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1 1 McKusick, V.A. (1969). On lumpers and splitters, or the nosology of genetic disease. Perspect Biol. Med. 12 (2): 298–312.

2 2 Simon‐Sanchez, J. and Gasser, T. (2015). Parkinson disease GWAS: the question of lumping or splitting is back again. Neurology 84 (10): 966–967.

3 3 Schofield, P.N., Bubela, T., Weaver, T. et al. (2009). Post‐publication sharing of data and tools. Nature 461 (7261): 171–173.

4 4 Low, B.E., Kutny, P.M., and Wiles, M.V. (2016). Simple, efficient CRISPR‐Cas9‐mediated gene editing in mice: strategies and methods. Methods Mol. Biol. 1438: 19–53.

5 5 Snell, G.D. (1941). Biology of the Laboratory Mouse, 1e. New York, NY: McGraw‐Hill.

6 6 Husler, M.R., Beamer, W.G., Boggess, D. et al. (1998). Neoplastic and hyperplastic lesions in aging C3H/HeJ mice. J. Exp. Anim. Sci. 38 (4): 165–180.

7 7 Sundberg, J.P., King, L.E. Jr., Bosenberg, M. et al. (2020). Animal models of skin disease. In: McKee's Pathology of the Skin with Clinical Correlations. 2, 5e (eds. E. Calonje, T. Brenn, A.H. Lazar and S.D. Billings), 1895–1917. China: Elsevier.

8 8 Li, Q., Berndt, A., Sundberg, B.A. et al. (2016). Mouse genome‐wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age‐related cardiac fibrosis. Mamm Genome. 27 (5‐6): 179–190. https://doi.org/10.1007/s00335‐016‐9634‐y. Epub 2016 Apr 28.

9 9 Giehl, K.A., Potter, C.S., Wu, B. et al. (2009). Hair interior defect in AKR/J mice. Clin. Exp. Dermatol. 34 (4): 509–517.

10 10 Wu, B., Potter, C.S., Silva, K.A. et al. (2010). Mutations in sterol O‐acyltransferase 1 (Soat1) result in hair interior defects in AKR/J mice. J. Invest. Dermatol. 130 (11): 2666–2668.

11 11 Davisson, M.T., Schmidt, C., Reeves, R.H. et al. (1993). Segmental trisomy as a mouse model for Down syndrome. Prog. Clin. Biol. Res. 384: 117–133.

12 12 Bisaillon, J.J., Radden, L.A. 2nd, Szabo, E.T. et al. (2014). The retarded hair growth (rhg) mutation in mice is an allele of ornithine aminotransferase (Oat). Mol. Genet. Metabol. Rep. 1: 378–390.

13 13 Fox, S. and Eicher, E.M. (1978). The retarded hair growth (rhg) mutation in mice is an allele of ornithine aminotransferase (Oat). Mouse News Lett. 58: 47.

14 14 Griffen, A. (1951). tc – truncate. Mouse News Lett. 5: 31.

15 15 Mulligan, M.K., Mozhui, K., Prins, P., and Williams, R.W. (2017). GeneNetwork: a toolbox for systems genetics. Methods Mol. Biol. 1488: 75–120.

16 16 Li, Q., Philip, V.M., Stearns, T.M. et al. (2019). Quantitative trait locus and integrative genomics revealed candidate modifier genes for ectopic mineralization in mouse models of pseudoxanthoma elasticum. J. Invest. Dermatol. 139 (12): 2447–2457. e7.

17 17 Chesler, E.J., Miller, D.R., Branstetter, L.R. et al. (2008). The Collaborative Cross at Oak Ridge National Laboratory: developing a powerful resource for systems genetics. Mamm. Genome 19 (6): 382–389.

18 18 Philip, V.M., Sokoloff, G., Ackert‐Bicknell, C.L. et al. (2011). Genetic analysis in the Collaborative Cross breeding population. Genome Res. 21 (8): 1223–1238.

19 19 Graham, J.B., Thomas, S., Swarts, J. et al. (2015). Genetic diversity in the collaborative cross model recapitulates human West Nile virus disease outcomes. mBio 6 (3): e00493–e00415.

20 20 Zeiss, C.J., Gatti, D.M., Toro‐Salazar, O. et al. (2019). Doxorubicin‐induced cardiotoxicity in Collaborative Cross (CC) mice recapitulates individual cardiotoxicity in humans. G3 9 (8): 2637–2646.

21 21 Gralinski, L.E., Ferris, M.T., Aylor, D.L. et al. (2015). Genome wide identification of SARS‐CoV susceptibility loci using the Collaborative Cross. PLoS Genet. 11 (10): e1005504.

22 22 Konger, R.L., Derr‐Yellin, E., Hojati, D. et al. (2016). Comparison of the acute ultraviolet photoresponse in congenic albino hairless C57BL/6J mice relative to outbred SKH1 hairless mice. Exp. Dermatol. 25 (9): 688–693.

23 23 Voigt, A.Y., Michaud, M., Tsai, K.Y. et al. (2019). Differential hairless mouse strain‐specific susceptibility to skin cancer and sunburn. J. Invest. Dermatol.

24 24 Papale, L.A., Beyer, B., Jones, J.M. et al. (2009). Heterozygous mutations of the voltage‐gated sodium channel SCN8A are associated with spike‐wave discharges and absence epilepsy in mice. Hum. Mol. Genet. 18 (9): 1633–1641.

25 25 Johnson, K.R., Tian, C., Gagnon, L.H. et al. (2017). Effects of Cdh23 single nucleotide substitutions on age‐related hearing loss in C57BL/6 and 129S1/Sv mice and comparisons with congenic strains. Sci. Rep. 7: 44450.

26 26 Thomas, M.K., Devon, O.N., Lee, J.H. et al. (2001). Development of diabetes mellitus in aging transgenic mice following suppression of pancreatic homeoprotein IDX‐1. J. Clin. Invest. 108 (2): 319–329.

27 27 Ohlrogge, W., Haag, F., Lohler, J. et al. (2002). Generation and characterization of ecto‐ADP‐ribosyltransferase ART2.1/ART2.2‐deficient mice. Mol. Cell. Biol. 22 (21): 7535–7542.

28 28 Serreze, D.V., Chapman, H.D., Post, C.M. et al. (2001). Th1 to Th2 cytokine shifts in nonobese diabetic mice: sometimes an outcome, rather than the cause, of diabetes resistance elicited by immunostimulation. J. Immunol. 166 (2): 1352–1359.

29 29 Dunn, L.C. (1937). Caracul, a dominant mutation. J. Heredity. 28: 334.

30 30 Bubier, J.A., Sproule, T.J., Alley, L.M. et al. (2010). A mouse model of generalized non‐Herlitz junctional epidermolysis bullosa. J. Invest. Dermatol. 130 (7): 1819–1828.

31 31 Sproule, T.J., Bubier, J.A., Grandi, F.C. et al. (2014). Molecular identification of collagen 17a1 as a major genetic modifier of laminin gamma 2 mutation‐induced junctional epidermolysis bullosa in mice. PLoS Genet. 10 (2): e1004068.

32 32 Nadeau, J.H., Singer, J.B., Matin, A., and Lander, E.S. (2000). Analysing complex genetic traits with chromosome substitution strains. Nat. Genet. 24 (3): 221–225.

33 33 Dietl, G., Langhammer, M., and Renne, U. (2004). Model simulations for genetic random drift in the outbred strain Fzt:DU. Arch. Anim. Breed 47 (6): 595–604.

34 34 Svenson, K.L., Gatti, D.M., Valdar, W. et al. (2012). High‐resolution genetic mapping using the mouse diversity outbred population. Genetics 190 (2): 437–447.

35 35 French, J.E., Gatti, D.M., Morgan, D.L. et al. (2015). Diversity outbred mice identify population‐based exposure thresholds and genetic factors that influence benzene‐induced genotoxicity. Environ. Health Perspect. 123 (3): 237–245.

36 36 Broman, K.W., Gatti, D.M., Svenson, K.L. et al. (2019). Cleaning genotype data from diversity outbred mice. G3 9 (5): 1571–1579.

37 37 Recla, J.M., Bubier, J.A., Gatti, D.M. et al. (2019). Genetic mapping in diversity outbred mice identifies a Trpa1 variant influencing late‐phase formalin response. Pain 160 (8): 1740–1753.

38 38 Sigmon, J.S., Blanchard, M.W., Baric, R.S. et al. (2020). Content and performance of the MiniMUGA genotyping array, a new tool to improve rigor and reproducibility in mouse research. Genetics 216 (4): 905–930. https://doi.org/10.1534/genetics.120.303596.

39 39 Stoye, J.P., Fenner, S., Greenoak, G.E. et al. (1988). Role of endogenous retroviruses as mutagens: the hairless mutation of mice. Cell 54 (3): 383–391.

40 40 Maddox, D.M., Hicks, W.L., Vollrath, D. et al. (2011). An ENU‐induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degeneration. Invest. Ophthalmol. Vis. Sci. 52 (7): 4703–4709.

41 41 Theiler, K. and Varnum, D.S. (1981). Development of coloboma (Cm/+), a mutation with anterior lens adhesion. Anat. Embryol. (Berl). 162 (1): 121–126.

42 42 Hess, E.J., Jinnah, H.A., Kozak, C.A., and Wilson, M.C. (1992). Spontaneous locomotor hyperactivity in a mouse mutant with a deletion including the Snap gene on chromosome 2. J. Neurosci. 12 (7): 2865–2874.

43 43 Birling, M.C., Schaeffer, L., Andre, P. et al. (2017). Efficient and rapid generation of large genomic variants in rats and mice using CRISMERE. Sci. Rep. 7: 43331.

44 44 Wang, X., Ria, M., Kelmenson, P.M. et al. (2005). Positional identification of TNFSF4, encoding OX40 ligand, as a gene that influences atherosclerosis susceptibility. Nat. Genet. 37 (4): 365–372.

45 45 Broccoli, V., Boncinelli, E., and Wurst, W. (1999). The caudal limit of Otx2 expression positions the isthmic organizer. Nature 401 (6749): 164–168.

46 46 Rickert, R.C., Rajewsky, K., and Roes, J. (1995). Impairment of T‐cell‐dependent B‐cell responses and B‐1 cell development in CD19‐deficient mice. Nature 376 (6538): 352–355.

47 47 Larsson, N.G., Wang, J., Wilhelmsson, H. et al. (1998). Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice. Nat. Genet. 18 (3): 231–236.

48 48 Knowlton, M.N. and Smith, C.L. (2017). Naming CRISPR alleles: endonuclease‐mediated mutation nomenclature across species. Mamm. Genome 28 (7–8): 367–376.

49 49 Cao, W., Kayama, H., Chen, M.L. et al. (2017). The xenobiotic transporter Mdr1 enforces T cell homeostasis in the presence of intestinal bile acids. Immunity 47 (6): 1182–1196. e10.

50 50 Mizuno, S., Takami, K., Daitoku, Y. et al. (2015). Peri‐implantation lethality in mice carrying megabase‐scale deletion on 5qc3.3 is caused by Exoc1 null mutation. Sci. Rep. 5: 13632.

51 51 Friedel, R.H. and Soriano, P. (2010). Gene trap mutagenesis in the mouse. Methods Enzymol. 477: 243–269.

52 52 Fritz, J.M., Dong, M., Apsley, K.S. et al. (2014). Deficiency of the BiP cochaperone ERdj4 causes constitutive endoplasmic reticulum stress and metabolic defects. Mol. Biol. Cell 25 (4): 431–440.

53 53 The Jackson Laboratory. (2009). Large‐scale enhancer trap project to generate transgenic cre alleles by Ron Davis at Baylor University [Internet]. http://www.informatics.jax.org (accessed 04 March 2021).

54 54 Li, L., Liu, P., Sun, L. et al. (2016). PiggyBac transposon‐based polyadenylation‐signal trap for genome‐wide mutagenesis in mice. Sci. Rep. 6: 27788.

55 55 Elso, C.M., Chu, E.P., Alsayb, M.A. et al. (2015). Sleeping beauty transposon mutagenesis as a tool for gene discovery in the NOD mouse model of type 1 diabetes. G3 5 (12): 2903–2911.

56 56 Echelard, Y., Vassileva, G., and McMahon, A.P. (1994). Cis‐acting regulatory sequences governing Wnt‐1 expression in the developing mouse CNS. Development 120 (8): 2213–2224.

57 57 Lewandoski, M., Wassarman, K.M., and Martin, G.R. (1997). Zp3‐cre, a transgenic mouse line for the activation or inactivation of loxP‐flanked target genes specifically in the female germ line. Curr. Biol. 7 (2): 148–151.

Pathology of Genetically Engineered and Other Mutant Mice

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