Pathology of Genetically Engineered and Other Mutant Mice. Группа авторов

Читать онлайн.
Название Pathology of Genetically Engineered and Other Mutant Mice
Автор произведения Группа авторов
Жанр Биология
Серия
Издательство Биология
Год выпуска 0
isbn 9781119624592



Скачать книгу

and PV).

      1 1 Sundberg, J.P., Roopenian, D.C., Liu, E.T., and Schofield, P.N. (2013). The Cinderella effect: searching for the best fit between mouse models and human diseases. J. Invest. Dermatol. 133 (11): 2509–2513.

      2 2 Seok, J., Warren, H.S., Cuenca, A.G. et al. (2013). Genomic responses in mouse models poorly mimic human inflammatory diseases. Proc. Natl. Acad. Sci. U.S.A. 110 (9): 3507–3512.

      3 3 Takao, K. and Miyakawa, T. (2015). Genomic responses in mouse models greatly mimic human inflammatory diseases. Proc. Natl. Acad. Sci. U.S.A. 112 (4): 1167–1172.

      4 4 Shay, T., Lederer, J.A., and Benoist, C. (2015). Genomic responses to inflammation in mouse models mimic humans: we concur, apples to oranges comparisons won't do. Proc. Natl. Acad. Sci. U.S.A. 112 (4): E346.

      5 5 Lu, Y.F., Goldstein, D.B., Angrist, M., and Cavalleri, G. (2014). Personalized medicine and human genetic diversity. Cold Spring Harb. Perspect. Med. 4 (9): a008581.

      6 6 Selman, C. and Swindell, W.R. (2018). Putting a strain on diversity. EMBO J. 37 (22): e100862. https://doi.org/10.15252/embj.2018100862.

      7 7 Threadgill, D.W., Dlugosz, A.A., Hansen, L.A. et al. (1995). Targeted disruption of mouse EGF receptor: effect of genetic background on mutant phenotype. Science 269 (5221): 230–234.

      8 8 Sibilia, M. and Wagner, E.F. (1995). Strain‐dependent epithelial defects in mice lacking the EGF receptor. Science 269 (5221): 234–238.

      9 9 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.

      10 10 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.

      11 11 Scarpelli, D.G., Capen, C.C., Cork, L.C. et al. (1985). Animal models of human disease. In: (ed. G. Migaki), 302–321. Washington, DC: Armed Forces Institute of Pathology.

      12 12 McElwee, K.J., Boggess, D., King, L.E. Jr., and Sundberg, J.P. (1998). Experimental induction of alopecia areata‐like hair loss in C3H/HeJ mice using full‐thickness skin grafts. J. Invest. Dermatol. 111 (5): 797–803.

      13 13 Nishina, P.M., Verstuyft, J., and Paigen, B. (1990). Synthetic low and high fat diets for the study of atherosclerosis in the mouse. J. Lipid Res. 31 (5): 859–869.

      14 14 Hudson, A., Trider, C.‐L., and Blake, K. (2017). CHARGE syndrome. Pediatr. Rev. 38 (1): 56.

      15 15 Jongmans, M.C.J., Admiraal, R.J., van der Donk, K.P. et al. (2006). CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene. J. Med. Genet. 43 (4): 306–314.

      16 16 Bosman, E.A., Penn, A.C., Ambrose, J.C. et al. (2005). Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. Hum. Mol. Genet. 14 (22): 3463–3476.

      17 17 van Ravenswaaij‐Arts, C. and Martin, D.M. (2017). New insights and advances in CHARGE syndrome: diagnosis, etiologies, treatments, and research discoveries. Am. J. Med. Genet. C Semin. Med. Genet. 175 (4): 397–406.

      18 18 Gage, P.J., Hurd, E.A., and Martin, D.M. (2015). Mouse models for the dissection of CHD7 functions in eye development and the molecular basis for ocular defects in CHARGE syndrome. Invest. Ophthalmol. Vis. Sci. 56 (13): 7923–7930.

      19 19 Lutzner, M.A., Lowrie, C.T., and Jordan, H.W. (1967). Giant granules in leukocytes of the beige mouse. J. Hered. 58 (6): 299–300.

      20 20 Penner, J.D. and Prieur, D.J. (1987). A comparative study of the lesions in cultured fibroblasts of humans and four species of animals with Chediak‐Higashi syndrome. Am. J. Med. Genet. 28 (2): 445–454.

      21 21 Penner, J.D. and Prieur, D.J. (1987). Interspecific genetic complementation analysis with fibroblasts from humans and four species of animals with Chediak‐Higashi syndrome. Am. J. Med. Genet. 28 (2): 455–470.

      22 22 Schofield, P.N., Vogel, P., Gkoutos, G.V., and Sundberg, J.P. (2012). Exploring the elephant: histopathology in high‐throughput phenotyping of mutant mice. Dis. Models Mech. 5 (1): 19–25.

      23 23 Mezick, J.A., Bhatia, M.C., and Capetola, R.J. (1984). Topical and systemic effects of retinoids on horn‐filled utriculus size in the rhino mouse. A model to quantify “antikeratinizing” effects of retinoids. J. Invest. Dermatol. 83 (2): 110–113.

      24 24 Ashton, R.E., Connor, M.J., and Lowe, N.J. (1984). Histologic changes in the skin of the rhino mouse (Hrrh/Hrrh) induced by retinoids. J. Invest. Dermatol. 82 (6): 632–635.

      25 25 Bryce, G.F., Bogdan, N.J., and Brown, C.C. (1988). Retinoic acids promote the repair of the dermal damage and the effacement of wrinkles in the UVB‐irradiated hairless mouse. J. Invest. Dermatol. 91 (2): 175–180.

      26 26 Kligman, L.H. (1989). Prevention and repair of photoaging: sunscreens and retinoids. Cutis 43 (5): 458–465.

      27 27 Sundberg, J.P., Dunstan, R.W., and Compton, J.G. (1989). Hairless mouse, HRS/J hr/hr. In: Integument and Mammary Glands Monographs on Pathology of Laboratory Animals (eds. T.C. Jones, U. Mohr and R.D. Hunt), 192–197. Heidelberg: Springer‐Verlag.

      28 28 Sundberg, J.P., Price, V.H., and King, L.E. Jr. (1999). The “hairless” gene in mouse and man. Arch. Dermatol. 135 (6): 718–720.

      29 29 Ahmad, W., Faiyaz ul Haque, M., Brancolini, V. et al. (1998). Alopecia universalis associated with a mutation in the human hairless gene. Science 279 (5351): 720–724.

      30 30 Ahmad, W., Irvine, A.D., Lam, H. et al. (1998). A missense mutation in the zinc‐finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers. Am. J. Hum. Genet. 63 (4): 984–991.

      31 31 Ahmad, W., Panteleyev, A.A., Henson‐Apollonio, V. et al. (1998). Molecular basis of a novel rhino (hrrhChr) phenotype: a nonsense mutation in the mouse hairless gene. Exp. Dermatol. 7 (5): 298–301.

      32 32 Ahmad, W., Panteleyev, A.A., Sundberg, J.P., and Christiano, A.M. (1998). Molecular basis for the rhino (Hrrh‐8J) phenotype: a nonsense mutation in the mouse hairless gene. Genomics 53 (3): 383–386.

      33 33 Panteleyev, A.A., Ahmad, W., Malashenko, A.M. et al. (1998). Molecular basis for the rhino Yurlovo (hr(rhY)) phenotype: severe skin abnormalities and female reproductive defects associated with an insertion in the hairless gene. Exp. Dermatol. 7 (5): 281–288.

      34 34 Panteleyev, A.A., Paus, R., Ahmad, W. et al. (1998). Molecular and functional aspects of the hairless (Hr) gene in laboratory rodents and humans. Exp. Dermatol. 7 (5): 249–267.

      35 35 Tuttle, A.H., Philip, V.M., Chesler, E.J., and Mogil, J.S. (2018). Comparing phenotypic variation between inbred and outbred mice. Nat. Methods 15 (12): 994–996.

      36 36 McElwee, K.J., Niiyama, S., Freyschmidt‐Paul, P. et al. (2003). Dietary soy oil content and soy‐derived phytoestrogen genistein increase resistance to alopecia areata onset in C3H/HeJ mice. Exp. Dermatol. 12 (1): 30–36.

      37 37 Ward, J.M. and Devor‐Henneman, D.E. (2004). Mouse models of human familial cancer syndromes. Toxicol. Pathol. 32 (Suppl 1): 90–98.

      38 38 Kuperwasser, C., Hurlbut, G.D., Kittrell, F.S. et al. (2000). Development of spontaneous mammary tumors in BALB/c p53 heterozygous mice. A model for Li‐Fraumeni syndrome. Am. J. Pathol. 157 (6): 2151–2159.

      39 39 Sundberg, J.P. and Schofield, P.N. (2018). Living inside the box: environmental effects on mouse models of human disease. Dis. Models Mech. 11 (10): dmm035360. https://doi.org/10.1242/dmm.035360.

      40 40 Sofaer, J.A. (1969). Aspects of the tabby‐crinkled‐downless syndrome. II. Observations on the reaction to changes of genetic background. J. Embryol. Exp. Morphol. 22 (2): 207–227.

      41 41 Sofaer, J.A. (1969). Aspects of the