User:Z5059996

From Embryology
    2017 Project Groups
Group 1 Group 2 Group 3 Group 4 Group 5 Group 6

Z5177691

Z5178570

Z5093005

Z5059696

Z5059949

Z5178275

Z5178407

Z5076039

Z5017644

Z5015446

Z5178463

Z5076019

Z5059996

Z5076466

Z5018962

Z5177670

Z5117343

Z5075309

Z5075778

Z3416557

Z5178462

Z5059373

Z5114217

Z5062492

Z5076351

Z5177699

Z5113034

Z5114433

Z5076158

Z5018156

Mark Hill - Lab 1 page

Student Page Here is the Student Page demonstration page I showed in the Practical class.

Use this page to practice editing and don't forget to add a topic to the 2017 Group Project 3 page.

Chicken embryo E-cad and P-cad gastrulation.png

Chicken embryo E-cadherin and P-cadherin in gastrulation[1]

 2017 ANAT2341 - Timetable | Course Outline | Group Projects | Moodle | Tutorial 1 | Tutorial 2 | Tutorial 3

Labs: 1 Fertility and IVF | 2 ES Cells to Genome Editing | 3 Preimplantation and Early Implantation | 4 Reproductive Technology Revolution | 5 Cardiac and Vascular Development | 6 CRISPR-Cas9 | 7 Somitogenesis and Vertebral Malformation | 8 Organogenesis | 9 Genetic Disorders | 10 Melanocytes | 11 Stem Cells | 12 Group

Lectures: 1 Introduction | 2 Fertilization | 3 Week 1/2 | 4 Week 3 | 5 Ectoderm | 6 Placenta | 7 Mesoderm | 8 Endoderm | 9 Research Technology | 10 Cardiovascular | 11 Respiratory | 12 Neural crest | 13 Head | 14 Musculoskeletal | 15 Limb | 16 Renal | 17 Genital | 18 Endocrine | 19 Sensory | 20 Fetal | 21 Integumentary | 22 Birth | 23 Stem cells | 24 Revision

 Student Projects: 1 Cortex | 2 Kidney | 3 Heart | 4 Eye | 5 Lung | 6 Cerebellum


Criteria Strengths Weaknesses
1. The choice of content shows a good understanding of the topic area Kidney development was done well Current research was not mentioned



Peer Reviews

Marking Criteria

Group Assessment Criteria (modified and condensed from the student page)


1. The choice of content shows a good understanding of the topic area

  • The choice of content, headings and sub-headings, diagrams, tables, graphs show a good understanding of the topic area
  • Project sub-heading structure is appropriate
  • No key topic areas have been missed.


2. Content is correctly cited and referenced

  • Text within the project page is correctly cited.
  • Research articles and reviews can both be used, but are clearly identified.
  • Images within the project page is correctly cited.
  • Reference list does not contain multiple copies of the same article.


3. The wiki has an element of teaching at a peer level

  • 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.
  • The content has been designed for an university undergraduate science student level.
  • Acronyms and terms are well explained.
  • Image summaries include a useful description in the context of the project page and not simply the original legends (though these can be included).


4. Relates the topic and content of the Wiki entry to learning aims of embryology

  • Well-structured project page showing a broad understanding of embryological development.
  • Includes relevant historic and current research.
  • Molecular signaling mechanisms are included within the project page.


5. The content of the wiki should demonstrate to the reader that your group has researched adequately on this topic

  • 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.
  • Includes links to other UNSW Embryology related topic/content pages.


Suggested topic sub-headings (obtained from the student page)

  • Developmental origin
  • Developmental timeline
  • Key discoveries
  • Developmental signaling processes
  • Identify review and research articles
  • Current research
  • Animal models
  • Abnormal development
  • Future questions

Group 1: Cerebral Cortex

Criteria Strengths Weaknesses
1. The choice of content shows a good understanding of the topic area The developmental origin of the cerebral cortex is addressed well under the sub-heading ‘Early development of the brain’.


The development timeline of the cerebral cortex is described clearly and in detail in the table of the ‘Timeline of corticogenesis’.

Abnormal development of the cerebral cortex and the associated conditions are covered in an immense amount of detail. The accompanying images and videos enhance the written information, as well as making it easier for the reader to comprehend. In addition, the sub-headings of this section compartmentalize the congenital diseases in a logical manner that highlights the link between abnormal development and specific diseases.

There are several key topic areas missing from the page:
  • There is no section covering key historical discoveries relevant to the cerebral cortex and its embryological development.
  • There is no information relating to developmental signalling processes
  • There is no section on current research in fields relevant to the embryological development of the cerebral cortex.
  • There is no section on animal models that have been used to advance scientific understanding of the cerebral cortex.
  • There is no section on future questions regarding the development of the cerebral cortex.
  • A glossary of terms has not been included.

Some sections that have been included are somewhat irrelevant to the subject matter. For example, there is a large (unfinished) section on the anatomy and functions of the cerebral cortex. While it is important to provide a bit of an anatomical background on the subject, it shouldn’t be a major focus of this assignment. Focus more on the sections mentioned above, and keep the project focused on the embryology of the cerebral cortex.

2. Content is correctly cited and referenced There have been attempts at referencing throughout the assignment. A reference list has been produced and appears mostly correct. References have not been repeated throughout the list.

Peer-reviewed primary research articles have been used in this assignment.

The student-drawn image has been cited correctly, as have most of the images used in the ‘abnormal development’ section.

Overall, referencing in this assignment is very poor. Most of the content is completely devoid of any references (see ‘introduction’, ‘anatomy of the cortex’ and ‘abnormal development), and sections that have been referenced have been referenced “by paragraph” (see ‘timeline of corticogenesis’)


Many of the sources used in this assignment are inappropriate and/or unreliable. Try to rely more on primary research articles and less on textbooks or websites.

Many of the images have been cited incorrectly and used without permission. Remember to include the full reference, the original summary and the copyright license information for each image.

3. The wiki has an element of teaching at a peer level The information presented is mostly at a level appropriate for peers. Images and hand-drawn diagrams have been included to facilitate the readers understanding of the subject matter. Some of the images contain useful descriptions of the subject matter, and aid in understanding of the topic. Many of the acronyms and terms used in this assignment are not well explained. Include a glossary of terms to make some of the content easier to follow and understand.
4. Relates the topic and content of the Wiki entry to learning aims of embryology The development of the cerebral cortex was covered extensively, which is a very important learning aim of embryology. There are certain learning aims of embryology that have not been included in this assignment, such as developmental signaling processes (see criteria 1 for more information). There has been no discussion of relevant historical or current research (adding in the subheadings “key developments” and “current research” would help rectify this).
5. The content of the wiki should demonstrate to the reader that your group has researched adequately on this topic Certain aspects have been researched and presented well (such as embryological development).

Links to other pages of the UNSW embryology wiki have been included, however they have been used as references rather than just links.

Information from the UNSW embryology wiki has been used as direct sources of information. Instead they should be included to relate this particular wiki page to other areas of learning.

The small number of sources cited in the reference list demonstrates a poor and narrow approach to researching this topic. A greater library of sources should be used to create this page (mainly primary research articles.

Cardiac Septation

This stage of heart morphogenesis refers to the development of the four main cardiac chambers from the primitive atrium and ventricle. Cardiac septation is comprised of three main events:

  • Division of the atrioventricular canal
  • Atrial septation
  • Ventricular septation


Division of the atrioventricular canal

Division of the atrioventricular canal (AVC) begins with the formation of the superior and inferior endocardial cushions, which are located on the dorsal and ventral aspects of the AVC respectively.[2] These cushions develop as mesenchymal cells invade and proliferate within swollen regions of cardiac jelly of the AVC; this mesenchyme is derived from endothelial cells that have transdifferentiated via the process of epithelial-mesenchymal transformation (EMT). Throughout the fifth week of development, the endocardial cushions project inwards and eventually fuse to partition the AVC into the left and right atrioventricular canals [1,2]. These canals will serve as the orifices in which the tricuspid and mitral valves are situated [1,2].

Atrial septation

As the AVC is undergoing division, a muscular outgrowth, referred to as the septum primum, extends inferiorly from the roof of the primordial atrium [3]. This septum partially divides the atrial chamber into left and right halves, leaving a temporary communication located between the inferior border of septum primum and the endocardial cushions known as the foramen primum [1]. As the size of the foramen primum diminishes, perforations in the superior portion of the septum primum develop as a result of apoptosis, forming a second communication between the atrial chambers called the foramen secundum [2]. Concurrently, an additional muscular septum, known as the septum secundum, projects inferiorly to the right of the septum primum [1]. Eventually, the septum secundum will extend beyond the length of the foramen secundum, generating a partial division of the atria that forms the upper boundary of the foramen ovale [3]. The development of the foramen ovale is critical as it allows oxygen-rich blood from the placenta to bypass pulmonary circulation of the embryo and directly enter systemic circulation [4]. Following birth, the foramen ovale is obliterated as the septum primum and septum secundum fuse, resulting in complete formation of the interatrial septum [1].

Stages of Atrial Septation.png


Ventricular septation

As with atrial septation, differentiation of the ventricles is initiated within week 4 of development [1]. A muscular ridge, referred to as the interventricular septum primordium, develops and extends superiorly from the caudal aspect of the primitive ventricular chamber [2]. Growth of the septum is attributed to the expansion of the ventricles, which involves the development of muscular trabeculae as cardiomyocytes proliferate within the chamber walls [3]. The end result is a partial division between the left and right ventricles, which forms the muscular portion of the interventricular septum [2]. A communication between the ventricles, known as the interventricular foramen, remains until approximately week 7 of development [5]. The foramen is obliterated by the fusion of the septum intermedium and the bulbar ridges of the bulbus cordis; this constitutes the membranous portion of the interventricular septum [1].

Abnormal Development

Ventricular Septal Defect

[1] [2]

Atrial Septal Defect

References

  1. <pubmed>27097030</pubmed>
  2. <pubmed>PMC3424040</pubmed>