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[[User:Dina|Dina Elantably, MD, MSc]][mailto:dina.antably@gmail.com]
[[User:Dina|Dina Elantably, MD, MSc]][mailto:dina.antably@gmail.com]<br />
 
 
 
<br />


* [[Cardiovascular|CVS]]<ref name="pmid255232322">{{cite journal| author=Spicer DE, Hsu HH, Co-Vu J, Anderson RH, Fricker FJ| title=Ventricular septal defect. | journal=Orphanet J Rare Dis | year= 2014 | volume= 9 | issue=  | pages= 144 | pmid=25523232 | doi=10.1186/s13023-014-0144-2 | pmc=4316658 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25523232  }}</ref>
* [[Cardiovascular|CVS]]<ref name="pmid255232322">{{cite journal| author=Spicer DE, Hsu HH, Co-Vu J, Anderson RH, Fricker FJ| title=Ventricular septal defect. | journal=Orphanet J Rare Dis | year= 2014 | volume= 9 | issue=  | pages= 144 | pmid=25523232 | doi=10.1186/s13023-014-0144-2 | pmc=4316658 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=25523232  }}</ref>
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Atrial fibrillation
Atrial fibrillation


==Insulin==
==Functions==
#Bind insulin receptors
##inducing glucose uptake into insulin dependent tissue
##gene transcription
:glucose is the major regulator of insulin release to incretins.
Diabetes mellitus
It could be due to genetic , enviromental or immune defects.
----
'''''Regulation of insulin'''''
{{cquote|Do or Die!}}
<br />
<font color="red">proinsulin and c-peptide</font>


==References==
==References==
{{reflist}}
{{reflist}}

Revision as of 03:31, 14 May 2020

Dina Elantably, MD, MSc[1]

AF

Atrial fibrillation

Insulin

Functions

  1. Bind insulin receptors
    1. inducing glucose uptake into insulin dependent tissue
    2. gene transcription
glucose is the major regulator of insulin release to incretins.

Diabetes mellitus It could be due to genetic , enviromental or immune defects.


Regulation of insulin

Do or Die!


proinsulin and c-peptide

References

  1. Spicer DE, Hsu HH, Co-Vu J, Anderson RH, Fricker FJ (2014). "Ventricular septal defect". Orphanet J Rare Dis. 9: 144. doi:10.1186/s13023-014-0144-2. PMC 4316658. PMID 25523232.