Chapter 3: Visual Anatomy and Physiology – Flashcards
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NUCLEAR PORES
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PASSAGEWAYS THAT PERMIT CHEMICAL COMMUNICATION BETWEEN THE NUCLEUS AND THE CYTOSOL
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NUCLEOPLASM
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FLUID, GEL-LIKE SUBSTANCE OF THE NUCLEUS
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NUCLEOLI
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TRANSCIENT NUCLEAR ORGANELLES THAT SYNTHESIZE RIBOSOMAL RNA
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CHOLESTROL
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STIFFENS PLASMA MEMBRANE, MAKES IT LESS FLUID AND PERMEABLE
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AMPHIPATHIC
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HAS BOTH HYDROPHOBIC AND HYDROPHILIC PORTIONS
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ANCHORING PROTEINS
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ATTACH THE PLASMA MEMBRANE TO OTHER STRUCTURES AND STABILIZE ITS POSITION
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RECOGNITION PROTEINS
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DETECTED BY CELLS OF THE IMMUNE SYSTEM
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ENZYMES
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PLASMA MEMBRANES MAY BE INTEGRAL OR PERIPHERAL PROTEINS
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RECEPTOR PROTEINS
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BIND TO SPECIFIC EXTRACELLULAR MOLECULES
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LIGANDS
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ANYTHING FROM A SMALL ION LIKE CALCIUM TO A RELATIVELY LARGE AND COMPLEX HORMONE
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CARRIER PROTEINS
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BIND SOLUTES AND TRANSPORT THEM ACROSS THE PLASMA MEMBRANE
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CHANNELS
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INTEGRAL PROTEINS CONTAINING A CENTRAL PORE THAT FORMS A PASSAGEWAY COMPLETELY THROUGH THE PLASMA MEMBRANE
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MICROVILLI
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FINGER SHAPED EXTENSIONS OF THE PLASMA MEMBRANES THAT INCREASE SURFACE AREA TO FACILITATE ABSORPTION OF EXTRACELLULAR MATERIALS
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MICROFILAMENTS
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THE SMALLEST OF THE CYTOSKELETAL ELEMENTS
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ACTIN
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THE PROTEIN THAT MAKES UP MICROFILAMENTS
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TERMINAL WEB
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LAYER OF MICROFILAMENTS JUST INSIDE THE PLASMA MEMBRANE AT THE EXPOSED SURFACE OF A CELL
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INTERMEDIATE FILAMENTS
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LARGEST COMPONENTS OF THE CYTOSKELETON, EXTEND FROM THE CENTROSOME
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CENTRIOLES
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ORGANIZE MICROTUBULES IN THE SPINDLE TO MOVE CHROMOSOMES DURING CELL DIVISION
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CILIA
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PROPEL FLUIDS OR SOLIDS ACROSS CELL SURFACE AND CAN DETECT ENVIRONMENTAL STIMULI
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FLAGELLA
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PROPELS SPERM
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SMOOTH ENDOPLASMIC RETICULUM
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LACKS RIBOSOMES, TUBULAR CISTERNAE
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ROUGH ENDOPLASMIC RETICULUM
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WHERE MANY NEWLY SYNTHESIZED PROTEINS ARE CHEMICALLY MODIFIED AND PACKAGED FOR THE GOLGI APPARATUS
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MEMBRANE RENEWAL VESICLES
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ADD TO THE SURFACE AREA OF THE PLASMA MEMBRANE
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SECRETORY VESICLES
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CONTAIN PRODUCTS THAT WILL BE DISCHARGED FROM THE CELL BY EXOCYTOSIS
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EXOCYTOSIS
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PROCESS WHERE VESICLES FUSE WITH THE PLASMA MEMBRANE AND EMPTY THEIR CONTENTS INTO THE EXTRACELLULAR ENVIRONMENT
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LYSOSOMES
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SPECIAL VESICLES THAT PROVIDE AN ISOLATED ENVIRONMENT FOR POTENTIALLY DANGEROUS CHEMICAL REACTIONS
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TRANS FACE
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"SHIPPING" SIDE WHICH IS USUALLY ORIENTED TOWARD THE FREE SURFACE
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TRANSPORT VESICLES
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DELIVER PROTEINS FROM THE ENDOPLASMIC RETICULUM TO THE GOLGI APPARATUS
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CIS FACE
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"RECEIVING SIDE"
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MEMBRANE FLOW
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CONTINUOUS MOVEMENT AND EXHANGE THROUGH MOVEMENT OF VESICLES
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AUTOLYSIS
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DIGESTIVE ENZYMES BECOME ACTIVE AND THEN ATTACK THE CYTOPLASM IN A DESTRUCTIVE PROCESS
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CRISTAE
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FOLDS IN THE INNER MEMBRANE
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MATRIX
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LIQUID ENCLOSED BY THE INNER MEMBRANE
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GLYCOLYSIS
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GLUCOSE MOLECULE IS BROKEN INTO TWO MOLECULES OF PYRUVATE
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CITRIC ACID CYCLE
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ENZYMATIC PATHWAY THAT SYSTEMATICALLY BREAKS DOWN THE ABSORBED PYRUVATE REMNANT INTO CARBON DIOXIDE AND HYDROGEN ATOMS
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AEROBIC METABOLISM
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ATP PRODUCTION IN MITOCHONDRIA USING OXYGEN
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PERINUCLEAR SPACE
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SEPARATES THE TWO LAYERS OF THE NUCLEAR ENVELOPE
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NUCLEAR ENVELOPE
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SURROUNDS THE NUCLEUS AND SEPARATES IT FROM THE CYTOPLASM
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HISTONES
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PROTEINS THAT MAKE UP NUCLEOLI
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NUCLEOSOMES
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WHEN THE COILS WRAP AROUND HISTONE MOLECULES AND FORM COMPLEX STRUCTURES
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CHROMATIN
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LOOSELY COILED TANGLE OF FINE FILAMENTS THAT FORM WHEN CELLS ARE NOT DIVIDING
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CHROMOSOMES
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STRUCTURES THAT FORM AT THE BEGINNING OF CELL DIVISION WHEN DNA COILING BECOMES TIGHTER
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CENTROMERE
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LOCATION WHERE TWO COPIES OF EACH CHROMOSOME ARE HELD TOGETHER
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GENETIC CODE
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THE CHEMICAL "LANGUAGE" THE CELL USES
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Gene Expression
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Transcription: long terms storage in DNA transcribed into similar elements in RNA Translation: -translating RNA from nucleic acids to amino acids DNA->RNA-> Protein. Protein is the product of gene expression
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GENE
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THE FUNCTIONAL UNIT OF HEREDITY
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TRIPLET CODE
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ANOTHER NAME FOR A GENETIC CODE
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THE CELL THEORY
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CELLS ARE THE BUILDING BLOCKS OF LIFE, NEW CELLS COME FROM DIVISION, THEY ARE THE SMALLEST STRUCTURAL UNITS THAT CARRY OUT ALL VITAL PHYSIOLOGICAL FUNCTIONS
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DIFFERENTION
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THE PROCESS OF GRADUAL SPECIALIZATION
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EXTRACELLULAR FLUID
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WATERY MEDIUM THAT SURROUNDS OUR BODY CELLS
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INTERSTITIAL FLUID
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EXTRACELLULAR FLUID FOUND IN MOST TISSUES
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CYTOPLASM
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MATERIAL LOCATED BETWEEN THE PLASMA MEMBRANE AND THE MEMBRANE SURROUNDING THE NUCLEUS
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CYTOSOL
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FLUID COMPONENT OF CYTOPLASM
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INTRACELLULAR FLUID
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MAY CONTAIN INSOLUBLE MATERIALS, ANOTHER NAME FOR THE CYTOSOL
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ORGANELLES
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INTRACELLULAR STRUCTURES SUSPENDED WITHIN THE CYTOSOL WITH SPECIFIC FUNCTIONS
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NONMEMBRANOUS ORGANELLES
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ALL COMPONENTS ARE IN DIRECT CONTACT WITH THE CYTOSOL
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PEROXISOME
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VESICLES CONTAINING DEGRADATIVE ENZYMES THAT BREAK DOWN ORGANIC COMPOUNDS AND NEUTRALIZES TOXIC COMPOUNDS
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LYSOSOME
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VESICLES CONTAINING DIGESTIVE ENZYMES THAT BREAK DOWN ORGANIC COMPOUNDS AND DAMAGED ORGANELLES
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GOLGI APPARATUS
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STACKS OF FLATTENED MEMBRANES CONTAINING CHAMBERS THAT STORE, ALTER, AND PACKAGE SYNTHESIZED PRODUCTS
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NUCLEUS
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A FLUID NUCLEOPLASM CONTAINING ENZYMES, PROTEINS, DNA, AND NUCLEOTIDES SURROUNDED BY A DOUBLE MEMBRANE THAT CONTROLS METABOLISM, STORES AND PROCESSES GENETIC INFORMATION, CONTROLS PROTEIN SYNTHESIS
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ENDOPLASMIC RETICULUM
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NETWORK OF MEMBRANOUS SHEETS AND CHANNELS EXTENDING THROUGHOUT THE CYTOPLASM THAT FACILITATES THE SYNTHESIS OF SECRETORY PRODUCTS; INTRACELLULAR STORAGE AND TRANSPORT; DETOXIFICATION OF DRUGS OR TOXIN
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RIBOSOMES
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RNA AND PROTEINS, FIXED RIBOSOMES BOUND TO ROUGH ENDOPLASMIC RETICULUM, FREE RIBOSOMES SCATTERED IN CYTOPLASM AND SYNTHESIZES PROTEINS
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MITOCHONDRION
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ENCLOSES IMPORTANT METABOLIC ENZYMES AND PRODUCES 95% OF ATP
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CYTOSKELETON
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ORGANIZING CENTER LOCATED AT THE CENTROSOME THAT STRENGTHENS AND SUPPORTS CELL, AIDS IN MOVEMENT OF CELLULAR STRUCTURES AND MATERIALS
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PLASMA MEMBRANE
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PHYSICAL BARRIER THAT SEPARATES THE INSIDE OF THE CELL FROM THE SURROUNDING EXTRACELLULAR FLUID
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GLYCOCALYX
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A LAYER FORMED BY A SUPERFICIAL MEMBRANE OF CARBOHYDRATES
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INTEGRAL PROTEINS
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PART OF THE MEMBRANE STRUCTURE AND CAN NOT BE REMOVED
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TRANSMEMBRANE PROTEINS
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WHEN INTEGRAL PROTEINS SPAN THE WIDTH OF THE MEMBRANE ONE OR MORE TIMES
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PERIPHERAL PROTEINS
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BOUND TO THE INNER OR OUTER SURFACE OF THE MEMBRANE
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PHOSPHOLIPID BILAYER
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PLASMA MEMBRANE DIFFERENT PHOSPHOLIPID MOLECULES IN IT FORM TWO LAYERS
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SEROUS MEMBRANE
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COVERS VISCERA AND LINES THE TRUE BODY CAVITIES OF THE TRUNK
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CONTROL SEGMENT
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THE FIRST SEGMENT OF A GENE
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TEMPLATE STRAND
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DNA STRAND THAT WILL BE USED TO SYNTHESIZE RNA
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Triplet Code DNA
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-AT- Lt. Dan was AT the -CG- coast guard
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Codons=
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RNA!! Triplets= DNA tRNA- carrying amino acid with it
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RNA POLYMERASE
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BINDS TO THE EXPOSED CONTROL SEGMENT AND, USING TRIPLETS AS A GUIDE, ASSEMBLES A STRAND OF mRNA
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IMMATURE mRNA
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THE mRNA STRAND ASSEMBLED DURING TRANSCRIPTION MUST BE EDITED BEFORE IT LEAVES THE NUCLEUS
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EXONS
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THE REMAINING CODING SEGMENTS IN RNA PROCESSING
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INTRONS
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SNIPPED OUT DURING RNA PROCESSING
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INITIATION
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PHASE OF TRANSLATION BEGINS WHEN mRNA STRAND BINDS TO A SMALL RIBOSOMAL SUBUNIT NEAR THE P SITE
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INITIATION COMPLEX
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WHEN THE SMALL AND LARGE RIBOSOMAL SUBUNITS INTERLOCK AROUND THE mRNA STRAND, FORMING A FUNCTIONAL RIBOSOME
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ELONGATION
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AMINO ACIDS ARE ADDED ONE BY ONE TO THE GROWING POLYPEPTIDE CHAIN
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TERMINATION
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OCCURS AS A PROTEIN RELEASING FACTOR, NOT A tRNA MOLECULE, RECOGNIZES THE STOP CODON
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DIFFUSION
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THE NET MOVEMENT OF A SUBSTANCE FROM AN AREA OF HIGHER CONCENTRATION TO AN AREA OF LOWER CONCENTRATION -all gasses move in the body by simple diffusion. only. -all diffusion is passive, even facilitated -"with its concentration gradient"= movement from an area of high concentration to ares of low concentration -"against its gradient"= opposite
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membrane channel proteins
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what water, small water soluble molecules, and ions diffuse through
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CONCENTRATION GRADIENT
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THE DIFFERENCE BETWEEN HIGH AND LOW CONCENTRATIONS
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Factors that influence diffusion rates
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-distance (shorter the distance_ -molecule or ion size (small diffuse faster) -temperature (higher the temperature-faster) -concentration gradient (steeper the concentration gradient- faster) -electrical forces (opposites attract)
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OSMOSIS
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THE DIFFUSION OF WATER ACROSS A SELECTIVELY PERMEABLE MEMBRANE- i.e. the solvent, not a solute -movement of water instead of solute to main similar overall solute concentrations between the cytosol and extracellular fluid
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OSMOTIC FLOW
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THE MOVEMENT OF WATER DRIVEN BY OSMOSIS The greater the initial difference in solute concentrations- stronger the osmotic flow
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OSMOTIC PRESSURE
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INDICATION OF THE FORCE WITH WHICH PURE WATER MOVES INTO A SOLUTION -indication od physical force of net water movement into a solution with higher solute concentration
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HYDROSTATIC PRESSURE
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THE RESULT OF PUSHING AGAINST A FLUID -measue how much physical pressure by applying force
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OSMOLARITY/OSMOTIC CONCENTRATION
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THE TOTAL SOLUTE CONCENTRATION IN AN AQUEOUS SOLUTION
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TONICITY
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SAME AS OSMOLARITY EXCEPT DESCRIbES HOW A SOLUTION AFFECTS A CELL. Has 3 types. -"how much stuff is dissolved" how much pull does that generate? -we always compare the fluid outside a cell to what is inside a cell. therefore, the solution is iso, hypo, or hyper tonic compared to a normal cell -word is describing the solution...not the cell
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ISOTONIC
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A SOLUTION THAT DOES NOT CAUSE AN OSMOTIC FLOW OF WATER INTO OR OUT OF A CELL.
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HYPOTONIC
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A SOLUTION THAT CAUSES OSMOTIC WATER FLOW INTO A CELL i.e.- hemolysis- when red blood cells swell up so much that they burst -"low amount of studs in water" low pull
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HARAMBE
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AN INSIDE JOB
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HEMOLYSIS
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WHEN A CELL BURSTS AND RELEASES ITS CONTENTS
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HYPERTONIC
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FORCES WATER OUT OF A CELL causes crenation
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CRENATION
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THE SHRINKING OF RED BLOOD CELLS
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NORMAL SALINE
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.9% SOLUTION OF SODIUM CHLORIDE .9% g/dL of NaCL -isotonic with blood -too much salt=hypertonic
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Carrier Proteins
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what nutrients that are insoluble in lipids and too large to fit through membrane channels must pass through
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COTRANSPORT
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WHEN CARRIER PROTEINS SIMULTANEOUSLY MOVE MORE THAN ONE SUBSTANCE IN ONE DIRECTION
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COUNTERTRANSPORT
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SIMULTANEOUSLY MOVES TWO SUBSTANCES IN OPPOSITE DIRECTIONS. Carrier protein is called an exchange pump.
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EXCHANGE PUMP
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WHAT CARRIER PROTEINS ARE REFERRED AS DURING COUNTERTRANSPORT
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FACILITATED DIFFUSION
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PROCESS WHERE SUBSTANCES ARE PASSIVELY TRANSPORTED ACROSS THE PLASMA MEMBRANE- no ATP is required -shape of the protein changes -all diffusion= passive -movement rate limited by number of available carrier proteins (=can become saturated)
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ACTIVE TRANSPORT
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ATP PROVIDES THE ENERGY NEEDED TO MOVE IONS OR MOLECULES ACROSS THE PLASMA MEMBRANE- non dependent on (& against) concentration gradient ION PUMPS- (Na, K, Ca, Mg) -sodium potassium pump pumps k in<--- pumpkin -primary active transport- because it uses ATP to change its shape -sodium ion concentration is high in extracellular -potassium is low in extracellular.
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Sodium-potassium ATPase
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the pump that the sodium and potassium concentration differences creates
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SECONDARY ACTIVE TRANSPORT
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DOES NOT REQUIRE ENERGY FROM ATP, BUT OFTEN NEEDS TO EXPEND IT LATER TO PRESERVE HOMEOSTASIS -since sodium is being taken in, Active transport is required to get sodium back out. "costs" about one ATP for every 3 glucose molecules it transports into the cell -sodium concentration to go up in the cell so the active transporter needs to pump sodium out -WHere the individual transport mechanism under consideration does not itself lyse ATP, but the overall process requires ATP usage on a linked process does
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VESICULAR TRANSPORT
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MATERIALS MOVE INTO AND OUT OF CELLS VIA VESICLES -small membranous sacs that form at, or fuse with, the plasma membrane
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RECEPTOR- MEDIATED ENDOCYTOSIS
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SMALL VESICLES FORM AT THE PLASMA MEMBRANE SURFACE containing a specific target molecule
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Process of Receptor-meditated endocytosis
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- the specific target molecules=ligands - a clathrin coated vesicle forms from this (proteins are recycled back to membrane) - lysosome fuses with endosome allowing ligands to enter cytoplasm by diffusion or active transport -endosome membrane detaches from the secondary lysosome and goes back up to the cell surface
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ENDOCYTOSIS
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THE IMPORTING OF EXTRACELLULAR SUBSTANCES THROUGH THE FORMATION OF VESICLES AT THE CELL SURFACE -active process!!
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ENDOSOMES
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THE VESICLES THAT FORM DURING ENDOCYTOSIS
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PINOCYTOSIS
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FORMATION OF ENDOSOMES FILLED WITH EXTRACELLULAR FLUID -not very selective because it doesn't involve ligands. sometimes it produces vesicles that are on one side of the cell that are discharged on the other -still forms deep groves that pinch off and enter the cytoplasm
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PSEUDOPODIA
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CYTOPLASMIC EXTENSIONS THAT BEGIN PHAGOCYTOSIS -forms to fuse a phagosome -vessicle fuses with lysosomes -nutrients diffuse into cytoplasm -residue is ejected from the cel; through exocytosis
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PHAGOCYTOSIS
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"CELL EATING" produces phagosomes
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PHAGOSOMES
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PRODUCED DURING PHAGOCYTOSIS -contain solid objects that may be as large as the cell itself
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Phagocytes/microphages
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-only specialized cells perform phagocytosis
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EXOCYTOSIS
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A VESICLE FORMED INSIDE THE CELL FUSES WITH, AND BECOMES PART OF, THE PLASMA MEMBRANE -may be waste products (lysosomal products) -or secretory products (mucins or hormones) -active process because it requires ATP
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Cell division
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- a form of cellular reproduction that makes transformation happen
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APOPTOSIS
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GENETICALLY CONTROLLED CELL DEATH -cells can last hours or decades. they age and get old or they contain "suicide genes ^^^"
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DAUGHTER CELLS
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PRODUCED BY THE DIVISION OF A SINGLE CELL produced by mitosis (contain a set of 46 chromosomes) -before they divide and reproduce, they themselves grow to the size of the original cell
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Meiosis
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-produces sex cells (sperm or oocytes) which contain only 23 chromosomes -sexual reproduction
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INTERPHASE
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THE PERIOD IN WHICH THE CELL IS PERFORMING NORMAL FUNCTIONS AND NOT ACTIVELY ENGAGED IN CELL DIVISION -preparing to divide by duplicating chromosomes and synthesizing proteins -doing normal cell business
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CYTOKINESIS
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THE DIVISION OF THE CYTOPLASM, WHICH PHYSICALLY SEPARATES THE TWO DAUGHTER CELLS- end of cell division -begins with the formation of a cleave furrow during anaphase and continues throughout telophase
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SOMATIC CELLS
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BODY CELLS- spends most of their time in interphase
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g1 phase
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-cell that are ready to divide enter this phase -starts producing and replicating all of the organelles and proteins -If not preforming its usual function it could take 8-12 hours. if it is preforming usual function, the process could go on for months -
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S phase
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-6-8 hours -DNA replication and synthesis of histones -DNA polymerase- adds nucleotides to make continuous copy of upper DNA strand - DNA Polymrease- adds nucleotides to make complementary copy of lower DNA strand -DNA helices- enzymes undoing strands of DNA
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G2 Phase
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-2-5 hours -dedicated to protein synthesis and centriole replication -pretty much ready to divide, but not quite yet
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M Phase
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-mitosis and cytokinesesis
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G0 phase
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-when cells are just preforming regular functions -skeletal (muscle cells) and neuron cells mostly just stay in this phase -cells that are not going to divide -muscle cells get bigger when you work out
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DNA Replcation
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-begins with DNA HELICASE enzymes disrupt hydrogen bonds between the bonds
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DNA polymerase
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-binds to the exposed nitrogenous bases promoting bonding between the nitrogenous bases of the DNA and Complementary DNA nucleotides -can only work in one direction -binds to the upper leading strand template and adds nucleotides to make a single, continuous complementary copay called the LEADING STRAND which grows toward the zipper
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2nd DNA polymerase
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-binds to the point of unzipping and assemble a complementary copy that goes until it bumps into the first segment created by the first DNA polymerase
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DNA ligases
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-enzymes that space together the two DNA segments into a strand called the lagging strand
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STEM CELLS
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DIVIDE REPEATEDLY WITH VERY BRIEF INTERPHASE PERIODS -purpose is to divide
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MITOSIS
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DUPLICATED CHROMOSOMES OF A CELL SEPARATE AND MIGRATE INTO TWO IDENTICAL NUCLEI -purposes= growth, replacement, repair - when you defecate- your gut is shedding lining so you need to make more cells -general process of becoming two cells (cell division)
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Cell cycle
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- takes about 22-24 hours for dividing human cells
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THE FOUR STAGES OF MITOSIS
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PROPHASE, METAPHASE, ANAPHASE, AND TELOPHASE
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PROPHASE
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CHROMOSOMES COIL SO TIGHTLY THAT THEY BECOME VISIBLE AS INDIVIDUAL STRUCTURES
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CHROMATID
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COPIES OF A CHROMOSOME- paired chromatids are connected at a region known as the centromere
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KINETOCHORE
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A RAISED REGION ON THE CENTROMERE WHERE THE SPINDLE FIBERS ATTACH TO THE CHROMATIDS
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ASTRAL RAYS
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MICROTUBULES THAT EXTEND INTO THE CYTOPLASM
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SPINDLE FIBERS
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MICROTUBULES THAT FORM BETWEEN CENTRIOLE PAIRS
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METAPHASE
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CHROMATIDS MOVE TO A NARROW CENTRAL ZONE AND ENDS WHEN ALL THE CHROMATIDS ARE ALIGNED IN THE PLANE OF THE METAPHASE PLATE
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ANAPHASE
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WHEN THE CENTROMERE OF EACH CHROMATID PAIR SPLITS AND THE CHROMATIDS SEPARATE -pulled along the spindle fibers
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Spindle Apparatus
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-two chromatids are now pulled apart by this -Anapahse ends when the chromatids arrive near the centrioles at opposite ends of the cell
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TELOPHASE
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CELL PREPARES TO RETURN TO INTERPHASE, THE NUCLEAR ENVELOPES RE-FORM, THE NUCLEI ENLARGE, AND THE CHROMOSOMES GRADUALLY UNCOIL TOO THE CHROMATIN STATE. LAST PHASE OF MITOSIS
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CLEAVAGE FURROW
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FORMS WHEN THE CYTOPLASM CONSTRICTS ALONG THE PLANE OF THE METAPHASE PLATE
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CANCER
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AN ILLNESS CHARACTERIZED BY MUTATIONS THAT DISRUPT NORMAL CONTROL MECHANISMS THAT REGULATE THE RATES OF CELL DIVISION
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TUMOR/NEOPLASM
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A MASS OR SWELLING PRODUCED BY ABNORMAL CELL GROWTH AND DIVISION
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BENIGN TUMOR
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CELLS REMAIN WITHIN THE ORIGINATING TISSUE- can be removed by surgery
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INVASION
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WHEN A TUMOR IS NO LONGER GROWING AS AN ISOLATED MASS OF CELLS AND BEGINS MIGRATING INTO SURROUNDING TISSUES
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MALIGNANT TUMOR
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CELLS DIVIDE RAPIDLY AND RELEASE CHEMICALS THAT STIMULATE THE GROWTH OF BLOOD VESSELS
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ANGEIOGENESIS
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THE GROWTH OF BLOOD VESSELS
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METASTASIS
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MALIGNANT CELLS MIGRATE INTO NEARBY BLOOD VESSELS AND TISSUES AND CAN PRODUCE SECONDARY TUMORS IS TISSUES REMOTE FROM THE PRIMARY SITE
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Where do cancer cells get their energy from
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-from healthy tissues, competing with normal cells for space and nutrients
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RNA
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-single stranded -uses codons -uces Uracial instead of
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rRNA, mRNA, tRNA
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rRNA- ribosomal rna mRNA- carries the genetic information tRNA- carries proteins
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translation
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-happens in the cytoplasm plasm "quam ribosome, mRNA pattern is translated - produces a typical protein in about 20 sec -mRNA can interact with multiple ribosomes simultaneously and produce multiple copies quickly
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transcription
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-happens in the nucleus