Genetics is a branch of biology concerned with the study of genes, genetic variation, and heredity in living organisms.[1][2][3]
The discoverer of genetics is Gregor Mendel, a late 19th-century scientist and Augustinian friar. Mendel studied "trait inheritance", patterns in the way traits are handed down from parents to offspring. He observed that organisms (pea plants) inherit traits by way of discrete "units of inheritance". This term, still used today, is a somewhat ambiguous definition of what is referred to as a gene.
Trait inheritance and molecular inheritance mechanisms of genes are still primary principles of genetics in the 21st century, but modern genetics has expanded beyond inheritance to studying the function and behavior of genes. Gene structure and function, variation, and distribution are studied within the context of the cell, the organism (e.g. dominance), and within the context of a population. Genetics has given rise to a number of subfields, including epigenetics and population genetics. Organisms studied within the broad field span the domains of life (archaea, bacteria, and eukarya).
Genetic processes work in combination with an organism's environment and experiences to influence development and behavior, often referred to as nature versus nurture. The intracellular or extracellular environment of a cell or organism may switch gene transcription on or off. A classic example is two seeds of genetically identical corn, one placed in a temperate climate and one in an arid climate. While the average height of the two corn stalks may be genetically determined to be equal, the one in the arid climate only grows to half the height of the one in the temperate climate due to lack of water and nutrients in its environment.
Answer:
Amniocentesis is an invasive method that involves the aspiration of 10-20 ml of fetal water through the abdominal wall under ultrasound-guided control. In most cases, the procedure is performed around the 16th week of gestation. The fetal water sample contains fetal cells, mostly cells of fetal skin and the epithelium of the urinary tract.
Chorionic Villus Sampling (CVS) biopsy is performed between weeks 11 and 12 of gestation. During biopsy, with ultrasound guidance, the tissue of the chorionic fossa is aspirated mainly across the abdomen (transabdominal pathway). The biopsy specimen is of fetal origin and belongs to the outer layer of blastocyst cells or the trophoblast (outer layer of the placenta). Very often, the biopsy specimen contains tissue of the decidua (mucous membrane of the uterus) that is of maternal origin, and it is necessary to remove the maternal tissue before any treatment of the sample.
Explanation:
The amniocentesis procedure carries a risk of miscarriage of 0.5-1%. After aspiration of the fruit of the water, the sample is centrifuged to separate the cells from the amniotic fluid. Separate cells are seeded on a nutrient medium (cell culture) that stimulates cell growth. After about 14 days, the cell culture is further used for various genetic or biochemical analyzes such as karyotyping.
The advantage of chorionic biopsy is the amount of biological material, which is sufficient for the whole a number of different laboratory procedures. Also, a great advantage is the timing of the procedure as it allows diagnosis in the first trimester of pregnancy, but the chorionic biopsy procedure itself carries a risk of miscarriage of 1-2%.
Hello, Leah082656. There are many heated arguments over discussing stem cell research because of these two moral principals: the duty to prevent or alleviate suffering and the duty to respect the value of human life. In order to get embryonic stem cells, the embryo has to be destroyed. Although this is a huge controversial problem, by researching this could actually save and treat many other people. Some people are for it because it saves multiple people in the process, and some do not like this because it is killing an embryo. Whatever your stance is on this debate, these are the two sides that people debate over. I hope I helped!! Have a great day. :)
Answer:
Ureteroplasty is surgery to remove the stricture.
Explanation:
Answer: Exons
Explanation:
In eukaryotic cell the primary transcript are very long the contains coding region (exons) and non coding region (introns)
The parts of the gene sequence that are expressed (coding region) in the protein are called exons, because they are expressed, while the parts of the gene sequence that are not expressed in the protein are called introns, because they come in between the exons.
Intron is a portion of a gene that does not code for amino acids. These Intron sequence are cleaved out and exons are spliced (I. E combine together) to form the mature mRNA molecule.
Exons are the mRNA parts that are kept and used to make protein.
