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58 Cards in this Set
- Front
- Back
Disease |
Any deviation from, or interruption of, the normal structure and function of the body |
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Cell degeneration |
Reversible injury to a cell |
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Cell Necrosis |
Irreversible injury to a cell that ultimately results in death, death of cells in living tissue |
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Apoptosis |
Active process whereby cells initiate and progress to death, cell causes its own death |
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Oncosis |
Passive process where cells are unable to maintain homeostasis and thus proceeds to cell death |
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Vascular thrombosis |
Inappropriate clot forms on interior wall of heart or vessel, causes paralysis |
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Acute Inflammation |
Characterized by predominate neutrophils, protein exudate on, redness, heat, swelling, pain, and loss of function. Only lasts a few days. Ex. Pneumonia |
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Chronic Inflammation |
Characterized by macrophages and lymphocytes, proliferation of blood vessels, fibrosis, and tissue necrosis. Lasts days to years building up scar tissue. |
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Neoplasia |
Disease process characterized by cells derived from normal tissues that have undergone heritable genetic changes allowing them to become unresponsive to normal growth controls. Can be benign or malignant. CANCER |
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Hyperplasia |
Increased tissue mass due to increased number of cells, non-neoplastic |
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Hypertrophy |
Increased tissue mass due to increased size of cells, non-neoplastic |
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Atrophy |
Decreased tissue mass due to decreased number and/or size of cells, non-neoplastic |
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Hypoplasia |
Decreased tissue mass due to failure to develop normally, non-neoplastic |
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Central dogma |
DNA - RNA - proteins |
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Exons |
Coding region of a gene on DNA |
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Exons |
Coding region of a gene on DNA |
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Introns |
Non coding regions of the gene, must be spliced out |
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Mitosis |
Copies of each chromosome separate to opposite poles in order for 2 daughter cells to form. Cell replication |
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Mitosis |
Copies of each chromosome separate to opposite poles in order for 2 daughter cells to form. Cell replication |
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G1 phase |
The time between cell replications where the cell is performing normal functions. |
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Mitosis |
The process of somatic cell division resulting in the formation of 2 genetically identical daughter cells |
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G1 phase |
The time between cell replications where the cell is performing normal functions. |
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S phase |
When DNA synthesis produces a precise copy of each chromosome forming two sister chromatids joined at a centromere |
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G2 phase |
A brief time gap between the S phase and mitosis |
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DNA polymerase |
An enzyme that uses each DNA strand as a template to synthesize new strands of DNA |
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Meiosis |
The process of germ cell division resulting in the formation of gametes containing half the number of chromosomes that are present in somatic cells |
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rRNA (ribosomal) |
Various types used along with proteins to assemble ribosomes used in translation of mRNA into protein |
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tRNA (transfer) |
Bring amino acids to the ribosome where they match up with codons of mRNA and add amino acids to the growing polypeptide chain. |
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RNA polymerase |
An enzyme that transcribes DNA to mRNA, #2 transcribes protein coding genes |
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Peptide bonds |
Join amino acids to one another, involve dehydration at the amino-group of one and the carboxyl-group of the other |
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Aminoacyl-tRNA synthetase |
Binds amino acids to tRNA using ATP |
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Synaptonemal Complex |
A protein that pairs chromosomes during meiosis 1 |
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Allele |
One of 2 or more alternative forms of a gene |
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Pseudoautosomal Regions (PAR) |
Regions of the X and Y chromosomes that connect to form the synopsis to link the X and Y chromosomes, may undergo homologous recombination |
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Meiotic Nondisjunction |
Failure of chromosome pairs to separate at meiosis, results in chromosomally abnormal fetuses, more likely to occur in eggs, |
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Mitotic Nondisjunction |
Failure of chromosome pairs to separate at Mitotic division resulting in 2 populations of cells with different karyotypes, usually results in a nonviable fetus, may contribute to cancer if it occurs late in life |
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Nucleotides |
Molecules that make up DNA and RNA, composed of a nitrogenous base, a sugar and a phosphate. Either A,T,G, and C |
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Heterochromatin |
Densely packed DNA that cannot be read |
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Euchromatin |
Loosely packed DNA that can easily be transcribed |
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mRNA (messenger) |
Copied from DNA, nucleotide sequence specifies sequence of amino acids in proteins |
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Epigenetics |
Heritable changes in gene expression that are not cause by changes to the underlying sequence of DNA. A change in phenotype without a change in genotype. Allow for cell differentiation. Caused by DNA methylation or histo me acetylation |
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Histone acetal transferases |
An enzyme that loosens DNA structure by adding acetyl groups to histone tails, allowing transcription to occur |
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Histone acetal transferases |
An enzyme that loosens DNA structure by adding acetyl groups to histone tails, allowing transcription to occur |
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Histone deacetylases |
An enzyme that tightens DNA by removing an acetyl group so the histone a can compact DNA to repress transcription |
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Histone acetal transferases |
An enzyme that loosens DNA structure by adding acetyl groups to histone tails, allowing transcription to occur |
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Histone deacetylases |
An enzyme that tightens DNA by removing an acetyl group so the histone a can compact DNA to repress transcription |
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Histone methyl transferase |
An enzyme that influences chromatin formation and DNA methylation |
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DNA methylation |
The addition of a methyl group to cytosine at G-C junctions of DNA which prevents transcription by attracting proteins that block transcription |
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Proteome |
The normal complement and amount of different proteins in a cell; measure of gene expression |
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Amyloid |
A generic term for aggregates of proteins that become misfiled into the wrong shape allowing many to stick together, lose their function, disrupt normal tissues, play a role iamb neurogenerative disorders such as Alzheimer's |
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Chaperones |
Assist in the correct folding of proteins and prevent misfiled proteins from causing a problem; originally known as heat shock proteins |
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Chaperonins |
Proteins that take up unfolded or misfiled proteins and create an internal environment for proper folding. |
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Proteosomes |
Enzymes that degrade proteins |
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Ubiquitin ligase |
An enzyme that recognizes old or misfiled proteins and marks them with ubiquitin proteins for degrading |
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Autophagosome |
A vesicles that contains damaged or old proteins and organelles that have been marked for destruction. |
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Locus |
Where a gene is on a chromosome, a segment of DNA that occupies a specific location on a specific chromosome |
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Allele |
Alternate versions of DNA sequence at a locus |
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Polymorphism |
A locus that has 2 or more common alleles |