After becoming chief pathologist at the University of Wisconsin-Madison Wisconsin Regional Primate Center in 1995, James A. Thomson began his pioneering work in deriving embryonic stem cells from isolated embryos. That same year, Thomson published his first paper, "Isolation of a Primate Embryonic Stem Cell Line," in Proceedings of the National Academy of Sciences of the United States of America, detailing the first derivation of primate embryonic stem cells. In the following years, Thomson and his team of scientists - Joseph Itskovitz-Eldor, Sander S. Shapiro, Michelle A. Waknitz, Jennifer J. Swiergiel, Vivienne S. Marshall, and Jeffry M. Jones - advanced their work with embryonic stem cells, eventually isolating and culturing human embryonic stem cells. Their work with human embryos was reported in the 1998 Nature article "Embryonic Stem Cell Lines Derived from Human Blastocysts."

Jacques Loeb broadened and corrected his earlier claims concerning artificial parthenogenesis in sea urchins in a series of experiments in 1900. He published these findings, "Further Experiments on Artificial Parthenogenesis and the Nature of The Process of Fertilization," in a 1900 issue of The American Journal of Physiology. His new results amended those from earlier experiments he summarized in 1899's "On the Nature of the Process of Fertilization and the Artificial Production of Norma Larvae (Plutei) from the Unfertilized Eggs of the Sea Urchin." Loeb's 1899 results were tainted by improperly prepared salts used in his experiments. Loeb's 1900 results corrected those of 1899 and led to more refined study of artificial parthenogenesis, the human-caused development of unfertilized eggs.

In "The Outgrowth of the Nerve Fiber as a Mode of Protoplasmic Movement," Ross Granville Harrison explores the growth of nerve fibers in vitro. The purpose of this experiment was to test two possible hypotheses for the growth of nerve fibers. Santiago Ramón y Cajal suggested that nerve growth is due to the extension of nerve fibers as they push through tissue. Victor Hensen's syncytial theory proposed an opposing view of nerve growth. He proposed that each neuron was connected by threads of cytoplasm and the successful connections stimulated further differentiation of the correct neural connections. Using hanging drop tissue cultures, Harrison provided significant evidence for Ramón y Cajal's theory by showing discrete cell membranes between cells and observing the growth of individual neurons.

Jacques Loeb showed that scientists could achieve artificial parthenogenesis with some types of annelid worm eggs through a series of experiments in 1900. Loeb published the results of his experiments in 1901 as "Experiments on Artificial Parthenogenesis in Annelids (Chaetopterus) and the Nature of the Process of Fertilization," in The American Journal of Physiology. Loeb 's results broadened the range of animals to which artificial parthenogenesis applied beyond sea urchins. Scientists could now also cause artificial parthenogenesis with the eggs of Chaetopterus, a segmented marine worm.

From 1987 to the late 1990s, James Haddow and his team of researchers at the Foundation for Blood Research in Scarborough, Maine, studied children born to women who had thyroid deficiencies while pregnant with those children. Haddow's team focused the study on newborns who had normal thyroid function at the time of neonatal screening. They tested the intelligence quotient, or IQ, of the children, ages eight to eleven years, and found that all of the children born to thyroid-hormone deficient mothers performed less well than the control group. Haddow and his colleagues published the experiment and results, Maternal Thyroid Deficiency during Pregnancy and Subsequent Neuropsychological Development of the Childin 1999. Haddow and his team proposed that undetected low thyroid hormone production in mothers, or maternal hypothyroidism, could adversely affect the neuropsychological development of children.

In 2008 researchers Daniel Warner and Richard Shine tested the Charnov-Bull model by conducting experiments on the Jacky dragon (Amphibolurus muricatus), in Australia. Their results showed that temperature-dependent sex determination(TSD) evolved in this species as an adaptation to fluctuating environmental temperatures. The Charnov-Bull model, proposed by Eric Charnov and James Bull in 1977, described the evolution of TSD, although the model was, for many years, untested. Many reptiles and some fish exhibit non-genetic sex determination, in which an embryos' environment can influence the sex of the adult organism. Environmental conditions such as humidity or population density can alter sex in some organisms, and a widespread form of non-genetic sex determination is temperature-dependent sex determination. TSD reveals how embryonic development can contribute to the evolution of physiological processes. Researchers have documented TSD in a wide range of species, and they continue to investigate how such a sex determining system has evolved.

The HeLa cell line was the first immortal human cell line that George Otto Gey, Margaret Gey, and Mary Kucibek first isolated from Henrietta Lacks and developed at The Johns Hopkins Hospital in Baltimore, Maryland, in 1951. An immortal human cell line is a cluster of cells that continuously multiply on their own outside of the human from which they originated. Scientists use immortal human cell lines in their research to investigate how cells function in humans. Though the HeLa cell line has contributed to many advancements in biomedical research since the twentieth century, its usage in medical research has been controversial because Lacks did not consent to having her cells used for such purposes. As of 2020, scientists continue to use the HeLa cell line for numerous scientific advancements, such as the development of vaccines and the identification of many underlying disease mechanisms.

In 1975 John Gurdon, Ronald Laskey, and O. Raymond Reeves published "Developmental Capacity of Nuclei Transplanted from Keratinized Skin Cells of Adult Frogs," in the Journal of Embryology and Experimental Morphology. Their article was the capstone of a series of experiments performed by Gurdon during his time at Oxford and Cambridge, using the frog species Xenopus laevis. Gurdon's first experiment in 1958 showed that the nuclei of Xenopus cells maintained their ability to direct normal development when transplanted. The goal of Gurdon's experiments was to show that specialized adult cells could maintain the information and capacity to direct normal development. He asked whether cells undergo permanent changes once they become fully specialized. Gurdon, Laskey, and Reeves's publication was important to embryology because it shed light on that very question.

In 'How do Embryos Assess Risk? Vibrational Cues in Predator-Induced Hatching of Red-Eyed Treefrogs' (2005), Karen Warkentin reported on experiments she conducted to see how red-eyed treefrog embryos, Agalychnis callidryas, can distinguish between vibrations due to predator attacks and other environmental occurrences, such as storms. Though the ability of red-eyed treefrogs to alter their hatch timing had been documented, the specific cues that induce early hatching were not well understood. Warkentin's study demonstrated that, based on vibration signals alone, treefrog embryos can determine whether they are under attack from a predator and respond accordingly.

In 1964, authors James Till, Ernest McCulloch, and Louis Siminovitch, published A Stochastic Model of Stem Cell Proliferation, Based on The Growth of Spleen Colony-Forming Cells, which discussed possible mechanisms that control stem cell division. The authors wrote the article following their experiments with spleens of irradiated mice to demonstrate the existence of stem cells, had unknown properties. In their previous experiments, Till and McCulloch noticed that many similar-looking colonies of cells formed on the spleens of irradiated mice, but those colonies had a highly variable number of stem cells. They could not explain why some stem cells gave rise to many stem cells while others only gave rise to a few. In the article, the authors propose an explanation for how stem cells divide and renew, and provide both a greater understanding as to how cancerous tissues may arise due to unchecked stem cell division as well how stem cells can aid in cancer therapy.