Počet záznamov: 1
myši SCID
SYS d016513 LBL 00000cx--j22000003--45-- 005 20240119200136.3 100 $a 19920103csloy0103----ba0 152 $b mesh 250 $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 $8 slo 300 1-
$a 92 $8 eng 300 1-
$a Mice, Mutant Strains (1983-1991) $8 eng 330 1-
$a 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. $8 eng 450 $a SCID Mice $5 e $8 eng 450 $a SCID-hu Mice $5 e $8 eng 450 $a Severe Combined Immunodeficient Mice $5 e $8 eng 450 $a myši, SCID mutanty $5 e $8 slo 450 $a myši SCID-hu $5 e $8 slo 450 $a myši s ťažkou kombinovanou imunodeficienciou $5 e $8 slo 686 $a B01.050.150.900.649.313.992.635.505.500.550.780 750 $a Mice, SCID $8 eng 801 -0
$a US $b DNLM $c 19920103 801 -2
$a SK $b BA006 $c 20011018 820 $a NIM with no qualifiers when experimental animal $8 eng 980 $x M
Počet záznamov: 1