The nucleotidic sequences of the primers allowing the amplification of mPins and Cyclophilin cDNA fragments are showh in the four upper panels of the table; whereas the oligonuclodidic squences of the 60 mer probes used for isotopic in situ hybridizatiuon experiments are shown in the three lower panels of the table. The first 60 mer oligoprobe corresponds to the antisense probe recognizing the mPins mRNA, The second mer oligoprobe corresponds to the sense probe which serves as a negative control. It does not recognize any mRNA. The Scramble probe serves also as a control probe providing a further garantee of the specificity of our in situ hybridization protocol.