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Student Learning Outcomes - BIO 131 - Google Docs.pdf

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‭Student Learning Outcomes‬ ‭Chapter 1 - MAJOR THEMES OF ANATOMY AND PHYSIOLOGY‬ ‭ ection 1.1‬ S ‭a.‬ ‭define‬‭anatomy‬‭and‬‭physiology‬‭and relate them to each‬‭other;‬ ‭‬ ‭Anatomy = the study of structure (inductive method)‬ ‭‬ ‭Physiology = the study of bodily...

‭Student Learning Outcomes‬ ‭Chapter 1 - MAJOR THEMES OF ANATOMY AND PHYSIOLOGY‬ ‭ ection 1.1‬ S ‭a.‬ ‭define‬‭anatomy‬‭and‬‭physiology‬‭and relate them to each‬‭other;‬ ‭‬ ‭Anatomy = the study of structure (inductive method)‬ ‭‬ ‭Physiology = the study of bodily function (hypothetico - deductive method)‬ ‭‬ ‭Always go in hand in hand: Form → Function‬ ‭b.‬ ‭describe several ways of studying human anatomy; and‬ ‭‬ ‭Observation of surface structure‬ ‭○‬ ‭Cadaver dissection - study the relationships of organs‬ ‭○‬ ‭Comparative anatomy - study more than one species to study the‬ ‭evolutionary trends‬ ‭‬ ‭Observation of external body structure‬ ‭○‬ ‭Physical examination‬ ‭‬ ‭Palpation - feeling the body to exam‬ ‭‬ ‭Auscultation - listening to internal organs (ex: stethoscope)‬ ‭‬ ‭Percussion - tapping w/ hands or small instruments (ex: testing‬ ‭reflex)‬ ‭‬ ‭Gross = see w/ naked eyes‬ ‭‬ ‭Histology = microscopy‬ ‭c.‬ ‭define a few subdisciplines of human physiology.‬ ‭‬ ‭Study of bodily function‬ ‭‬ ‭Comparative histology - other species‬ ‭○‬ ‭Test on animals before on humans for new drugs or medical procedures‬ ‭ ection 1.2‬ S ‭a.‬ ‭describe the contributions of some key people who helped to bring about this‬ ‭transformation. (‬‭Don’t have to know exact years)‬ ‭‬ ‭Anatomy: Andreas Vesalius - perform own dissections‬ ‭‬ ‭Physiology: William Harvey‬‭- experimental physiology‬‭(blood flow in/out of the‬ ‭heart)‬ ‭‬ ‭Maimonides - Jewish rabbi & physician who write 10 medical book‬ ‭‬ ‭Compound light microscope:‬ ‭○‬ ‭Jassen‬‭- discovered 2 lenses (ocular and objective‬‭lens)‬ ‭○‬ ‭Robert Hook -‬‭specimen stage, illuminator, coarse‬‭& fine focus controls‬ ‭‬ ‭Only x30 magnification‬ ‭‬ ‭First to see “animalcules” = cells‬ ‭‬ ‭Published a book about Microscopy‬ ‭ ection 1.3‬ S ‭a.‬ ‭describe the inductive and hypothetico–deductive methods of obtaining‬ ‭scientific knowledge;‬ ‭‬ ‭Francis Bacon & Rene Decartes‬‭→ philosophers that‬‭propose new way to a‬ ‭approach to science - scientific method‬ ‭‬ ‭Inductive method = Anatomy‬ ‭‬ ‭Hypothetico - deductive method = Physiology‬ ‭b.‬ ‭describe some aspects of experimental design that help to ensure objective and‬ ‭reliable results;‬ ‭‬ ‭Tested repeatedly‬ ‭‬ ‭Supported by reliable observations‬ ‭‬ ‭Not falsified by any credible observation‬ ‭‬ ‭Peer review‬ ‭c.‬ ‭explain what is meant by‬‭hypothesis, fact, law,‬‭and‬‭theory‬‭in science.‬ ‭‬ ‭Hypothesis - an educated speculation‬ ‭‬ ‭Fact - verified by any trained person‬ ‭‬ ‭Law - described how matter and energy behave ( from inductive reasoning and‬ ‭repeated observations)‬ ‭‬ ‭Theory - explanatory statement derived from facts, laws, and confirmed‬ ‭hypothesis‬ ‭ ection 1.4‬ S ‭a.‬ ‭explain why evolution is relevant to understanding human form and function;‬ ‭‬ ‭Charles Darwin - Theory of evolution by natural selection‬ ‭‬ ‭Model how species originate and change over time‬ ‭b.‬ ‭define‬‭evolution‬‭and‬‭natural selection;‬ ‭‬ ‭Evolution - change in genetic composition of population of organisms‬ ‭‬ ‭Natural selection - how evolution works, evolve to survive for that specific‬ ‭environment‬ ‭c.‬ d ‭ escribe some human characteristics that can be attributed to the tree-dwelling‬ ‭habits of earlier primates‬‭(‭A ‬ rboreal = treetop)‬ ‭‬ ‭Mobile shoulders - swinging among branches‬ ‭‬ ‭Opposable thumbs and prehensile hands - grab and manipulate objects‬ ‭‬ ‭Forward facing eyes w/ stereoscopic vision - depth perception‬ ‭‬ ‭Color vision - ripe fruit‬ ‭‬ ‭Large brain - memory‬ ‭d.‬ ‭describe some human characteristics that evolved later in connection with upright‬ ‭walking.‬‭Bipedalism‬ ‭‬ ‭Wider pelvis with a shorter, more curved hip joint‬ ‭‬ ‭Pronounced lumbar curve in the lower back‬ ‭‬ ‭Longer legs, a more developed gluteus medius muscle, and a modified knee joint‬ ‭ ection 1.5‬ S ‭a.‬ ‭list the levels of human structure from the most complex to the simplest;‬ ‭Smallest to biggest‬ ‭1.‬ ‭Atoms‬ ‭2.‬ ‭Molecules (Carbohydrates, lipids, proteins & nucleic acids)‬ ‭3.‬ ‭Organelles‬ ‭4.‬ ‭Cells (Smallest living unit)‬ ‭5.‬ ‭Tissues (2 or more type)‬ ‭6.‬ ‭Organs‬ ‭7.‬ ‭Organ systems‬ ‭8.‬ ‭Organisms‬ ‭b.‬ ‭discuss the clinical significance of anatomical variation among humans.‬ ‭‬ ‭different from theory but still function normally‬ ‭‬ ‭need to be aware during medical procedures‬ ‭‬ ‭Examples: Horseshoe kidneys, Aorta‬ ‭ ection 1.6‬ S ‭a.‬ ‭state the characteristics that distinguish living organisms from nonliving objects;‬ ‭C.O.R.M.H.E.R.D‬ ‭‬ ‭C‬‭ellular composition‬ ‭‬ ‭O‬‭rganization‬ ‭‬ ‭R‬‭esponsiveness & movement‬ ‭‬ ‭M‭e ‬ tabolism (Anabolism, catabolism & excretion)‬ ‭‬ ‭H‬‭omeostasis‬ ‭‬ ‭E‭v‬ olution‬ ‭‬ ‭R‬‭eproduction‬ ‭‬ ‭D‬‭evelopment‬ ‭b.‬ ‭explain the importance of physiological variation among persons;‬ ‭‬ ‭everyone is different, therefore need to consider the variation so it won't lead to‬ ‭overmedication‬ ‭c.‬ d ‭ efine‬‭homeostasis‬‭and explain why this concept is central to physiology;‬ ‭‬ ‭Claude Bernard - describe homeostasis‬ ‭‬ ‭Walter Cannon - coined “ homeostasis”‬ ‭○‬ ‭Homeostasis - physiological phenomena fluctuate narrowly around a set‬ ‭point by negative feedback, loss of control causes illness or death‬ ‭d.‬ d ‭ efine‬‭negative feedback,‬‭give an example of it, and‬‭explain its importance to‬ ‭homeostasis‬‭; and‬ ‭‬ ‭Negative feedback - reduces an excessive response‬ ‭‬ ‭Examples:‬ ‭○‬ ‭Too cold - thermostat activated - heat output - goes a little above set point‬ ‭- shuts off - room cools down - REPEAT‬ ‭○‬ ‭Thermoregulation‬ ‭‬ ‭Too hot - blood vessels dilate - sweating‬ ‭‬ ‭Too cold - vasoconstriction in the skin - shivering‬ ‭○‬ ‭Low blood pressure - baroreceptors respond to accelerates heartbeat -‬ ‭blood pressure rises to normal‬ ‭e.‬ d ‭ efine‬‭positive feedback‬‭and give examples of its‬‭beneficial and harmful effects;‬‭and‬ ‭‬ ‭Positive feedback - amplify a response‬ ‭‬ ‭Examples:‬ ‭○‬ ‭Oxytocin during childbirth‬ ‭○‬ ‭Fever if doesn’t stop → dangerous‬ ‭f.‬ ‭define‬‭gradients‬‭, describe the variety of gradients‬‭in human physiology, and identify‬ ‭some forms of matter and energy that flow down gradients.‬ ‭‬ G ‭ radient - a difference in chemical concentration, charge, temperature, or‬ ‭pressure between two points‬ ‭○‬ ‭Blood flow down pressure gradient‬ ‭○‬ ‭Glucose or ions flow down concentration or electrical gradient‬ ‭○‬ ‭Heat flow down thermal gradient‬ ‭ ection 1‬‭.‭7 S ‬‬ ‭a.‬ ‭explain why modern anatomical terminology is so heavily based on Greek and Latin‬ ‭‬ ‭Scientific investigation began in Greece and Rome - 90% of words‬ ‭‬ ‭Prefix and suffix can change the core meaning of the word‬ ‭○‬ ‭Root - cardi, my, path‬ ‭○‬ ‭Prefix - epi, hypo‬ ‭○‬ ‭Suffix -ia‬ ‭b.‬ d ‭ escribe the efforts to achieve an internationally uniform anatomical terminology;‬ ‭‬ ‭Prevent people from naming after themselves - Eponym‬ ‭c.‬ d ‭ iscuss why precise spelling is important in anatomy and physiology.‬ ‭‬ ‭Can mean VERY different things‬ ‭○‬ ‭Malleus = middle-ear bone | Malleolus = bony part in ankle‬ ‭○‬ ‭Hip bone = ilium | Small intestine = ileum‬ ‭○‬ ‭Trapezium = bone | trapezius = muscle‬ ‭Chapter 3 - CELLULAR FORM AND FUNCTION‬ ‭Cytology -‬‭study of cells‬ ‭ ection 3.1‬ S ‭a.‬ ‭discuss the development and modern tenets of the cell theory;‬ ‭‬ ‭Organisms are made of cells and their products‬ ‭‬ ‭Cell is the simplest unit of life‬ ‭‬ ‭Cell processes determine organism structure and function‬ ‭‬ ‭All cells arise from existing cells‬ ‭‬ ‭All cells share fundamental similarities in chemical composition and metabolic‬ ‭mechanisms‬ ‭b.‬ ‭describe cell shapes from their descriptive terms -‬‭9‬ ‭c.‬ ‭state the size range of human cells and discuss factors that limit their size;‬ ‭‬ ‭usually ~ 10-15 µm diameter‬ ‭○‬ ‭Egg cell > 100 µm‬ ‭○‬ ‭Neurons > 1 m long‬ ‭‬ S ‭ urface area to volume ratio - cells that are too large can absorb nutrients‬ ‭/remove waste efficiently - like LARGE SA:V ratio‬ ‭d.‬ ‭discuss the way that developments in microscopy have changed our view of cell‬ ‭structure; and‬ ‭‬ ‭Light microscopy (LM)‬ ‭○‬ ‭Light directed through sample‬ ‭○‬ ‭Illuminates material under magnification‬ ‭‬ ‭Transmission electron microscopy (TEM)‬ ‭○‬ ‭Shoots beams of electrons at the sample‬ ‭○‬ ‭Greater resolution at higher magnification‬ e‭.‬ ‭outline the major components of a cell.‬ ‭‬ P ‭ lasma membrane‬ ‭‬ ‭Cytoplasm‬ ‭○‬ ‭Cytoskeleton - hold structure‬ ‭○‬ ‭Organelles‬ ‭○‬ ‭Inclusion (oil, pigment,bacteria or cell debris) - not enclosed by membrane‬ ‭○‬ ‭Cytosol - aqueous fluid of cytoplasm‬ ‭ ection 3.2‬ S ‭a.‬ ‭describe the structure of a plasma membrane;‬ ‭‬ ‭Phospholipids bilayer w/ hydrophilic head facing out and hydrophobic tails facing in‬ ‭b.‬ ‭explain the functions of the lipid, protein, and carbohydrate components of the plasma‬ ‭membrane;‬ ‭Lipids‬ ‭‬ ‭Phospholipids - 75%‬ ‭○‬ ‭Bilayer + keep membrane fluid‬ ‭‬ ‭Cholesterol - 20%‬ ‭○‬ ‭Low concentration - stiffen membrane‬ ‭○‬ ‭High concentration - increase fluidity‬ ‭‬ ‭Glycolipids - 5%‬ ‭○‬ ‭Contribute to‬‭glycocalyx‬ ‭‬ ‭Project into extracellular space‬ ‭‬ ‭To distinguish intrinsic from foreign cells‬ ‭‬ ‭Protection, cell adhesion and fertilization‬ ‭‬ ‭Unique for everyone but twins‬ ‭Protein‬ ‭‬ ‭Transmembrane proteins - completely pass through the bilayer‬ ‭‬ ‭Peripheral proteins - adhere to the membrane (anchored down by filaments)‬ ‭‬ ‭Some functions of membrane proteins‬ ‭1.‬ ‭Receptor‬ ‭2.‬ ‭Enzyme‬ ‭3.‬ ‭Channel‬ ‭4.‬ ‭Gated channel‬ ‭5.‬ ‭Cell-identity marker‬ ‭6.‬ ‭Cell-adhesion molecule (CAM)‬ ‭c.‬ ‭describe a second-messenger system and discuss its importance in human physiology;‬ ‭1.‬ ‭Messenger (Epinephrine) = → Receptor @ plasma membrane‬ ‭2.‬ ‭Receptor → Releases G protein‬ ‭3.‬ ‭G protein freely travel in cytoplasm → bind to an enzyme (Adenylate‬ ‭cyclase) → convert ATP to cAMP‬ ‭4.‬ ‭cAMP = second messenger → active kinase → kinase active enzymes‬ ‭Importance - transmitting signals and allow metabolic steps to occur‬ ‭d.‬ ‭explain the composition and functions of the glycocalyx that coats cell surfaces; and‬ ‭ ‬ ‭Glycocalyx is a cell surface coating made of glycolipids and glycoproteins‬ ‭‬ ‭Functions: physical cushion, protection, adhesion, fertilization and embryonic‬ ‭development‬ ‭e.‬ ‭describe the structure and functions of microvilli, cilia, and flagella, and pseudopods‬ ‭‬ M ‭ icrovilli - finger like projections, help with absorption → small intestines‬ ‭‬ ‭Cilia - hair like projections, longer and have stroke movement → respiratory tract,‬ ‭fallopian tubes → Cystic Fibrosis‬ ‭‬ ‭Flagella - movement → human sperm‬ ‭‬ ‭Pseudopods = “false feet” cytoplasm filled extension of the cells, temporary‬ ‭1.‬ ‭Amoeba (freshwater) → use to catch food‬ ‭a.‬ ‭Pinocytosis - cellular drinking‬ ‭b.‬ ‭Phagocytosis - cellular eating‬ ‭2.‬ ‭Neutrophil (White blood cells → catch foreign particles in immune system‬ ‭3.‬ ‭Macrophage → filamentous pseudopods to bring in bacteria‬ ‭ ection 3.3‬ S ‭a.‬ ‭explain what is meant by a‬‭selectively permeable membrane‬‭;‬ ‭ ‬ ‭A membrane that allows certain molecules to pass through while blocking others‬ ‭b.‬ ‭describe the various mechanisms for transporting material through cellular‬ ‭membranes; and‬ ‭1.‬ ‭Filtration‬‭- by‬‭hydrostatic pressure, no ATP‬‭required‬‭→ blood capillaries‬ ‭2.‬ ‭Simple diffusion‬‭- net movement from‬‭high → low w/‬‭no ATP‬ ‭3.‬ ‭Osmosis‬‭- movement of‬‭water‬ ‭from high → low‬ ‭a.‬ ‭Hydrostatic pressure = pushing force‬ ‭(Larger V = Larger hydrostatic pressure)‬ ‭b.‬ ‭Osmotic = pulling force‬ ‭4.‬ ‭Carrier - mediated transport‬‭-‬‭via transport protein‬ ‭a.‬ ‭Types of carriers‬ ‭‬ ‭Uniport → gated ion channel‬ ‭‬ ‭Symport → Na+ / Glucose transporters‬ ‭‬ ‭Antiport → Na+ / K+ pump‬ ‭b.‬ ‭‬ ‭Facilitated diffusion‬‭: High → Low no ATP for molecules‬‭that are‬ ‭too big, charged or hydrophobic‬ ‭‬ ‭Pumps‬‭: Low → High‬‭NEED ATP →‬‭Na+ / K+ pump‬ ‭○‬ ‭3 Na+ out / 2 K+ in‬ ‭○‬ ‭50% of daily energy use‬ ‭5.‬ V ‭ esicular transport‬‭- move large particles or quantities in enclosed vesicles -‬ ‭NEED ATP‬ ‭a.‬ ‭Endocytosis (phagocytosis, pinocytosis and receptor-mediated cytosis)‬ ‭i.‬ ‭Receptor - Mediated Cytosis (most selective)‬ ‭1.‬ ‭Clathrin-coated vesicle‬ ‭2.‬ ‭Ex: Second messenger system‬ ‭b.‬ ‭Exocytosis‬ ‭c.‬ ‭Transcytosis - transfer material across the cell and release it on the other‬ ‭side → Golgi Apparatus‬ ‭c.‬ ‭define‬‭osmolarity‬‭and‬‭tonicity‬‭and explain their importance.‬ ‭‬ O ‭ smolarity - the number of particles of solute in a solution‬ ‭‬ ‭Tonicity - the ability of a solution to affect the fluid volume‬ ‭ ection 3.4‬ S ‭a.‬ ‭describe the cytoskeleton and its functions;‬ ‭‬ ‭Microtubules → centrioles‬ ‭○‬ ‭Protein tubulin‬ ‭‬ ‭Intermediate filaments → nuclear lamina‬ ‭○‬ ‭Variety of fibrous proteins‬ ‭‬ ‭Microfilaments → villi‬ ‭○‬ ‭α & β tubulin‬ ‭‬ F ‭ unction: supports and shapes a cell, helps position and transport organelles,‬ ‭provides strength, assists in cell division, and aids cell movement.‬ ‭b.‬ l‭ist the main organelles of a cell, describe their structure, and explain their functions;‬ ‭and‬ ‭1.‬ ‭Nucleus‬ ‭a.‬ ‭Nuclear pore: mRNA exit the nucleus‬ ‭b.‬ ‭Nucleolus: produces parts that form ribosomes‬ ‭c.‬ ‭Chromatin: genetic material‬ ‭d.‬ ‭Nuclear lamina : protein structural components, intermediate filaments‬ ‭2.‬ ‭ER‬ ‭a.‬ ‭Rough ER‬ ‭i.‬ ‭Studded with ribosomes → protein synthesis‬ ‭b.‬ ‭Smooth ER‬ ‭i.‬ ‭Make lipids, phospholipids, cholesterol and steroid hormones‬ ‭3.‬ ‭Golgi Complex‬ ‭a.‬ ‭Process → Package → Transport proteins in vesicles‬ ‭4.‬ ‭Lysosomes‬ ‭a.‬ ‭Digestive system of cell‬ ‭5.‬ ‭Peroxisomes‬ ‭a.‬ ‭Generate hydrogen peroxide → oxidative purpose‬ ‭6.‬ ‭Proteasomes‬ ‭a.‬ ‭Protein disposal by tagging them‬ ‭7.‬ ‭Mitochondria‬ ‭a.‬ ‭Make ATP‬ ‭b.‬ ‭Cristae: the folds → increase SA = increase rate‬ ‭c.‬ ‭Matrix: hold enzymes, proteins and pH for Kreb’s cycle‬ ‭d.‬ ‭Inner membrane : ETC‬ ‭e.‬ ‭Outer membrane: transport protein to pull in pyruvate‬ ‭8.‬ ‭Centrioles‬ ‭a.‬ ‭microtubules‬ ‭b.‬ ‭mitosis - separating the sister chromatids‬ ‭c.‬ ‭meiosis - separate homologous chromosomes and sister chromatids‬ ‭9.‬ ‭Ribosomes‬ ‭a.‬ ‭Make protein from RNA‬ ‭b.‬ ‭Free in cytosol or studded on rough ER‬ ‭c.‬ ‭No unit membrane‬ ‭c.‬ ‭give some examples of cell Inclusions and explain how Inclusions differ from‬ ‭organelles.‬ ‭‬ ‭ igments like melatonin, chloroplast‬ P ‭‬ ‭Oils, bacteria or cell debris‬ ‭‬ ‭Inclusion are NOT enclosed by membrane and NOT essential for survival‬ ‭‬ ‭But important for the function of the cells‬ ‭Chapter 4-GENETICS AND CELLULAR FUNCTION‬ ‭ ection 4.1‬ S ‭a.‬ ‭describe the structure of DNA and relate this to its function;‬ ‭‬ ‭Made of nucleotides:‬ ‭○‬ ‭Sugar - deoxyribose‬ ‭○‬ ‭Phosphate group - phosphate backbone‬ ‭○‬ ‭Nitrogenous base - what changes‬ ‭‬ ‭Purines: Adenine , Guanine = 2 rings‬ ‭(‬‭P‭u‬ re‬‭A‬‭s‬‭G‭o‬ ld)‬ ‭‬ ‭Pyrimidines: Cytosine Thymine and Uracil‬ ‭(Pyramids has one top = 1 ring)‬ ‭‬ ‭Law of complementary base - pairing‬ ‭‬ ‭A - T (2 H bonds)‬ ‭‬ ‭C - G (3H bonds)‬ ‭‬ ‭Double helix, antiparallel → semi-conservative replication‬ ‭b.‬ ‭explain how DNA and proteins are organized to form the chromosomes; and‬ ‭‬ ‭DNA wound around histones → form nucleosomes → condense and fold over further‬ ‭into chromosomes‬ ‭c.‬ ‭describe the types of RNA, their structural and functional differences, and how they‬ ‭compare with DNA.‬ ‭‬ ‭mRNA = transcription / transcript region of DNA‬ ‭‬ ‭tRNA = translation / find amino acids in cytosol → bring to ribosomes‬ ‭‬ ‭rRNA = special RNA that forms part of ribosome‬ ‭Section 4.2‬ ‭a.‬ g‭ ive a working definition of the‬‭gene‬‭and explain‬‭why new discoveries in genetics‬ ‭have changed our concept of what a gene is;‬ ‭ ‬ ‭Gene - segments of DNA that code for proteins‬ ‭‬ ‭Recent discoveries in genetics have revealed that the concept of a gene is more complex‬ ‭than simply coding for proteins,‬ b‭.‬ ‭explain what the human genome is and what relationship it has to the health sciences;‬ ‭ ‬ ‭Genome - sum of all genes‬ ‭‬ ‭Human genome project - know where the location and function of each gene‬ ‭‬ ‭Gene therapy, prediction, diagnosis and treatment‬ ‭c.‬ ‭define‬‭genetic code‬‭and describe how DNA codes for‬‭protein structure;‬ ‭‬ G‭ enetic code/ Central dogma: DNA → mRNA → Protein‬ ‭d.‬ ‭describe the process of assembling amino acids to form a protein;‬ ‭‬ ‭mRNA’s codon is read by ribosomes‬ ‭‬ ‭tRNA read the anticodon → pick up the amino acid and go back to‬ ‭ribosome @A‬ ‭‬ ‭Polypeptide form @P‬ ‭‬ ‭tRNA exits @E‬ ‭○‬ ‭tRNA and mRNA goes in opposite directions‬ ‭e.‬ ‭explain what happens to a protein after its amino acid sequence has been synthesized;‬ ‭golgi‬ ‭f.‬ d ‭ escribe some ways that a gene can be turned on or off; and‬ ‭‬ ‭casein - milk production‬ ‭○‬ ‭Prolactin → activates Prolactin receptor‬ ‭○‬ ‭Activation of regulatory protein‬ ‭○‬ ‭Casein gene is turn on‬ ‭○‬ ‭Casein is produced in breast tissues‬ ‭g.‬ ‭explain how DNA indirectly regulates the synthesis of nonprotein molecules.‬ ‭‬ ‭testosteron‬ ‭○‬ ‭DNA codes for mRNA → enzyme is produced‬ ‭○‬ ‭Luteinizing hormone from pituitary gland = second messenger activates‬ ‭dormant enzyme‬ ‭○‬ ‭Activate enzyme convert cholesterol → Testosterone → secrets‬ ‭ ection 4.3‬ S ‭a.‬ ‭describe how DNA is replicated; -‬‭semiconservative‬ ‭‬ ‭b.‬ ‭describe the life history of a cell, including the events of mitosis; and‬ ‭‬ ‭c.‬ ‭explain how the timing of cell division is regulated.‬ ‭‬ ‭ ection 4.4‬ S ‭a.‬ ‭describe the paired arrangement of chromosomes in the human karyotype;‬ ‭b.‬ ‭define‬‭allele‬‭and discuss how alleles affect the traits‬‭of an individual; and‬ ‭c.‬ ‭discuss the interaction of heredity and environment in producing individual traits.‬ ‭d.‬ ‭discuss the consequences of replication errors; mutations.‬ ‭Vocab (Chap 1 → 4)‬

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