Marion Kubitza
Overview
Explore the profile of Marion Kubitza including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
108
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0
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Recent Articles
1.
Gross S, Danielyan L, Buechler C, Kubitza M, Klein K, Schwab M, et al.
Int J Mol Sci
. 2024 Aug;
25(16).
PMID: 39201455
Amyloid beta (Aβ) plays a major role in the pathogenesis of Alzheimer's disease and, more recently, has been shown to protect against liver fibrosis. Therefore, we studied Aβ-42 levels and...
2.
Schilcher K, Dayoub R, Kubitza M, Riepl J, Klein K, Buechler C, et al.
Int J Mol Sci
. 2023 Sep;
24(17).
PMID: 37686029
Metabolic dysfunction-associated steatotic liver disease (MASLD) comprises a spectrum of liver diseases, ranging from liver steatosis to metabolic dysfunction-associated steatohepatitis (MASH), increasing the risk of developing cirrhosis and hepatocellular carcinoma...
3.
Nimphy J, Ibrahim S, Dayoub R, Kubitza M, Melter M, Weiss T
Int J Mol Sci
. 2023 May;
24(9).
PMID: 37175814
Inflammasomes and innate immune cells have been shown to contribute to liver injury, thereby activating Kupffer cells, which release several cytokines, including IL-6, IL-1ß, and TNFα. Augmenter of liver regeneration...
4.
Grosch M, Brunner K, Ilyaskin A, Schober M, Staudner T, Schmied D, et al.
J Cell Sci
. 2021 Aug;
134(16).
PMID: 34345895
Mutations in the PKD2 gene cause autosomal-dominant polycystic kidney disease but the physiological role of polycystin-2, the protein product of PKD2, remains elusive. Polycystin-2 belongs to the transient receptor potential...
5.
Burghardt T, Kastner J, Suleiman H, Rivera-Milla E, Stepanova N, Lottaz C, et al.
J Am Soc Nephrol
. 2013 Aug;
24(11):1830-48.
PMID: 23990680
Mutations of the LMX1B gene cause nail-patella syndrome, a rare autosomal-dominant disorder affecting the development of the limbs, eyes, brain, and kidneys. The characterization of conventional Lmx1b knockout mice has...
6.
Osten L, Kubitza M, Gallagher A, Kastner J, Olbrich H, de Vries U, et al.
Histochem Cell Biol
. 2009 Apr;
132(2):199-210.
PMID: 19381676
Nephronophthisis belongs to a family of recessive cystic kidney diseases and may arise from mutations in multiple genes. In this report we have used a spontaneous mouse mutant of type...
7.
Pina A, Kubitza M, Brawanski A, Tombran-Tink J, Kloth S
Cell Tissue Res
. 2007 May;
329(2):329-38.
PMID: 17497179
Inhibitors and stimulators of endothelial cell growth are essential for the coordination of blood vessel formation during organ growth and development. In the adult kidney, one of the major inhibitors...
8.
Rothoerl R, Schebesch K, Kubitza M, Woertgen C, Brawanski A, Pina A
Cerebrovasc Dis
. 2006 May;
22(2-3):143-9.
PMID: 16691023
Background: The pathophysiology of ischemic cerebral lesions following aneurysmal subarachnoid hemorrhage (SAH) is poorly understood. There is growing evidence that inflammatory reactions could be involved in the pathogenesis of such...
9.
Proescholdt M, Mayer C, Kubitza M, Schubert T, Liao S, Stanbridge E, et al.
Neuro Oncol
. 2005 Oct;
7(4):465-75.
PMID: 16212811
Malignant brain tumors exhibit distinct metabolic characteristics. Despite high levels of lactate, the intracellular pH of brain tumors is more alkaline than normal brain. Additionally, with increasing malignancy, brain tumors...