Difference between revisions of "Molecular pathology"

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split-out cytogenetics
(split-out cytogenetics)
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==Cytogenetics==
==Cytogenetics==
===General===
{{Main|Cytogenetics}}
*Large changes (chromosomal).
This deals with karyotyping and ISH.
**Maximum resolution 3-4 megabase pairs (3-4 million base pairs); may be less - dependent on band density.<ref>{{Ref WMSP|695}}</ref>
*Morphologic data.
 
===Techniques===
*ISH = in situ hybridization.
**FISH = fluorescent in situ hybridization.
**SISH = silver in situ hybridization.<ref>URL: [http://www.immunoportal.com/modules.php?name=News&file=article&sid=186 http://www.immunoportal.com/modules.php?name=News&file=article&sid=186]. Accessed on: 2 May 2011.</ref>
*Karyotyping.
 
====Karyotyping====
What?
*Metaphase nuclei.
 
How?
*Chromosomes are identified by:
**Size (chromosome 1 = largest, chromosome 22 = smallest).
**Position of centromere.
**Banding pattern - using (special) stains:
***Several different techniques (stains) are used:<ref>URL: [http://www.ncbi.nlm.nih.gov/pmc/articles/PMC355922/ http://www.ncbi.nlm.nih.gov/pmc/articles/PMC355922/]. Accessed on: 10 May 2011.</ref>
****Examples: Q-banding (Q=Quinacrine), C-banding (C=constitutive heterchromatin), G-banding (G=Giemsa), R-banding (R=reverse).
*****Q-banding is the standard at UHN.
 
Image:
*[http://commons.wikimedia.org/wiki/File:NHGRI_human_male_karyotype.png Karyotype (WC)].
 
Notes:
*Quinacrine dye - AT-rich regions brighter than GC-rich regions.
 
====ISH====
*Usu. interphase nuclei.
 
May be prepared from:
*In situ paraffin sections (section 4 micrometers thick).
*Isolated nuclei (section 10 micrometers thick).
*Cytospin.
*Cultured cells.
 
=====Probe types=====
Types:
*Fusion (two colours).
*Breakapart (two colours).
*Deletion/duplication (e.g. trisomy).
 
Image:
*[http://commons.wikimedia.org/wiki/File:Bcrablmet.jpg Bcr-Abl translocation (WC)].


==Other garbage==
==Other garbage==
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