T. Hanck

发表

Peroxisome Proliferator-Activated Receptor (PPAR)-γ Positively Controls and PPARα Negatively Controls Cyclooxygenase-2 Expression in Rat Brain Astrocytes through a Convergence on PPARβ/δ via Mutual Control of PPAR Expression Levels

G. Reiser, M. Sergeeva, S. Aleshin, 2009, Molecular Pharmacology.

Research Article Endocytosis mechanism of P2Y 2 nucleotide receptor tagged with green fluorescent protein: clathrin and actin cytoskeleton dependence

G. Reiser, R. Schäfer, G. Weisman, 2005 .

Endocytosis mechanism of P2Y2 nucleotide receptor tagged with green fluorescent protein: clathrin and actin cytoskeleton dependence

G. Reiser, R. Schäfer, G. Weisman, 2005, Cellular and Molecular Life Sciences.

Hetero-oligomerization of the P2Y 11 and P2Y 1 receptor controls

G. Reiser, R. Schäfer, D. Ecke, 2020 .

Hetero-oligomerization of the P 2 Y 11 receptor with the P 2 Y 1 receptor controls the internalization and ligand selectivity of the P 2 Y 11 receptor

G. Reiser, R. Schäfer, M. Kassack, 2007 .

Interaction of the brain‐specific protein p42IP4/centaurin‐α1 with the peptidase nardilysin is regulated by the cognate ligands of p42IP4, PtdIns(3,4,5)P3 and Ins(1,3,4,5)P4, with stereospecificity

L. Hersh, G. Reiser, D. Walther, 2006, Journal of neurochemistry.

Lipid kinase and protein kinase activities of G-protein-coupled phosphoinositide 3-kinase gamma: structure-activity analysis and interactions with wortmannin.

R. Wetzker, R. Klinger, T. Hanck, 1997, The Biochemical journal.

Cellular expression and subcellular localization of the human Ins(1,3,4,5)P(4)-binding protein, p42(IP4), in human brain and in neuronal cells.

G. Reiser, F. Sedehizade, H. Bernstein, 2002, Brain research. Molecular brain research.

Oligomerization controls in tissue-specific manner ligand binding of native, affinity-purified p42(IP4)/centaurin alpha1 and cytohesins-proteins with high affinity for the messengers D-inositol 1,3,4,5-tetrakisphosphate/phosphatidylinositol 3,4,5-trisphosphate.

J. Vandekerckhove, J. Falck, G. Reiser, 2003, Biochimica et biophysica acta.

Recombinant p42IP4, a brain-specific 42-kDa high-affinity Ins(1,3,4,5)P4 receptor protein, specifically interacts with lipid membranes containing Ptd-Ins(3,4,5)P3.

Y. Chang, G. Reiser, J. Falck, 1999, European journal of biochemistry.

αA‐crystallin and αB‐crystallin, newly identified interaction proteins of protease‐activated receptor‐2, rescue astrocytes from C2‐ceramide‐ and staurosporine‐induced cell death

G. Reiser, T. Hanck, Rongyu Li, 2009, Journal of neurochemistry.

Identification of gene structure and subcellular localization of human centaurin α2, and p42IP4, a family of two highly homologueous, Ins 1,3,4,5‐P4‐/PtdIns 3,4,5‐P3‐binding, adapter proteins

G. Reiser, F. Sedehizade, T. Hanck, 2003, Journal of neurochemistry.

Polyoxometalates--potent and selective ecto-nucleotidase inhibitors.

C. Müller, J. Sévigny, K. Brylev, 2015, Biochemical pharmacology.

Imidazopyridine- and purine-thioacetamide derivatives: potent inhibitors of nucleotide pyrophosphatase/phosphodiesterase 1 (NPP1).

C. Müller, P. Herdewijn, J. Rozenski, 2014, Journal of medicinal chemistry.

p42IP4/Centaurin α1, a Brain-specific PtdIns(3,4,5)P3/Ins(1,3,4,5)P4-binding Protein: Membrane Trafficking Induced by Epidermal Growth Factor is Inhibited by Stimulation of Phospholipase C-coupled Thrombin Receptor

G. Reiser, F. Sedehizade, T. Hanck, 2005, Neurochemical Research.

Thiazolo[3,2-a]benzimidazol-3(2H)-one derivatives: Structure-activity relationships of selective nucleotide pyrophosphatase/phosphodiesterase1 (NPP1) inhibitors.

Piet Herdewijn, C. Müller, P. Herdewijn, 2016, Bioorganic & medicinal chemistry.

Gβγ Stimulates Phosphoinositide 3-Kinase-γ by Direct Interaction with Two Domains of the Catalytic p110 Subunit*

R. Wetzker, D. Leopoldt, B. Nürnberg, 1998, The Journal of Biological Chemistry.

Development of Potent and Selective Antagonists for the UTP-Activated P2Y4 Receptor.

C. Müller, Y. Baqi, Alexander Neumann, 2017, Journal of medicinal chemistry.

Cloning and characterization of a G protein-activated human phosphoinositide-3 kinase.

S. Volinia, B. Vanhaesebroeck, B. Nürnberg, 1995, Science.

Extracellular binding sites of positive and negative allosteric P2X4 receptor modulators.

V. Namasivayam, R. Hausmann, T. Hanck, 2022, Life sciences.

Rapid Ribosequencing – an Effective Diagnostic Tool for Detecting Microbial Infection

W. König, B. König, T. Hanck, 2001, Infection.

Hetero-oligomerization of the P2Y11 receptor with the P2Y1 receptor controls the internalization and ligand selectivity of the P2Y11 receptor.

G. Reiser, R. Schäfer, M. Kassack, 2008, The Biochemical journal.

Gbetagamma stimulates phosphoinositide 3-kinase-gamma by direct interaction with two domains of the catalytic p110 subunit.

R. Wetzker, D. Leopoldt, B. Nürnberg, 1998, The Journal of biological chemistry.

Jab1, a Novel Protease-activated Receptor-2 (PAR-2)-interacting Protein, Is Involved in PAR-2-induced Activation of Activator Protein-1*

G. Reiser, W. Luo, Yingfei Wang, 2006, Journal of Biological Chemistry.