Investigation of X-linked histocompatibility may offer an opportunity to find CD and HD minor H haplotype components which are widely separated on the X chromosome. The presence of the HX antigen is detected by placing parental strain grafts onto...
The mouse frizzy (fr) mutation arose on a genetically mixed background and was first described by G.D. Snell of The Jackson Laboratory in 1951. Mice carrying this recessive mutation have curly vibrissae which can be observed as early as one to two...
The mouse frizzy (fr) mutation is a Mendelian recessive trait that affects hair structure and formation in mice. The mutation arose in a mouse of mixed origin at the Jackson Lab (Bar Harbor, ME) in 1951. Frizzy is known to be linked to other genes...
Parental behavior in animals; Rats -- Physiology; Animal mutation
Rats that are hypotrichotic (lacking normal hair) due to the autosomal recessive
shorn (shn) mutation showed a low survival rate in brother by sister matings in a breeding
colony of SU/Csu rats. The majority of rats died before weaning. Subsequent...
The pairing and recombination of homologous regions of the X and Y chromosomes, in an area known as the pseudoautosomal region (PAR), has been a phenomenon of interest since its discovery in 1934. Its presence seems to be limited to eutherian...
The male sterility and histoincompatibility mutant, mshi, results from a recessive mutation that arose spontaneously in the BALB/cBy inbred mouse strain. Using a 402-member BALB/cBy-mshi/mshi (BALB/cBy-mshi C57BL/6J) F1 backcross panel, the...
