-
1
-
-
0029069941
-
The germinal center reaction
-
Kelsoe, G. 1995. The germinal center reaction. Immunol. Today. 16:324-326.
-
(1995)
Immunol. Today
, vol.16
, pp. 324-326
-
-
Kelsoe, G.1
-
2
-
-
0029888843
-
The molecular basis of somatic hypermutation of immunoglobulin genes
-
Storb, U. 1996. The molecular basis of somatic hypermutation of immunoglobulin genes. Curr. Opin. Immunol. 8:206-214.
-
(1996)
Curr. Opin. Immunol.
, vol.8
, pp. 206-214
-
-
Storb, U.1
-
3
-
-
0031443534
-
Somatic hypermutation of immunoglobulin genes is linked to transcription
-
Storb, U., A. Peters, E. Klotz, N. Kim, H.M. Shen, K. Kage, and B. Rogerson. 1998. Somatic hypermutation of immunoglobulin genes is linked to transcription. Curr. Top. Microbid. Immunol. 229:11-19.
-
(1998)
Curr. Top. Microbid. Immunol.
, vol.229
, pp. 11-19
-
-
Storb, U.1
Peters, A.2
Klotz, E.3
Kim, N.4
Shen, H.M.5
Kage, K.6
Rogerson, B.7
-
4
-
-
0031569118
-
Analysis of the frequency and pattern of somatic mutations within nonproductively rearranged human variable heavy chain genes
-
Doerner, T., H.-P. Brezinschek, R. Brezinschek, S. Foster, R. Domiati-Saad, and P. Lipsky. 1997. Analysis of the frequency and pattern of somatic mutations within nonproductively rearranged human variable heavy chain genes. J. Immunol. 158:2779-2789.
-
(1997)
J. Immunol.
, vol.158
, pp. 2779-2789
-
-
Doerner, T.1
Brezinschek, H.-P.2
Brezinschek, R.3
Foster, S.4
Domiati-Saad, R.5
Lipsky, P.6
-
5
-
-
0029947265
-
Di- and trinucleotide target preferences of somatic mutagenesis in normal and autoreactive B cells
-
Smith, D., G. Creadon, P. Jena, J. Portanova, B. Kotzin, and L. Wysocki. 1996. Di- and trinucleotide target preferences of somatic mutagenesis in normal and autoreactive B cells. J. Immunol. 156:2642-2652.
-
(1996)
J. Immunol.
, vol.156
, pp. 2642-2652
-
-
Smith, D.1
Creadon, G.2
Jena, P.3
Portanova, J.4
Kotzin, B.5
Wysocki, L.6
-
6
-
-
0030063726
-
Somatic hypermutation of immunoglobulin genes is linked to transcription initiation
-
Peters, A., and U. Storb. 1996. Somatic hypermutation of immunoglobulin genes is linked to transcription initiation. Immunity. 4:57-65.
-
(1996)
Immunity
, vol.4
, pp. 57-65
-
-
Peters, A.1
Storb, U.2
-
7
-
-
0032127810
-
Somatic hypermutation in the heavy chain locus correlates with transcription
-
Fukita, Y., H. Jacobs, and K. Rajewsky. 1998. Somatic hypermutation in the heavy chain locus correlates with transcription. Immunity. 9:105-114.
-
(1998)
Immunity
, vol.9
, pp. 105-114
-
-
Fukita, Y.1
Jacobs, H.2
Rajewsky, K.3
-
8
-
-
0028270307
-
Elements regulating somatic hypermutation of an immunoglobulin κ gene: Critical role for the intron enhancer/matrix attachment region
-
Betz, A., C. Milstein, R. Gonzalez-Fernandes, R. Pannell, T. Larson, and M. Neuberger. 1994. Elements regulating somatic hypermutation of an immunoglobulin κ gene: critical role for the intron enhancer/matrix attachment region. Cell. 77:239-248.
-
(1994)
Cell
, vol.77
, pp. 239-248
-
-
Betz, A.1
Milstein, C.2
Gonzalez-Fernandes, R.3
Pannell, R.4
Larson, T.5
Neuberger, M.6
-
9
-
-
0028596398
-
Transcription-coupled repair and human disease
-
Hanawalt, P.C. 1994. Transcription-coupled repair and human disease. Science. 266:1957-1958.
-
(1994)
Science
, vol.266
, pp. 1957-1958
-
-
Hanawalt, P.C.1
-
10
-
-
0030761761
-
B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes
-
Kim, N., K. Kage, F. Matsuda, M.-P. Lefranc, and U. Storb. 1997. B lymphocytes of xeroderma pigmentosum or Cockayne syndrome patients with inherited defects in nucleotide excision repair are fully capable of somatic hypermutation of immunoglobulin genes. J. Exp. Med. 186:413-419.
-
(1997)
J. Exp. Med.
, vol.186
, pp. 413-419
-
-
Kim, N.1
Kage, K.2
Matsuda, F.3
Lefranc, M.-P.4
Storb, U.5
-
11
-
-
0029871507
-
Somatic hypermutation of Ig genes in patients with xeroderma pigmentosum (XP-D)
-
Wagner, S., J. Elvin, P. Norris, J. McGregor, and M. Neuberger. 1996. Somatic hypermutation of Ig genes in patients with xeroderma pigmentosum (XP-D). Int. Immunol. 8:701-705.
-
(1996)
Int. Immunol.
, vol.8
, pp. 701-705
-
-
Wagner, S.1
Elvin, J.2
Norris, P.3
McGregor, J.4
Neuberger, M.5
-
12
-
-
0000542120
-
The inactivation of the XP-C gene does not affect somatic hypermutation or class switch recombination of immunoglobulin genes
-
Shen, H.M., D.L. Cheo, E. Friedberg, and U. Storb. 1997. The inactivation of the XP-C gene does not affect somatic hypermutation or class switch recombination of immunoglobulin genes. Mol. Immunol. 34:527-533.
-
(1997)
Mol. Immunol.
, vol.34
, pp. 527-533
-
-
Shen, H.M.1
Cheo, D.L.2
Friedberg, E.3
Storb, U.4
-
13
-
-
0032101017
-
Hypermutation of immunoglobulin genes in memory B cells of DNA repair-deficient mice
-
Jacobs, H., Y. Fujita, G. van der Horst, J. de Boer, G. Weeda, J. Essers, N. de Wind, B. Engelward, L. Samson, S. Verbeek, et al. 1998. Hypermutation of immunoglobulin genes in memory B cells of DNA repair-deficient mice. J. Exp. Med. 187:1735-1743.
-
(1998)
J. Exp. Med.
, vol.187
, pp. 1735-1743
-
-
Jacobs, H.1
Fujita, Y.2
Van Der Horst, G.3
De Boer, J.4
Weeda, G.5
Essers, J.6
De Wind, N.7
Engelward, B.8
Samson, L.9
Verbeek, S.10
-
14
-
-
13144250122
-
Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2
-
Winter, D., Q. Phung, A. Umar, S. Baker, R. Tarone, R. Tanaka, R. Liskay, T. Kunkel, V. Bohr, and P. Gearhart. 1998. Altered spectra of hypermutation in antibodies from mice deficient for the DNA mismatch repair protein PMS2. Proc. Natl. Acad. Sci. USA. 95:6953-6958.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 6953-6958
-
-
Winter, D.1
Phung, Q.2
Umar, A.3
Baker, S.4
Tarone, R.5
Tanaka, R.6
Liskay, R.7
Kunkel, T.8
Bohr, V.9
Gearhart, P.10
-
15
-
-
0004228157
-
-
ASM Press, Washington, DC
-
Friedberg, E., G. Walker, and W. Siede. 1995. DNA Repair and Mutagenesis. ASM Press, Washington, DC.
-
(1995)
DNA Repair and Mutagenesis
-
-
Friedberg, E.1
Walker, G.2
Siede, W.3
-
16
-
-
0026355962
-
Mechanisms and biological effects of mismatch repair
-
Modrich, P. 1991. Mechanisms and biological effects of mismatch repair. Annu. Rev. Genet. 25:229-253.
-
(1991)
Annu. Rev. Genet.
, vol.25
, pp. 229-253
-
-
Modrich, P.1
-
17
-
-
0029099989
-
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis
-
Baker, S.M., C.E. Bronner, L. Zhang, A.W. Plug, M. Robatzek, G. Warren, E.A. Elliott, J. Yu, T. Ashley, N. Arnheim, et al. 1995. Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis. Cell. 82:309-319.
-
(1995)
Cell
, vol.82
, pp. 309-319
-
-
Baker, S.M.1
Bronner, C.E.2
Zhang, L.3
Plug, A.W.4
Robatzek, M.5
Warren, G.6
Elliott, E.A.7
Yu, J.8
Ashley, T.9
Arnheim, N.10
-
18
-
-
8944232867
-
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over
-
Baker, S.M., A.W. Plug, T.A. Prolla, C.E. Bronner, A.C. Harris, X. Yao, D.-M. Christie, C. Monell, N. Arnheim, A. Bradley, et al. 1996. Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over. Nat. Genet. 13: 336-342.
-
(1996)
Nat. Genet.
, vol.13
, pp. 336-342
-
-
Baker, S.M.1
Plug, A.W.2
Prolla, T.A.3
Bronner, C.E.4
Harris, A.C.5
Yao, X.6
Christie, D.-M.7
Monell, C.8
Arnheim, N.9
Bradley, A.10
-
19
-
-
0029101616
-
Inactivation of the mouse MSH2 gene results in mismatch repair deficiency, methylation tolerance, hyper-recombination, and predisposition to cancer
-
de Wind, N., M. Dekker, A. Berns, M. Radman, and H. te Riele. 1995. Inactivation of the mouse MSH2 gene results in mismatch repair deficiency, methylation tolerance, hyper-recombination, and predisposition to cancer. Cell. 82:321-330.
-
(1995)
Cell
, vol.82
, pp. 321-330
-
-
De Wind, N.1
Dekker, M.2
Berns, A.3
Radman, M.4
Te Riele, H.5
-
20
-
-
0032101611
-
Increased hypermutation at G and C nucleotides in immunoglobulin variable genes from mice deficient for the MSH2 mismatch repair protein
-
Phung, Q., D. Winter, A. Cranston, R. Tarone, W. Bohr, R. Fishel, and P. Gearhart. 1998. Increased hypermutation at G and C nucleotides in immunoglobulin variable genes from mice deficient for the MSH2 mismatch repair protein. J. Exp. Med. 187:1745-1751.
-
(1998)
J. Exp. Med.
, vol.187
, pp. 1745-1751
-
-
Phung, Q.1
Winter, D.2
Cranston, A.3
Tarone, R.4
Bohr, W.5
Fishel, R.6
Gearhart, P.7
-
21
-
-
0032127804
-
Hot spot focusing of somatic hypermutation in MSH2-deficient mice suggests two stages of mutational targeting
-
Rada, C., M.R. Ehrenstein, M.S. Neuberger, and C. Milstein. 1998. Hot spot focusing of somatic hypermutation in MSH2-deficient mice suggests two stages of mutational targeting. Immunity. 9:135-141.
-
(1998)
Immunity
, vol.9
, pp. 135-141
-
-
Rada, C.1
Ehrenstein, M.R.2
Neuberger, M.S.3
Milstein, C.4
-
22
-
-
0032127811
-
Mismatch repair deficiency interferes with the accumulation of mutations in chronically stimulated B cells and no with the hypermutation process
-
Frey, S., B. Bertocci, F. Delbos, L. Quint, J.-C. Weill, and C.-A. Reynaud. 1998. Mismatch repair deficiency interferes with the accumulation of mutations in chronically stimulated B cells and no with the hypermutation process. Immunity. 9:127-134.
-
(1998)
Immunity
, vol.9
, pp. 127-134
-
-
Frey, S.1
Bertocci, B.2
Delbos, F.3
Quint, L.4
Weill, J.-C.5
Reynaud, C.-A.6
-
23
-
-
0028983486
-
Somatic hypermutation of VHS107 genes is not associated with gene conversion among family members
-
Rogerson, B. 1995. Somatic hypermutation of VHS107 genes is not associated with gene conversion among family members. Int. Immunol. 7:1225-1235.
-
(1995)
Int. Immunol.
, vol.7
, pp. 1225-1235
-
-
Rogerson, B.1
-
24
-
-
0032528421
-
Somatic hypermutation of an artificial test substrate within an Ig kappa transgene
-
Klotz, E., J.J. Hackett, and U. Storb. 1998. Somatic hypermutation of an artificial test substrate within an Ig kappa transgene. J. Immunol. 161:782-790.
-
(1998)
J. Immunol.
, vol.161
, pp. 782-790
-
-
Klotz, E.1
Hackett, J.J.2
Storb, U.3
-
25
-
-
0024595101
-
Detection of polymorphism of human DNA by gel electrophoresis as single-strand conformation polymorphism
-
Orita, M., H. Iwahana, H. Kanazawa, K. Hayashi, and S. Takao. 1989. Detection of polymorphism of human DNA by gel electrophoresis as single-strand conformation polymorphism. Proc. Natl. Acad. Sci. USA. 86:2766-2770.
-
(1989)
Proc. Natl. Acad. Sci. USA.
, vol.86
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Takao, S.5
-
26
-
-
0032541394
-
A hypermutable insert in an immunoglobulin transgene contains hotspots of somatic mutation and sequences predicting highly stable structures in the RNA transcript
-
Storb, U., E. Klotz, J. Hackett, K. Kage, G. Bozek, and T.E. Martin. 1998. A hypermutable insert in an immunoglobulin transgene contains hotspots of somatic mutation and sequences predicting highly stable structures in the RNA transcript. J. Exp. Med. 188:689-698.
-
(1998)
J. Exp. Med.
, vol.188
, pp. 689-698
-
-
Storb, U.1
Klotz, E.2
Hackett, J.3
Kage, K.4
Bozek, G.5
Martin, T.E.6
-
27
-
-
0033558532
-
Hypermutation in Ig V genes from mice deficient in the MLH1 mismatch repair protein
-
Phung, Q., D. Winter, R. Alrefai, and P. Gearhart. 1999. Hypermutation in Ig V genes from mice deficient in the MLH1 mismatch repair protein. J. Immunol. 162:3121-3124.
-
(1999)
J. Immunol.
, vol.162
, pp. 3121-3124
-
-
Phung, Q.1
Winter, D.2
Alrefai, R.3
Gearhart, P.4
-
28
-
-
0033081331
-
Severe attenuation of the B cell immune response in Msh2-deficient mice
-
Vora, K., K. Tuma-Brundage, V. Lentz, A. Cranston, R. Fishel, and T. Manser. 1999. Severe attenuation of the B cell immune response in Msh2-deficient mice. J. Exp. Med. 189: 471-481.
-
(1999)
J. Exp. Med.
, vol.189
, pp. 471-481
-
-
Vora, K.1
Tuma-Brundage, K.2
Lentz, V.3
Cranston, A.4
Fishel, R.5
Manser, T.6
-
29
-
-
0032100485
-
The role of DNA repair in somatic hypermutation of immunoglobulin genes
-
Kim, N., and U. Storb. 1998. The role of DNA repair in somatic hypermutation of immunoglobulin genes. J. Exp. Med. 187:1729-1733.
-
(1998)
J. Exp. Med.
, vol.187
, pp. 1729-1733
-
-
Kim, N.1
Storb, U.2
-
30
-
-
0029887819
-
Transcription-coupled repair deficiency and mutations in human mismatch repair genes
-
Mellon, I., D. Rajpal, M. Koi, C. Boland, and G. Champe. 1996. Transcription-coupled repair deficiency and mutations in human mismatch repair genes. Science. 272:557-560.
-
(1996)
Science
, vol.272
, pp. 557-560
-
-
Mellon, I.1
Rajpal, D.2
Koi, M.3
Boland, C.4
Champe, G.5
-
31
-
-
0030034077
-
Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli
-
Mellon, I., and G.N. Chanpe. 1996. Products of DNA mismatch repair genes mutS and mutL are required for transcription-coupled nucleotide-excision repair of the lactose operon in Escherichia coli. Proc. Natl. Acad. Sci. USA. 93:1292-1297.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 1292-1297
-
-
Mellon, I.1
Chanpe, G.N.2
-
32
-
-
0032549125
-
Mismatch repair co-opted by hypermutation
-
Cascalho, M., J. Wong, C. Steinberg, and M. Wabl. 1998. Mismatch repair co-opted by hypermutation. Science. 279: 1207-1210.
-
(1998)
Science
, vol.279
, pp. 1207-1210
-
-
Cascalho, M.1
Wong, J.2
Steinberg, C.3
Wabl, M.4
-
33
-
-
0032402306
-
Isolated human germinal center centroblasts have an intact mismatch repair system
-
Park, K., J. Kim, H.-S. Kim, and H.S. Shin. 1998. Isolated human germinal center centroblasts have an intact mismatch repair system. J. Immunol. 161:6128-6132.
-
(1998)
J. Immunol.
, vol.161
, pp. 6128-6132
-
-
Park, K.1
Kim, J.2
Kim, H.-S.3
Shin, H.S.4
|