Memorisation Flashcards
HLA A3
Hemochromatosis
HLA B8
Addison’s
Myasthenia Gravis
Graves disease
My m8 kennedy
HLA DQ2/8
Celiac disease
HLA DR2
Good Morning Lu
Goodpastures
Multiple Sclerosis
SLE
HLA DR3
Great SAiD Hermionie Graves SLE Addison's DM1 Hashimotos
HLA DR4
Ron At the Door
Rheumatoid
Addisons
DM1
HLA DR5
Harry Potter stays alive
Hashimotos
Pernicious anaemia
CD16, CD56
NK cells
CD25, FOXP3
regulatory T cells
CD80/86 (B7)
Dendritic cells which interact with CD28
CD40L
Th2 cells which interact with B cells
CD14
macrophages
CD34
Haemopoietic stem cells
hot t bone steak
Hot - fever T cell stimulation Bone marrow stimulation st IgE IgA K (Acute phase proteins)
IL 8
neutrophil chemotaxis
IL10
decrease MHCII and Th1
IL12
Th1, NK cells
TNFa
septic shock, increase WBC migration and vascular leakage
INF-y
macrophage stimulation
INFa+b
against viruses - break down nucleic acids and proteins
respiratory burst
catalase positive organisms
complement cascade (early and late)
early - encapsulated bacteria
MAC - gram negatives - neisseria
MHCII
antigen presenting cells
dendritic cells, macrophages, B cells
mitochondrial permeability
irreversible
nuclear pyknosis, karyohexis, karyolysis
irreversible
plasma membrane damage
irreversible
lysosomal rupture
irreversible
cellular/mitochondrial swelling
reversible
chromatin clumping
reversible
blebbing
reversible
ribosomal detachment
reversible
dispersal of Nissl substance throughout the cytoplasm, nucleus in the periphery
chromatolysis
reaction to axonal cell injury
collagen types wound healing
Type III, after 1 week –> type I
tap with high LDH
exudate (inflammatory, lymphatic, malignancy)
pure red cell aplasia
thymoma
good syndrome (hypogammaglobulinemia)
thymoma
migratory superficial thrombophlebitis
trosseau sign
adenocarcinoma - pancreas
anti-NMDA encephalitis
ovarian teratoma
opsoclonus-myoclonus ataxia
neuroblastoma
small cell lung cancer
paraneoplastic cerebellar degeneration
small cell lung cancer
gynae and breast
Hodgkins
antibodies against Hu
small cell lung cancer
ALK
oncogene
lung adenocarcinoma
BRAF
oncogene
melanoma
non-Hodgkin lymphoma
c-KIT
oncogene
GIST
c-MYC
oncogene
Burkitt’s
KRAS
oncogene
colon, lung, pancreas
MYCL1
oncogene
lung
MYCN
oncogene
neuroblastoma
APC
tumour suppressor gene
colon
CDKN2A
tumour suppressor gene
melanoma, pancreas
p16
CDKN2A
blocks G1-S phase
DCC
tumour suppressor gene
colon cancer
PDC4
SMAD4
pancreas
Juvenile polyposis syndrome
NF2
tumour suppressor gene
Merlin
PTEN
tumour suppressor gene
breast, prostate, endometrial
TP53
tumour suppressor gene
Li-Fraumeni
TSC1 + 2
tumour suppressor gene
Tuberous sclerosis
Harmatin + tuberin
thyroid radiation
papillary cancer
vinyl chloride
angiosarcoma of liver
carbon tetrachloride
centrilobular liver necrosis, fatty change
psammoma bodies
papillary thyroid cancer
serous papillary cystadenocarcinoma of ovary
meningioma
malignant mesothelioma
CA125
ovary
CA15-3/27-29
breast
CEA
pancreas, colon, breast
medullary thyroid
p-glycoprotein
adrenal cell carcinoma
sarcoma spread
blood
carcinoma spread
lymph
minus HCC, RCC, follicular, choriocarcinoma
HCC spread
hematoganous
RCC spread
heme
follicular carcinoma spread
heme
choriocarcinoma spread
hemea
Bcl2
antiapoptotic
BAX/BAK
proapoptotic
STAT3 mutation
hyper-IgE
Th17 deficiency
ATM gene
ataxia-telangectasia
DNA break repair
CD40L defect
hyper IgM
LFA-1 defect
leukocyte adhesion deficiency type 1
CD18
LYST gene
lysosomal trafficking gene
Chediak-Higashi
NADPH oxidase
chronic granulomatous disease
inheritance IL-12 receptor deficiency
AR
inheritance SICD
XR
AR
inheritance hyper-IgM
XR
inheritance Wiskott-Aldrich
XR
inheritance leukocyte adhesion deficiency type 1
AR
inheritance Chediak-Higashi
AR
adenosine deaminase deficiency
SCID
defective IL-2R gamma chain
SCID
anticentromere
LIMITED scleroderma (CREST)
anti-desmoglein/ anti-desmosome
pemphigus vulgaris
antiGAD
glutamic acid decarboxylase
diabetes mellitus type 1
antihemidesmosome
bullous pemphygoid
anti-histome
drug induced lupus
anti-Jo-1
polymyositis, dermatomyositis
Anti-SRP, anti Mi2, histidyl tRNA synthetase
polymyositis, dermatomyositis
antimicrosomal
hashimoto’s
antimitochondrial
primary biliary cirrhosis
antiphospholipase A2 receptor
primary membranous nephropahy
anti DNA topoisomerase I
anti-Scl-70
scleroderma - DIFFUSE
anti smooth muscle
autoimmune hepatitis type I
anti SSA, SSB
sjogrens
anti Ro, La
anti TSH
Graves
Anti-U1 RNP
mixed connective tissue disease
p-ANCA (Myeloperoxidase)
UC, PSC, Churg-Strauss, microscopic polyangitis
Proteinase3-ANCA (c-ANCA)
Granulomatosis with polyangitis
prevents IL-2 transcription
cyclosporine
binds FK506
tacrolimus
sirolimus
rapamycin
mTOR inhibitor
sirolimus
FKBP
sirolimus
inhibits IMP dehydrogenase
mycophenolate
NFkB inhibition
corticosteroids
alemtuzumab
CD52
bevacizumab
VEGF
cetiximab
ECFR
Rituximab
CD20
Trastuzumab
HER2
Adalimumab
TNF-a
Infliximab
TNF-a
etanercept
Certolizumab
TNF-a
Eculizumab
Complement protein C5
Natalizumab
a4 integrin
Denosumab
RANKL
Platelet glycoproteins IIb/IIIa
Acbiximab
Omalizumab
IgE
Palivizumab
RSV F protein
Ranibizumab, bevacizumab
VEFG
increases Km
reversible competitive inhibitors
doesn’t change Vmax
decreases Vmax
irreversible competitive inhibitors
and noncompetitive inhibitors
don’t change Km
potency
Km
efficacy
Vmax
-stigmine
anticholinesterase
-chol
cholinomimetic
edrophonium
anticholinesterase
organophosphate poisoning
anticholinesterase poisoning
Rx organophosphate poisoning
atropine + pralidoxime
- pine, -mine, -pium
muscarinic antagonists
oxybutynin, solifenacin, tolterodine
muscarinic agonist for overactive bladder
Rx atropine poisoning
pyridostigmine
isoproterenol
selective B agonist
NE
E
alpha
equal alpha and beta
toxin binding fast Na+ channels in heart/nerves
tetrodotoxin
pufferfish
toxin opens Na+ channels causing depolarisation
ciguatoxin
reef fish
bacterial histidine –> histamine
scombroid poisoning
spoiled dark meat fish
arsenic poisoning
succimer, dimercaprol
amphetamine poisoning
NH4Cl - acidify urine
Metal poisoning
penicillamine
Copper, Gold, Lead
cyanide poisoning
nitrite + thiosulfate + hydroxocolbamin
dimercaprol
gold, lead, mercury
-ivir
neuraminidase inhibitor
-navir
protease inhibitor
-ovir
DNA polymerase inhibitor
-curium
nondepolarising paralytic
a1
contraction, fight or flight
a2
inhibition, decreases sympathetic system
B3
lipolysis, thermogenesis
M1
CNS, enteric nervous system
M2
heart rate and contractility decrease
M3
relaxation state - rest and digest
D1
increases renal blood flow
V=
vasopressin
case-control
odds ratio
with and without disease
cohort study
risk ratio
with and without risk
rule out test
negative
negative skew
mean lowest
type I error
study finding there is a difference when there isn’t
type II error
study doesn’t find a difference, when one exists
power =
1 - chance of type II error (study not finding anything when there was a correlation)
liklihood of a type I error
p vaue
ANOVA
difference between 3 or more means
chi-squared
difference between 2 or more percentage or proportions of categorical outcomes
NAD requires
B3
FAD requires
B2
hexokinase
everywhere minus liver and pancreas
glucokinase
liver and pancreas
glycolysis
2 pyruvate + 2ATP + 2NADH + 2H+ + 2H2O
Hot water PAN
arsenic inhibits
causes
lipolic acid
TCA to not produce ATP
pyruvate dehydrogenase complex cofactors
B1, 2, 3, 5, lipolic acid
TCA cycle produces
10 ATP, 3 NADH, 2CO2, FADH2, GTP
double for per glucose
neuro problems, lactic acidosis, high serum alanine
pyruvate dehydrogenase deficiency
high fat diet with high lysine and leucine
cells that don’t have sorbitol dehydrogenase
schwann cells, retina, kidneys, lens (mainly)
cherry red spot on mecula
Tay-Sachs
+ hepatosplenomegaly = Nieman-Pick
long bone aseptic necrosis
Gaucher disease
worsening eyesight, peripheral neuropathy, regressive milestones
Krabbe disease
clumsy, ataxia, dementia - child
Metachromatic leukodystrophy
XR lysosomal storage disease
Fabry
Hunter
small purple blemishes, neuropathy, increased sweating
Fabry disease
corneal clouding, lung and liver issues, low IQ
Hurler
low IQ, gargoyle, Aggression
Hunter (XR)
hexosaminidase A deficiency
tay-sachs
increased GM2
spingomyelinase deficiency
Nieman-Pick
glucocerebrosidase deficiency
Gaucher disease
galactocerebrosidase deficiency
Krabbe disease
arylsulfatase A deficiency
metachromatic leukodystrophy
increased cerebroside sulfate
alpha galactosidase A deficiency
Fabry disease
increased ceramide trihexoside