000 01390 a2200409 4500
005 20250514214659.0
264 0 _c20050728
008 200507s 0 0 eng d
022 _a0007-4888
024 7 _a10.1007/s10517-005-0060-5
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aStenina, M A
245 0 0 _aHereditary muscular dystrophy in MDX mice as a homologous model for introduction of cell technologies in the treatment of progressive muscular dystrophies in humans.
_h[electronic resource]
260 _bBulletin of experimental biology and medicine
_cOct 2004
300 _a425-8 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAnimals
650 0 4 _aDystrophin
_xgenetics
650 0 4 _aExons
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMice
650 0 4 _aMice, Inbred mdx
650 0 4 _aMotor Activity
650 0 4 _aMuscle, Skeletal
_xpathology
650 0 4 _aMuscular Dystrophy, Animal
_xgenetics
650 0 4 _aPoint Mutation
700 1 _aSavchuk, V I
700 1 _aSitnikov, V F
700 1 _aKrivov, L I
700 1 _aKuznetsov, A B
700 1 _aVoevodin, D A
700 1 _aYarygin, V N
700 1 _aSukhikh, G T
773 0 _tBulletin of experimental biology and medicine
_gvol. 138
_gno. 4
_gp. 425-8
856 4 0 _uhttps://doi.org/10.1007/s10517-005-0060-5
_zAvailable from publisher's website
999 _c15344587
_d15344587