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| =Oral presentation of group projects part 1=
| | Lab 7 |
| ==There will be no short answer/multiple choice test this week and next week due to time constraints==
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| However, please arrive on-time as we need the whole 2 hours to complete the oral presentations
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| ===Dividing the tasks===
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| '''The oral and written reports should be divided into 3 equal sections.'''
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| #Developmental abnormalities of the disease, diagnosis and human genetics
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| #Genetics of the relevant mouse mutants and the resulting developmental abnormalities
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| #Using the mouse mutants to understand the developmental, cellular and molecular basis of the disease
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| Each member of the group should assume responsibility for one of these sections. The marks will be divided into 2 parts. A mark for the overall project and a mark for the section for which you have taken responsibility. Therefore, it is important to edit each others work and ensure that the overall product is integrated and well finished. Each person should identify which section they have taken chief responsibility for.
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| Groups that only have 2 members should divide their work by one student taking responsibility for part 1 and the other part 2, then part 3 should be shared equally. During the oral presentation, only one student should present part 3.
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| ===Topics===
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| The selected topics will be updated when they have been chosen
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| {| class="pretty table"
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| |-bgcolor="lightsteelblue"
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| | <center>''' System '''</center>
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| | <center>''' Human disease '''</center>
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| | <center>''' OMIM '''</center>
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| | <center>''' Gene '''</center>
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| | <center>''' Relevant mouse models '''</center>
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| |-
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| | Skin
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| | Gorlin Sydndrome/Basal Cell Nevus Syndrome
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| | 109400
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| | ''PTCH1''
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| | K14-Cre Ptc mutants
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| |-
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| | Craniofacial
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| | Treacher-Collins Syndrome 1
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| | 154500
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| | ''TCOF1''
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| | Tcof1 mutants
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| |-
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| | Limb development
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| | Split-hand/foot malformation 1 with sensorineural hearing loss
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| | 220600
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| | ''DLX5''
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| | Dlx5/6 mutants
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| |-
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| | Gonadal development
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| | Campomelic Dysplasia
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| | 114290
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| | ''SOX9''
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| | Sox9 transgenics/LOF mutants
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| |-
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| | Heart development
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| | Holt-Oram Syndrome
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| | 142900
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| | ''TBX5''
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| | Tbx5 mutants
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| |-
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| | Kidney development
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| | Polycystic kidney disease, adult type I
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| | 173900
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| | ''PKD1''
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| | Pkd1,2 mutants
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| | |
| |-
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| |Multisystemic
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| |DiGeorge Syndrome
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| |188400
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| | ''TBX1''
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| | Multiple
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| |-
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| |Eye
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| |Aniridia
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| |106210
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| |''PAX6''
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| |Small eye (Sey)
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| |-
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| |Blood
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| |Omenn Syndrome
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| |603554
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| |''RAG1'' and ''RAG2''
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| |''Rag1'' mutant and ''Rag2'' knockin
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| |-
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| |Bone
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| |Cleidocranial Dysplasia
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| |119600
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| |''RUNX2''
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| |''Runx2'' mutant and knockout
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| |-
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| |Neural tube
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| |Neural tube defects including spina bifida
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| |182940
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| |''T''
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| |Tailless Brachyury mutants
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| |-
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| |Sexual differentiation
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| |Androgen Insensitivity Syndrome
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| |300068
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| |''AR''
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| |Tfm mice
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| |-
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| |Neural Crest Derivatives
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| |Waardenburg Syndrome Type 4
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| |277580
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| |''EDNRB''
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| |Endothelin-B receptor mutant
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| |}
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