The existence of a polar definition of a human embryo has been revealed by scientists in a paper published in the journal Nature.
Researchers have now identified a number of genes that can be used to determine the precise age of the human embryo.
The discovery is important as it opens up the possibility of studying human embryos for genetic clues that could be used for the treatment of genetic diseases.
The genes involved in the process were identified as the “biosynaptic” genes, meaning they are expressed in cells of the developing embryo.
They are the ones that allow the embryos to sense its environment and make decisions about whether to continue developing.
The researchers identified about 100 genes that were involved in regulating the timing of the development of these genes.
This allows for the precise timing of each gene to be used as a template to determine an embryo’s age.
In addition to the human genes, another gene that was involved in determining the age of human embryos was also identified.
The scientists identified these genes as the polar gene and it controls the expression of the polar receptor gene.
This gene was originally discovered to be involved in maintaining the integrity of the endometrium and therefore was thought to be the polar definition gene.
However, in recent years it has been discovered that other genes also control the polar receptors and that these genes also play a role in regulating both the polar and the endomechial processes.
The polar gene is also important for the formation of the oocyte and the oocytes themselves.
The researchers say that the genes responsible for controlling the formation and development of oocytes and the embryo are found in the human brain and the somatosensory cortex.
The research team has identified the polar genes as “bioynaptic”, meaning they regulate the expression in cells that express them in the embryo.
This is a common function in the brain and other parts of the body.
The team says that the gene involved in controlling the expression has been previously shown to be active in other cells.
However, this particular gene is very specific for the brain, which means it was not only present in other tissues, but also in cells in the ova itself.
This makes the study a very promising development for the development and development in the field of gene therapies.
The study, published in Nature, found that the polar function of the gene is associated with the formation, differentiation and eventual differentiation of oocyte, which are key components of the embryo and are key to its success in the developing human embryo and its development.
These oocytes are then capable of developing into oocytes with the potential to become functional human beings.
The findings also revealed that the ovarian gene plays a role for oocyte development.
This discovery opens the door to investigating the genetic basis of human diseases and genetic disorders that affect human embryos.
The finding of a gene that controls the polar functions of the embryos is important, said the researchers, who are affiliated to the Hebrew University of Jerusalem.
It opens the doors to studying the genetics of human disease, genetic diseases and diseases of development in human embryos and their potential to be targeted for therapeutic intervention.
The results could have implications for treating genetic diseases, especially in cases where there is a known genetic disease or genetic defect, said Dr. Daniel A. Goldin, a geneticist from the Hebrew U.S. Department of Genetics.
Dr. Goldins team will soon publish a follow-up study that will investigate whether these genes are active in the embryos of other animals and in humans.
