-
1
-
-
0024149641
-
The immunoglobulin superfamily - Domains for cell surface recognition
-
Williams, A. F., and Barclay, A. N., The immunoglobulin superfamily - domains for cell surface recognition. Annu. Rev. Immunol. 6, 381-405, 1988.
-
(1988)
Annu. Rev. Immunol.
, vol.6
, pp. 381-405
-
-
Williams, A.F.1
Barclay, A.N.2
-
2
-
-
0023650302
-
Physical map of the human immunoglobulin K locus and its implications for the mechanisms of VK-JK rearrangement
-
Lorenz, W., Straubinger, B., and Zachau, H. G., Physical map of the human immunoglobulin K locus and its implications for the mechanisms of VK-JK rearrangement. Nucleic Acids Res. 15, 9667-9676, 1987.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 9667-9676
-
-
Lorenz, W.1
Straubinger, B.2
Zachau, H.G.3
-
3
-
-
0023487171
-
Human immunoglobulin C lambda 6 gene encodes the Kern+Oz-lambda chain and C lambda 4 and C lambda 5 are pseudogenes
-
Dariavach, P., Lefranc, G., and Lefranc, M. P., Human immunoglobulin C lambda 6 gene encodes the Kern+Oz-lambda chain and C lambda 4 and C lambda 5 are pseudogenes. Proc. Natl. Acad. Sci. USA 84, 9074-9078, 1987.
-
(1987)
Proc. Natl. Acad. Sci. USA
, vol.84
, pp. 9074-9078
-
-
Dariavach, P.1
Lefranc, G.2
Lefranc, M.P.3
-
4
-
-
0029031724
-
Organization of the human immunoglobulin lambda light-chain locus on chromosome 22q11.2
-
Frippiat, J. P., Williams, S. C., Tomlinson, I. M., Cook, G. P., Cherif, D., Le Paslier, D., Collins, J. E., Dunham, I., Winter, G., and Lefranc, M. P., Organization of the human immunoglobulin lambda light-chain locus on chromosome 22q11.2. Hum. Mol. Genet. 4, 983-991, 1995.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 983-991
-
-
Frippiat, J.P.1
Williams, S.C.2
Tomlinson, I.M.3
Cook, G.P.4
Cherif, D.5
Le Paslier, D.6
Collins, J.E.7
Dunham, I.8
Winter, G.9
Lefranc, M.P.10
-
5
-
-
0019830478
-
Gene conversion: Some implications for immunoglobulin genes
-
Baltimore, D., Gene conversion: Some implications for immunoglobulin genes. Cell 24, 592-594, 1981.
-
(1981)
Cell
, vol.24
, pp. 592-594
-
-
Baltimore, D.1
-
6
-
-
0001957475
-
Molecular mechanisms for gene conversion in higher cells
-
Kourilsky, P., Molecular mechanisms for gene conversion in higher cells. Trends Genet. 2, 60-63, 1986.
-
(1986)
Trends Genet.
, vol.2
, pp. 60-63
-
-
Kourilsky, P.1
-
7
-
-
0023114469
-
Homology requirement for efficient gene conversion between duplicated chromosomal sequences in mammalian cells
-
Liskay, R. M., Letsou, A., and Stachelek, J. L., Homology requirement for efficient gene conversion between duplicated chromosomal sequences in mammalian cells. Genetics 115, 161-167, 1987.
-
(1987)
Genetics
, vol.115
, pp. 161-167
-
-
Liskay, R.M.1
Letsou, A.2
Stachelek, J.L.3
-
8
-
-
0023652339
-
A hyperconversion mechanism generates the chicken light chain preimmune repertoire
-
Reynaud, C. A., Anquez, V., Grimal, H., and Weill, J. C., A hyperconversion mechanism generates the chicken light chain preimmune repertoire. Cell 48, 379-388, 1987.
-
(1987)
Cell
, vol.48
, pp. 379-388
-
-
Reynaud, C.A.1
Anquez, V.2
Grimal, H.3
Weill, J.C.4
-
9
-
-
0023652303
-
Somatic diversification of the chicken immunoglobulin light chain gene is limited to the rearranged variable gene segment
-
Thompson, C. B., and Neiman, P. E., Somatic diversification of the chicken immunoglobulin light chain gene is limited to the rearranged variable gene segment. Cell 48, 369-378, 1987.
-
(1987)
Cell
, vol.48
, pp. 369-378
-
-
Thompson, C.B.1
Neiman, P.E.2
-
10
-
-
0026464440
-
Creation of immunoglobulin diversity by intrachromosomal gene conversion
-
Thompson, C.B., Creation of immunoglobulin diversity by intrachromosomal gene conversion. Trends Genet. 8, 416-422, 1992.
-
(1992)
Trends Genet.
, vol.8
, pp. 416-422
-
-
Thompson, C.B.1
-
11
-
-
0033120988
-
Gene conversion and hypermutation during diversification of VH sequences in developing splenic germinal centers of immunized rabbits
-
Schiaffella, E., Sehgal, D., Anderson, A. O., and Mage, R. G., Gene conversion and hypermutation during diversification of VH sequences in developing splenic germinal centers of immunized rabbits. J. Immunol. 162, 3984-3995, 1999.
-
(1999)
J. Immunol.
, vol.162
, pp. 3984-3995
-
-
Schiaffella, E.1
Sehgal, D.2
Anderson, A.O.3
Mage, R.G.4
-
12
-
-
0033555381
-
A role for RAD51 in the generation of immunoglobulin gene diversity in rabbits
-
Barrington, R. A., Fasullo, M., and Knight, K. L., A role for RAD51 in the generation of immunoglobulin gene diversity in rabbits. J. Immunol. 162, 911-919, 1999.
-
(1999)
J. Immunol.
, vol.162
, pp. 911-919
-
-
Barrington, R.A.1
Fasullo, M.2
Knight, K.L.3
-
13
-
-
0020700687
-
Evolution of immunoglobulin V genes: Evidence indicating that recently duplicated human V kappa sequences have diverged by gene conversion
-
Bentley, D. L., and Rabbitts, T. H., Evolution of immunoglobulin V genes: Evidence indicating that recently duplicated human V kappa sequences have diverged by gene conversion. Cell 32, 181-189, 1983.
-
(1983)
Cell
, vol.32
, pp. 181-189
-
-
Bentley, D.L.1
Rabbitts, T.H.2
-
14
-
-
0027477152
-
A de novo pathological point mutation at the 21-hydroxylase locus: Implications for gene conversion in the human genome
-
Collier, S., Tassabehji, M., Sinnott, P., and Strachan, T., A de novo pathological point mutation at the 21-hydroxylase locus: Implications for gene conversion in the human genome. Nat. Genet. 3, 260-265, 1993.
-
(1993)
Nat. Genet.
, vol.3
, pp. 260-265
-
-
Collier, S.1
Tassabehji, M.2
Sinnott, P.3
Strachan, T.4
-
15
-
-
0028345761
-
Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence
-
Eikenboom, J. C., Vink, T., Briet, E., Sixma, J. J., and Reitsma, P. H., Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence. Proc. Natl. Acad. Sci. USA 91, 2221-2224, 1994.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 2221-2224
-
-
Eikenboom, J.C.1
Vink, T.2
Briet, E.3
Sixma, J.J.4
Reitsma, P.H.5
-
16
-
-
0040945789
-
A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease
-
Gorlach, A., Lee, P. L., Roesler, J., Hopkins, P. J., Christensen, B., Green, E. D., Chanock, S. J., and Curnutte, J. T., A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease. J. Clin. Invest. 100, 1907-1918, 1997.
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 1907-1918
-
-
Gorlach, A.1
Lee, P.L.2
Roesler, J.3
Hopkins, P.J.4
Christensen, B.5
Green, E.D.6
Chanock, S.J.7
Curnutte, J.T.8
-
17
-
-
0031594211
-
Mutations in the human λ5/ 14.1 gene result in B cell deficiency and agammaglobulinemia
-
Minegishi, Y., Coustan-Smith, E., Wang, Y.-H., Cooper, M. D., Campana, D., and Conley, M. E., Mutations in the human λ5/ 14.1 gene result in B cell deficiency and agammaglobulinemia. J. Exp. Med. 187, 71-77, 1998.
-
(1998)
J. Exp. Med.
, vol.187
, pp. 71-77
-
-
Minegishi, Y.1
Coustan-Smith, E.2
Wang, Y.-H.3
Cooper, M.D.4
Campana, D.5
Conley, M.E.6
-
18
-
-
0027465094
-
The surrogate light chain in B-cell development
-
Melchers, F., Karasuyama, H., Haasner, D., Bauer, S., Kudo, A., Sakaguchi, N., Jameson, B., and Rolink, A., The surrogate light chain in B-cell development. Immunol. Today 14, 60-68, 1993.
-
(1993)
Immunol. Today
, vol.14
, pp. 60-68
-
-
Melchers, F.1
Karasuyama, H.2
Haasner, D.3
Bauer, S.4
Kudo, A.5
Sakaguchi, N.6
Jameson, B.7
Rolink, A.8
-
19
-
-
0023390930
-
A second gene, VpreB in the lambda 5 locus of the mouse, which appears to be selectively expressed in pre-B lymphocytes
-
Kudo, A., and Melchers, F., A second gene, VpreB in the lambda 5 locus of the mouse, which appears to be selectively expressed in pre-B lymphocytes. EMBO J. 6, 2267-2272, 1987.
-
(1987)
EMBO J.
, vol.6
, pp. 2267-2272
-
-
Kudo, A.1
Melchers, F.2
-
20
-
-
0023035608
-
Lambda 5, a new light-chain-related locus selectively expressed in pre-B lymphocytes
-
Sakaguchi, N., and Melchers, F., Lambda 5, a new light-chain-related locus selectively expressed in pre-B lymphocytes. Nature 324, 579-582, 1986.
-
(1986)
Nature
, vol.324
, pp. 579-582
-
-
Sakaguchi, N.1
Melchers, F.2
-
21
-
-
0026551809
-
Pre-B lymphocyte-specific transcriptional control of the mouse VpreB gene
-
Okabe, T., Bauer, S. R., and Kudo, A., Pre-B lymphocyte-specific transcriptional control of the mouse VpreB gene. Eur. J. Immunol. 22, 31-36, 1992.
-
(1992)
Eur. J. Immunol.
, vol.22
, pp. 31-36
-
-
Okabe, T.1
Bauer, S.R.2
Kudo, A.3
-
22
-
-
0022577255
-
Identification of three new Ig lambda-like genes in man
-
Chang, H., Dmitrovsky, E., Hieter, P. A., Mitchell, K., Leder, P., Turoczi, L., Kirsch, I. R., and Hollis, G. F., Identification of three new Ig lambda-like genes in man. J. Exp. Med. 163, 425-435, 1986.
-
(1986)
J. Exp. Med.
, vol.163
, pp. 425-435
-
-
Chang, H.1
Dmitrovsky, E.2
Hieter, P.A.3
Mitchell, K.4
Leder, P.5
Turoczi, L.6
Kirsch, I.R.7
Hollis, G.F.8
-
23
-
-
0026077398
-
Organization and expression of the lambda-like genes that contribute to the mu-surrogate light chain complex in human pre-B cells
-
Bossy, D., Milili, M., Zucman, J., Thomas, G., Fougereau, M., and Schiff, C., Organization and expression of the lambda-like genes that contribute to the mu-surrogate light chain complex in human pre-B cells. Int. Immunol. 3, 1081-1090, 1991.
-
(1991)
Int. Immunol.
, vol.3
, pp. 1081-1090
-
-
Bossy, D.1
Milili, M.2
Zucman, J.3
Thomas, G.4
Fougereau, M.5
Schiff, C.6
-
24
-
-
0027494505
-
Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2
-
Bauer, T. R., Jr., McDermid, H. E., Budarf, M. L., Van Keuren, M. L., and Blomberg, B. B., Physical location of the human immunoglobulin lambda-like genes, 14.1, 16.1, and 16.2. Immunogenetics 38, 387-399, 1993.
-
(1993)
Immunogenetics
, vol.38
, pp. 387-399
-
-
Bauer T.R., Jr.1
McDermid, H.E.2
Budarf, M.L.3
Van Keuren, M.L.4
Blomberg, B.B.5
-
25
-
-
0019776489
-
Clustered arrangement of immunoglobulin lambda constant region genes in man
-
Hieter, P. A., Hollis, G. F., Korsmeyer, S. J., Waldmann, T. A., and Leder, P., Clustered arrangement of immunoglobulin lambda constant region genes in man. Nature 294, 536-540, 1981.
-
(1981)
Nature
, vol.294
, pp. 536-540
-
-
Hieter, P.A.1
Hollis, G.F.2
Korsmeyer, S.J.3
Waldmann, T.A.4
Leder, P.5
-
26
-
-
0020636838
-
Variable amplification of immunoglobulin lambda light-chain genes in human populations
-
Taub, R. A., Hollis, G. F., Hieter, P. A., Korsmeyer, S., Waldmann, T. A., and Leder, P., Variable amplification of immunoglobulin lambda light-chain genes in human populations. Nature 304, 172-174, 1983.
-
(1983)
Nature
, vol.304
, pp. 172-174
-
-
Taub, R.A.1
Hollis, G.F.2
Hieter, P.A.3
Korsmeyer, S.4
Waldmann, T.A.5
Leder, P.6
-
27
-
-
0026058478
-
Genomic structure of the human Ig lambda 1 gene suggests that it may be expressed as an Ig lambda 14.1-like protein or as a canonical B cell Ig lambda light chain: Implications for Ig lambda gene evolution
-
Evans, R. J., and Hollis, G. F., Genomic structure of the human Ig lambda 1 gene suggests that it may be expressed as an Ig lambda 14.1-like protein or as a canonical B cell Ig lambda light chain: Implications for Ig lambda gene evolution. J. Exp. Med. 173, 305-311, 1991.
-
(1991)
J. Exp. Med.
, vol.173
, pp. 305-311
-
-
Evans, R.J.1
Hollis, G.F.2
-
28
-
-
0032980196
-
Novel mechanisms control the folding and assembly of lambda5/14.1 and VpreB to produce an intact surrogate light chain
-
Minegishi, Y., Hendershot, L. M., and Conley, M. E., Novel mechanisms control the folding and assembly of lambda5/14.1 and VpreB to produce an intact surrogate light chain. Proc. Natl. Acad. Sci. USA 96, 3041-3046, 1999.
-
(1999)
Proc. Natl. Acad. Sci. USA
, vol.96
, pp. 3041-3046
-
-
Minegishi, Y.1
Hendershot, L.M.2
Conley, M.E.3
-
29
-
-
0028137136
-
Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase
-
Conley, M. E., Fitch-Hilgenberg, M. E., Cleveland, J. L., Parolini, O., and Rohrer, J., Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase. Hum. Mol. Genet. 3, 1751-1756, 1994.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1751-1756
-
-
Conley, M.E.1
Fitch-Hilgenberg, M.E.2
Cleveland, J.L.3
Parolini, O.4
Rohrer, J.5
-
30
-
-
0018654090
-
Three-dimensional structure of immunoglobulins
-
Amzel, L. M., and Poljak, R. J., Three-dimensional structure of immunoglobulins. Annu. Rev. Biochem. 48, 961-997, 1979.
-
(1979)
Annu. Rev. Biochem.
, vol.48
, pp. 961-997
-
-
Amzel, L.M.1
Poljak, R.J.2
-
31
-
-
0033358728
-
Sequence diversity in 36 candidate genes for cardiovascular disorders
-
Cambien, F., Poirier, O., Nicaud, V., Herrmann, S. M., Mallet, C., Ricard, S., Behague, I., Hallet, V., Blanc, H., Loukaci, V., Thillet, J., Evans, A., Ruidavets, J. B., Arveiler, D., Luc, G., and Tiret, L., Sequence diversity in 36 candidate genes for cardiovascular disorders. Am. J. Hum. Genet. 65, 183-191, 1999.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 183-191
-
-
Cambien, F.1
Poirier, O.2
Nicaud, V.3
Herrmann, S.M.4
Mallet, C.5
Ricard, S.6
Behague, I.7
Hallet, V.8
Blanc, H.9
Loukaci, V.10
Thillet, J.11
Evans, A.12
Ruidavets, J.B.13
Arveiler, D.14
Luc, G.15
Tiret, L.16
-
32
-
-
0032990407
-
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
Halushka, M. K., Fan, J. B., Bentley, K., Hsie, L., Shen, N., Weder, A., Cooper, R., Lipshutz, R., and Chakravarti, A., Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis. Nat. Genet. 22, 239-247, 1999.
-
(1999)
Nat. Genet.
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
Hsie, L.4
Shen, N.5
Weder, A.6
Cooper, R.7
Lipshutz, R.8
Chakravarti, A.9
-
33
-
-
7144227286
-
Susceptibility locus for IgA deficiency and common variable immunodeficiency in the HLA-DR3, -B8, -A1 haplotypes
-
Schroeder, H. W. J., Zhu, Z. B., March, R. E., Campbell, R. D., Berney, S. M., Nedospasov, S. A., Turetskaya, R. L., Atkinson, T. P., Go, R. C., Cooper, M. D., and Volanakis, J. E., Susceptibility locus for IgA deficiency and common variable immunodeficiency in the HLA-DR3, -B8, -A1 haplotypes. Mol. Med. 4, 72-86, 1998.
-
(1998)
Mol. Med.
, vol.4
, pp. 72-86
-
-
Schroeder, H.W.J.1
Zhu, Z.B.2
March, R.E.3
Campbell, R.D.4
Berney, S.M.5
Nedospasov, S.A.6
Turetskaya, R.L.7
Atkinson, T.P.8
Go, R.C.9
Cooper, M.D.10
Volanakis, J.E.11
-
34
-
-
0031573549
-
TNF and lymphotoxin-alpha polymorphisms associated with common variable immunodeficiency: Role in the pathogenesis of granulomatous disease
-
Mullighan, C. G., Fanning, G. C., Chapel, H. M., and Welsh, K. I., TNF and lymphotoxin-alpha polymorphisms associated with common variable immunodeficiency: Role in the pathogenesis of granulomatous disease. J. Immunol. 159, 6236-6241, 1997.
-
(1997)
J. Immunol.
, vol.159
, pp. 6236-6241
-
-
Mullighan, C.G.1
Fanning, G.C.2
Chapel, H.M.3
Welsh, K.I.4
-
35
-
-
0032535301
-
Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease
-
Foster, C. B., Lehrnbecher, T., Mol, F., Steinberg, S. M., Venzon, D. J., Walsh, T. J., Noack, D., Rae, J., Winkelstein, J. A., Curnutte, J. T., and Chanock, S. J., Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease. J. Clin. Invest. 102, 2146-2155, 1998.
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 2146-2155
-
-
Foster, C.B.1
Lehrnbecher, T.2
Mol, F.3
Steinberg, S.M.4
Venzon, D.J.5
Walsh, T.J.6
Noack, D.7
Rae, J.8
Winkelstein, J.A.9
Curnutte, J.T.10
Chanock, S.J.11
-
36
-
-
0032231888
-
Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase
-
Clark, A. G., Weiss, K. M., Nickerson, D. A., Taylor, S. L., Buchanan, A., Stengard, J., Salomaa, V., Vartiainen, E., Perola, M., Boerwinkle, E., and Sing, C. F., Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. Am. J. Hum. Genet. 63, 595-612, 1998.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 595-612
-
-
Clark, A.G.1
Weiss, K.M.2
Nickerson, D.A.3
Taylor, S.L.4
Buchanan, A.5
Stengard, J.6
Salomaa, V.7
Vartiainen, E.8
Perola, M.9
Boerwinkle, E.10
Sing, C.F.11
-
37
-
-
0007383587
-
Mutation in the CYP21B gene (Ile-172 - Asn) causes steroid 21-hydroxylase deficiency
-
Amor, M., Parker, K. L., Globerman, H., New, M. I., and White, P. C., Mutation in the CYP21B gene (Ile-172 - Asn) causes steroid 21-hydroxylase deficiency. Proc. Natl. Acad. Sci. USA 85, 1600-1604, 1988.
-
(1988)
Proc. Natl. Acad. Sci. USA
, vol.85
, pp. 1600-1604
-
-
Amor, M.1
Parker, K.L.2
Globerman, H.3
New, M.I.4
White, P.C.5
-
38
-
-
0026542050
-
A possible example of gene conversion with a common beta-thalassemia mutation and Chi sequence present in the beta-globin gene
-
Matsuno, Y., Yamashiro, Y., Yamamoto, K., Hattori, Y., Ohba, Y., and Miyaji, T., A possible example of gene conversion with a common beta-thalassemia mutation and Chi sequence present in the beta-globin gene. Hum. Genet. 88, 357-358, 1992.
-
(1992)
Hum. Genet.
, vol.88
, pp. 357-358
-
-
Matsuno, Y.1
Yamashiro, Y.2
Yamamoto, K.3
Hattori, Y.4
Ohba, Y.5
Miyaji, T.6
-
39
-
-
0015257040
-
Correlations between the concentrations of the four sub-classes of IgG and Gm allotypes in normal human sera
-
Morell, A., Skvaril, F., Steinberg, A. G., Van Loghem, E., and Terry, W. D., Correlations between the concentrations of the four sub-classes of IgG and Gm allotypes in normal human sera. J. Immunol. 108, 195-206, 1972.
-
(1972)
J. Immunol.
, vol.108
, pp. 195-206
-
-
Morell, A.1
Skvaril, F.2
Steinberg, A.G.3
Van Loghem, E.4
Terry, W.D.5
-
40
-
-
0021971575
-
Correlation between G2m(n) immunoglobulin allotype and human antibody response and susceptibility to polysaccharide encapsulated bacteria
-
Ambrosino, D. M., Schiffman, G., Gotschlich, E. C., Schur, P. H., Rosenberg, G. A., DeLange, G. G., Van Loghem, E., and Siber, G. R., Correlation between G2m(n) immunoglobulin allotype and human antibody response and susceptibility to polysaccharide encapsulated bacteria. J. Clin. Invest. 75, 1935-1942, 1985.
-
(1985)
J. Clin. Invest.
, vol.75
, pp. 1935-1942
-
-
Ambrosino, D.M.1
Schiffman, G.2
Gotschlich, E.C.3
Schur, P.H.4
Rosenberg, G.A.5
DeLange, G.G.6
Van Loghem, E.7
Siber, G.R.8
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