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77 Cards in this Set
- Front
- Back
Part of chromatin transcribed
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Euchromatin
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Number of bonds in G and C
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3 bonds between these nucleic acids
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Purines
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Adenosine and Guanine
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Number of bonds between A and T
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2 bonds between these nucleic acids
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Amino acids necessary for purine synthesis
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Glycine Asparate and Glutamine
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Transition vs Transversion
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purine to purine vs purine to pyrimadine (or vice versa)
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Number of rings in pyrimadines (C, T and U)
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1 ring nucleotides
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Number of rings in purines (A and G)
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2 rings nucleotides
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Direction DNA is opened up and read from
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3' to 5'
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Direction DNA and RNA are made and RNA read
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5' to 3', its all down hill
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most, largest, smallest RNAs
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rRNA, mRNA, tRNA
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DNA Gyrase
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A prokaryotic topoisomerase that relieves supercoils for replication (blocked by fluroquinolones)
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Problem with mismatch repair
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HNPColorectal Cancer has this DNA repair problem
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Problem with thymidine dimer repair (base eXcision repair)
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Xeroderma pigmentosum (dry skin w/ melanoma ect) have this problem w/ DNA repair
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Start and Stop Codons
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AUG and UGA,UAA,UAG
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Promoter vs Enhancer
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Promoter binds both TF and RNA polymerase
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RNA polymerases that make tRNA, rRNA, and mRNA
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RNA polymerase III, I, and II
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Death cap mushrooms (alpha-amanitin) do what?
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This toxin inhibits RNA polymerase II
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RNA processing (steps inside nucleus before it gets out, INtrons stay IN the nucleus) turning hnRNA (heterogenous) into mRNA, by snRNPs/spliceosome
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5' capping w/ 7-methylguanosine, Polyadenylation on 3' (AAUAAA), splicing of introns with
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size of Eukaroyotic and Prokaryotic rRNA
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even (80) and odd (70)
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50S blocking
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Chlorophemicol, Clindamycin, Linezolid, Erythromycin (Macrolides- Clarithromycin and Azithromycin)
CLEAN |
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30S blocking
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Tetracyclin (and Doxycyclin), Aminoglycosides (amikacin, gentamicin, neomycin, streptomycin, tobramycin) TAG- AmiNoGlycoSides
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Energy to aminoacyclate, load tRNA onto ribosome or Translocate, total energy
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ATP-> AMP. GTP-> GDP, total energy is 4 high energy bonds
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Cell Cycle
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G1 (growth), S phase (synthesis), G2 (growth), Mitosis (prophase, metaphase, anaphase, telophase), G1
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Rb and p53 inhibit this
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these tumor suppressor genes inhibit the passage from G1 to S phase
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These are permanent, not replicating cells, these are stable (quiescent), these are labile
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Neurons, skeletal and cardiac muscle, RBCs
Hepatocytes, lymphocytes Bone marrow, gut epithelium, skin/hair |
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Site of packaging and secretion of proteins through glycosylation, rich in goblet cells (mucous), and Ab secreting plasma cells
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Rough ER role in protein transport
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Site of steroid synthesis and detoxification
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Smooth ER (Hepatocytes and adrenal cortex)
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Golgi apparatus function
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Distribute proteins from ER to plasma membrane, lysosomes and secretory vessicles, adds oligosaccharides, targets proteins to lysosomes, makes proteoglycans and sulfation of these sugars and other tyrosines
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How does the Golgi target proteins to lysosomes
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mannose-6-phosphate to protein
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Clathrin does what?
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This protein does plasma-membrane receptor mediated endocytosis, and moving things from trans-Golgi network to lysosomes
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Microtubules structure and function
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alpha and beta tubulin make flagella, cilia, axoplasmic transport, and mitotic spindles
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Motor proteins that go forward on microtubules)
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Kinesin (vs Dynein)
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Drugs that act on microtubules
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Vincristine/vinblastin (anti-cancer), Colchicine (gout, also raises pH to stop uric acid crystalization and NSAID by blocking PMNs), Griseofulvin (antifungal), and Mebendazole/thiabendazole (anti-helminthic), Paclitaxel (anti-breast cancer)
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Chediak-Higashi syndrome ((ashy white skin, checked phagocytosis leads to pyogenic infection)
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Microtubule polymerization defect -> low phagocytosis: PYOGENIC INFECTIONS, PARTIAL ALBANISM, PERIPHERAL NEUROPATHY
ashy white skin, checked phagocytosis leads to pyogenic infection) |
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Kartagener's Syndrome
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Immotile cilia from dynein arm defect on cilia. Infertility, bronchiectasis, sinusitis, related to sinus inversus
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Cilia
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cilia are 9+2 arrangement of microtubule doublets
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Intermediate filaments
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desmin (Dsg) of skin, GFAP, neurofilaments, cytokeratin
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What is I-Cell Dz
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No mannose-6-P to lysosomal bound proteins -> accumulation -> course facial features, clouded cornea, restricted ROM, high plasma lysosymal enxymes (often childhood fatal)
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Vimentin stains
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Connective tissue is stained by
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Desmin stains
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Muscle is stained by
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Cytokeratin stains
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Epithelial cells are stained by
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GFAP stains (glial fibrillary acid proteins)
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Neuroglia stain
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Neurofilaments stain
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Neurons are stained by
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Digoxin/Digitoxin mechanism of action
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This drug inhibits Na/K ATPase, indirectly inhibiting Na/Ca exchange which gets rid of Ca by letting in Na, increasing [Ca+], increasing CTY
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Collagen Type I
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Collagen in Bone, Skin, Tendon, dentin, fascia, cornea, late wound repair
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Collagen Type II
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Collagen in cartilage, nucleus pulposus, vitreous body
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Type III Collagen
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Collagen in skin, blood vessels, uterus, fetal tissue, granulation tissue (aka Reticulin)
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Type IV col
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Collagen in basement membrane (FLOOR), kidneys, eyes, ears
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Type VII collagen
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Collagen in dermis (epidermolysis bullosa)
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Collagen synthesis inside fibroblasts
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Vit C, glycine, proline, anydroxyproline, or hydroxylysine, glycosylation, formation of triple-helix and exocytosis
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Outside fibroblasts collagen gets
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Proteolytic processing of procollagen (terminal regions get cleaved) to make tropocollagen, and cross-linking to make collagen fibrils (by lysyl oxidase)
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Osteogensis imperfect (brittle bone dz)
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Collagen type I stops formation of triple helix to make procollagen
blue sclera, hearing loss, dental problems, AUTOSOMAL DOMINANT |
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Ehlers-Danlos syndrome
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Hyper extensible skin, bleeding, hyperflexibilty from Type III collagen mutation (berry aneurysms, organ rupture, joint dyslocation)
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Alports Syndrome
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Type IV col disorder, X-linked recessive
progressive nephritis and deafness, vision changes |
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Marfans
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fibrillin-1 defect (AD) (makes elastin which makes making lungs, arteries, ligmants, vertebrae flexible),
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Regulation of Elastin
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This molecule is broken down by elastase, which is inhibited by alpha1-antitrypsin (emphysem can be caused by anti-trypsin deficiency)
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cDNA
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library of all a organisms translated genetic material that w/ introns
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Imprinting Diseases
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Prader-Willi (retardation, developmental delay followed by hyperphagia, parental is deleted in dz) and AngelMan's Syndrome (maternal is deleted in dz,intellectual and developmental delay, hand flapping, happy super smiley), both on 15
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Locus Heterogeneity
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When one phenotype can be produced by mutations in different places
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Heteroplasmy
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A result of inheriting lots of mtDNA, it describes how the expression is very variable in mitochondrial inherited diseases
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Hardy Weinberg
carrier frequency affected frequency allele frequency prevalence in men if x-linked |
1 = p2 + 2pq + q2
carrier = 2pq affected = q^2 allele frequency= p and q, p+q = 1 if x-linked, male prev = q |
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Vit D resistant rickets inheritance pattern
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X-linked dominate, (phosphate wasting in proximal tubules)
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Leber's hereditary optic neuropathy, other myopathies
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Mitochondrial inheritance
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Location of FA oxidation (beta-oxidation)
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Mitochondria
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Location of acetyl-CoA production
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Mitochondria
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Location of TCA cycle
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Mitochondria
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Location of oxydative phosphorylation
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Mitochondria
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Location of glycolysis
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cytoplasm
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Location of FA synthesis
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cytoplasm
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Location of HMP shunt
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Cytoplasm
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Location of Protein synthesis
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cytoplasm (RER)
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Location of steroid synth
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cytoplasm (SER)
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Location of Heme synth
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Both Mito and Cyto
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Location of Urea Cycle
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Both Mito and Cyto
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Location of Gluconeogensis
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Both Mito and Cyto
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what goes up the most in ketoacidosis
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Beta-hydroxybuterate
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