-
1
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome. Nature 409, 860-921 (2001).
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
-
2
-
-
0035895505
-
The sequence of the human genome
-
Venter, J. C. et al. The sequence of the human genome. Science 291, 1304-1351 (2001).
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
-
3
-
-
0000260488
-
Evidence that ultraviolet light induced thymine dimers in DNA cause biological damage
-
Setlow, R. B. & Setlow, J. K. Evidence that ultraviolet light induced thymine dimers in DNA cause biological damage. Proc Natl Acad. Sci. USA 48, 1250-1257 (1962).
-
(1962)
Proc. Natl. Acad. Sci. USA
, vol.48
, pp. 1250-1257
-
-
Setlow, R.B.1
Setlow, J.K.2
-
4
-
-
78651191735
-
The disappearance of the thymine dimers from DNA: An error correcting mechanism
-
Setlow, R. B. & Carrier, W. L. The disappearance of the thymine dimers from DNA: An error correcting mechanism. Proc Natl Acad. Sci. USA 51, 226-231 (1964).
-
(1964)
Proc. Natl. Acad. Sci. USA
, vol.51
, pp. 226-231
-
-
Setlow, R.B.1
Carrier, W.L.2
-
5
-
-
0014421995
-
Defective repair replication of DNA in xeroderma pigmentosum
-
Cleaver, J. E. Defective repair replication of DNA in xeroderma pigmentosum. Nature 218, 652-656 (1968).
-
(1968)
Nature
, vol.218
, pp. 652-656
-
-
Cleaver, J.E.1
-
6
-
-
0024797804
-
Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19
-
Mohrenweiser, H. W. et al. Refined mapping of the three DNA repair genes, ERCC1, ERCC2, and XRCC1, on human chromosome 19. Cytogenet. Cell Genet. 52, 11-14 (1989).
-
(1989)
Cytogenet. Cell Genet.
, vol.52
, pp. 11-14
-
-
Mohrenweiser, H.W.1
-
7
-
-
0031520887
-
The Human Genome Project: View from the Department of Energy
-
Patrinos, A. & Drell, D. W. The Human Genome Project: view from the Department of Energy. J. Am. Med. Womens Assoc. 52, 8-10 (1997).
-
(1997)
J. Am. Med. Womens Assoc.
, vol.52
, pp. 8-10
-
-
Patrinos, A.1
Drell, D.W.2
-
8
-
-
0028866218
-
An integrated metric physical map of human chromosome 19
-
Ashworth, L. K. et al. An integrated metric physical map of human chromosome 19. Nature Genet. 11, 422-427 (1995).
-
(1995)
Nature Genet.
, vol.11
, pp. 422-427
-
-
Ashworth, L.K.1
-
9
-
-
0001038798
-
Human chromosome-specific partial digest libraries in lambda and cosmid vectors
-
de Jong, P. et al. Human chromosome-specific partial digest libraries in lambda and cosmid vectors. Cytogenet. Cell Genet. 51, 985 (1989).
-
(1989)
Cytogenet. Cell Genet.
, vol.51
, pp. 985
-
-
De Jong, P.1
-
10
-
-
0028075854
-
Human chromosome 19p: A fluorescence in situ hybridization map with genomic estimates for 79 intervals spanning 20 Mbp
-
Brandiff, B. F. et al. Human chromosome 19p: A fluorescence in situ hybridization map with genomic estimates for 79 intervals spanning 20 Mbp. Genomics 23, 582-591 (1994).
-
(1994)
Genomics
, vol.23
, pp. 582-591
-
-
Brandiff, B.F.1
-
11
-
-
0028887026
-
A 30-Mb metric fluorescence in situ hybridization map of human chromosome 19q
-
Gordon, L. A. et al. A 30-Mb metric fluorescence in situ hybridization map of human chromosome 19q. Genomics 30, 187-192 (1995).
-
(1995)
Genomics
, vol.30
, pp. 187-192
-
-
Gordon, L.A.1
-
12
-
-
0033047270
-
Assessing the quality of the DNA sequence from the Human Genome Project
-
Felsenfeld, A., Peterson, J., Schloss, J. & Guyer, M. Assessing the quality of the DNA sequence from the Human Genome Project. Genome Res. 9, 1-4 (1999).
-
(1999)
Genome Res.
, vol.9
, pp. 1-4
-
-
Felsenfeld, A.1
Peterson, J.2
Schloss, J.3
Guyer, M.4
-
13
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib, C. et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380, 152-154 (1996).
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
-
14
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong, A. et al. A high-resolution recombination map of the human genome. Nature Genet. 31, 241-247 (2002).
-
(2002)
Nature Genet.
, vol.31
, pp. 241-247
-
-
Kong, A.1
-
15
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman, K. W., Murray, J. C., Sheffield, V. C., White, R. L. & Weber, J. L. Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am. J. Hum. Genet. 63, 861-869 (1998).
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
16
-
-
0035865094
-
Comparison of human genetic and sequence-based physical maps
-
Yu, A. et al. Comparison of human genetic and sequence-based physical maps. Nature 409, 951-953 (2001).
-
(2001)
Nature
, vol.409
, pp. 951-953
-
-
Yu, A.1
-
17
-
-
0242300182
-
The DNA sequence and analysis of human chromosome 6
-
Mungali, A. J. et al. The DNA sequence and analysis of human chromosome 6. Nature 425, 805-811 (2003).
-
(2003)
Nature
, vol.425
, pp. 805-811
-
-
Mungali, A.J.1
-
18
-
-
0038495746
-
The DNA sequence of human chromosome 7
-
Hillier, L. W. et al. The DNA sequence of human chromosome 7. Nature 424, 157-164 (2003).
-
(2003)
Nature
, vol.424
, pp. 157-164
-
-
Hillier, L.W.1
-
19
-
-
0037421899
-
The DNA sequence and analysis of human chromosome 14
-
Hellig, R. et al. The DNA sequence and analysis of human chromosome 14. Nature 421, 601-607 (2003).
-
(2003)
Nature
, vol.421
, pp. 601-607
-
-
Hellig, R.1
-
20
-
-
0035924324
-
The DNA sequence and comparative analysis of human chromosome 20
-
Deloukas, P. et al. The DNA sequence and comparative analysis of human chromosome 20. Nature 414, 865-871 (2001).
-
(2001)
Nature
, vol.414
, pp. 865-871
-
-
Deloukas, P.1
-
21
-
-
0034682403
-
The DNA sequence of human chromosome 21
-
Hattori, M. et al. The DNA sequence of human chromosome 21. Nature 405, 311-319 (2000).
-
(2000)
Nature
, vol.405
, pp. 311-319
-
-
Hattori, M.1
-
22
-
-
79960655760
-
The DNA sequence of human chromosome 22
-
Dunham, I. et al. The DNA sequence of human chromosome 22. Nature 402, 489-495 (1999).
-
(1999)
Nature
, vol.402
, pp. 489-495
-
-
Dunham, I.1
-
23
-
-
0035162594
-
RefSeq and LocusLink: NCBI gene-centered resources
-
Pruitt, K. D. & Maglott, D. R. RefSeq and LocusLink: NCBI gene-centered resources. Nucleic Acids Res. 29, 137-140 (2001).
-
(2001)
Nucleic Acids Res.
, vol.29
, pp. 137-140
-
-
Pruitt, K.D.1
Maglott, D.R.2
-
24
-
-
0036560755
-
The CA 125 gene: A newly discovered extension of the glycosylated N-terminal domain doubles the size of this extracellular superstructure
-
O'Brien, T. J., Beard, J. B., Underwood, L. J. & Shigemasa, K. The CA 125 gene: a newly discovered extension of the glycosylated N-terminal domain doubles the size of this extracellular superstructure. Tumour Biol. 23, 154-169 (2002).
-
(2002)
Tumour Biol.
, vol.23
, pp. 154-169
-
-
O'Brien, T.J.1
Beard, J.B.2
Underwood, L.J.3
Shigemasa, K.4
-
25
-
-
18744390284
-
Selecting for functional alternative splices in ESTs
-
Kan, Z., States, D. & Gish, W. Selecting for functional alternative splices in ESTs. Genome Res. 12, 1837-1845 (2002).
-
(2002)
Genome Res.
, vol.12
, pp. 1837-1845
-
-
Kan, Z.1
States, D.2
Gish, W.3
-
26
-
-
0038278868
-
Different noses for different people
-
Menashe, I., Man, O., Lancet, D. & Gilad, Y. Different noses for different people. Nature Genet. 34, 143-144 (2003).
-
(2003)
Nature Genet.
, vol.34
, pp. 143-144
-
-
Menashe, I.1
Man, O.2
Lancet, D.3
Gilad, Y.4
-
27
-
-
6644225936
-
Human chromosome 19 and related regions in mouse: Conservative and lineage-specific evolution
-
Dehal, P. et al. Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolution. Science 293, 104-111 (2001).
-
(2001)
Science
, vol.293
, pp. 104-111
-
-
Dehal, P.1
-
28
-
-
0038104885
-
Complex evolution of 7E olfactory receptor genes in segmental duplications
-
Newman, T. & Trask, B. J. Complex evolution of 7E olfactory receptor genes in segmental duplications. Genome Res. 13, 781-793 (2003).
-
(2003)
Genome Res.
, vol.13
, pp. 781-793
-
-
Newman, T.1
Trask, B.J.2
-
29
-
-
0038141095
-
Differential expansion of zinc-finger transcription factor loci in homologous human and mouse gene clusters
-
Shannon, M., Hamilton, A. T., Gordon, L., Branscomb, E. & Stubbs, L. Differential expansion of zinc-finger transcription factor loci in homologous human and mouse gene clusters. Genome Res. 13, 1097-1110 (2003).
-
(2003)
Genome Res.
, vol.13
, pp. 1097-1110
-
-
Shannon, M.1
Hamilton, A.T.2
Gordon, L.3
Branscomb, E.4
Stubbs, L.5
-
30
-
-
0031686366
-
Complex β-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12
-
Eichler, E. E. et al. Complex β-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12. Genome Res. 8, 791-808 (1998).
-
(1998)
Genome Res.
, vol.8
, pp. 791-808
-
-
Eichler, E.E.1
-
31
-
-
0034895149
-
The genomic context of natural killer receptor extended gene families
-
Trowsdale, J. et al. The genomic context of natural killer receptor extended gene families. Immunol. Rev. 181, 20-38 (2001).
-
(2001)
Immunol. Rev.
, vol.181
, pp. 20-38
-
-
Trowsdale, J.1
-
32
-
-
0036945657
-
The killer cell immunoglobulin-like receptor (KIR) genomic region: Gene-order, haplotypes and allelic polymorphism
-
Hsu, K. C. et al. The killer cell immunoglobulin-like receptor (KIR) genomic region: gene-order, haplotypes and allelic polymorphism. Immunol. Rev. 190, 40-52 (2002).
-
(2002)
Immunol. Rev.
, vol.190
, pp. 40-52
-
-
Hsu, K.C.1
-
33
-
-
0035175053
-
Organization, structure and evolution of the CYP2 gene cluster on human chromosome 19
-
Hoffmann, S. M., Nelson, D. R. & Keeney, D. S. Organization, structure and evolution of the CYP2 gene cluster on human chromosome 19. Pharmacogenetics 11, 687-698 (2001).
-
(2001)
Pharmacogenetics
, vol.11
, pp. 687-698
-
-
Hoffmann, S.M.1
Nelson, D.R.2
Keeney, D.S.3
-
34
-
-
0035018273
-
The new human tissue kallikrein gene family: Structure, function, and association to disease
-
Yousef, G. M. & Diamandis, E. P. The new human tissue kallikrein gene family: structure, function, and association to disease. Endocr. Rev. 22, 184-204 (2001).
-
(2001)
Endocr. Rev.
, vol.22
, pp. 184-204
-
-
Yousef, G.M.1
Diamandis, E.P.2
-
35
-
-
1542563409
-
Initial sequencing and comparative analysis of the mouse genome
-
Mouse Genome Sequencing Consortium. Initial sequencing and comparative analysis of the mouse genome. Nature 420, 520-562 (2002).
-
(2002)
Nature
, vol.420
, pp. 520-562
-
-
-
36
-
-
0003157183
-
Noncoding RNA gene detection using comparative sequence analysis
-
Rivas, E. & Eddy, S. R. Noncoding RNA gene detection using comparative sequence analysis. BMC Bioinformatics 2, 8 (2001).
-
(2001)
BMC Bioinformatics
, vol.2
, pp. 8
-
-
Rivas, E.1
Eddy, S.R.2
-
37
-
-
0142084743
-
Scanning human gene deserts for long-range enhancers
-
Nobrega, M. A., Ovcharenko, I., Afzal, V. & Rubin, E. M. Scanning human gene deserts for long-range enhancers. Science 302, 413 (2003).
-
(2003)
Science
, vol.302
, pp. 413
-
-
Nobrega, M.A.1
Ovcharenko, I.2
Afzal, V.3
Rubin, E.M.4
-
38
-
-
0021742599
-
The human LDL receptor: A cysteine-rich protein with multiple Alu sequences in its mRNA
-
Yamamoto, T. et al. The human LDL receptor: a cysteine-rich protein with multiple Alu sequences in its mRNA. Cell 39, 27-38 (1984).
-
(1984)
Cell
, vol.39
, pp. 27-38
-
-
Yamamoto, T.1
-
39
-
-
0025597137
-
The LDL receptor locus in familial hypercholesterolemia: Mutational analysis of a membrane protein
-
Hobbs, H. H., Russell, D. W., Brown, M. S. & Goldstein, J. L. The LDL receptor locus in familial hypercholesterolemia: mutational analysis of a membrane protein. Annu. Rev. Genet. 24, 133-170 (1990).
-
(1990)
Annu. Rev. Genet.
, vol.24
, pp. 133-170
-
-
Hobbs, H.H.1
Russell, D.W.2
Brown, M.S.3
Goldstein, J.L.4
-
40
-
-
0025885417
-
Autosomal dominant erythrocytosis caused by increased sensitivity to erythropoietin
-
Juvonen, E., Ikkala, E., Fyhrquist, F. & Ruutu, T. Autosomal dominant erythrocytosis caused by increased sensitivity to erythropoietin. Blood 78, 3066-3069 (1991).
-
(1991)
Blood
, vol.78
, pp. 3066-3069
-
-
Juvonen, E.1
Ikkala, E.2
Fyhrquist, F.3
Ruutu, T.4
-
41
-
-
7344244286
-
Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease
-
Doray, B. et al. Mutation of the RET ligand, neurturin, supports multigenic inheritance in Hirschsprung disease. Hum. Mol. Genet. 7, 1449-1452 (1998).
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1449-1452
-
-
Doray, B.1
-
42
-
-
0037146578
-
Finding genes that underlie complex traits
-
Glazier, A. M., Nadeau, J. H. & Aitman, T. J. Finding genes that underlie complex traits. Science 298, 2345-2349 (2002).
-
(2002)
Science
, vol.298
, pp. 2345-2349
-
-
Glazier, A.M.1
Nadeau, J.H.2
Aitman, T.J.3
-
43
-
-
0036226603
-
The BLAST-like alignment tool
-
Kent, W. J. The BLAST-like alignment tool. Genome Res. 12, 656-664 (2002).
-
(2002)
Genome Res.
, vol.12
, pp. 656-664
-
-
Kent, W.J.1
-
45
-
-
0034098730
-
Using GeneWise in the Drosophila annotation experiment
-
Birney, E. & Durbin, R. Using GeneWise in the Drosophila annotation experiment. Genome Res. 10, 547-548 (2002).
-
(2002)
Genome Res.
, vol.10
, pp. 547-548
-
-
Birney, E.1
Durbin, R.2
-
46
-
-
0012306021
-
Apollo: A sequence annotation editor
-
research0082.1-0082.14
-
Lewis, S. E. et al. Apollo: a sequence annotation editor. Genome Biol. 3, research0082.1-0082.14 (2002).
-
(2002)
Genome Biol.
, vol.3
-
-
Lewis, S.E.1
-
47
-
-
0037267806
-
Human-mouse alignments with BLASTZ
-
Schwartz, S. et al. Human-mouse alignments with BLASTZ. Genome Res. 13, 103-107 (2003).
-
(2003)
Genome Res.
, vol.13
, pp. 103-107
-
-
Schwartz, S.1
-
48
-
-
0034831138
-
Segmental duplications: Organization and impact within the current human genome project assembly
-
Bailey, J. A., Yavor, A. M., Massa, H. F., Trask, B. J. & Eichler, E. E. Segmental duplications: organization and impact within the current human genome project assembly. Genome Res. 11, 1005-1017 (2001).
-
(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
|