-
1
-
-
0025973822
-
In situ hybridisation banding of human chromosomes with Alu-PCR. products: A simultaneous karyotype for gene mapping studies
-
Baldini, A. and Ward, D.C. (1991) In situ hybridisation banding of human chromosomes with Alu-PCR. products: a simultaneous karyotype for gene mapping studies. Genomics 9, 770-774.
-
(1991)
Genomics
, vol.9
, pp. 770-774
-
-
Baldini, A.1
Ward, D.C.2
-
2
-
-
0027525876
-
Human biliary glycoprotein gene: Characterisation of a family of novel alternatively spliced RNAs and their expressed proteins
-
Barnett, T.R., Drake, L. and Pickle, W. II. (1993) Human biliary glycoprotein gene: characterisation of a family of novel alternatively spliced RNAs and their expressed proteins. Mol. Cell. Biol. 13, 1273-1282.
-
(1993)
Mol. Cell. Biol.
, vol.13
, pp. 1273-1282
-
-
Barnett, T.R.1
Drake, L.2
Pickle, W.I.I.3
-
3
-
-
0342596934
-
Sources and evolution of human Alu repeated sequences
-
Britten, R.J., Baron, W.F., Stout, D.B. and Davidson, E.H. (1988) Sources and evolution of human Alu repeated sequences. Proc. Natl. Acad. Sci. USA 85, 4770-4774.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 4770-4774
-
-
Britten, R.J.1
Baron, W.F.2
Stout, D.B.3
Davidson, E.H.4
-
4
-
-
0023092626
-
Cloning of decay-accelerating factor sugests novel use of splicing to generate two proteins
-
Caras, I.W., Davitz, M.A., Rhee, L., Weddell, G., Martin Jr., D.W. and Nussenzweig, V. (1987) Cloning of decay-accelerating factor sugests novel use of splicing to generate two proteins. Nature 325, 545-548.
-
(1987)
Nature
, vol.325
, pp. 545-548
-
-
Caras, I.W.1
Davitz, M.A.2
Rhee, L.3
Weddell, G.4
Martin D.W., Jr.5
Nussenzweig, V.6
-
5
-
-
0025852429
-
Complete nucleotide sequence of the gene for human C1 inhibitor with an unusually high density of Alu elements
-
Carter, P.E., Duponchel, C., Tosi, M. and Fothergill, J.E. (1991) Complete nucleotide sequence of the gene for human C1 inhibitor with an unusually high density of Alu elements. Eur. J. Biochem. 197, 301-308.
-
(1991)
Eur. J. Biochem.
, vol.197
, pp. 301-308
-
-
Carter, P.E.1
Duponchel, C.2
Tosi, M.3
Fothergill, J.E.4
-
6
-
-
0024504147
-
Structural alterations of the BCR and ABL genes in Ph1 positive acute leukemias with rearrangements in the BCR gene first intron: Further evidence implicating Alu sequences in the chromosome translocation
-
Chen, S.J., Chen, Z., D'Auriol, L., Le Coniat, M., Grausz, D. and Berger, R. (1989) Structural alterations of the BCR and ABL genes in Ph1 positive acute leukemias with rearrangements in the BCR gene first intron: further evidence implicating Alu sequences in the chromosome translocation. Oncogene 4, 195-202.
-
(1989)
Oncogene
, vol.4
, pp. 195-202
-
-
Chen, S.J.1
Chen, Z.2
D'Auriol, L.3
Le Coniat, M.4
Grausz, D.5
Berger, R.6
-
7
-
-
0022429759
-
Integration site preferences of the Alu family and similar repetitive DNA sequences
-
Daniels, G.R. and Deininger, P.L. (1985) Integration site preferences of the Alu family and similar repetitive DNA sequences. Nucleic Acids Res. 13, 8939-8954.
-
(1985)
Nucleic Acids Res.
, vol.13
, pp. 8939-8954
-
-
Daniels, G.R.1
Deininger, P.L.2
-
8
-
-
0025730415
-
An unusual Alu repeat within the CAD gene
-
Davidson, J.N., Khattar, N.H. and Chen, K.-C. (1991) An unusual Alu repeat within the CAD gene. J. Mol. Evol. 32, 162-166.
-
(1991)
J. Mol. Evol.
, vol.32
, pp. 162-166
-
-
Davidson, J.N.1
Khattar, N.H.2
Chen, K.-C.3
-
9
-
-
0001383133
-
SINEs: Short intespersed repeated DNA elements in higher eukaryotes
-
Berg, D.E. and Howe, M.M. (Eds.), Washington, DC
-
Deininger, P.L. (1989) SINEs: Short intespersed repeated DNA elements in higher eukaryotes. In: Berg, D.E. and Howe, M.M. (Eds.), Mobile DNA. Am. Soc. Microbiol., Washington, DC, pp. 619-636.
-
(1989)
Mobile DNA. Am. Soc. Microbiol.
, pp. 619-636
-
-
Deininger, P.L.1
-
10
-
-
0023047033
-
Molecular analysis of both translocation products of a Philadelphia-positive CML patient
-
de Klein, A., van Agthoven, T., Groffen, C., Heisterkamp, J., Groffen, J. and Grosveld, G. (1986) Molecular analysis of both translocation products of a Philadelphia-positive CML patient. Nucleic Acids Res. 14, 7071-7082.
-
(1986)
Nucleic Acids Res.
, vol.14
, pp. 7071-7082
-
-
Klein, A.1
Van Agthoven, T.2
Groffen, C.3
Heisterkamp, J.4
Groffen, J.5
Grosveld, G.6
-
11
-
-
0024341561
-
A novel mRNa of the A4 amyloid precursor gene coding for a possibly secreted protein
-
de Sauvage, F. and Octave, J.N. (1989) A novel mRNA of the A4 amyloid precursor gene coding for a possibly secreted protein. Science 245, 651-653.
-
(1989)
Science
, vol.245
, pp. 651-653
-
-
Sauvage, F.1
Octave, J.N.2
-
12
-
-
0021760092
-
A comprehensive set of sequence analysis programs for the VAX
-
Devereux, J., Haeberli, P. and Smithies, O. (1984) A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Res. 12, 387-395.
-
(1984)
Nucleic Acids Res.
, vol.12
, pp. 387-395
-
-
Devereux, J.1
Haeberli, P.2
Smithies, O.3
-
13
-
-
0025097959
-
Partial gene duplication involving exon-alu interchange results in lipoprotein lipase deficiency
-
Devlin, R.H., Deeb, S., Brunzell, J. and Hayden, M.R. (1990) Partial gene duplication involving exon-alu interchange results in lipoprotein lipase deficiency. Am. J. Hum. Genet. 46, 112-119.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 112-119
-
-
Devlin, R.H.1
Deeb, S.2
Brunzell, J.3
Hayden, M.R.4
-
14
-
-
0025283215
-
Automated DNA sequencing of the human HPRT locus
-
Edwards, A., Voss, H., Rice, P., Civitello, A., Stegemann, J., Schwager, C., Zimmermann, J., Erfle, H., Caskey, C.T. and Assorge, W. (1990) Automated DNA sequencing of the human HPRT locus. Genomics 6, 593-608.
-
(1990)
Genomics
, vol.6
, pp. 593-608
-
-
Edwards, A.1
Voss, H.2
Rice, P.3
Civitello, A.4
Stegemann, J.5
Schwager, C.6
Zimmermann, J.7
Erfle, H.8
Caskey, C.T.9
Assorge, W.10
-
15
-
-
0027073138
-
Junctions between genes in the haptoglobin gene cluster of primates
-
Erickson, L.M., Kim, H.S. and Maeda, N. (1992) Junctions between genes in the haptoglobin gene cluster of primates. Genomics 14, 948-958.
-
(1992)
Genomics
, vol.14
, pp. 948-958
-
-
Erickson, L.M.1
Kim, H.S.2
Maeda, N.3
-
16
-
-
0027958632
-
Molecular description of a hypoxanthine phosphoribosyltransferase gene deletion in Lesch-Nyhan syndrome
-
Fuscoe, J.C. and Nelsen, A.J. (1994) Molecular description of a hypoxanthine phosphoribosyltransferase gene deletion in Lesch-Nyhan syndrome. Hum. Mol. Genet. 3, 199-200.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 199-200
-
-
Fuscoe, J.C.1
Nelsen, A.J.2
-
17
-
-
0028437683
-
Sequence analysis of the breakpoint cluster region in the ALL-1 gene involved in acute leukemia
-
Gu, Y., Alder, H., Nakamura, T., Schichman, S.A., Prasad, R., Canaani, O., Saito, H., Croce, C.M. and Canaani, E. (1994) Sequence analysis of the breakpoint cluster region in the ALL-1 gene involved in acute leukemia. Cancer Res. 54, 2327-2330.
-
(1994)
Cancer Res.
, vol.54
, pp. 2327-2330
-
-
Gu, Y.1
Alder, H.2
Nakamura, T.3
Schichman, S.A.4
Prasad, R.5
Canaani, O.6
Saito, H.7
Croce, C.M.8
Canaani, E.9
-
18
-
-
0026022865
-
Complete cDNA sequence of human complement pro-C5
-
Haviland, D.L., Haviland, J.C., Fleischer, D.T., Hunt, A. and Wetsel, R.A. (1991) Complete cDNA sequence of human complement pro-C5. Evidence of truncated transcripts derived from a single copy gene. J. Immunol. 146, 362-368.
-
(1991)
Evidence of Truncated Transcripts Derived from a Single Copy Gene. J. Immunol.
, vol.146
, pp. 362-368
-
-
Haviland, D.L.1
Haviland, J.C.2
Fleischer, D.T.3
Hunt, A.4
Wetsel, R.A.5
-
19
-
-
0022422948
-
Oncogene chromosome break-points and Alu sequences
-
Heisterkamp, N. and Groffen, J. (1985) Oncogene chromosome break-points and Alu sequences. Nature 317, 559.
-
(1985)
Nature
, vol.317
, pp. 559
-
-
Heisterkamp, N.1
Groffen, J.2
-
20
-
-
0021811764
-
Structural organisation of the bcr gene and its role in the Ph' translocation
-
Heisterkamp, N., Stam, K., Groffen, J., de Klein, A. and Grosveld, G. (1985) Structural organisation of the bcr gene and its role in the Ph' translocation. Nature 315, 715-761.
-
(1985)
Nature
, vol.315
, pp. 715-761
-
-
Heisterkamp, N.1
Stam, K.2
Groffen, J.3
De Klein, A.4
Grosveld, G.5
-
21
-
-
0025891865
-
Complete nucleotide sequence of the gene for human heparin cofactor II and mapping to chromosomal band 22q11
-
Herzog, R., Lutz, S., Blin, N., Marasa, J.C., Blinder, M.A. and Tollefsen, D.M. (1991) Complete nucleotide sequence of the gene for human heparin cofactor II and mapping to chromosomal band 22q11. Biochemistry 30, 1350-1357.
-
(1991)
Biochemistry
, vol.30
, pp. 1350-1357
-
-
Herzog, R.1
Lutz, S.2
Blin, N.3
Marasa, J.C.4
Blinder, M.A.5
Tollefsen, D.M.6
-
22
-
-
0023120569
-
Unequal crossing-over between two Alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene
-
Horsthemke, B., Beisiegel, U., Dunning, A., Havinga, J.R. and Williamson, R. (1987) Unequal crossing-over between two Alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene. Eur. J. Biochem. 164, 77-81.
-
(1987)
Eur. J. Biochem.
, vol.164
, pp. 77-81
-
-
Horsthemke, B.1
Beisiegel, U.2
Dunning, A.3
Havinga, J.R.4
Williamson, R.5
-
23
-
-
0024410226
-
Hypobetalipoproteinemia due to an apolipoprotein B gene exon 21 deletion derived by Alu-Alu recombination
-
Huang, L-S., Ripps, M.E., Korman, S.H., Deckelbaum, R.J. and Breslow, J.L. (1989) Hypobetalipoproteinemia due to an apolipoprotein B gene exon 21 deletion derived by Alu-Alu recombination. J. Biol. Chem. 264, 11394-11400.
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 11394-11400
-
-
Huang, L.-S.1
Ripps, M.E.2
Korman, S.H.3
Deckelbaum, R.J.4
Breslow, J.L.5
-
24
-
-
0026697245
-
The human serglycin gene. Nucleotide sequence and methylation pattern in human promyelcytic leukemia HL-60 cells and T-lymphoblast Molt-4 cells
-
Humphries, D.E., Nicodemus, C.F., Schiller, V. and Stevens, R.L. (1992) The human serglycin gene. Nucleotide sequence and methylation pattern in human promyelcytic leukemia HL-60 cells and T-lymphoblast Molt-4 cells. J. Biol. Chem. 267, 13558-13563.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 13558-13563
-
-
Humphries, D.E.1
Nicodemus, C.F.2
Schiller, V.3
Stevens, R.L.4
-
25
-
-
0025736539
-
Reconstruction and analysis of Human Alu genes
-
Jurka, J. and Milosavljevic, A. (1991) Reconstruction and analysis of Human Alu genes. J. Mol. Evol. 32, 105-121.
-
(1991)
J. Mol. Evol.
, vol.32
, pp. 105-121
-
-
Jurka, J.1
Milosavljevic, A.2
-
26
-
-
0342298816
-
A fundamental division in the Alu family of repeated sequences
-
Jurka, J. and Smith, T. (1988) A fundamental division in the Alu family of repeated sequences. Proc. Natl. Acad. Sci. USA 85, 4774-4778.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 4774-4778
-
-
Jurka, J.1
Smith, T.2
-
27
-
-
0026049457
-
Free left arms as precursor molecules in the evolution of Alu sequences
-
Jurka, J. and Zuckerkandl, E. (1991) Free left arms as precursor molecules in the evolution of Alu sequences. J. Mol. Evol. 33, 49-56.
-
(1991)
J. Mol. Evol.
, vol.33
, pp. 49-56
-
-
Jurka, J.1
Zuckerkandl, E.2
-
28
-
-
0022869029
-
Expression of human gastrin gene in normal and gastrinoma tissues
-
Kariya, Y., Kato, K., Hayashizaki, Y., Himeno, S., Tarui, S. and Marsubara, K. (1986) Expression of human gastrin gene in normal and gastrinoma tissues. Gene 50, 345-352.
-
(1986)
Gene
, vol.50
, pp. 345-352
-
-
Kariya, Y.1
Kato, K.2
Hayashizaki, Y.3
Himeno, S.4
Tarui, S.5
Marsubara, K.6
-
29
-
-
0028969936
-
Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome
-
Knebelmann, B., Forestier, L., Drouot, L., Quinones, S., Chuet, C., Benessy, F., Saus, J. and Antignac, C. (1995) Splice-mediated insertion of an Alu sequence in the COL4A3 mRNA causing autosomal recessive Alport syndrome. Hum. Mol. Genet. 4, 675-679.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 675-679
-
-
Knebelmann, B.1
Forestier, L.2
Drouot, L.3
Quinones, S.4
Chuet, C.5
Benessy, F.6
Saus, J.7
Antignac, C.8
-
30
-
-
0023946286
-
Human genome organisation: Alu, lines, and the molecular structure of metaphase chromosome bands
-
Korenberg, J.R. and Rykowski, M.C. (1988) Human genome organisation: Alu, lines, and the molecular structure of metaphase chromosome bands. Cell 53, 391-400.
-
(1988)
Cell
, vol.53
, pp. 391-400
-
-
Korenberg, J.R.1
Rykowski, M.C.2
-
31
-
-
0026575429
-
Duplication-targeted DNA methylation and mutagenesis in the evolution of eukaryotic chromosomes
-
Kricker, M.C., Drake, J.W. and Radman, M. (1992) Duplication-targeted DNA methylation and mutagenesis in the evolution of eukaryotic chromosomes. Proc. Natl. Acad. Sci. USA 89, 1075-1079.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 1075-1079
-
-
Kricker, M.C.1
Drake, J.W.2
Radman, M.3
-
32
-
-
0021770770
-
Sequence of an expressed human ß-tubulin gene containing ten Alu family members
-
Lee, M.G.-S., Loomis, C. and Cowan, N.J. (1984) Sequence of an expressed human ß-tubulin gene containing ten Alu family members. Nucleic Acids Res. 12, 5823-5836.
-
(1984)
Nucleic Acids Res.
, vol.12
, pp. 5823-5836
-
-
Lee, M.G.-S.1
Loomis, C.2
Cowan, N.J.3
-
33
-
-
0022536609
-
Exon-Alu recombination deletes 5 kilobases from the low density lipoprotein receptor gene, producing a null phenotype in familial hypercholesterolemia
-
Lehrman, M.A., Russell, D.W., Goldstein, J.L. and Brown, M.S. (1986) Exon-Alu recombination deletes 5 kilobases from the low density lipoprotein receptor gene, producing a null phenotype in familial hypercholesterolemia. Proc. Natl. Acad. Sci. USA 83, 3679-3683.
-
(1986)
Proc. Natl. Acad. Sci. USA
, vol.83
, pp. 3679-3683
-
-
Lehrman, M.A.1
Russell, D.W.2
Goldstein, J.L.3
Brown, M.S.4
-
34
-
-
0023610526
-
Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia
-
Lehrman, M.A., Goldstein, J.L., Russell, D.W. and Brown, M.S. (1987a) Duplication of seven exons in LDL receptor gene caused by Alu-Alu recombination in a subject with familial hypercholesterolemia. Cell 48, 827-835.
-
(1987)
Cell
, vol.48
, pp. 827-835
-
-
Lehrman, M.A.1
Goldstein, J.L.2
Russell, D.W.3
Brown, M.S.4
-
35
-
-
0023262783
-
Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia
-
Lehrman, M.A., Russell, D.W., Goldstein, J.L. and Brown, M.S. (1987b) Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia. J. Biol. Chem. 262, 3354-3361.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 3354-3361
-
-
Lehrman, M.A.1
Russell, D.W.2
Goldstein, J.L.3
Brown, M.S.4
-
36
-
-
0027437275
-
Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia
-
Li, L. and Bray, P. (1993) Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia. Am. J. Hum. Genet. 53, 140-149.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 140-149
-
-
Li, L.1
Bray, P.2
-
37
-
-
0027416569
-
Characterisation and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy
-
Mahadevan, M.S., Foitzik, M.A., Surh, L.C. and Korneluk, R.G. (1993) Characterisation and polymerase chain reaction (PCR) detection of an Alu deletion polymorphism in total linkage disequilibrium with myotonic dystrophy. Genomics 15, 446-448.
-
(1993)
Genomics
, vol.15
, pp. 446-448
-
-
Mahadevan, M.S.1
Foitzik, M.A.2
Surh, L.C.3
Korneluk, R.G.4
-
38
-
-
0028356158
-
Alu sequences in the coding regions of mRNA: A source of protein variability
-
Makalowski, W., Mitchell, G. and Labuda, D. (1994) Alu sequences in the coding regions of mRNA: a source of protein variability. Trends Genet. 10, 188-193.
-
(1994)
Trends Genet.
, vol.10
, pp. 188-193
-
-
Makalowski, W.1
Mitchell, G.2
Labuda, D.3
-
39
-
-
0027401877
-
Duplication in the hypoxanthine phosphoribosyltransferase gene caused by Alu-Alu recombination in a patient with Lesch-Nyhan syndrome
-
Marcus, S., Hellgren, D., Lambert, B., Fallstrom, S.P. and Wahlstrom, J. (1993) Duplication in the hypoxanthine phosphoribosyltransferase gene caused by Alu-Alu recombination in a patient with Lesch-Nyhan syndrome. Hum. Genet. 90, 477-482.
-
(1993)
Hum. Genet.
, vol.90
, pp. 477-482
-
-
Marcus, S.1
Hellgren, D.2
Lambert, B.3
Fallstrom, S.P.4
Wahlstrom, J.5
-
40
-
-
0023941754
-
Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements
-
Markert, M.L., Hutton, J.J., Wiginton, D.A., States, J.C. and Kaufman, R.E. (1988) Adenosine deaminase (ADA) deficiency due to deletion of the ADA gene promoter and first exon by homologous recombination between two Alu elements. J. Clin. Invest. 81, 1323-1327.
-
(1988)
J. Clin. Invest.
, vol.81
, pp. 1323-1327
-
-
Markert, M.L.1
Hutton, J.J.2
Wiginton, D.A.3
States, J.C.4
Kaufman, R.E.5
-
41
-
-
0026082569
-
Splice mediated insertion of an Alu sequence inactivates ornithine d-aminotransferase: A role for Alu elements in human mutation
-
Mitchell, G.A., Labuda, D., Fontaine, G., Saudubray, J.M., Bonnefort, J.P., Lyonnet, S., Brody, L.C., Steel, G., Obie, C. and Valle, D. (1991) Splice mediated insertion of an Alu sequence inactivates ornithine d-aminotransferase: a role for Alu elements in human mutation. Proc. Natl. Acad. Sci. USA 88, 815-819.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 815-819
-
-
Mitchell, G.A.1
Labuda, D.2
Fontaine, G.3
Saudubray, J.M.4
Bonnefort, J.P.5
Lyonnet, S.6
Brody, L.C.7
Steel, G.8
Obie, C.9
Valle, D.10
-
42
-
-
0026764345
-
Molecular structure and genetic stability of human hypoxanthine phosphoribosyltransferase (HPRT) gene duplications
-
Monnat, R.J., Chiaverotti, T.A., Hackmann, A.F.M. and Maresh, G.A. (1992) Molecular structure and genetic stability of human hypoxanthine phosphoribosyltransferase (HPRT) gene duplications. Genomics 13, 788-796.
-
(1992)
Genomics
, vol.13
, pp. 788-796
-
-
Monnat, R.J.1
Chiaverotti, T.A.2
Hackmann, A.F.M.3
Maresh, G.A.4
-
43
-
-
0024650990
-
The distribution of interspersed repetitive DNA sequences in the human genome
-
Moyzis, R.K., Torney, D.C., Meyne, J., Buckingham, J.M., Wu, J.R., Burks, C., Sirotkin, K.M. and Goad, W.B. (1989) The distribution of interspersed repetitive DNA sequences in the human genome. Genomics 4, 273-289.
-
(1989)
Genomics
, vol.4
, pp. 273-289
-
-
Moyzis, R.K.1
Torney, D.C.2
Meyne, J.3
Buckingham, J.M.4
Wu, J.R.5
Burks, C.6
Sirotkin, K.M.7
Goad, W.B.8
-
44
-
-
0026322613
-
Inactivation of the cholinesterase gene by Alu insertion - Possible mechanism for human gene transposition
-
Muratani, K., Hada, T., Yamamoto, Y., Kaneko, T., Shigeto, Y., Ohue, T., Furuyama, J. and Higashino, K. (1991) Inactivation of the cholinesterase gene by Alu insertion - possible mechanism for human gene transposition. Proc. Natl. Acad. Sci. USA 88, 11315-11319.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 11315-11319
-
-
Muratani, K.1
Hada, T.2
Yamamoto, Y.3
Kaneko, T.4
Shigeto, Y.5
Ohue, T.6
Furuyama, J.7
Higashino, K.8
-
45
-
-
0025198437
-
Chracterization of the translocation breakpoint sequences in Philadelphia-positive acute lymphoblastic leukemia
-
Papadopoulos, P.C., Greenstein, A.M., Gaffney, R.A., Westbrook, C. A. and Wiedemann, L.M. (1990) Chracterization of the translocation breakpoint sequences in Philadelphia-positive acute lymphoblastic leukemia. Genes Chromosomes Cancer 1, 223-239.
-
(1990)
Genes Chromosomes Cancer
, vol.1
, pp. 223-239
-
-
Papadopoulos, P.C.1
Greenstein, A.M.2
Gaffney, R.A.3
Westbrook, C.A.4
Wiedemann, L.M.5
-
46
-
-
0023916853
-
The Alu family developed through successive waves of fixation closely connected with primate lineage history
-
Quentin, Y. (1988) The Alu family developed through successive waves of fixation closely connected with primate lineage history. J. Mol. Evol. 27, 194-202.
-
(1988)
J. Mol. Evol.
, vol.27
, pp. 194-202
-
-
Quentin, Y.1
-
47
-
-
0026749958
-
Origin of the Alu family: A family of Alu-like monomers gave birth to the left and the right arms of the Alu elements
-
Quentin, Y. (1992) Origin of the Alu family: a family of Alu-like monomers gave birth to the left and the right arms of the Alu elements. Nucleic Acids Res. 20, 3397-3401.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 3397-3401
-
-
Quentin, Y.1
-
48
-
-
0029091672
-
Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch-Nyhan syndrome
-
Renwick, P.J., Birley, A.J., Mckeown, C.M.E. and Hultén, M. (1995) Southern analysis reveals a large deletion at the hypoxanthine phosphoribosyltransferase locus in a patient with Lesch-Nyhan syndrome. Clin. Genet. 48, 80-84.
-
(1995)
Clin. Genet.
, vol.48
, pp. 80-84
-
-
Renwick, P.J.1
Birley, A.J.2
Mckeown, C.M.E.3
Hultén, M.4
-
49
-
-
0023646823
-
A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination
-
Rouyer, F., Simmler, M.-C., Page, D.C. and Weissenbach, J. (1987) A sex chromosome rearrangement in a human XX male caused by Alu-Alu recombination. Cell 51, 417-425.
-
(1987)
Cell
, vol.51
, pp. 417-425
-
-
Rouyer, F.1
Simmler, M.-C.2
Page, D.C.3
Weissenbach, J.4
-
50
-
-
0027298903
-
DNA sequence analysis of the type II breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias
-
Sowerby, S.J., Kennedy, M.A., Fitzgerald, P.H. and Morris, C.M. (1993) DNA sequence analysis of the type II breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias. Oncogene 8, 1679-1683.
-
(1993)
Oncogene
, vol.8
, pp. 1679-1683
-
-
Sowerby, S.J.1
Kennedy, M.A.2
Fitzgerald, P.H.3
Morris, C.M.4
-
51
-
-
0025174888
-
Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements
-
Stoppa-Lyonnet, D., Carter, P.E., Meo, T. and Tosi, M. (1990) Clusters of intragenic Alu repeats predispose the human C1 inhibitor locus to deleterious rearrangements. Proc. Natl. Acad. Sci. USA 87, 1551-1555.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 1551-1555
-
-
Stoppa-Lyonnet, D.1
Carter, P.E.2
Meo, T.3
Tosi, M.4
-
52
-
-
0024497357
-
Nucleotide sequence of both reciprical translocation junction regions in a patient with Ph positive acute lymphoblastic leukaemia, with a breakpoint within the first intron of the BCR gene
-
van der Feltz, M.J.M., Shiviji, M.K.K., Allen, P.B., Heisterkamp, N., Groffen, J. and Wiedemann, L.M. (1989) Nucleotide sequence of both reciprical translocation junction regions in a patient with Ph positive acute lymphoblastic leukaemia, with a breakpoint within the first intron of the BCR gene. Nucleic Acids Res. 17, 1-10
-
(1989)
Nucleic Acids Res.
, vol.17
, pp. 1-10
-
-
Feltz, M.J.M.1
Shiviji, M.K.K.2
Allen, P.B.3
Heisterkamp, N.4
Groffen, J.5
Wiedemann, L.M.6
-
53
-
-
0027874926
-
Haemophilia B due to a de novo insertion of a human specific Alu subfamily member within the coding region of the Factor IX gene
-
Viduad, D., Viduad, M., Bahnak, B.R., Siguret, V., Gispert-Sanchez, S., Laurian, Y., Meyer, D., Goossens, M. and Lavergne, J.M. (1993) Haemophilia B due to a de novo insertion of a human specific Alu subfamily member within the coding region of the Factor IX gene. Eur. J. Hum. Genet. 1, 30-36.
-
(1993)
Eur. J. Hum. Genet.
, vol.1
, pp. 30-36
-
-
Viduad, D.1
Viduad, M.2
Bahnak, B.R.3
Siguret, V.4
Gispert-Sanchez, S.5
Laurian, Y.6
Meyer, D.7
Goossens, M.8
Lavergne, J.M.9
-
54
-
-
0025951042
-
A de novo Alu insertion results in neurofibromatosis type I
-
Wallace, M.R., Andersen, L.B., Saulino, A.M., Gregory, P.E., Glover, T.W. and Collins, F.S. (1991) A de novo Alu insertion results in neurofibromatosis type I. Nature 353, 864-866.
-
(1991)
Nature
, vol.353
, pp. 864-866
-
-
Wallace, M.R.1
Andersen, L.B.2
Saulino, A.M.3
Gregory, P.E.4
Glover, T.W.5
Collins, F.S.6
-
55
-
-
0022887765
-
Complete sequence and structure of the gene for human adenosine deaminase
-
Wiginton, D.A., Kaplan, D.J., States, C., Akeson, A.L., Perme, C.M., Bilyk, I.J., Vaughn, A.J., Lattier, D.L. and Hutton, J.J. (1986) Complete sequence and structure of the gene for human adenosine deaminase. Biochemistry 25, 8234-8244.
-
(1986)
Biochemistry
, vol.25
, pp. 8234-8244
-
-
Wiginton, D.A.1
Kaplan, D.J.2
States, C.3
Akeson, A.L.4
Perme, C.M.5
Bilyk, I.J.6
Vaughn, A.J.7
Lattier, D.L.8
Hutton, J.J.9
-
56
-
-
0027958672
-
The human gene (CSNK2A1) coding for the casein kinase II subunit a is located on chromsome 20 and contains tandemly arranged Alu repeats
-
Wirkner, U., Voss, H., Lichter, P., Ansorge, W. and Pyerin, W. (1994) The human gene (CSNK2A1) coding for the casein kinase II subunit a is located on chromsome 20 and contains tandemly arranged Alu repeats. Genomics 19, 257-265.
-
(1994)
Genomics
, vol.19
, pp. 257-265
-
-
Wirkner, U.1
Voss, H.2
Lichter, P.3
Ansorge, W.4
Pyerin, W.5
-
57
-
-
0021219230
-
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients
-
Yang, T.P., Patel, P.I., Chinault, A.C., Stout, J.T., Jackson, L.G., Hildebrand, B.M. and Caskey, C.T. (1984) Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients. Nature 310, 412-414.
-
(1984)
Nature
, vol.310
, pp. 412-414
-
-
Yang, T.P.1
Patel, P.I.2
Chinault, A.C.3
Stout, J.T.4
Jackson, L.G.5
Hildebrand, B.M.6
Caskey, C.T.7
-
58
-
-
0027409758
-
Hydroxymethylbilane synthase: Complete genomic sequence and amplifiable polymorphisms in the human gene
-
Yoo, H.-W., Warner, C.A., Chen, C.-H. and Desnick, R.J. (1993) Hydroxymethylbilane synthase: complete genomic sequence and amplifiable polymorphisms in the human gene. Genomics 15, 21-29.
-
(1993)
Genomics
, vol.15
, pp. 21-29
-
-
Yoo, H.-W.1
Warner, C.A.2
Chen, C.-H.3
Desnick, R.J.4
|