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Revision as of 15:14, 16 September 2011 by Z3329495 (talk | contribs) (→‎Lab 7)

Lab 4 Online Assessment

  1. The allantois, identified in the placental cord, is continuous with what anatomical structure?
  2. Identify the 3 vascular shunts, and their location, in the embryonic circulation.
  3. Identify the Group project sub-section that you will be researching. (Add to project page and your individual assessment page)



Group Project notes

Cardiomyopathy is caused by build up of iron overload in mitochondria producing excessive amounts of free radicals and anti-oxidants which damages cells. As Frataxin is most expressed in the heart, skeletal muscles, (as well as liver and pancreas)[1], it impacts most significantly on musculature and cardiac muscles.

Prior to 1996, FA could not be genetically confirmed and many older individuals with FA were not diagnosed with FA as their presenting age went over the norm of FA onset. Now with genetic testing available, the mean age of onset for symptoms of FA has increased[2].

Availability of genetic testing Diagnostic symptoms
Prior to genetic testing availability Only physical complaints, age of onset and typical FA progression could identify it as FA.
After genetic testing is available Physical complaints are used in conjunction with genetic testing to confirm FA. Due to genetic testing, [2]it has been discovered that FA can occur in individuals older than the typical diagnostic age (first two decades of life[3]).
  1. <pubmed>10633128 </pubmed>
  2. 2.0 2.1 <pubmed>21315377</pubmed>
  3. <pubmed>19283344</pubmed>
Diagnostic tool What it does How it diagnoses FRDA Image if available
Electromyogram (EMG) Measures the electrical activity of muscle cells by inserting needles into muscle fibers that is to be tested and asking the patient to tense the muscle[1]. EMG can detect denervation[1] such as present in motor neuron diseases or muscle denervation as present in FRDA.
Electrocardiogram (ECG) Provides graphic presentation of the electrical activity or beat pattern of the heart If T wave inversion is present, it may be an indication myocardial hypertrophy[2] which is a hallmark of cardiac involvment in FRDA. T wave inversions are also common findings in patients with FRDA[3].
File:Schematic ECG.jpg
Schematic drawing of ECG waves
Echocardiogram (ECHO) Records the position and motion of the heart muscle Identifies abnormalities in heart muscle such as hypertrophy of ventricles(useful for determining cardiac involvement)[4].
Blood tests Checks for elevated glucose levels (in the event of diabetes developing) and vitamin E levels as individuals with FRDA often have low Vitamin E serum levels [5] Blood tests work to identify any possible complication of FRDA (ie: diabetes) and identifies patients who require vitamin E supplements to increase the body's antioxidant capabilities[5].
Blood test results for glucose and iron
Magnetic resonance imaging (MRI) Provide brain and spinal cord images that are useful for ruling out other neurological conditions and confirming dorsal root degeneration. Changes in the dorsal root or related neural structures involved in motor coordination can be monitored and identified with MRI. In a recent pilot study, the globus pallidus (involved in motor coordination) was found to improve with iron-chelation treatment using MRI technology[6]. Another paper found that MRI may be a useful tool in diagnosing FRDA and allows researchers to track neural atrophy[7].
Computed tomography scans (CT scan) CT scans work similarly to the MRI in that it is used as an imaging tool to identify neurodegeneration. While CT scans can be used in a similar fashion to MRIs, it has been noted that CT scans only identified mild cerebellar atrophy in advanced patients perhaps due to low CT resolution in the neck[7].
Nerve conduction studies (NCS) Measures the speed with which nerves transmit impulses by using two electrodes (one to send the impulse and the other to measure the response)[1]. Nerve conduction studies determines how far and if neurodegeneration has occurred by analysing amplitude, latency, duration, and conduction. Each item assessed will inform the clinician of the number of nerve fibers activated, integrity of myelin sheaths or axonal loss[1]. FRDA diagnosis may be considered if nerve conduction studies indicates nerve degeneration.
Genetic Testing
Prenatal Testing


  1. 1.0 1.1 1.2 1.3 <pubmed>21894276</pubmed>
  2. <pubmed>19486532</pubmed>
  3. <pubmed>3593615</pubmed>
  4. <pubmed>2940284</pubmed>
  5. 5.0 5.1 <pubmed>11554913</pubmed>
  6. <pubmed>21791473</pubmed>
  7. 7.0 7.1 <pubmed>2759158</pubmed>

Lab 1

Questions

  1. Identify the origin of In Vitro Fertilization and the 2010 nobel prize winner associated with this technique.
  2. Identify a recent paper on fertilisation and describe its key findings.
  3. Identify 2 congenital anomalies.

Answers

  1. Robert G. Edwards won the 2010 Nobel Prize for his IVF work which led to the birth of the first IVF baby Louise Brown, born at the Royal Oldham Hospital Manchester, England.
  2. A recent paper on predicting how sucessful IVF treatment would be for specific individuals has come out with its finding that predetermined factors (such as maternal age, how long infertility has persisted for and if the maternal oocyte was used) can indicate the sucess of fertility treatment as opposed to a simple probability for a sucessful treatment. PLoS Medicine: Predicting Live Birth Preterm Delivery, and Low Birth Weight in Infants Born from In Vitro Fertilisation: A Prospective Study of 144,018 Treatment Cycles
  3. Downs Syndrome and hemophilia

--Z3329495 14:14, 28 July 2011 (EST)

--Z3329495 12:55, 28 July 2011 (EST)

--Mark Hill 10:07, 3 August 2011 (EST)These answers are fine.

Lab 2

--Z3329495 13:00, 4 August 2011 (EST)

Questions

  1. Identify the ZP protein that spermatozoa binds and how is this changed (altered) after fertilisation.
  2. Identify a review and a research article related to your group topic. (Paste on both group discussion page with signature and on your own page)

Answers

  1. the ZP protein that spermatozoa binds to is ZP3. After fertilisation, enzymes in the cortical reaction alters ZP3 so that it no longer binds to sperm.
  2. Angelman's Syndrome:

Review article: http://jmg.bmj.com/content/40/2/87.short Research article: http://jmg.bmj.com/content/38/12/834.abstract --Z3329495 12:07, 9 August 2011 (EST)

Lab 3

--Amanda Tan 11:07, 11 August 2011 (EST)

Differentially expressed RefSeq genes in human trisomy 21

Differentially expressed RefSeq genes in human trisomy 21.jpg


Differentially expressed RefSeq genes in human trisomy 21

Questions

  1. What is the maternal dietary requirement for late neural development?
  2. Upload a picture relating to you group project.

Answers

  1. Folate has been found to reduce the incidence of neural tube defects and many countries have fotified food staples (flour etc) with folic acid. A recent study found that more cases of neural tube defects can be avoided if more countries implemented policies to fortify foods with folic acid. Update on prevention of folic acid-preventable spina bifida and anencephaly.

Iodine also prevents Cretin from developing and has been recommended that pregnant women consume supplemented iodine. http://www.thyroid.org/professionals/publications/statements/documents/ATAIodineRec.pdf

  1. Pathogenesis of Friedreich Ataxia

Pathogenesis of Friedreich Ataxia.jpg


A model of Pathogenesis of Friedreich Ataxia

--z3329495 20:58, 13 August 2011 (EST)

--Mark Hill 12:22, 16 August 2011 (EST) Not bad and the image contains all the correct citation information. The file would more correctly be named "A Model of....."


Lab 4

--Z3329495 11:07, 18 August 2011 (EST)

Questions

  1. The allantois, identified in the placental cord, is continuous with what anatomical structure?
  2. Identify the 3 vascular shunts, and their location, in the embryonic circulation.
  3. Identify the Group project sub-section that you will be researching. (Add to project page and your individual assessment page)

Answers

  1. It is an invagination of the developing hindgut and is connected to the yolk sac via the connecting stalk.
  2. Foramen Ovale (between right and left atrium), Ductus arteriosus (connects pulmonary artery to aortic arch) and Ductus venosus (allow portal and umbilical veins to connect to inferior vena cava - lets oxygenated blood bypass liver)
  3. pahology of cardiomyopathy and musculature sections of Friedreich's Ataxia and parts of pathogenesis.

Lab 5

--z3329495 12:27, 25 August 2011 (EST)

Questions

  1. Which side (L/R) is most common for diaphragmatic hernia and why?

Answers

  1. left side is more common because during embryonic development the left pericardioperitoneal canal is much larger than the right side and is takes longer than the right side to close up.

Lab 6

--z3329495 11:08, 1 September 2011 (EST)

Questions

  1. What week of development do the palatal shelves fuse?
  2. What animal model helped elucidate the neural crest origin and migration of cells?
  3. What abnormality results from neural crest not migrating into the cardiac outflow tract?

Answers

  1. week 10 is when the palatal shelves fuse.
  2. Chicken-quail model - a genetic mix of chicken and quail allowed researchers to identify origin and migration of neural crest cells before fluorescent marking of genes were available.
  3. Shortening or truncation of cardiac outflow tract.

Lab 7

--z3329495 11:21, 15 September 2011 (EST)

Questions

  1. Are satellite cells (a) necessary for muscle hypertrophy and (b) generally involved in hypertrophy?
  2. Why does chronic low frequency stimulation cause a fast to slow fibre type shift?
  3. Evaluation of Trisomy 21

Answers

  1. a) No satellite cells are not necessary for muscle hypertrophy b)yes, it is generally involved in hypertrophy
  2. Chronic low frequency stimulation is found in slow fiber type shifts such as in tonically active muscles of the back and stimulating fast fibers with chronic low frequency stimulation can cause the type of fiber to respond to the stimulus by its change from a fast to slow fiber type. However, the change will only be in small increments and total change of fast to slow fibers will more likely happen as a mix of fast and slow fibers with slow fibers dominating.
  3. Group Assessment Criteria
  • The key points relating to the topic that your group allocated are clearly described.
  • The choice of content, headings and sub-headings, diagrams, tables, graphs show a good understanding of the topic area.
  • Content is correctly cited and referenced.
  • The wiki has an element of teaching at a peer level using the student's own innovative diagrams, tables or figures and/or using interesting examples or explanations.
  • Evidence of significant research relating to basic and applied sciences that goes beyond the formal teaching activities.
  • Relates the topic and content of the Wiki entry to learning aims of embryology.
  • Clearly reflects on editing/feedback from group peers and articulates how the Wiki could be improved (or not) based on peer comments/feedback. Demonstrates an ability to review own work when criticised in an open edited wiki format. Reflects on what was learned from the process of editing a peer's wiki.
  • Evaluates own performance and that of group peers to give a rounded summary of this wiki process in terms of group effort and achievement.
  • The content of the wiki should demonstrate to the reader that your group has researched adequately on this topic and covered the key areas necessary to inform your peers in their learning.
  • Develops and edits the wiki entries in accordance with the above guidelines.

Lab 8

Lab 9

Lab 10