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

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 +1  (nbme24#13)
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ceDltryi omrf apidwi:ike

Acu"et eipeifvtlorar uoirloelpimernthsg si a drserodi fo teh eirlumogl ml,spo(iehrogulir)net ro lslma ldobo ssvlese in teh .eikndsy It is a nmcmoo ipmtacnoiocl of ialecatrb iofctnsnei, iatlylcyp knsi nofnetiic yb ecupsrSoctoct bacrieta syetp ,21 4 adn 1 igt)o(mepi tub olas aerft srotelactocpc giastr,hnipy rfo iwhch ti is aols onwnk as tutseisonicfpo ro rsotlecpttcpoosac ip.setrl"hunroigolme

 +4  (nbme20#22)
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oFmr Absoms on eoriPnt oniatgdeDa:r

sd"gnEuonoe psroneti ear edrdadeg yb so.eptoesram Exoensuog tisenpor rae eegdrdad yb osley"msso

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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G-1IF is oueddrpc laprymrii yb eht rlive sa na endoricen nrhmoeo as elwl as in taegrt ueitsss ni a eci/aapnnouirearcrt hf.saoin Pucotirdno is tsmduateil by rwghot oonhmre GH() nda can eb redratde yb t,nurutineodirn otgrhw mornheo yittnvi,issnie kacl fo twhrgo moohren trcreosp,e or usaielrf of het saowtmrned gligsainn tpaawhy psto GH eotcrepr uilcgnndi P2SH dan ST5.TBA

rmFo i;aieidkpw ceusrod ot :ma/ea/r?cpc5etd3s0.3=4.eccoptxt1dstl71-7hor6/0iFfbtcdnr/uee2:muer///doe5ot3tmiil/aratalc

 -13  (nbme20#20)
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The ewsarn si ltyaclau oakpmyile,ha cndgroaci ot N.EBM

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The wsenra si luytalca ak,opmyleiah drccgaion ot ENB.M