Number of the records: 1
myši inbredné CFTR
SYS d018181 LBL 00000nz--a2200000o--4500 005 20250606214810.1 008 930603|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a B01.050.050.199.520.520.445 065 $a B01.050.150.900.649.313.992.635.505.500.400.445 066 $a 01 $c 03 150 $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 $2 slo 450 $w v $a myši inbrídované CFTR $2 slo 450 $w v $a myši inbredné, s inaktivovaným génom cystic fibrosis transmembrane conductance regulator $2 slo 450 $w v $a myši inbrídované, s inaktivovaným génom cystic fibrosis transmembrane conductance regulator $2 slo 550 $7 sllk_us_auth*d003550 $Y Cystic Fibrosis $w b $a fibróza cystická 665 $a 94 $2 eng 665 $a Mice (1992-1993) $2 eng 680 9-
$i 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. $2 eng 680 $a NIM with no qualifiers when experimental animal $2 eng 750 -2
$a Mice, Inbred CFTR $2 eng 980 $x M
Number of the records: 1