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Test Bank For Lippincott Illustrated Reviews Pharmacology 7th Edition by Karen Whalen 9781496384133 Chapter 1-48 All Chapters with Answers and Rationals 2

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Test Bank For Lippincott Illustrated Reviews Pharmacology 7th Edition by Karen Whalen 9781496384133 Chapter 1-48 All Chapters with Answers and Rationals 2

Instelling
Vak

Voorbeeld van de inhoud

Test Bank for Lippincott Illustrated Reviews: Pharmacolo
q q q q q q



gy 8th Edition by Karen Whalen|
q q q q q




KNOW qTHIS:q-
qANSWERqqq1)qRNAqisqsusceptibleqtoqalkalineqhydrolysis,qwhereasqDNAqisqnot.




2)qUnderqalkalineqconditions,qtheqhydroxylqgroupqcanqactqasqaqnucleophileqandqattackqth
eqphosphodiesterqlinkageqbetweenqadjacentqnucleotides,qbreakingqtheqlinkageqandqlea
dingqtoqtheqtransientqformationqofqaqcyclicqnucleotide.q

3)qAsqthisqcanqoccurqatqeveryqphosphodiesterqlinkageqinqRNA,qhydrolysisqofqtheqRNAqwil
lqoccurqdueqtoqtheseqreactions.qAsqDNAqlacksqtheq2′-
hydroxylqgroup,qthisqreactionqcannotqoccur,qand
DNAqisqveryqstablequnderqalkalineqconditions.

Symptomsqofqadenosineqdeaminaseqdeficiency:q-
qANSWERqqq1)qHistoryqofqchronicqdiarrheaqandqmultipleqpneumonias




2)qTheqchestqX-rayqshowsqaqpneumonia,qbutqalsoqrevealsqanqabnormallyqsmallqthymus.q

3)qBloodqworkqshowsqaqdistinctqlackqofqcirculatingqlymphocytes.q

*HereqyouqhaveqnoqworkingqBqorqTqcells*

*qThisqdisorderqleadsqtoqanqaccumulationqofqdeoxyadenosineqandqS-
adenosylhomocysteine,
whichqareqtoxicqtoqimmatureqlymphocytesqinqtheqthymus.*

4)qTheqmostqlikelyqinheritedqenzymaticqdefectqinqthisqchildqleadsqtoqanqinabilityqtoqalterqaq
purineqnucleotideqatqpositionq6qofqtheqringqstructureq(whereqdeaminationqoccursqandqisqr
eplacedqwithqaqcarbonylqgroup)

InosineqandqWobblingq-qANSWERqqqInosineqisqaqwobbleqbaseqpairqformer,qhavingqthe
abilityqtoqbaseqpairqwithq*adenine,quracil,qorqcytosine*

KNOW qTHIS:q-qANSWERqqqLactaseqwillqsplitqtheqβ-1,4qlinkageqbetween
galactoseqandqglucoseqinqlactose.q

Theqlactoseqthusqpassesqunmetabolizedqtoqtheqbacteriaqinhabitingqtheqgut,qandqtheirqme
tabolismqofqtheqdisaccharideqleadsqtoqtheqobservedqsymptoms.q

Combiningqtwoqsugarsqinqaqdehydrationqreactionqcreatesqaqglycosidicqbond.q

AddingqaqsugarqtoqtheqnitrogenqofqaqnitrogenousqbaseqalsoqcreatesqanqN-
glycosidicqbond.

,KNOW qTHIS:q-
qANSWERqqqTheqalphaqcarbonqdeterminesqwhetherqtheqaminoqacidqisqinqtheqDqorqLqconfi

guration

*Manyqbiochemicalqcompoundsq(includingqdrugs)qareqonlyqactiveqasqeitherqtheqDqorqLqis
omer.*

Yourqpatientqhasqaqmechanicalqheartqvalveqandqisqchronicallyqanemicqdueqtoqdamageqto
qredqbloodqcellsqasqtheyqpassqthroughqthisqvalve.qOneqofqtheqsignalsqthatqtargetqdamage

dqredqbloodqcellsqforqremovalqfromqtheqcirculationqisqtheqpresenceqofqphosphatidylserine
qinqtheqouterqleafletqofqtheqredqcellqmembrane.qPhosphatidylserineqisqanqintegralqpartqofq

cellqmembranesqandqisqnormallyqfoundqinqtheqinnerqleafletqofqtheqredqcellqmembrane.qThi
sqflip-
flopqofqphosphatidylserineqbetweenqmembraneqleafletsqexposesqwhichqpartqofqtheqphos
phatidylserineqto
theqenvironment?

(A)qTheqheadqgroup
(B)qFattyqacids
(C)qSphingosine
(D)qGlycerol
(E)qCeramideq-qANSWERqqqA.

Thus,qwhenqaqphospholipidqflqip-
flqopsqacrossqtheqmembrane,qtheqheadqgroupqwillqalwaysqendqupqfacingqtheqaqueousqen
vironment.

Aqcoupleqhasqhadqfiveqchildren,qallqofqwhoqexhibitqshort
stature,qeyelidqdroop,qandqsomeqdegreeqofqmuscleqweaknessqandqhearingqlossq(someqs
evere,qsomeqmild).qTheqmotherqalsoqhasqsuchqproblems,qalthoughqatqaqmildqlevel.qTheqf
atherqhasqnoqsymptoms.qTheqmutationqthatqafflictsqtheqchildrenqmostqlikelyqresidesqinqD
NAqfoundqinqwhichqintracellularqorganelle?

(A)qMitochondria
(B)qPeroxisome
(C)qLysosome
(D)qEndoplasmicqreticulum
(E)qNucleusq-qANSWERqqqA.

Theqmotherqandqchildrenqareqexperiencingqtheqeffectsqofqaqmitochondrialqdisorder.


*Theyqkeyqhereqisqthatqallqofqtheqkidsqhaveqtheqissueqandqtheqmotherqasqwellqbutqtheqfath
erqshowsqnoqsymptoms*

Thereqareqmultipleqmitochondrialqdisordersqassociatedqwithqmuscularqdystrophy:
q




1)qKearns-Sayerqsyndrome(thisqcase)
2)qLeighqsyndromeq(non-X-linked)
3)qPearsonqsyndrome

,4)qMitochondrialqDNAqdepletionqsyndrome
5)qMitochondrialqencephalomyopathy

Membraneqformationqoccurs,qinqpart,qdueqtoqlowqlipidqsolubilityqinqwaterqdueqtoqprimarilyq
whichqofqtheqfollowing?

(A)qHydrogenqbondqformationqbetweenqlipidsqandqwater
(B)qCovalentqbondqformationqbetweenqlipidsqandqwater
(C)qAqdecreaseqinqwaterqentropy
(D)qAnqincreaseqinqwaterqentropy
(E)qIonicqbondqformationqbetweenqlipidsqandqwaterq-qANSWERqqqD.

Cageqformingqdecreasesqwaterqentropy,qwhichqis
unfavorable,qandqthisqleadsqtoqtheqhydrophobicqeffect,qinqwhichqtheqlipidqmoleculesqallqc
omeqtogetherqsuchqthatqonlyqoneqlargeqcageqneedsqtoqbeqformedqaboutqtheqlipidqmolecu
les,qratherqthanqmanyqsmallqcagesqaboutqeachqindividualqlipidqmolecule.q

Theqlipidsqdoqnotqformqcovalentqorqionicqbondsqwithqwater,qand,qasqmentionedqabove,qlip
idsqinqwaterqleadsqtoqaqdecreaseqinqwaterqentropyq(whichqisqunfavorable),qratherqthanqan
qincreaseqinqtheqentropyqofqwaterq(whichqwouldqbeqaqfavorableqevent).




KNOW qTHIS:q-
qANSWERqqqPrecipitationqofquricqacidqoccursqinq"cold"qareasqofqtheqbody,qsuchqasqtheqgr

eatqtoe.

Aqsingle-strandedqDNAqmoleculeqcontainsq20%A,q25%T,
30%G,qandq25%C.qWhenqtheqcomplementqofqthisqstrand
isqsynthesized,qtheqTqcontentqofqtheqresultingqduplexqwill
beqwhichqoneqofqtheqfollowing?

(A)q20%
(B)q22.5%
(C)q25%
(D)q27.5%
(E)q30%q-qANSWERqqqB.

Forqtheqentireqduplexqthen,qtheqTqcontent
isqtheqaverageqofq25%qandq20%,qorq22.5%qforqtheqduplex.qTheq[A]qinqtheqduplexqwillqalso
qbeq22.5%q(again,qsinceq[A]q=q[T]),qandqtheqconcentrationsqofq[G]qandq[C]qwillqeachqbeq27

.5%qforqtheqduplex.

KNOW qTHIS:q-qANSWERqqqTheqglycosylationqofqhemoglobinqprimarilyqoccursqonqtheqN-
terminalqvalineqresiduesqofqtheqβqchainsq(whichqcontainqaqfreeqaminoqgroup).

TheqrateqofqdegradationqofqnonmodifiedqhemoglobinqandqHbA1cqareqtheqsame.

KNOW qTHIS:q-
qANSWERqqq1)qInqorderqtoqmakeqaqxenobioticqmoreqsoluble,qaqhydrophilicqgroupqneedsqt

oqbeqadded
toqtheqxenobiotic.q

, 2)qGlucuronicqacidq(glucoseqwithqaqcarboxylicqacidqatqpositionq6qinsteadqofqanqalcoholqgr
oup)qisqaqhydrophilicqmolecule.

3)qGlucuronicqacidqisqaddedqtoqtheqxenobioticqatqpositionq1,qusingqtheqactivatedqinterme
diateqUDPqglucuronate.

EarlyqclinicalqsignsqofqCreutzfeldt-Jakobqdisease:q-qANSWERqqq1)qMoodqchanges
2)qMinorqlossqofqmemory
3)qDecreasedqmotorqskills

Causedqbyqaqmisfoldedqprionqprotein,qleadingqtoqproteinqaggregatesqinqtheqbrain.q

Thisqpatientqwillqprobablyqdieqwithinq1qyear.q

Thereqisqnoqcurrentqtreatmentqforqtheqdisease.q

Asqtheqdiseaseqprogresses,qheqwillqprobablyqdevelopqblindness,qinvoluntaryqmovement
s,qandqsevereqdeteriorationqofqmentalqfunction.

KNOW qTHIS:q-
qANSWERqqqBisphosphonatesqdecreaseqboneqresorptionqbyqtheqosteoclasts,qtherebyqst

rengtheningqtheqbone,qevenqwithqtheqdefectiveqcollagenqmolecule.

Youqareqvisitedqbyqaq40-year-
oldqfemaleqpatientqcomplainingqofqweightqloss,qnumbnessqinqtheqhandsqandqfeet,qfatigue
,qandqdifficultyqswallowing.qPhysicalqexam
notesqanqenlargedqtongue,qenlargedqliver,qaqrubbery
feelingqaroundqtheqjoints,qandqbruisingqaroundqthe
eyes.qAqboneqmarrowqbiopsyqshowsqanqabnormal
stainingqofqdenaturedqproteinq(seeqbelow).qThese
denaturedqproteinsqareqmostqlikelyqtoqbeqwhichqofqthe
following?

(A)qAntibodyqlightqchains
(B)qCollagen
(C)qFibrillin
(D)qAlbumin
(E)qTransaminasesq-qANSWERqqqA.

*Theqpatientqisqexhibitingqtheqsymptomsqofqprimaryqamyloidosis*

Primaryqamyloidosisq-
qANSWERqqq1)qAqproteinqfoldingqdiseaseqinqwhichqimmunoglobulinqlightqchainsqareqimpr

operlyqprocessedqandqcannotqbeqdegraded.q

2)qTheseqproteinsqthenqformqfibrilsqinqtissues,
whichqareqinsoluble.qThisqdisruptsqtheqnormalqfunctionqofqtheqtissue,qandqmanyqtissuesq
canqaccumulateqtheseqfibrils.

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