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عنوان
Nörominidaz 1 ve gm3 sentaz enzimlerinin glikolipit metabolizmasındaki birleşik biyolojik rolünün araştırılması

پدید آورنده
Can, Melike

موضوع
Genetics,Molecular biology

رده

کتابخانه
Center and Library of Islamic Studies in European Languages

محل استقرار
استان: Qom ـ شهر: Qom

Center and Library of Islamic Studies in European Languages

تماس با کتابخانه : 32910706-025

NATIONAL BIBLIOGRAPHY NUMBER

Number
TL58119

LANGUAGE OF THE ITEM

.Language of Text, Soundtrack etc
انگلیسی

TITLE AND STATEMENT OF RESPONSIBILITY

Title Proper
Nörominidaz 1 ve gm3 sentaz enzimlerinin glikolipit metabolizmasındaki birleşik biyolojik rolünün araştırılması
General Material Designation
[Thesis]
First Statement of Responsibility
Can, Melike
Subsequent Statement of Responsibility
Seyrantepe, Volkan

.PUBLICATION, DISTRIBUTION, ETC

Name of Publisher, Distributor, etc.
Izmir Institute of Technology (Turkey)
Date of Publication, Distribution, etc.
2020

GENERAL NOTES

Text of Note
158 p.

DISSERTATION (THESIS) NOTE

Dissertation or thesis details and type of degree
Master's
Body granting the degree
Izmir Institute of Technology (Turkey)
Text preceding or following the note
2020

SUMMARY OR ABSTRACT

Text of Note
Gangliosides are sialic acid-containing glycosphingolipids, and commonly expressed in nervous system. GM3 Synthase is responsible for production of GM3 ganglioside known as precursor of a- and b- series gangliosides. Sialidases catalyze removing of sialic acid residues from sialoglycoconjugates and classified based on subcellular localization. Lysosomal Neu1 sialidase is responsible for catabolism of glycolipids, glycoproteins and oligosaccharides. Mutations of lysosomal Neu1 sialidase cause sialidosis and Neu1-/- mice mimic symptoms seen in patients. Glycosphingolipid accumulation in visceral organs of sialidosis patients was notified previously, and it was also reported the GM3 ganglioside as substrate of lysosomal sialidase in vitro. However, effect of Neu1 sialidase in the case of complex ganglioside deficiency in brain remains unclear. In the concept of research, we aimed to understand biological role of lysosomal Neu1 sialidase alone and combined with GM3S in ganglioside metabolism in vivo. In accordance with this purpose, cortex, cerebellum and thalamus tissues of 2- and 5-month old Neu1-/-GM3S-/-, Neu1-/- and GM3S-/- mice were compared with age-matched control group using molecular biological, histological, immunohistochemistry and behavioral analyses. Alterations in ganglioside metabolism, oligosaccharide pattern and cellular processes (ER-oxidative stress, apoptosis), structural abnormalities, glycoconjugate accumulation, loss of neurons and oligodendrocytes in addition to age dependent behavioral impairments in motor function, memory and muscle strength were demonstrated in single and double knock-out mice. In regard of these results, we have concluded that altered glycosphingolipid metabolism with accumulated secondary metabolites like oligosaccharides affect cellular processes and brain pathology resulting in behavioral abnormalities in age dependent and region specific manner.

UNCONTROLLED SUBJECT TERMS

Subject Term
Genetics
Subject Term
Molecular biology

PERSONAL NAME - PRIMARY RESPONSIBILITY

Can, Melike

PERSONAL NAME - SECONDARY RESPONSIBILITY

Seyrantepe, Volkan

CORPORATE BODY NAME - SECONDARY RESPONSIBILITY

Izmir Institute of Technology (Turkey)

ELECTRONIC LOCATION AND ACCESS

Electronic name
 مطالعه متن کتاب 

p

[Thesis]
276903

a
Y

Proposal/Bug Report

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