
Kamelia Mirdamadi- Doctor of Philosophy
- PhD Student at University of Toronto
Kamelia Mirdamadi
- Doctor of Philosophy
- PhD Student at University of Toronto
Pharmacokinetics Scientist
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10
Publications
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Publications
Publications (10)
Activated T helper 17 (Th-17) cytokines play a role in the pathophysiology of autoimmune and infectious diseases. While these diseases affect many women of childbearing age, little is known about the effect of these cytokines on placental transporters. As several pro-inflammatory cytokines impact the expression of ABC and SLC placental transporters...
ackground: Sleep disturbances during pregnancy are associated with higher risks of maternal depression, hypertension, gestational diabetes and preterm labor. Nocturnal plasma melatonin levels are known to increase as pregnancy proceeds, reaching their peak near term. While insomnia is frequently seen in pregnancy, the possible role of maternal mela...
Background
Autoimmune arthritic diseases affect many women of child-bearing age. Tumour necrosis factor (TNF)-α inhibitors are currently used for the treatment of various immune-mediated diseases during pregnancy. However, there has been no evaluation of safety in the treatment of arthritic diseases during gestation.
Objective
To analyze the risk o...
Insomnia in pregnancy is associated with depression, preeclampsia, gestational diabetes, and preterm labor. In normal pregnancies, maternal plasma melatonin levels increase significantly as pregnancy proceeds, reaching its peak near term. However, the role of melatonin in insomnia during pregnancy is not known. The objective of this study was to me...
Mental health disorders such as schizophrenia and bipolar disorder are common among the women of child bearing age. Obstetric complications and infant outcome of untreated psychiatric illnesses have been studied. Meanwhile there is limited information on the safety of psychotropic medications in pregnancy. Studies demonstrated that treatment with c...
Question:
I have been encouraging pregnant women to receive both the H1N1 and influenza vaccines since I became aware of Health Canada's guidelines. However, some of the women in my practice have heard conflicting information, often from media sources, and they are hesitant to be vaccinated. What is the evidence behind these guidelines, and should...
During the H1N1 influenza pandemic in 2009, The Motherisk Program, a counselling service providing teratology information, received many calls from pregnant women inquiring about the safety of the H1N1 vaccine. We wished to explore pregnant women's perception of risk and the factors associated with deciding whether or not to receive the vaccine.
Pr...
Questions
Questions (6)
I started using "RNA storage solution (1mM sodium citrate) from THermoFisher to dissolve RNA pellets and store in -20 or -80.
However, there is no amplification in the Q-PCR. it is frustrating and I am not sure if the solution affects the RNA, and if no do I have to change the RNA input?
I use 2 mcg RNA to make cDNA with high capacity superscriptII RT-kit (20 ul). but no luck so far in q-PCR?
I am trying to run RNA on 1% agarose/formaldehyde gel using 5x MOP buffer and SybrSafe staining instead of ethidium bromide.
what is the proper voltage and time? it says 5-6V/cm, but how can I calculate how much that is?
I ran with 90V and 90minutes! but results were weird. I also tried 75V 60 minutes, didn't get the optimal results either meaning the 18s and 28s do not separate.
what is the problem?
I am trying to run RNA on 1% agarose/formaldehyde gel using 5x MOP buffer and SybrSafe staining instead of ethidium bromide.
what is the proper voltage and time? it says 5-6V/cm, but how can I calculate how much that is?
I ran with 90V and 90minutes! but results were weird. I also tried 75V 60 minutes, didn't get the optimal results either meaning the 18s and 28s do not deparate.
what is the problem
Hello, I did multi-analyte ELISA to detect the concentrations of several cytokines, but how should I calculate the concentration as each well represents a different sample and a different cytokine. there are rows of negative control and positive controls but each is a different cytokine. I am confused.
Hi,
My samples (placental tissue) were collected and stored using RNALater. in the process of protein extraction and at the end, I was not able to dissolve the protein pallets in the homogenizing buffer.
Does RNAlater play a role? or what are some possible explanations?