-
1
-
-
0026207423
-
Vectorette PCR: A novel approach to genomic walking
-
Arnold C., Hodgson I.J. Vectorette PCR: A novel approach to genomic walking. PCR Methods Appl. 1991, 1:39-42.
-
(1991)
PCR Methods Appl.
, vol.1
, pp. 39-42
-
-
Arnold, C.1
Hodgson, I.J.2
-
2
-
-
0034612238
-
Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis
-
Bailey J.A., Carrel L., Chakravarti A., Eichler E.E. Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: the Lyon repeat hypothesis. Proc. Natl. Acad. Sci. USA 2000, 97:6634-6639.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 6634-6639
-
-
Bailey, J.A.1
Carrel, L.2
Chakravarti, A.3
Eichler, E.E.4
-
3
-
-
77953880842
-
LINE-1 retrotransposition activity in human genomes
-
this issue
-
Beck C.R., Collier P., Macfarlane C., Malig M., Kidd J.M., Eichler E.E., Badge R.M., Moran J.V. LINE-1 retrotransposition activity in human genomes. Cell 2010, 141:1159-1170. this issue.
-
(2010)
Cell
, vol.141
, pp. 1159-1170
-
-
Beck, C.R.1
Collier, P.2
Macfarlane, C.3
Malig, M.4
Kidd, J.M.5
Eichler, E.E.6
Badge, R.M.7
Moran, J.V.8
-
4
-
-
39749182717
-
The impact of multiple splice sites in human L1 elements
-
Belancio V.P., Roy-Engel A.M., Deininger P. The impact of multiple splice sites in human L1 elements. Gene 2008, 411:38-45.
-
(2008)
Gene
, vol.411
, pp. 38-45
-
-
Belancio, V.P.1
Roy-Engel, A.M.2
Deininger, P.3
-
5
-
-
8544229065
-
Natural genetic variation caused by transposable elements in humans
-
Bennett E.A., Coleman L.E., Tsui C., Pittard W.S., Devine S.E. Natural genetic variation caused by transposable elements in humans. Genetics 2004, 168:933-951.
-
(2004)
Genetics
, vol.168
, pp. 933-951
-
-
Bennett, E.A.1
Coleman, L.E.2
Tsui, C.3
Pittard, W.S.4
Devine, S.E.5
-
6
-
-
0034086210
-
L1 (LINE-1) retrotransposon evolution and amplification in recent human history
-
Boissinot S., Chevret P., Furano A.V. L1 (LINE-1) retrotransposon evolution and amplification in recent human history. Mol. Biol. Evol. 2000, 17:915-928.
-
(2000)
Mol. Biol. Evol.
, vol.17
, pp. 915-928
-
-
Boissinot, S.1
Chevret, P.2
Furano, A.V.3
-
7
-
-
3543151399
-
The insertional history of an active family of L1 retrotransposons in humans
-
Boissinot S., Entezam A., Young L., Munson P.J., Furano A.V. The insertional history of an active family of L1 retrotransposons in humans. Genome Res. 2004, 14:1221-1231.
-
(2004)
Genome Res.
, vol.14
, pp. 1221-1231
-
-
Boissinot, S.1
Entezam, A.2
Young, L.3
Munson, P.J.4
Furano, A.V.5
-
8
-
-
0037965788
-
Hot L1s account for the bulk of retrotransposition in the human population
-
Brouha B., Schustak J., Badge R.M., Lutz-Prigge S., Farley A.H., Moran J.V., Kazazian H.H. Hot L1s account for the bulk of retrotransposition in the human population. Proc. Natl. Acad. Sci. USA 2003, 100:5280-5285.
-
(2003)
Proc. Natl. Acad. Sci. USA
, vol.100
, pp. 5280-5285
-
-
Brouha, B.1
Schustak, J.2
Badge, R.M.3
Lutz-Prigge, S.4
Farley, A.H.5
Moran, J.V.6
Kazazian, H.H.7
-
9
-
-
33745276315
-
Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements
-
Chen J., Rattner A., Nathans J. Effects of L1 retrotransposon insertion on transcript processing, localization and accumulation: lessons from the retinal degeneration 7 mouse and implications for the genomic ecology of L1 elements. Hum. Mol. Genet. 2006, 15:2146-2156.
-
(2006)
Hum. Mol. Genet.
, vol.15
, pp. 2146-2156
-
-
Chen, J.1
Rattner, A.2
Nathans, J.3
-
10
-
-
34347354302
-
Mutational and selective effects on copy-number variants in the human genome
-
Cooper G.M., Nickerson D.A., Eichler E.E. Mutational and selective effects on copy-number variants in the human genome. Nat. Genet. 2007, 39:S22-S29.
-
(2007)
Nat. Genet.
, vol.39
-
-
Cooper, G.M.1
Nickerson, D.A.2
Eichler, E.E.3
-
11
-
-
70349318211
-
The impact of retrotransposons on human genome evolution
-
Cordaux R., Batzer M.A. The impact of retrotransposons on human genome evolution. Nat. Rev. Genet. 2009, 10:691-703.
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 691-703
-
-
Cordaux, R.1
Batzer, M.A.2
-
12
-
-
73349101053
-
Transglutaminase 1-deficient recessive lamellar ichthyosis associated with a LINE-1 insertion in Jack Russell terrier dogs
-
Credille K.M., Minor J.S., Barnhart K.F., Lee E., Cox M.L., Tucker K.A., Diegel K.L., Venta P.J., Hohl D., Huber M., et al. Transglutaminase 1-deficient recessive lamellar ichthyosis associated with a LINE-1 insertion in Jack Russell terrier dogs. Br. J. Dermatol. 2009, 161:265-272.
-
(2009)
Br. J. Dermatol.
, vol.161
, pp. 265-272
-
-
Credille, K.M.1
Minor, J.S.2
Barnhart, K.F.3
Lee, E.4
Cox, M.L.5
Tucker, K.A.6
Diegel, K.L.7
Venta, P.J.8
Hohl, D.9
Huber, M.10
-
13
-
-
33846927932
-
Characterization of pre-insertion loci of de novo L1 insertions
-
Gasior S.L., Preston G., Hedges D.J., Gilbert N., Moran J.V., Deininger P.L. Characterization of pre-insertion loci of de novo L1 insertions. Gene 2007, 390:190-198.
-
(2007)
Gene
, vol.390
, pp. 190-198
-
-
Gasior, S.L.1
Preston, G.2
Hedges, D.J.3
Gilbert, N.4
Moran, J.V.5
Deininger, P.L.6
-
14
-
-
33645068168
-
The human LINE-1 retrotransposon creates DNA double-strand breaks
-
Gasior S.L., Wakeman T.P., Xu B., Deininger P.L. The human LINE-1 retrotransposon creates DNA double-strand breaks. J. Mol. Biol. 2006, 357:1383-1393.
-
(2006)
J. Mol. Biol.
, vol.357
, pp. 1383-1393
-
-
Gasior, S.L.1
Wakeman, T.P.2
Xu, B.3
Deininger, P.L.4
-
16
-
-
62549134411
-
Mechanisms for human genomic rearrangements
-
Gu W., Zhang F., Lupski J.R. Mechanisms for human genomic rearrangements. Pathogenetics 2008, 1:4.
-
(2008)
Pathogenetics
, vol.1
, pp. 4
-
-
Gu, W.1
Zhang, F.2
Lupski, J.R.3
-
17
-
-
24644516249
-
LINE-1 retrotransposons: modulators of quantity and quality of mammalian gene expression?
-
Han J.S., Boeke J.D. LINE-1 retrotransposons: modulators of quantity and quality of mammalian gene expression?. Bioessays 2005, 27:775-784.
-
(2005)
Bioessays
, vol.27
, pp. 775-784
-
-
Han, J.S.1
Boeke, J.D.2
-
18
-
-
2442667886
-
Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes
-
Han J.S., Szak S.T., Boeke J.D. Transcriptional disruption by the L1 retrotransposon and implications for mammalian transcriptomes. Nature 2004, 429:268-274.
-
(2004)
Nature
, vol.429
, pp. 268-274
-
-
Han, J.S.1
Szak, S.T.2
Boeke, J.D.3
-
19
-
-
79959503826
-
The International HapMap Project
-
International HapMap Consortium
-
The International HapMap Project. Nature 2003, 426:789-796. International HapMap Consortium.
-
(2003)
Nature
, vol.426
, pp. 789-796
-
-
-
20
-
-
18244384210
-
Multiple-laboratory comparison of microarray platforms
-
Irizarry R.A., Warren D., Spencer F., Kim I.F., Biswal S., Frank B.C., Gabrielson E., Garcia J.G., Geoghegan J., Germino G., et al. Multiple-laboratory comparison of microarray platforms. Nat. Methods 2005, 2:345-350.
-
(2005)
Nat. Methods
, vol.2
, pp. 345-350
-
-
Irizarry, R.A.1
Warren, D.2
Spencer, F.3
Kim, I.F.4
Biswal, S.5
Frank, B.C.6
Gabrielson, E.7
Garcia, J.G.8
Geoghegan, J.9
Germino, G.10
-
21
-
-
77953889472
-
Natural mutagenesis of human genomes by endogenous retrotransposons
-
this issue
-
Iskow R.C., McCabe M.T., Mills R.E., Torene S., Pittard W.S., Neuwald A.F., Van Meir E.G., Vertino P.M., Devine S.E. Natural mutagenesis of human genomes by endogenous retrotransposons. Cell 2010, 141:1253-1261. this issue.
-
(2010)
Cell
, vol.141
, pp. 1253-1261
-
-
Iskow, R.C.1
McCabe, M.T.2
Mills, R.E.3
Torene, S.4
Pittard, W.S.5
Neuwald, A.F.6
Van Meir, E.G.7
Vertino, P.M.8
Devine, S.E.9
-
22
-
-
66149168927
-
L1 retrotransposition occurs mainly in embryogenesis and creates somatic mosaicism
-
Kano H., Godoy I., Courtney C., Vetter M.R., Gerton G.L., Ostertag E.M., Kazazian H.H. L1 retrotransposition occurs mainly in embryogenesis and creates somatic mosaicism. Genes Dev. 2009, 23:1303-1312.
-
(2009)
Genes Dev.
, vol.23
, pp. 1303-1312
-
-
Kano, H.1
Godoy, I.2
Courtney, C.3
Vetter, M.R.4
Gerton, G.L.5
Ostertag, E.M.6
Kazazian, H.H.7
-
23
-
-
0023867459
-
Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man
-
Kazazian H.H., Wong C., Youssoufian H., Scott A.F., Phillips D.G., Antonarakis S.E. Haemophilia A resulting from de novo insertion of L1 sequences represents a novel mechanism for mutation in man. Nature 1988, 332:164-166.
-
(1988)
Nature
, vol.332
, pp. 164-166
-
-
Kazazian, H.H.1
Wong, C.2
Youssoufian, H.3
Scott, A.F.4
Phillips, D.G.5
Antonarakis, S.E.6
-
24
-
-
0036079158
-
The human genome browser at UCSC
-
Kent W.J., Sugnet C.W., Furey T.S., Roskin K.M., Pringle T.H., Zahler A.M., Haussler D. The human genome browser at UCSC. Genome Res. 2002, 12:996-1006.
-
(2002)
Genome Res.
, vol.12
, pp. 996-1006
-
-
Kent, W.J.1
Sugnet, C.W.2
Furey, T.S.3
Roskin, K.M.4
Pringle, T.H.5
Zahler, A.M.6
Haussler, D.7
-
25
-
-
0036778597
-
The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors
-
Kolomietz E., Meyn M.S., Pandita A., Squire J.A. The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors. Genes Chromosomes Cancer 2002, 35:97-112.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 97-112
-
-
Kolomietz, E.1
Meyn, M.S.2
Pandita, A.3
Squire, J.A.4
-
26
-
-
33846897374
-
Identification and characterization of novel polymorphic LINE-1 insertions through comparison of two human genome sequence assemblies
-
Konkel M.K., Wang J., Liang P., Batzer M.A. Identification and characterization of novel polymorphic LINE-1 insertions through comparison of two human genome sequence assemblies. Gene 2007, 390:28-38.
-
(2007)
Gene
, vol.390
, pp. 28-38
-
-
Konkel, M.K.1
Wang, J.2
Liang, P.3
Batzer, M.A.4
-
27
-
-
35348988679
-
Paired-end mapping reveals extensive structural variation in the human genome
-
Korbel J.O., Urban A.E., Affourtit J.P., Godwin B., Grubert F., Simons J.F., Kim P.M., Palejev D., Carriero N.J., Du L., et al. Paired-end mapping reveals extensive structural variation in the human genome. Science 2007, 318:420-426.
-
(2007)
Science
, vol.318
, pp. 420-426
-
-
Korbel, J.O.1
Urban, A.E.2
Affourtit, J.P.3
Godwin, B.4
Grubert, F.5
Simons, J.F.6
Kim, P.M.7
Palejev, D.8
Carriero, N.J.9
Du, L.10
-
28
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander E.S., Linton L.M., Birren B., Nusbaum C., Zody M.C., Baldwin J., Devon K., Dewar K., Doyle M., FitzHugh W., et al. Initial sequencing and analysis of the human genome. Nature 2001, 409:860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
Devon, K.7
Dewar, K.8
Doyle, M.9
FitzHugh, W.10
-
29
-
-
35648976118
-
The diploid genome sequence of an individual human
-
Levy S., Sutton G., Ng P.C., Feuk L., Halpern A.L., Walenz B.P., Axelrod N., Huang J., Kirkness E.F., Denisov G., et al. The diploid genome sequence of an individual human. PLoS Biol. 2007, 5:e254.
-
(2007)
PLoS Biol.
, vol.5
-
-
Levy, S.1
Sutton, G.2
Ng, P.C.3
Feuk, L.4
Halpern, A.L.5
Walenz, B.P.6
Axelrod, N.7
Huang, J.8
Kirkness, E.F.9
Denisov, G.10
-
30
-
-
0033936876
-
The retinal determination gene, dachshund, is required for mushroom body cell differentiation
-
Martini S.R., Roman G., Meuser S., Mardon G., Davis R.L. The retinal determination gene, dachshund, is required for mushroom body cell differentiation. Development 2000, 127:2663-2672.
-
(2000)
Development
, vol.127
, pp. 2663-2672
-
-
Martini, S.R.1
Roman, G.2
Meuser, S.3
Mardon, G.4
Davis, R.L.5
-
31
-
-
0026503996
-
Disruption of the APC gene by a retrotransposal insertion of L1 sequence in a colon cancer
-
Miki Y., Nishisho I., Horii A., Miyoshi Y., Utsunomiya J., Kinzler K.W., Vogelstein B., Nakamura Y. Disruption of the APC gene by a retrotransposal insertion of L1 sequence in a colon cancer. Cancer Res. 1992, 52:643-645.
-
(1992)
Cancer Res.
, vol.52
, pp. 643-645
-
-
Miki, Y.1
Nishisho, I.2
Horii, A.3
Miyoshi, Y.4
Utsunomiya, J.5
Kinzler, K.W.6
Vogelstein, B.7
Nakamura, Y.8
-
32
-
-
0030606320
-
High frequency retrotransposition in cultured mammalian cells
-
Moran J.V., Holmes S.E., Naas T.P., DeBerardinis R.J., Boeke J.D., Kazazian H.H. High frequency retrotransposition in cultured mammalian cells. Cell 1996, 87:917-927.
-
(1996)
Cell
, vol.87
, pp. 917-927
-
-
Moran, J.V.1
Holmes, S.E.2
Naas, T.P.3
DeBerardinis, R.J.4
Boeke, J.D.5
Kazazian, H.H.6
-
33
-
-
77954540079
-
Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion
-
Morisada N., Rendtorff N.D., Nozu K., Morishita T., Miyakawa T., Matsumoto T., Hisano S., Iijima K., Tranebjaerg L., Shirahata A., et al. Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion. Pediatr. Nephrol. 2010, 25:1343-1348.
-
(2010)
Pediatr. Nephrol.
, vol.25
, pp. 1343-1348
-
-
Morisada, N.1
Rendtorff, N.D.2
Nozu, K.3
Morishita, T.4
Miyakawa, T.5
Matsumoto, T.6
Hisano, S.7
Iijima, K.8
Tranebjaerg, L.9
Shirahata, A.10
-
34
-
-
20544466648
-
Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition
-
Muotri A.R., Chu V.T., Marchetto M.C., Deng W., Moran J.V., Gage F.H. Somatic mosaicism in neuronal precursor cells mediated by L1 retrotransposition. Nature 2005, 435:903-910.
-
(2005)
Nature
, vol.435
, pp. 903-910
-
-
Muotri, A.R.1
Chu, V.T.2
Marchetto, M.C.3
Deng, W.4
Moran, J.V.5
Gage, F.H.6
-
35
-
-
0036073862
-
A comprehensive analysis of recently integrated human Ta L1 elements
-
Myers J.S., Vincent B.J., Udall H., Watkins W.S., Morrish T.A., Kilroy G.E., Swergold G.D., Henke J., Henke L., Moran J.V., et al. A comprehensive analysis of recently integrated human Ta L1 elements. Am. J. Hum. Genet. 2002, 71:312-326.
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 312-326
-
-
Myers, J.S.1
Vincent, B.J.2
Udall, H.3
Watkins, W.S.4
Morrish, T.A.5
Kilroy, G.E.6
Swergold, G.D.7
Henke, J.8
Henke, L.9
Moran, J.V.10
-
36
-
-
0344826526
-
RNA truncation by premature polyadenylation attenuates human mobile element activity
-
Perepelitsa-Belancio V., Deininger P. RNA truncation by premature polyadenylation attenuates human mobile element activity. Nat. Genet. 2003, 35:363-366.
-
(2003)
Nat. Genet.
, vol.35
, pp. 363-366
-
-
Perepelitsa-Belancio, V.1
Deininger, P.2
-
37
-
-
34347348166
-
Challenges and standards in integrating surveys of structural variation
-
Scherer S.W., Lee C., Birney E., Altshuler D.M., Eichler E.E., Carter N.P., Hurles M.E., Feuk L. Challenges and standards in integrating surveys of structural variation. Nat. Genet. 2007, 39:S7-S15.
-
(2007)
Nat. Genet.
, vol.39
-
-
Scherer, S.W.1
Lee, C.2
Birney, E.3
Altshuler, D.M.4
Eichler, E.E.5
Carter, N.P.6
Hurles, M.E.7
Feuk, L.8
-
38
-
-
17344363489
-
Positional cloning of the gene for X-linked retinitis pigmentosa 2
-
Schwahn U., Lenzner S., Dong J., Feil S., Hinzmann B., van Duijnhoven G., Kirschner R., Hemberger M., Bergen A.A., Rosenberg T., et al. Positional cloning of the gene for X-linked retinitis pigmentosa 2. Nat. Genet. 1998, 19:327-332.
-
(1998)
Nat. Genet.
, vol.19
, pp. 327-332
-
-
Schwahn, U.1
Lenzner, S.2
Dong, J.3
Feil, S.4
Hinzmann, B.5
van Duijnhoven, G.6
Kirschner, R.7
Hemberger, M.8
Bergen, A.A.9
Rosenberg, T.10
-
39
-
-
0023948714
-
Unit-length line-1 transcripts in human teratocarcinoma cells
-
Skowronski J., Fanning T.G., Singer M.F. Unit-length line-1 transcripts in human teratocarcinoma cells. Mol. Cell. Biol. 1988, 8:1385-1397.
-
(1988)
Mol. Cell. Biol.
, vol.8
, pp. 1385-1397
-
-
Skowronski, J.1
Fanning, T.G.2
Singer, M.F.3
-
40
-
-
77953907075
-
-
RepeatMasker: Open-3.0. 1996-2004
-
Smit, A.F.A., Hubley, R., and Green, P. (2004). RepeatMasker: Open-3.0. 1996-2004 http://www.repeatmasker.org.
-
(2004)
-
-
Smit, A.F.A.1
Hubley, R.2
Green, P.3
-
41
-
-
0034999474
-
Antisense promoter of human L1 retrotransposon drives transcription of adjacent cellular genes
-
Speek M. Antisense promoter of human L1 retrotransposon drives transcription of adjacent cellular genes. Mol. Cell. Biol. 2001, 21:1973-1985.
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 1973-1985
-
-
Speek, M.1
-
42
-
-
77949831756
-
Structural variation in the human genome and its role in disease
-
Stankiewicz P., Lupski J.R. Structural variation in the human genome and its role in disease. Annu. Rev. Med. 2010, 61:437-455.
-
(2010)
Annu. Rev. Med.
, vol.61
, pp. 437-455
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
43
-
-
0037249501
-
PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification
-
Thomas P.D., Kejariwal A., Campbell M.J., Mi H., Diemer K., Guo N., Ladunga I., Ulitsky-Lazareva B., Muruganujan A., Rabkin S., et al. PANTHER: a browsable database of gene products organized by biological function, using curated protein family and subfamily classification. Nucleic Acids Res. 2003, 31:334-341.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 334-341
-
-
Thomas, P.D.1
Kejariwal, A.2
Campbell, M.J.3
Mi, H.4
Diemer, K.5
Guo, N.6
Ladunga, I.7
Ulitsky-Lazareva, B.8
Muruganujan, A.9
Rabkin, S.10
-
44
-
-
33749627376
-
Long L1 insertions in human gene introns specifically reduce the content of corresponding primary transcripts
-
Ustyugova S.V., Lebedev Y.B., Sverdlov E.D. Long L1 insertions in human gene introns specifically reduce the content of corresponding primary transcripts. Genetica 2006, 128:261-272.
-
(2006)
Genetica
, vol.128
, pp. 261-272
-
-
Ustyugova, S.V.1
Lebedev, Y.B.2
Sverdlov, E.D.3
-
45
-
-
0031976478
-
A 20.7 kb deletion within the factor VIII gene associated with LINE-1 element insertion
-
Van de Water N., Williams R., Ockelford P., Browett P. A 20.7 kb deletion within the factor VIII gene associated with LINE-1 element insertion. Thromb. Haemost. 1998, 79:938-942.
-
(1998)
Thromb. Haemost.
, vol.79
, pp. 938-942
-
-
Van de Water, N.1
Williams, R.2
Ockelford, P.3
Browett, P.4
-
46
-
-
34447320759
-
L1 retrotransposition can occur early in human embryonic development
-
van den Hurk J.A., Meij I.C., Del Carmen Seleme M., Hoefsloot L.H., Sistermans E.A., de Wijs I.J., Plomp A.S., de Jong P.T., Kazazian H.H., Cremers F.P. L1 retrotransposition can occur early in human embryonic development. Hum. Mol. Genet. 2007, 16:1587-1592.
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 1587-1592
-
-
van den Hurk, J.A.1
Meij, I.C.2
Del Carmen Seleme, M.3
Hoefsloot, L.H.4
Sistermans, E.A.5
de Wijs, I.J.6
Plomp, A.S.7
de Jong, P.T.8
Kazazian, H.H.9
Cremers, F.P.10
-
47
-
-
0035895505
-
The sequence of the human genome
-
Venter J.C., Adams M.D., Myers E.W., Li P.W., Mural R.J., Sutton G.G., Smith H.O., Yandell M., Evans C.A., Holt R.A., et al. The sequence of the human genome. Science 2001, 291:1304-1351.
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
Smith, H.O.7
Yandell, M.8
Evans, C.A.9
Holt, R.A.10
-
48
-
-
33645786590
-
DbRIP: a highly integrated database of retrotransposon insertion polymorphisms in humans
-
Wang J., Song L., Grover D., Azrak S., Batzer M.A., Liang P. dbRIP: a highly integrated database of retrotransposon insertion polymorphisms in humans. Hum. Mutat. 2006, 27:323-329.
-
(2006)
Hum. Mutat.
, vol.27
, pp. 323-329
-
-
Wang, J.1
Song, L.2
Grover, D.3
Azrak, S.4
Batzer, M.A.5
Liang, P.6
-
49
-
-
23744454779
-
Gene-breaking: a new paradigm for human retrotransposon-mediated gene evolution
-
Wheelan S.J., Aizawa Y., Han J.S., Boeke J.D. Gene-breaking: a new paradigm for human retrotransposon-mediated gene evolution. Genome Res. 2005, 15:1073-1078.
-
(2005)
Genome Res.
, vol.15
, pp. 1073-1078
-
-
Wheelan, S.J.1
Aizawa, Y.2
Han, J.S.3
Boeke, J.D.4
-
50
-
-
33845204670
-
Eukaryotic Transposable Elements and Genome Evolution Special Feature: Transposon insertion site profiling chip (TIP-chip)
-
Wheelan S.J., Scheifele L.Z., Martinez-Murillo F., Irizarry R.A., Boeke J.D. Eukaryotic Transposable Elements and Genome Evolution Special Feature: Transposon insertion site profiling chip (TIP-chip). Proc. Natl. Acad. Sci. USA 2006, 103:17632-17637.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 17632-17637
-
-
Wheelan, S.J.1
Scheifele, L.Z.2
Martinez-Murillo, F.3
Irizarry, R.A.4
Boeke, J.D.5
-
51
-
-
33750165708
-
Human population genetic structure and diversity inferred from polymorphic L1(LINE-1) and Alu insertions
-
Witherspoon D.J., Marchani E.E., Watkins W.S., Ostler C.T., Wooding S.P., Anders B.A., Fowlkes J.D., Boissinot S., Furano A.V., Ray D.A., et al. Human population genetic structure and diversity inferred from polymorphic L1(LINE-1) and Alu insertions. Hum. Hered. 2006, 62:30-46.
-
(2006)
Hum. Hered.
, vol.62
, pp. 30-46
-
-
Witherspoon, D.J.1
Marchani, E.E.2
Watkins, W.S.3
Ostler, C.T.4
Wooding, S.P.5
Anders, B.A.6
Fowlkes, J.D.7
Boissinot, S.8
Furano, A.V.9
Ray, D.A.10
-
52
-
-
67649982842
-
Mobile elements create structural variation: analysis of a complete human genome
-
Xing J., Zhang Y., Han K., Salem A.H., Sen S.K., Huff C.D., Zhou Q., Kirkness E.F., Levy S., Batzer M.A., et al. Mobile elements create structural variation: analysis of a complete human genome. Genome Res. 2009, 19:1516-1526.
-
(2009)
Genome Res.
, vol.19
, pp. 1516-1526
-
-
Xing, J.1
Zhang, Y.2
Han, K.3
Salem, A.H.4
Sen, S.K.5
Huff, C.D.6
Zhou, Q.7
Kirkness, E.F.8
Levy, S.9
Batzer, M.A.10
-
53
-
-
0032815964
-
An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness
-
Yajima I., Sato S., Kimura T., Yasumoto K., Shibahara S., Goding C.R., Yamamoto H. An L1 element intronic insertion in the black-eyed white (Mitf[mi-bw]) gene: the loss of a single Mitf isoform responsible for the pigmentary defect and inner ear deafness. Hum. Mol. Genet. 1999, 8:1431-1441.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1431-1441
-
-
Yajima, I.1
Sato, S.2
Kimura, T.3
Yasumoto, K.4
Shibahara, S.5
Goding, C.R.6
Yamamoto, H.7
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