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Former Names J.Cg-p+ Tyr+ Lystbg/J (Changed: 11-FEB-08 ) SJL.Cg-p+ Tyr+ Lystbg (Changed: 15-DEC-04 ) Type Congenic; Mutant Strain; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Species laboratory mouse Background Strain SJL/J Donor Strain Lystbg Oak Ridge irr.; Oca2+ C57BL/6 ?; +Tyr-c C57BL/6 ? Generation NE13F50p Appearance
brown agouti, retinal degeneration, affected
Related Genotype: A/A Lystbg/Lystbg Pde6brd1/Pde6brd1Description
Mice homozygous for the beige spontaneous mutation (Lystbg) are characterized by a condition that closely resembles Chediak-Higashi disease in man and similar conditions in mink and cattle. Abnormal giant lysosomal granules occur in all tissues with granule-containing cells, including granulocytes, lymphocytes, cells of the liver, kidney, central nervous system, pancreas, and thyroid, and the ducts of most glands; in type II pneumocytes; in mast cells; and in retinal pigment epithelium. Granulocytes from beige homozygous mutant mice mice show defective chemotaxis and reduced bactericidal activity. Beige mice are more susceptible than controls to pneumonitis and to various viral, bacterial, and parasitic infections. Natural killer (NK) cells from beige mice exhibit decreased endogenous cytotoxic activity. Beige mice also have a defective cytotoxic T-cell and cytotoxic antibody response to allogeneic tumor cells. Syngeneic tumor cells grow better in beige mice than in littermate controls, an effect thought to be due to the deficiency of NK cells. Beige mice have platelet storage pool deficiency, leading to a prolonged bleeding time. The immunodeficiency of beige mutant mice has been used, especially in combination with the scid mutation (Prkdcscid), in tissue graft and disease studies.
| Control | ||
|---|---|---|
| 000686 SJL/J | ||
| Considerations for Choosing Controls | ||
Strains carrying Lystbg allele
000204 B6.C3Rl-Lystbg/J 000269 SB/LeJ View Strains carrying Lystbg (2 strains)
Strains carrying Oca2+ allele
000090 129S1/Sv-Oca2+ Tyr+ KitlSl-J/J 000091 129T1/Sv-Oca2+ Tyrc-ch Dnd1Ter/J 001279 129T1/Sv-Oca2+ Tyrc-ch-Aft/J 000822 B6 x 129S1/SvEi Oca2+ Tyr+-Vsx2or-J/J View Strains carrying Oca2+ (4 strains)
Strains carrying Tyr+ allele
000090 129S1/Sv-Oca2+ Tyr+ KitlSl-J/J 005445 A.B6 Tyr+-Cybanmf333/J 005012 A.B6 Tyr+-Myo5ad-l31J/J 002565 A.B6-Tyr+/J 000822 B6 x 129S1/SvEi Oca2+ Tyr+-Vsx2or-J/J 000899 C.B6-Tyr+ Hbbs/J 002281 NFS.C58-Tyr+/J 004304 NOD.CBALs-Tyr+/LtJ View Strains carrying Tyr+ (8 strains)
Strains carrying other alleles of Lyst
000604 B6C3 a/A-T(10;13)199H +/+ Lystbg-J/J or Lystbg-2J/J 000509 C3.Cg-Lystbg-2J/J 000629 C57BL/6J-Lystbg-J/J View Strains carrying other alleles of Lyst (3 strains)
Strains carrying other alleles of Oca2
000004 ABP/LeJ 000577 B6 x STOCK a Oca2p Hps5ru2 Ednrbs/J 001059 B6By.Cg-Oca2p/J 002460 C3H/HeJ-Oca2p-J Is(7;1)40H/J 000513 C3H/HeJ-Oca2p-J/J 001136 C57BL/6J-Oca2p-un+2J/J 001506 C57BL/6J-Oca2p-un+3J/J 001810 C57BL/6J-Oca2p-un+4J/J 001513 C57BL/6J-Oca2p-un+5J/J 001499 C57BL/6J-Oca2p-un+6J/J 001033 C57BL/6J-Oca2p-un+J/J 000028 C57BL/6J-Oca2p-un/J 000619 FS/EiJ 000306 STOCK Dll3pu + Tyrc-ch/+ Oca2p Tyrc-ch/J 001584 STOCK Oca2p-J/Oca2p-bs/J 001585 STOCK Oca2p-d/Oca2p-25H/J 000823 STOCK Oca2p-d/Oca2p-6H/J 001747 STOCK Oca2p-d/Oca2p-cp/J 001618 STOCK Oca2p/Oca2p Prop1df/J View Strains carrying other alleles of Oca2 (19 strains)
Strains carrying other alleles of Tyr
View Strains carrying other alleles of Tyr (38 strains)
JAX® NOTES, Spring 1991; 445. Why C57BL/6J-bgJ (beige) Mice are not Beige.
JAX® NOTES, Winter 1992; 448. The Beige (BgJ) Mutation.
View Related Disease (OMIM) Terms
Related Disease (OMIM) Terms
Chediak-Higashi Syndrome; CHS - Models with phenotypic similarity to human disease where etiologies involve orthologs.1
1 Human genes are associated with this disease. Orthologs of those genes appear in the mouse genotype(s).
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Lystbg/Lystbg
C3H/Rl
- pigmentation phenotype
- abnormal eye pigmentation (MGI Ref ID J:29744)
- diluted coat color (MGI Ref ID J:29744)
- irregular coat pigmentation (MGI Ref ID J:29744)
- skin/coat/nails phenotype
- diluted coat color (MGI Ref ID J:29744)
- irregular coat pigmentation (MGI Ref ID J:29744)
- vision/eye phenotype
- abnormal eye pigmentation (MGI Ref ID J:29744)
Lystbg/Lystbg
B6.C3Rl-Lystbg
- tumorigenesis
- increased incidence of induced tumors (MGI Ref ID J:6302)
- pigmentation phenotype
- abnormal melanosome morphology (MGI Ref ID J:5346)
- enlarged hair follicle melanin granules (MGI Ref ID J:5078)
- cellular phenotype
- abnormal lysosome morphology (MGI Ref ID J:29294)
- accumulation of giant lysosomes in kidney/renal tubule cells (MGI Ref ID J:5590)
- lysosomal protein accumulation (MGI Ref ID J:5338)
- hematopoietic system phenotype
- abnormal eosinophil morphology (MGI Ref ID J:5078)
- presence of giant granules in cells
- abnormal lymphocyte morphology (MGI Ref ID J:5078)
- presence of giant granules in cells
- abnormal neutrophil morphology (MGI Ref ID J:5078)
- presence of giant granules in cells
- immune system phenotype
- abnormal eosinophil morphology (MGI Ref ID J:5078)
- presence of giant granules in cells
- abnormal lymphocyte morphology (MGI Ref ID J:5078)
- presence of giant granules in cells
- abnormal neutrophil morphology (MGI Ref ID J:5078)
- presence of giant granules in cells
- defective cytotoxic T cell cytolysis (MGI Ref ID J:6692)
- impaired NK cell cytolysis (MGI Ref ID J:6213)
- increased susceptibility to parasitic infection (MGI Ref ID J:6946)
- renal/urinary system phenotype
- accumulation of giant lysosomes in kidney/renal tubule cells (MGI Ref ID J:5590)
- skin/coat/nails phenotype
- enlarged hair follicle melanin granules (MGI Ref ID J:5078)
- nervous system phenotype
- abnormal hippocampal mossy fiber morphology (MGI Ref ID J:4978)
- ectopic Bergmann glia cells (MGI Ref ID J:4978)
- ectopic Purkinje cell (MGI Ref ID J:4978)
- ectopic granule cells (MGI Ref ID J:4978)
- ectopic pyramidal neurons (MGI Ref ID J:4978)
- behavior/neurological phenotype
- abnormal vestibuloocular reflex (MGI Ref ID J:29747)
- mice exhibit an inverted optokinetic nystagmus in response to stimulation of only the temporal retina
- mice exhibit eye movements with a vertical component in response to horizontally moving, full-field stimuli
- enhanced behavioral response to xenobiotics (MGI Ref ID J:29294)
- sleep time is increased in mice exposed to pentobarbital, tribromoethanol, or alphaxalone compared to controls
- hearing/vestibular/ear phenotype
- abnormal vestibuloocular reflex (MGI Ref ID J:29747)
- mice exhibit an inverted optokinetic nystagmus in response to stimulation of only the temporal retina
- mice exhibit eye movements with a vertical component in response to horizontally moving, full-field stimuli
Lystbg/Lystbg
B6.C3Rl-Lystbg/J
- cellular phenotype
- abnormal lysosome morphology (MGI Ref ID J:6629)
- light and electron microscopic cytochemistry of cultured fibroblasts shows large dense bodies have an origin through fusion of lysosomes
- abnormal lysosome physiology (MGI Ref ID J:6801)
- significant increase in lysosomal enzyme activity of beta-galactosidase and beta-glucuronidase, and to a lesser extent N-acetyl-beta-hexoseaminidase, in kidney extracts
- immune system phenotype
- abnormal NK cell physiology (MGI Ref ID J:6801)
- lower natural killer cell activity
- respiratory system phenotype
- abnormal lung development (MGI Ref ID J:149429)
- impaired respiratory alveologenesis (MGI Ref ID J:149429)
- alveolar maturation is impaired, resulting in abnormally large alveoli
- emphysema (MGI Ref ID J:149429)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Lystbg related
Tyr+ relatedCardiovascular Research
Atherosclerosis
Dermatology Research
Color and White Spotting Defects
Hematological Research
Immunological Defects
Platelet Defects
platelet storage pool deficiency
Immunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Immunodeficiency
Intracellular Signaling Molecules
Internal/Organ Research
Kidney Defects
lysosomal enzyme abnormalities
Metabolism Research
Mouse/Human Gene Homologs
Chediak-Higashi syndrome
Research Tools
Immunology and Inflammation Research
NK Cell Deficiency
Dermatology Research
Color and White Spotting Defects
oculocutaneous albinism, type I
Mouse/Human Gene Homologs
albinism, tyrosine negative
wildtype
| Allele Symbol | Lystbg | ||
|---|---|---|---|
| Allele Name | beige | ||
| Allele Type | Radiation induced | ||
| Common Name(s) | 30B/22B; CHS mice; bg; | ||
| Strain of Origin | C3H/Rl | ||
| Gene Symbol and Name | Lyst, lysosomal trafficking regulator | ||
| Chromosome | 13 | ||
| Gene Common Name(s) | Beige; CHS; CHS1; D13Sfk13; DNA segment, Chr 13, Stephen F. Kingsmore 13; beige; bg; | ||
| Molecular Note | This allele is an insertion of a partial LINE 1 repetitive element into an intron of the gene. The insertion included only the most 3' 1097 bp of the element producing a frameshift mutation resulting in a truncated protein predicted to be missing the last 1442 amino acids. [MGI Ref ID J:33734] [MGI Ref ID J:41243] | ||
| Allele Symbol | Oca2+ | ||
| Allele Name | wild type | ||
| Allele Type | Not Specified | ||
| Gene Symbol and Name | Oca2, oculocutaneous albinism II | ||
| Chromosome | 7 | ||
| Gene Common Name(s) | BEY; BEY1; BEY2; BOCA; D15S12; D7H15S12; D7Icr28RN; D7Nic1; DNA segment, Chr 7, Institute for Cancer Research 28RN; DNA segment, Chr 7, Nicholls 1; DNA segment, Chr 7, human D15S12; EYCL; EYCL2; EYCL3; HCL3; P; PED; SHEP1; p; pink-eyed dilution; | ||
| Allele Symbol | Tyr+ | ||
| Allele Name | wild type | ||
| Allele Type | Not Applicable | ||
| Gene Symbol and Name | Tyr, tyrosinase | ||
| Chromosome | 7 | ||
| Gene Common Name(s) | C; OCA1A; OCAIA; SHEP3; albino; c; skc35; skin/coat color 35; | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Genotyping resources and troubleshooting
Gallin JI; Bujak JS; Patten E; Wolff SM. 1974. Granulocyte function in the Chediak-Higashi syndrome of mice. Blood 43(2):201-6. [PubMed: 4589319] [MGI Ref ID J:5405]
Perou CM; Moore KJ; Nagle DL; Misumi DJ; Woolf EA; McGrail SH; Holmgren L; Brody TH; Dussault BJ Jr; Monroe CA; Duyk GM; Pryor RJ; Li L; Justice MJ; Kaplan J. 1996. Identification of the murine beige gene by YAC complementation and positional cloning. Nat Genet 13(3):303-8. [PubMed: 8673129] [MGI Ref ID J:33734]
Roder JC. 1979. The beige mutation in the mouse. I. A stem cell predetermined impairment in natural killer cell function. J Immunol 123(5):2168-73. [PubMed: 489978] [MGI Ref ID J:6213]
Schiller NK; Black AS; Bradshaw GP; Bonnet DJ; Curtiss LK. 2004. Participation of macrophages in atherosclerotic lesion morphology in LDLr-/- mice. J Lipid Res 45(8):1398-409. [PubMed: 15175354] [MGI Ref ID J:91367]
Lystbg relatedOca2+ relatedAhmed F; Lundin LG; Shire JG. 1989. Lysosomal mutations increase susceptibility to anaesthetics. Experientia 45(11-12):1133-5. [PubMed: 2513223] [MGI Ref ID J:29294]
Ahmed F; Shire JG. 1985. Lysosomal mutations inhibit lipofuscinosis of the spleen in C57BL mice. J Hered 76(4):311-2. [PubMed: 4031470] [MGI Ref ID J:7980]
Andoh M; Zhang G; Russell-Lodrigue KE; Shive HR; Weeks BR; Samuel JE. 2007. T Cells Are Essential for Bacterial Clearance, and Gamma Interferon, Tumor Necrosis Factor Alpha, and B Cells Are Crucial for Disease Development in Coxiella burnetii Infection in Mice. Infect Immun 75(7):3245-55. [PubMed: 17438029] [MGI Ref ID J:122426]
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Barthold SW; de Souza M. 1995. Exacerbation of Lyme arthritis in beige mice. J Infect Dis 172(3):778-84. [PubMed: 7658072] [MGI Ref ID J:28297]
Bertin A. 1992. Comparison of susceptibility of inbred and outbred infant mice to Escherichia coli heat-stable enterotoxin STa. Infect Immun 60(8):3117-21. [PubMed: 1639480] [MGI Ref ID J:2117]
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Brandt EJ; Elliott RW; Swank RT. 1975. Defective lysosomal enzyme secretion in kidneys of Chediak-Higashi (beige) mice. J Cell Biol 67(3):774-88. [PubMed: 408] [MGI Ref ID J:5590]
Cavarra E; Martorana PA; de Santi M; Bartalesi B; Cortese S; Gambelli F; Lungarella G. 1999. Neutrophil influx into the lungs of beige mice is followed by elastolytic damage and emphysema. Am J Respir Cell Mol Biol 20(2):264-9. [PubMed: 9922217] [MGI Ref ID J:53722]
Chi EY; Ignacio E; Lagunoff D. 1978. Mast cell granule formation in the beige mouse. J Histochem Cytochem 26(2):131-7. [PubMed: 624833] [MGI Ref ID J:5935]
Chow LH. 1993. Studies of virus-induced myocardial injury in mice: value of the scid mutation on different genetic backgrounds and combined with other mutations. Lab Anim Sci 43(2):133-5. [PubMed: 8391609] [MGI Ref ID J:12476]
Clark EA; Roths JB; Murphy ED; Ledbetter JA; Clagett JA. 1982. The beige (bg) gene influences the development of autoimmune disease in SB/Le male mice. In: NK Cells and Other Natural Effector Cells. Academic Press, New York. [MGI Ref ID J:30716]
Clark EA; Shultz LD; Pollack SB. 1981. Mutations in mice that influence natural killer (NK) cell activity. Immunogenetics 12(5-6):601-13. [PubMed: 6971254] [MGI Ref ID J:6485]
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Dominique V; Francis L. 1995. Interactions of the scid or beige mutations with the viable motheaten mutation. Autoimmunity 22(4):199-207. [PubMed: 8781712] [MGI Ref ID J:33985]
Elin RJ; Edelin JB; Wolff SM. 1974. Infection and immunoglobulin concentrations in Chediak-Higashi mice. Infect Immun 10(1):88-91. [PubMed: 4601767] [MGI Ref ID J:5471]
Enriquez FJ; Sterling CR. 1991. Cryptosporidium infections in inbred strains of mice. J Protozool 38(6):100S-102S. [PubMed: 1818124] [MGI Ref ID J:598]
Feith GW; Assmann KJ; Bogman MJ; van Gompel AP; Schalkwijk J; Koene RA. 1993. Lack of albuminuria in the early heterologous phase of anti-GBM nephritis in beige mice. Kidney Int 43(4):824-7. [PubMed: 8479118] [MGI Ref ID J:12891]
Fernandez NC; Lozier A; Flament C; Ricciardi-Castagnoli P; Bellet D; Suter M; Perricaudet M; Tursz T; Maraskovsky E; Zitvogel L. 1999. Dendritic cells directly trigger NK cell functions: cross-talk relevant in innate anti-tumor immune responses in vivo. Nat Med 5(4):405-11. [PubMed: 10202929] [MGI Ref ID J:54135]
Galli SJ; Hammel I. 1984. Unequivocal delayed hypersensitivity in mast cell-deficient and beige mice. Science 226(4675):710-3. [PubMed: 6494907] [MGI Ref ID J:127346]
Gallin JI; Bujak JS; Patten E; Wolff SM. 1974. Granulocyte function in the Chediak-Higashi syndrome of mice. Blood 43(2):201-6. [PubMed: 4589319] [MGI Ref ID J:5405]
Gallo-Hendrikx E; Percy D; Copps J; McKeown B; Quinton M; McMillan I; Croy BA; Wildeman AG. 1999. Evaluation of three lines of immunodeficient mice for the study of spontaneous metastatic tumors. APMIS 107(2):245-56. [PubMed: 10225324] [MGI Ref ID J:54114]
Guo H; Sekiguchi M; Shimai K. 1992. Cytoarchitectonic abnormalities in cerebellum and hippocampal formation of beige mutant mouse. Tokai J Exp Clin Med 17(1):53-61. [PubMed: 1523694] [MGI Ref ID J:4978]
Haliotis T; Ball JK; Dexter D; Roder JC. 1985. Spontaneous and induced primary oncogenesis in natural killer (NK)-cell-deficient beige mutant mice. Int J Cancer 35(4):505-13. [PubMed: 2985510] [MGI Ref ID J:80649]
Harkness RE; Guimond MJ; McBey BA; Klein MH; Percy DH; Croy BA. 1993. Branhamella catarrhalis pathogenesis in SCID and SCID/beige mice. Brief report. APMIS 101(10):805-10. [PubMed: 8267959] [MGI Ref ID J:16050]
Hearing VJ; Phillips P; Lutzner MA. 1973. The fine structure of melanogenesis in coat color mutants of the mouse. J Ultrastruct Res 43(1):88-106. [PubMed: 4634048] [MGI Ref ID J:5346]
Hua C; Chang B; Ma B-L; Li Y; Wang G. 1992. Reduction of lymphokine-activated killer cell activity by the introduction of the beige gene into SCID mice ILAR News 34(1-2):S15-S16. [MGI Ref ID J:2627]
Ishigaki Y; Hayakawa J; Hashimoto N; Nikaido H; Nikaido O. 1996. New immunodeficient mouse strains bred by introducing beige and xid mutations into the KSN nude strain. (Correction: 1996 Dec;46(6):691) Lab Anim Sci 46(4):418-24. [PubMed: 8872993] [MGI Ref ID J:36125]
Ishigaki Y; Yasuda K; Hashimoto N; Hayakawa J; Hiai H; Nikaido O. 1998. A comparison of UVB-carcinogenesis between nude mice and nude beige mice. J Radiat Res (Tokyo) 39(2):119-27. [PubMed: 9735600] [MGI Ref ID J:52659]
Ishigaki Y; Yasuda K; Hashimoto N; Nikaido H; Nikaido O; Hayakawa JI. 1998. Enhanced human tumor cell transplantability in a new congenic immunodeficient mouse; KSN-BNX. Folia Microbiol (Praha) 43(5):493-4. [PubMed: 9821307] [MGI Ref ID J:52313]
Jensen BL; Rasch R; Nyengaard JR; Skott O. 1997. Giant renin secretory granules in beige mouse renal afferent arterioles. Cell Tissue Res 288(2):399-406. [PubMed: 9082976] [MGI Ref ID J:41539]
Johnson LL; Sayles PC. 1995. Strong cytolytic activity of natural killer cells is neither necessary nor sufficient for preimmune resistance to Toxoplasma gondii infection. Nat Immun 14(4):209-15. [PubMed: 8696010] [MGI Ref ID J:113057]
Jones-Carson J; Vazquez-Torres A; Balish E. 1995. Defective killing of Candida albicans hyphae by neutrophils from beige mice. J Infect Dis 171(6):1664-7. [PubMed: 7769315] [MGI Ref ID J:25930]
Kaido T; Gresser I; Maury C; Maunoury MT; Vignaux F; Belardelli F. 1993. Sensitized T lymphocytes render DBA/2 beige mice responsive to IFN alpha/beta therapy of Friend erythroleukemia visceral metastases. Int J Cancer 54(3):475-81. [PubMed: 8509222] [MGI Ref ID J:12190]
Karre K; Klein GO; Kiessling R; Klein G; Roder JC. 1980. Low natural in vivo resistance to syngeneic leukaemias in natural killer-deficient mice. Nature 284(5757):624-6. [PubMed: 7366734] [MGI Ref ID J:6302]
Keil M; Lungarella G; Cavarra E; van Even P; Martorana PA. 1996. A scanning electron microscopic investigation of genetic emphysema in tight-skin, pallid, and beige mice, three different C57 BL/6J mutants. Lab Invest 74(2):353-62. [PubMed: 8780155] [MGI Ref ID J:31735]
Kelly EM. 1957. Beige, bg Mouse News Lett 16:36. [MGI Ref ID J:29744]
Kirkpatrick CE; Farrell JP. 1982. Leishmaniasis in beige mice. Infect Immun 38(3):1208-16. [PubMed: 6218091] [MGI Ref ID J:6946]
Kisucka J; Butterfield CE; Duda DG; Eichenberger SC; Saffaripour S; Ware J; Ruggeri ZM; Jain RK; Folkman J; Wagner DD. 2006. Platelets and platelet adhesion support angiogenesis while preventing excessive hemorrhage. Proc Natl Acad Sci U S A 103(4):855-60. [PubMed: 16418262] [MGI Ref ID J:105659]
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Lane PW; Murphy ED. 1972. Susceptibility to spontaneous pneumonitis in an inbred strain of beige and satin mice. Genetics 72(3):451-60. [PubMed: 4643821] [MGI Ref ID J:5311]
Lode HN; Xiang R; Pertl U; Forster E; Schoenberger SP; Gillies SD; Reisfeld RA. 2000. Melanoma immunotherapy by targeted IL-2 depends on CD4(+) T-cell help mediated by CD40/CD40L interaction. J Clin Invest 105(11):1623-30. [PubMed: 10841521] [MGI Ref ID J:62762]
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Lutzner MA; Lowrie CT; Jordan HW. 1967. Giant granules in leukocytes of the beige mouse. J Hered 58(6):299-300. [PubMed: 5590154] [MGI Ref ID J:5078]
Maruo K; Shimamura K; Hioki K; Itoh M; Ueyama Y; Tamaoki N. 1993. Role of X-linked immunodeficiency (xid) and NK activity in rejection of human tumor xenotransplants in nude mice. APMIS 101(5):345-52. [PubMed: 8329195] [MGI Ref ID J:14379]
Mathiasen JR; Raffa RB; Vaught JL. 1987. C57BL/6J-bgJ (beige) mice: differential sensitivity in the tail flick test to centrally administered mu- and delta-opioid receptor agonists. Life Sci 40(20):1989-94. [PubMed: 3033418] [MGI Ref ID J:29746]
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McGarry RC; Walker R; Roder JC. 1984. The cooperative effect of the satin and beige mutations in the suppression of NK and CTL activities in mice. Immunogenetics 20(5):527-34. [PubMed: 6334024] [MGI Ref ID J:7649]
McLeod R; Estes RG; Mack DG; Cohen H. 1984. Immune response of mice to ingested Toxoplasma gondii: a model of toxoplasma infection acquired by ingestion. J Infect Dis 149(2):234-44. [PubMed: 6699433] [MGI Ref ID J:39992]
Mosier DE; Stell KL; Gulizia RJ; Torbett BE; Gilmore GL. 1993. Homozygous scid/scid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation. J Exp Med 177(1):191-4. [PubMed: 8418200] [MGI Ref ID J:3479]
Murphy ED; Roths JB. 1978. Purkinje cell degeneration, a late effect of beige mutations in mice Jackson Lab Ann Rep 49:108-9. [MGI Ref ID J:15166]
Mutwiri G K; Kosecka U; Benjamin M; Rosendal S; Perdue M; Butler D G. 2001. Mycobacterium avium subspecies paratuberculosis triggers intestinal pathophysiologic changes in beige/scid mice. Comp Med 51(6):538-44. [PubMed: 11924817] [MGI Ref ID J:73720]
Nakagawa R; Nagafune I; Tazunoki Y; Ehara H; Tomura H; Iijima R; Motoki K; Kamishohara M; Seki S. 2001. Mechanisms of the antimetastatic effect in the liver and of the hepatocyte injury induced by alpha-galactosylceramide in mice. J Immunol 166(11):6578-84. [PubMed: 11359810] [MGI Ref ID J:69484]
Nonoyama S; Smith FO; Bernstein ID; Ochs HD. 1993. Strain-dependent leakiness of mice with severe combined immune deficiency. J Immunol 150(9):3817-24. [PubMed: 8473734] [MGI Ref ID J:4610]
Novak EK; Hui SW; Swank RT. 1984. Platelet storage pool deficiency in mouse pigment mutations associated with seven distinct genetic loci. Blood 63(3):536-44. [PubMed: 6696991] [MGI Ref ID J:7327]
Novak EK; McGarry MP; Swank RT. 1985. Correction of symptoms of platelet storage pool deficiency in animal models for Chediak-Higashi syndrome and Hermansky-Pudlak syndrome. Blood 66(5):1196-201. [PubMed: 3902123] [MGI Ref ID J:8056]
Ohsugi T; Kiuchi Y; Shimoda K; Oguri S; Maejima K. 1996. Translocation of bacteria from the gastrointestinal tract in immunodeficient mice. Lab Anim 30(1):46-50. [PubMed: 8709573] [MGI Ref ID J:31261]
Oliver C; Essner E. 1973. Distribution of anomalous lysosomes in the beige mouse: a homologue of Chediak-Higashi syndrome. J Histochem Cytochem 21(3):218-28. [PubMed: 4697831] [MGI Ref ID J:5338]
Oliver C; Essner E. 1975. Formation of anomalous lysosomes in monocytes, neutrophils, and eosinophils from bone marrow of mice with Chediak-Higashi syndrome. Lab Invest 32(1):17-27. [PubMed: 1113502] [MGI Ref ID J:5514]
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Diet Information LabDiet® 5K52/5K67
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
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