References
Bailey, D.W.: Genetics of histocompatibility in mice. I. New loci and congenic lines.Immunogenetics 2: 249–256, 1975.
Barker, P.E., Royer, H.-D., Ruddle, F.H., and Reinherz, E.L.: Human T cell receptor gene TCRA lies in region 14pter-q21.Cytogenet Cell Genet 40: 576–577, 1985.
Beisel, K.W. and Booth, B.J.M.: Identification of three alleles forMus musculus at theMyhc-a locus which co-segregates withNp-2, Tcra andRib-1 on chromosome 14.Nucl Acids Res 17: 10519, 1989.
Belin, D., Vassalli, J.-D., Combépine, C., Godeau, F., Nagamine, Y., Reich, E., Kocher, H.P., and Duvoisin, R.M.: Cloning, nucleotide sequencing and expression of cDNAs encoding mouse urokinase-type plasminogen activator.Eur J Biochem 148: 225–232, 1985.
Berman, J.W., Rocha, A.J.D., and Basch, R.: Restriction length polymorphism in the variable region of theTcr locus linked to histocompatibility antigenH-8 on murine chromosome 14.Immunogenetics 24: 328–330, 1986.
Bessis, A., Simon-Chazottes, D., Devillers-Thiéry, A., Guénet, J.-L., and Changeux, J.-P.: Chromosomal localization of the mouse genes coding for α2, α3, α4, and β2 subunits of neuronal nicotinic acetylcholine receptor.FEBS Lett 264: 48–52, 1990.
Bishop, D.T.: The information content of phase known matings for ordering genetic loci.Genet Epidemiol 2: 349–361, 1985.
Bode, V.C., Bonhomme, F., and Guénet, J.-L.: Personal communication.Mouse News Lett 74: 97, 1986.
Bode, V.C., McDonald, J.D., Guénet, J.-L., and Simon, D.:hph-1: A mouse mutant with hereditary hyperphenylalaninemia induced by ethylnitrosourea mutagenesis.Genetics 118: 299–305, 1988.
Boehm, T., Baer, R., Lavenir, I., Forster, A., Waters, J.J., Nacheva, E., and Rabbitts, T.H.: The mechanism of chromosomal translocation t(11;14) involving the T-cell receptor C-delta locus on human chromosome 14q11 and a transcribed region of chromosome 11p15.EMBO J 7: 385–394, 1988.
Bowcock, A.M., Farrer, L.A., Hebert, J.M., Agger, M., Sternlieb, I., Scheinberg, I.H., Buys, C.H.C.M., Scheffer, H., Frydman, M., Chajek-Saul, T., Bonne-Tamir, B., and Cavalli-Sforza, L.L.: Eight closely linked loci place the Wilson disease locus within 13q14–q21.Am J Hum Genet 43: 664–674, 1988.
Brand, N., Petkovich, M., Krust, A., Chambon, P., de Thé, H., Marchio, A., Tiollais, P., and Dejean, A.: Identification of a second human retinoic acid receptor.Nature 332: 850–853, 1988.
Bremmer, T.A., Premkumar-Reddy, E., Nayar, K., and Kouri, R.E.: Nucleoside phosphorylase 2 (Np-2) inmice.Biochem Genet 16: 1143–1151, 1978.
Brooke, H.C.: Hairless mice.J Hered 17: 173–174, 1926.
Brunet, J.-F., Dosseto, M., Denizot, F., Mattei, M.-G., Clark, W.R., Haqqi, T.M., Ferrier, P., Nabholz, M., Schmitt-Verhulst, A.-M., Luciani, M.-F., and Golstein, P.: The inducible cytotoxic T-lymphocyte-associated gene transcriptCTLA-1 sequence and gene localization to mouse chromosome 14.Nature 322: 268–271, 1986.
Carson, N.L. and Simpson, N.E.: A physical map of 13 markers on chromosome 10 from dosage studies on abnormal cell lines.Cytogenet Cell Genet 40: 974–975, 1989.
Cattanach, B.M.: Crossover suppression in mice heterozygous for tobacco mouse metacentrics.Cytogenet Cell Genet 20: 264–281, 1978.
Ceci, J.D., Kingsley, D.M., Silan, C.M., Copeland, N.G., and Jenkins, N.A.: An interspecific backcross linkage map of the proximal half of mouse chromosome 14.Genomics 6: 673–678, 1990.
Chan, T.-S., Creagan, R.P., and Reardon, M.P.: Adenosine kinase as a new selective marker in somatic cell genetics: Isolation of adenosine kinase-deficient mouse cell lines and human-mouse hybrid cell lines containing adenosine kinase.Som Cell Genet 4: 1–12, 1978.
Chang, H.-Y., Guerrero, I., Lake, R., Pellicer, A., and D'Eustachio, P.: MouseN-ras genes: Organization of the functional locus and of a truncated cDNA-like pseudogene.Oncogene Res 1: 129–136, 1987.
Chen, S., Creagan, R.P., Nichols, E.A., and Ruddle, F.H.: Assignment of human esterase-D gene to chromosome 13.Cytogenet Cell Genet 14: 269–272, 1975.
Chien, Y.-H., Iwashima, M., Kaplan, K.B., Elliott, J.F., and Davis, M.M.: A new T-cell receptor gene located within the α locus and expressed early in T-cell differentiation.Nature 327: 677–682, 1987.
Collins, M.K.L., Goodfellow, P.N., Spurr, N.K., Solomon, E., Tanigawa, G., Tonegawa, S., and Owen, M.J.: The human T-cell receptor α-chain maps to chromosome 14.Nature 314: 273–274, 1985.
Committee on Standardized Genetic Nomenclature for Mice: Standard karyotype of the mouse,Mus musculus.J Hered 63: 69–72, 1985.
Cox, D.W., Billingsley, G.D., Willard, H.F., and Grzeschik, K.-H.: Localization of markers on chromosome 14.Cytogenet Cell Genet 40: 980, 1989.
Croce, C.M., Isobe, M., Palumbo, A., Puck, J., Ming, J., Tweardy, D., Erikson, J., and Davis, M.: Gene for α-chain for T-cell receptor: Location on chromosome 14 region involved in T-cell neoplasms.Science 227: 1044–1047, 1985.
Crosby, J.L., Bleackley, R.C., and Nadeau, J.H.: A complex of serine protease genes expressed preferentially in cytotic T-lymphocytes is closely linked to the T-cell receptor α- and β-chain genes on mouse chromosome 14.Genomics 6: 252–259, 1990.
Cumming, R.B., Walton, W.F., Fuscoe, J.C., Taylor, B.A., Womack, J.E., and Gaertner, F.H.: Genetics of formamidase-5 (brain formamidase) in the mouse: Localization of the structural gene on chromosome 14.Biochem Genet 17: 415–431, 1979.
Cumming, R.B., Gaertner, F.H., Walton, M.F., and O'Donnell, S.C.: A structural gene for formamidase.Mouse News Lett 56: 53, 1977.
Czosnek, H.H., Bienz, B., Givol, D., Zakut-Houri, R., Pravtcheva, D., Ruddle, F.H., and Oren, M.: The gene and the pseudogene for mouse p53 cellular tumor antigen are located on different chromosomes.Mol Cell Biol 4: 1638–1640, 1984.
Danciger, M., Kozak, C.A., Nickerson, J., Redmond, T.M., and Farber, D.B.: Localization of the gene for interphotoreceptor retinoid-binding protein to mouse chromosome 14 nearNp-1.Genomics 8: 727–731, 1990.
Datta, S.K., Owen, F.L., Womack, J.E., and Riblet, R.J.: Analysis of recombinant inbred lines derived from “autoimmune” (NZB) and “high leukemia” (C58) strain: Independent multigenic systems control B cell hyperactivity, retrovirus expression, and autoimmunity.J Immunol 129: 1539–1544, 1982.
Davisson, M.T., Roderick, T.H., and Hillyard, A.: Recombination percentages and chromosomal assignments.In M.F. Lyon and A.G. Searle (eds.);Genetic Variants and Strains of the Laboratory Mouse, pp. 432–505. Oxford University Press, New York, 1989.
Dembic, Z., Bannwarth, W., Taylor, B.A., and Steinmetz, M.: The gene encoding the T-cell receptor α-chain maps close to theNp-2 locus on mouse chromosome 14.Nature 314: 271–273, 1985.
de Thé, H., Marchio, A., Tiollais, P., and Dejean, A.: A novel steroid thyroid hormone receptor-related gene inappropriately expressed in human heptocellular carcinoma.Nature 330: 667–670, 1987.
Dickie, M.M.: Gunmetal.Mouse News Lett 30: 30, 1964.
Dickie, M.M., Schneider, J., and Harman, P.J.: A juvenile wabblerlethal in the house mouse.J Hered 43: 283–286, 1952.
Dickinson, M.E., Kobrin, M.S., Silan, C.M., Kingsley, D.M., Justice, M.J., Miller, D.A., Ceci, J.D., Lock, L.F., Lee, A., Buchberg, A.M., Siracusa, L.D., Lyons, K.M., Derynck, R., and Hogan, B.L.M.: Chromosomal localization of seven members of the murine TGF-β superfamily suggests close linkage to several morphogenetic mutant loci.Genomics 6: 505–520, 1990.
Donis-Kellor, H., Green, P., Helms, C., Cartinhour, S., Weiffenbach, B., Stephens, K., Keith, T.P., Bowden, B.W., Smith, D.R., Lander, E.S., Botstein, D., Akots, G., Rediker, K.S., Gravius, T., Brown, V.A., Rising, M.B., Parker, C., Powers, J.A., Watt, D.E., Kaufman, E.R., Bricker, A., Phipps, P., Muller-Kahle, H., Fulton, T.R., Ng, S., Schumm, J., Braman, J.C., Knowlton, R.G., Barker, D.F., Crooks, S.M., Lincoln, S.E., Daly, M.J., and Abrahamson, J.: A genetic linkage map of the human genome.Cell 51: 319–337, 1987.
Dunn, L.C.: Types of white spotting in mice.Am Nat 54: 465–495, 1920.
Dymecki, S.M., Niederhuber, J.E., and Desiderio, S.V.: Specific expression of a tyrosine kinase gene,blk, in B lymphoid cells.Science 247: 332–336, 1990.
Eicher, E.M.: Personal communication, 1972.
Eicher, E.M. and Green, M.C.: TheT6 translocation in the mouse: Its use in trisomy mapping, centromere localization, and cytological identification of linkage group III.Genetics 71: 621–632, 1972.
Elliott, R.W.: Identification and mapping of new loci using cloned cDNA.Mouse New Lett 64: 87, 1981.
Elliott, R.W., Samuelson, L.C., Lambert, M.S., and Meisler, M.H.: Assignment of pancreatic ribonuclease gene to mouse chromosome 14.Cytogenet Cell Genet 42: 110–112, 1986.
Eppig, J.T. and Eicher, E.M.: Application of the ovarian teratoma mapping method in the mouse.Genetics 103: 797–812, 1983.
Epstein, R., Sham, G., Womack, J., Yagüe, J., Palmer, E., and Cohn, M.: The cytotoxic T cell response to the male-specific histocompatibility antigen (H-Y) is controlled by two dominant immune response genes, one in the MHC, the other in the T-α locusJ Exp Med 163: 759–773, 1986.
Farrer, L.A., Castiglione, C.M., Kidd, J.R., Myers, S., Carson, N., Simpson, N.E., and Kidd, K.K.: A linkage group of five DNA markers on human chromosome 10.Genomics 3: 72–77, 1988.
Francke, U., Busby, N., Shaw, D., Hansen, S., and Brown, M.G.: Intrachromosomal gene mapping in man: Assignment of nucleoside phosphorylase to region 14cen->14q21 by interspecific hybridization of cells with a t(X;14)(p22;q21) translocation.Som Cell Genet 2: 27–40, 1976.
Francke, U., Lalley, P.A., Moss, W., Ivy, J., and Minna, J.D.: Gene mapping inMus musculus by interspecific cell hybridization: Assignment of the gene tripeptidase-1 to chromosome 10, dipeptidase-2 to chromosome 18, acid phosphatase-1 to chromosome 12, and adenylate kinase-1 to chromosome 2.Cytogenet Cell Genet 19: 57–84, 1977.
Francke, U. and Thompson, L.: Regional mapping by exclusion of adenosine kinase (ADOK) on human chromosome 10 using gene dosage.Cytogenet Cell Genet 25: 156, 1979.
Frankel, W.N., Stoye, J.P., Taylor, B.A., and Coffin, J.M.: Genetic analysis of endogenous xenotropic murine leukemia viruses: Association with two common mouse mutations and the viral restriction locusFv-1.J Virol 63: 1763–1774, 1989.
Frecker, M., Dallaire, L., Young, S.R., Chen, G.C.C., and Simpson, N.E.: Confirmation of regional assignment of nucleoside phosphorylase (NP) on chromosome 14 by gene dosage studies:Hum Genet 45: 167–173, 1978.
Friend, S.H., Bernards, R., Rogelj, S., Weinberg, R.A., Rapaport, J.M., Albert, D.M., and Dryja, T.P.: A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma.Nature 323: 643–646, 1986.
Gey, W.: Multiple missbildungen und retinoblastom.Humangenetik 10: 362–365, 1970.
Gleditsch, L., Snodgrass, R., and Bogen, B.: No recombinations betweenTcra-V andTcra-C gene segments in 699 backcross mice.Immunogenetics 32: 297–303, 1990.
Green, M.C.: Personal communication.Mouse News Lett 34: 31, 1966.
Green, M.C.: Personal communication.Mouse News Lett 44: 30, 1971.
Green, M.C.: Slaty (slt).Mouse News Lett 47: 36, 1972a.
Green, M.C.: Waved coat (Wc).Mouse News Lett 47: 36, 1972b.
Green, M.C.: Chromosome 14.Mouse News Lett 48: 35, 1973a.
Green, M.C.: Personal communication.Mouse News Lett 49: 32, 1973b.
Green, M.C.: Personal communication.Mouse News Lett 51: 23, 1974.
Green, M.C. and Sweet, H.O.: Chromosome 14.Mouse News Lett 55: 17, 1976.
Hammer, M.F., Schimenti, J., and Silver, L.M.: Evolution of mouse chromosome 17 and the origin of inversions associated witht haplotypes.Proc Natl Acad Sci USA 86: 3261–3265, 1989.
Hanauer, A., Mandel, J.-L., and Mattei, M.-G.: X linked and autosomal sequences corresponding to glutamate dehydrogenase (GLUD) and to an anonymous cDNA.Cytogenet Cell Genet 40: 647–648, 1985.
Hanauer, A., Mattei, M.-G., and Mandel, J.-L.: Presence of aTaqII polymorphism in the human glutamate dehydrogenase (GLUD) gene on chromosome 10.Nucl Acids Res 15: 6308, 1987.
Harper, K., Mattei, M.-G., Simon, D., Suzan, M., Guénet, J.-L., Haddad, P., Sasportes, M., and Golstein, P.: Proximity of the CTLA-1 serine protease andTcr α loci in mouse and man.Immunogenetics 28: 439–444, 1988.
Hayday, A.C., Diamond, D.J., Tanigawa, G., Heilig, J.S., Folsom, V., Saito, H., and Tonegawa, S.: Unusual organization and diversity of T-cell receptor α-chain genes.Nature 316: 828–832, 1985.
Hearne, C.M., McAleer, M.A., Love, J., Aitman, T.J., Cornall, R.J., Ghosh, S., Knight, A., Prins, J.-B., and Todd, J.A.: Additional microsatellite markers for mouse genome mapping.Mammalian Genome, in press, 1991.
Heidmann, O., Buonanno, A., Geoffroy, B., Robert, B., Guénet, J.-L., Merlie, J.P., and Changeux, J.-P.: Chromosomal localization of muscle nicotinic acetylcholine receptor genes in the mouse.Science 234: 866–868 1986.
Hoecker, G., Martinez, A., Markovic, S., and Pizarro, O.: Agitans, a new mutation in the house mouse with neurological effects.J Hered 45: 10–14, 1954.
Hsieh, C.-L., Bowcock, A.M., Farrer, L.A., Hebert, J.M., Huang, K.N., Cavalli-Sforza, L.L., Julius, D., and Francke, U.: The seratonin receptor subtype 2 locusHTR2 is on human chromosome 13 near genes for esterase D and retinoblastoma-1 and on mouse chromosome 14.Som Cell Mol Genet 16: 567–574, 1990.
Hsieh, C.-L., Lee, W.H., Lee, E.Y.-H.P., Killary, A.M., Lalley, P.A., and Naylor, S.A.: Assignment of retinoblastoma susceptibility gene to mouse chromosome 14.Som Cell Mol Genet 15: 461–464, 1989.
Hummel, K.P.: Personal communication, 1985.
Hummel, K.P.: The inheritance and expression of disorganization, an unusual mutation in the mouse.J Exp Zool 137: 389–423, 1958.
Hurst, J., Flavell, D., Julien, J.P., Meijer, P., Mushinski, W., and Grosveld, F.: The human neurofilament gene (NFL) is located on the short arm of chromosome 8.Cytogenet Cell Genet 45: 30–32, 1987.
Jeffreys, A.J., Wilson, V., Kelly, R., Taylor, B.A., and Bulfield, G.: Mouse DNA “fingerprints”; analysis of chromosome localization and germ-line stability of hypervariable loci in recombinant inbred strains.Nucl Acids Res 15: 2823–2836, 1987.
Kidwell, J.F., Gowen, J.W., and Stadler, J.: Pugnose—a recessive mutation in linkage group of 3 mice.J Hered 52: 145–148, 1961.
Kidwell, J.F., Gowen, J.W., and Stadler, J.: Pugnose linkage in the mouse.J Hered 57: 229–230, 1967.
Kozak, C.A.: Personal communication, 1990.
Kozak, C., Danciger, M., and Farber, D.: Chromosome assignment in the mouse of the genes for several proteins involved in visual transduction.Cytogenet Cell Genet 10: 1025–1026, 1989.
Kozak, C.A. and Ruddle, F.H.: Sexual and parasexual approaches to the genetic analysis of the laboratory mouse,Mus musculus.In Vitro 12: 720–725, 1976.
Krangel, M.S., Band, H., Hata, S., McLean, J., and Brenner, M.B.: Structurally divergent human T-cell receptor γ proteins encoded by distinct C-γ genes.Science 237: 64–67, 1987.
Kranz, D.M., Saito, H., Disteche, C.M., Swisshelm, K., Pravtcheva, D., Ruddle, F.H., Eisen, H.N. and Tonegawa, S.: Chromosomal locations of the murine T-cell receptor α-chain gene and the T-cell γ gene.Science 227: 941–945 1985.
Lai, E., Wilson, R.K., and Hood, L.E.: Physical maps of the mouse and human immunoglobulin-like loci.Adv Immunol 46: 1–59, 1989.
Lane, P.W.: Personal communication, 1963.
Lane, P.W.: Personal communication, 1966.
Lane, P.W.: Personal communication, 1970.
Lane, P.W. and Dickie, M.M.: Linkage of wabbler-lethal and hair-less in the mouse.J Hered 52: 159–160, 1961.
Lee, W.H., Bookstein, R., Hong, F., Young, L.-J., Shew, J.-Y., and Lee, E.Y.-H.P.: Human retinoblastoma susceptibility gene: Cloning, identification and sequencing.Science 235: 1394–1399, 1987.
Lee, B.K. and Eicher, E.M.: Segregation patterns of endogenous mouse mammary tumor viruses in five recombinant inbred strain sets.J Virol 64: 4568–4572, 1990.
Lee, E.Y.-H.P. and Lee, W.H.: Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma.Proc Natl Acad Sci USA 83: 6337–6341, 1986.
Leinwand, L., Fournier, R.E.K., Nichols, E.A., and Ruddle, F.H.: Assignment of the gene for adenosine kinase to chromosome 14 inMus musculus by somatic cell hybridization.Cytogenet Cell Genet 21: 77–85, 1978.
Lewis, W.H., Michalopoulos, E.E., Williams, D.L., Minden, M.D., and Mak, T.W.: Breakpoints in the human T-cell antigen receptor α-chain locus in two T-cell leukemia patients with chromosomal translocations.Nature 317: 544–546, 1985.
Liesi, P., Julien, J.-P.,Vilja, P., Grosveld, F., and Rechardt, L.: Specific detection of neuronal cell bodies: In situ hybridization with a biotin-labeled neurofilament cDNA probe.J Histochem Cytochem 7: 923–926, 1986.
Liou, G.I., Li, Y., Wang, C., Fong, S.-L., Bhattacharya, S., and Bridges, C.D.B.:BgIII RFLP recognized by a human IRBP cDNA localized to chromosome 10.Nucl Acids Res 15: 3196, 1987.
Lobe, C.G., Finlay, B.B., Paranchych, W., Paetkus, V.H., and Bleackley, R.C.: Cloning of two genes that are specifically expressed in activated cytotoxic T lymphocytes.Proc Natl Acad Sci USA 83: 1448–1452, 1986.
Love, J.M., Knight, A.M., McLeer, M.A., and Todd, J.A.: Toward construction of a high resolution map of the mouse genome using PCR-analyzed microsatellites.Nucl Acids Res 18: 4123–4130, 1990.
Lukey, T., Neote, K., Loman, J.F., Unger, A.E., Biddle, F.G., and Snyder, F.F.: Purine nucleoside phosphorylase (Np) in the mouse: Linkage relationship ofNp-2 to esterase-10 (Es-10) andNp-1 on chromosome 14.Biochem Genet 23: 347–356 1985.
Lyon, M.F. and Glenister, P.H.: Roan and freckled.Mouse News Lett 59: 18, 1978.
Lyon, M.F. and Newport, P.R.: Personal communication.Mouse News Lett 49: 30, 1973.
MacGregor, G.R., Russell, L.D., Van Beck, M.E.A.B., Hanten, G.R., Kovac, M.J., Kozak, C.A., Meistrich, M.L., and Overbeek, P.A.: Symplastic spermatids (sys): A recessive insertional mutation in mice causing a defect in spermatogenesis.Proc Natl Acad Sci USA 87: 5016–5020, 1990.
Mathew, C., Nakamura, Y., Easton, D., Wakeling, W., Jones, E., Chin, K., Telenius, H., Clark, J., Smith, S., Strong, C., Bragg, T., Little, P., Jones, C.A., Povey, S., White, R., and Ponder, B.: MEN2A and the developing map of chromosome 10.Cytogenet Cell Genet 40: 1040, 1989.
Matsuoka, R., Chambers, A., Kimura, M., Kanda, N., Bruns, G., Yoshida, M., and Takao, A.: Molecular cloning and chromosomal localization of a gene coding for human cardiac myosin heavy chain.Am J Med Genet 29: 369–376, 1988.
Matsuoka, R., Yoshida, M.C., Kanda, N., Kimura, M., Ozasa, H., and Takao, A.: Human cardiac myosin heavy chain mapped within chromosomal region 14q11.2–q13.Cytogenet Cell Genet 40: 1040–1041, 1989a.
Matsuoka, R., Yoshida, M.C., Kanda, N., Kimura, M., Ozasa, H., and Takao, A.: Human cardiac myosin heavy chain gene mapped within chromosomal region 14q11.2–q13.Am J Med Genet 32: 279–284, 1989b.
Mattei, M.-G., de Thé, H., Mattei, J.-F., Marchio, A., Tiollais, P., and Dejean, A.: Assignment of the human hap retinoic acid receptor RAR-β gene to the p24 band of chromosome 3.Hum Genet 80: 189–190, 1988.
Mattei, M.-G., Duprey, P., Li, Z.L., Mattei, J.-F., and Paulin, D.: Chromosomal localization of the mouse gene coding for the 68 kDa neurofilament subunit.Biol Cell 67: 235–237, 1989.
Mattei, M.-G., Harper, K., Brunet, J.F., Denizot, F., Mattei, J.-F., Golstein, P., and Giraud, F.: In situ mapping of four cytotoxic T-lymphocyte associated proteins (CTLA) to the mouse genome.Cytogenet Cell Genet 46: 657–658, 1987.
Miret-Duvaux, O., Frederic, F., Simon, D., Guénet, J.-L., Hanauer, A., Delhaye-Bouchaud, N., and Mariani, J.: Glutamate dehydrogenase in cerebellar mutant mice: Gene localization and enzyme activity in different tissues.J Neurochem 54: 23–29, 1990.
Nadeau, J.H., Herrmann, B., Bucan, M., Burkhart, D., Crosby, J.L., Erhart, M.A., Kosowsky, M., Kraus, J.P., Michiels, F., Schnattinger, A., Tchetgen, M.-B., Varnum, D., Willison, K., Lehrach, H., and Barlow, D.: Genetic maps of mouse Chromosome 17 including 12 new anonymous DNA loci and 25 anchor loci.Genomics: 78–89, 1991.
Nakamura, Y., Lathrop, M., Bragg, T., Leppert, M., O'Connell, P., Jones, C., Lalouel, J.-M., and White, R.: An extended genetic linkage map of markers for human chromosome 10.Genomics 3: 389–392, 1988.
Naylor, S.L., Marshall, A., Killary, A.M., Lalley, P.A., Belin, D., Rickles, R., Stickland, S., and Rajput, B.: The gene for mouse plasminogen activator and urokinase map to chromosomes 8 and 14, respectively.Cytogenet Cell Genet 46: 669, 1987.
Nesbitt, M., Pugh, S.L., and Pigen, B.: Strain distribution pattern of thirteen genetic loci in the AXB and BXA recombinant inbred set.Mouse Genome 88: 113, 1990.
Nichols, E.A. and Ruddle, R.H.: A review of enzyme polymorphism, linkage and electrophoretic conditions for mouse and somatic cells hybrids in starch gels.J Histochem Cytochem 21: 1066–1081, 1973.
Owerbach, D. and Hjorth, J.P.: Genetic determination of a parotid secretory protein in mouse.Hereditas 89: 146, 1978.
Prakash, O., Kozak, C., and Sarkar, N.H.: Molecular cloning, characterization, and genetic mapping of an endogenous murine mammary tumor virus proviral unit I of C3H/He mice.J Virol 54: 285–294, 1985.
Peterson, T.C., Killary, A.M., and Fournier, R.E.K.: Chromosomal assignment and trans regulation of the tyrosine amino transferase structural gene in hepatoma hybrid cells.Mol Cell Biol 5: 2491–2494, 1985.
Rajput, B., Degen, S.F., Reich, E., Waller, E.K., Axelrod, J., Eddy, R.L., and Shows, T.B.: Chromosomal locations of human tissue plasminogen activator and urokinase genes.Science 230: 672–674, 1985.
Rajput, B., Marshall, A., Killary, A.M., Lalley, P.A., Naylor, S.L., Belin, D., Rickles, R.J., and Strickland, S.: Chromosomal assignments of genes for tissue plasminogen activator and urokinase in mouse.Som Cell Mol Genet 13: 581–586, 1987.
Rasberry, C. and Cattanach, B.: Location of talipes (Tal).Mouse Genome 87: 89, 1990.
Ricciuti, F. and Ruddle, F.H.: Assignment of nucleoside phosphorylase to D-14 and localization of X-linked loci in many by somatic cell genetics.Nature New Biol 241: 180–182, 1973.
Richards-Smith, B., and Elliott, R.W.: Mapping of repeated sequences in the mouse genome.Mouse News Lett 71: 46–47, 1984.
Roderick, T.H., Hawes, N.L., Davisson, M.T., and Hillyard, A.L.: Map of inversions.In M.F. Lyon and A.G. Searle (eds.),Genetic Variants and Strains of the Laboratory Mouse, pp. 626–631, Oxford University Press, New York, 1989.
Roderick, T.H. and Hillyard, A.L.: Differences in recombination due to sex in mice.Mouse News Lett 85: 87, 1989.
Russell, W.L. and Russell, L.B.: The genetic and phenotypic characteristics of radiation-induced mutations in mice.Rad Res Suppl 1: 296–305, 1959.
Rutledge, J.C., Cain, K.T., Cachiero, N.L.A., Cornett, C.V., Wright, C.G., and Generoso, W.M.: A balanced translocation in mice with a neurological defect.Science 231: 395–397, 1985.
Ryan, J., Hart, C.P., and Ruddle, F.H.: Molecular cloning and chromosomal assignment of murine.N-ras.Nucl Acids Res 12: 6063–6072, 1984.
Saez, L.J., Gianola, K.M., McNalley, E.M., Feghali, R., Eddy, R., Shows, T.B., and Leinwand, L.: Human cardiac myosin heavy chain genes and their linkage in the genome.Nucl Acids Res 15: 5443–5459, 1987.
Samuelson, L.C. and Farber, R.A.: Cytological localization of three genes on chromosome 14 inMus musculus. Am J Huma Genet 36: 207s, 1984.
Samuelson, L.C. and Farber, R.A.: Cytological localization of adenosine kinase, nucleoside phosphorylase-1 and esterase-10 genes on mouse chromosome 14.Som Cell Mol Genet 11: 157–165, 1985.
Searle, A.G. and Beechey, C.V.: Maps of chromosomal variants.In M.F. Lyon and A.G. Searle (eds.);Genetic Variants and Strains of the Laboratory Mouse, pp. 620–625, Oxford University Press, New York, 1989.
Sebastio, G., Riccio, A., Verde, P., Scarpato, N., and Blasi, F.:Bam HI RFLP linked to the human urokinase gene.Nucl Acids Res 13: 5404, 1985.
Schugart, K., Pravtcheva, D., Newman, M.S., Hunihan, L.W., Jiang, Z., and Ruddle, F.H.: Isolation and regional localization of the murine homeobox-containing geneHox-3.3 to mouse chromosome region 15E.Genomics 5: 76–83, 1989.
Seldin, M.: Personal communication, 1990.
Sharpe, P.T., Miller, J.R., Evans, E.P., Burtenshaw, M.D., and Gaunt, S.J.: Isolation and expression of a new mouse homeobox gene.Development 102: 397–407, 1988.
Shaughnessy, J., Mock, B., Duncan, R., Potter, M., and Banner, C.: A restriction fragment length polymorphism at murineGlud locus co-segregates withRib-1, Es-10, andTcra on chromosome 14.Nucl Acids Res 17: 2881, 1989.
Silver, J.: Confidence limits for estimates of gene linkage based on analysis of recombinant inbred strains.J Hered 76: 436–440, 1985.
Siracusa, L.D., Buchberg, A.M., Copeland, N.G., and Jenkins, N.A.: Recombinant inbred strain and interspecific backcross analysis of molecular markers flanking the murine agouti coat color locus.Genetics 122: 669–679, 1989.
Siracusa, L.D., Jenkins, N.A., and Copeland, N.G.: Identification and application of repetitive probes for gene mapping in the mouse.Genetics 127: 169–179, 1990.
Siracusa, L.D., Rosner, M.H., Vigano, M.A., Gilbert, D.J., Staudt, L.M., Copeland, N.G., and Jenkins, N.A.: Chromosomal location of the octamer transcription factors,Otf-1, Otf-2 andOtf-3, suggests close linkage to several mutant loci and defines multiple-Otf-3-related sequences dispersed in the mouse genome.Genomics, in press, 1991.
Snell, G.D.: Inheritance in the house mouse, the linkage of shortear, hairless, and naked.Genetics, 16: 42–74, 1931.
Snell, G.D. and Bunker, H.P.: Histocompatibility genes of mice. V. Five new histocompatibility loci identified by congenic resistant lines on a C57BL/10 background.Transplantation 3: 235–252, 1965.
Snyder, F.: Regulation of purine metabolism.Mouse News Lett 65: 10, 1981.
Snyder, F.F., Biddle, F.G., Lukey, T., and Sparling, M.J.: Genetic variability of purine nucleoside phosphorylase activity in the mouse: Relationship toNP-1 andNP-2.Biochem Genet 21: 323–332, 1983.
Snyder, F.F., Lin, C.C., Rudd, N.L., Shearer, J.E., Heikkila, E.M., and Hoo, J.J.: A de novo case of trisomy 10p: Gene dosage studies of hexokinase, inorganic phosphatase and adenosine kinase.Hum Genet 67: 187–189, 1984.
Sorokina, J.D. and Blandova, Z.K.: Waved alopecia.Mouse News Lett 73: 23, 1985.
Stone, J.C., Crosby, J.L., Kozak, C.A., Schievella, A., Bernards, R., and Badeau, J.H.: The murine retinoblastoma homolog maps to chromosome 14 nearEs-10.Genomics 5: 70–75, 1989.
Strobel, M.: Personal communication, 1990.
Taylor, B.A.: Linkage ofNp-2.Mouse News Lett 65: 28, 1981.
Traina, V.L., Taylor, B.A., and Cohen, J.C.: Genetic mapping of endogenous mammary tumor viruses: Locus characterization, segregation, and chromosomal distribution.J Virol 40: 735–744, 1981.
Tripputi, P., Blasi, F., Verde, P., Cannizzaro, L.A., Emanuel, B.S., and Croce, C.M.: Human urokinase gene located on the long arm of chromosome 10.Proc Natl Acad Sci USA 82: 4448–4452, 1985.
Ward, P., Packman, S., Loughman, W., Sparkes, M., Sparkes, R., McMahon, A., Gregory, T., and Ablin, A.: Location of the retinoblastoma susceptibility gene(s) and the human esteraseD locus.J Med Genet 21: 92–95, 1984.
Weber, J.L. and May, P.E.: Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction.Am J Hum Genet 44: 388–396, 1989.
Weller, P.A., Ogryzko, E.P., Corben, E.B., Zhidkova, N.I., Patel, B., Price, G.J., Spurr, N.K., Koteliansky, V.E., and Critchley, D.R.: Complete sequence of human vinculin and assignment of the gene to chromosome 10.Proc Natl Acad Sci USA 87: 5667–5671, 1990.
Weydert, A., Daubas, P., Lazaridis, I., Barton, P., Garner, I., Leader, D.P., Bonhomme, F., Catalan, J., Simon, D., Guénet, J.-L., Gros, F., and Buckingham, M.E.: Genes for skeletal muscle myosin heavy chains are clustered and are not located on the same mouse chromosome as a cardiac myosin heavy chain gene.Proc Natl Acad Sci USA 82: 7183–7187, 1985.
Womack, J.E., Davisson, M.T., Eicher, E.M., and Kendall, D.A.: Mapping of nucleoside phosphorylase (Np-1) and esterase 10 (Es-10) on mouse chromosome 14.Biochem Genet 15: 347–355, 1977.
Womack, J.E. and Sharp, M.: Comparative autosomal linkage in mammals: Genetics of esterase inMus musculus andRattus norvegicus.Genetics 82: 665–675, 1976.
Wozney, J.M., Rosen, V., Celeste, A.J., Mitsock, L.M., Whitters, M.J., Kriz, R.W., Hewick, R.M., and Wang, E.A.: Novel regulators of bone formation: Molecular clones and activities.Science 242: 1528–1534, 1988.
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Nadeau, J.H., Ceci, J.D. & Cox, R. Mouse chromosome 14. Mammalian Genome 1 (Suppl 1), S221–S240 (1991). https://doi.org/10.1007/BF00656495
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DOI: https://doi.org/10.1007/BF00656495