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1989: Thomas Cech discovered that RNA can catalyze chemical reactions, [60] making for one of the most important breakthroughs in molecular genetics, because it elucidates the true function of poorly understood segments of DNA. 1989: The human gene that encodes the CFTR protein was sequenced by Francis Collins and Lap-Chee Tsui.
In 1960, Jacob and collaborators discovered the operon which consists of a sequence of genes whose expression is coordinated by operator DNA. [30] In the period 1961 – 1967, through work in several different labs, the nature of the genetic code was determined (e.g. [31]).
This gene produces a testis-determining factor ("TDF"), which initiates testis development in humans and other mammals. The SRY sequence's prominence in sex determination was discovered when the genetics of sex-reversed XX men (i.e. humans who possess biological male-traits but actually have XX allosomes) were studied. After examination, it was ...
Many other genes found on other autosomes, including WT1, SOX9 and SF1 also play a role in gonadal development. [9] Females: Without testosterone and AMH, the mesonephric ducts degenerate and disappear. The paramesonephric ducts develop into the uterus, fallopian tubes, and upper vagina (the lower vagina develops from the urogenital sinus). [9]
Haplodiploidy is found in insects belonging to Hymenoptera, such as ants and bees. Sex determination is controlled by the zygosity of a complementary sex determiner ( csd ) locus. Unfertilized eggs develop into haploid individuals which have a single, hemizygous copy of the csd locus and are therefore males.
Sexual differentiation is the process of development of the sex differences between males and females from an undifferentiated zygote. [1] [2] Sex determination is often distinct from sex differentiation; sex determination is the designation for the development stage towards either male or female, while sex differentiation is the pathway towards the development of the phenotype.
The human genome consists of two copies of each of 23 chromosomes (a total of 46). [1] One set of 23 comes from the mother and one set comes from the father. [1] Of these 23 pairs of chromosomes, 22 are autosomes, and one is a sex chromosome. [1]
Gender-based medicine, also called "gender medicine", is the field of medicine that studies the biological and physiological differences between the human sexes and how that affects differences in disease. Traditionally, medical research has mostly been conducted using the male body as the basis for clinical studies.