-
1
-
-
0019230217
-
The striking resemblance of high-resolution G-banded chromosomes of man and chimpanzee
-
PID: 7375922, COI: 1:STN:280:DyaL3c7ptF2gsw%3D%3D
-
Yunis JJ, Sawyer JR, Dunham K: The striking resemblance of high-resolution G-banded chromosomes of man and chimpanzee. Science. 1980, 208: 1145-1148. DOI: 10.1126/science.7375922
-
(1980)
Science
, vol.208
, pp. 1145-1148
-
-
Yunis, J.J.1
Sawyer, J.R.2
Dunham, K.3
-
2
-
-
0020027910
-
The origin of man: a chromosomal pictorial legacy
-
PID: 7063861, COI: 1:STN:280:DyaL387lt1OktQ%3D%3D
-
Yunis JJ, Prakash O: The origin of man: a chromosomal pictorial legacy. Science. 1982, 215: 1525-1530. DOI: 10.1126/science.7063861
-
(1982)
Science
, vol.215
, pp. 1525-1530
-
-
Yunis, J.J.1
Prakash, O.2
-
3
-
-
0016669094
-
Evolution at two levels in humans and chimpanzees
-
PID: 1090005, COI: 1:CAS:528:DyaE2MXhs1Orur4%3D
-
King MC, Wilson AC: Evolution at two levels in humans and chimpanzees. Science. 1975, 188: 107-116. DOI: 10.1126/science.1090005
-
(1975)
Science
, vol.188
, pp. 107-116
-
-
King, M.C.1
Wilson, A.C.2
-
4
-
-
6644225936
-
Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution
-
PID: 11441184, COI: 1:CAS:528:DC%2BD3MXltFCntbw%3D
-
Dehal P, Predki P, Olsen AS, Kobayashi A, Folta P, Lucas S, Land M, Terry A, Ecale Zhou CL, Rash S, et al: Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution. Science. 2001, 293: 104-111. 10.1126/science.1060310. DOI: 10.1126/science.1060310
-
(2001)
Science
, vol.293
, pp. 104-111
-
-
Dehal, P.1
Predki, P.2
Olsen, A.S.3
Kobayashi, A.4
Folta, P.5
Lucas, S.6
Land, M.7
Terry, A.8
Ecale Zhou, C.L.9
Rash, S.10
-
5
-
-
1542563409
-
Initial sequencing and comparative analysis of the mouse genome
-
Mouse Genome Sequencing Consortium: Initial sequencing and comparative analysis of the mouse genome. Nature. 2002, 420: 520-562. 10.1038/nature01262. DOI: 10.1038/nature01262
-
(2002)
Nature
, vol.420
, pp. 520-562
-
-
-
6
-
-
0014406287
-
Models of speciation. New concepts suggest that the classical sympatric and allopatric models are not the only alternatives
-
PID: 5636340, COI: 1:STN:280:DyaF1c7isVyhsA%3D%3D
-
White MJ: Models of speciation. New concepts suggest that the classical sympatric and allopatric models are not the only alternatives. Science. 1968, 159: 1065-1070. DOI: 10.1126/science.159.3819.1065
-
(1968)
Science
, vol.159
, pp. 1065-1070
-
-
White, M.J.1
-
7
-
-
0032526478
-
Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees
-
PID: 9676431, COI: 1:CAS:528:DyaK1cXks1Smt7Y%3D
-
Nickerson E, Nelson DL: Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees. Genomics. 1998, 50: 368-372. 10.1006/geno.1998.5332. DOI: 10.1006/geno.1998.5332
-
(1998)
Genomics
, vol.50
, pp. 368-372
-
-
Nickerson, E.1
Nelson, D.L.2
-
8
-
-
0034924052
-
The evolutionary chromosome translocation 4;19 in Gorilla gorillais associated with microduplication of the chromosome fragment syntenic to sequences surrounding the human proximal CMT1A-REP
-
PID: 11435402, COI: 1:CAS:528:DC%2BD3MXltFaitLY%3D
-
Stankiewicz P, Park SS, Inoue K, Lupski JR: The evolutionary chromosome translocation 4;19 in Gorilla gorilla is associated with microduplication of the chromosome fragment syntenic to sequences surrounding the human proximal CMT1A-REP. Genome Res. 2001, 11: 1205-1210. 10.1101/gr.181101. DOI: 10.1101/gr.181101
-
(2001)
Genome Res
, vol.11
, pp. 1205-1210
-
-
Stankiewicz, P.1
Park, S.S.2
Inoue, K.3
Lupski, J.R.4
-
9
-
-
0036071239
-
Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17
-
PID: 12094327, COI: 1:CAS:528:DC%2BD38XlvV2qtb0%3D
-
Kehrer-Sawatzki H, Schreiner B, Tanzer S, Platzer M, Muller S, Hameister H: Molecular characterization of the pericentric inversion that causes differences between chimpanzee chromosome 19 and human chromosome 17. Am J Hum Genet. 2002, 71: 375-388. 10.1086/341963. DOI: 10.1086/341963
-
(2002)
Am J Hum Genet
, vol.71
, pp. 375-388
-
-
Kehrer-Sawatzki, H.1
Schreiner, B.2
Tanzer, S.3
Platzer, M.4
Muller, S.5
Hameister, H.6
-
10
-
-
0029068854
-
The genomic sequence for Prader-Willi/Angelman syndromes' loci of human is apparently conserved in the great apes
-
PID: 7666455, COI: 1:CAS:528:DyaK2MXntVSltL8%3D
-
Luke S, Verma RS: The genomic sequence for Prader-Willi/Angelman syndromes' loci of human is apparently conserved in the great apes. J Mol Evol. 1995, 41: 250-252. DOI: 10.1007/BF00170680
-
(1995)
J Mol Evol
, vol.41
, pp. 250-252
-
-
Luke, S.1
Verma, R.S.2
-
11
-
-
0032971379
-
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)
-
PID: 10332034, COI: 1:CAS:528:DyaK1MXjs1Wls7k%3D
-
Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH: Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13). Hum Mol Genet. 1999, 8: 1025-1037. 10.1093/hmg/8.6.1025. DOI: 10.1093/hmg/8.6.1025
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1025-1037
-
-
Christian, S.L.1
Fantes, J.A.2
Mewborn, S.K.3
Huang, B.4
Ledbetter, D.H.5
-
12
-
-
0343362695
-
Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human
-
PID: 10720573, COI: 1:CAS:528:DC%2BD3cXitVWkt74%3D
-
Ji Y, Rebert NA, Joslin JM, Higgins MJ, Schultz RA, Nicholls RD: Structure of the highly conserved HERC2 gene and of multiple partially duplicated paralogs in human. Genome Res. 2000, 10: 319-329. 10.1101/gr.10.3.319. DOI: 10.1101/gr.10.3.319
-
(2000)
Genome Res
, vol.10
, pp. 319-329
-
-
Ji, Y.1
Rebert, N.A.2
Joslin, J.M.3
Higgins, M.J.4
Schultz, R.A.5
Nicholls, R.D.6
-
13
-
-
0033361765
-
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
-
PID: 10417280, COI: 1:CAS:528:DyaK1MXlsFSgsr8%3D
-
Amos-Landgraf JM, Ji Y, Gottlieb W, Depinet T, Wandstrat AE, Cassidy SB, Driscoll DJ, Rogan PK, Schwartz S, Nicholls RD: Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints. Am J Hum Genet. 1999, 65: 370-386. 10.1086/302510. DOI: 10.1086/302510
-
(1999)
Am J Hum Genet
, vol.65
, pp. 370-386
-
-
Amos-Landgraf, J.M.1
Ji, Y.2
Gottlieb, W.3
Depinet, T.4
Wandstrat, A.E.5
Cassidy, S.B.6
Driscoll, D.J.7
Rogan, P.K.8
Schwartz, S.9
Nicholls, R.D.10
-
14
-
-
0036079158
-
The human genome browser at UCSC
-
PID: 12045153, COI: 1:CAS:528:DC%2BD38Xks12hs7s%3D
-
Kent WJ, Sugnet CW, Furey TS, Roskin KM, Pringle TH, Zahler AM, Haussler D: The human genome browser at UCSC. Genome Res. 2002, 12: 996-1006. 10.1101/gr.229102. Article published online before print in May 2002. DOI: 10.1101/gr.229102. Article published online before print in May 2002
-
(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
-
16
-
-
0034831138
-
Segmental duplications: organization and impact within the current human genome project assembly
-
PID: 11381028, COI: 1:CAS:528:DC%2BD3MXkt12rurg%3D
-
Bailey JA, Yavor AM, Massa HF, Trask BJ, Eichler EE: Segmental duplications: organization and impact within the current human genome project assembly. Genome Res. 2001, 11: 1005-1017. 10.1101/gr.GR-1871R. DOI: 10.1101/gr.GR-1871R
-
(2001)
Genome Res
, vol.11
, pp. 1005-1017
-
-
Bailey, J.A.1
Yavor, A.M.2
Massa, H.F.3
Trask, B.J.4
Eichler, E.E.5
-
17
-
-
0035704937
-
A 3-Mb map of a large segmental duplication overlapping the alpha7-nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14
-
PID: 11829490, COI: 1:CAS:528:DC%2BD38Xpslyksg%3D%3D
-
Riley B, Williamson M, Collier D, Wilkie H, Makoff A: A 3-Mb map of a large segmental duplication overlapping the alpha7-nicotinic acetylcholine receptor gene (CHRNA7) at human 15q13-q14. Genomics. 2002, 79: 197-209. 10.1006/geno.2002.6694. DOI: 10.1006/geno.2002.6694
-
(2002)
Genomics
, vol.79
, pp. 197-209
-
-
Riley, B.1
Williamson, M.2
Collier, D.3
Wilkie, H.4
Makoff, A.5
-
18
-
-
0034671109
-
Cloning and characterization of a Golgin-related gene from the large-scale polymorphism linked to the PML gene
-
PID: 11161787, COI: 1:CAS:528:DC%2BD3MXjt1Oqsw%3D%3D
-
Gilles F, Goy A, Remache Y, Manova K, Zelenetz AD: Cloning and characterization of a Golgin-related gene from the large-scale polymorphism linked to the PML gene. Genomics. 2000, 70: 364-374. 10.1006/geno.2000.6388. DOI: 10.1006/geno.2000.6388
-
(2000)
Genomics
, vol.70
, pp. 364-374
-
-
Gilles, F.1
Goy, A.2
Remache, Y.3
Manova, K.4
Zelenetz, A.D.5
-
19
-
-
0035154373
-
Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26
-
PID: 11156619, COI: 1:CAS:528:DC%2BD3MXmsVCrsA%3D%3D
-
Pujana MA, Nadal M, Gratacos M, Peral B, Csiszar K, Gonzalez-Sarmiento R, Sumoy L, Estivill X: Additional complexity on human chromosome 15q: identification of a set of newly recognized duplicons (LCR15) on 15q11-q13, 15q24, and 15q26. Genome Res. 2001, 11: 98-111. 10.1101/gr.155601. DOI: 10.1101/gr.155601
-
(2001)
Genome Res
, vol.11
, pp. 98-111
-
-
Pujana, M.A.1
Nadal, M.2
Gratacos, M.3
Peral, B.4
Csiszar, K.5
Gonzalez-Sarmiento, R.6
Sumoy, L.7
Estivill, X.8
-
20
-
-
17944367325
-
A polymorphic genomic duplication on human chromosome 15 is a susceptibility factor for panic and phobic disorders
-
PID: 11509185, COI: 1:CAS:528:DC%2BD3MXmtFKntro%3D
-
Gratacos M, Nadal M, Martin-Santos R, Pujana MA, Gago J, Peral B, Armengol L, Ponsa I, Miro R, Bulbena A, et al: A polymorphic genomic duplication on human chromosome 15 is a susceptibility factor for panic and phobic disorders. Cell. 2001, 106: 367-379. DOI: 10.1016/S0092-8674(01)00447-0
-
(2001)
Cell
, vol.106
, pp. 367-379
-
-
Gratacos, M.1
Nadal, M.2
Martin-Santos, R.3
Pujana, M.A.4
Gago, J.5
Peral, B.6
Armengol, L.7
Ponsa, I.8
Miro, R.9
Bulbena, A.10
-
21
-
-
85047695990
-
Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons
-
PID: 11896453, COI: 1:CAS:528:DC%2BD38XjtFSmu7g%3D
-
Pujana MA, Nadal M, Guitart M, Armengol L, Gratacos M, Estivill X: Human chromosome 15q11-q14 regions of rearrangements contain clusters of LCR15 duplicons. Eur J Hum Genet. 2002, 10: 26-35. 10.1038/sj.ejhg.5200760. DOI: 10.1038/sj.ejhg.5200760
-
(2002)
Eur J Hum Genet
, vol.10
, pp. 26-35
-
-
Pujana, M.A.1
Nadal, M.2
Guitart, M.3
Armengol, L.4
Gratacos, M.5
Estivill, X.6
-
22
-
-
0034028921
-
Structure of chromosomal duplicons and their role in mediating human genomic disorders
-
PID: 10810082, COI: 1:CAS:528:DC%2BD3cXjsFegtLw%3D
-
Ji Y, Eichler EE, Schwartz S, Nicholls RD: Structure of chromosomal duplicons and their role in mediating human genomic disorders. Genome Res. 2000, 10: 597-610. 10.1101/gr.10.5.597. DOI: 10.1101/gr.10.5.597
-
(2000)
Genome Res
, vol.10
, pp. 597-610
-
-
Ji, Y.1
Eichler, E.E.2
Schwartz, S.3
Nicholls, R.D.4
-
23
-
-
0031946990
-
Molecular cytogenetic evidence for a common breakpoint in large (class III) inverted duplications of chromosome 15
-
PID: 9529335, COI: 1:CAS:528:DyaK1cXlvVahsb0%3D
-
Wandstrat A, Lena CJ, Jenkins L, Schwartz S: Molecular cytogenetic evidence for a common breakpoint in large (class III) inverted duplications of chromosome 15. Am J Hum Genet. 1998, 62: 925-936. 10.1086/301777. DOI: 10.1086/301777
-
(1998)
Am J Hum Genet
, vol.62
, pp. 925-936
-
-
Wandstrat, A.1
Lena, C.J.2
Jenkins, L.3
Schwartz, S.4
-
24
-
-
0033652564
-
Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation
-
PID: 11151680, COI: 1:CAS:528:DC%2BD3cXotVKntrw%3D
-
Wandstrat AE, Schwartz S: Isolation and molecular analysis of inv dup(15) and construction of a physical map of a common breakpoint in order to elucidate their mechanism of formation. Chromosoma. 2000, 109: 498-505. DOI: 10.1007/s004120000103
-
(2000)
Chromosoma
, vol.109
, pp. 498-505
-
-
Wandstrat, A.E.1
Schwartz, S.2
-
25
-
-
0037047628
-
Recent segmental duplications in the human genome
-
PID: 12169732, COI: 1:CAS:528:DC%2BD38Xmt1Cktr4%3D
-
Bailey JA, Gu Z, Clark RA, Reinert K, Samonte RV, Schwartz S, Adams MD, Myers EW, Li PW, Eichler EE: Recent segmental duplications in the human genome. Science. 2002, 297: 1003-1007. 10.1126/science.1072047. DOI: 10.1126/science.1072047
-
(2002)
Science
, vol.297
, pp. 1003-1007
-
-
Bailey, J.A.1
Gu, Z.2
Clark, R.A.3
Reinert, K.4
Samonte, R.V.5
Schwartz, S.6
Adams, M.D.7
Myers, E.W.8
Li, P.W.9
Eichler, E.E.10
-
26
-
-
0035566862
-
Divergent origins and concerted expansion of two segmental duplications on chromosome 16
-
PID: 11948212, COI: 1:CAS:528:DC%2BD38XjslCktrg%3D
-
Eichler EE, Johnson ME, Alkan C, Tuzun E, Sahinalp C, Misceo D, Archidiacono N, Rocchi M: Divergent origins and concerted expansion of two segmental duplications on chromosome 16. J Hered. 2001, 92: 462-468. 10.1093/jhered/92.6.462. DOI: 10.1093/jhered/92.6.462
-
(2001)
J Hered
, vol.92
, pp. 462-468
-
-
Eichler, E.E.1
Johnson, M.E.2
Alkan, C.3
Tuzun, E.4
Sahinalp, C.5
Misceo, D.6
Archidiacono, N.7
Rocchi, M.8
-
27
-
-
0036591666
-
Molecular-evolutionary mechanisms for genomic disorders
-
PID: 12076675, COI: 1:CAS:528:DC%2BD38XktFSiu7k%3D
-
Stankiewicz P, Lupski JR: Molecular-evolutionary mechanisms for genomic disorders. Curr Opin Genet Dev. 2002, 12: 312-319. 10.1016/S0959-437X(02)00304-0. DOI: 10.1016/S0959-437X(02)00304-0
-
(2002)
Curr Opin Genet Dev
, vol.12
, pp. 312-319
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
29
-
-
26344469243
-
Sequence analysis of the breakpoints of a pericentric inversion distinguishing the human and chimpanzee chromosomes 12
-
Nickerson E, Gibbs RA, Nelson DL: Sequence analysis of the breakpoints of a pericentric inversion distinguishing the human and chimpanzee chromosomes 12. Am J Hum Genet. 1999, 65 (Supplement): A56-
-
(1999)
Am J Hum Genet
, vol.65Supplement
, pp. A56
-
-
Nickerson, E.1
Gibbs, R.A.2
Nelson, D.L.3
-
30
-
-
0031937488
-
Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb
-
PID: 9477342, COI: 1:CAS:528:DyaK1cXhsFSlsbw%3D
-
Christian SL, Bhatt NK, Martin SA, Sutcliffe JS, Kubota T, Huang B, Mutirangura A, Chinault AC, Beaudet AL, Ledbetter DH: Integrated YAC contig map of the Prader-Willi/Angelman region on chromosome 15q11-q13 with average STS spacing of 35 kb. Genome Res. 1998, 8: 146-157.
-
(1998)
Genome Res
, vol.8
, pp. 146-157
-
-
Christian, S.L.1
Bhatt, N.K.2
Martin, S.A.3
Sutcliffe, J.S.4
Kubota, T.5
Huang, B.6
Mutirangura, A.7
Chinault, A.C.8
Beaudet, A.L.9
Ledbetter, D.H.10
-
31
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Sequencing Consortium: Initial sequencing and analysis of the human genome. Nature. 2001, 409: 860-921. 10.1038/35057062. DOI: 10.1038/35057062
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
-
32
-
-
85038540134
-
Recombination between large, transcriptionally active repeated elements at the proximal and distal breakpoints in Prader-Willi and Angelman syndromes
-
Amos-Landgraf J, Ji Y, Wandstrat A, Driscoll D, Schartz S, Nicholls R: Recombination between large, transcriptionally active repeated elements at the proximal and distal breakpoints in Prader-Willi and Angelman syndromes. Am J Hum Genet. 1997, 61 (Supplement): A3-
-
(1997)
Am J Hum Genet
, vol.61Supplement
, pp. A3
-
-
Amos-Landgraf, J.1
Ji, Y.2
Wandstrat, A.3
Driscoll, D.4
Schartz, S.5
Nicholls, R.6
-
33
-
-
0033016617
-
The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities
-
PID: 9949213, COI: 1:CAS:528:DyaK1MXhslKksrg%3D
-
Ji Y, Walkowicz MJ, Buiting K, Johnson DK, Tarvin RE, Rinchik EM, Horsthemke B, Stubbs L, Nicholls RD: The ancestral gene for transcribed, low-copy repeats in the Prader-Willi/Angelman region encodes a large protein implicated in protein trafficking, which is deficient in mice with neuromuscular and spermiogenic abnormalities. Hum Mol Genet. 1999, 8: 533-542. 10.1093/hmg/8.3.533. DOI: 10.1093/hmg/8.3.533
-
(1999)
Hum Mol Genet
, vol.8
, pp. 533-542
-
-
Ji, Y.1
Walkowicz, M.J.2
Buiting, K.3
Johnson, D.K.4
Tarvin, R.E.5
Rinchik, E.M.6
Horsthemke, B.7
Stubbs, L.8
Nicholls, R.D.9
-
34
-
-
0025128991
-
High-resolution mapping of human chromosome 11 by in situhybridization with cosmid clones
-
PID: 2294592, COI: 1:CAS:528:DyaK3cXptlajsw%3D%3D
-
Lichter P, Tang CJ, Call K, Hermanson G, Evans GA, Housman D, Ward DC: High-resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science. 1990, 247: 64-69. DOI: 10.1126/science.2294592
-
(1990)
Science
, vol.247
, pp. 64-69
-
-
Lichter, P.1
Tang, C.J.2
Call, K.3
Hermanson, G.4
Evans, G.A.5
Housman, D.6
Ward, D.C.7
-
35
-
-
0004239562
-
-
RepeatMasker. [http://ftp.genome.washington.edu/RM/RepeatMasker.html]
-
Repeatmasker.
-
-
-
36
-
-
85182672897
-
-
Webcutter. [http://www.firstmarket.com/cutter/cut2.html]
-
Webcutter.
-
-
-
37
-
-
0033916868
-
The mosaic structure of a human pericentromeric segment: a strategy for characterizing complex regions of the human genome
-
PID: 10854415, COI: 1:CAS:528:DC%2BD3cXkt1eisb4%3D
-
Horvath J, Schwartz S, Eichler E: The mosaic structure of a human pericentromeric segment: a strategy for characterizing complex regions of the human genome. Genome Res. 2000, 10: 839-852. 10.1101/gr.10.6.839. DOI: 10.1101/gr.10.6.839
-
(2000)
Genome Res
, vol.10
, pp. 839-852
-
-
Horvath, J.1
Schwartz, S.2
Eichler, E.3
|