DOI: 10.1007/bf02341614. The mouse mutation severe combined immune deficiency (scid) is on chromosome 16

The mouse mutation severe combined immune deficiency (scid) is on chromosome 16

10.1007/bf02341614

Crossref journal-article

Springer Science and Business Media LLC

Immunogenetics (297)

Bibliography

Bosma, G. C., Davisson, M. T., Ruetsch, N. R., Sweet, H. O., Shultz, L. D., & Bosma, M. J. (1989). The mouse mutation severe combined immune deficiency (scid) is on chromosome 16. Immunogenetics, 29(1), 54â57.

Authors 6

G. C. Bosma (first)
M. T. Davisson (additional)
N. R. Ruetsch (additional)
H. O. Sweet (additional)
L. D. Shultz (additional)
M. J. Bosma (additional)

References 28 Referenced 80

Ackert, C., Plüss, H. J., and Hitzig, W. H.: Hereditary severe combined immunodeficiency and adenosine deaminase deficiency.Pediarr Res 10: 67–70, 1976 (10.1203/00006450-197601000-00013) / Pediarr Res by C. Ackert (1976)
Arp, B., McMullen, M. D., and Storb, U.: Sequences of immunoglobulin λ1 genes in a λ1 defective mouse strain.Nature 298: 184–186, 1982 (10.1038/298184a0) / Nature by B. Arp (1982)
Bosma, G. C., Custer, R. P., and Bosma, M. J.: A severe combined immunodeficiency mutation in the mouse.Nature 301: 527–530, 1983 (10.1038/301527a0) / Nature by G. C. Bosma (1983)
Bosma, G. C., Fried, M., Custer, R. P., Carroll, A., Gibson, D. M., and Bosma, M. J.: Evidence of functional lymphocytes in some (leaky)scid mice.J Exp Med 167: 1016–1033, 1988 (10.1084/jem.167.3.1016) / J Exp Med by G. C. Bosma (1988)
Custer, R. P., Bosma, G. C., and Bosma, M. J.: Severe combined immunodeficiency (SCID) in the mouse.Am J Pathol 120: 464–477, 1985 / Am J Pathol by R. P. Custer (1985)
Davisson, M. T.: The Jackson Laboratory. 56th Annual Report, 1984–85, p. 40 (1985) (10.1080/08102597.1985.11800574)
Epstein, R., Lehmann, K., Cohn, M., Buckler, C., Rowe, W., and Davisson, M.: Linkage of theIgl-1 structural and regulatory genes toAkv-2 on chromosome 16.Immunogenetics 19: 527–537, 1984 (10.1007/BF00403444) / Immunogenetics by R. Epstein (1984)
Epstein, R., Davisson, M., Lehmann, K., Akeson, E. C., and Cohn, M.: Position ofIgl-1 md, andBst loci on chromosome 16 of the mouse.Immunogenetics 23: 78–83, 1986 (10.1007/BF00377965) / Immunogenetics by R. Epstein (1986)
Glanzmann, E. and Riniker, P.: Essentielle lymphocytophthise. Ein neues Krankheitsbild aus der Säuglingspathologie.Ann Pediatr 175: 1–32, 1950 / Ann Pediatr by E. Glanzmann (1950)
Green, E. L: Tables and a computer program for analyzing linkage data.Mouse News Letter 73: 20–21, 1985 / Mouse News Letter by E. L Green (1985)
Hendrickson, E. A., Schatz, D. G., and Weaver, D. T.: The scid gene encodes atrans-acting factor that mediates the rejoining even of Ig gene rearrangement.Genes & Development 2: 817–829, 1988 (10.1101/gad.2.7.817) / Genes & Development by E. A. Hendrickson (1988)
Hesse, J. E., Lieber, M. R., Gellert, M., and Mizuuchi, K.: Extrachromosomal DNA substrates in pre-B cells undergo inversion or deletion at immunoglobulin V-(D)-J joining signals.Cell 49: 775–783, 1987 (10.1016/0092-8674(87)90615-5) / Cell by J. E. Hesse (1987)
Hirayoshi, K., Nishikawa, S., Kina, T., Hatanaka, M., Habi, S., Nomura, T., and Katsura, Y.: Immunoglobulin heavy chain gene diversification in the long-term bone marrow culture of normal mice and mice with severe combined immunodeficiency.Eur J Immunol 17: 1051–1057, 1987 (10.1002/eji.1830170723) / Eur J Immunol by K. Hirayoshi (1987)
Hirschhorn, R., Vawter, G. F., Kirkpatrick, J. A., and Rosen, F. S.: Adenosine deaminase deficiency: Frequency and comparative pathology in autosomal recessive severe combined immunodeficiency.Clin Imunol Immunopathol 14: 107–120, 1979 (10.1016/0090-1229(79)90131-4) / Clin Imunol Immunopathol by R. Hirschhorn (1979)
Hitzig, W. H., Biró, Z., Bosch, H., and Huser, H. J.: Agammaglobulindmie und Alymphocytose mit Schwund des lymphatischen Gewebes.Helv Paediatr Acta 13: 551–585, 1958 / Helv Paediatr Acta by W. H. Hitzig (1958)
Julius, M. H., Heusser, C. H., and Hartmann, K. U.: Induction of resting B cells to DNA synthesis by soluble monoclonal anti-immunoglobulin.Eur J Immunol 14: 753–757, 1984 (10.1002/eji.1830140816) / Eur J Immunol by M. H. Julius (1984)
Kim, M., Schuler, W., Bosma, M. J., and Marcu, K.: Abnormal recombination of immunoglobulin D and J gene segments in transformed pre-B cells of scid mice.J Immunol 141: 1341–1347, 1988 (10.4049/jimmunol.141.4.1341) / J Immunol by M. Kim (1988)
Lieber, M. R., Hesse, J. E., Lewis, S., Bosma, G. C., Rosenberg, N., Mizuuchi, K., Bosma, M. J., and Gellert, M.: The defect in murine severe combined immune deficiency: joining of signal sequences but not coding segments in V(D)J recombination. Cell, in press, 1988 (10.1016/0092-8674(88)90004-9)
Malynn, B., Blackwell, T. K., Fulop, G., Rathbun, G., Furley, A., Ferrier, P., Heinke, B., Phillips, R., Yancopoulos, G., and Alt, F.: The scid defect affects the final step of the immunoglobulin VDJ recombinase mechanism.Cell 154: 453–460, 1988 (10.1016/0092-8674(88)90066-9) / Cell by B. Malynn (1988)
Mather, K.:Statistical Analysis in Biology, p. 56, Interscience Publishers, Inc., New York, 1938 / Statistical Analysis in Biology by K. Mather (1938)
Okazaki, K., Nishikawa, S., and Sakano, H.: Aberrant immunoglobulin gene rearrangement in SLID mouse bone marrow cells.J Immunol 141: 1348–1352, 1988 (10.4049/jimmunol.141.4.1348) / J Immunol by K. Okazaki (1988)
Rosen, F. S., Cooper, M. D, and Wedgwood, J. P.: The primary immunodeficiencies.N Engl J Med 311: 300–310, 1984 (10.1056/NEJM198408023110506) / N Engl J Med by F. S. Rosen (1984)
Schuler, W., Weiler, I. J., Schuler, A., Phillips, R. A., Rosenberg, N., Mak, T. W., Kearney, J. F., Perry, R. P., and Bosma, M. J.: Rearrangement of antigen receptor genes is defective in mice with severe combined immune deficiency.Cell 46: 963–972, 1986 (10.1016/0092-8674(86)90695-1) / Cell by W. Schuler (1986)
Schuler, W., Schuler, A., Lennon, G. G., Bosma, G. C., and Bosma, M. J.: Transcription of unrearranged antigen receptor genes inscid mice.EMBO J 7: 2019–2024, 1988 (10.1002/j.1460-2075.1988.tb03041.x) / EMBO J by W. Schuler (1988)
Siciliano, M. J., Fournier, R. E. K., and Stallings, R. L.: Regional assignment of ADA and ITPA to mouse chromosome 2(C1→ter). A demonstration of the conserved linkage of enzyme and protooncogene loci.J Hered 75: 175–180, 1984 (10.1093/oxfordjournals.jhered.a109907) / J Hered by M. J. Siciliano (1984)
Southern, E.: Detection of specific sequences among DNA fragments separated by gel electrophoresis.J Mol Biol 98: 503–517, 1975 (10.1016/S0022-2836(75)80083-0) / J Mol Biol by E. Southern (1975)
Tobler, R. and Cottier, H.: Familiäre lymphopenie mit Agammaglobulinämia und schwere Moniliasis. Die essentielle Lymphocytophthise’ als besondere Form der frühkindlichen Agammaglobulinämia.Helv Paediatr Acta 13: 313–338, 1958 / Helv Paediatr Acta by R. Tobler (1958)
Witte, P. L., Burrows, P. D., Kincade, P. W., and Cooper, M. D.: Characterization of B lymphocyte lineage progenitor cells from mice with severe combined immune deficiency disease (SCID) made possible by long term culture.J Immunol 138: 2698–2705, 1987 (10.4049/jimmunol.138.8.2698) / J Immunol by P. L. Witte (1987)

Dates

Type	When
Created	19 years, 5 months ago (March 15, 2006, 1:09 a.m.)
Deposited	1 year, 7 months ago (Feb. 3, 2024, 4:38 a.m.)
Indexed	5 months, 1 week ago (March 27, 2025, 4:18 a.m.)
Issued	36 years, 8 months ago (Jan. 1, 1989)
Published	36 years, 8 months ago (Jan. 1, 1989)
Published Print	36 years, 8 months ago (Jan. 1, 1989)

Funders 0

None

BibTeX

@article{Bosma_1989, title={The mouse mutation severe combined immune deficiency (scid) is on chromosome 16}, volume={29}, ISSN={1432-1211}, url={http://dx.doi.org/10.1007/bf02341614}, DOI={10.1007/bf02341614}, number={1}, journal={Immunogenetics}, publisher={Springer Science and Business Media LLC}, author={Bosma, G. C. and Davisson, M. T. and Ruetsch, N. R. and Sweet, H. O. and Shultz, L. D. and Bosma, M. J.}, year={1989}, month=jan, pages={54–57} }

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