Acad Sci U S A 107 : 19945 ~ 19948 [2010]
  • The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors
    Kolomietz E Genes Chromosomes Cancer 35 : 97 ~ 112 [2005]
  • The origin and behavior of mutable loci in maize
    McClintock B Proc Natl Acad Sci U S A 36 : 344 ~ 355 [1950]
  • The impact of retrotransposons on human genome evolution
    Cordaux R Nat Rev Genet 10 : 691 ~ 703 [2009]
  • The human LINE-1 retrotransposon creates DNA double-strand breaks
    Gasior SL J Mol Biol 357 : 1383 ~ 1393 [2006]
  • The evolutionary history of human DNA transposons: evidence for intense activity in the primate lineage
    Pace JK 2nd Genome Res 17 : 422 ~ 432 [2007]
  • TEMP: a computational method for analyzing transposable element polymorphism in populations
    Zhuang J Nucleic Acids Res 42 : 6826 ~ 6838 [2014]
  • Structural determinants of BRCA1translational regulation
    Sobczak K J Biol Chem 277 : 14349 ~ 17358 [2002]
  • Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation
    Mitchell GA Proc Natl Acad Sci U S A 88 : 815 ~ 819 [1991]
  • Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome
    Knebelmann B Hum Mol Genet 4 : 675 ~ 679 [1995]
  • SVA elements: a hominid-specific retroposon family
    Wang H J Mol Biol 354 : 994 ~ 1007 [2005]
  • SVA elements are nonautonomous retrotransposons that cause disease in humans
    Ostertag EM Am J Hum Genet 73 : 1444 ~ 1451 [2003]
  • SINEs and LINEs: the art of biting the hand that feeds you
    Weiner AM Curr Opin Cell Biol 14 : 343 ~ 350 [2002]
  • Retrotransposable elements and human disease
    Callinan PA Genome Dyn 1 : 104 ~ 115 [2006]
  • Replication stalling at unstable inverted repeats: interplay between DNA hairpins and fork stabilizing proteins
    Voineagu I Proc Natl Acad Sci U S A 105 : 9936 ~ 9941 [2008]
  • Repetitive elements in the 5' untranslated region of a human zinc-finger gene modulate transcription and translation efficiency
    Landry JR Genomics 76 : 110 ~ 116 [2001]
  • Repbase update: a database and an electronic journal of repetitive elements
    Jurka J Trends Genet 16 : 418 ~ 420 [2000]
  • Regulation of the mammalian alcohol dehydrogenase genes
    Edenberg HJ Prog Nucleic Acid Res Mol Biol 64 : 295 ~ 341 [2000]
  • Recently mobilized transposons in the human and chimpanzee genomes
    Mills RE Am J Hum Genet 78 : 671 ~ 679 [2006]
  • Recently integrated human Alu repeats: finding needles in the haystack
    Roy AM Genetica 107 : 149 ~ 161 [1999]
  • Rearrangement of the human tre oncogene by homologous recombination between Alu repeats of nucleotide sequences from two different chromosomes
    Onno M Oncogene 7 : 2519 ~ 2523 [1992]
  • Progress in understanding the biology of the human mutagen LINE-1
    Babushok DV Hum Mutat 28 : 527 ~ 539 [2007]
  • Potential gene conversion and source genes for recently integrated Alu elements
    Roy AM Genome Res 10 : 1485 ~ 1495 [2000]
  • Positional cloning of the gene for X-linked retinitis pigmentosa 2
    Schwahn U Nat Genet 19 : 327 ~ 332 [1998]
  • Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD)
    Kondo-Iida E Hum Mol Genet 8 : 2303 ~ 2309 [1999]
  • Non-traditional Alu evolution and primate genomic diversity
    Roy-Engel AM J Mol Biol 316 : 1033 ~ 1040 [2002]
  • Nested retrotransposons in the intergenic regions of the maize genome
    SanMiguel P Science 274 : 765 ~ 768 [1996]
  • Mutation analysis in the BRCA2 gene in primary breast cancers
    Miki Y Nat Genet 13 : 245 ~ 247 [1996]
  • Monocyte activation and differentiation augment human endogenous retrovirus expression: implications for inflammatory brain diseases
    Johnston JB Ann Neurol 50 : 434 ~ 442 [2001]
  • Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients
    Mukherjee S Haemophilia 10 : 259 ~ 263 [2004]
  • Mobile elements: drivers of genome evolution
    Kazazian HH Jr Science 303 : 1626 ~ 1632 [2004]
  • Mobile DNA II
    Craig NL ASM Press [2002]
  • Mesothelin targeted cancer immunotherapy
    Hassan R Eur J Cancer 44 : 46 ~ 53 [2008]
  • Mammalian non-LTR retrotransposons: for better or worse, in sickness and in health
    Belancio VP Genome Res 18 : 343 ~ 358 [2008]
  • Loss of LINE-1 activity in the megabats
    Cantrell MA Genetics 178 : 393 ~ 404 [2008]
  • Large-scale analysis of the Alu Ya5 and Yb8subfamilies and their contribution to human genomic diversity
    Carroll ML J Mol Biol 311 : 17 ~ 40 [2001]
  • LINE-mediated retrotransposition of marked Alu sequences
    Dewannieux M Nat Genet 35 : 41 ~ 48 [2003]
  • LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease:mutation detection bias and multiple mechanisms of target gene disruption
    Chen JM J Biomed Biotechnol 2006 : 56182 ~ [2006]
  • LINE dancing in the human genome: transposable elements and disease
    Belancio VP Genome Med 1 : 97 ~ [2009]
  • L1recombination-associated deletions generate human genomic variation
    Han K Proc Natl Acad Sci U S A 105 : 19366 ~ 19371 [2008]
  • Isolation of cancer-specific chimeric transcripts induced by hypomethylation of the LINE-1antisense promoter
    Cruickshanks HA Genomics 94 : 397 ~ 406 [2009]
  • Inviting instability: transposable elements, double-strand breaks, and the maintenance of genome integrity
    Hedges DJ Mutat Res 616 : 46 ~ 59 [2007]
  • Inverted Alu repeats unstable in yeast are excluded from the human genome
    Lobachev KS EMBO J 19 : 3822 ~ 3830 [2000]
  • Insertion of an Alu SINE in the human homologue of the Mlvi-2 locus
    Economou-Pachnis A Nucleic Acids Res 13 : 8379 ~ 8387 [1985]
  • 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
    Narita N J Clin Invest 91 : 1862 ~ 1867 [1993]
  • Initial sequencing and analysis of the human genome
    Lander ES Nature 409 : 860 ~ 921 [2001]
  • Inactivation of the Fas gene by Alu insertion: retrotransposition in an intron causing splicing variation and autoimmune lymphoproliferative syndrome
    Tighe PJ Genes Immun 3 (3Suppl 1) : S66 ~ S70 [2002]
  • Identification, characterization, and cell specificity of a human LINE-1 promoter
    Swergold GD Mol Cell Biol 10 : 6718 ~ 6729 [1990]
  • Identification of a unique Alu-based polymorphism and its use in human population studies
    Kass DH Gene 390 : 146 ~ 152 [2007]
  • Hypomethylation of retrotransposable elements correlates with genomic instability in non-small cell lung cancer
    Daskalos A Int J Cancer 124 : 81 ~ 87 [2009]
  • Hypomethylation of L1 retrotransposons in colorectal cancer and adjacent normal tissue
    Suter CM Int J Colorectal Dis 19 : 95 ~ 101 [2004]
  • Human genomic deletions mediated by recombination between Alu elements
    Sen SK Am J Hum Genet 79 : 41 ~ 53 [2006]
  • Hot L1s account for the bulk of retrotransposition in the human population
    Brouha B Proc Natl Acad Sci U S A 100 : 5280 ~ 5285 [2003]
  • Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC gene
    Halling KC Hum Hered 49 : 97 ~ 102 [1999]
  • Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man
    Kazazian HH Jr Nature 332 : 164 ~ 166 [1988]
  • Genomic rearrangements of the APC tumor-suppressor gene in familial adenomatous polyposis
    Su LK Hum Genet 106 : 101 ~ 107 [2000]
  • Genomic gems: SINE RNAs regulate mRNA production
    Ponicsan SL Curr Opin Genet Dev 20 : 149 ~ 155 [2010]
  • Gene regulation by SINES and inosines:biological consequences of A-to-I editing of Alu element inverted repeats
    Chen LL Cell Cycle 7 : 3294 ~ 3301 [2008]
  • Exon skipping caused by an intronic insertion of a young Alu Yb9 element leads to severe hemophilia A
    Ganguly A Hum Genet 11 : 348 ~ 352 [2003]
  • Endogenous retroviruses and human evolution
    Khodosevich K Comp Funct Genomics 3 : 494 ~ 498 [2002]
  • Disruption of the APC gene by a retrotransposal insertion of L1 sequence in a colon cancer
    Miki Y Cancer Res 52 : 643 ~ 645 [1992]
  • Direct competition between hnRNP C and U2AF65 protects the transcriptome from the exonization of Alu elements
    Zarnack K Cell 152 : 453 ~ 466 [2013]
  • De novo Alu element insertions targeted to a sequence common to the BRCA1 and BRCA2 genes
    Teugels E Hum Mutat 26 : 284 ~ [2005]
  • DNA methylation and expression of LINE-1 and HERV-K provirus sequences in urothelial and renal cell carcinomas
    Florl AR Br J Cancer 80 : 1312 ~ 1321 [1999]
  • DNA hypomethylation and human diseases
    Wilson AS Biochim Biophys Acta 1775 : 138 ~ 162 [2007]
  • Cytosine methylation and the ecology of intragenomic parasites
    Yoder JA Trends Genet 13 : 335 ~ 340 [1997]
  • Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT
    Carlton VE Nat Genet 34 : 91 ~ 96 [2003]
  • Association between endometriosis and genetic polymorphisms of the estradiol-synthesizing enzyme genes HSD17B1 and CYP19
    Tsuchiya M Hum Reprod 20 : 974 ~ 978 [2005]
  • Antisense promoter of human L1 retrotransposon drives transcription of adjacent cellular genes
    Speek M Mol Cell Biol 21 : 1973 ~ 1985 [2001]
  • Alu repeats and human genomic diversity
    Batzer MA Nat Rev Genet 3 : 370 ~ 379 [2002]
  • Alu repeats and human disease
    Deininger PL Mol Genet Metab 67 : 183 ~ 193 [1999]
  • Alu insertion polymorphisms for the study of human genomic diversity
    Roy-Engel AM Genetics 159 : 279 ~ 290 [2001]
  • A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease
    Chen JM Hum Genet 117 : 411 ~ 427 [2005]
  • A new exon created by intronic insertion of a rearranged LINE-1 element as the cause of chronic granulomatous disease
    Meischl C Eur J Hum Genet 8 : 697 ~ 703 [2000]
  • A mutation (IVS8+0.6kbdelTC) creating a new donor splice site activates a cryptic exon in an Alu-element in intron 8 of the human beta-glucuronidase gene
    Vervoort R Hum Genet 103 : 686 ~ 693 [1998]
  • A mobile threat to genome stability:the impact of non-LTR retrotransposons upon the human genome
    Konkel MK Semin Cancer Biol 20 : 211 ~ 221 [2010]
  • A large genomic deletion in the PDHX gene caused by the retrotranspositional insertion of a full-length LINE-1 element
    Mine M Hum Mutat 28 : 137 ~ 142 [2007]
  • A de novo Alu insertion results in neurofibromatosis type 1
    Wallace MR Nature 353 : 864 ~ 866 [1991]