-
1
-
-
0043264447
-
Translocations and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs
-
Abeysinghe SS, Chuzhanova N, Krawczak M, Ball EV, Cooper DN. 2003. Translocations and gross deletion breakpoints in human inherited disease and cancer I: nucleotide composition and recombination-associated motifs. Hum Mutat 22:229-244.
-
(2003)
Hum Mutat
, vol.22
, pp. 229-244
-
-
Abeysinghe, S.S.1
Chuzhanova, N.2
Krawczak, M.3
Ball, E.V.4
Cooper, D.N.5
-
2
-
-
0031838697
-
Translocations, cancer and the puzzle of specificity
-
Barr FG. 1998. Translocations, cancer and the puzzle of specificity. Nat Genet 19:121-124.
-
(1998)
Nat Genet
, vol.19
, pp. 121-124
-
-
Barr, F.G.1
-
3
-
-
0037245984
-
GenBank
-
Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Wheeler DL. 2003. GenBank. Nucleic Acids Res 31:23-27.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 23-27
-
-
Benson, D.A.1
Karsch-Mizrachi, I.2
Lipman, D.J.3
Ostell, J.4
Wheeler, D.L.5
-
4
-
-
0041761326
-
Translocations and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends
-
Chuzhanova N, Abeysinghe SS, Krawczak M, Cooper DN. 2003. Translocations and gross deletion breakpoints in human inherited disease and cancer II: potential involvement of repetitive sequence elements in secondary structure formation between DNA ends. Hum Mutat 22:245-251.
-
(2003)
Hum Mutat
, vol.22
, pp. 245-251
-
-
Chuzhanova, N.1
Abeysinghe, S.S.2
Krawczak, M.3
Cooper, D.N.4
-
6
-
-
0036480427
-
Double strand breaks and translocations in cancer
-
Elliot B, Jasin M. 2002. Double strand breaks and translocations in cancer. Cell Mol Life Sci 59:373-385.
-
(2002)
Cell Mol Life Sci
, vol.59
, pp. 373-385
-
-
Elliot, B.1
Jasin, M.2
-
7
-
-
0031731487
-
Genomic disorders: Structural features of the genome can lead to DNA rearrangements and human disease traits
-
Lupski JR. 1998. Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits. Trends Genet 14:417-422.
-
(1998)
Trends Genet
, vol.14
, pp. 417-422
-
-
Lupski, J.R.1
-
8
-
-
0033855389
-
Mechanisms of DNA double-strand break repair and their potential to induce chromosomal aberrations
-
Pfeiffer P, Goedecke W, Obe G. 2000. Mechanisms of DNA double-strand break repair and their potential to induce chromosomal aberrations. Mutagenesis 15:289-302.
-
(2000)
Mutagenesis
, vol.15
, pp. 289-302
-
-
Pfeiffer, P.1
Goedecke, W.2
Obe, G.3
-
9
-
-
0030929515
-
Recombination hot spots and human disease
-
Purandare SM, Patel PI. 1997. Recombination hot spots and human disease. Genome Res 7:773-786.
-
(1997)
Genome Res
, vol.7
, pp. 773-786
-
-
Purandare, S.M.1
Patel, P.I.2
-
10
-
-
0027970838
-
Chromosomal translocations in human cancer
-
Rabbitts TH. 1994. Chromosomal translocations in human cancer. Nature 372:143-149.
-
(1994)
Nature
, vol.372
, pp. 143-149
-
-
Rabbitts, T.H.1
-
11
-
-
0031453254
-
Consequences of chromosomal abnormalities in tumor development
-
Sánchez-García I. 1997. Consequences of chromosomal abnormalities in tumor development. Annu Rev Genet 31:429-453.
-
(1997)
Annu Rev Genet
, vol.31
, pp. 429-453
-
-
Sánchez-García, I.1
-
12
-
-
0036468807
-
Genome architecture, rearrangements and genomic disorders
-
Stankiewicz P, Lupski JR. 2002. Genome architecture, rearrangements and genomic disorders. Trends Genet 18:74-82.
-
(2002)
Trends Genet
, vol.18
, pp. 74-82
-
-
Stankiewicz, P.1
Lupski, J.R.2
-
13
-
-
0037903275
-
Human Gene Mutation Database (HGMD®): 2003 Update
-
Stenson PD, Ball EV, Mort M, Phillips AD, Shiel JA, Thomas NST, Abeysinghe S, Krawczak M, Cooper DN. 2003. Human Gene Mutation Database (HGMD®): 2003 update. Hum Mutat 21:577-581.
-
(2003)
Hum Mutat
, vol.21
, pp. 577-581
-
-
Stenson, P.D.1
Ball, E.V.2
Mort, M.3
Phillips, A.D.4
Shiel, J.A.5
Thomas, N.S.T.6
Abeysinghe, S.7
Krawczak, M.8
Cooper, D.N.9
-
14
-
-
0037252616
-
The EMBL Nucleotide Sequence Database: Major new developments
-
Stoesser G, Baker W, van den Broek A, Garcia-Pastor M, Kanz C, Kulikova T, Leinonen R, Lin Q, Lombard V, Lopez R, Mancuso R, Nardone F, Stoehr P, Tuli MA, Tzouvara K, Vaughan R. 2003. The EMBL Nucleotide Sequence Database: Major new developments. Nucleic Acids Res 31:17-22.
-
(2003)
Nucleic Acids Res
, vol.31
, pp. 17-22
-
-
Stoesser, G.1
Baker, W.2
Van Den Broek, A.3
Garcia-Pastor, M.4
Kanz, C.5
Kulikova, T.6
Leinonen, R.7
Lin, Q.8
Lombard, V.9
Lopez, R.10
Mancuso, R.11
Nardone, F.12
Stoehr, P.13
Tuli, M.A.14
Tzouvara, K.15
Vaughan, R.16
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