Retrovirus, Quiescence and Heterogenous Germ Cells Turnover

Precussor cells in Human in vitro to divide and produce all the differentiated cells. Higher numbers of heterogenous stem cells are considered to be an advantage over, non dividing quiescent cell lines. (THSC 1987) Totipotent precussors an agrigate divide into pluripotent (PHSC) cells endo-, ecto- & mesoderm, able to differentiate and divide into most cell types. Embriologic Trisomy 21 fetus, germ cell tumor markers evaluate the a potential method for deletion in standard testing, respectively in normal pregnancies, for expression of octamer binding (Germ cell neoplasia; OCT3/4; TSPY) oncogens Y+ DNA and the X (Precussor cell cannot survive.) implications of RNA inactivation. Based on fetal tandem repeat varityping and spermatogenesis proliferation from the lower, primary gonocytes that lose the ‘phenotype‘\ Such as HSF6 (heat shock) and sperm cell nucleus differentiation, of cold-impaired recessive mutation ( tcp1-1) is weaker (Microtubule folding stabilization where it occurs in place.) in situ/intratubular neoplasia, and results in the eventual loss of genetic RNA-dependent, DNA retrovirus information. And highly repetitive DNA only active in germ cells pluripotency, differentation into most cell types. Most antibodies (Mab) do not bind to human progenator cells. Embryonic stem cells, having the complete set of all chromosomes, to form embroid bodies expression analysis and genotyping polymorphisms; incubated for primary antibodies. And the regression results in cell turnover.