-
1
-
-
0015029187
-
Postnatal development of fiber types in normal and dystrophic skeletal muscle of the chick
-
Ashmore, C. R. and Doerr, L. 1971. Postnatal development of fiber types in normal and dystrophic skeletal muscle of the chick. Exp. Neurol. 30: 431-446.
-
(1971)
Exp. Neurol.
, vol.30
, pp. 431-446
-
-
Ashmore, C.R.1
Doerr, L.2
-
2
-
-
0032850960
-
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B
-
Bittner, R. E., Anderson, L. V., Burkhardt, E., Bashir, R., Vafiadaki, E., Ivanova, S., Raffelsberger, T., Maerk, I., Hoger, H., Jung, M., Karbasiyan, M., Storch, M., Lassmann, H., Moss, J. A., Davison, K., Harrison, R., Bushby, K. M. and Reis, A. 1999. Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B. Nat. Genet. 23: 141-142.
-
(1999)
Nat. Genet.
, vol.23
, pp. 141-142
-
-
Bittner, R.E.1
Anderson, L.V.2
Burkhardt, E.3
Bashir, R.4
Vafiadaki, E.5
Ivanova, S.6
Raffelsberger, T.7
Maerk, I.8
Hoger, H.9
Jung, M.10
Karbasiyan, M.11
Storch, M.12
Lassmann, H.13
Moss, J.A.14
Davison, K.15
Harrison, R.16
Bushby, K.M.17
Reis, A.18
-
3
-
-
0345731966
-
X chromosome-linked muscular dystrophy (mdx) in the mouse
-
Bulfield, G., Siller, W. G., Wight, P. A. and Moore, K. J. 1984. X chromosome-linked muscular dystrophy (mdx) in the mouse. Proc. Natl. Acad. Sci. U.S.A. 81: 1189-1192.
-
(1984)
Proc. Natl. Acad. Sci. U.S.A.
, vol.81
, pp. 1189-1192
-
-
Bulfield, G.1
Siller, W.G.2
Wight, P.A.3
Moore, K.J.4
-
4
-
-
0024346882
-
Feline muscular dystrophy with dystrophin deficiency
-
Carpenter, J. L., Hoffman, E. P., Romanul, F. C., Kunkel, L. M., Rosales, R. K., Ma, N. S., Dasbach, J. J., Rae, J. F., Moore, F. M., McAfee, M. B. and Pearce, L. K. 1989. Feline muscular dystrophy with dystrophin deficiency. Am. J. Pathol. 135: 909-919.
-
(1989)
Am. J. Pathol.
, vol.135
, pp. 909-919
-
-
Carpenter, J.L.1
Hoffman, E.P.2
Romanul, F.C.3
Kunkel, L.M.4
Rosales, R.K.5
Ma, N.S.6
Dasbach, J.J.7
Rae, J.F.8
Moore, F.M.9
McAfee, M.B.10
Pearce, L.K.11
-
5
-
-
0033814140
-
Molecular basis of muscular dystrophies
-
Cohn, R. D. and Campbell, K. P. 2000. Molecular basis of muscular dystrophies. Muscle. Nerve. 23: 1456-1471.
-
(2000)
Muscle. Nerve.
, vol.23
, pp. 1456-1471
-
-
Cohn, R.D.1
Campbell, K.P.2
-
6
-
-
0023883621
-
The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs
-
Cooper, B. J., Winand, N. J., Stedman, H., Valentine, B. A., Hoffman, E. P., Kunkel, L. M., Scott, M. O., Fischbeck, K. H., Kornegay, J. N., Avery, R. J., Williams, J. R., Schmickel, R. D. and Sylvester, J.E. 1988. The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs. Nature (Lond.) 334: 154-156.
-
(1988)
Nature (Lond.)
, vol.334
, pp. 154-156
-
-
Cooper, B.J.1
Winand, N.J.2
Stedman, H.3
Valentine, A.B.4
Hoffman, P.E.5
Kunkel, L.M.6
Scott, M.O.7
Fischbeck, K.H.8
Kornegay, J.N.9
Avery, R.J.10
Williams, J.R.11
Schmickel, D.R.12
Sylvester, J.E.13
-
7
-
-
0024242853
-
Ultrastructure of the skeletal muscle in the X chromosome-linked dystrophic (mdx) mouse. Comparison with Duchenne muscular dystrophy
-
Cullen, M. J. and Jaros, E. 1988. Ultrastructure of the skeletal muscle in the X chromosome-linked dystrophic (mdx) mouse. Comparison with Duchenne muscular dystrophy. Acta Neuropathol (Berl.) 77: 69-81.
-
(1988)
Acta Neuropathol (Berl.)
, vol.77
, pp. 69-81
-
-
Cullen, M.J.1
Jaros, E.2
-
8
-
-
25444444984
-
Procedures for morphologic studies of skeletal muscle, rat, mouse, and hamster
-
(Jones, T. C., Mohr, U. and Hunt, R. D. eds.), Springer-Verlag, Berlin
-
Donald McGavin, M. 1991.Procedures for morphologic studies of skeletal muscle, rat, mouse, and hamster. pp. 101-108. In: Cardiovascular and Musculoskeletal Systems (Jones, T. C., Mohr, U. and Hunt, R. D. eds.), Springer-Verlag, Berlin.
-
(1991)
Cardiovascular and Musculoskeletal Systems
, pp. 101-108
-
-
Donald McGavin, M.1
-
9
-
-
0036188005
-
Distal mdx muscle groups exhibiting up-regulation of utrophin and rescue of dystrophin-associated glycoproteins exemplify a protected phenotype in muscular dystrophy
-
Dowling, P., Culligan, K. and Ohlendieck, K. 2002. Distal mdx muscle groups exhibiting up-regulation of utrophin and rescue of dystrophin-associated glycoproteins exemplify a protected phenotype in muscular dystrophy. Naturwissenschaften 89: 75-78.
-
(2002)
Naturwissenschaften
, vol.89
, pp. 75-78
-
-
Dowling, P.1
Culligan, K.2
Ohlendieck, K.3
-
10
-
-
0038823857
-
Comparative analysis of Dp427-deficient mdx tissues shows that the milder dystrophic phenotype of extraocular and toe muscle fibres is associated with a persistent expression of beta-dystroglycan
-
Dowling, P., Lohan, J. and Ohlendieck, K. 2003. Comparative analysis of Dp427-deficient mdx tissues shows that the milder dystrophic phenotype of extraocular and toe muscle fibres is associated with a persistent expression of beta-dystroglycan. Eur. J. Cell. Biol. 82: 222-230.
-
(2003)
Eur. J. Cell. Biol.
, vol.82
, pp. 222-230
-
-
Dowling, P.1
Lohan, J.2
Ohlendieck, K.3
-
11
-
-
0037160782
-
The muscular dystrophies
-
Emery, A. E. 2002. The muscular dystrophies. Lancet 359: 687-695.
-
(2002)
Lancet
, vol.359
, pp. 687-695
-
-
Emery, A.E.1
-
12
-
-
0014135640
-
Nemaline (Z disk) myopathy: Observations on the origin, structure, and solubility properties of the nemaline structures
-
Engel, A. G. and Gomez, M. R. 1967. Nemaline (Z disk) myopathy: observations on the origin, structure, and solubility properties of the nemaline structures. J. Neuropathol. Exp. Neurol. 26: 601-619.
-
(1967)
J. Neuropathol. Exp. Neurol.
, vol.26
, pp. 601-619
-
-
Engel, A.G.1
Gomez, M.R.2
-
13
-
-
0034793617
-
The ABC's of limb-girdle muscular dystrophy: Alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more
-
Gordon, E. S. and Hoffman, E. P. 2001. The ABC's of limb-girdle muscular dystrophy: alpha-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more. Curr. Opin. Neurol. 14: 567-573.
-
(2001)
Curr. Opin. Neurol.
, vol.14
, pp. 567-573
-
-
Gordon, E.S.1
Hoffman, E.P.2
-
14
-
-
4243243654
-
Muscle biopsy in neuromuscular disorders
-
(Sternberg, S. ed.), Raven Press Ltd., New York
-
Heffner, R. R. 1989. Muscle biopsy in neuromuscular disorders. pp. 119-139. In: Diagnostic Surgical Pathology (Sternberg, S. ed.), Raven Press Ltd., New York.
-
(1989)
Diagnostic Surgical Pathology
, pp. 119-139
-
-
Heffner, R.R.1
-
15
-
-
0002273549
-
Dystrophinopathies
-
(Karpati, G., Hilton-Jones, D., Griggs, R. eds.), Cambridge Univ. Press, Cambridge, UK
-
Hoffman, E. P. 2001. Dystrophinopathies. pp. 385-432. In: Disorders of Voluntary Muscle (Karpati, G., Hilton-Jones, D., Griggs, R. eds.), Cambridge Univ. Press, Cambridge, UK.
-
(2001)
Disorders of Voluntary Muscle
, pp. 385-432
-
-
Hoffman, E.P.1
-
16
-
-
0024332141
-
Dystrophin abnormalities in Duchenne/Becker muscular dystrophy
-
Hoffman, E. P. and Kunkel, L. M. 1989. Dystrophin abnormalities in Duchenne/Becker muscular dystrophy. Neuron 2: 1019-1029.
-
(1989)
Neuron
, vol.2
, pp. 1019-1029
-
-
Hoffman, E.P.1
Kunkel, L.M.2
-
17
-
-
0000357470
-
Primary, generalized polymyopathy and cardiac necrosis in an inbred line of Syrian hamsters
-
Homburger, F., Baker, J. R., Nixon, C. W. and Whitney, R. 1962. Primary, generalized polymyopathy and cardiac necrosis in an inbred line of Syrian hamsters. Med. Exp. 6: 339-345.
-
(1962)
Med. Exp.
, vol.6
, pp. 339-345
-
-
Homburger, F.1
Baker, J.R.2
Nixon, C.W.3
Whitney, R.4
-
18
-
-
0014936580
-
Muscular dystrophy in the mouse caused by an allele at the dy-locus
-
Meier, H. and Southard, J. L. 1970. Muscular dystrophy in the mouse caused by an allele at the dy-locus. Life. Sci. 9: 137-144.
-
(1970)
Life. Sci.
, vol.9
, pp. 137-144
-
-
Meier, H.1
Southard, J.L.2
-
20
-
-
3042868147
-
Muscle diseases
-
(Benirschke, K., Garner, F. and Jones, T. eds.), Springer-Verlag, New York
-
Montgomery, C. A. 1978. Muscle diseases. pp. 821-887. In: Pathology of Laboratory Animals (Benirschke, K., Garner, F. and Jones, T. eds.), Springer-Verlag, New York.
-
(1978)
Pathology of Laboratory Animals
, pp. 821-887
-
-
Montgomery, C.A.1
-
21
-
-
8244259185
-
Identification of the Syrian hamster cardiomyopathy gene
-
Nigro, V., Okazaki, Y., Belsito, A., Piluso, G., Matsuda, Y., Politano, L., Nigro, G., Ventura, C., Abbondanza, C., Molinari, A. M., Acampora, D., Nishimura, M., Hayashizaki, Y. and Puca, G. A. 1997. Identification of the Syrian hamster cardiomyopathy gene. Hum. Mol. Genet. 6: 601-607.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 601-607
-
-
Nigro, V.1
Okazaki, Y.2
Belsito, A.3
Piluso, G.4
Matsuda, Y.5
Politano, L.6
Nigro, G.7
Ventura, C.8
Abbondanza, C.9
Molinari, A.M.10
Acampora, D.11
Nishimura, M.12
Hayashizaki, Y.13
Puca, G.A.14
-
22
-
-
0028673167
-
Muscle pathologic diagnosis-mechanism in muscle fiber degeneration
-
in Japanese
-
Nonaka, I. 1994. Muscle pathologic diagnosis-mechanism in muscle fiber degeneration. Rinsho Shinkeigaku 34: 1279-1281 (in Japanese).
-
(1994)
Rinsho Shinkeigaku
, vol.34
, pp. 1279-1281
-
-
Nonaka, I.1
-
23
-
-
0019808737
-
Intracytoplasmic vacuoles in alpha W fibers of dystrophic chicken muscle-probable early pathologic event initiates massive fiber necrosis
-
Nonaka, I. and Sugita, H. 1981. Intracytoplasmic vacuoles in alpha W fibers of dystrophic chicken muscle-probable early pathologic event initiates massive fiber necrosis. Acta Neuropathol. (Berl.) 55: 173-181.
-
(1981)
Acta Neuropathol. (Berl.)
, vol.55
, pp. 173-181
-
-
Nonaka, I.1
Sugita, H.2
-
24
-
-
0033120705
-
Covert persistence of mdx mouse myopathy is revealed by acute and chronic effects of irradiation
-
Pagel, C. N. and Partridge, T. A. 1999. Covert persistence of mdx mouse myopathy is revealed by acute and chronic effects of irradiation. J. Neurol. Sci. 164: 103-116.
-
(1999)
J. Neurol. Sci.
, vol.164
, pp. 103-116
-
-
Pagel, C.N.1
Partridge, T.A.2
-
25
-
-
0017883349
-
Central core disease: Histochemical and ultrastructural study of muscle biopsies of father and daughter
-
Palmucci, L., Schiffer, D., Monga, G., Mollo, F. and de Marchi, M. 1978. Central core disease: histochemical and ultrastructural study of muscle biopsies of father and daughter. J. Neurol. 218: 55-62.
-
(1978)
J. Neurol.
, vol.218
, pp. 55-62
-
-
Palmucci, L.1
Schiffer, D.2
Monga, G.3
Mollo, F.4
De Marchi, M.5
-
26
-
-
0031830818
-
Commentary: Extraocular muscle sparing in muscular dystrophy: A critical evaluation of potential protective mechanisms
-
Porter, J. D. 1998. Commentary: extraocular muscle sparing in muscular dystrophy: a critical evaluation of potential protective mechanisms. Neuromuscul. Disord. 8: 198-203.
-
(1998)
Neuromuscul. Disord.
, vol.8
, pp. 198-203
-
-
Porter, J.D.1
-
27
-
-
0031824850
-
The sparing of extraocular muscle in dystrophinopathy is lost in mice lacking utrophin and dystrophin
-
Porter, J. D., Rafael, J. A., Ragusa, R. J., Brueckner, J. K., Trickett, J. I. and Davies, K. E. 1998. The sparing of extraocular muscle in dystrophinopathy is lost in mice lacking utrophin and dystrophin. J. Cell. Sci. 111 (Pt 13): 1801-1811.
-
(1998)
J. Cell. Sci.
, vol.111
, Issue.13 PART
, pp. 1801-1811
-
-
Porter, J.D.1
Rafael, J.A.2
Ragusa, R.J.3
Brueckner, J.K.4
Trickett, J.I.5
Davies, K.E.6
-
28
-
-
1042268862
-
Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy
-
Porter, J. D., Merriam, A. P., Leahy, P., Gong, B., Feuerman, J., Cheng, G. and Khanna, S. 2004. Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy. Hum. Mol. Genet. 13: 257-269.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 257-269
-
-
Porter, J.D.1
Merriam, A.P.2
Leahy, P.3
Gong, B.4
Feuerman, J.5
Cheng, G.6
Khanna, S.7
-
29
-
-
0031871858
-
The International Life Sciences Institute's role in the evaluation of alternative methodologies for the assessment of carcinogenic risk
-
Robinson, D. 1998. The International Life Sciences Institute's role in the evaluation of alternative methodologies for the assessment of carcinogenic risk. Toxicol. Pathol. 26: 474-475.
-
(1998)
Toxicol. Pathol.
, vol.26
, pp. 474-475
-
-
Robinson, D.1
-
30
-
-
0004211516
-
-
Butterworth-Heinemann, Boston
-
Rosenberg, R. N., Prusiner, S. B., DiMauro, S., Barchi, R. L. and Kunkel, L. M. 1993. The Molecular and Genetic Basis of Neurological Disease, Butterworth-Heinemann, Boston.
-
(1993)
The Molecular and Genetic Basis of Neurological Disease
-
-
Rosenberg, R.N.1
Prusiner, S.B.2
DiMauro, S.3
Barchi, R.L.4
Kunkel, L.M.5
-
31
-
-
0025121594
-
Most tumors in transgenic mice with human c-Ha-ras gene contained somatically activated transgenes
-
Saitoh, A., Kimura, M., Takahashi, R., Yokoyama, M., Nomura, T., Izawa, M., Sekiya, T., Nishimura, S. and Katsuki, M. 1990. Most tumors in transgenic mice with human c-Ha-ras gene contained somatically activated transgenes. Oncogene 5: 1195-1200.
-
(1990)
Oncogene
, vol.5
, pp. 1195-1200
-
-
Saitoh, A.1
Kimura, M.2
Takahashi, R.3
Yokoyama, M.4
Nomura, T.5
Izawa, M.6
Sekiya, T.7
Nishimura, S.8
Katsuki, M.9
-
32
-
-
0031471956
-
Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: An animal model of disrupted dystrophin-associated glycoprotein complex
-
Sakamoto, A., Ono, K., Abe, M., Jasmin, G., Eki, T., Murakami, Y., Masaki, T., Toyo-oka, T. and Hanaoka, F. 1997. Both hypertrophic and dilated cardiomyopathies are caused by mutation of the same gene, delta-sarcoglycan, in hamster: an animal model of disrupted dystrophin-associated glycoprotein complex. Proc. Natl. Acad. Sci. U.S.A. 94: 13873-13878.
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 13873-13878
-
-
Sakamoto, A.1
Ono, K.2
Abe, M.3
Jasmin, G.4
Eki, T.5
Murakami, Y.6
Masaki, T.7
Toyo-oka, T.8
Hanaoka, F.9
-
33
-
-
0015180411
-
Fiber types and preclinical changes in chicken muscular dystrophy
-
Shafiq, S. A., Askanas, V. and Milhorat, A. T. 1971. Fiber types and preclinical changes in chicken muscular dystrophy. Arch. Neurol. 25: 560-571.
-
(1971)
Arch. Neurol.
, vol.25
, pp. 560-571
-
-
Shafiq, S.A.1
Askanas, V.2
Milhorat, A.T.3
-
34
-
-
0019810179
-
Calcium release and ionic changes in the sarcoplasmic reticulum of tetanized muscle: An electron-probe study
-
Somlyo, A. V., Gonzalez-Serratos, H. G., Shuman, H., McClellan, G. and Somlyo, A. P. 1981. Calcium release and ionic changes in the sarcoplasmic reticulum of tetanized muscle: an electron-probe study. J. Cell. Biol. 90: 577-594.
-
(1981)
J. Cell. Biol.
, vol.90
, pp. 577-594
-
-
Somlyo, A.V.1
Gonzalez-Serratos, H.G.2
Shuman, H.3
McClellan, G.4
Somlyo, A.P.5
-
35
-
-
0036235994
-
Transgene stability and features of rasH2 mice as an animal model for short-term carcinogenicity testing
-
Suemizu, H., Muguruma, K., Maruyama, C., Tomisawa, M., Kimura, M., Hioki, K., Shimozawa, N., Ohnishi, Y., Tamaoki, N. and Nomura, T. 2002. Transgene stability and features of rasH2 mice as an animal model for short-term carcinogenicity testing. Mol. Carcinog. 34: 1-9.
-
(2002)
Mol. Carcinog.
, vol.34
, pp. 1-9
-
-
Suemizu, H.1
Muguruma, K.2
Maruyama, C.3
Tomisawa, M.4
Kimura, M.5
Hioki, K.6
Shimozawa, N.7
Ohnishi, Y.8
Tamaoki, N.9
Nomura, T.10
-
36
-
-
0005567541
-
X chromosome-linked muscular dystrophy (mdx) of the skeletal muscle, mouse
-
(Jones, T. C., Mohr, U. and Hunt, R. D. eds.), Springer-Verlag, Berlin
-
Tanabe, Y., Woo, M. and Nonaka, I. 1991. X chromosome-linked muscular dystrophy (mdx) of the skeletal muscle, mouse, pp. 149-155. In: Cardiovascular and Musculoskeletal Systems (Jones, T. C., Mohr, U. and Hunt, R. D. eds.), Springer-Verlag, Berlin.
-
(1991)
Cardiovascular and Musculoskeletal Systems
, pp. 149-155
-
-
Tanabe, Y.1
Woo, M.2
Nonaka, I.3
-
37
-
-
0036628962
-
Skeletal myopathy in transgenic mice carrying human prototype c-Ha-ras gene
-
Tsuchiya, T., Kobayashi, K., Sakairi, T., Goto, K., Okada, M., Sano, F., Sugimoto, J., Morohashi, T., Usui, T. and Mutai, M. 2002. Skeletal myopathy in transgenic mice carrying human prototype c-Ha-ras gene. Toxicol. Pathol. 30: 501-506.
-
(2002)
Toxicol. Pathol.
, vol.30
, pp. 501-506
-
-
Tsuchiya, T.1
Kobayashi, K.2
Sakairi, T.3
Goto, K.4
Okada, M.5
Sano, F.6
Sugimoto, J.7
Morohashi, T.8
Usui, T.9
Mutai, M.10
-
38
-
-
0021813838
-
The mechanism of muscle fiber breakdown in Duchenne muscular dystrophy-with particular reference to the significance of opaque muscle fibers
-
Uchino, M., Araki, S. and Yoshida, O. 1985. The mechanism of muscle fiber breakdown in Duchenne muscular dystrophy-with particular reference to the significance of opaque muscle fibers. Rinsho Shinkeigaku 25: 944-948.
-
(1985)
Rinsho Shinkeigaku
, vol.25
, pp. 944-948
-
-
Uchino, M.1
Araki, S.2
Yoshida, O.3
-
39
-
-
0026597535
-
Canine X-linked muscular dystrophy as an animal model of Duchenne muscular dystrophy: A review
-
Valentine, B. A., Winand, N. J., Pradhan, D., Moise, N. S., de Lahunta, A., Kornegay, J. N. and Cooper, B. J. 1992. Canine X-linked muscular dystrophy as an animal model of Duchenne muscular dystrophy: a review. Am. J. Med. Genet. 42: 352-356.
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 352-356
-
-
Valentine, B.A.1
Winand, N.J.2
Pradhan, D.3
Moise, N.S.4
De Lahunta, A.5
Kornegay, J.N.6
Cooper, B.J.7
-
40
-
-
0036021778
-
Functional characteristics of dystrophic skeletal muscle: Insights from animal models
-
Watchko, J. F., O'Day, T. L. and Hoffman, E. P. 2002. Functional characteristics of dystrophic skeletal muscle: insights from animal models. J. Appl. Physiol. 93: 407-417.
-
(2002)
J. Appl. Physiol.
, vol.93
, pp. 407-417
-
-
Watchko, J.F.1
O'Day, T.L.2
Hoffman, E.P.3
-
41
-
-
0023832469
-
Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy
-
Webster, C., Silberstein, L., Hays, A. P. and Blau, H. M. 1988. Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy. Cell 52: 503-513.
-
(1988)
Cell
, vol.52
, pp. 503-513
-
-
Webster, C.1
Silberstein, L.2
Hays, A.P.3
Blau, H.M.4
-
42
-
-
0028334735
-
Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse
-
Xu, H., Christmas, P., Wu, X. R., Wewer, U. M. and Engvall, E. 1994. Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse. Proc. Natl. Acad. Sci. U.S.A. 91: 5572-5576.
-
(1994)
Proc. Natl. Acad. Sci. U.S.A.
, vol.91
, pp. 5572-5576
-
-
Xu, H.1
Christmas, P.2
Wu, X.R.3
Wewer, U.M.4
Engvall, E.5
-
43
-
-
0031977910
-
Validation of transgenic mice carrying the human prototype c-Ha-ras gene as a bioassay model for rapid carcinogenicity testing
-
Yamamoto, S., Urano, K., Koizumi, H., Wakana, S., Hioki, K., Mitsumori, K., Kurokawa, Y., Hayashi, Y. and Nomura, T. 1998. Validation of transgenic mice carrying the human prototype c-Ha-ras gene as a bioassay model for rapid carcinogenicity testing. Environ. Health Perspect. 106 (Suppl. 1): 57-69.
-
(1998)
Environ. Health Perspect.
, vol.106
, Issue.1 SUPPL.
, pp. 57-69
-
-
Yamamoto, S.1
Urano, K.2
Koizumi, H.3
Wakana, S.4
Hioki, K.5
Mitsumori, K.6
Kurokawa, Y.7
Hayashi, Y.8
Nomura, T.9
|