Your browser does not allow JavaScript!
JavaScript is necessary for the proper functioning of this website. Please enable JavaScript or use a modern browser.
Open Science Slovenia
Open Science
DiKUL
slv
|
eng
Search
Browse
New in RUL
About RUL
In numbers
Help
Sign in
Molecular pathways involved in the development of congenital erythrocytosis
ID
Tomc, Jana
(
Author
),
ID
Debeljak, Nataša
(
Author
)
PDF - Presentation file,
Download
(1,83 MB)
MD5: E172E654ADD3E49571EB2A4E93E3CBF6
URL - Source URL, Visit
https://www.mdpi.com/2073-4425/12/8/1150
Image galllery
Abstract
Patients with idiopathic erythrocytosis are directed to targeted genetic testing including nine genes involved in oxygen sensing pathway in kidneys, erythropoietin signal transduction in pre-erythrocytes and hemoglobin-oxygen affinity regulation in mature erythrocytes. However, in more than 60% of cases the genetic cause remains undiagnosed, suggesting that other genes and mechanisms must be involved in the disease development. This review aims to explore additional molecular mechanisms in recognized erythrocytosis pathways and propose new pathways associated with this rare hematological disorder. For this purpose, a comprehensive review of the literature was performed and different in silico tools were used. We identified genes involved in several mechanisms and molecular pathways, including mRNA transcriptional regulation, post-translational modifications, membrane transport, regulation of signal transduction, glucose metabolism and iron homeostasis, which have the potential to influence the main erythrocytosis-associated pathways. We provide valuable theoretical information for deeper insight into possible mechanisms of disease development. This information can be also helpful to improve the current diagnostic solutions for patients with idiopathic erythrocytosis.
Language:
English
Keywords:
erythrocytosis
,
disease mechanisms
,
metabolomics
,
congenital
,
familial
,
signal transduction
,
transcriptomic
,
proteomic
Work type:
Article
Typology:
1.02 - Review Article
Organization:
MF - Faculty of Medicine
Publication status:
Published
Publication version:
Version of Record
Year:
2021
Number of pages:
20 str.
Numbering:
Vol. 12, iss. 8, art. 1150
PID:
20.500.12556/RUL-135705
UDC:
616.1
ISSN on article:
2073-4425
DOI:
10.3390/genes12081150
COBISS.SI-ID:
72028419
Publication date in RUL:
29.03.2022
Views:
747
Downloads:
111
Metadata:
Cite this work
Plain text
BibTeX
EndNote XML
EndNote/Refer
RIS
ABNT
ACM Ref
AMA
APA
Chicago 17th Author-Date
Harvard
IEEE
ISO 690
MLA
Vancouver
:
Copy citation
Share:
Record is a part of a journal
Title:
Genes
Shortened title:
Genes
Publisher:
Multidisciplinary Digital Publishing Institute (MDPI)
ISSN:
2073-4425
COBISS.SI-ID:
523100185
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:
01.08.2021
Secondary language
Language:
Slovenian
Keywords:
eritrocitoza
,
mehanizmi bolezni
,
metabolomika
Projects
Funder:
ARRS - Slovenian Research Agency
Project number:
L3-9279
Name:
Genetska osnova eritrocitoz v Sloveniji
Funder:
ARRS - Slovenian Research Agency
Project number:
P1-0390
Name:
Funkcijska genomika in biotehnologija za zdravje
Similar documents
Similar works from RUL:
Similar works from other Slovenian collections:
Back