Filter my results
Angelman syndrome is a disorder in humans that causes neurological symptoms such as lack of speech, jerky movements, and insomnia. A human cell has…
Angelman syndromeGenomic imprintingHuman chromosome 15--AbnormalitiesHuman chromosome 15Happy Puppet SyndromeShoukhrat Mitalipov, Masahito Tachibana, and their team of researchers replaced the mitochondrial genes of primate embryonic stem cells via spindle…
monkeysrhesus macaqueSendai virusEmbryonic Stem CellsMitochondrial DiseasesY-chromosomes exist in the body cells of many kinds of male animals.
Y ChromosomeX chromosomeSex ChromosomesChromosomesSex ChromatinEdmund Beecher Wilson contributed to cell biology, the study of cells, in the US during the end of the nineteenth and the beginning of the twentieth…
EmbryologyCellsCytologyHeredityEvolutionKurt Benirschke studied cells, placentas, and endangered species in Germany and the US during the twentieth century. Benirschke was professor at the…
Developmental BiologyGeneticsEndangered SpeciesGene librariesEmbryologyTelomeres are sequences of DNA on the ends of chromosomes that protect chromosomes from sticking to each other or tangling, which could cause…
TelomeraseGreider, Carol W.Wistar Institute of Anatomy and BiologyAgingDNAThe Hayflick Limit is a concept that helps to explain the mechanisms behind cellular aging. The concept states that a normal human cell can only…
CellsCell populationsCell DeathApoptosisCell ProliferationAmong other functions, the Notch signaling pathway forestalls the process of myogenesis in animals. The Notch signaling pathway is a pathway in…
MyogenesisNotch genesNotch ProteinsMusclesMyoblastsBetween 1953 and 1957, before the Meselson-Stahl experiment verified semi-conservative replication of DNA, scientists debated how DNA replicated. In…
ChromosomesCalifornia Institute of TechnologyCold Spring Harbor LaboratoryDNA ReplicationJulia Bell worked in twentieth-century Britain, discovered Fragile X Syndrome, and helped find heritable elements of other developmental and genetic…
Genetic Disordersfetal developmentRubella in pregnancyRubella virusHeredity