ord Forum Junior
Topics: 15 Posts: 30
| | 07/01/06 - 01:35 PM  
 
   
 
|   #1 |
mutations in the cystic fibrosis transmembrane conductance regulator(CFTR) protein alter which of the following ion transport mechanisms? a)Ca2+ activated Cl-secretion b)Ca2+ activated Cl-uptake C)cyclic Amp(cAMP) stimulated Cl-secretion d)cAMP stimulated Na+secretion e)cAMP stimulated Na+uptake
|
| ord Forum Junior
Topics: 15 Posts: 30
| | 07/01/06 - 01:35 PM  
 
   
 
|   #2 |
Is it A?
Edited by ord on 07/01/06 - 01:45 PM
|
| alpha12 Forum Senior
Topics: 6 Posts: 70
| | 07/01/06 - 05:42 PM  
 
   
 
|   #3 |
I'd go with C, but not sure. I guess the second messenger should be the same than secretin (cAMP)
___________________ Flex
|
| robin082006 Forum Hero

Topics: 471 Posts: 5,125
| | 07/01/06 - 06:30 PM  
 
   
 
|   #4 |
THIS HAS BEEN DISCUSSED SOME AGRED WITH C, SOME WITH D I GO WITH C
___________________ The Key to Succeed is Patience.
|
| Cedrick Forum Fanatic

Topics: 320 Posts: 1,928
| | 07/04/06 - 11:40 AM  
 
   
 
|   #5 |
C
|
| waqastariq
| | 07/04/06 - 03:50 PM  
 
   
 
|   #6 |
it's C people
|
| waqastariq
| | 07/04/06 - 03:52 PM  
 
   
 
|   #7 |
lemme find some links for it then..
|
| waqastariq
| | 07/04/06 - 03:52 PM  
 
   
 
|   #8 |
http://humrep.oxfordjournals.org/cgi/content/abst... http://www.bioscience.org/knockout/cftr.htm
|
| zzzz Forum Elite
Topics: 9 Posts: 167
| | 07/08/06 - 03:46 PM  
 
   
 
|   #9 |
i think it was in kaplan d bank & it is c .
|
| tolito Forum Fanatic
Topics: 119 Posts: 2,164
| | 07/11/06 - 05:32 PM  
 
   
 
|   #10 |
C. cl secretion occurs via camp activation of protein kinase A. prot kin A phosphorylates CFTR resulting in opening of cl channel.... source, robbins.
___________________ It has been a looooong hard journey but I am inches away from my destination...
|
| dericanthony Forum Newbie
Topics: 2 Posts: 28
| | 07/21/06 - 05:37 AM  
 
   
 
|   #11 |
very resorceful wasaspas
|
| what to do Forum Senior

Topics: 29 Posts: 88
| | 12/06/06 - 09:26 PM  
 
   
 
|   #12 |
ans C there is gene mutation in long arm of chromosome 7 (7q21.3 --> 7q22.1) the commonest abnormality is a specific deletion in position 508 in the aminoacid sequence which results in defective CFTR . it is a Cl channel. the mutation alters the secondary and tertiary structure of the protein, leading to the failure of the opening of the of the chloride channel in response to elevated cAMP in epithelial cells. this results the decreased excreation of Cl and increased reabsorption of Na. 30% ashkenazi, 50% european, 70% USA
___________________ saif
|
| what to do Forum Senior

Topics: 29 Posts: 88
| | 12/06/06 - 09:26 PM  
 
   
 
|   #13 |
ans C there is gene mutation in long arm of chromosome 7 (7q21.3 --> 7q22.1) the commonest abnormality is a specific deletion in position 508 in the aminoacid sequence which results in defective CFTR . it is a Cl channel. the mutation alters the secondary and tertiary structure of the protein, leading to the failure of the opening of the of the chloride channel in response to elevated cAMP in epithelial cells. this results the decreased excreation of Cl and increased reabsorption of Na. 30% ashkenazi, 50% european, 70% USA
___________________ saif
|
| Ancylostoma Forum Guru
Topics: 42 Posts: 642
| | 12/25/06 - 11:39 AM  
 
   
 
|   #14 |
C is right, it cant be d because normall there is secretion of cloride and reabsorbion of na. The clhorid keeps the water in the lumen. When there is a problem in secretion of chloride, there is nothing to keep the water on that side. the sodium is reabsorbed as it is normall, but because of lask of chloride water goes with it leading to thick secretions.
|
|
| |
| | | | | | | | | | | | | | |