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Welcome to dontwanttofail’s page.
Contributor score: -6

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 +1  (nbme24#13)
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rylciDte omfr iwk:apiide

eAuct" plrtieafiover lrsnielpmgutreioho is a rrddesio of hte eoiumrlgl rrnt(pge,)ieusillomoh ro mslal lodbo sessevl ni het yids.kne tI si a cnmmoo nacictimoplo fo cbalieatr oeci,nnsfti ytiypclal nsik tiocnenif by eutScotsopccr reabitca tspey ,21 4 and 1 ietop)(gim tub saol rafte cerasctplocto hirtpngi,say for hihwc it is saol nknwo as ssiouettpinfoc ro solstractopepcoct egsm.tunerlolpi"ohir

 +4  (nbme20#22)
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mFro somsAb no tnerPoi ria:agDodten

dne"sgnoEuo rtnoeips rae derdadeg yb amsptsoroee. geusnEoxo rnpistoe aer dereddag by loesmsoy"s

azibird  According to UWorld question ID 11674: Referring to the presentation of viral antigens on MHC class I, it says "The ubiquitin proteasome pathway (UPP) is essential to this process because of its role in breaking down native and foreign intracellular proteins." In the AMBOSS protein degradation card it says, "endogenous proteins (those synthesized as cells)." Would viral proteins synthesized by host machinery count both foreign and endogenous? If so, then this post is correct but a bit misleading. +
azibird  *synthesized IN cells +

 +1  (nbme20#30)
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FIG-1 is puddroce rralmpiyi yb hte lvire sa an edroecnin romhoen sa well sa ni grttea ssutesi in a p/canaeitarinrrcoue aih.nfso codiurntPo is smuilteatd yb trghow erhmnoo GH)( dna can eb tdaerred by utnd,rtneiinruo owhrgt ohenmor seisityitnvin, akcl fo rhotgw omhrone tsr,ecpreo ro railefsu fo teh drawonsetm angiisgnl aytwhpa ospt GH rerepoct iiunclgdn S2PH dna B5TAST.

Fmro dikeaiiw;p rouscde :to ral:u0t6r?a/t3523rpait.d.ludteea7/btnm51ctaecis0ei=-Fomdc/sec7/xo/r/l/o4efohp1ctecm3t/dr

 -13  (nbme20#20)
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heT wrensa is yltclaau oyakm,apelhi gcianrdco ot BNE.M

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heT rnwase is acluylat ohaelkya,imp rcaicndgo ot EBM.N