References (continued)

Previous

1

2

3

4

Next

Lamoreux, M.L.: A Study of Gene Interaction Using Coat Color Mutants in the Mouse and Selected Mammals. Ph.D. thesis, University of Maine, Orono, 1973.

Lamoreux, M.L., and Mayer, T.C.: Site of gene action in the development of hair pigment in recessive yellow ( e/e) mice. Develop. Biol. 46: 160-166, 1975.
See also MGI.

Lamoreux, M.L., and Russell, E.S.: Effects of agouti-locus alleles ( Ay/a vs a/a) on amount of white spotting when combined with two different spotting genotypes ( s/sl and Wj2/+). Genetics 68: s36, 1971 (Abstract).

Lane, P.W.: Private communication. Mouse News Letter 22: 35, 1960a.
See also MGI.

Lane, P.W.: Private communication. Mouse News Letter 23: 36, 1960b.
See also MGI.

Lane, P.W.: Private communication. Mouse News Letter 26: 35, 1962.
See also MGI.

Lane, P.W.: Private communication. Mouse News Letter 32: 47, 1965.
See also MGI.

Lane, P.W.: Association of megacolon with two recessive spotting genes in the mouse. J. Hered. 57: 29-31, 1966.
See also MGI.

Lane, P.W.: Private communication. Mouse News Letter 44: 30, 1971.
See also MGI.

Lane, P.W.: Two new mutations in linkage group XVI of the house mouse. Flaky tail and varitint-waddler-J. J. Hered. 63: 135-140, 1972.
See also MGI.

Lane, P.W., and Deol, M.S.: Mocha, a new coat color and behavior mutation on chromosome 10 of the mouse. J. Hered. 65: 362-364, 1974.
See also MGI.

Lane, P.W., and Green, M.C.: Mahogany, a recessive color mutation in linkage group V of the mouse. J. Hered. 51: 228-230, 1960.
See also MGI.

Lane, P.W., and Green, E.L.: Pale ear and light ear in the house mouse. Mimic mutations in linkage groups XII and XVII. J. Hered. 58: 17-20, 1967.
See also MGI.

Lane, P.W., and Murphy, E.D.: Susceptability to spontaneous pneumonitis in an inbred strain of beige and satin mice. Genetics 72: 451-460, 1972.
See also MGI.

Lane, P.W., and Womack, J.E.: Private communication. Mouse News Letter 57: 18, 1977.
See also MGI.

Larsen, M.M.: Private communication. Mouse News Letter 34: 41, 1966.
See also MGI.

LaVail, M.M., and Sidman, R.L.: C57BL/6J mice with inherited retinal degeneration. Arch. Ophthalmol. 91: 394-400, 1974.
See also MGI.

Law, L.W.: The flexed-tail-anemia gene ( f) and induced leukemia in mice. J. Nat. Cancer Inst. 12: 1119-1126, 1952.

Lerner, A.B.: Melanin pigmentation. Amer. J. Med. 19: 902-924, 1955.

Lerner, A.B., and Case, J.D.: Pigment cell regulatory factors. J. Invest. Dermatol. 32: 211-221, 1959.

Lewis, E.B.: Pseudoallelism and gene evolution. Cold Spring Harbor Symp. Quant. Biol. 16: 159-174, 1961.

Lewis, J.P., O'Grady, L.F., Bernstein, S.E., Russell, E.S., and Trobaugh, F.E., Jr.: Growth and differentiation of transplanted W/Wv marrow. Blood 30: 601-616, 1967.
See also PubMed.

Lewis, S.E., Turchin, H.A., and Gluecksohn-Waelsch, S.: The developmental analysis of an embryonic lethal ( c6H) in the mouse. J. Embryol. Exp. Morphol. 36: 363-371, 1976.
See also MGI.

Lilly, F.: Private communication. Mouse News Letter 34: 14, 1966.
See also MGI.

Little, C.C.: Experimental studies of the inheritance of color in mice. Publ. Carneg. Instn., No. 179: 13-102, 1913.

Little, C.C.: "Dominant" and "recessive" spotting in mice. Amer. Nat. 48: 74-82, 1914.

Little, C.C.: The inheritance of black-eyed white spotting in mice. Amer. Nat. 49: 727-740, 1915.

Little, C.C.: The occurrence of three recognized color mutations in mice. Amer. Nat. 50: 3335-349, 1916.

Little, C.C.: The relation of yellow coat color to black-eyed white spotting of mice, in heredity. Anat. Rec. 11: 501, 1917a (Abstract).

Little, C.C.: The relation of yellow coat color and black-eyed white spotting in mice. Genetics 2: 433-444, 1917b.

Little, C.C.: Evidence of multiple factors in mice and rats. Amer. Nat. 51: 457-480, 1917c.

Little, C.C.: The genetics of spotting. Carnegie Inst. Wash. Yearbook 23: 42, 1924.

Little, C.C.: The inheritance of blaze spotting in mice. Anat. Rec. 34: 171, 1926 (Abstract).

Little, C.C.: Coat color genes in rodents and carnivores. Quart. Rev. Biol. 33: 103-137, 1958.

Little, C.C., and Cloudman, A.M.: The occurrence of a dominant spotting mutation in the house mouse. Proc. Nat. Acad. Sci. USA 23: 535-537, 1937.
See also MGI.

Little, C.C., and Hummel, K.P.: A reverse mutation to a "remote" allele in the house mouse. Proc. Nat. Acad. Sci. USA 33: 42-43, 1947.

Littleford, R.A.: Occurrence of piebald spotting in a wild house mouse. Amer. Nat. 80: 283-288, 1946.

Loosli, R.: Tanoid — a new agouti mutant in the mouse. J. Hered. 54: 26-29, 1963.
See also MGI.

Loutit, J.F.: Bone Marrow grafts in mature osteopetrotic mice. Space not a requirement. Transplantation 24: 299-301, 1977.
See also PubMed.

Loutit, J.F., and Sansom, J.M.: Osteopetrosis of microphthalmic mice — a defect of the hematopoietic stem cell? Calcif. Tissue Res. 20: 251-259, 1976.
See also PubMed.

Lund, R.D.: Uncrossed visual pathways of hooded and albino rats. Science 149: 1506-1507, 1965.

Lutzner, M.: Ultrastructure of giant melanin granules in the beige mouse during ontogeny. J. Invest. Dermatol. 54: 91, 1970 (Abstract).

Lutzner, M.A., and Lowrie, C.T.: Ultrastructure of the development of the normal black and giant beige melanin granules in the mouse. In Pigmentation: Its Genesis and Biologic Control, V. Riley (ed.), pp. 89-105. Appleton-Century-Crofts, New York, 1972.

Lutzner, M.A., Lowrie, C.T., and Jordan, H.W.: Giant granules in leukocytes of the beige mouse. J. Hered. 58: 299-300, 1967.
See also MGI.

Lyon, M.F.: Hereditary absence of otoliths in the house mouse. J. Physiol. 114: 410-418, 1951.

Lyon, M.F.: Absence of otoliths in the mouse: An effect of the pallid mutant. J. Genet. 51: 638-650, 1953.
See also MGI.

Lyon, M.F.: Stage of action of the litter-size effect on absence of otoliths in mice. Z. induckt. Abstamm.-u. VererbLehre 86: 289-292, 1954.

Lyon, M.F.: The development of otoliths in the mouse. J. Embryol. Exp. Morphol. 3: 213-229, 1955a.

Lyon, M.F.: The developmental origin of hereditary absence of otoliths in mice. J. Embryol. Exp. Morphol. 3: 230-241, 1955b.
See also MGI.

Lyon, M.F.: A further mutation of the mottled type in the house mouse. J. Hered. 51: 116-120, 1960.
See also MGI.

Lyon, M.F.: Gene action in the X-chromosome of the mouse ( Mus musculus L.). Nature (London) 190: 372-373, 1961.
See also MGI.

Lyon, M.F.: Attempts to test the inactive-X theory of dosage compensation in mammals. Genet. Res. (Camb.) 4: 93-103, 1963.
See also MGI.

Lyon, M.F.: Private communication. Mouse News Letter 34: 28, 1966.
See also MGI.

Lyon, M.F.: Chromosomal and subchromosomal inactivation. Ann. Rev. Genet. 2: 31-52, 1968.

Lyon, M.F.: Genetic activity of sex chromosomes in somatic cells of mammals. Phil. Trans. Roy. Soc. (London) B 259: 41-53, 1970.
See also MGI.

Lyon, M.F.: Possible mechanisms of X chromosome inactivation. Nature New Biol. 232: 229-232, 1971.
See also PubMed.

Lyon, M.F.: X-chromosome inactivation and developmental patterns in mammals. Biol. Rev. 47: 1-35, 1972a.
See also PubMed.

Lyon, M.F.: Private communication. Mouse News Letter 47: 34, 1972b.
See also MGI.

Lyon, M.F.: Mechanisms and evolutionary origins of variable X-chromosome activity in mammals. Proc. Roy. Soc. (London) B 187: 243-268, 1974.
See also PubMed.

Lyon, M.F.: Private communication. Mouse News Letter 53: 29, 1975.

Lyon, M.F., and Glenister, P.H.: Private communication. Mouse News Letter 45: 24, 1971.

Lyon, M.F., and Glenister, P.H.: Private communication. Mouse News Letter 48: 31, 1973.
See also MGI.

Lyon, M.F., and Glenister, P.H.: Private communication. Mouse News Letter 59: 18, 1978.
See also MGI.

Lyon, M.F., and Meredith, R.: Private communication. Mouse News Letter 32: 38, 1965a.
See also MGI.

Lyon, M.F., and Meredith, R.: Private communication. Mouse News Letter 33: 29, 1965b.
See also MGI.

Lyon, M.F., and Meredith, R.: Muted, a new mutant affecting coat color and otoliths of the mouse, and its position in linkage group XIV. Genet. Res. (Camb.) 14: 163-166, 1969.
See also MGI.

Lyon, M.F., and Morris, T.: Mutation rates at a new set of specific loci in the mouse. Genet. Res. (Camb.) 7: 12-17, 1966.
See also PubMed.

Lyons, R.T. and Pitot, H.C.: Protein degradation in normal and beige (Chediak-Higashi) mice. J. Clin. Invest. 61: 260-268, 1978.
See also PubMed.

MacDowell, E.C.: "Light" — a new mouse color. J. Hered. 41: 35-36, 1950.
See also MGI.

Maloney, M.A., Dorie, M.J., Lamela, R.A., Rogers, Z.R., and Patt, H.M.: Hematopoietic stem cell regularoty volumes as revealed in the studies of the bgJ/bgJ:W/Wv chimera. J. Exp. Med. 147: 1189-1197, 1978.
See also PubMed.

Margolis, F.L. and Russell, E.S.: Delta-amino-levulinate dehydratase actvity in mice with hereditary anemia. Science 144: 844-846, 1965.
See also PubMed.

Markert, C.L.: Substrate utilization in cell differentiation. Ann. N.Y. Acad. Sci. 60: 1003-1014, 1955.

Markert, C.L.: Biochemical embryology and genetics. In Symposium on Normal and Abnormal Differentiation and Development. N. Kaliss (ed.) Nat. Cancer Inst. Monogr. 2: 3-17, 1960.
See also MGI.

Markert, C.L. and Petters, R.M.: Manufactured hexaparental mice show that adults are derived from three embryonic cells. Science 202: 56-58, 1978.
See also PubMed.

Markert, C.L. and Silvers, W.K.: The effects of genotype and cell environment on melanoblast differentiation in the house mouse. Genetics 41: 429-450, 1956.
See also MGI.

Markert, C.L. and Silvers, W.K.: Effects of genotype and cellular environment on melanocyte morphology. In Pigment Cell Biology, M. Gordon (ed.), pp. 241-248, Academic Press, New York, 1959.

Marks, S.C., Jr.: Studies of the mechanism of spleen cell cure for osteopetrosis in ia rats: Appearance of osteoclasts with ruffled borders. Amer. J. Anat. 151: 119-130, 1978a.
See also PubMed.

Marks, S.C., Jr.: Studies of the cellular cure for osteopetrosis by transplanted cells: Specificity of the cell type in ia rats. Amer. J. Anat. 151: 131-137, 1978b.
See also PubMed.

Marks, S.C., Jr., and Lane, P.W.: Osteopetrosis, a new recessive skeletal mutation on chromosome 12 of the mouse. J. Hered. 67: 11-18, 1976.
See also MGI.

Marks, S.C., Jr., and Walker, D.G.: The role of the parafollicular cell of the thyroid gland in the pathogenesis of congenital osteopetrosis in mice. Amer. J. Anat. 126: 299-314, 1969.
See also MGI.

Marks, S.C., Jr., and Walker, D.G.: Mammalian osteopetrosis: A model for studying cellular and humoral factors in bone resorption. In The Biochemistry and Physiology of Bone, Chap. 6, G. Bourne (ed.), pp. 227-301, Academic Press, New York, 1976.

Mather, K., and North, S.B.: Umbrous: A case of dominance modification in mice. J. Genet. 40: 229-241, 1940.
See also MGI.

Mauer, I., and Sideman, M.B.: Phenylalanine metabolism in a dilute-lethal strain of mice. J. Hered 58: 14-16, 1967.
See also PubMed.

Mayer, T.C.: The development of piebald spotting in mice. Develop. Biol. 11: 319-334, 1965.
See also MGI.

Mayer, T.C.: Pigment cell migration in piebald mice. Develop. Biol. 15: 521-535, 1967a.
See also MGI.

Mayer, T.C.: Temporal skin factors influencing the development of melanoblasts in piebald mice. J. Exp. Zool. 166: 397-403, 1967b.
See also MGI.

Mayer, T.C.: A comparison of pigment cell development in albino, steel, and dominant spotting mutant mouse embryos. Develop. Biol. 23: 297-309, 1970.
See also MGI.

Mayer, T.C.: Site of gene action in steel mice. Analysis of the pigment defect by mesoderm-ectoderm recombinations. J. Exp. Zool. 184: 345-352, 1973a.
See also MGI.

Mayer, T.C.: The migratory pathway of neural crest cells into the skin of mouse embryos. Develop. Biol. 34: 39-46, 1973b.
See also PubMed.

Mayer, T.C.: Tissue environmental influences on the development of melanoblasts in steel mice. In Extracellular Matrix Influences on Gene Expression, H.C. Slavkin and R.C. Grevlich (eds.), pp. 555-560, Academic Press, New York, 1975.

Mayer, T.C., and Fishbane, J.L.: Mesoderm-ectoderm interaction in the production of the agouti pigmentation pattern in mice. Genetics 71: 297-303, 1972.
See also MGI.

Mayer, T.C., and Green, M.C.: An experimental analysis of the pigment defect caused by mutations at the W and Sl loci in mice. Develop. Biol. 18: 62-75, 1968.
See also MGI.

Mayer, T.C., and Maltby, E.L.: An experimental investigation of pattern development in lethal spotting and belted mouse embryos. Develop. Biol. 9: 269-286, 1964.
See also MGI.

Mayer, T.C., and Oddis, L.: Pigment cell differentiation in embryonic mouse skin and isolated epidermis: An in vitro study. J. Exp. Zool. 202: 415-424, 1977.
See also PubMed.

Mayer, T.C., and Reams, W.M., Jr.: An experimental analysis and description of the melanocytes in the leg musculature of the PET strain of mice. Anat. Rec. 142: 431-442, 1962.

McCarthy, K.F.: In vivo colony formation by hematopoietic cells from mice of genotype Sl/Sld. Cell Tissue Kinet. 8: 397-398, 1975.
See also PubMed.

McCarthy, K.F., Ledney, G.D., and Mitchell, R.: A deficiency of hematopoietic stem cells in steel mice. Cell Tissue Kinet. 10: 121-126, 1977.
See also PubMed.

McClintock, B.: Chromosome organization and genic expression. Cold Spring Harbor Symp. Quant. Biol. 16: 13-47, 1951.

McCoshen, J.A., and McCallion, D.J.: A study of primordial germ cells during their migratory phase in steel mutant mice. Experientia 31: 589-590, 1975.
See also MGI.

McCulloch, E.A., Siminovitch, L., and Till, J.E.: Spleen-colony formation in anemic mice of genotype W/Wv. Science 144: 844-846, 1964.

McCulloch, E.A., Siminovitch, L., Till, J.E., Russell, E.S., and Bernstein, S.E.: The cellular basis of the genetically determined hemopoietic defect in anemic mice of genotype Sl/Sld. Blood 26: 399-410, 1965.
See also PubMed.

McCuskey, R.S., and Meineke, H.A.: The cellular basis of the genetically determined hemopoietic defect in anemic mice of genotype Sl/Sld. Blood 26: 399-410, 1965.

McGrath, E.P., and Quevedo, W.C., Jr.: Genetic regulation of melanocyte function during hair growth in the mouse: Cellular events leading to "pigment clumping" within developing hairs. In Biology of the Skin and Hair Growth, A.G. Lyne and B.F. Short (eds.), pp. 727-745, Angus and Robertson, Sydney, 1965.

McLaren, A., and Bowman, P.: Mouse chimeras derived from fusion of embryos differing by nine genetic factors. Nature (London) 224: 238-240, 1969.
See also MGI.

McLaren, A., Gauld, I.K., and Bowman, P.: Comparison between mice chimaeric and heterozygous for the X-linked gene tabby. Nature New Biol. 241: 180-183, 1973.

Meisler, M.H.: Synthesis and secretion of kidney beta-galactosidase in the mutant le/le mice. J. Biol. Chem. 253: 3129-3134, 1978.
See also MGI.

Mekori, T., and Phillips, R.A.: The immune response in mice of genotypes W/Wv and Sl/Sld. Proc. Soc. Exp. Biol. Med. 132: 115-119, 1969.
See also PubMed.

Melvold, R.W.: Spontaneous somatic reversion in mice. Effects of parental genotype in stability at the p-locus. Mutation Res. 12: 171-174, 1971.
See also MGI.

Melvold, R.W.: Private communication. Mouse News Letter 46: 32, 1972.

Melvold, R.W.: The effects of mutant p-alleles on the reproductive system in mice. Genet. Res. (Camb.) 23: 319-325, 1974.
See also MGI.

Menkes, J.H., Alter, M., Steigleder, G.K., Weakly, D.R., and Sung, J.H.: A sex-linked, recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cellular degeneration. Pediatrics 29: 764-779, 1962.

Milhaud, G., Labat, M., Parant, M., Damais, C., and Chedid, L.: Immunological defect and its correction in the osteopetrotic mutant rat. Proc. Nat. Acad. Sci. USA 74: 339-342, 1977.
See also PubMed.

Miller, D.A., Dev, V.G., Tantravahi, R., Miller, O.J., Schiffman, M.B., Yates, R.A., and Gluecksohn-Waelsch, S.: Cytological detection of the c25H deletion involving the albino (c) locus on chromosome 7 in the mouse. Genetics 78: 905-910, 1974.
See also MGI.

Miller, D.S.: Coat color and behavior mutations in inbred mice under chronic low-level gamma-irradiation. Radiat. Res. 19: 184-185, 1963 (Abstract).
See also MGI.

Miller, D.S., and Potas, M.Z.: Cordovan, a new allele of black and brown color in the mouse. J. Hered. 46: 293-296, 1955.
See also MGI.

Miner, G.: Private communication. Mouse News Letter 38: 25, 1968.

Mintz, B.: Embryological development of primordial germ-cells in the mouse: Influence of a new mutation, Wj. J. Embryol. Exp. Morphol. 5: 396-403, 1957a.

Mintz, B.: Interaction between two allelic series modifying primordial germ cell development in the mouse embryo. Anat. Rec. 128: 591, 1957b (Abstract).

Mintz, B.: Embryological phases of mammalian gametogenesis. J. Cell Comp. Physiol. 56 (suppl. 1): 31-48, 1960.

Mintz, B.: Gene control of mammalian pigmentary differentiation. I. Clonal origin of melanocytes. Proc. Natl. Acad. Sci. USA 58: 344-351, 1967.
See also PubMed.

Mintz, B.: Developmental mechanisms found in allophenic mice with sex chromosomal and pigmentary mosaicism. In Birth Defects: Orig. Art. Ser. 5, First Conf. Clin. Delineation Birth Defects, D. Bergsma and V. McKusick (eds.), pp. 11-22, National Found., New York, 1969a.

Mintz, B.: Gene Control of the mouse pigmentary system. Genetics 61: s41, 1969b (Abstract).

Mintz, B.: Gene expression in allophenic mice. In Control Mech. Expression Cellular Phenotypes, Symp. Int. Soc. Cell Biol., H. Padylkula (ed.), pp. 15-42, Academic Press, New York, 1970.
See also MGI.

Mintz, B.: Clonal basis of mammalian differentiation. In: Control Mechanisms of Growth and Differentiation. 25th Symp. Soc. Exp. Biol., D.D. Davies and M. Balls (eds.), pp. 345-369, University Press, Cambridge, 1971a.

Mintz, B.: Allophenic mice of multi-embryo origin. In Methods in Mammalian Embryology, J. Daniel, Jr. (ed.), pp. 186-214, Freeman, San Francisco, 1971b.

Mintz, B.: Genetic mosaicism in vivo: Development and disease in allophenic mice. Fed. Proc. 30: 935-943, 1971c.
See also PubMed.

Mintz, B.: Gene control of mammalian differentiation. Ann. Rev. Genet. 8: 411-470, 1974.
See also PubMed.

Mintz, B., and Cronmiller, C.: Normal blood cells of anemic genotype in teratocarcinoma-derived mosaic mice. Proc. Nat. Acad. Sci. USA 75: 6247-6251, 1978.
See also PubMed.

Mintz, B., and Palm, J.: Gene control of hematopoiesis. I. Erythrocyte mosaicism and permanent immunological tolerance in allophenic mice. J. Exp. Med. 129: 1013-1027, 1969.
See also PubMed.

Mintz, B. and Russell, E.S.: Gene-induced embryological modifications of primordial germ cells in the mouse. J. Exp. Zool. 134: 207-237, 1957.
See also MGI.

Mintz, B., and Silvers, W.K.: Histocompatibility antigens on melanoblasts and hair follicle cells. Transplantation 9: 497-505, 1970.
See also PubMed.

Misuraca, G., Nicolaus, R.A., Prota, G., and Ghiara, G.: A cytochemical study of phaeomelanin formation in feather papillae of New Hampshire chick embryos. Experientia 25: 920-922, 1969.
See also PubMed.

Mixter, R., and Hunt, H.R.: Anemia in the flexed tailed mouse, Mus musculus. Genetics 18: 367-387, 1933.

Mohr, E.: Akromelanismus bei Mus musculus. Zool. Anz. 126: 45-46, 1939.

Moyer, F.H.: Electron microscope studies on the origin, development, and genetic control of melanin granules in the mouse eye. In The Structure of the Eye, C.K. Smelser (ed.), pp. 469-486, Academic Press, New York, 1961.

Moyer, F.H.: Genetic effects on melanosome fine structure and ontogeny in normal and malignant cells. Ann. N.Y. Acad. Sci. 100: 584-606, 1963.

Moyer, F.H.: Genetic variations in the fine structure and ontogeny of mouse melanin granules. Amer. Zool. 6: 43-66, 1966.
See also MGI.

Mullen, R.J., and Whitten, W.K.: Relationship of genotype and degree of chimerism in coat color to sex ratios and gametogenesis in chimeric mice. J. Exp. Zool. 178: 165-176, 1971.
See also PubMed.

Müller, G.: Eine entwicklungsgeschichtliche Untersuchung über das erbliche Kolobom mit Mikrophthalmus bei der Hausmaus. Z. Mikr.-anta. Forsch. 56: 520-558, 1950.

Müller, G.: Die embryonale Entwicklung eines sich rezessiv vererbenden Merkmals. (Kolobom bei der Hausmaus). Wiss. Z. Martin-Luther-Univ. 1: 27-43, 1951.

Munford, R.E.: Private communication. Mouse News Letter 33: 52, 1965.
See also MGI.

Murphy, E.D.: Steel alleles and leukemia. In 40th Annual Report, The Jackson Laboratory, 1968-1969, pp. 29-30, 1969.

Murphy, E.D., and Russell, E.S.: Ovarian Tumorigenesis following deletion of germ cells in hybrid mice. Acta Unio Int. Contra Cancrum 19: 779-782, 1963.

Murphy, E.D., Harrison, D.E., and Roths, J.B.: Giant granules of beige mice: A quantitative marker for granulocytes in bone marrow transplantation. Transplantation 15: 526-530, 1973.
See also PubMed.

Murphy, H.M.: Calcium and phosphorus metabolism in the grey-lethal mouse. Genet. Res. (Camb.) 11: 7-14, 1968.
See also PubMed.

Murphy, H.M.: A review of inherited osteopetrosis in the mouse. Man and other mammals also considered. Clin. Orthopaed. Related Res. 65: 97-109, 1969.
See also PubMed.

Murphy, H.M.: Calcitonin-like activity in the circulation of osteopetrotic grey-lethal mice. J. Endocrinol. 53: 139-150, 1972.
See also MGI.

Murphy, H.M.: The osteopetrotic syndrome in the microphthalmic mutant mouse. Calc. Tissue Res. 13: 19-26, 1973.
See also PubMed.

Murray, J.M.: A preliminary note on the occurrence of a color mutation in the house mouse (Mus musculus). Science 73: 482, 1931.

Murray, J.M.: "Leaden", a recent color mutation in the house mouse. Amer. Nat. 67: 278-283, 1933.
See also MGI.

Murray, J.M., and Green, G.D.: Inheritance of ventral spotting in mice. Genetics 18: 481-486, 1933.

Murray, J.M., and Snell, G.D.: Belted, a new sixth chromosome mutation in the mouse. J. Hered. 36: 266-268, 1945.
See also MGI.

Mysttkowska, E.T., and Tarkowski, A.K.: Observations on CBA-p/CBA-T6T6 mouse chimeras. J. Embryol. Exp. Morphol. 20: 33-52, 1968.

Nachmias, V.T.: Tryptophan oxidation by yellow mouse skin. Proc. Soc. Exp. Biol. Med. 101: 247-250, 1959.

Nash, D.J.: Private Communication. Mouse News Letter 29: 84, 1959.

Newsome, A.E.: A population study of house-mice temporarily inhabiting a South Australian wheat field. J. Anim. Ecol. 38: 341-359, 1969a.

Newsome, A.E.: A population study of house-mice permanently inhabiting a reedbed in South Australia. J. Anim. Ecol. 38: 361-377, 1969b.

Nicolaus, R.A., and Piattelli, M.: Progress in the chemistry of natural black pigments. Rendiconti Accad. Sci. Fisiche Matemat. (Naples) 32: 1-17, 1965.

Nichols, S.E., and Reams, W.M., Jr.: The occurence and morphogenesis of melanocytes in the connective tissues of the PET/MCV mouse strain. J. Embryol. Exp. Morphol. 8: 24-32, 1960.

Niece, R.L., McFarland, E.C., and Russell, E.S.: Erythroid homeostasis in normal and genetically anemic mice: Reaction to induced polycythemia. Science 142: 1468-1469, 1963.

Nisbet, N.W., Menage, J., and Loutit, J.F.: Host-donor cellular interactions in the treatment of experimental osteopetrosis. Nature (London) 271: 464-466, 1978.
See also PubMed.

Novak, E.K., and Swank, R.T.: Lysosomal dysfunctions associated with mutations at mouse pigment genes. Genetics 92: 189-204, 1979.
See also MGI.

Ohno, S., and Cattanach, B.M.: Cytological study of an X-autosome translocation in Mus musculus. Cytogenetics 1: 129-140, 1962.

Okun, M.R.: Mast cells and melanocytes. Int. J. Dermatol. 15: 711-722, 1976.
See also PubMed.

Oliver, C., and Essner, E.: Distribution of anomalous lysosomes in the beige mouse: A homologue of Chediak-Higashi syndrome. J. Histochem Cytochem. 21: 218-228, 1973.
See also MGI.

Oliver, C., and Essner, E.: Formation of anomalous lysosomes in monocytes, neutrophils, and eosinophils from bone marrow of mice with Chediak-Higashi syndrome. Lab. Invest. 32: 17-27, 1975.
See also MGI.

Oliver, C., Essner, E., Zimring, A., and Haimes, H.: Age-related accumulation of ceroid-like pigment in mice with Chediak-Higashi syndrome. Amer. J. Pathol. 84: 225-238, 1976.
See also PubMed.

Oliver, J.M.: Impaired microtubule function correctable by cyclic GMP and cholinergic agonists in the Chediak-Higashi syndrome. Amer. J. Pathol. 85: 395-418, 1976.
See also MGI.

Oliver, J.M., Krawiec, J.A., and Berlin, R.D.: Carbamylcholine prevents giant granule formation in cultured fibroblasts from beige (Chediak-Higashi) mice. J. Cell Biol. 69: 205-210, 1976.
See also PubMed.

Onslow, H.: A contribution to our knowledge of the chemistry of coat-colour in animals and of dominant and recessive whiteness. Proc. Roy. Soc. (London) B 89: 36-58, 1915.

Owens, J.: Private Communication. Mouse News Letter 47: 61, 1972.
See also MGI.

Padgett, G.A.: The Chediak-Higashi syndrome. Adv. Vet. Sci. 12: 239-284, 1968.

Padgett, G.A., Leader, R.W., Gorham, J.R., and O'Mary, C.C.: The familal occurrence of the Chediak-Higashi syndrome in mink and cattle. Genetics 49: 505-512, 1964.

Padgett, G.A., Holland, J.M., Prieur, D.J., Davis, W.C., and Gorham, J.R.: The Chediak-Higashi syndrome. A review of the disease in man, mink, cattle, and mice. In Animal models For Biomedical Research, pp. 1-12, Nat. Acad. Sci. Printing and Publishing Office, Washington, D.C., 1970.

Papaioannou, V., and Mardon, H.: Private Communication. Mouse News Letter 58: 66, 1978.

Parsons, P.A.: A balanced four-point linkage experiment for linkage group XIII of the house mouse. Heredity 12: 77-95, 1958.
See also MGI.

Patt, H.M., and Maloney, M.A.: The bgJ/bgJ:W/Wv bone marrow chimera. Blood Cells 4: 27-35, 1978.
See also PubMed.

Pederson, R.A.: Development of lethal yellow ( Ay/Ay) mouse embryos in vitro. J. Exp. Zool. 188: 307-320, 1974.

Pederson, R.A., and Spindle, A.I.: Genetic effects of mammalian development during and after implantation. In Embryogenesis in Mammals. Ciba Foundation Symposium 40, I. Elliott and M. O'Conner (eds.), pp. 133-154, Elsevier-North Holland, Amsterdam, 1976.

Phillips, R.J.S.: Private Communication. Mouse News Letter 19: 22, 1958.

Phillips, R.J.S.: Private Communication. Mouse News Letter 21: 39, 1959.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 22: 30, 1960.

Phillips, R.J.S.: A comparison of mutation induced by acute x and chronic gamma irradiation in mice. Brit. J. Radiol. 34: 261-264, 1961a.

Phillips, R.J.S.: "Dappled", a new allele at the mottled locus in the house mouse. Genet. Res, (Camb.) 2: 290-295, 1961b.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 27: 34, 1962.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 29: 38, 1963.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 32: 39, 1965.
See also MGI.

Phillips, R.J.S.: A cis-trans position effect at the A locus of the house mouse. Genetics 54: 485-495, 1966a.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 34: 27, 1966b.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 39: 25, 1968.

Phillips, R.J.S.: Private Communication. Mouse News Letter 42: 26, 1970a.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 42: 27, 1970b.

Phillips, R.J.S.: Private Communication. Mouse News Letter 45: 25, 1971.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 48: 30, 1973.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 50: 42, 1974.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 53: 29, 1975.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 55: 14, 1976.
See also MGI.

Phillips, R.J.S.: Private Communication. Mouse News Letter 56: 38, 1977.
See also MGI.

Phillips, R.J.S., and Hawker, S.G.: Private Communication. Mouse News Letter 49: 29, 1973.
See also MGI.

Phillips, R.J.S., Hawker, S.G., and Moseley, H.J.: Private Communication. Mouse News Letter 48: 30-31, 1973.
See also MGI.

Pierro, L.J.: Effects of the light mutation of the mouse coat color on eye pigmentation. J. Exp. Zool. 153: 81-87, 1963a.
See also MGI.

Pierro, L.J.: Pigment granule formation in slate, a coat color mutant in the mouse. Anat. Rec. 146: 365-371, 1963b.

Pierro, L.J.: Private Communication. Mouse News Letter 32: 82, 1965.

Pierro, L.J., and Chase, H.B.: Slate — a new coat color in the mouse. J. Hered. 54: 46-50, 1963.
See also MGI.

Pierro, L.J., and Chase, H.B.: Temporary hair loss associated with the slate mutation of coat color in the mouse. Nature (London) 205: 579-580, 1965.
See also MGI.

Pierro, L.J., and Spiggle, J.: Gene interaction and hair pigmentation in the mouse. J. Invest. Dermatol. 54: 95, 1970 (Abstract).

Pincus, G.: A spontaneous mutation in the house mouse. Proc. Natl. Acad. Sci. USA 15: 85-88, 1929.

Pincus, G.: A modifier of piebald spotting in mice. Amer. Nat. 65: 283-286, 1931.

Pizarro, O.: Private Communication. Mouse News Letter 17: 95, 1957.

Pomerantz, S.H., and Chang, L.: Effects of beta-MSH, cortisol and ACTH on tyrosinase in the skin of newborn hamsters and mice. Endocrinology 87: 302-310, 1970.

Pomerantz, S.H., and Li, J.P-C.: Tyrosinase in the skin of albino hamsters and mice. Nature (London) 252: 241-243, 1974.
See also PubMed.

Poole, T.W.: Dermal-epidermal interactions and the site of action of the yellow ( Ay) and nonagouti ( a) coat color genes in the mouse. Develop. Biol. 36: 208-211, 1974.
See also PubMed.

Poole, T.W.: Dermal-epidermal interactions and the action of alleles at the agouti locus in the mouse. Develop. Biol. 42: 203-210, 1975.
See also MGI.

Poole, T.W., and Silvers, W.K.: The development of regional pigmentation patterns in black and tan ( at) mice. J. Exp. Zool. 197: 115-120, 1976a.
See also MGI.

Poole, T.W., and Silvers, W.K.: An experimental analysis of the recessive yellow coat color in the mouse. Develop. Biol. 48: 377-381, 1976b.
See also MGI.

Potten, C.S.: Radiation depigmentation of mouse hair: A study of follicular melanocyte populations. Cell Tissue Kinet. 1: 239-254, 1968.

Prieur, D.J., and Collier, L.L.: Animal model of human disease. Chediak-Higashi syndrome. Amer. J. Pathol. 90: 533-536, 1978.
See also PubMed.

Prieur, D.J., Davis, W.C., and Padgett, G.A.: Defective function of renal lysosomes in mice with Chediak-Higashi syndrome. Amer. J. Pathol. 67: 227-235, 1972.
See also PubMed.

Prota, G.: Structure and biogenesis of phaeomelanins. J. Invest. Dermatol. 54: 95, 1970 (Abstract).

Prota, G.: Strcture and biogenesis of phaeomelanins. In Pigmentation: Its Genesis and Biologic Control, V. Riley (ed.), pp. 615-630, Appleton-Century-Crofts, New York, 1972.

Prota, G., and Nicolaus, R.A.: On the biogenesis of phaeomelanins. In The Pigmentary System, Advances in Biology of Skin, Vol. 8, W. Montagna and F. Hu (eds.), pp. 323-328, Pergamon Press, Oxford, 1967.

Prota, G., and Thomson, R.H.: Melanin pigmentation in mammals. Endeavor 35: 32-38, 1976.
See also PubMed.

Pullig, T.: A new recessive spotting gene. J. Hered. 40: 229-230, 1949.

Quevedo, W.C., Jr.: Effect of biotin deficiency on follicular melanocytes of mice. Proc. Soc. Exp. Biol. Med. 93: 260-263, 1956.

Quevedo, W.C., Jr.: Loss of clear cells in the hair follicles of x-irradiated albino mice. Anat. Rec. 127: 725-734, 1957.

Quevedo, W.C., Jr.: Genetic regulation of melanocyte responses to U.V. In Recent Progress in Photobiology, E.J. Bowen (ed.), pp. 383-386, Blackwell, Oxford, 1965.

Quevedo, W.C., Jr.: The control of color in mammals. Amer. Zool. 9: 531-540, 1969a.
See also PubMed.

Quevedo, W.C., Jr.: Genetics of mammalian pigmentation. In The Biologic Effects of Ultraviolet Radiation, F. Urbach (ed.), pp. 315-324, Pergamon Press, Oxford, 1969b.

Quevedo, W.C., Jr.: Genetic regulation of pigmentation in mammals. In Biology of Normal and Abnormal Melanocytes, T. Kawamura, T.B. Fitzpatrick, and M. Seiji (eds.), pp. 99-115, Univ. of Tokyo Press, 1971.

Quevedo, W.C., Jr.: Epidermal melanin units: Melanocyte-keratinocyte interactions. Amer. Zool. 12: 35-41, 1972.

Quevedo, W.C., Jr., and Chase, H.B.: An analysis of the light mutation of coat color in mice. J. Morphol. 102: 329-346, 1958.
See also MGI.

Quevedo, W.C., Jr., and McTague, C.F.: Genetic influences on the response of mouse melanocytes to ultraviolet light: The melanocyte system of hair-covered skin. J. Exp. Zool. 152: 159-168, 1963.

Quevedo, W.C., Jr.: and Smith, J.A.: Studies on radiation-induced tanning of skin. Ann. N.Y. Acad. Sci. 100: 364-388, 1963.

Quevedo, W.C., Jr., and Smith, J.: Electron microscopic observations on the postnatal "loss" of interfollicilar epidermal melanocytes in mice. J. Cell Biol. 39: 103a, 1968 (Abstract).

Quevedo, W.C., Jr., Youle, M.C., Rovee, D.T., and Bienieki, T.C.: The developmental fate of melanocytes in murine skin. In Structure and Control of the Melanocyte, G. Della Porta (ed.), pp. 228-241, Springer-Verlag, Berlin, 1966.

Quevedo, W.C., Jr., Bienieki, T.C., McMorris, F.A., and Hepinstall, M.J.: Environmental and genetic influences on radiation-induced tanning of murine skin. In The Pigmentary System, Advances in Biology of Skin, Vol. 8, W. Montagna and F. Hu (eds.), pp. 361-377, Pergamon Press, Oxford, 1967.

Previous

1

2

3

4

Next