-
1
-
-
0027476083
-
Identification of new genes required for meiotic recombination in Saccharomyces cerevisiae
-
Ajimura, M., Leem, S.H., and Ogawa, H. (1993). Identification of new genes required for meiotic recombination in Saccharomyces cerevisiae. Genetics 133, 51-66.
-
(1993)
Genetics
, vol.133
, pp. 51-66
-
-
Ajimura, M.1
Leem, S.H.2
Ogawa, H.3
-
2
-
-
0024590169
-
Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia
-
Bigbee, W.L., Langlois, R.G., Swift, M., and Jensen, R.H. (1989). Evidence for an elevated frequency of in vivo somatic cell mutations in ataxia telangiectasia. Am. J. Hum. Genet. 44, 402-408.
-
(1989)
Am. J. Hum. Genet.
, vol.44
, pp. 402-408
-
-
Bigbee, W.L.1
Langlois, R.G.2
Swift, M.3
Jensen, R.H.4
-
3
-
-
0025734394
-
Fibroblasts from ataxia telangiectasia (AT) and AT heterozygotes show an enhanced level of residual DNA double-strand breaks after low dose-rate γ-irradiation as assayed by pulsed field gel electrophoresis
-
Blocher, D., Sigut, D., and Hannan, M.A. (1991). Fibroblasts from ataxia telangiectasia (AT) and AT heterozygotes show an enhanced level of residual DNA double-strand breaks after low dose-rate γ-irradiation as assayed by pulsed field gel electrophoresis. Int. J. Radiat. Biol. 60, 791-802.
-
(1991)
Int. J. Radiat. Biol.
, vol.60
, pp. 791-802
-
-
Blocher, D.1
Sigut, D.2
Hannan, M.A.3
-
4
-
-
0023262454
-
Effects of Bloom's syndrome fibroblasts on genetic recombination and mutagenesis of herpes simplex virus type 1
-
Bubley, G.J., and Schnipper, L.E. (1987). Effects of Bloom's syndrome fibroblasts on genetic recombination and mutagenesis of herpes simplex virus type 1. Somat. Cell Mol. Genet. 13, 111-117.
-
(1987)
Somat. Cell Mol. Genet.
, vol.13
, pp. 111-117
-
-
Bubley, G.J.1
Schnipper, L.E.2
-
5
-
-
0346351375
-
A many fold increase in sister chromatid exchange in Bloom's syndrome lymphocytes
-
Chaganti, R.S.K., Schonberg, S., and German, J.A. (1974). A many fold increase in sister chromatid exchange in Bloom's syndrome lymphocytes. Proc. Natl. Acad. Sci. USA 71, 4508-4512.
-
(1974)
Proc. Natl. Acad. Sci. USA
, vol.71
, pp. 4508-4512
-
-
Chaganti, R.S.K.1
Schonberg, S.2
German, J.A.3
-
6
-
-
0024569179
-
DNA repair in man
-
Cleaver, J.E. (1989). DNA repair in man. Birth Defects 25, 61-82.
-
(1989)
Birth Defects
, vol.25
, pp. 61-82
-
-
Cleaver, J.E.1
-
7
-
-
0030089480
-
The sbcC and sbcD genes of Escherichia coli encode a nuclease involved in palindrome inviability and genetic recombination
-
Connelly, J.C., and Leach, D.R.F. (1996). The sbcC and sbcD genes of Escherichia coli encode a nuclease involved in palindrome inviability and genetic recombination. Genes Cells 1, 285-291.
-
(1996)
Genes Cells
, vol.1
, pp. 285-291
-
-
Connelly, J.C.1
Leach, D.R.F.2
-
8
-
-
0030756165
-
Overexpression, purification, and characterization of the SbcCD protein from Escherichia coli
-
Connelly, J.C., de Leau, E.S., Okely, E.A., and Leach, D.R. (1997). Overexpression, purification, and characterization of the SbcCD protein from Escherichia coli. J. Biol. Chem. 272, 19819-19826.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 19819-19826
-
-
Connelly, J.C.1
De Leau, E.S.2
Okely, E.A.3
Leach, D.R.4
-
9
-
-
0021978722
-
On the nature of a defect in cells from individuals with ataxia-telangiectasia
-
Cornforth, M.N., and Bedford, J.S. (1985). On the nature of a defect in cells from individuals with ataxia-telangiectasia. Science 227, 1589-1591.
-
(1985)
Science
, vol.227
, pp. 1589-1591
-
-
Cornforth, M.N.1
Bedford, J.S.2
-
10
-
-
0029742576
-
Human Rad50 is physically associated with hMre11: Identification of a conserved multiprotein complex implicated in recombinational DNA repair
-
Dolganov, G.M., Maser, R.S., Novikov, A., Tosto, L., Chong, S., Bressan, D.A., and Petrini, J.H.J. (1996). Human Rad50 is physically associated with hMre11: identification of a conserved multiprotein complex implicated in recombinational DNA repair. Mol. Cell. Biol. 16, 4832-4841.
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 4832-4841
-
-
Dolganov, G.M.1
Maser, R.S.2
Novikov, A.3
Tosto, L.4
Chong, S.5
Bressan, D.A.6
Petrini, J.H.J.7
-
11
-
-
0027251721
-
The retinoblastoma protein associates with the protein phosphatase type 1 catalytic subunit
-
Durfee, T., Becherer, K., Chen, P.-L., Yeh, S.-H., Yang, Y., Kilburn, A.E., Lee, W.H., and Elledge, S.J. (1993). The retinoblastoma protein associates with the protein phosphatase type 1 catalytic subunit. Genes Dev. 7, 555-569.
-
(1993)
Genes Dev.
, vol.7
, pp. 555-569
-
-
Durfee, T.1
Becherer, K.2
Chen, P.-L.3
Yeh, S.-H.4
Yang, Y.5
Kilburn, A.E.6
Lee, W.H.7
Elledge, S.J.8
-
12
-
-
0030861685
-
DNA helicases in inherited human disorders
-
Ellis, N.A. (1997). DNA helicases in inherited human disorders. Curr. Opin. Genet. Dev. 7, 354-363.
-
(1997)
Curr. Opin. Genet. Dev.
, vol.7
, pp. 354-363
-
-
Ellis, N.A.1
-
13
-
-
0000857494
-
An approach to correlate MS/MS data to amino acid sequences in protein database
-
Eng, J., McCormack, A.L., and Yates, J.R., III. (1994). An approach to correlate MS/MS data to amino acid sequences in protein database. J. Am. Soc. Mass Spectrom. 5, 976-989.
-
(1994)
J. Am. Soc. Mass Spectrom.
, vol.5
, pp. 976-989
-
-
Eng, J.1
McCormack, A.L.2
Yates J.R. III3
-
14
-
-
0024465870
-
Mutator phenotype of Werner syndrome is characterized by extensive deletions
-
Fukuchi, K.-I., Martin, G.M., and Monnat, R.J.(1989). Mutator phenotype of Werner syndrome is characterized by extensive deletions. Proc. Natl. Acad. Sci. USA 86, 5893-5897.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 5893-5897
-
-
Fukuchi, K.-I.1
Martin, G.M.2
Monnat, R.J.3
-
15
-
-
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. Cancer Biol. 4, 73-83.
-
(1993)
Cancer Biol.
, vol.4
, pp. 73-83
-
-
Game, J.C.1
-
16
-
-
0025780420
-
Ataxia-telangiectasia: An interdisciplinary approach to pathogenesis
-
Gatti, R.A., Boder, E., Vinters, H.V., Sparkes, R.S., Norman, A., and Lange, K. (1991). Ataxia-telangiectasia: an interdisciplinary approach to pathogenesis. Medicine 70, 99-117.
-
(1991)
Medicine
, vol.70
, pp. 99-117
-
-
Gatti, R.A.1
Boder, E.2
Vinters, H.V.3
Sparkes, R.S.4
Norman, A.5
Lange, K.6
-
17
-
-
0030966099
-
Recent advances in understanding V(D)J recombination
-
Geliert, M. (1997). Recent advances in understanding V(D)J recombination. Adv. Immunol. 64, 39-64.
-
(1997)
Adv. Immunol.
, vol.64
, pp. 39-64
-
-
Geliert, M.1
-
18
-
-
0001863965
-
Patterns of neoplasia associated with the chromosome-breakage syndromes
-
J. German, ed. (New York: Alan R. Liss)
-
German, J. (1983). Patterns of neoplasia associated with the chromosome-breakage syndromes. In Chromosome Mutation and Neoplasia, J. German, ed. (New York: Alan R. Liss), pp. 11-21.
-
(1983)
Chromosome Mutation and Neoplasia
, pp. 11-21
-
-
German, J.1
-
19
-
-
0026551842
-
Identification of sbcD mutations as cosuppressors of recBC that allow propagation of DNA palindromes in Escherichia coli K-12
-
Gibson, F.P., Leach, D.R.F., and Lloyd, R.G. (1992). Identification of sbcD mutations as cosuppressors of recBC that allow propagation of DNA palindromes in Escherichia coli K-12. J. Bacteriol. 174, 1222-1228.
-
(1992)
J. Bacteriol.
, vol.174
, pp. 1222-1228
-
-
Gibson, F.P.1
Leach, D.R.F.2
Lloyd, R.G.3
-
21
-
-
0030977349
-
Responses to DNA damage and regulation of cell cycle checkpoints by the ATM protein kinase family
-
Hoekstra, M.F. (1997). Responses to DNA damage and regulation of cell cycle checkpoints by the ATM protein kinase family. Curr. Opin. Genet. Dev. 7, 170-175.
-
(1997)
Curr. Opin. Genet. Dev.
, vol.7
, pp. 170-175
-
-
Hoekstra, M.F.1
-
22
-
-
0028796434
-
Spontaneous chromosomal aberrations in Fanconi anaemia, ataxia telangiectasia fibroblast and Bloom's syndrome lymphoblastoid cell lines as detected by conventional cytogenetic analysis and fluorescence in situ hybridisation (FISH) technique
-
Hojo, E.T., van Diemen, P.C., Darroudi, F., and Natarajan, A.T. (1995). Spontaneous chromosomal aberrations in Fanconi anaemia, ataxia telangiectasia fibroblast and Bloom's syndrome lymphoblastoid cell lines as detected by conventional cytogenetic analysis and fluorescence in situ hybridisation (FISH) technique. Mut. Res. 334, 59-69.
-
(1995)
Mut. Res.
, vol.334
, pp. 59-69
-
-
Hojo, E.T.1
Van Diemen, P.C.2
Darroudi, F.3
Natarajan, A.T.4
-
23
-
-
0027304013
-
V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder
-
Hsieh, C.-L., Arlett, C.F., and Leiber, M.R. (1993). V(D)J recombination in ataxia telangiectasia, Bloom's syndrome, and a DNA ligase I-associated immunodeficiency disorder. J. Biol. Chem. 268, 20105-20109.
-
(1993)
J. Biol. Chem.
, vol.268
, pp. 20105-20109
-
-
Hsieh, C.-L.1
Arlett, C.F.2
Leiber, M.R.3
-
24
-
-
0028212415
-
Mutations in XRS2 and RAD50 delay but do not prevent mating-type switching in Saccharomyces cerevisiae
-
Ivanov, E.L., Sugawara, N., White, C.I., Fabre, F., and Haber, J.E. (1994). Mutations in XRS2 and RAD50 delay but do not prevent mating-type switching in Saccharomyces cerevisiae. Mol. Cell. Biol. 14, 3414-3425.
-
(1994)
Mol. Cell. Biol.
, vol.14
, pp. 3414-3425
-
-
Ivanov, E.L.1
Sugawara, N.2
White, C.I.3
Fabre, F.4
Haber, J.E.5
-
25
-
-
0030000946
-
Genetic requirements for the single-strand annealing pathway of double-strand break repair in Saccharomyces cerevisiae
-
Ivanov, E.L., Sugawara, N., Fishman-Lobell, J., and Haber, J.E. (1996). Genetic requirements for the single-strand annealing pathway of double-strand break repair in Saccharomyces cerevisiae. Genetics 142, 693-704.
-
(1996)
Genetics
, vol.142
, pp. 693-704
-
-
Ivanov, E.L.1
Sugawara, N.2
Fishman-Lobell, J.3
Haber, J.E.4
-
26
-
-
0029397873
-
Cancer predisposition. Ataxia-telangiectasia at the crossroads
-
Jackson, S.P. (1995). Cancer predisposition. Ataxia-telangiectasia at the crossroads. Curr. Biol. 5, 1210-1212.
-
(1995)
Curr. Biol.
, vol.5
, pp. 1210-1212
-
-
Jackson, S.P.1
-
27
-
-
0030455820
-
Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast
-
James, P., Halladay, J., and Craig, E.A. (1996). Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast. Genetics 144, 1425-1436.
-
(1996)
Genetics
, vol.144
, pp. 1425-1436
-
-
James, P.1
Halladay, J.2
Craig, E.A.3
-
28
-
-
0029906133
-
Cloning and expression of the multifunctional human fatty acid synthase and its subdomains in Escherichia coli
-
Jayakumar, A., Huang, W.Y., Raetz, B., Chirala, S.S., and Wakil, S.J. (1996). Cloning and expression of the multifunctional human fatty acid synthase and its subdomains in Escherichia coli. Proc. Natl. Acad. Sci. USA 93, 14509-14514.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 14509-14514
-
-
Jayakumar, A.1
Huang, W.Y.2
Raetz, B.3
Chirala, S.S.4
Wakil, S.J.5
-
29
-
-
0028914077
-
Interaction of Mre11 and Rad50: Two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae
-
Johzuka, K., and Ogawa, H. (1995). Interaction of Mre11 and Rad50: two proteins required for DNA repair and meiosis-specific double-strand break formation in Saccharomyces cerevisiae. Genetics 139, 1521-1532.
-
(1995)
Genetics
, vol.139
, pp. 1521-1532
-
-
Johzuka, K.1
Ogawa, H.2
-
30
-
-
0030786912
-
Nijmegen breakage syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation
-
Jongmans, W., Vuillaume, M., Chrzanowska, K., Smeets, D., Sperling, K., and Hall, J. (1997). Nijmegen breakage syndrome cells fail to induce the p53-mediated DNA damage response following exposure to ionizing radiation. Mol. Cell. Biol. 17, 5016-5022.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 5016-5022
-
-
Jongmans, W.1
Vuillaume, M.2
Chrzanowska, K.3
Smeets, D.4
Sperling, K.5
Hall, J.6
-
31
-
-
0028867842
-
Mismatch repair: Mechanisms and relationship to cancer susceptibility
-
Kolodner, R.D. (1995). Mismatch repair: mechanisms and relationship to cancer susceptibility. Trends Biochem. Sci. 20, 397-401.
-
(1995)
Trends Biochem. Sci.
, vol.20
, pp. 397-401
-
-
Kolodner, R.D.1
-
32
-
-
3142544243
-
Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome
-
Langlois, R.G., Bigbee, W.L., Jensen, R.H., and German, J. (1989). Evidence for increased in vivo mutation and somatic recombination in Bloom's syndrome. Proc. Natl. Acad. Sci. USA 86, 670-674.
-
(1989)
Proc. Natl. Acad. Sci. USA
, vol.86
, pp. 670-674
-
-
Langlois, R.G.1
Bigbee, W.L.2
Jensen, R.H.3
German, J.4
-
33
-
-
0030751012
-
Identifying the major proteome components of Haemophilus influenzae type-strain NCTC 8143
-
Link, A.J., Hays, L.G., Carmack, E.B., and Yates, J.R., III. (1997). Identifying the major proteome components of Haemophilus influenzae type-strain NCTC 8143. Electrophoresis 18, 1314-1334.
-
(1997)
Electrophoresis
, vol.18
, pp. 1314-1334
-
-
Link, A.J.1
Hays, L.G.2
Carmack, E.B.3
Yates J.R. III4
-
34
-
-
0030764691
-
hMre11 and hRad50 nuclear foci are induced during the normal cellular response to DNA double strand breaks
-
Maser, R.S., Monsen, K.J., Nelms, B.E., and Petrini, J.H.J. (1997). hMre11 and hRad50 nuclear foci are induced during the normal cellular response to DNA double strand breaks. Mol. Cell. Biol. 17, 6087-6096.
-
(1997)
Mol. Cell. Biol.
, vol.17
, pp. 6087-6096
-
-
Maser, R.S.1
Monsen, K.J.2
Nelms, B.E.3
Petrini, J.H.J.4
-
35
-
-
16944367119
-
Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24
-
Matsuura, S., Weemaes, C., Smeets, D., Takami, H., Kondo, N., Sakamoto, S., Yano, N., Nakamura, A., Tauchi, H., Endo, S., et al. (1997). Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24. Am. J. Hum. Genet. 60, 1487-1494.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1487-1494
-
-
Matsuura, S.1
Weemaes, C.2
Smeets, D.3
Takami, H.4
Kondo, N.5
Sakamoto, S.6
Yano, N.7
Nakamura, A.8
Tauchi, H.9
Endo, S.10
-
36
-
-
0027306104
-
High spontaneous rates of intrachromosomal recombination in ataxia-telangiectasia
-
Meyn, M.S. (1993). High spontaneous rates of intrachromosomal recombination in ataxia-telangiectasia. Science 260, 1327-1330.
-
(1993)
Science
, vol.260
, pp. 1327-1330
-
-
Meyn, M.S.1
-
37
-
-
0028880649
-
Ataxia-telangiectasia and cellular responses to DNA damage
-
Meyn, M.S. (1995). Ataxia-telangiectasia and cellular responses to DNA damage. Cancer Res. 55, 5991-6001.
-
(1995)
Cancer Res.
, vol.55
, pp. 5991-6001
-
-
Meyn, M.S.1
-
38
-
-
0028932603
-
Cell cycle regulation in response to DNA damage in mammalian cells: A historical perspective
-
Murnane, J.P. (1995). Cell cycle regulation in response to DNA damage in mammalian cells: a historical perspective. Cancer Metastasis Rev. 14, 17-29.
-
(1995)
Cancer Metastasis Rev.
, vol.14
, pp. 17-29
-
-
Murnane, J.P.1
-
39
-
-
0032562595
-
In situ visualization of double strand break repair in human fibroblasts
-
in press
-
Nelms, B.E., Maser, R.S., MacKay, J.F., Lagally, M.G., and Petrini, J.H.J. (1998). In situ visualization of double strand break repair in human fibroblasts. Science, in press.
-
(1998)
Science
-
-
Nelms, B.E.1
Maser, R.S.2
MacKay, J.F.3
Lagally, M.G.4
Petrini, J.H.J.5
-
40
-
-
0023931298
-
DNA repair synthesis in human fibroblasts requires DNA polymerase δ
-
Nishida, C., Reinhard, P., and Linn, S. (1988). DNA repair synthesis in human fibroblasts requires DNA polymerase δ. J. Biol. Chem. 263, 501-510.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 501-510
-
-
Nishida, C.1
Reinhard, P.2
Linn, S.3
-
41
-
-
0028943378
-
Functions of the yeast meiotic recombination genes, MRE11 and MRE2
-
Ogawa, H., Johzuka, K., Nakagawa, T., Leem, S., and Hagihara, A. (1995). Functions of the yeast meiotic recombination genes, MRE11 and MRE2. Adv. Biophys. 31, 67-76.
-
(1995)
Adv. Biophys.
, vol.31
, pp. 67-76
-
-
Ogawa, H.1
Johzuka, K.2
Nakagawa, T.3
Leem, S.4
Hagihara, A.5
-
42
-
-
0026663777
-
Initial chromosome damage but not DNA damage is greater in ataxia telangiectasia cells
-
Pandita, T.K., and Hittelman, W.N. (1992). Initial chromosome damage but not DNA damage is greater in ataxia telangiectasia cells. Radiat. Res. 130, 94-103.
-
(1992)
Radiat. Res.
, vol.130
, pp. 94-103
-
-
Pandita, T.K.1
Hittelman, W.N.2
-
43
-
-
0030997558
-
Chromosome instability with bleomycin and X-ray hypersensitivity in a boy with Nijmegen breakage syndrome
-
Perez-Vera, P., Gonzalez-del Angel, A., Molina, B., Gomez, L., Frias, S., Gatti, R.A., and Carnevale, A. (1997). Chromosome instability with bleomycin and X-ray hypersensitivity in a boy with Nijmegen breakage syndrome. Am. J. Med. Genet. 70, 24-27.
-
(1997)
Am. J. Med. Genet.
, vol.70
, pp. 24-27
-
-
Perez-Vera, P.1
Gonzalez-Del Angel, A.2
Molina, B.3
Gomez, L.4
Frias, S.5
Gatti, R.A.6
Carnevale, A.7
-
44
-
-
0027953084
-
Normal V(D)J coding junction formation in DNA ligase I deficiency syndromes
-
Petrini, J.H.J., Donovan, J.W., DiMare, C., and Weaver, D.T. (1994). Normal V(D)J coding junction formation in DNA ligase I deficiency syndromes. J. Immunol. 152, 176-183.
-
(1994)
J. Immunol.
, vol.152
, pp. 176-183
-
-
Petrini, J.H.J.1
Donovan, J.W.2
Dimare, C.3
Weaver, D.T.4
-
45
-
-
0029095108
-
Isolation and characterization of the human MRE11 homologue
-
Petrini, J.H.J., Walsh, M.E., Di Mare, C., Korenberg, J.R., Chen, X.-N., and Weaver, D.T. (1995). Isolation and characterization of the human MRE11 homologue. Genomics 29, 80-86.
-
(1995)
Genomics
, vol.29
, pp. 80-86
-
-
Petrini, J.H.J.1
Walsh, M.E.2
Di Mare, C.3
Korenberg, J.R.4
Chen, X.-N.5
Weaver, D.T.6
-
46
-
-
0031171269
-
The RAD52 epistasis group in mammalian double strand break repair
-
Petrini, J.H., Bressan, D.A., and Yao, M.S. (1997). The RAD52 epistasis group in mammalian double strand break repair. Semin. Immunol. 9, 181-188.
-
(1997)
Semin. Immunol.
, vol.9
, pp. 181-188
-
-
Petrini, J.H.1
Bressan, D.A.2
Yao, M.S.3
-
47
-
-
0027970838
-
Chromosomal translocations in human cancer
-
Rabbitts, T.H. (1994). Chromosomal translocations in human cancer. Nature 372, 143-149.
-
(1994)
Nature
, vol.372
, pp. 143-149
-
-
Rabbitts, T.H.1
-
48
-
-
0028229975
-
Chromosome translocations: Dangerous liaisons
-
Rowley, J.D. (1994). Chromosome translocations: dangerous liaisons. Leukemia 8 Suppl. 1, S1-S6.
-
(1994)
Leukemia
, vol.8
, Issue.SUPPL. 1
-
-
Rowley, J.D.1
-
49
-
-
0025633261
-
Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: Identification of 11q23 translocation break points with a yeast artifical chromosome
-
Rowley, J.D., Diaz, M.O., Espinosa, R., Patel, Y.D., van Melle, E., Ziemin, S., Taillon-Miller, P., Lichter, P., Evans, G.A., Kersey, J.D., et al. (1990). Mapping chromosome band 11q23 in human acute leukemia with biotinylated probes: identification of 11q23 translocation break points with a yeast artifical chromosome. Proc. Natl. Acad. Sci. USA 87, 9358-9362.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 9358-9362
-
-
Rowley, J.D.1
Diaz, M.O.2
Espinosa, R.3
Patel, Y.D.4
Van Melle, E.5
Ziemin, S.6
Taillon-Miller, P.7
Lichter, P.8
Evans, G.A.9
Kersey, J.D.10
-
50
-
-
16944366639
-
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21
-
Saar, K., Chrzanowska, K.H., Stumm, M., Jung, M., Nurnberg, G., Wienker, T.F., Seemanova, E., Wegner, R.D., Reis, A., and Sperling, K. (1997). The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21. Am. J. Hum. Genet. 60, 605-610.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 605-610
-
-
Saar, K.1
Chrzanowska, K.H.2
Stumm, M.3
Jung, M.4
Nurnberg, G.5
Wienker, T.F.6
Seemanova, E.7
Wegner, R.D.8
Reis, A.9
Sperling, K.10
-
51
-
-
0031472370
-
Association of BRCA1 with Rad51 in mitotic and meiotic cells
-
Scully, R., Chen, J., Plug, A., Xiao, Y., Weaver, D., Feunteun, J., Ashley, T., and Livingston, D.M. (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
-
52
-
-
0028857690
-
Structural and functional similarities between the SbcCD proteins of Escherichia coli and the RAD50 and MRE11 (RAD32) recombination and repair proteins of yeast
-
Sharples, G.J., and Leach, D.R. (1995). Structural and functional similarities between the SbcCD proteins of Escherichia coli and the RAD50 and MRE11 (RAD32) recombination and repair proteins of yeast. Mol. Microbiol. 17, 1215-1217.
-
(1995)
Mol. Microbiol.
, vol.17
, pp. 1215-1217
-
-
Sharples, G.J.1
Leach, D.R.2
-
53
-
-
0029927505
-
Mass spectrometric sequencing of proteins from silver-stained polyacrylamide gels
-
Shevchenko, A., Wilm, M., Vorm, O., and Mann, M. (1996). Mass spectrometric sequencing of proteins from silver-stained polyacrylamide gels. Anal. Chem. 68, 850-858.
-
(1996)
Anal. Chem.
, vol.68
, pp. 850-858
-
-
Shevchenko, A.1
Wilm, M.2
Vorm, O.3
Mann, M.4
-
54
-
-
0031466618
-
Ataxia-telangiectasia and the Nijmegen breakage syndrome: Related disorders but genes apart
-
Shiloh, Y. (1997). Ataxia-telangiectasia and the Nijmegen breakage syndrome: related disorders but genes apart. Annu. Rev. Genet. 31, 635-662.
-
(1997)
Annu. Rev. Genet.
, vol.31
, pp. 635-662
-
-
Shiloh, Y.1
-
55
-
-
0030022218
-
Antibody class switching
-
Stavnezer, J. (1996). Antibody class switching. Adv. Immunol. 61, 79-146.
-
(1996)
Adv. Immunol.
, vol.61
, pp. 79-146
-
-
Stavnezer, J.1
-
56
-
-
0030955042
-
Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons
-
Stumm, M., Sperling, K., and Wegner, R.D. (1997). Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons. Am. J. Hum. Genet. 60, 1246-1251.
-
(1997)
Am. J. Hum. Genet.
, vol.60
, pp. 1246-1251
-
-
Stumm, M.1
Sperling, K.2
Wegner, R.D.3
-
57
-
-
0031035628
-
Cell cycle checkpoints and DNA repair in Nijmegen breakage syndrome
-
Sullivan, K.E., Veksler, E., Lederman, H., and Lees-Miller, S.P. (1997). Cell cycle checkpoints and DNA repair in Nijmegen breakage syndrome. Clin. Immunol. Immunopathol. 82, 43-48.
-
(1997)
Clin. Immunol. Immunopathol.
, vol.82
, pp. 43-48
-
-
Sullivan, K.E.1
Veksler, E.2
Lederman, H.3
Lees-Miller, S.P.4
-
58
-
-
0020684242
-
Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen breakage syndrome
-
Taalman, R.D., Jaspers, N.G., Scheres, J.M., de Wit, J., and Hustinx, T.W. (1983). Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen breakage syndrome. Mut. Res. 112, 23-32.
-
(1983)
Mut. Res.
, vol.112
, pp. 23-32
-
-
Taalman, R.D.1
Jaspers, N.G.2
Scheres, J.M.3
De Wit, J.4
Hustinx, T.W.5
-
59
-
-
0023800238
-
Diseases with DNA damage-processing defects
-
Timme, T.L., and Moses, R.E. (1988). Diseases with DNA damage-processing defects. Am. J. Med. Sci. 295, 40-48.
-
(1988)
Am. J. Med. Sci.
, vol.295
, pp. 40-48
-
-
Timme, T.L.1
Moses, R.E.2
-
60
-
-
0031983191
-
A novel mre11 mutation impairs processing of double-strand breaks of DNA during both mitosis and meiosis
-
Tsubouchi, H., and Ogawa, H. (1998). A novel mre11 mutation impairs processing of double-strand breaks of DNA during both mitosis and meiosis. Mol. Cell. Biol. 18, 260-268.
-
(1998)
Mol. Cell. Biol.
, vol.18
, pp. 260-268
-
-
Tsubouchi, H.1
Ogawa, H.2
-
61
-
-
0030022497
-
Nijmegen breakage syndrome
-
van der Burgt, I., Chrzanowska, K.H., Smeets, D., and Weemaes, C. (1996). Nijmegen breakage syndrome. J. Med. Genet. 33, 153-156.
-
(1996)
J. Med. Genet.
, vol.33
, pp. 153-156
-
-
Van Der Burgt, I.1
Chrzanowska, K.H.2
Smeets, D.3
Weemaes, C.4
-
62
-
-
0032076190
-
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
-
this issue
-
Varan, R., Vissinga, C., Platzer, M., Cerosaletti, K.M., Chrzanowska, K.H., Saar, K., Beckmann, G., Seemanová, E., Cooper, P.R., Nowak, N.J., et al. (1998). Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 93, this issue, 467-476.
-
(1998)
Cell
, vol.93
, pp. 467-476
-
-
Varan, R.1
Vissinga, C.2
Platzer, M.3
Cerosaletti, K.M.4
Chrzanowska, K.H.5
Saar, K.6
Beckmann, G.7
Seemanová, E.8
Cooper, P.R.9
Nowak, N.J.10
-
63
-
-
0019478575
-
A new chromosomal instability disorder: The Nijmegen breakage syndrome
-
Weemaes, C.M., Hustinx, T.W., Scheres, J.M., van Munster, P.J., Bakkeren, J.A., and Taalman, R.D. (1981). A new chromosomal instability disorder: the Nijmegen breakage syndrome. Acta. Paediatr. 70, 557-564.
-
(1981)
Acta. Paediatr.
, vol.70
, pp. 557-564
-
-
Weemaes, C.M.1
Hustinx, T.W.2
Scheres, J.M.3
Van Munster, P.J.4
Bakkeren, J.A.5
Taalman, R.D.6
-
64
-
-
0028598517
-
Nijmegen breakage syndrome: A progress report
-
Weemaes, C.M., Smeets, D.F., and van der Burgt, C.J. (1994). Nijmegen breakage syndrome: a progress report. Int. J. Radiat. Biol. 66, S185-S188.
-
(1994)
Int. J. Radiat. Biol.
, vol.66
-
-
Weemaes, C.M.1
Smeets, D.F.2
Van Der Burgt, C.J.3
-
65
-
-
0030749867
-
Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells
-
Xiao, Y., and Weaver, D.T. (1997). Conditional gene targeted deletion by Cre recombinase demonstrates the requirement for the double-strand break repair Mre11 protein in murine embryonic stem cells. Nucleic Acids Res. 25, 2985-2991.
-
(1997)
Nucleic Acids Res.
, vol.25
, pp. 2985-2991
-
-
Xiao, Y.1
Weaver, D.T.2
-
66
-
-
0029645432
-
Mining genomes: Correlating tandem mass spectra of modifed and unmodified peptides to nucleotide sequences
-
Yates, J.R., III., Eng, J., and McCormack, A.L. (1995). Mining genomes: correlating tandem mass spectra of modifed and unmodified peptides to nucleotide sequences. Anal. Chem. 67, 3203-3210.
-
(1995)
Anal. Chem.
, vol.67
, pp. 3203-3210
-
-
Yates J.R. III1
Eng, J.2
McCormack, A.L.3
-
67
-
-
0024313378
-
Radioresistant DNA synthesis and human genetic diseases
-
Young, B.R., and Painter, R.B. (1989). Radioresistant DNA synthesis and human genetic diseases. Hum. Genet. 82, 113-117.
-
(1989)
Hum. Genet.
, vol.82
, pp. 113-117
-
-
Young, B.R.1
Painter, R.B.2
|