Počet záznamov: 1
myši inbredné CFTR
SYS d018181 LBL 00000nx--j22000003--45-- 005 20240119200924.3 100 $a 19930603csloy0103----ba0 152 $b mesh 250 $a myši inbredné CFTR $x AB $x AH $x BL $x CF $x CL $x EM $x GD $x GE $x IM $x IN $x ME $x MI $x PH $x PS $x PX $x SU $x UR $x VI $8 slo 300 1-
$a 94 $8 eng 300 1-
$a Mice (1992-1993) $8 eng 330 1-
$a A strain of mice widely studied as a model for cystic fibrosis. These mice are generated from embryonic stem cells in which the CFTR (cystic fibrosis transmembrane conductance regulator) gene is inactivated by gene targeting. As a result, all mice have one copy of this altered gene in all their tissues. Mice homozygous for the disrupted gene exhibit many features common to young cystic fibrosis patients, including failure to thrive, meconium ileus, and alteration of mucous and serous glands. $8 eng 450 $a myši inbrídované CFTR $5 e $8 slo 450 $a myši inbredné, s inaktivovaným génom cystic fibrosis transmembrane conductance regulator $5 e $8 slo 450 $a myši inbrídované, s inaktivovaným génom cystic fibrosis transmembrane conductance regulator $5 e $8 slo 550 $3 sllk_un_auth*d003550 $Y Cystic Fibrosis $5 B $a fibróza cystická 686 $a B01.050.050.199.520.520.445 686 $a B01.050.150.900.649.313.992.635.505.500.400.445 750 $a Mice, Inbred CFTR $8 eng 801 -0
$a US $b DNLM $c 19930603 801 -2
$a SK $b BA006 $c 20010606 820 $a NIM with no qualifiers when experimental animal $8 eng 980 $x M
Počet záznamov: 1