Markus Schueler
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Explore the profile of Markus Schueler including associated specialties, affiliations and a list of published articles.
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41
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2813
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Recent Articles
1.
Boeckhaus J, Gale D, Simon J, Ding J, Zhang Y, Bergmann C, et al.
Kidney Int Rep
. 2024 Dec;
9(12):3490-3500.
PMID: 39698346
Introduction: Large-scale trials showed positive outcomes of sodium-glucose cotransporter-2 inhibitors (SGLT2i) in adults with chronic kidney disease (CKD). Whether the use of SGLT2i is safe and effective in patients with...
2.
Beagrie R, Thieme C, Annunziatella C, Baugher C, Zhang Y, Schueler M, et al.
Nat Methods
. 2023 Jun;
20(7):1037-1047.
PMID: 37336949
Technology for measuring 3D genome topology is increasingly important for studying gene regulation, for genome assembly and for mapping of genome rearrangements. Hi-C and other ligation-based methods have become routine...
3.
Gulluni F, Prever L, Li H, Krafcikova P, Corrado I, Lo W, et al.
Science
. 2021 Dec;
374(6573):eabk0410.
PMID: 34882480
Cytokinetic membrane abscission is a spatially and temporally regulated process that requires ESCRT (endosomal sorting complexes required for transport)–dependent control of membrane remodeling at the midbody, a subcellular organelle that...
4.
Mansour F, Boivin F, Shaheed I, Schueler M, Schmidt-Ott K
Int J Mol Sci
. 2021 Nov;
22(22).
PMID: 34830133
The primary cilium is found in most mammalian cells and plays a functional role in tissue homeostasis and organ development by modulating key signaling pathways. Ciliopathies are a group of...
5.
Schwarz H, Popp B, Airik R, Torabi N, Knaup K, Stoeckert J, et al.
Hum Mol Genet
. 2021 Nov;
31(9):1357-1369.
PMID: 34740236
Nephronophthisis-related ciliopathies (NPHP-RC) comprises a group of inherited kidney diseases, caused by mutations in genes encoding proteins localizing to primary cilia. NPHP-RC represents one of the most frequent monogenic causes...
6.
Wiesener A, Knaup K, Buttner-Herold M, Dieterle A, Stoeckert J, Riedl B, et al.
Am J Transplant
. 2019 Dec;
20(5):1410-1416.
PMID: 31814324
In light of the organ shortage, there is a great responsibility to assess postmortal organs for which procurement has been consented and to increase the life span of transplanted organs....
7.
Maurer M, Papotto N, Sertel-Nakajima J, Schueler M, de Col R, Mohrlen F, et al.
PLoS One
. 2019 Aug;
14(8):e0211175.
PMID: 31412038
Olfactory and trigeminal chemosensory systems reside in parallel within the mammalian nose. Psychophysical studies in people indicate that these two systems interact at a perceptual level. Trigeminal sensations of pungency...
8.
Airik R, Airik M, Schueler M, Bates C, Hildebrandt F
Kidney Int
. 2019 Jun;
96(2):320-326.
PMID: 31248650
Nephronophthisis is an autosomal recessive kidney disease with high genetic heterogeneity. Understanding the functions of the individual genes contributing to this disease is critical for delineating the pathomechanisms of this...
9.
Tiosano D, Baris H, Chen A, Hitzert M, Schueler M, Gulluni F, et al.
PLoS Genet
. 2019 Apr;
15(4):e1008088.
PMID: 31034465
PIK3C2A is a class II member of the phosphoinositide 3-kinase (PI3K) family that catalyzes the phosphorylation of phosphatidylinositol (PI) into PI(3)P and the phosphorylation of PI(4)P into PI(3,4)P2. At the...
10.
Widmeier E, Airik M, Hugo H, Schapiro D, Wedel J, Ghosh C, et al.
J Am Soc Nephrol
. 2019 Feb;
30(3):393-405.
PMID: 30737270
Background: Although studies have identified >55 genes as causing steroid-resistant nephrotic syndrome (SRNS) and localized its pathogenesis to glomerular podocytes, the disease mechanisms of SRNS remain largely enigmatic. We recently...