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- Publications
- Influence
p21-Activated Kinase 1 Phosphorylates the Death Agonist Bad and Protects Cells from Apoptosis
- A. Schürmann, A. Mooney, +4 authors G. Bokoch
- Biology, Medicine
- Molecular and Cellular Biology
- 15 January 2000
ABSTRACT Bad is a critical regulatory component of the intrinsic cell death machinery that exerts its death-promoting effect upon heterodimerization with the antiapoptotic proteins Bcl-2 and Bcl-xL.… Expand
Na+-d-glucose Cotransporter SGLT1 is Pivotal for Intestinal Glucose Absorption and Glucose-Dependent Incretin Secretion
- V. Gorboulev, A. Schürmann, +20 authors H. Koepsell
- Chemistry, Medicine
- Diabetes
- 12 December 2011
To clarify the physiological role of Na+-d-glucose cotransporter SGLT1 in small intestine and kidney, Sglt1−/− mice were generated and characterized phenotypically. After gavage of d-glucose, small… Expand
HIV-1 Nef associated PAK and PI3-Kinases stimulate Akt-independent Bad-phosphorylation to induce anti-apoptotic signals
A highly conserved signaling property of Nef proteins encoded by human or simian immunodeficiency virus is the binding and activation of a PAK kinase whose function is unclear. Here we show that… Expand
The glucose transporter families SGLT and GLUT: molecular basis of normal and aberrant function.
- A. Scheepers, H. Joost, A. Schürmann
- Biology, Medicine
- JPEN. Journal of parenteral and enteral nutrition
- 1 September 2004
Glucose enters eucaryotic cells via 2 different types of membrane associated carrier proteins, the Na+-coupled glucose transporters (SGLT) and glucose transporter facilitators (GLUT). Three members… Expand
Regulation of macropinocytosis by p21-activated kinase-1.
- S. Dharmawardhane, A. Schürmann, M. Sells, J. Chernoff, S. Schmid, G. Bokoch
- Biology, Medicine
- Molecular biology of the cell
- 1 October 2000
The process of macropinocytosis is an essential aspect of normal cell function, contributing to both growth and motile processes of cells. p21-activated kinases (PAKs) are targets for activated Rac… Expand
The central melanocortin system directly controls peripheral lipid metabolism.
- R. Nogueiras, P. Wiedmer, +23 authors M. Tschöp
- Biology, Medicine
- The Journal of clinical investigation
- 1 November 2007
Disruptions of the melanocortin signaling system have been linked to obesity. We investigated a possible role of the central nervous melanocortin system (CNS-Mcr) in the control of adiposity through… Expand
Adipocyte Accumulation in the Bone Marrow during Obesity and Aging Impairs Stem Cell-Based Hematopoietic and Bone Regeneration
- Thomas H Ambrosi, Antonio Scialdone, +9 authors T. Schulz
- Biology, Medicine
- Cell stem cell
- 1 June 2017
Summary Aging and obesity induce ectopic adipocyte accumulation in bone marrow cavities. This process is thought to impair osteogenic and hematopoietic regeneration. Here we specify the cellular… Expand
Ghrelin action in the brain controls adipocyte metabolism.
- C. Theander-Carrillo, P. Wiedmer, +9 authors F. Rohner-Jeanrenaud
- Biology, Medicine
- The Journal of clinical investigation
- 3 July 2006
Many homeostatic processes, including appetite and food intake, are controlled by neuroendocrine circuits involving the CNS. The CNS also directly regulates adipocyte metabolism, as we have shown… Expand
Nomenclature of the GLUT/SLC2A family of sugar/polyol transport facilitators.
- H. Joost, G. Bell, +13 authors B. Thorens
- Biology, Medicine
- American journal of physiology. Endocrinology and…
- 1 April 2002
The recent identification of several additional members of the family of sugar transport facilitators (gene symbol SLC2A, protein symbol GLUT) has created a heterogeneous and, in part, confusing… Expand
GLUT8, a Novel Member of the Sugar Transport Facilitator Family with Glucose Transport Activity*
- H. Doege, A. Schürmann, G. Bahrenberg, A. Brauers, H. Joost
- Biology, Medicine
- The Journal of Biological Chemistry
- 26 May 2000
GLUT8 is a novel glucose transporter-like protein that exhibits significant sequence similarity with the members of the sugar transport facilitator family (29.4% of amino acids identical with GLUT1).… Expand