Basic Science Flashcards
Mechanism to decrease effectiveness of beta lactams
Altered membrane-binding protein
Mechanism to decrease effectiveness of quinolones
Mutations of bacterial DNA gyrase
Mechanism to decrease effectiveness of Tetracyclines
increased tetracycline efflux, ribosome protection, and tetracycline modification
Mechanism to decrease effectiveness of rifampin
Alteration of RNA polymerase
Vitronectin
important receptor involved in Osteoclasts attach to bone surfaces by means of integrins and then seal the space below.
also integrin avß3
RANK
receptor on osteoclasts that when activated by RANKL stimulates osteoclasts. RANKL is found on osteoblasts.
Osteoprotegerin (OPG)
decreases osteoclast differentiation by it’s interaction with RANKL (receptor activator of NF-kappaB ligand). OPG is made by osteoblasts and binds to RANKL (RANK Ligand) to competitively inhibit RANK binding.
PDGF (Platelet Derived Growth Factor)
involved in fracture healing. It is chemotactic and attracts inflammatory cells to the fracture site and is important in early fracture healing, especially the hematoma formation.
TGF-B (transforming growth factor Beta)
induces mesenchymal cells to produce type II collagen & proteoglycans. It is important in the early stages of fracture callus formation.
Doxycycline MOA
inhibit protein synthesis by binding to the 30s ribosomal subunit.
clindamycin MOA
inhibit the 50s ribosomal subunit.
Penicillin MOA
cell wall synthesis.
vancomycin MOA
inhibit cell wall synthesis.
linezolid MOA
inhibit the 50s ribosomal subunit.
Sulfonamides MOA
folic acid inhibitors.
Rifampin MOA
RNA synthesis inhibitor.
Inhibits cell-wall production by preventing peptidoglycan cross-linkage
Cephalosporins
Inhibits cell-wall production by interfering with the addition of cell-wall subunits
Glycopeptides - vancomycin
Inhibits translation through irreversible binding of the 30S ribosomal subunit
Aminoglycosides
Inhibits DNA-dependent RNA polymerase F
Rifamycins
Inhibits DNA gyrase
Fluoroquinolones
amphotericin
binds to sterols and disrupting the cell membrane also nystatin
Alveolar rhabdomyosarcoma
PAX3-FKHR fusion gene - 1:13
PAX7-FKHR fusion gene - 2:13
Ewings Sarcoma
EWS-Fli1 fusion gene - 11:22
Multiple hereditary exostosis
EXT1, EXT2, EXR3
Multiple Osteochondromas
Trabecular bone is remodeled through the formation of?
Howship lacunae : After the pit is formed, osteoclasts are replaced by osteoblasts that form new bone matrix
Synovial sarcoma
SYT-SSX fusion gene - t(x,18)
foot
15-20
Parosteal osteosarcoma
Ring chromosomes
Stress
force per cross-sectional area
Strain
Strain is the deformation of a material in response to an applied force
change in length/original length
Modulus of Elasticity
slope of the stress-strain curve
measure of an object’s ability to resist deformation under an external load.
Toughness
the area under the stress-strain curve and is a measure of the amount of energy a material can absorb before failure
Creep
increased displacement over time attributable to the same force
What molecules have been shown to promote fibrosis during muscle injury
TGF-ß1
important trophic factors in muscle regeneration
Insulin growth factor 1 (IGF-1)
Basic fibroblast growth factor (bFGF)
What dominant intracellular proteins become directly phosphorylated as a result of bone morphogenetic protein (BMP) binding to its receptors - See more at:
SMADS
myasthenia gravis
loss of acetylcholine receptors secondary to autoimmune antibodies at the NM junction.
Mann-Whitney U test
used when data are nonparametric, meaning either not normally distributed or variances are not equal among groups
Low Molecular weight Heparin
bind to antithrombin
increases the ability of antithrombin to inhibit thrombin and Factor Xa
Warfarin
Inhibition of vitamin K-dependent carboxylation
intervenes with cyclic interconversion of vitamin K and its 2, 3 epoxide
leading to hepatic synthesis of factors II, VII, IX, and X with reduced activity
Fondaparinux
Inhibition of factor Xa through antithromin binding
Enoxaparin
Inhibition of factor Xa through antithromin binding
Aspirin
Binding of cyclooxygenase (COX)-1 and COX-2
Argatroban
YOUR RESPONSE: 4- Direct thrombin inhibition
Hemophilia
X linked
Factor 8
Hemarthrosis
Von Willebrand disease is a and not hemarthroses.
lack of von Willebrand factor that leads to decreased platelet aggregation;
mucosal bleeding
Protein C and S deficiencies
AD
lead to thrombosis
protein C and S shut off thrombin formation.
Calcitonin
directly interfering with osteoclast maturation via receptors
inhibits phosphate reabsorption
decreases calcium reabsorption in the kidneys
Dkk-1 (dickkopf-1) & sclerostin
inhibit the binding of the Wnt molecule to receptors LRP5/6
Wnt
binds LRP5/6
inhibits phosphorylation of the ß-catenin
ß-catenin
part of Wnt pathway
osteoblast formation differentiation
Dystrophin
Duchenne muscular dystrophy (DMD)
X-linked muscular disorder
Runt-related transcription factor 2 (Runx2)
cleidocranial dysplasia
Mutations of collagen type
OI
Neurofibromin
protein product of the NF-1 gene
associated with neurofibromatosis
FGFR3
achondroplasia
Fibrin
Marfan syndrome
Cartilage oligomeric matrix protein mutations
pseudoachondroplasia
have short stature (3.5-4.5 feet)
Radiographically, patient appearance is normal at birth but severely abnormal with growth.
multiple joint deformities and normal facies
COL2A
spondyloepiphyseal dysplasias
facies with mild midface flattening, short necks, and barrel-shaped chests
Drug Resistance : quinolones
Mutations of bacterial DNA gyrase
Drug Resistance : beta -lactams
Altered membrane-binding protein
Drug Resistance: Tetracyclines
increased tetracycline efflux, ribosome protection, and tetracycline modification
Drug Resistance: rifampin
Alteration of RNA polymerase
Integrin
promotes tumor cell attachment to bone during metastasis
Heuter-Volkmann
bone placed in longitudinal tension will tend to stimulate longitudinal growth, and that compressive longitudinal forces inhibit longitudinal growth
Wolff’s law
bone remodels in response to mechanical stress, with the correlate that increased stress causes increased growth, and decreased stress leads to bone loss.
Adult Lyme Dx Abx
amoxicillin
doxycycline
cefuroxime
PITX1-TBX4
Club foot,
Single nuclear polymorphism (SNP)
COLIA-1
osteoporosis
COL5A / COL3A
Ehlers-Danlos syndrome
Activating missense mutations of GNAS
Fibrous Dysplasia
Fusion transcripts of HEY1-NCOA2
Mesenchymal chondrosarcoma
Ring chromosomes with CDK4 and MDMK amplification
low-grade central osteosarcoma or parosteal osteosarcoma
Fibrous Dysplasia
Activating missense mutations of GNAS
CDH11-USP6
aneurysmal bone cysts
Poland syndrome /Sprengel deformity
interruption of the embryonic subclavian blood supply
Fibular hemimelia
NO known genetic component absent ACL absent rays of the foot tarsal coalition hypoplastic or aplastic fibula leg-length discrepancy femoral and tibial hypoplasia lower extremity angular deformity
Distal arthrogryposis
MYH3 mutation
gene which codes for myosin heavy chain 3
The NF1
Chromosome 17, codes for neurofibromin, a tumor suppressor
autosomal dominant inheritance
50% of new cases are due to sporadic mutation
Dystrophic scoliosis
typical of NF1 scalloped vertebra penciled ribs severe rotation sharp and short (4-6 vertebrae) kyphoscoliosis
MYH3 mutation
Distal arthrogryposis
Beckwith-Wiedemann syndrome
Chromosome 11 near the IGF gene Neonatal hypoglycemia macroglossia visceromegaly hemihypertrophy embryonal tumors, especially Wilms tumor
Etanercept
Soluble receptor that binds TNF-α
Infliximab
Monoclonal antibody that binds TNF-α
Warfarin
inhibits clotting factors II,VII,IX,X.
inhibition of hepatic enzymes, vitamin Kepoxide = lack of carboxylation of vitamin K dependent proteins (II,VII,IX,X)
Factor V Leiden
caused by anabnormality of factor V that leads to decreased inactivation of factor Va by activated proteinC (aPC) and increased blood clotting.
Single AA substitution
LMWH
Factor Xa