Marijana Samardzija
Overview
Explore the profile of Marijana Samardzija including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
64
Citations
1730
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Ebner L, Karademir D, Notzli S, Wogenstein G, Samardzija M, Grimm C
Exp Eye Res
. 2024 Dec;
251:110190.
PMID: 39638278
Restricted oxygen supply in the aging eye may lead to hypoxic conditions in the outer retina and contribute not only to physiological aging but also to nonhereditary degenerative retinal diseases....
2.
Todorova V, Stauffacher M, Ravotto L, Notzli S, Karademir D, Ebner L, et al.
Mol Neurodegener
. 2023 Mar;
18(1):15.
PMID: 36882871
Background: Major retinal degenerative diseases, including age-related macular degeneration, diabetic retinopathy and retinal detachment, are associated with a local decrease in oxygen availability causing the formation of hypoxic areas affecting...
3.
Todorova V, Merolla L, Karademir D, Wogenstein G, Behr J, Ebner L, et al.
Sci Rep
. 2022 Nov;
12(1):20195.
PMID: 36424523
Understanding the physiology of the retina, and especially of the highly polarized photoreceptors, is essential not only to broaden our knowledge of the processes required for normal vision, but also...
4.
Kaplan L, Drexler C, Pfaller A, Brenna S, Wunderlich K, Dimitracopoulos A, et al.
Glia
. 2022 Nov;
71(2):391-414.
PMID: 36334068
The human macula is a highly specialized retinal region with pit-like morphology and rich in cones. How Müller cells, the principal glial cell type in the retina, are adapted to...
5.
Ail D, Samardzija M, Chang A, Keck J, Reddel R, Grimm C
Front Neurosci
. 2022 Jul;
16:882559.
PMID: 35812222
The quest for neuroprotective factors that can prevent or slow down the progression of retinal degeneration is still ongoing. Acute hypoxic stress has been shown to provide transient protection against...
6.
Miller A, Fuller-Carter P, Masarini K, Samardzija M, Carter K, Rashwan R, et al.
Cell Mol Life Sci
. 2022 Jul;
79(8):409.
PMID: 35810394
Inherited retinal diseases (IRDs) are a heterogeneous group of blinding disorders, which result in dysfunction or death of the light-sensing cone and rod photoreceptors. Despite individual IRDs (Inherited retinal disease)...
7.
Kiessling E, Peters F, Ebner L, Merolla L, Samardzija M, Baumgartner M, et al.
Biochim Biophys Acta Gen Subj
. 2022 May;
1866(9):130175.
PMID: 35636712
The MMACHC gene encodes for an enzyme involved in intracellular vitamin B metabolism, and autosomal recessive defects in MMACHC represent the most common disorder of intracellular vitamin B metabolism. Recent...
8.
Karademir D, Todorova V, Ebner L, Samardzija M, Grimm C
BMC Biol
. 2022 Apr;
20(1):86.
PMID: 35413909
Background: In inherited retinal disorders such as retinitis pigmentosa (RP), rod photoreceptor-specific mutations cause primary rod degeneration that is followed by secondary cone death and loss of high-acuity vision. Mechanistic...
9.
Zang J, Gesemann M, Keim J, Samardzija M, Grimm C, Neuhauss S
Elife
. 2021 Sep;
10.
PMID: 34550876
Eukaryotes generally display a circadian rhythm as an adaption to the reoccurring day/night cycle. This is particularly true for visual physiology that is directly affected by changing light conditions. Here...
10.
Kiessling E, Notzli S, Todorova V, Forny M, Baumgartner M, Samardzija M, et al.
Biochim Biophys Acta Mol Basis Dis
. 2021 Jun;
1867(10):166201.
PMID: 34147638
Combined methylmalonic aciduria with homocystinuria (cblC type) is a rare disease caused by mutations in the MMACHC gene. MMACHC encodes an enzyme crucial for intracellular vitamin B metabolism, leading to...