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mendelian genetics
mendelian genetics

... These are carried out to identify if the phenotypically dominant organism is heterozygous or homozygous.  If the dominant organism is homozygous all offspring will show the dominant characteristic.  If the dominant organism is heterozygous 50% of the offspring will show the dominant trait and 50% ...
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...  Affects the mucus-producing glands, digestive enzymes, and sweat glands  Chloride ions are not absorbed into the cells of a person with cystic fibrosis but are excreted in the sweat.  Without sufficient chloride ions in the cells, a thick mucus is secreted. ...
The Genetics of Microcephaly
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... We know that any gene in the total of 20,000 may become damaged. Usually, this does not matter because, just like the chromosomes, genes come in pairs, one inherited from father and the other inherited from mother. When one gene is faulty, the second copy of that gene usually compensates for it. How ...
chapter14_Sections 1
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... Red–Green Color Blindness • Most genes involved in proper function of pigment-containing receptors in the eyes are on the X chromosome • Color blindness includes a range of conditions in which an individual cannot distinguish among some or all colors • Some types of color blindness confuse red and ...
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toxicity in bread wheat - BMC Plant Biology
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... Comparative embryology of the vertebrates shown clearly indicates similarities between the different organisms in the early stages of development. Such similarities suggest an evolutionary relationship between the organisms such that at some point in the history of their development they shared a co ...
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... Mendel’s second law concerns independent inheritance of different traits. We will not examine these experiments in great detail; they are fundamentally not different from the first set of experiments, although more complicated because of the large number of possible outcomes that can be observed whe ...
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... Telomerase is not present in most cells of multicellular organisms. Therefore, the DNA of dividing somatic cells and cultured cells does tend to become shorter. Thus, telomere length may be a limiting factor in the life span of certain tissues and the organism. Telomerase is present in germ-line cel ...
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Gene mapping and medical genetics Human chromosome 8
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... The association of osteopetrosis and renal tubular using somatic cell hybrids.99 Enzyme activity has acidosis has been recognised as a rare recessive been assayed in a variety of patients with chromodisorder.8385 Cerebral calcifications are a feature of some 8 anomalies. These dosage studies showed ...
Jumbo Powerpoint - Warren County Public Schools
Jumbo Powerpoint - Warren County Public Schools

... Improved microscopy techniques, and a better understanding of cellular processes converged with Mendel’s work during the late 1800’s and early 1900’s. It was discovered that Mendelian inheritance has its physical basis in the behavior of chromosomes during sexual life cycles. ...
Unit 05 - Delivery guide
Unit 05 - Delivery guide

... One form of a gene; e.g. tall and dwarf are the alleles for the height of a pea plant. More than two alleles can exist for any specific gene, but only two of them will be found within any individual. ...
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Chromosome



A chromosome (chromo- + -some) is a packaged and organized structure containing most of the DNA of a living organism. It is not usually found on its own, but rather is complexed with many structural proteins called histones as well as associated transcription (copying of genetic sequences) factors and several other macromolecules. Two ""sister"" chromatids (half a chromosome) join together at a protein junction called a centromere. Chromosomes are normally visible under a light microscope only when the cell is undergoing mitosis. Even then, the full chromosome containing both joined sister chromatids becomes visible only during a sequence of mitosis known as metaphase (when chromosomes align together, attached to the mitotic spindle and prepare to divide). This DNA and its associated proteins and macromolecules is collectively known as chromatin, which is further packaged along with its associated molecules into a discrete structure called a nucleosome. Chromatin is present in most cells, with a few exceptions - erythrocytes for example. Occurring only in the nucleus of eukaryotic cells, chromatin composes the vast majority of all DNA, except for a small amount inherited maternally which is found in mitochondria. In prokaryotic cells, chromatin occurs free-floating in cytoplasm, as these cells lack organelles and a defined nucleus. The main information-carrying macromolecule is a single piece of coiled double-stranded DNA, containing many genes, regulatory elements and other noncoding DNA. The DNA-bound macromolecules are proteins, which serve to package the DNA and control its functions. Chromosomes vary widely between different organisms. Some species such as certain bacteria also contain plasmids or other extrachromosomal DNA. These are circular structures in the cytoplasm which contain cellular DNA and play a role in horizontal gene transfer.Compaction of the duplicated chromosomes during cell division (mitosis or meiosis) results either in a four-arm structure (pictured to the right) if the centromere is located in the middle of the chromosome or a two-arm structure if the centromere is located near one of the ends. Chromosomal recombination during meiosis and subsequent sexual reproduction plays a vital role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe and die, or it may unexpectedly evade apoptosis leading to the progression of cancer.In prokaryotes (see nucleoids) and viruses, the DNA is often densely packed and organized. In the case of archaea by homologs to eukaryotic histones, in the case of bacteria by histone-like proteins. Small circular genomes called plasmids are often found in bacteria and also in mitochondria and chloroplasts, reflecting their bacterial origins.
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