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Galbraith, D.B.: The agouti pigment pattern of the mouse: A quantitative and experimental study. J. Exp. Zool. 155: 71-90, 1964.

Galbraith, D.B.: Cell mass, hair type and expression of the agouti gene. Nature (London) 222: 288-290, 1969.
See also PubMed.

Galbraith, D.B.: Expression of genes at the agouti locus and mitotic activity of the hair bulb of the mouse. Genetics 67: 559-568, 1971.
See also PubMed.

Galbraith, D.B., and Arceci, R.J.: Melanocyte populations of yellow and black hair bulbs in the mouse. J. Hered. 65: 381-382, 1974.
See also MGI.

Galbraith, D.B., and Patrignani, A.M.: Sulfhydryl compounds in melanocytes of yellow ( Ay/a), nonagouti ( a/a), and agouti ( A/A) mice. Genetics 84: 587-591, 1976.
See also MGI.

Galbraith, D.B., and Wolff, G.L.: Aberrant regulation of the agouti pigment pattern in the viable yellow mouse. J. Hered. 65: 137-140, 1974.
See also MGI.

Gallin, J.L., Bujak, J.S., Patten, E., and Wolff, S.M.: Granulocyte function in the Chediak-Higashi syndrome of mice. Blood 43: 201-206, 1974.
See also MGI.

Gardner, R.L., and Lyon, M.F.: X chromosome inactivation studied by injection of a single cell into the mouse blastocyst. Nature (London) 231: 385-386, 1971.
See also PubMed.

Garland, R.C., Satrustegui, J., Gluecksohn-Waelsch, S., and Cori, C.F.: Deficiency in plasma protein synthesis caused by x-ray-induced lethal albino alleles in mouse. Proc. Nat. Acad. Sci. USA 73: 3376-3380, 1976.
See also MGI.

Gasser, D.L., and Fischgrund, T.: Genetic control of the immune response in mice. IV. Relationship between graft vs host reactivity and possession of the high tumor genotypes Aya and Avya. J. Immunol. 110: 305-308, 1973.
See also MGI.

Gates, W.H.: The Japanese waltzing mouse; its origin, heredity and relation to the genetic characters of other varieties of mice. Pub. Carnegie Inst. Wash. No. 337: 83-138, 1926.

Geissler, E.N., and Russell, E.S.: Private communication. Mouse News Letter 59: 26, 1978.

Gerson, D.E., and Szabó, G.: Effect of single gene substitution on the melanocyte system of the C57BL mouse: Quantitative and qualitative histology. Nature (London) 218: 381-382, 1968.
See also PubMed.

Geschwind, I.I.: Change in hair color in mice induced by injection od alpha MSH. Endocrinology 79: 1165-1167, 1966.
See also PubMed.

Geschwind, I.I., and Huseby, R.A.: Melanocyte-stimulating activity in a transplantable mouse pituitary tumor. Endocrinology 79: 97-105, 1966.
See also PubMed.

Geschwind, I.I., and Huseby, R.A.: Hormonal modification of coat color in the laboratory mouse. In Pigmentation: Its Genesis and Biologic Control, V. Riley (ed.), pp. 207-214, Appleton-Century-Crofts, New York, 1972.

Geschwind, I.I., and Huseby, R.A., and Nishioka, R.: The effect of melanocyte-stimulating hormone on coat color in the mouse. Recent Prog. Hormone Res. 28: 91-130, 1972.
See also MGI.

Gluecksohn-Waelsch, S.: Private communication. Mouse News Letter 30: 14, 1964a.

Gluecksohn-Waelsch, S.: Private communication. Mouse News Letter 31: 10, 1964b.
See also MGI.

Gluecksohn-Waelsch, S.: Private communication. Mouse News Letter 32: 15, 1965.

Gluecksohn-Waelsch, S., Schiffman, M.B., Thorndike, J., and Cori, C.F.: Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase. Proc. Nat. Acad. Sci. USA 71: 825-829, 1974.
See also MGI.

Gluecksohn-Waelsch, S., Schiffman, M.B., and Moscona, M.H.: Glutamine synthetase in newborn mice homozygous for lethal albino alleles. Develop. Biol. 45: 369-371, 1975.
See also MGI.

Goka, T.J., Stevenson, R.E., Hefferan, P.M., and Howell, R.R.: Menkes disease: A biochemical abnormality in cultured human fibroblasts. Proc. Nat. Acad. Sci. USA 73: 604-606, 1976.
See also PubMed.

Goodale, H.D.: Evidence that size of head-spot (headdot, Keeler) in the mouse is not controlled by modifiers distributed among many chromosomes. Genetics 22: 193, 1937a (Abstract).

Goodale, H.D.: Can artificial selection produce unlimited change? Amer. Nat. 71: 433-459, 1937b.

Goodale, H.D.: Further progress with artificial selection. Amer. Nat. 76: 515-519, 1942.

Goodale, H.D.: New extreme variants in a selection experiment. Genetics 28: 75, 1943 (Abstract).

Goodale, H.D.: Transformation of black mice into white mice. Genetics 33: 106, 1948 (Abstract).

Goodman, R.M.: Effect of Wv locus in mouse on differential excretion of isomers of several amino acids. Proc. Soc. Exp. Biol. Med. 88: 283-287, 1955.

Goodman, R.M.: The effect of Wv allele in the mouse on the differential excretion of the optical isomers of several amino acids. J. Exp. Zool. 132: 189-217, 1956.

Goodman, R.M.: In vitro amino acid metabolism of tissues from a mouse mutant showing differential patterns of amino acid excretion. Fed. Proc. 17: 57, 1958 (Abstract).

Gordon, J.: Failure of XX cells containing the sex reversed gene to produce gametes in allophenic mice. J. Exp. Zool. 198: 367-373, 1976.
See also PubMed.

Gordon, J.: Modification of pigmentation patterns in allophenic mice by the W gene. Differentiation 9: 19-28, 1977.
See also MGI.

Grahn, D., and Craggs, R.: Mammalian genetics: An unusual occurrence of XXY tortoise males and presumed XY/XY mosaic. Argonne National Laboratory Biological and Medical Division Annual Report 7409 111-113, 1967.
See also PubMed.

Grahn, D., Fry, R.J.M., and Hamilton, K.F.: Genetic and pathologic analysis of the sex-linked allelic series, mottled, in the mouse. Genetics 61: s22-s23, 1969a (Abstract).

Grahn, D., Allen, K.H., Fry, R.J.M., and Hulesh, J.: Genetics of the "mottled" alleles of the X chromosome of the mouse. Argonne National Laboratory Biological and Medical Research Division Annual Report 7635 154-156, 1969b.
See also PubMed.

Grahn, D., Fry, R.J.M., and Allen, K.: Private communication. Mouse News Letter 44: 16, 1971.

Grahn, D., Fry, R.J.M., and Hulesch, J.L.: Private communication. Mouse News Letter 47: 20, 1972.
See also MGI.

Granholm, N.H. and Johnson, P.M.: Enhanced identification of lethal yellow ( Ay/Ay) mouse embryos by means of delayed development of four-cell stages. J. Exp. Zool. 205: 327-333, 1978.
See also PubMed.

Green, M.C.: Himalayan, a new allele of albino in the mouse. J. Hered. 52: 73-75, 1961.
See also MGI.

Green, M.C.: Mutant genes and linkages. In Biology of the Laboratory Mouse, 2nd ed., E.L. Green (ed.), pp. 87-150, McGraw-Hill, New York, 1966a.
See also Biology of the Laboratory Mouse at MGI.

Green, M.C.: Private communication. Mouse News Letter 34: 31, 1966b.
See also MGI.

Green, M.C.: Private communication. Mouse News Letter 44: 30, 1971.
See also MGI.

Green, M.C.: Private communication. Mouse News Letter 47: 36, 1972.
See also MGI.

Green, M.C.: Private communication. Mouse News Letter 49: 32, 1973.
See also MGI.

Green, M.C., and Sweet, H.O.: Private communication. Mouse News Letter 49: 32, 1973.
See also MGI.

Gregory, C.J., McCulloch, E.A., and Till, J.E.: The cellular basis for the defect in haemopoiesis in flexed-tailed mice. III. Restriction of the defect to erythropoietic progenitors capable of transient colony formation in vivo. Brit. J. Haematol. 30: 401-410, 1975.
See also MGI.

Grobman, A.B., and Charles, D.R.: Mutant white mice. J. Hered. 38: 381-384, 1947.
See also MGI.

Gropp, A., Tettenborn, U., and von Lehmann, E.: Chromosomenuntersuchungen bei der Tobakmaus (M. poschiavinus) und bei Tobakmaus-Hybriden. Experientia 25: 875-876, 1969.
See also MGI.

Gropp, A., Tettenborn, U., and von Lehmann, E.: Chromosomenvariation vom Roberton'schen Typus bei der Tabakmaus, M. poschiavinus, und ihren Hybriden mit der Laboratoriumsmaus. Cytogenetics 9: 9-23, 1970.
See also MGI.

Grüneberg, H.: A new sub-lethal colour mutation in the house mouse. Proc. Roy. Soc. (London) B 118: 321-342, 1935.
See also MGI.

Grüneberg, H.: Grey-lethal, a new mutation in the house mouse. J. Hered. 27: 105-109, 1936a.
See also MGI.

Grüneberg, H.: The inheritance of tail tip pigmentation in the house mouse. J. Genet 33: 343-345, 1936b.

Grüneberg, H.: Some new data on the grey-lethal mouse. J. Genet 36: 153-170, 1938.

Grüneberg, H.: Inherited macrocytic anemias in the house mouse. Genet. 24: 777-810, 1939.

Grüneberg, H.: Siderocytes: A new kind of erythrocytes. Nature (London) 148: 114-115, 1941.

Grüneberg, H.: Inherited macrocytic anaemias in the house mouse. II. Dominance relationships. J. Genet 43: 285-293, 1942a.
See also MGI.

Grüneberg, H.: The anemia of flexed-tailed mice (Mus musculus L.). I. Static and dynamic hematology. J. Genet 43: 45-68, 1942b.

Grüneberg, H.: The anemia of flexed-tailed mice (Mus musculus L.). II. Siderocytes. J. Genet. 44: 246-271, 1942c.
See also MGI.

Grüneberg, H.: Some observations on the micropthalmia gene in the mouse. J. Genet 49: 1-13, 1948.
See also MGI.

Grüneberg, H.: The Genetics of the Mouse, 2nd ed., Nijhoff, The Hague, 1952.
See also MGI.

Grüneberg, H.: The relationships of micropthalmia and white in the mouse. J. Genet. 51:359-362, 1953.
See also MGI.

Grüneberg, H.: The Pathology of Development; a Study of Inherited Skeletal Disorders in Animals, Wiley, New York, 1963.

Grüneberg, H.: The case for somatic crossing over in the mouse. Genet. Res. (Camb.) 7: 58-75, 1966a.
See also PubMed.

Grüneberg, H.: The molars of the tabby mouse, and a test of the 'single-active- X-chromosome' hypothesis. J. Embryol. Exp. Morphol. 15: 223-244, 1966b.
See also MGI.

Grüneberg, H.: More about the tabby mouse and about the Lyon hypothesis. J. Embryol. Exp. Morphol. 16: 569-590, 1966c.
See also PubMed.

Grüneberg, H.: Gene action in the mammalian X-chromosome. Genet. Res. (Camb.) 9: 343-357, 1967a.
See also PubMed.

Grüneberg, H.: Sex-linked genes in man and the Lyon hypothesis. Ann. Human Genet. 30: 239-237, 1967b.
See also PubMed.

Grüneberg, H.: Threshold phenomena versus cell heredity in the manifestation of sex-linked genes in mammals. J. Embryol. Exp. Morphol. 22: 145-179, 1969.
See also MGI.

Grüneberg, H.: The tabby syndrome in the mouse. Proc. Roy. Soc. (London) B. 179: 139-156, 1971a.
See also MGI.

Grüneberg, H.: The glandular aspects of the tabby syndrome in the mouse. J. Embryol. Exp. Morphol. 25: 1-19, 1971b.
See also MGI.

Grüneberg, H., and Truslove, G.M.: Two closely linked genes in the mouse. Genet. Res. (Camb.) 1: 69-90, 1960.
See also MGI.

Grüneberg, H., Cattanach, B.M., McLaren, A., Wolfe, H.G., and Bowman, P.: The molars of tabby chimeras in the mouse. Proc. Roy. Soc. (London) B 182: 183-192, 1972.
See also PubMed.

Guénet, J.L., and Mercier-Balaz, M.: Private communication. Mouse News Letter 53: 57-58, 1975.

Guénet, J.L., Marchal, G., Milon, G., Tambourin, P., and Wendling, F.: Fertile dominant spotting ( Wf): A new allele at the W locus. J. Hered. 70: 9-12, 1979.
See also PubMed.

Guillery, R.W., Amorn, C.S., and Eighmy, B.B.: Mutants with abnormal visual pathways: An explanation of anomalous geniculate laminae. Science 174: 831-832, 1971.
See also PubMed.

Guillery, R.W., Scott, G.L., Cattanach, B.M., and Deol, M.S.: Genetic mechanisms determining the central visual pathways of mice. Science 179: 1014-1016, 1973.
See also PubMed.

Guy-Grand, D., Griscelli, C., and Vassalli, P.: The mouse gut T lymphocyte a novel type of T cell. Nature, origin, and traffic in mice in normal and graft-versus-host conditions. J. Exp. Med. 148: 1661-1677, 1978.
See also PubMed.

Hadley, M.E., and Quevedo, W.C., Jr.: Vertebrate epidermal melanin unit. Nature (London) 209: 1334-1335, 1966.
See also PubMed.

Hagedoorn, A.L.: The genetic factors in the development of the house mouse which influence coat color. Z. induckt. Abstamm.-u. VererbLehre 6: 97-136, 1912.

Håkansson, E.M., and Lundin, L.G.: Effect of a coat color locus on kidney lysosomal glycosidases in the house mouse. Biochem. Genet. 15: 75-85, 1977.
See also MGI.

Haldane, J.B.S., Sprunt, A.D., and Haldane, N.M.: Reduplication in mice. J. Genet. 5: 133-135, 1915.
See also MGI.

Hance, R.T.: Detection of heterozygotes with x-rays. J. Hered. 19: 481-485, 1928.

Harrison, D.E.: Normal function of transplanted mouse erythrocyte precursors for 21 months beyond donor life spans. Nature New Biol. 237: 220-222, 1972a.
See also PubMed.

Harrison, D.E.: Lifesparing ability (in lethally irradiated mice) of W/Wv mouse marrow with no macroscopic clonies. Radiat. Res. 52: 553-563, 1972b.
See also PubMed.

Harrison, D.E.: Normal function of transplanted marrow cell lines from aged mice. J. Gerontol. 30: 279-285, 1975a.
See also PubMed.

Harrison, D.E.: Defective erythropoietic responses of aged mice not improved by young marrow. J. Gerontol. 30: 286-288, 1975b.
See also PubMed.

Harrison, D.E., and Cherry, M.: Survival of marrow allografts in W/Wv anemic mice: Effect of disparity at the Ea-2 locus. Immunogenet. 2: 219-229, 1975.
See also MGI.

Harrison, D.E., and Russell, E.S.: The response of W/Wv and Sl/Sld anaemic mice to haemopoietic stimuli. Brit. J. Haematol. 22: 155-168, 1972.
See also PubMed.

Harrison, D.E., Malathi, V.G., and Silber, R.: Elevated erythrocyte nucleoside deaminase levels in genetically anemic W/Wv and Sl/Sld mice. Blood Cells 1: 605-614, 1975.

Hauschka, T.S., Jacobs, B.B., and Holdridge, B.A.: Recessive yellow and it interaction with belted in the mouse. J. Hered. 59: 339-341, 1968.
See also MGI.

Hearing, V.J.: Tyrosinase activity in subcellular fractions of black and albino mice. Nature New Biol. 245: 81-83, 1973.
See also PubMed.

Hearing, V.J., Phillips, P., and Lutzner, M.A.: The fine structure of melanogenesis in coat color mutants of the mouse. J. Ultrastruct. Res. 43: 88-106, 1973.
See also MGI.

Heath, J.: Private communication. Mouse News Letter 58: 66, 1978.

Hertwig, P.: Neue Mutationen und koppelungsgruppen bei der Hausmaus. Z. induckt. Abstamm.-u. VererbLehre 80: 220-246, 1942a.
See also MGI.

Hertwig, P.: Sechs neue Mutationen bei der Hausmaus in ihrer Bedeutung für allgemeine Vererbungsfragen. Z. menschl. Vererbungs-u. KonstL. 26: 1-21, 1942b.

Heston, W.E.: Relationship between the lethal yellow ( Ay) gene of the mouse and susceptibility to induced pulmonary tumors. J. Natl. Cancer Inst. 3: 303-308, 1942.

Heston, W.E., and Deringer, M.K.: Relationship between the lethal yellow ( Ay) gene of the mouse and susceptability to spontaneous pulmonary tumors. J. Nat. Cancer Inst. 7: 463-465, 1947.

Heston, W.E., and Vlahakis, G.: Influence of the Ay gene on mammary-gland tumors, hepatomas, and normal growth in mice. J. Nat. Cancer Inst. 26: 969-983, 1961a.

Heston, W.E., and Vlahakis, G.: Elimination of the effect of the Ay gene on pulmonary tumors in mice by alteration of its effect on normal growth. J. Nat. Cancer Inst. 27: 1189-1196, 1961b.

Heston, W.E., and Vlahakis, G.: C3H- Avy — a high hepatoma and high mammary tumor strain of mice. J. Nat. Cancer Inst. 40: 1161-1166, 1968.
See also PubMed.

Hetherington, C: Private communication. Mouse News Letter 54: 34, 1976.
See also MGI.

Hirobe, T., and Takeuchi, T.: Induction of melanogenesis in the epidermal melanoblasts of newborn mouse skin by MSH. J. Embryol. Exp. Morphol. 37: 79-90, 1977a.
See also PubMed.

Hirobe, T., and Takeuchi, T.: Induction of melanogenesis in vitro in the epidermal melanoblasts of newborn mouse skin by MSH. In Vitro 13: 311-315, 1977b.
See also PubMed.

Hirobe, T., and Takeuchi, T.: Changes of organelles associated with the differentiation of epidermal melanocytes in the mouse. J. Embryol. Exp. Morphol. 43: 107-121, 1978.
See also PubMed.

Hirsch, M.S.: Studies on the response of osteopetrotic bone explants to parathyroid explants in vitro. Bull. Johns Hopkins Hosp. 110: 257-263, 1962.

Hoecker, G.: Mutaciones dominantes reversivas en mosaico en la cepa pura de ratones C58 negra. Biológica, Santiago 12: 25-37, 1950.

Holland, J.M.: Serotonin deficiency and prolonged bleeding in beige mice. Proc. Soc. Exp. Biol. Med. 151: 32-39, 1976.
See also PubMed.

Hollander, W.F.: Private communication. Mouse News Letter 15: 32-39, 1956.

Hollander, W.F.: Private communication. Mouse News Letter 20: 34, 1959.

Hollander, W.F.: Private communication. Mouse News Letter 25: 9, 1961.

Hollander, W.F.: Private communication. Mouse News Letter 30: 29, 1964.
See also MGI.

Hollander, W.F.: Complementary alleles at the mi-locus in the mouse. Genetics 60: 189, 1968 (Abstract).
See also MGI.

Hollander, W.F., and Gowen, J.W.: An extreme non-agouti mutant in the mouse. J. Hered. 47: 221-224, 1956.
See also MGI.

Hollander, W.F., Bryan, J.H.D., and Gowen, J.W.: Pleiotropic effects of a mutant at the P locus from x-irradiated mice. Genetics 45: 413-418, 1960a.
See also MGI.

Hollander, W.F., Bryan, J.H.D., and Gowen, J.W.: A male sterile pink-eyed mutant type in the mouse. Fertil. Steril. 11: 316-324, 1960b.
See also MGI.

Hollinshead, M.B., and Schneider, L.C.: Identification of neonatal grey lethal mice. Anat. Rec. 176: 273-278, 1973.
See also PubMed.

Hollinshead, M.B., Schneider, L.C., and Smith, M.E.: Prenatal development of the grey lethal mouse. I. Teeth and jaws. Anat. Rec. 182: 305-320, 1975.
See also MGI.

Holstein, M.B., Burnett, J.B., and Quevedo, W.C., Jr.: Genetic regulation of multiple forms of tyrosinase in mice: Action of a and b loci. Proc. Soc. Exp. Biol. Med. 126: 415-418, 1967.
See also PubMed.

Holstein, T.J., Quevedo, W.C., Jr., and Burnett, J.B.: Multiple forms of tyrosinase in rodents and lagomorphs with special reference to their genetic control in mice. J. Exp. Zool. 177: 173-184, 1971.
See also PubMed.

Hrubant, E.H.: Urinary amino acids differences in C57BL/6 and C3Heb/Fe inbred mice, and their F1 hybrid. Canad. J. Genet. Cytol. 7: 530-535, 1965.
See also PubMed.

Hsu, C.Y., and van Dyke, J.H.: An analysis of growth rates in neural epithelium of normal and spina bifidous (myeloschisis) mouse embryos. Anat. Rec. 100: 745, 1948 (Abstract).

Huff, S.D., and Fuller, J.L.: Audiogenic seizures, the dilute locus, and phenylalanine hydroxylase in DBA/1 mice. Science 144: 304-305, 1964.

Huff, S.D., and Huff, R.L.: Dilute locus and audiogenic seizures in mice. Science 136: 318-319, 1962.

Hummel, K.P., Coleman, D.L., and Lane, P.W.: The influence of genetic background on expression of mutations at the diabetes locus in the mouse. I. C57BL/KsJ and C57BL/6J strains. Biochem. Genet. 7: 1-13, 1972.
See also PubMed.

Hunsicker, P.R.: Private communication. Mouse News Letter 38: 31, 1968.
See also MGI.

Hunsicker, P.R.: Private communication. Mouse News Letter 40: 41, 1969.
See also MGI.

Hunt, D.M.: Primary defect in copper transport underlies mottled mutants in the mouse. Nature (London) 249: 852-854, 1974a.
See also MGI.

Hunt, D.M.: Private communication. Mouse News Letter 50: 36, 1974b.

Hunt, D.M., and Johnson, D.R.: Abnormal spermiogenesis in two pink-eyed sterile mutants in the mouse. J. Embryol. Exp. Morphol. 26: 111-121, 1971.
See also MGI.

Hunt, D.M., and Johnson, D.R.: Aromatic amino acid metabolism in brindled ( Mobr) and viable-brindled ( Movbr), two alleles at the mottled locus in the mouse. Biochem. Genet. 6: 31-40, 1972a.
See also MGI.

Hunt, D.M., and Johnson, D.R.: An inherited deficiency in noradrenalin biosynthesis in the brindled mouse. J. Neurochem. 19: 281-2819, 1972b.
See also MGI.

Hunt, D.M., and Skinner, D.F.: Private communication. Mouse News Letter 54: 42, 1976.

Hunt, H.R.: The flexed tailed mouse. Proc. VI Int. Congr. Genet. 2: 91-93, 1932 (Abstract).

Hunt, H.R., Mixter, R., and Permar, D.: Flexed tail in the mouse, Mus Musculus. Genetics 18: 335-366, 1933.
See also MGI.

Hurley, L.S., and Everson, G.J.: Influence of timing of short-term supplementation during gestation on congenital abnormalities of manganese-deficient rats. J. Nutrit. 79: 23-27, 1963.

Hurley, L.S., Everson, G.J., and Geiger, J.F.: Manganese deficiency in rats. Congenital nature of ataxia. J. Nutrit. 66: 309-320, 1958.

Hurley, L.S., Theriault, L.L., and Dreosti, I.E.: Liver mitochondria from manganese-deficient and pallid mice: Function and ultrastructure. Science 170: 1316-1318, 1970.
See also PubMed.

Ibsen, H.L., and Steigleder, E.: Evidence for the death in utero of the homozygous yellow mouse. Amer. Nat. 51: 740-752, 1917.

Ikejima, T., and Takeuchi, T.: Fluorescence spectrophotometric analysis of melanins in the house mouse. Biochem. Genet. 16: 673-679, 1978.
See also PubMed.

Iljin, N.A., and Iljin, V.N.: Temperature effects on the color of the siamese cat. J. Hered. 21: 309-318, 1930.

Isherwood, J.E., Strong, L.C., and Quevedo, W.C., Jr.: A new mutation of a to at in the mouse. J. Hered. 51: 121-135, 1960.

Ives, P.T.: The importance of mutation rate genes in evolution. Evolution 4: 236-252, 1950.

Jimbow, K., Quevedo, W.C., Jr., Fitzpatrick, T.B., and Szabó, G.: Some aspects of melanin biology: 1950-1975. J. Invest. Dermatol. 67: 72-89, 1976.
See also PubMed.

Johnson, D.R., and Hunt, D.M.: Private communication. Mouse News Letter 47: 52, 1972.
See also MGI.

Kales, A.N., Fried, W., and Gurney, C.W.: Mechanism of the hereditary anemia of Slm mutant mice. Blood 28: 387-397, 1966.
See also MGI.

Kaliss, N.: The morphogenesis of pigment in the hair follicles of the house mouse. J. Morphol. 70: 209-219, 1942.

Kamenoff, R.J.: Effects of the flexed-tailed gene on the development of the house mouse. J. Morphol. 58: 117-155, 1935.
See also MGI.

Kamenoff, R.J.: A cytological study of the embryonic livers (16-18 days) of normal and flexed-tailed (anemic) mice. Genetics 27: 150, 1942 (Abstract).

Kaplan, S.S., Boggs, S.S., Nardi, M.A., Basford, R.E., and Holland, J.M.: Leukocyte-platelet interactions in a murine model of Chediak-Higashi syndrome. Blood 52: 719-725, 1978.
See also PubMed.

Keeler, C.E.: A probable new mutation to white-belly in the house mouse, Mus musculus. Proc. Nat. Acad. Sci. USA 17: 700-703, 1931.

Keeler, C.E.: Akhissar spotting in the mouse. Proc. Nat. Acad. Sci. USA 19: 477-481, 1933.

Keeler, C.E.: Headdot: An incompletely recessive white spotting character of the house mouse. Proc. Nat. Acad. Sci. USA 21: 379-383, 1935.

Keeler, C.E., and Goodale, H.D.: A second occurrence of headdot spotting in the house mouse. J. Mammal. 17: 263-265, 1936.

Keighley, G., Russell, E.S., and Lowy, P.H.: Response of normal and genetically anaemic mice to erythropoietic stimuli. Brit. J. Hematol. 8: 429-441, 1962.

Keighley, G.H., Lowy, P., Russell, E.S., and Thompson, M.W.: Analysis of homeostatic mechanisms in normal and genetically anaemic mice. Brit. J. Haematol. 12: 461-477, 1966.

Kelley, E.M.: Private communication. Mouse News Letter 16: 36, 1957.

Kelley, E.M.: Private communication. Mouse News Letter 38: 31, 1968.

Kelley, E.M.: Private communication. Mouse News Letter 43: 59, 1970.

Kelley, E.M.: Private communication. Mouse News Letter 50: 52, 1974.

Kelley, E.M.: Private communication. Mouse News Letter 52: 46, 1975.

Kelton, D.E., and Rauch, H.: Myelination and myelin degeneration in the central nervous system of dilute-lethal mice. Exp. Neurol. 6: 252-262, 1962.

Kindred, B.: Some observations on the skin and hair of tabby mice. J. Hered. 58: 197-199, 1967.

King, R.A., and Rush, W.A.: Alcohol sensitivity in the albino mouse. In Pigment Cell, V. Riley (ed.), Vol. 3, pp. 211-219, Karger, Basal, 1976.

Kirby, G.C.: Greying with age: A coat-color variant in wild Australian populations of mice. J. Hered. 65: 126-128, 1974.
See also MGI.

Kirchner, C.E.J.: The effects of the mutator gene on molecular changes and mutations in Salmonella Typhimurium. J. Mol. Biol. 2: 331-338, 1960.

Kirkham, W.B.: The fate of homozygous yellow mice. J. Exp. Zool. 28: 125-135, 1919.

Kitamura, Y., Shimada, M., Hatanaka, K., and Miyano, Y.: Development of mast cells from grafted bone marow in irradiated mice. Nature (London) 268: 442-443, 1977.
See also PubMed.

Kitamura, Y., Go, S., and Hatanaka, K.: Decrease of mast cells in W/Wv mice and their increase by bone marrow transplantation. Blood 52: 447-452, 1978.
See also PubMed.

Klein, A., and Sitarz, K.: The influence of the mosaic ( Ms) mutation on the amino acid composition of blood plasma and the osmotic resistance of erythrocytes. Acta Biol. Cracov. Ser. Zool. 14: 129-136, 1971.

Klein, A., and Styrna, J.: Ninhydrin positive substances present in the urine of mice carrying the lethal mosaic ( Ms) mutation. Acta Biol. Cracov. Ser. Zool. 14: 121-127, 1971.

Klein, J.: Biology of the Mouse Histocompatibility-2 Complex. Springer-Verlag, New York, 1975.
See also MGI.

Knisely, A.S., Gasser, D.L., and Silvers, W.K.: Expression in organ culture of agouti locus genes of the mouse. Genetics 79: 471-475, 1975.
See also MGI.

Knospe, W.H., Hinrichs, B., Fried, W., Robinson, W., and Trobaugh, F.E., Jr.: Normal colony stimulating factor (CSF) production by bone marrow stromal cells and abnormal granulopoiesis with decreased CFUc in Sl/Sld mice. Exp. Hematol. 4: 125-130, 1976.
See also PubMed.

Konyukhov, B.V., and Sazhina, M.V.: Eye development in mutant mice strain microphthalmia. J. Gen. Biol. 24: 285-295, 1963 (in Russian).

Konyukhov, B.V., and Sazhina, M.V.: Interaction of the genes of ocular retardation and microphthalmia in mice. Folia Biol. (Praha) 12: 116-123, 1966.
See also PubMed.

Konyukhov, B.V., Osipov, V.V., Vachruscheva, M.P.: Damage of derivatives of neural crest in mice of mutant lines Microphthalmia and White. Arch. Anat. Histol. Embryol. 8: 100-107, 1965 (in Russian).

Kramer, J.W., Davis, W.C., and Prieur, D.J.: The Chediak-Higashi syndrome of cats. Lab. Invest. 36: 554-562, 1977.
See also PubMed.

Kreitner, P.C.: Linkage studies in a new black-eyed white mutation in the house mouse (not W). J. Hered. 48: 300-304, 1957.
See also MGI.

Krzanowska, H.: Private communication. Mouse News Letter 35: 35, 1966.
See also MGI.

Krzanowska, H.: Private communication. Mouse News Letter 38: 25, 1968.

Krzanowska, H., and Wabik, B.: Selection for expression of sex linked gene Ms (mosaic) in heterozygous mice. Genet. Pol. 12: 537-544, 1971.

Krzanowska, H., and Wabik, B.: Further studies on the expression of sex-linked gene Ms (mosaic) in heterozygous mice. Genet. Pol. 14: 193-198, 1973.

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