Number of the records: 1
myši SCID
SYS d016513 LBL 00000cz--a2200000o--4500 005 20250606214831.8 008 920103|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 065 $a B01.050.150.900.649.313.992.635.505.500.550.780 066 $a 01 $c 03 150 $a myši SCID $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 SCID-hu Mice $2 eng 450 $w v $a SCID Mice $2 eng 450 $w v $a Severe Combined Immunodeficient Mice $2 eng 450 $w v $a myši, SCID mutanty $2 slo 450 $w v $a myši SCID-hu $2 slo 450 $w v $a myši s ťažkou kombinovanou imunodeficienciou $2 slo 665 $a 92 $2 eng 665 $a Mice, Mutant Strains (1983-1991) $2 eng 680 9-
$i Mice homozygous for the mutant autosomal recessive gene scid which is located on the centromeric end of chromosome 16. These mice lack mature, functional lymphocytes and are thus highly susceptible to lethal opportunistic infections if not chronically treated with antibiotics. The lack of B- and T-cell immunity resembles severe combined immunodeficiency (SCID) syndrome in human infants. SCID mice are useful as animal models since they are receptive to implantation of a human immune system producing SCID-human (SCID-hu) hematochimeric mice. $2 eng 680 $a NIM with no qualifiers when experimental animal $2 eng 750 -2
$a Mice, SCID $2 eng 980 $x M
Number of the records: 1