-
1
-
-
0026751086
-
Semidominant suppressors of Srs2 helicase mutations of Saccharomyces cerevisiae map in the RAD51 gene, whose sequence predicts a protein with similarities to prokaryotic RecA proteins
-
Aboussekhra, A., R. Chanet, A. Adjiri, and F. Fabre. 1992. Semidominant suppressors of Srs2 helicase mutations of Saccharomyces cerevisiae map in the RAD51 gene, whose sequence predicts a protein with similarities to prokaryotic RecA proteins. Mol. Cell. Biol. 12: 3224-3234.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 3224-3234
-
-
Aboussekhra, A.1
Chanet, R.2
Adjiri, A.3
Fabre, F.4
-
2
-
-
0028209370
-
Nuclear proteins binding to a novel target sequence within the recombination hotspot regions of Bcl-2 and the immunoglobulin DH family
-
Aoki, K., K. Nakahara, C. Ikegawa, M. Seto, T. Takahashi, J. Minowada, J.L. Strominger, R.T. Maziarz, and M. Kasai. 1994. Nuclear proteins binding to a novel target sequence within the recombination hotspot regions of Bcl-2 and the immunoglobulin DH family. Oncogene 9: 1109-1115.
-
(1994)
Oncogene
, vol.9
, pp. 1109-1115
-
-
Aoki, K.1
Nakahara, K.2
Ikegawa, C.3
Seto, M.4
Takahashi, T.5
Minowada, J.6
Strominger, J.L.7
Maziarz, R.T.8
Kasai, M.9
-
3
-
-
0029040211
-
A novel gene Translin encodes a recombination hotspot binding protein associated with chromosome translocations
-
Aoki, K., K. Suzuki, T. Sugano, T. Tasaka, K. Nakahara, O. Kuge, A. Omori, and M. Kasai. 1995. A novel gene Translin encodes a recombination hotspot binding protein associated with chromosome translocations. Nature Genet. 10: 167-174.
-
(1995)
Nature Genet.
, vol.10
, pp. 167-174
-
-
Aoki, K.1
Suzuki, K.2
Sugano, T.3
Tasaka, T.4
Nakahara, K.5
Kuge, O.6
Omori, A.7
Kasai, M.8
-
4
-
-
0015812080
-
Hemoglobin P Nilotic containing a β-δ chain
-
Badr, F.M., P.A. Lorkin, and H. Lehmann 1973. Hemoglobin P Nilotic containing a β-δ chain. Nature 242: 107-110.
-
(1973)
Nature
, vol.242
, pp. 107-110
-
-
Badr, F.M.1
Lorkin, P.A.2
Lehmann, H.3
-
5
-
-
0000328467
-
The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion
-
Baglioni, C. 1962. The fusion of two peptide chains in hemoglobin Lepore and its interpretation as a genetic deletion. Proc. Natl. Acad. Sci. 48: 1880-1886.
-
(1962)
Proc. Natl. Acad. Sci.
, vol.48
, pp. 1880-1886
-
-
Baglioni, C.1
-
6
-
-
0024802646
-
Contiguous gene syndrome due to deletions in the distal short arm of the human X chromosome
-
Ballabio, A., B. Bardoni, R. Carrozzo, G. Andria, D. Bick, L. Campbell, B. Hamell, M.A. Ferguson-Smith, G. Gimelli, M. Fraccaro, P. Maraschio, O. Zuffardi, S. Guioli, and G. Camerino. 1989a. Contiguous gene syndrome due to deletions in the distal short arm of the human X chromosome. Proc. Natl. Acad. Sci. 86: 10001-10005.
-
(1989)
Proc. Natl. Acad. Sci.
, vol.86
, pp. 10001-10005
-
-
Ballabio, A.1
Bardoni, B.2
Carrozzo, R.3
Andria, G.4
Bick, D.5
Campbell, L.6
Hamell, B.7
Ferguson-Smith, M.A.8
Gimelli, G.9
Fraccaro, M.10
Maraschio, P.11
Zuffardi, O.12
Guioli, S.13
Camerino, G.14
-
7
-
-
0024527636
-
Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients at DNA and protein levels
-
Ballabio, A., R. Carozzo, G. Parenti, A. Gil, M. Zollo, M.G. Perisco, E. Gillard, N. Affara, J. Yates, M.A. Ferguson-Smith, R.R. Frants, A.W. Eriksso, and G. Andria. 1989b. Molecular heterogeneity of steroid sulfatase deficiency: A multicenter study on 57 unrelated patients at DNA and protein levels. Genomics 4: 36-40.
-
(1989)
Genomics
, vol.4
, pp. 36-40
-
-
Ballabio, A.1
Carozzo, R.2
Parenti, G.3
Gil, A.4
Zollo, M.5
Perisco, M.G.6
Gillard, E.7
Affara, N.8
Yates, J.9
Ferguson-Smith, M.A.10
Frants, R.R.11
Eriksso, A.W.12
Andria, G.13
-
8
-
-
0001052681
-
Hemoglobin Lepore Hollandia
-
Barnabus, J. and C.J. Muller. 1962. Hemoglobin Lepore Hollandia. Nature 194: 931-932.
-
(1962)
Nature
, vol.194
, pp. 931-932
-
-
Barnabus, J.1
Muller, C.J.2
-
9
-
-
0026643384
-
Nucleotide sequence and transcriptional regulation of the yeast recombinational repair gene RAD51
-
Basile, G., M. Aker, and R.K. Mortimer. 1992. Nucleotide sequence and transcriptional regulation of the yeast recombinational repair gene RAD51. Mol. Cell. Biol. 12: 3235-3246.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 3235-3246
-
-
Basile, G.1
Aker, M.2
Mortimer, R.K.3
-
10
-
-
0029877516
-
Replicational model for DNA recombination between direct repeats
-
Bi, X. and L.F. Liu. 1996. Replicational model for DNA recombination between direct repeats. J. Mol. Biol. 256: 849-858.
-
(1996)
J. Mol. Biol.
, vol.256
, pp. 849-858
-
-
Bi, X.1
Liu, L.F.2
-
11
-
-
0028600050
-
RecA homologs Dmc1 and Rad51 interact to form multiple nuclear complexes prior to meiotic chromosome synapsis
-
Bishop, D.K. 1994. RecA homologs Dmc1 and Rad51 interact to form multiple nuclear complexes prior to meiotic chromosome synapsis. Cell 79: 1081-1092.
-
(1994)
Cell
, vol.79
, pp. 1081-1092
-
-
Bishop, D.K.1
-
12
-
-
0026697166
-
DMC1: A meiosis-specific yeast homologue of E. coli RecA required for recombination, synaptonemal complex formation, and cell cycle progression
-
Bishop, D.K., D. Park, L. Xu, and N. Kleckner. 1992. DMC1: A meiosis-specific yeast homologue of E. coli RecA required for recombination, synaptonemal complex formation, and cell cycle progression. Cell 9: 439-456.
-
(1992)
Cell
, vol.9
, pp. 439-456
-
-
Bishop, D.K.1
Park, D.2
Xu, L.3
Kleckner, N.4
-
13
-
-
0030030169
-
Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease type 1a - First report of a de novo duplication with a maternal origin
-
Blair, I.P., J. Nash, M.J. Gordon, and G.A. Nicholson. 1996. Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease type 1a - first report of a de novo duplication with a maternal origin. Am. J. Hum. Genet. 58: 472-476.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 472-476
-
-
Blair, I.P.1
Nash, J.2
Gordon, M.J.3
Nicholson, G.A.4
-
14
-
-
0028926890
-
Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome
-
Bondeson, M.L., N. Dahl, H. Malmgren, W.J. Kleijer, T. Tonnesen, B.M. Carlberg, and U. Pettersson. 1995. Inversion of the IDS gene resulting from recombination with IDS-related sequences is a common cause of the Hunter syndrome. Hum. Mol. Genet. 4: 615-621.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 615-621
-
-
Bondeson, M.L.1
Dahl, N.2
Malmgren, H.3
Kleijer, W.J.4
Tonnesen, T.5
Carlberg, B.M.6
Pettersson, U.7
-
15
-
-
0023473993
-
Cloning of a cDNA for steroid sulfatase: Frequent occurrence of gene deletions in patients with recessive X chromosome linked icthyosis
-
Bonifas, J.M., B.J. Morley, R.E. Oakley, Y.W. Kan, and E.H. Epstein, Jr. 1987. Cloning of a cDNA for steroid sulfatase: Frequent occurrence of gene deletions in patients with recessive X chromosome linked icthyosis. Proc. Natl. Acad. Sci. 84: 9248-9251.
-
(1987)
Proc. Natl. Acad. Sci.
, vol.84
, pp. 9248-9251
-
-
Bonifas, J.M.1
Morley, B.J.2
Oakley, R.E.3
Kan, Y.W.4
Epstein Jr., E.H.5
-
16
-
-
0027972378
-
Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
-
Chance, P.F., N. Abbas, M.W. Lensch, L. Pentao, B.B. Roa, P.I. Patel, and J.R. Lupski. 1994. Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17. Hum. Mol. Genet. 3: 223-228.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 223-228
-
-
Chance, P.F.1
Abbas, N.2
Lensch, M.W.3
Pentao, L.4
Roa, B.B.5
Patel, P.I.6
Lupski, J.R.7
-
17
-
-
9244234493
-
Long-range sequence analysis in Xq28: Thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci
-
Chen, E.Y., M. Zollo, R. Mazzarella, A. Ciccodicola, C.-N. Chen, L. Zuo, C. Heiner, F. Burrough, M. Repetto, D. Schlessinger, and M. D'Urso. 1996. Long-range sequence analysis in Xq28: Thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci. Hum. Mol. Genet. 5: 659-668.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 659-668
-
-
Chen, E.Y.1
Zollo, M.2
Mazzarella, R.3
Ciccodicola, A.4
Chen, C.-N.5
Zuo, L.6
Heiner, C.7
Burrough, F.8
Repetto, M.9
Schlessinger, D.10
D'Urso, M.11
-
18
-
-
0029812441
-
Analysis of the organisation and localisation of the FSHD-associated tandem array in primates-implications for the origin and evolution of the 3.3 kb repeat family
-
Clark, L.N., U. Koehler, D.C. Ward, J. Wienberg, and J.E. Hewitt. 1996. Analysis of the organisation and localisation of the FSHD-associated tandem array in primates-implications for the origin and evolution of the 3.3 kb repeat family. Chromosoma 105: 180-189.
-
(1996)
Chromosoma
, vol.105
, pp. 180-189
-
-
Clark, L.N.1
Koehler, U.2
Ward, D.C.3
Wienberg, J.4
Hewitt, J.E.5
-
19
-
-
0027477152
-
A de novo pathological point mutation at the 21-hydroxylase locus: Implications for gene conversion in the human genome
-
Collier, P.S., M. Tassabehji, P.J. Sinnott, and T. Strachan. 1993. A de novo pathological point mutation at the 21-hydroxylase locus: Implications for gene conversion in the human genome. Nature Genet. 3: 260-265.
-
(1993)
Nature Genet.
, vol.3
, pp. 260-265
-
-
Collier, P.S.1
Tassabehji, M.2
Sinnott, P.J.3
Strachan, T.4
-
20
-
-
0023241709
-
Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase
-
Conary, J.T., G. Lorkowski, B. Schmidt, R. Pohlmann, G. Nagel, H.E. Meyer, C. Krentler, J. Tully, A. Hasilik, and K. von Figura. 1987. Genetic heterogeneity of steroid sulfatase deficiency revealed with cDNA for human steroid sulfatase. Biochem. Biophys. Res. Commun. 144: 1010-1017.
-
(1987)
Biochem. Biophys. Res. Commun.
, vol.144
, pp. 1010-1017
-
-
Conary, J.T.1
Lorkowski, G.2
Schmidt, B.3
Pohlmann, R.4
Nagel, G.5
Meyer, H.E.6
Krentler, C.7
Tully, J.8
Hasilik, A.9
Von Figura, K.10
-
21
-
-
0018581641
-
α-Globin gene organisation in blacks precludes the severe form of α-thalassemia
-
Dozy, A.M., Y.W. Kan, S.H. Embury, W.C. Mentzer, W.C. Wang, B. Lubin, J.R. Davis, and H.M. Koenig. 1979. α-Globin gene organisation in blacks precludes the severe form of α-thalassemia. Nature 280: 605-607.
-
(1979)
Nature
, vol.280
, pp. 605-607
-
-
Dozy, A.M.1
Kan, Y.W.2
Embury, S.H.3
Mentzer, W.C.4
Wang, W.C.5
Lubin, B.6
Davis, J.R.7
Koenig, H.M.8
-
22
-
-
0027433563
-
Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families
-
Easton, D.F., D.T. Bishop, D. Ford, G.P. Crockford, and the Breast Cancer Linkage Consortium. 1993. Genetic linkage analysis in familial breast and ovarian cancer: Results from 214 families. Am. J. Hum. Genet. 52: 678-701.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 678-701
-
-
Easton, D.F.1
Bishop, D.T.2
Ford, D.3
Crockford, G.P.4
-
23
-
-
0019219843
-
Two different molecular organizations account for the single α-globin gene of the α-thalassemia-2 genotype
-
Embury, S.H., J.A. Miller, A.M. Dozy, Y.W. Kan, V. Chan, and D. Todd. 1980. Two different molecular organizations account for the single α-globin gene of the α-thalassemia-2 genotype. J. Clin. Invest. 66: 1319-1324.
-
(1980)
J. Clin. Invest.
, vol.66
, pp. 1319-1324
-
-
Embury, S.H.1
Miller, J.A.2
Dozy, A.M.3
Kan, Y.W.4
Chan, V.5
Todd, D.6
-
24
-
-
0030948789
-
Disruption of mouse RAD54 reduces ionizing radiation reistance and homologous recombination
-
Essers, J., R.W. Hendriks, S.M.A. Swagemakers, C. Troelstra, J. de Wit, D. Bootsma, J.H.J. Hoeijmakers, and R. Kanaar. 1997. Disruption of mouse RAD54 reduces ionizing radiation reistance and homologous recombination. Cell 89: 195-204.
-
(1997)
Cell
, vol.89
, pp. 195-204
-
-
Essers, J.1
Hendriks, R.W.2
Swagemakers, S.M.A.3
Troelstra, C.4
De Wit, J.5
Bootsma, D.6
Hoeijmakers, J.H.J.7
Kanaar, R.8
-
25
-
-
0027587771
-
DNA double-strand breaks and the RAD50-RAD57 genes in Saccharomyces
-
Game, J.C. 1993. DNA double-strand breaks and the RAD50-RAD57 genes in Saccharomyces. Semin. Cancer Biol. 4: 73-83.
-
(1993)
Semin. Cancer Biol.
, vol.4
, pp. 73-83
-
-
Game, J.C.1
-
26
-
-
0031012305
-
Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene
-
Gayther, S.A., J. Mangion, P. Russell, S. Seal, R. Barfoot, B.A. Ponder, M.R. Stratton, and D. Easton. 1997. Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene. Nature Genet. 15: 103-105.
-
(1997)
Nature Genet.
, vol.15
, pp. 103-105
-
-
Gayther, S.A.1
Mangion, J.2
Russell, P.3
Seal, S.4
Barfoot, R.5
Ponder, B.A.6
Stratton, M.R.7
Easton, D.8
-
27
-
-
0000376354
-
A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with the thalassemia trait
-
Gerald, P.S. and L.K. Diamond. 1958. A new hereditary hemoglobinopathy (the Lepore trait) and its interaction with the thalassemia trait. Blood 13: 835-844.
-
(1958)
Blood
, vol.13
, pp. 835-844
-
-
Gerald, P.S.1
Diamond, L.K.2
-
28
-
-
0039276808
-
Triplicated α-globin loci in humans
-
Goosens, M., A.M. Dozy, S.H. Embury, Z. Zachariades, M.G. Hadjiminas, G. Stamatoyannopoulos, and Y.W. Kan. 1980. Triplicated α-globin loci in humans. Proc. Natl. Acad. Sci. 77: 518-521.
-
(1980)
Proc. Natl. Acad. Sci.
, vol.77
, pp. 518-521
-
-
Goosens, M.1
Dozy, A.M.2
Embury, S.H.3
Zachariades, Z.4
Hadjiminas, M.G.5
Stamatoyannopoulos, G.6
Kan, Y.W.7
-
29
-
-
0024435039
-
Molecular aspects of heavy-chain class switching
-
Gritzmacher, C.A. 1989. Molecular aspects of heavy-chain class switching. Crit. Immunol. 9: 173-200.
-
(1989)
Crit. Immunol.
, vol.9
, pp. 173-200
-
-
Gritzmacher, C.A.1
-
30
-
-
0028957889
-
Nuclear foci of mammalian Rad51 recombination protein in somatic cells after DNA damage and its localization in synaptonemal complexes
-
Haaf, T., E.I. Golub, G. Reddy, C.M. Radding, and D.C. Ward. 1995. Nuclear foci of mammalian Rad51 recombination protein in somatic cells after DNA damage and its localization in synaptonemal complexes. Proc. Natl. Acad. Sci. 92: 2298-2302.
-
(1995)
Proc. Natl. Acad. Sci.
, vol.92
, pp. 2298-2302
-
-
Haaf, T.1
Golub, E.I.2
Reddy, G.3
Radding, C.M.4
Ward, D.C.5
-
31
-
-
0029858451
-
Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy - New insights into molecular mechanisms responsible for the disease
-
Hahnen, E., J. Schonling, S. Rudnikschoneborn, K. Zerres, and B. Wirth. 1996. Hybrid survival motor neuron genes in patients with autosomal recessive spinal muscular atrophy - new insights into molecular mechanisms responsible for the disease. Am. J. Hum. Genet. 59: 1057-1065.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1057-1065
-
-
Hahnen, E.1
Schonling, J.2
Rudnikschoneborn, S.3
Zerres, K.4
Wirth, B.5
-
32
-
-
15844371372
-
The tumor suppressor gene Brca1 is required for embryonic cellular proliferation in the mouse
-
Hakem, R., J.L. de la Pompa, C. Sirard, R. Mo, M. Woo, A. Hakem, A. Wakeham, J. Potter, A. Reitmair, F. Billia, E. Firpo, C.C. Hui, J. Roberts, J. Rossant, and T.W. Mak. 1996. The tumor suppressor gene Brca1 is required for embryonic cellular proliferation in the mouse. Cell 85: 1009-1023.
-
(1996)
Cell
, vol.85
, pp. 1009-1023
-
-
Hakem, R.1
De La Pompa, J.L.2
Sirard, C.3
Mo, R.4
Woo, M.5
Hakem, A.6
Wakeham, A.7
Potter, J.8
Reitmair, A.9
Billia, F.10
Firpo, E.11
Hui, C.C.12
Roberts, J.13
Rossant, J.14
Mak, T.W.15
-
33
-
-
0027106891
-
Sex chromosome pairing and activity during mammalian meiosis
-
Handel, M.A. and P.A. Hunt. 1992. Sex chromosome pairing and activity during mammalian meiosis. BioEssays 12: 817-822.
-
(1992)
BioEssays
, vol.12
, pp. 817-822
-
-
Handel, M.A.1
Hunt, P.A.2
-
34
-
-
0023049029
-
Structure and function of repetitve DNA in eukaryotes
-
Hardman, N. 1986. Structure and function of repetitve DNA in eukaryotes. Biochem. J. 234: 1-11.
-
(1986)
Biochem. J.
, vol.234
, pp. 1-11
-
-
Hardman, N.1
-
35
-
-
0027949179
-
Charcot-Marie-Tooth disease type 1A: The parental origin of a de novo 17p11.2-p12 duplication
-
Hertz, J.M., A.D. Borglum, C.A. Brandt, T. Flint, and C. Bisgaard. 1994. Charcot-Marie-Tooth disease type 1A: The parental origin of a de novo 17p11.2-p12 duplication. Clin. Genet. 46: 291-294.
-
(1994)
Clin. Genet.
, vol.46
, pp. 291-294
-
-
Hertz, J.M.1
Borglum, A.D.2
Brandt, C.A.3
Flint, T.4
Bisgaard, C.5
-
36
-
-
0028040601
-
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy
-
Hewitt, J.E., R. Lyle, L.N. Clark, E.M. Valleley, T.J. Wright, C. Wijmenga, J.C. van Deutekom, F. Francis, P.T. Sharpe, M. Hofker, R.R. Frants, and R. Williamson. 1994. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. Hum. Mol. Genet. 3: 1287-1295.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1287-1295
-
-
Hewitt, J.E.1
Lyle, R.2
Clark, L.N.3
Valleley, E.M.4
Wright, T.J.5
Wijmenga, C.6
Van Deutekom, J.C.7
Francis, F.8
Sharpe, P.T.9
Hofker, M.10
Frants, R.R.11
Williamson, R.12
-
37
-
-
0028273997
-
The search for the right partner: Homologous pairing and DNA strand exchange proteins in eukaryotes
-
Heyer, W.D. 1994. The search for the right partner: Homologous pairing and DNA strand exchange proteins in eukaryotes. Experientia 50: 223-233.
-
(1994)
Experientia
, vol.50
, pp. 223-233
-
-
Heyer, W.D.1
-
38
-
-
0018649276
-
Negro α-thalassemia is caused by deletion of a single α-globin gene
-
Higgs, D.R., J.M. Old, J.B. Clegg, L. Pressley, D.M. Hunt, D.J. Weatherall, and G.R. Serjeant. 1979. Negro α-thalassemia is caused by deletion of a single α-globin gene. Lancet 2: 272-276.
-
(1979)
Lancet
, vol.2
, pp. 272-276
-
-
Higgs, D.R.1
Old, J.M.2
Clegg, J.B.3
Pressley, L.4
Hunt, D.M.5
Weatherall, D.J.6
Serjeant, G.R.7
-
39
-
-
0024509622
-
A review of the molecular genetics of the α-globin gene cluster
-
Higgs, D.R., M.A. Vickers, A.O.M. Wilkie, I-M. Pretorius, A.P. Jarman, and D.J. Weatherall. 1989. A review of the molecular genetics of the α-globin gene cluster. Blood 73: 1081-1104.
-
(1989)
Blood
, vol.73
, pp. 1081-1104
-
-
Higgs, D.R.1
Vickers, M.A.2
Wilkie, A.O.M.3
Pretorius, I.-M.4
Jarman, A.P.5
Weatherall, D.J.6
-
40
-
-
0018226990
-
Unbalanced globin chain synthesis by Hb Lincoln Park (anti-Lepore) reticulocytes
-
Honig, G.R., R.G. Mason, L.M. Tremaine, and L.N. Vida. 1978. Unbalanced globin chain synthesis by Hb Lincoln Park (anti-Lepore) reticulocytes. Am. J. Hematolol. 5: 335-340.
-
(1978)
Am. J. Hematolol.
, vol.5
, pp. 335-340
-
-
Honig, G.R.1
Mason, R.G.2
Tremaine, L.M.3
Vida, L.N.4
-
41
-
-
0015454803
-
Hemoglobin Kenya, the product of a fusion of γ and β polypeptide chains
-
Huisman, T.H.J., R.N. Wrightstone, J.B. Wilson, W.A. Schroeder, and A.G. Kendal. 1972. Hemoglobin Kenya, the product of a fusion of γ and β polypeptide chains. Arch. Biochem. Biophys. 153: 850-853.
-
(1972)
Arch. Biochem. Biophys.
, vol.153
, pp. 850-853
-
-
Huisman, T.H.J.1
Wrightstone, R.N.2
Wilson, J.B.3
Schroeder, W.A.4
Kendal, A.G.5
-
42
-
-
0020024303
-
Repititive sequences in eukaryotic DNA and their expression
-
Jelinek, W.R., and C.W. Schmid. 1982. Repititive sequences in eukaryotic DNA and their expression. Annu. Rev. Biochem. 51: 831-844.
-
(1982)
Annu. Rev. Biochem.
, vol.51
, pp. 831-844
-
-
Jelinek, W.R.1
Schmid, C.W.2
-
43
-
-
0028221280
-
Recombination hotspot associated factors specifically recognize novel target sequences at the site of interchromosomal rearrangements in T-ALL patients with t(8;14)(q24;q11) and t(1;14) (p32;q11)
-
Kasai, M., K. Aoki, Y. Matsuo, J. Minowada, R.T. Maziarz, and J.L. Strominger. 1994. Recombination hotspot associated factors specifically recognize novel target sequences at the site of interchromosomal rearrangements in T-ALL patients with t(8;14)(q24;q11) and t(1;14) (p32;q11). Int. Immunol. 6: 1017-1025.
-
(1994)
Int. Immunol.
, vol.6
, pp. 1017-1025
-
-
Kasai, M.1
Aoki, K.2
Matsuo, Y.3
Minowada, J.4
Maziarz, R.T.5
Strominger, J.L.6
-
44
-
-
0029999248
-
Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombination hotspot
-
Kiyosawa, H. and P.F. Chance. 1996. Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombination hotspot. Hum. Mol. Genet. 5: 745-754.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 745-754
-
-
Kiyosawa, H.1
Chance, P.F.2
-
45
-
-
9044227270
-
Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis
-
Konrad, M., S. Saunie, L. Heidet, F. Silbermann, F. Benessy, J. Calado, D. Lepaslier, M. Broyer, M.C. Gubler, and C. Antignac. 1996. Large homozygous deletions of the 2q13 region are a major cause of juvenile nephronophthisis. Hum. Mol. Genet. 5: 367-371.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 367-371
-
-
Konrad, M.1
Saunie, S.2
Heidet, L.3
Silbermann, F.4
Benessy, F.5
Calado, J.6
Lepaslier, D.7
Broyer, M.8
Gubler, M.C.9
Antignac, C.10
-
46
-
-
0028308710
-
Homologous pairing and DNA strand-exchange proteins
-
Kowalczykowski, S.C. and A.K. Eggleston. 1994. Homologous pairing and DNA strand-exchange proteins. Annu. Rev. Biochem. 63: 991-1043.
-
(1994)
Annu. Rev. Biochem.
, vol.63
, pp. 991-1043
-
-
Kowalczykowski, S.C.1
Eggleston, A.K.2
-
47
-
-
0028102267
-
Biochemistry of homologous recombination in Escherichia coli
-
Kowalczykowski, S.C., D.A. Dixon, A.K. Eggleston, S.D. Lauder, and W.M. Rehrauer. 1994. Biochemistry of homologous recombination in Escherichia coli. Microbiol. Rev. 58: 401-465.
-
(1994)
Microbiol. Rev.
, vol.58
, pp. 401-465
-
-
Kowalczykowski, S.C.1
Dixon, D.A.2
Eggleston, A.K.3
Lauder, S.D.4
Rehrauer, W.M.5
-
48
-
-
0025762012
-
Gene deletions causing human genetic disease: Mechanisms of mutagenesis and the role of the local DNA sequence environment
-
Krawczak, M. and D.N. Cooper. 1991. Gene deletions causing human genetic disease: Mechanisms of mutagenesis and the role of the local DNA sequence environment. Hum. Genet. 86: 425-441.
-
(1991)
Hum. Genet.
, vol.86
, pp. 425-441
-
-
Krawczak, M.1
Cooper, D.N.2
-
49
-
-
0027520025
-
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A
-
Lakich, D., H.H. Kazazian, Jr., S.E. Antonarakis, and J. Gitschier. 1993. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A. Nature Genet. 5: 236-241.
-
(1993)
Nature Genet.
, vol.5
, pp. 236-241
-
-
Lakich, D.1
Kazazian Jr., H.H.2
Antonarakis, S.E.3
Gitschier, J.4
-
50
-
-
0018903047
-
The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions
-
Lauer, J., C.-K.J. Chen, and T. Maniatis. 1980. The chromosomal arrangement of human α-like globin genes: Sequence homology and α-globin gene deletions. Cell 20: 119-130.
-
(1980)
Cell
, vol.20
, pp. 119-130
-
-
Lauer, J.1
Chen, C.-K.J.2
Maniatis, T.3
-
51
-
-
0028925370
-
Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35
-
Lee, J.H., K. Goto, C. Matsuda, and K. Arahata. 1995. Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35. Muscle & Nerve 2: 6-13.
-
(1995)
Muscle & Nerve
, vol.2
, pp. 6-13
-
-
Lee, J.H.1
Goto, K.2
Matsuda, C.3
Arahata, K.4
-
52
-
-
0014860374
-
Observations on hemoglobin P (Congo type)
-
Lehmann, H. and D. Charlesworth. 1970. Observations on hemoglobin P (Congo type). Biochem J. 119: 43.
-
(1970)
Biochem J.
, vol.119
, pp. 43
-
-
Lehmann, H.1
Charlesworth, D.2
-
53
-
-
0021918948
-
Mutation in LDL receptor: Alu-Alu recombination deletes exons encoding transmembrane and cytoplasmic domains
-
Lehrman, M.A., W.J. Schneider, T.C. Sudhof, M.S. Brown, J.L. Goldstein, and D.W. Russell. 1985. Mutation in LDL receptor: Alu-Alu recombination deletes exons encoding transmembrane and cytoplasmic domains. Science 227: 140-146.
-
(1985)
Science
, vol.227
, pp. 140-146
-
-
Lehrman, M.A.1
Schneider, W.J.2
Sudhof, T.C.3
Brown, M.S.4
Goldstein, J.L.5
Russell, D.W.6
-
54
-
-
0023262783
-
Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia
-
Lehrman, M.A., D.W. Russell, J.L. Goldstein, and M.S. Brown. 1987. Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia. J. Biol. Chem. 262: 3354-3356.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 3354-3356
-
-
Lehrman, M.A.1
Russell, D.W.2
Goldstein, J.L.3
Brown, M.S.4
-
55
-
-
0029556272
-
Evolution and biological significance of human retroelements
-
Leib-Mosch, C. and W. Seifarth. 1995. Evolution and biological significance of human retroelements. Virus Genes 11: 133-145.
-
(1995)
Virus Genes
, vol.11
, pp. 133-145
-
-
Leib-Mosch, C.1
Seifarth, W.2
-
56
-
-
0026548122
-
Characterization of a low copy repetitive element S232 involved in the generation of frequent deletions of the distal short arm of the human X chromosome
-
Li, X-M., P.H. Yen, and L.J. Shapiro. 1992. Characterization of a low copy repetitive element S232 involved in the generation of frequent deletions of the distal short arm of the human X chromosome. Nucleic Acids Res. 20: 1117-1122.
-
(1992)
Nucleic Acids Res.
, vol.20
, pp. 1117-1122
-
-
Li, X.-M.1
Yen, P.H.2
Shapiro, L.J.3
-
57
-
-
0026580019
-
A chimaeric 11-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension
-
Lifton, R.P., R.G. Dluhy, M. Powers, M. Rich, S. Cook, S. Ulick, and J.-M. Lalouel. 1992. A chimaeric 11-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension. Nature 355: 262-265.
-
(1992)
Nature
, vol.355
, pp. 262-265
-
-
Lifton, R.P.1
Dluhy, R.G.2
Powers, M.3
Rich, M.4
Cook, S.5
Ulick, S.6
Lalouel, J.-M.7
-
58
-
-
0029909565
-
A mutation in Mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53
-
Lim, D.-S. and P. Hasty. 1996. A mutation in Mouse rad51 results in an early embryonic lethal that is suppressed by a mutation in p53. Mol. Cell. Biol. 16: 7133-7143.
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 7133-7143
-
-
Lim, D.-S.1
Hasty, P.2
-
59
-
-
0029113034
-
The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes
-
Lyle, R., T.J. Wright, L.N. Clark, and J.E. Hewitt. 1995. The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes. Genomics 28: 389-397.
-
(1995)
Genomics
, vol.28
, pp. 389-397
-
-
Lyle, R.1
Wright, T.J.2
Clark, L.N.3
Hewitt, J.E.4
-
60
-
-
0027511117
-
Sex chromosomes, recombination and chromatin conformation
-
McKee, B.D. and M.A. Handel. 1993. Sex chromosomes, recombination and chromatin conformation. Chromosoma 102: 71-80.
-
(1993)
Chromosoma
, vol.102
, pp. 71-80
-
-
McKee, B.D.1
Handel, M.A.2
-
61
-
-
0027255247
-
A mouse homologue of the Escherichia coli RecA and Saccharomyces cerevisiae RAD51 genes
-
Morita, T., Y. Yoshimura, A. Yamamoto, K. Murata, M. Mori, H. Yamamoto, and A. Matsushiro. 1993. A mouse homologue of the Escherichia coli RecA and Saccharomyces cerevisiae RAD51 genes. Proc. Natl. Acad. Sci. 90: 6577-6580.
-
(1993)
Proc. Natl. Acad. Sci.
, vol.90
, pp. 6577-6580
-
-
Morita, T.1
Yoshimura, Y.2
Yamamoto, A.3
Murata, K.4
Mori, M.5
Yamamoto, H.6
Matsushiro, A.7
-
62
-
-
0022695490
-
Molecular genetics of human color vision: The genes encoding blue, green and red pigments
-
Nathans, J., D. Thomas, and D.S. Hogness. 1986. Molecular genetics of human color vision: The genes encoding blue, green and red pigments. Science 232: 193-202.
-
(1986)
Science
, vol.232
, pp. 193-202
-
-
Nathans, J.1
Thomas, D.2
Hogness, D.S.3
-
63
-
-
0023647951
-
Recombination at the human alpha-globin gene cluster: Sequence features and topological constraints
-
Nicholls, R.D., N. Fischel-Ghodsian, and D.R. Higgs. 1987. Recombination at the human alpha-globin gene cluster: Sequence features and topological constraints. Cell 49: 369-378.
-
(1987)
Cell
, vol.49
, pp. 369-378
-
-
Nicholls, R.D.1
Fischel-Ghodsian, N.2
Higgs, D.R.3
-
64
-
-
85036482272
-
Two structural and synthetical variants, Hb Miyada and homozygous δ-thalassemia, discovered in Japanese
-
Verlag, Munich, Germany
-
Ohta, Y., K. Yamaoka, I. Sumida, S. Fujita, T. Fujimura, M. Hadana, and T. Yanase. 1970. Two structural and synthetical variants, Hb Miyada and homozygous δ-thalassemia, discovered in Japanese. XIII International Congress of Haematology, Verlag, Munich, Germany.
-
(1970)
XIII International Congress of Haematology
-
-
Ohta, Y.1
Yamaoka, K.2
Sumida, I.3
Fujita, S.4
Fujimura, T.5
Hadana, M.6
Yanase, T.7
-
65
-
-
0014570210
-
Hemoglobin-Lepore-Baltimore, a third type of a δ-β crossover (δ50,β86)
-
Ostertag W. and E.W. Smith. 1969. Hemoglobin-Lepore-Baltimore, a third type of a δ-β crossover (δ50,β86). Eur. J. Biochem. 10: 371-376.
-
(1969)
Eur. J. Biochem.
, vol.10
, pp. 371-376
-
-
Ostertag, W.1
Smith, E.W.2
-
66
-
-
0027759563
-
Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: Unequal nonsister chromatid exchange during spermatogenesis
-
Palau, F., A. Lofgren, P. De Jonghe, S. Bort, E. Nelis, T. Sevilla, J.J. Martin, J. Vilchez, F. Prieto, and C. Van Broeckhoven. 1993. Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis. Hum. Mol. Genet. 2: 2031-2035.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 2031-2035
-
-
Palau, F.1
Lofgren, A.2
De Jonghe, P.3
Bort, S.4
Nelis, E.5
Sevilla, T.6
Martin, J.J.7
Vilchez, J.8
Prieto, F.9
Van Broeckhoven, C.10
-
67
-
-
0028231331
-
Charcot-Marie Tooth disease: A new paradigm for the mechanism of inherited disease
-
Patel, P.I., and J.R. Lupski. 1994. Charcot-Marie Tooth disease: A new paradigm for the mechanism of inherited disease. Trends Genet. 10: 128-133.
-
(1994)
Trends Genet.
, vol.10
, pp. 128-133
-
-
Patel, P.I.1
Lupski, J.R.2
-
68
-
-
0027017033
-
Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit
-
Pentao, L., C.A. Wise, A.C. Chinault, P.I. Patel, and J.R. Lupski. 1992. Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit. Nature Genet. 2: 292-300.
-
(1992)
Nature Genet.
, vol.2
, pp. 292-300
-
-
Pentao, L.1
Wise, C.A.2
Chinault, A.C.3
Patel, P.I.4
Lupski, J.R.5
-
69
-
-
15844409417
-
Presynaptic association of Rad51 protein with selected sites in meiotic chromatin
-
Plug, A.W., J. Xu, G. Reddy, E.I. Golub, and T. Ashley. 1996. Presynaptic association of Rad51 protein with selected sites in meiotic chromatin. Prof. Natl. Acad. Sci. 93: 5920-5924.
-
(1996)
Prof. Natl. Acad. Sci.
, vol.93
, pp. 5920-5924
-
-
Plug, A.W.1
Xu, J.2
Reddy, G.3
Golub, E.I.4
Ashley, T.5
-
70
-
-
0025997898
-
Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT1A)
-
Raeymaekers P., V. Timmerman, E. Nelis, P. De Jonghe, J.E. Hoogendijk, F. Bass, D.F Barker, J.J. Martin, M. De Visser, P.A. Bolhuis, and C. Van Broeckhoven. 1991. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT1A). Neuromusc. Disord. 1: 93-97.
-
(1991)
Neuromusc. Disord.
, vol.1
, pp. 93-97
-
-
Raeymaekers, P.1
Timmerman, V.2
Nelis, E.3
De Jonghe, P.4
Hoogendijk, J.E.5
Bass, F.6
Barker, D.F.7
Martin, J.J.8
De Visser, M.9
Bolhuis, P.A.10
Van Broeckhoven, C.11
-
71
-
-
0028842154
-
Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28
-
Rathmann, M., S. Bunge, C. Steglich, E. Schwinger, and A. Gal. 1995. Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28. Hum. Genet. 95: 34-38.
-
(1995)
Hum. Genet.
, vol.95
, pp. 34-38
-
-
Rathmann, M.1
Bunge, S.2
Steglich, C.3
Schwinger, E.4
Gal, A.5
-
72
-
-
0029962292
-
A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element
-
Reiter, L.T., T. Murakami, T. Koeuth, L. Pentao, D. Muzny, R. Gibbs, and J. Lupski. 1996. A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element. Nature Genet. 12: 288-297.
-
(1996)
Nature Genet.
, vol.12
, pp. 288-297
-
-
Reiter, L.T.1
Murakami, T.2
Koeuth, T.3
Pentao, L.4
Muzny, D.5
Gibbs, R.6
Lupski, J.7
-
73
-
-
0029001828
-
Sex-specific meitoic recombination in the Prader-Willi/Angelman syndrome imprinted region
-
Robinson, W.P. and M. Lalande. 1995. Sex-specific meitoic recombination in the Prader-Willi/Angelman syndrome imprinted region. Hum. Mol. Genet. 4: 801-806.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 801-806
-
-
Robinson, W.P.1
Lalande, M.2
-
74
-
-
0028180964
-
Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells
-
Rossiter, J.P., M. Young, M.L. Kimberland, P. Hutter, R.P. Ketterling, J. Gitschier, J. Horst, M.A. Morris, D.J. Schaid, P. deMoerloose, S. Sommer, H.H. Kazazian, and S.E. Antonarakis. 1994. Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells. Hum. Mol. Genet 3: 1035-1039.
-
(1994)
Hum. Mol. Genet
, vol.3
, pp. 1035-1039
-
-
Rossiter, J.P.1
Young, M.2
Kimberland, M.L.3
Hutter, P.4
Ketterling, R.P.5
Gitschier, J.6
Horst, J.7
Morris, M.A.8
Schaid, D.J.9
DeMoerloose, P.10
Sommer, S.11
Kazazian, H.H.12
Antonarakis, S.E.13
-
75
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and meiotic cells
-
Scully, R., J. Chen, A. Plug, Y. Xiao, D. Weaver, J. Feunteun, T. Ashley, and D.M. Livingston. 1997. Association of BRCA1 with Rad51 in mitotic and meiotic cells. Cell 88: 265-275.
-
(1997)
Cell
, vol.88
, pp. 265-275
-
-
Scully, R.1
Chen, J.2
Plug, A.3
Xiao, Y.4
Weaver, D.5
Feunteun, J.6
Ashley, T.7
Livingston, D.M.8
-
76
-
-
0030933762
-
Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2
-
Sharan, S.K., M. Morimatsu, U. Albrecht, D.-S. Lim, E. Regel, C. Dinh, A. Sands, G. Eichele, P. Hasty, and A. Bradley. 1997. Embryonic lethality and radiation hypersensitivity mediated by Rad51 in mice lacking Brca2. Nature 386: 804-810.
-
(1997)
Nature
, vol.386
, pp. 804-810
-
-
Sharan, S.K.1
Morimatsu, M.2
Albrecht, U.3
Lim, D.-S.4
Regel, E.5
Dinh, C.6
Sands, A.7
Eichele, G.8
Hasty, P.9
Bradley, A.10
-
77
-
-
0026751113
-
Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein
-
Shinohara, A., H. Ogawa, and T. Ogawa. 1992. Rad51 protein involved in repair and recombination in S. cerevisiae is a RecA-like protein. Cell 69: 457-470.
-
(1992)
Cell
, vol.69
, pp. 457-470
-
-
Shinohara, A.1
Ogawa, H.2
Ogawa, T.3
-
78
-
-
0027325816
-
Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and RecA
-
Shinohara, A., H. Ogawa, Y. Matsuda, N. Ushio, K. Ikeo, and T. Ogawa. 1993. Cloning of human, mouse and fission yeast recombination genes homologous to RAD51 and RecA. Nature Genet. 4: 239-243.
-
(1993)
Nature Genet.
, vol.4
, pp. 239-243
-
-
Shinohara, A.1
Ogawa, H.2
Matsuda, Y.3
Ushio, N.4
Ikeo, K.5
Ogawa, T.6
-
79
-
-
0020044638
-
SINEs and LINEs: Highly repeated short and long interspersed sequences in mammalian genomes
-
Singer, M.F. 1982. SINEs and LINEs: Highly repeated short and long interspersed sequences in mammalian genomes. Cell 28: 433-434.
-
(1982)
Cell
, vol.28
, pp. 433-434
-
-
Singer, M.F.1
-
80
-
-
0025218871
-
Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency
-
Sinnott, P.J., S. Collier, C. Costigan, P.A. Dyer, R. Harris, and T. Strachan. 1990. Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency. Proc. Natl. Acad. Sci. 87: 2107-2111.
-
(1990)
Proc. Natl. Acad. Sci.
, vol.87
, pp. 2107-2111
-
-
Sinnott, P.J.1
Collier, S.2
Costigan, C.3
Dyer, P.A.4
Harris, R.5
Strachan, T.6
-
81
-
-
0031005848
-
Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats
-
Small, K., J. Iber, and S.T. Warren. 1997. Emerin deletion reveals a common X-chromosome inversion mediated by inverted repeats. Nature Genet. 16: 96-99.
-
(1997)
Nature Genet.
, vol.16
, pp. 96-99
-
-
Small, K.1
Iber, J.2
Warren, S.T.3
-
82
-
-
0026935108
-
Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome
-
Smith S.A., D.F. Easton, D.G. Evans, and B.A. Ponder. 1992. Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome. Nature Genet. 2: 128-131.
-
(1992)
Nature Genet.
, vol.2
, pp. 128-131
-
-
Smith, S.A.1
Easton, D.F.2
Evans, D.G.3
Ponder, B.A.4
-
83
-
-
0024435146
-
Homologous recombination in E. coli: Multiple pathways for multiple reasons
-
Smith, G.R. 1989. Homologous recombination in E. coli: Multiple pathways for multiple reasons. Cell 58: 807-809.
-
(1989)
Cell
, vol.58
, pp. 807-809
-
-
Smith, G.R.1
-
84
-
-
0028844757
-
Homologous unequal cross-over involving a 2.8 kb direct repeat as a mechanism for the generation of allelic variants of human cytochrome P450 CYP2D6 gene
-
Steen, V.M., A. Molven, N.K. Aarskog, and A.K. Gulbrandsen. 1995. Homologous unequal cross-over involving a 2.8 kb direct repeat as a mechanism for the generation of allelic variants of human cytochrome P450 CYP2D6 gene. Hum. Mol. Genet. 4: 2251-2257.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2251-2257
-
-
Steen, V.M.1
Molven, A.2
Aarskog, N.K.3
Gulbrandsen, A.K.4
-
85
-
-
0025997032
-
Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients
-
Stoppa-Lyonnet, D., C. Duponchel, T. Meo, J. Laurent, P.E. Carter, M. Arala-Chaves, J.H. Cohen, G. Dewald, J. Goetz, G. Hauptmann, G. Lagrue, P. Lesavre, M. Lopez-Trascasa, G. Misiano, C. Moraine, A. Sobel, P.J. Spath, and M. Tosi. 1991. Recombinational biases in the rearranged C1-inhibitor genes of hereditary angioedema patients. Am. J. Hum. Genet. 49: 1055-1062.
-
(1991)
Am. J. Hum. Genet.
, vol.49
, pp. 1055-1062
-
-
Stoppa-Lyonnet, D.1
Duponchel, C.2
Meo, T.3
Laurent, J.4
Carter, P.E.5
Arala-Chaves, M.6
Cohen, J.H.7
Dewald, G.8
Goetz, J.9
Hauptmann, G.10
Lagrue, G.11
Lesavre, P.12
Lopez-Trascasa, M.13
Misiano, G.14
Moraine, C.15
Sobel, A.16
Spath, P.J.17
Tosi, M.18
-
86
-
-
0029969418
-
p53 is linked directly to homologous recombination processes via RAD51/RECA protein interaction
-
Sturzbecher, H.W., B. Donzelmann, W. Henning, U. Knippschild, and S. Buchop. 1996. p53 is linked directly to homologous recombination processes via RAD51/RECA protein interaction. EMBO J. 15: 1992-2002.
-
(1996)
EMBO J.
, vol.15
, pp. 1992-2002
-
-
Sturzbecher, H.W.1
Donzelmann, B.2
Henning, W.3
Knippschild, U.4
Buchop, S.5
-
87
-
-
0028200226
-
Identification of illegitimate recombination hot spot of the retinoic acid receptor alpha gene involved in 15;17 chromosomal translocation of acute promyelocytic leukemia
-
Tashiro, S., N. Kotomura, K. Tanaka, K. Suzuki, T. Kyo, H. Dohy, O. Niwa, and N. Kamada. 1994. Identification of illegitimate recombination hot spot of the retinoic acid receptor alpha gene involved in 15;17 chromosomal translocation of acute promyelocytic leukemia. Oncogene 9: 1939-1945.
-
(1994)
Oncogene
, vol.9
, pp. 1939-1945
-
-
Tashiro, S.1
Kotomura, N.2
Tanaka, K.3
Suzuki, K.4
Kyo, T.5
Dohy, H.6
Niwa, O.7
Kamada, N.8
-
88
-
-
0028894976
-
Nuclear proteins binding to the recombination hotspot region of the retinoic acid receptor alpha gene
-
Tashiro S., Z.W. Wang, N. Kotomura, M. Eguchi, O. Niwa, K. Ueda, and N. Kamada. 1995. Nuclear proteins binding to the recombination hotspot region of the retinoic acid receptor alpha gene. Cancer Res. Ther. Control 4: 293.
-
(1995)
Cancer Res. Ther. Control
, vol.4
, pp. 293
-
-
Tashiro, S.1
Wang, Z.W.2
Kotomura, N.3
Eguchi, M.4
Niwa, O.5
Ueda, K.6
Kamada, N.7
-
89
-
-
0029987450
-
Targeted disruption of the rad51 gene leads to lethality in embryonic mice
-
Tsuzuki, T., Y. Fujii, K. Sakumi, Y. Tominaga, K. Nakao, M. Sekiguchi, A. Matsuhiro, Y. Yoshimura, and T. Morita. 1996. Targeted disruption of the rad51 gene leads to lethality in embryonic mice. Proc. Natl. Acad. Sci. 93: 6236-6240.
-
(1996)
Proc. Natl. Acad. Sci.
, vol.93
, pp. 6236-6240
-
-
Tsuzuki, T.1
Fujii, Y.2
Sakumi, K.3
Tominaga, Y.4
Nakao, K.5
Sekiguchi, M.6
Matsuhiro, A.7
Yoshimura, Y.8
Morita, T.9
-
90
-
-
0027744223
-
FSHD-associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit
-
van Deutekom, J.C., C. Wijmenga, E.A. van Tienhoven, A.M. Gruter, J.E. Hewitt, G.W. Padberg, G.J. van Ommen, M.H. Hofker, and R.R. Frants. 1993. FSHD-associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit. Hum. Mol. Genet. 2: 2037-2042.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 2037-2042
-
-
Van Deutekom, J.C.1
Wijmenga, C.2
Van Tienhoven, E.A.3
Gruter, A.M.4
Hewitt, J.E.5
Padberg, G.W.6
Van Ommen, G.J.7
Hofker, M.H.8
Frants, R.R.9
-
91
-
-
1842329056
-
Molecular basis of human growth hormone gene deletions
-
Vnencak-Jones, C.L., J.A. Phillips III, E.Y. Chen, and P.H. Seeburg. 1988. Molecular basis of human growth hormone gene deletions. Proc. Natl. Acad. Sci. 85: 5615-5619.
-
(1988)
Proc. Natl. Acad. Sci.
, vol.85
, pp. 5615-5619
-
-
Vnencak-Jones, C.L.1
Phillips III, J.A.2
Chen, E.Y.3
Seeburg, P.H.4
-
92
-
-
0025673701
-
Hot spots for growth hormone gene deletions in homologous regions outside of Alu repeats
-
Vnencak-Jones, C.L, and J.A. Phillips III. 1990. Hot spots for growth hormone gene deletions in homologous regions outside of Alu repeats. Science 250: 1745-1748.
-
(1990)
Science
, vol.250
, pp. 1745-1748
-
-
Vnencak-Jones, C.L.1
Phillips III, J.A.2
-
93
-
-
0025189579
-
Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code."
-
Vogt, P. 1990. Potential genetic functions of tandem repeated DNA sequence blocks in the human genome are based on a highly conserved "chromatin folding code." Hum. Genet. 84: 301-306.
-
(1990)
Hum. Genet.
, vol.84
, pp. 301-306
-
-
Vogt, P.1
-
94
-
-
0025190946
-
Hypervariable minisatellite DNA is a hotspot for homologous recombination in human cells
-
Wahls, W.P., L.J. Wallace, and P.D. Moore. 1990. Hypervariable minisatellite DNA is a hotspot for homologous recombination in human cells. Cell 60: 95-103.
-
(1990)
Cell
, vol.60
, pp. 95-103
-
-
Wahls, W.P.1
Wallace, L.J.2
Moore, P.D.3
-
95
-
-
0021846940
-
Meiotic chromosome pairing in the normal female
-
Wallace, B.M.K. and M.A. Hulten. 1985. Meiotic chromosome pairing in the normal female. Annu. Hum. Genet. 49: 215-226.
-
(1985)
Annu. Hum. Genet.
, vol.49
, pp. 215-226
-
-
Wallace, B.M.K.1
Hulten, M.A.2
-
96
-
-
0020490330
-
Specific sequences in native DNA that arrest synthesis by DNA polymerase α
-
Weaver, D.T. and M.L. DePamphilis. 1982. Specific sequences in native DNA that arrest synthesis by DNA polymerase α. J. Biol. Chem. 257: 2075-2086.
-
(1982)
J. Biol. Chem.
, vol.257
, pp. 2075-2086
-
-
Weaver, D.T.1
DePamphilis, M.L.2
-
97
-
-
0029798271
-
The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region
-
Winokur, S.T., U. Bengtsson, J.C. Vargas, J.J. Wasmuth, and M.R. Altherr. 1996. The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region. Hum. Mol. Genet. 5: 1567-1575.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 1567-1575
-
-
Winokur, S.T.1
Bengtsson, U.2
Vargas, J.C.3
Wasmuth, J.J.4
Altherr, M.R.5
-
98
-
-
0027374931
-
Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggests a high frequency of the CMT1A duplication
-
Wise, C.A., C.A. Garcia, S.N. Davis, Z. Heju, L. Pentao, P.I. Patel, and J.R. Lupski. 1993. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggests a high frequency of the CMT1A duplication. Am. J. Hum. Genet. 53: 853-863.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 853-863
-
-
Wise, C.A.1
Garcia, C.A.2
Davis, S.N.3
Heju, Z.4
Pentao, L.5
Patel, P.I.6
Lupski, J.R.7
-
99
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster, R., S.L. Neuhausen, J. Mangion, Y. Quirk, D. Ford, N. Collins, K. Nguyen, S. Seal, T. Tran, D. Averill, P. Fields, G. Marshall, S. Narod, G.M. Lenoir, H. Lynch, J. Feunteun, P. Devilee, C.J. Cornelisse, F.H. Menko, P.A. Daly, W. Orminston, R. McMannus, C. Pye, C.M. Lewis, L.A. Cannon-Albright, J. Peto, B.A.J. Ponder, M.H. Skolnick, D.F. Easton, D.E. Goldgar, and M.R. Stratton. 1994. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 265: 2088-2090.
-
(1994)
Science
, vol.265
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
Nguyen, K.7
Seal, S.8
Tran, T.9
Averill, D.10
Fields, P.11
Marshall, G.12
Narod, S.13
Lenoir, G.M.14
Lynch, H.15
Feunteun, J.16
Devilee, P.17
Cornelisse, C.J.18
Menko, F.H.19
Daly, P.A.20
Orminston, W.21
McMannus, R.22
Pye, C.23
Lewis, C.M.24
Cannon-Albright, L.A.25
Peto, J.26
Ponder, B.A.J.27
Skolnick, M.H.28
Easton, D.F.29
Goldgar, D.E.30
Stratton, M.R.31
more..
-
100
-
-
0025280088
-
Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repititive elements
-
Yen, P.H., X-M. Li, S.-P. Tsai, C. Johnson, T. Mohandas, and L.J. Shapiro. 1990. Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repititive elements. Cell 61: 603-610.
-
(1990)
Cell
, vol.61
, pp. 603-610
-
-
Yen, P.H.1
Li, X.-M.2
Tsai, S.-P.3
Johnson, C.4
Mohandas, T.5
Shapiro, L.J.6
-
101
-
-
0027278710
-
Cloning and sequence of the human RecA-like gene cDNA
-
Yoshimura, Y., T. Morita, A. Yamamoto, A. Matsushiro. 1993. Cloning and sequence of the human RecA-like gene cDNA. Nucleic Acids Res. 21: 1665.
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 1665
-
-
Yoshimura, Y.1
Morita, T.2
Yamamoto, A.3
Matsushiro, A.4
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