References

Adler, S.S., and Trobaugh, F.E., Jr.: Pluripotent (CFU-S) and granulocyte-committed (CFU-C) stem cells in intact and ⁸⁹Sr marrow-ablated Sl/Sl^d mice. Cell Tissue Kinet. 11:555-566, 1978.
See also PubMed.

Altman, K.I., and Russell, E.S.: Heme synthesis in normal and genetically anemic mice. J. Cell. Comp. Physiol. 64: 293-301, 1964.

Altus, M.S., Bernstein, S.E., Russell, E.S., Carsten, A.L., and Upton, A.C.: Defect extrinsic to stem cells in spleens of steel anemic mice. Proc. Soc. Exp. Biol. Med. 138: 985-988, 1971.
See also PubMed.

Andrews, E.J., White, W.J., and Bullock, L.P.: Spontaneous aortic aneurysms in blotchy mice. Amer. J. Pathol. 78: 199-208, 1975.
See also MGI.

Artzt, K., and Bennett, D.: Analogies between embryonic (T/t) antigens and adult major histocompatibility (H-2) antigens. Nature (London) 256: 545-547, 1975.
See also PubMed.

Attfield, M.: Inherited macrocytic anemias in the house mouse. III. Red blood cell diameters. J. Genet. 50: 250-263, 1951.

Auerbach, R.: Analysis of the developmental effects of a lethal mutation in the house mouse. J. Exp. Zool. 127: 305-329, 1954.
See also MGI.

Bagnara, J.T., Matsumoto, J., Ferris, W., Frost, S.K., Turner, W.A., Jr., Tchen, T.T., and Taylor, J.D.: Common origin of pigment cells. Science 203: 410-415, 1979.
See also PubMed.

Ballantyne, J., Bock, F.G., Strong, L.C., and Quevedo, W.C., Jr.: Another allele at the W locus of the mouse. J. Hered. 52: 200-202, 1961.
See also MGI.

Bangham, J.W.: Private communication. Mouse News Letter 38: 31, 1968.
See also MGI.

Barnes, D.W.H., Loutit, J.F., and Sansom, J.M.: Histocompatible cells for the resolution of osteopetrosis in microphthalmic mice. Proc. Roy. Soc. (London) B 188: 501-505, 1975.
See also PubMed.

Barnicot, N.A.: Studies on the factors involved in bone absorption. I. The effect of subcutaneous transplantation of bones of the grey-lethal house mouse into normal hosts and of normal bones into grey-lethal hosts. Amer. J. Anat. 68: 497-531, 1941.

Barnicot, N.A.: Some data on the effect of parathormone on the grey-lethal mouse. J. Anat. 79: 497-531, 1945.

Barnicot, N.A.: The local action of the parathyroid and other tissues on bone in intracerebral grafts. J. Anat. 82: 233-248, 1948.

Barrows, E.F.: Modification of the dominance of agouti to nonagouti in the mouse. J. Genet. 29: 9-15, 1934.

Barrows, E.F.: Selection for tail-spotting in the house mouse. J. Exp. Zool. 80: 107-111, 1939.

Batchelor, A.L., Phillips, R.J.S., and Searle, A.G.: A comparison of the mutagenic effectiveness of chronic neutron- and gamma-irradiation of mouse spermatogonia. Mutat. Res. 3: 218-229, 1966.
See also MGI.

Bateman, A.E., and Cole, R.J.: Colony forming cells in the livers of prenatal flexed (f/f) anaemic mice. Cell Tissue Kinet. 5: 165-173, 1972.
See also PubMed.

Bateman, A.E., Cole, R.J., Regan, T., and Tarbutt, R.G.: The role of erythropoietin in prenatal erythropoiesis of congenitally anaemic flexed-tail (f/f) mice. Brit. J. Haematol. 22: 415-427, 1972.
See also PubMed.

Bateman, A.J.: A probable case of mitotic crossing-over in the mouse. Genet. Res. (Camb.) 9: 375, 1967.
See also PubMed.

Bateman, N.: Bone growth: A study of the grey-lethal and microphthalmic mutants of the mouse. J. Anat. 88: 212-262, 1954.
See also MGI.

Bateman, N.: Private communication. Mouse News Letter 16: 7, 1957.
See also MGI.

Bateman, N.: Sombre, a viable dominant mutant in the house mouse. J. Hered. 52: 186-189, 1961.
See also MGI.

Beechy, C.V., and Searle, A.G.: Private communication. Mouse News Letter 44: 27, 1971.

Beechy, C.V., and Searle, A.G.: Private communication. Mouse News Letter 46: 27, 1972.

Beechy, C.V., and Searle, A.G.: Private communication. Mouse News Letter 55: 15, 1976.

Beechy, C.V., and Searle, A.G.: Private communication. Mouse News Letter 59: 19, 1978.

Benestad, H.B., Boyum, A., and Warhuus, K.: Haematopoietic defects of W/W^v mice studied with the spleen colony, agar colony, and diffusion chamber techniques. Scand. J. Haematol. 15: 219-227, 1975.
See also PubMed.

Bennett, D.: Developmental analysis of a mutant with pleiotropic effects in the mouse. J. Morphol. 98: 199-234, 1956.
See also MGI.

Bennett, D.: The T-locus of the mouse. Cell 6: 441-454, 1975.
See also MGI.

Bennett, J.M., Blume, R.S., and Wolff, S.M.: Characterization and significance of abnormal leukocyte granules in the beige mouse. A possible homologue for Chediak-Higashi Aleutian trait. J. Lab. Clin. Med. 73: 235-243, 1969.
See also PubMed.

Bennett, M., Cudkowicz, G., Foster, R.A., and Metcalf, D.: Hemopoietic progenitor cells of W anemic mice studied in vivo and in vitro. J. Cell. Physiol. 71: 211-226, 1968a.
See also PubMed.

Bennett, M., Steeves, R.A., Cudkowicz, G., Mirand, E.A., and Russell, L.B.: Mutant Sl alleles of mice affect susceptibility to Friend spleen focus-forming virus. Science 162: 564-565, 1968b.
See also MGI.

Bernstein, S.E.: Private communication. Mouse News Letter 23: 33-34, 1960.
See also MGI.

Bernstein, S.E.: Acute radiosensitivity in mice of differing W genotype. Science 137: 428-429, 1962.

Bernstein, S.E.: Modification of radiosensitivity of genetically anemic mice by implantation of blood-forming tissue. Radiat. Res. 20: 695-702, 1963.

Bernstein, S.E.: Tissue transplantation as an analytic and therapeutic tool in hereditary anemias. Amer. J. Surg. 119: 448-451, 1970.
See also PubMed.

Bernstein, S.E., and Russell, E.S.: Implantation of normal blood-forming tissue in genetically anemic mice, without x-irradiation of host. Proc. Soc. Exp. Biol. Med. 101: 769-773, 1959.

Bernstein, S.E., Russell, E.S., and Keighley, G: Two hereditary mouse anemias ( Sl/Sl^d and W/W^v) deficient in response to erythropoietin. Ann. N.Y. Acad. Sci 149: 475-485, 1968.

Bhat, N.R.: A dominant mutant mosaic house mouse. Heredity 3: 243-248, 1949.

Bielschowsky, M., and Schofield, G.C.: Studies on the inheritance and neurohistology of megacolon in mice. Proc. Univ. Ontago Med. Sch. 38: 14-15, 1960.

Bielschowsky, M. and Schofield, G.C.: Studies on megacolon in piebald mice. Aust. J. Exp. Biol. Med. Sci. 40: 395-404, 1962.

Billingham, R.E., and Silvers, W.K.: The melanocytes of mammals. Quart. Rev. Biol. 35: 1-40, 1960.
See also MGI.

Bolois, M.S., Zahlan, A.B., and Maling, J.E.: Electron spin-resonance studies on melanin. Biophys. J. 4: 471-490, 1964.

Bloom, J.L., and Falconer, D.S.: "Grizzled", a mutant in linkage group X of the mouse. Genet. Res. (Camb.) 7: 159-167, 1966.
See also MGI.

Blume, R.S., and Wolff, S.M.: The Chediak-Higashi syndrome. Studies in four patients and a review of the literature. Medicine 51: 247-280, 1972.
See also PubMed.

Blume, R.S., Bennett, J.M., Yankee, R.A., and Wolff, S.M.: Defective granulocyte regulation in the Chediak-Higashi syndrome. New Eng. J. Med. 279: 1009-1015, 1968.
See also PubMed.

Blume, R.S., Padgett, G.A., Wolff, S.M., and Bennett, J.M.: Giant neutrophil granules in the Chediak-Higashi syndrome of man, mink, cattle, and mice. Canad. J. Comp. Med. 33: 271-274, 1969.
See also PubMed.

Boggs, S.S., Wilson, S.M., and Smith, W.W.: Effects of endotoxin on hematopoiesis in irradiated and nonirradiated W/W^v mice. Radiat. Res. 56: 481-493, 1973.
See also PubMed.

Borghese, E.: Gonads of W mice cultured in vitro. Anat. Rec. 124: 481-482, 1956 (Abstract).

Borghese, E.: The present state of research on WW mice. Acta Anat. 36: 185-220, 1959.

Boxer, L.A., Watanabe, A.M., Rister, M., Besch, H.R., Jr., Allen, J., and Baehner, R.L.: Correction of leukocyte function in Chediak-Higashi syndrome by ascorbate. New Eng. J. Med. 295: 1041-1045, 1976.
See also PubMed.

Brandt, E.J., and Swank, R..: The Chediak-Higashi (beige) mutation in two mouse strains. Allelism and similarity in lysosomal dysfunction. Amer. J. Pathol. 82: 573-588, 1976.
See also PubMed.

Brandt, E.S., Elliott, R.W., and Swank, R.T.: Defective lysosomal enzyme secretion in kidneys of Chediak-Higashi (beige) mice. J. Cell Biol. 67: 774-788, 1975.
See also MGI.

Brauch, L.R., and Russell, W.L.: Colorimetric measurement of the effects of the major coat color genes in the mouse on the quantity of yellow pigment in extracts. Genetics 31: 212, 1946 (Abstract).

Bulfield, G.: Private communication. Mouse News Letter 50: 35, 1974.

Burnett, J.B.: The tyrosinases of mouse melanoma. Isolation and molecular properties. J. Biol. Chem. 246: 3079-3091, 1971.
See also PubMed.

Burnett, J.B., and Seiler, H.: Separation and properties of solubilized tyrosinase from mouse melanoma. Fed. Proc. 25: 294, 1966 (Abstract).

Burnett, J.B., Seiler, H., and Brown, I.V.: Separation and characterization of multiple forms of tyrosinase from mouse melanoma. Cancer Res. 27: 880-889, 1967.
See also PubMed.

Burnett, J.B., Holstein, T.J., and Quevedo, W.C., Jr.: Electrophoretic variations of tyrosinase in follicular melanocytes during the hair growth cycle in mice. J. Exp. Zool. 171: 369-376, 1969.
See also PubMed.

Burrows, E.F.: Selection for tail-spotting in the house mouse. J. Exp. Zool. 80: 107-111, 1939.

Butler, J. and Lyon, M.F.: Private Communication. Mouse News Letter 40: 25, 1969.
See also MGI.

Butler, L.: The effect of the coat colour dilution gene on body size in the mouse. Heredity 8: 275-278, 1954.

Cacheiro, N.L.A., and Russell, L.B.: Evidence that linkage group IV as well as linkage group X of the mouse are in chromosome 10. Genet. Res. (Camb.) 25: 193-195, 1975.
See also MGI.

Calarco, P.G., and Pederson, R.A.: Ultrastructural observations of lethal yellow ( A^y/A^y) mouse embryos. J. Embryol. Exp. Morphol. 35: 73-80, 1976.
See also MGI.

Carnes, W.H.: Copper and connective tissue metabolism. Int. Rev. Connect. Tissue Res. 4: 197-232, 1968.
See also PubMed.

Carter, T.C.: A mosaic mouse with an anomalous segregation ratio. J. Genet. 51: 1-6, 1952.

Carter, T.C.: Private Communication. Mouse News Letter 21: 40, 1959.
See also MGI.

Carter, T.C., Lyon, M.F., and Philips, R.J.S.: Genetic hazard of ionizing radiations. Nature (Lond.) 182: 409, 1958.

Castle, W.E.: Mammalian Genetics. Harvard Univ. Press, Cambridge, 1940.

Castle, W.E.: Influence of certain color mutations on body size in mice, rats, and rabbits. Genetics 26: 177-191, 1941.

Castle, W.E.: Size genes of mice. Proc. Nat. Acad. Sci. USA 28: 69-72, 1942.

Castle, W.E., and Allan, G.M.: The heredity of albinism. Proc. Amer. Acad. Arts Sci. 38: 603-622, 1903.

Castle, W.E., and Little, C.C.: On a modified Mendelian ratio among yellow mice. Science 32: 603-622, 1910.
See also MGI.

Castle, W.E., Gates, W.H., Reed, S.C., and Law, L.W.: Studies of a size cross in mice. II. Genetics 21: 310-323, 1936.

Cattanach, B.M.: A chemically-induced variegation-type position effect in the mouse. Z. Vererbungslehre 92: 165-182, 1961.

Cattanach, B.M.: Position effect variegation in the mouse. Genet. Res. (Camb.) 23: 291-306, 1974.
See also PubMed.

Cattanach, B.M.: Private Communication. Mouse News Letter 59: 18, 1978.
See also MGI.

Cattanach, B.M., and Williams, C.E.: Private Communication. Mouse News Letter 47: 34-35, 1972.

Cattanach, B.M., Pollard, C.E., and Perez, J.N.: Controlling elements in the mouse X-chromosome. I. Interaction with the X-linked genes. Genet. Res. (Camb.) 14: 223-235, 1969.
See also MGI.

Cattanach, B.M., Wolfe, H.G., and Lyon, M.F.: A comparative study of the coats of chimeric mice and those of heterozygotes for X-linked genes. Genet. Res. (Camb.) 19: 213-228, 1972.
See also MGI.

Charles, D.R.: Studies on spotting patterns. IV. Pattern variation and its developmental significance. Genetics 23: 523-547, 1938.

Chase, H.B.: Studies on the tricolor pattern of the guinea pig. II. The distribution of black and yellow as affected by white spotting and by imperfect dominance in the tortoise shell series of alleles. Genetics 24: 622-643, 1939.

Chase, H.B.: Greying of hair. I. Effects produced by single doses of x-rays on mice. J. Morphol. 84: 57-80, 1949.

Chase, H.B.: Number of entities inactivated by x-rays in greying of hair. Science 113: 714-716, 1951.

Chase, H.B.: Growth of the hair. Physiol. Rev. 34: 113-126, 1954.

Chase, H.B.: The behavior of pigment cells and epithelial cells in the hair follicle. In The Biology of Hair Growth, W. Montagna and R.A. Ellis (eds.), pp. 229-237, Academic Press, New York, 1958.

Chase, H.B.: Private Communication. Mouse News Letter 21: 21, 1959.
See also MGI.

Chase, H.B.: Private Communication. Mouse News Letter 33: 17, 1965.
See also MGI.

Chase, H.B., and Mann, S.J.: Phenogenetic aspects of some hair and pigment mutants. J. Cell. Comp. Physiol. 56: 103-112, 1960.

Chase, H.B., and Rauch, H.: Greying of hair. II. Response of individual hairs in mice to variations in x-radiation. J. Morphol. 87: 381-392, 1950.

Chase, H.B., and Silver, A.F.: The biology of hair growth. In The Biological Basis of Medicine, Vol. 6, Part I. Hair and Skin, E.E. Bittar (ed.), pp. 3-19, Academic Press, London, 1969.

Chase, H.B., Rauch, H., and Smith, V.W.: Critical stages of hair development and pigmentation in the mouse. Physiol. Zool. 24: 1-8, 1951.

Chervenick, P.A., and Boggs, D.A.: Decreased neutrophils and megakaryocytes in anemic mice of genotype W/W^v. J. Cell Physiol. 73: 25-30, 1969.
See also PubMed.

Chi, E.Y., and Lagunoff, D.: Abnormal mast cell granules in the beige (Chediak-Higashi syndrome) mouse. J. Histochem. Cytochem. 23: 117-122, 1975.
See also PubMed.

Chi, E.Y., Prueitt, J.L., and Lagunoff, D.: Abnormal lamellar bodies in type II pneumocytes and increased lung surface active material in the beige mouse. J. Histochem. Cytochem. 23: 863-866, 1975.
See also PubMed.

Chi, E.Y., Lagunoff, D., and Koehler, J.K.: Abnormally large lamellar bodies in type II pneumocytes in Chediak-Higashi syndrome in beige mice. Lab. Invest. 34: 166-173, 1976.
See also PubMed.

Chi, E.Y., Ignacio, E., and Lagunoff, D.: Mast cell granule formation in the beige mouse. J. Histochem. Cytochem. 26: 131-137, 1978.
See also MGI.

Chian, L.T.Y., and Wilgram, G.F.: Tyrosinase inhibition: Its role in suntanning and in albinism. Science 155: 198-200, 1967.
See also PubMed.

Chiquoine, A.D.: The identification, origin and migration of the primordial germ cells in the mouse embryo. Anat. Rec. 118: 135-146, 1954.

Chui, D.H.K., and Loyer, B.V.: Foetal erythropoiesis in steel mutant mice. II. Haemopoietic stem cells in foetal livers during development. Brit. J. Haematol. 29: 553-565, 1975a.
See also PubMed.

Chui, D.H.K., and Loyer, B.V.: Erythropoiesis in steel mutant mice: Effects of erythropoietin in vitro. Blood 45: 427-433, 1975b.
See also PubMed.

Chui, D.H.K., and Russell, E.S.: Fetal erythropoiesis in steel mutant mice. I. A morphological study of erythroid cell development in fetal liver. Develop. Biol. 40: 256-269, 1974.
See also PubMed.

Chui, D.H.K., Loyer, B.V., and Russell, E.S.: Steel ( Sl) mutation in mice. Identification of mutant embryos early in development. Develop. Biol. 49: 300-303, 1976.
See also PubMed.

Chui, D.H.K., Sweeney, G.D., Patterson, M., and Russell, E.S.: Hemoglobin synthesis in siderocytes of flexed-tail ( f/f) fetal mice. Blood 50: 165-177, 1977.
See also MGI.

Cizadlo, G.R., and Granholm, N.H.: In vivo development of the lethal yellow ( A^y/A^y) mouse embryo at 105 hours post coitum. Genetica 48: 89-93, 1978a.

Cizadlo, G.R., and Granholm, N.H.: Ultrastructural analysis of preimplantation lethal yellow ( A^y/A^y) mouse embryos. J. Embryol. Exp. Morphol. 45: 13-24, 1978b.
See also PubMed.

Clark, F.H.: The inheritance and linkage relations of a new recessive spotting in the house mouse. Genetics 19: 365-393, 1934.

Clarke, W.E.: Notes on the mice of St. Kilda. Scot. Natural. (Edinburgh) pp. 124-128, 1914.

Cleffmann, G.: Untersuchen über die Fellzeichnung des Wildkaninchens Ein Betrag zur Wirkungsweise des Agutifacktors. Z. induct. Abstamm.-u. VererbLehre 85: 137-162, 1953.

Cleffmann, G.: Uber den Einfluss des Milieus in situ and in vitro auf die Manifestierung der Agutizeichung. In Verhandl. Deutsch. Zool. Gesellsch., pp. 263-268, Geest and Portig K.-G., Leipzig, 1960.

Cleffmann, G.: Agouti pigment cells in situ and in vitro. Ann. N.Y. Acad. Sci. 100: 749-760, 1963.

Cleffmann, G.: Function-specific changes in the metabolism of agouti pigment cells. Exp. Cell Res. 35: 590-600, 1964.

Cloudman, A.M., and Bunker, L.E.: The varitint-waddler mouse. A dominant mutation in Mus musculus. J. Hered. 36: 259-263, 1945.
See also MGI.

Cole, R.J., Tarbutt, R.G., Cheek, E.M., and White, S.L.: Expression of congenital defects in the haemopoietic micro-environment: Pre-natal erythropoiesis in anaemic "steel" ( Sl^j/Sl^j) mice. Cell Tissue Kinet. 7: 463-477, 1974.
See also PubMed.

Coleman, D.L.: Phenylalanine hydroxylase activity in dilute and non-dilute strains of mice. Arch. Biochem. Biophys. 91: 300-306, 1960.

Coleman, D.L.: Effect of genic substitution on the incorporation of tyrosine into the melanin of mouse skin. Arch. Biochem. Biophys. 96: 562-568, 1962.
See also MGI.

Coleman, D.L.: Tactics in pigment cell research. (Discussion). In Methodology in Mammalian Genetics, W.J. Burdette (ed.), pp. 342, Holden-Day, San Francisco, 1963.

Coleman, D.L., Russell, E.S., and Levin, E.Y.: Enzymatic studies of the hemopoietic defect in flexed mice. Genetics 61:631-642, 1969.
See also PubMed.

Cotzias, G.C., Papavasilov, P.S., and Miller, S.T.: Manganese in melanin. Nature (London) 201: 1228-1229, 1964.

Coulombre, J.L., and Russell, E.S.: Analysis of the pleiotropism at the W-locus in the mouse: The effects of W and W^v substitution upon postnatal development of germ cells. J. Exp. Zool. 126: 277-296, 1954.

Creel, D.J.: Visual system anomaly associated with albinism in the cat. Nature (London) 231: 465-466, 1971.
See also PubMed.

Cúenot, L.: La loi de Mendel et l'hereditie de la pigmentation chez la souris. Arch. Zool. exp. gen., 3e ser., 10: xxvii-xxx, 1902.

Cúenot, L.: Les races pures et leurs combinaisons chez les souris (4e note). Arch. Zool. exp. gen., 4e ser., 3: cxxiii-cxxxii, 1905.

Dancis, J., Jansen, V., Brown, G.F., Gorstein, F., and Balis, M.E.: Treatment of hypoplastic anemia in mice with placental transplants. Blood 50: 663-670, 1977.
See also PubMed.

Danks, D.M., Campbell, P.E., Stevens, B.J., Mayne, V., and Cartwright, E.: Menkes's kinky hair syndrome: An inherited defect in copper absorption with wide-spread effects. Pediatrics 50: 188-201, 1972a.

Danks, D.M., Campbell, P.E., Walker-Smith, J., Stevens, B.J., Gillespie, J.M., Blomfield, J., and Turner, B.: Menkes' kinky-hair syndrome. Lancet ii: 1100-1103, 1972b.
See also PubMed.

Davidson, G.E., and Dawson, G.W.P.: Chemically induced presumed somatic mutations in the mouse. Mutat. Res. 38: 151-154, 1976.
See also PubMed.

Davidson, G.E., and Dawson, G.W.P.: The induction of somatic mutations in mouse embryos by benzo(a)pyrene. Arch. Toxicol. 38: 99-103, 1977.
See also PubMed.

Davis, W.C., and Douglas, S.D.: Defective granule formation and function in the Chediak-Higashi syndrome in man and animals. Semin. Hematol. 9: 431-450, 1972.
See also PubMed.

Davisson, M.T.: Private communication. Mouse News Letter 57: 22, 1977.

deAberle, S.: A study of hereditary anemia in mice. Amer. J. Anat. 40: 219-247, 1927.

Demerec, M.: Frequency of spontaneous mutations in certain stocks of Drosophila melanogaster. Genetics 22: 469-478, 1937.

Deol, M.S.: The anomalies of the labyrinth of the mutants varitint-waddler, shaker-2 and jerker in the mouse. J. Genet. 52: 562-588, 1954.
See also MGI.

Deol, M.S.: Inheritance of coat color in laboratory rodents. In Animals for Research, W. Lane-Petter (ed.), pp. 177-198, Academic Press, London, 1963.

Deol, M.S.: The neural crest and the acoustic ganglion. J. Embryol. Exp. Morphol. 17: 533-541, 1967.
See also MGI.

Deol, M.S.: Inherited diseases of the inner ear in man in the light of studies on the mouse. J. Med. Genet. 5: 137-158, 1968.
See also PubMed.

Deol, M.S.: The determination and distribution of coat colour variation in the house mouse. Symp. Zool. Soc. London 26: 239-250, 1970a.

Deol, M.S.: The relationship between abnormalities of pigmentation and of the inner ear. Proc. Roy. Soc. (London) A 175: 201-217, 1970b.
See also PubMed.

Deol, M.S.: The origin of the acoustic ganglion and effects of the gene dominant spotting ( W^v) in the mouse. J. Embryol. Exp. Morphol. 23: 773-784, 1970c.
See also MGI.

Deol, M.S.: Spotting genes and internal pigmentation patterns in the mouse. J. Embryol. Exp. Morphol. 26: 123-133, 1971.
See also MGI.

Deol, M.S.: The role of the tissue environment in the expression of spotting genes in the mouse. J. Embryol. Exp. Morphol. 30: 483-489, 1973.
See also MGI.

Deol, M.S., and Whiten, W.K.: Time of X chromosome inactivation in retinal melanocytes of the mouse. Nature New Biol. 238: 159-160, 1972.
See also PubMed.

Deringer, M.K.: Influence of the lethal yellow ( A^y) gene on the development of reticular neoplasms. J. Nat. Cancer Inst. 45: 1205-1210, 1970.
See also PubMed.

Detlefsen, J.A.: A new mutation in the house mouse. Amer. Nat. 55: 469-473, 1921.
See also MGI.

Dexter, T.M., and Moore, M.A.S.: In vitro duplication and "cure" of haemopoietic defects in genetically anaemic mice. Nature (London) 269: 412-414, 1977.
See also PubMed.

Dickerson, G.E., and Gowen, J.W.: Food utilization in genetic obesity of mice. Genetics 31: 214-215, 1946 (Abstract).

Dickerson, G.E., and Gowen, J.W.: Hereditary obesity and efficient food utilization in mice. Science 105: 496-498, 1947.

Dickie, M.M.: The tortoise shell house mouse. J. Hered. 45: 158-159, 1954.
See also MGI.

Dickie, M.M.: A new viable yellow mutation in the house mouse. J. Hered. 53: 84-86, 1962a.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 27: 37, 1962b.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 30: 30, 1964a.
See also MGI.

Dickie, M.M.: New splotch alleles in the mouse. J. Hered. 55: 97-101, 1964b.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 32: 43, 1965a.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 32: 44, 1965b.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 34: 30, 1966a.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 35: 31, 1966b.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 36: 39, 1967a.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 37: 33, 1967b.
See also MGI.

Dickie, M.M.: Mutations at the agouti locus in the mouse. J. Hered. 60: 20-25, 1969a.
See also MGI.

Dickie, M.M.: Private communication. Mouse News Letter 41: 31, 1969b.
See also MGI.

Doolittle, C.H., and Rauch, H.: Epinephrin and norepinephrin levels in dilute-lethal mice. Biochem. Biophys. Res. Commun. 18: 43-47, 1965.

Doykos, J.D., Cohen, M.M., and Shklar, G.: Physical, histological and roentgenographic characteristics of the grey lethal mouse. Amer. J. Anat. 121: 29-40, 1967.
See also PubMed.

Dry, F.W.: The coat of the mouse. J. Genet. 16: 287-340, 1926.

Dry, F.W.: The agouti coloration of the mouse (Mus musculus) and the rat (Mus norvegicus). J. Genet. 20: 131-144, 1928.
See also MGI.

Dunn, L.C.: The genetic behavior of mice of the color varieties "black-and-tan" and "red". Amer. Nat. 50: 664-675, 1916.

Dunn, L.C.: The sable varieties of mice. Amer. Nat. 54: 247-261, 1920a.

Dunn, L.C.: Types of white spotting in mice. Amer. Nat. 54: 465-495, 1920b.
See also MGI.

Dunn, L.C.: A fifth allelomorph in the agouti series of the house mouse. Proc. Natl. Acad. Sci. USA 14: 816-819, 1928.
See also MGI.

Dunn, L.C.: Analysis in a case of mosaicism in the house mouse. J. Genet. 29: 317-326, 1934.

Dunn, L.C.: Studies of multiple allelomorphic series in the house mouse. I. Description of agouti and albino series of allelomorphs. J. Genet. 33: 443-453, 1936.
See also MGI.

Dunn, L.C.: Studies on spotting patterns. II. Genetic analysis of variegated spottingin the house mouse. Genetics 22: 43-64, 1937.
See also MGI.

Dunn, L.C.: Studies on spotting patterns. V. Further analysis of minor spotting genes in the house mouse. Genetics 27: 258-267, 1942.

Dunn, L.C.: A new eye color mutant in the mouse with asymmetrical expression. Proc. Nat. Acad. Sci. USA 31: 343-346, 1945.
See also MGI.

Dunn, L.C., and Charles, D. R.: Studies on spotting patterns. I. Analysis of quantitative variations in the pied spotting of the house mouse. Genetics 22: 14-42, 1937.
See also MGI.

Dunn, L.C., and Einsele, W.: Studies of multiple allelomorphic series in the house mouse. IV. Quantitative comparisons of melanins from members of the albino series. J. Genet. 36: 145-152, 1938.

Dunn, L.C., and Mohr, J.: An association of hereditary eye defects with white spotting. Proc. Nat. Acad. Sci. USA 38: 872-875, 1952.
See also MGI.

Dunn, L.C., and Thigpen, L.W.: The silver mouse, a recessive color variation. J. Hered. 21: 495-498, 1930.
See also MGI.

Dunn, L.C., MacDowell, E.C., and Lebedeff, G.A.: Studies on spotting patterns. III. Interaction between genes affecting white spotting and those affecting color in the mouse. Genetics 22: 307-318, 1937.
See also MGI.

Durham, F.M.: A preliminary account of the inheritance of coat colour in mice. Rep. Evol. Com. Roy. Soc. Rep. 4: 41-53, 1908.

Durham, F.M.: Further experiments on the inheritance of coat colour in mice. J. Genet. 1: 159-178, 1911.

Eaton, G.J.: Stimulation of trophoblastic giant cell differentiation in the homozygous yellow mouse embryo. Genetica 39: 371-378, 1968.
See also PubMed.

Eaton, G.J., and Green, M.M.: Implantation and lethality of the yellow mouse. Genetica 33: 106-112, 1962.

Eaton, G.J., and Green, M.M: Giant cell differentiation and lethality of homozygous yellow mouse embryos. Genetica 34: 155-161, 1963.
See also MGI.

Ebbe, S., and Phalen, E.: Regulation of megakaryocytes in W/W^v. J. Cell Physiol. 96: 73-79, 1978.
See also PubMed.

Ebbe, S., Phalen, E., and Stohlman, F., Jr.: Abnormalities of megakaryocytes in W/W^v mice. Blood 42: 857-864, 1973a.
See also PubMed.

Ebbe, S., Phalen, E., and Stohlman, F., Jr.: Abnormalities of megakaryocytes in Sl/Sl^d mice. Blood 42: 865-871, 1973b.
See also PubMed.

Ebbe, S., Phalen, E., and Ryan, M.K.: The production of megakaryocytic macrocytosis by systemic factors in Sl/Sl^d mice. Proc. Soc. Exp. Biol. Med. 155: 243-246, 1977.
See also PubMed.

Ebbe, S., Phalen, E., and Howard, D.: Parabiotic demonstration of a humoral factor affecting megakaryocyte size in Sl/Sl^d. Proc. Soc. Exp. Biol. Med. 158: 637-642, 1978.
See also PubMed.

Eicher, E.M.: The position of ru-2 and qv with respect to the flecked translocation in the mouse. Genetics 64: 495-510, 1970a.
See also MGI.

Eicher, E.M.: X-autosome translocation in the mouse: Total inactivation versus partial inactivation of the X chromosome. Adv. Genetics 15: 175-259, 1970b.

Eicher, E.M.: Private communication. Mouse News Letter 47: 36, 1972.
See also MGI.

Eicher, E.M., and Fox, S.: Private communication. Mouse News Letter 56: 42, 1977.
See also MGI.

Erickson, R.P., Gluecksohn-Waelsch, S., and Cori, C.F.: Glucose-6-phosphatase deficiency caused by radiation induced alleles at the albino locus in the mouse. Proc. Nat. Acad. Sci. USA 59: 437-444, 1968.
See also MGI.

Erickson, R.P., Eicher, E.M., and Gluecksohn-Waelsch, S.: Demonstration in mouse of x-ray-induced deletions for a known enzyme structural locus. Nature (London) 248: 416-418, 1974a.
See also MGI.

Erickson, R.P., Siekevitz, P., Jacobs, K., and Gluecksohn-Waelsch, S.: Chemical and immunological studies of liver microsomes from mouse mutants with ultrastructurally normal hepatic endoplasmic reticulum. Biochem. Genet. 12: 81-95, 1974b.
See also PubMed.

Erway, L., Hurley, L.S., and Fraser, A.: Neurological defect: Manganese in phenocopy and prevention of a genetic abnormality of inner ear. Science 152: 1766-1768, 1966.
See also PubMed.

Erway, L., Hurley, L.S., and Fraser, A.: Congenital ataxia and otolith defects due to manganese deficiency in mice. J. Nutrit. 100: 643-654, 1970.
See also PubMed.

Erway, L.C., Fraser, A.S., and Hurley, L.S.: Prevention of congenital otolith defect in pallid mutant mice by manganese supplementation. Genetics 67: 97-108, 1971.
See also MGI.

Essner, E., and Oliver, C.: A hereditary alteration in kidneys of mice with Chediak-Higashi syndrome. Amer. J. Pathol. 73: 217-232, 1973.
See also PubMed.

Essner, E., and Oliver, C.: Lysosome formation in hepatocytes of mice with Chediak-Higashi syndrome. Lab. Invest. 30: 596-607, 1974.
See also PubMed.

Evans, E.P., and Phillips, R.J.S.: Private communication. Mouse News Letter 58: 44-45, 1968.

Fahrig, R.: A mammalian spot test: Induction of genetic alterations in pigment cells of mouse embryos with x-rays and chemical mutagens. Mol. Gen. Genet. 138: 309-314, 1975.
See also PubMed.

Fahrig, R.: The mammalian spot test (Fellfleckentest) with mice. Arch. Toxicol. 38: 87-98, 1977.
See also PubMed.

Fahrig, R.: The mammalian spot test: A sensitive in vivo method for the detection of genetic alterations of somatic cells of mice. In Chemical Mutagens, Vol. 5, A. Hollaender and F.J. de Serres (eds.). pp. 151-176, Plenum, New York, 1978.

Falconer, D.S.: Total sex linkage in the house mouse. Z. induckt. Abstamm.-u. VererbLehre 85: 210-219, 1953.
See also MGI.

Falconer, D.S.: Private communication. Mouse News Letter 15: 23, 1956a.
See also MGI.

Falconer, D.S.: Private communication. Mouse News Letter 15: 24-25, 1956b.
See also MGI.

Falconer, D.S., and Isaacson, J.H.: Private communication. Mouse News Letter 27: 30, 1962.
See also MGI.

Falconer, D.S., and Avery, P.J.: Variability of chimeras and mosaics. J. Embryol. Exp. Morphol. 43: 195-219, 1978.
See also PubMed.

Falconer, D.S., and Isaacson, J.H.: Selection for expression of a sex linked gene (brindled) in mice. Heredity 24: 180, 1969 (Abstract).

Falconer, D.S., and Isaacson, J.H.: Sex-linked variegation modified by selection in brindled mice. Genet. Res. (Camb.) 20: 291-316, 1972.
See also MGI.

Fattorusso, E., Minale, L., De Stefano, S., Cimino, G., and Nicolaus, R.A.: Struttura e biogenesi della feomelanine. IX. Feomelanine biosintetiche. Gazetta Chim. Ital. 99: 969-992, 1969.

Feldman, H.W.: A fourth allelomorph in the albino series in mice. Amer. Nat. 56: 573-574, 1922.
See also MGI.

Feldman, H.W.: A fifth allelomorph in the albino series of the house mouse. J. Mammal. 16: 207-210, 1935.
See also MGI.

Ferguson, J.M., and Wallace, M.E.: Private communication. Mouse News Letter 57: 11, 1977.
See also MGI.

Fielder, J.H.: The taupe mouse. A new coat color mutation. J. Hered. 43: 75-76, 1952.
See also MGI.

Fisher, H. and Tost, M.: Missbildungen im fasciculus opticus beim hereditären mikropthalmus der Hausmaus. Biol. Zentralbl. 78: 759-776, 1959.

Fisher, R.A., and Landauer, W.: Sex differences of crossing-over in close linkage. Amer. Nat. 87: 116, 1953.
See also MGI.

Fisher, R.A., and Mather, K.: A linkage test with mice. Ann. Eugen. 7: 265-280, 1936.
See also MGI.

Fitzpatrick, T.B., and Breathnach, A.S.: Das epidermale Melanin-Einheit-System. Dermatol. Wochenschrift 147: 481-489, 1963.

Fitzpatrick, T.B., and Kukita, A.: Tyrosinase activity in vertebrate melanocytes. In Pigment Cell Biology, M. Gordon (ed.), pp. 489-524, Academic Press, New York, 1959.

Fitzpatrick, T.B., and Lerner, A.B.: Biochemical basis of human melanin pigmentation. Arch. Dermatol. Syphilol. 69: 133-149, 1954.

Fitzpatrick, T.B., Brunet, P., and Kukita, A.: The nature of hair pigment. In The Biology of Hair Growth, W. Montagna and R.A. Ellis (eds.), pp. 255-303, Academic Press, New York, 1958.

Fitzpatrick, T.B., Miyamoto, M., and Ishikawa, K.: The evolution of concepts of melanin biology. In The Pigmentary System, Advances in Biology of Skin, Vol. 8 W. Montagna and F. Hu (eds.), pp. 1-30, Pergamon Press, Oxford, 1967.

Flaherty, L., Cantor, L., Zimmerman, D., and Bennett, D.: Cell surface antigens on erythroid cells. A comparison of normal and anemic ( W/W) mice. Develop. Biol. 59: 237-240, 1977.
See also MGI.

Flesch, P.: Studies of the red pigmentary system. Arch. Dermatol. 101: 475-481, 1970.
See also PubMed.

Foster, M.: Enzymatic studies of pigment-forming abilities in mouse skin. J. Exp. Zool. 117: 211-246, 1951.

Foster, M.: Physiological studies of melanogenesis. In Pigment Cell Biology, M. Gordon (ed.), pp. 301-314, Academic Press, New York, 1959.

Foster, M.: Tactics in pigment-cell research. (Discussion). In Methodology in Mammalian Genetics, W.J. Burdette (ed.), pp. 336-339, Holden-Day, San Francisco, 1963.

Foster, M.: Mammalian pigment genetics. Adv. Genet. 13: 311-339, 1965.
See also PubMed.

Foster, M.: Genetic aspects of mammalian melanogenesis. In The Pigmentary System, Advances in Biology of Skin, Vol. 8, W. Montagna and F. Hu (eds.), pp. 467-477, Pergamon Press, Oxford, 1967.

Foster, M. and Thomson, L.: The effects of substitution at the leaden (ln) locus on melanogenic attributes of the mouse. Proc. X Int. Congr. Genet. 2: 84, 1958 (Abstract).

Foster, M., Barto, E., and Thomson, L.: Genetic control of mammalian melanogenesis. In Pigmentation: Its Genesis and Biologic Control, V. Riley (ed.), pp. 387-400, Appleton-Century-Crofts, New York, 1972.

Foulks, J.G.: An analysis of the source of melanophores in regenerating feathers. Physiol. Zool. 16: 351-380, 1943.

Fowler, J.H., Till, J.E., McCulloch, E.A., and Siminovitch, L.: The cellular basis for the defect in haemopoiesis in flexed-tailed mice. II. The specificity of the defect for erythropoiesis. Brit. J. Haematol. 13: 256-264, 1967.
See also PubMed.

Fox, S., and Eicher, E.M.: Private communication. Mouse News Letter 58: 47, 1978.
See also MGI.

Frankel, F.R., Tucker, R.W., Bruce, J., and Stenberg, R.: Fibroblasts and macrophages of mice with the Chediak-Higashi-like syndrome have microtubules and actin cables. J. Cell Biol. 79: 401-408, 1978.
See also PubMed.

Fraser, A.S., Sobey, S., and Spicer, C.C.: Mottled, a sex-modified lethal in the house mouse. J. Genet. 51: 217-221, 1953.
See also MGI.

Fried, W., Rishpon-Meyerstein, N., and Gurney, C.W.: The effect of testosterone on erythropoiesis of W/W^v mice. J. Lab. Clin. Med. 70: 813-819, 1967.
See also PubMed.

Fried, W., Chamberlain, W., Knospe, W.H., Husseini, S., and Trobaugh, F.E., Jr.: Studies on the defective hematopoietic microenvironment of Sl/Sl^d mice. Brit. J. Haematol. 24: 643-650, 1973.

Fry, R.J.M., Slaughter, B., Grahn, D., Wasserman, F., Maelis, F., Hamilton, K.F., and Staffeldt, E.: Inherited connective tissue defect in tortoise mice. US AEC Argonne Nat. Lab. 7409: 44-117, 1967.
See also PubMed.

Fuller, J.L.: Effects of the albino gene upon behavior of mice. Anim. Behav. 15: 467-470, 1967.
See also PubMed.