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GM all, sorry didnt update yesterday as time was running fast & in btn had to do some chores.
yesterday i also read bio & some other quest of resp physio.
for micro i am not reading it yet i am just memorizing as a whole as i dont have time now. after completing patho then will read c/f in detail. but along with patho i am simultaneously reading some of its c/f ,transmission etc & also whiled doing some of uw quest it covered micro & drugs which i dint expect so thats a good thing .
i am focusing more on difficults like phsio, immuno, bio, path.
its been awhile since i revised bio & pharma cant find the time as its going by fast & some times my mind is tempting me u need more time to do all nbme etc but the key is in short time to cover all mainly with concepts behind it.
ok now will study , will update later
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GM all...days r just flying by. cant believe it's end of feb already. it helps when we discuss things here, the more we discuss, the more we may remember!
@owl: just wanted to clear up neurocutaneous disorders, u mixed them up in ur previous posts...
vHl- Hemangiomas
Tuberous sclerosis - hamarTomas
(this is a way to remember them)
sturge weber- has port wine stain in V1 distribution & AVM's (leptomeningeal angiomas), mental retardation
osler weber rendu (aka "hereditary hemorrhagic telangiectasia") as the name states has telangiectasias & AVM's, skin discoloration (but no port wine stain?)
drugs prolonging QT interval: Class IA & III antiarrhythmics, macrolides, haloperidol/risperidone, antimalarials (chloroquine, mefloquine), methadone, HIV protease inhibitors, fluoroquinolones (list is extensive)
@2177: it takes some time to get back to studying properly once there's been a break as has happened to me many times in my studying. keep going with the flow. i agree with raw, everyone's circumstances r different & some have it easier than others.
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@all: had posted a q in one of my previous posts
follicular lymphoma is c/b translocation of bcl2 oncogene from chromosome 18 to next to Ig heavy chain region on chromosome 14 ---> over expression of bcl2 & inc bcl2 protein
(this is what i have in my notes from uw i think cuz those r the only notes i have in my fa so far) can u guys clarify is the actual translation the other way around, oncogene on 14 moves next to 18?
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hey guys done with my first block..phew! can't believe im doing it second time..felt like the first time...i didnt remember the questions at all..maybe 2 or 3..lol need to work harder i guess!!
good to see u up and workin carpe and thanks for sharing
ok starting dit day 6 lecture 1
by the way guys...what should be the percentage in UW when u do it second time..80 or 90?? just wondering!! i took it as a learing tool first time round but now i just wonder!!
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@owl: typical antipsychotics block D2 receptors found in brain. tx- + symptoms of schiz.
high potency- more extrapyramidal SE
low potency- more anti-cholinergic SE
atypicals block 5HT2, alpha, H1 & DA receptors. tx- both + & - symptoms
DA normally inhibits prolactin, without DA ----> hyperprolactinemia
what are the EPS SE guys?
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so from the table i think it seems to say first IGg on chr 14 makes fusio protein and then bcl2 present on chr 18 induces fusion protien to become anti apoptotic
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@raw: thanks...my q was something different though, does 18 translocate over to 14 or 14 to 18? i know it's t(14:18) but i have it written same as i wrote above (which seems to be the opposite)
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GM guys .. another brand new day with fa .. another hopeful attempt foa another 40 pgs ,,
todays target -- hemat and musculo sk ..
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GM all
yesterday i only studied a bout 2 hr ,,,now starting with neuro again ........
thereis heavy snow at fargo ,,,they said it would be about 6inch.....
happy studing
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