His primary areas of investigation include Immunology, Internal medicine, Endocrinology, Pathology and Cell biology. His work investigates the relationship between Immunology and topics such as Angiogenesis that intersect with problems in Tube formation, Cancer and Pericyte. Hermann Josef Gröne is interested in Kidney, which is a field of Endocrinology.
Hermann Josef Gröne interconnects CCL2, Epithelium, Kidney disease, Renal function and Vascular endothelial growth factor A in the investigation of issues within Kidney. His biological study spans a wide range of topics, including Glomerulosclerosis, Laser capture microdissection and Monocyte. His Cell biology study incorporates themes from Regulation of gene expression and Biochemistry.
His scientific interests lie mostly in Internal medicine, Endocrinology, Pathology, Immunology and Cell biology. Hermann Josef Gröne frequently studies issues relating to Nephropathy and Internal medicine. In most of his Endocrinology studies, his work intersects topics such as Receptor.
His work on Immunology is being expanded to include thematically relevant topics such as Cancer research. His Cell biology research integrates issues from Regulation of gene expression, Biochemistry and Gene expression. Hermann Josef Gröne works mostly in the field of Kidney, limiting it down to topics relating to Transplantation and, in certain cases, Urology, as a part of the same area of interest.
Hermann Josef Gröne spends much of his time researching Internal medicine, Cell biology, Endocrinology, Pathology and Immunology. His Internal medicine research is multidisciplinary, incorporating perspectives in Gastroenterology and General surgery. His research integrates issues of T cell, Angiogenesis and Caspase 8 in his study of Cell biology.
Hermann Josef Gröne has included themes like Heart failure, Gene and Mitochondrion in his Endocrinology study. His studies in Pathology integrate themes in fields like Kidney disease, Inflammation, Focal segmental glomerulosclerosis, Kidney and Pulmonary edema. His work on Immune system as part of general Immunology research is frequently linked to Administration, bridging the gap between disciplines.
His primary areas of study are Cell biology, Internal medicine, Endocrinology, Pathology and Diabetic nephropathy. His research in Cell biology tackles topics such as Heart failure which are related to areas like Repressor, Orphan receptor and STIM1. In general Endocrinology study, his work on Albuminuria often relates to the realm of Myofilament, thereby connecting several areas of interest.
The Pathology study combines topics in areas such as Focal segmental glomerulosclerosis, Glomerular disease and CD44. Hermann Josef Gröne has researched Diabetic nephropathy in several fields, including Glomerulosclerosis, Apolipoprotein E, Tissue homeostasis and Glycocalyx. The various areas that Hermann Josef Gröne examines in his Diabetes mellitus study include Renin–angiotensin system, Receptor, Angiotensin II, Superoxide and Mitochondrion.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Human Y Chromosome Azoospermia Factors (AZF) Mapped to Different Subregions in Yq11
P. H. Vogt;A. Edelmann;S. Kirsch;O. Henegariu.
Human Molecular Genetics (1996)
Definition of Estrogen Receptor Pathway Critical for Estrogen Positive Feedback to Gonadotropin-Releasing Hormone Neurons and Fertility
Tim M. Wintermantel;Rebecca E. Campbell;Robert Porteous;Dagmar Bock.
Neuron (2006)
Vascular normalization in Rgs5-deficient tumours promotes immune destruction
Juliana Hamzah;Manfred Jugold;Fabian Kiessling;Paul Rigby.
Nature (2008)
Endostatin's antiangiogenic signaling network
Amir Abdollahi;Philip Hahnfeldt;Christian Maercker;Hermann Josef Gröne.
Molecular Cell (2004)
Localization of cyclooxygenase-1 and -2 in adult and fetal human kidney: implication for renal function
Martin Kömhoff;Hermann Josef Gröne;Thomas Klein;Hannsjoerg W. Seyberth.
American Journal of Physiology-renal Physiology (1997)
Constitutive Activation of Hypoxia-inducible Genes Related to Overexpression of Hypoxia-inducible Factor-1α in Clear Cell Renal Carcinomas
Michael S. Wiesener;Philine M. Münchenhagen;Irina Berger;Neil V. Morgan.
Cancer Research (2001)
Biglycan: A danger signal that activates the NLRP3 inflammasome via toll-like and P2X receptors
Andrea Babelova;Kristin Moreth;Kristin Moreth;Wasiliki Tsalastra-Greul;Jinyang Zeng-Brouwers;Jinyang Zeng-Brouwers.
Journal of Biological Chemistry (2009)
Inhibition of platelet-derived growth factor signaling attenuates pulmonary fibrosis
Amir Abdollahi;Minglun Li;Minglun Li;Gong Ping;Gong Ping;Christian Plathow.
Journal of Experimental Medicine (2005)
Modular Activation of Nuclear Factor-κB Transcriptional Programs in Human Diabetic Nephropathy
Holger Schmid;Anissa Boucherot;Anissa Boucherot;Yoshinari Yasuda;Anna Henger;Anna Henger.
Diabetes (2006)
Decrease and gain of gene expression are equally discriminatory markers for prostate carcinoma: A gene expression analysis on total and microdissected prostate tissue
Thomas Ernst;Manfred Hergenhahn;Marc Kenzelmann;Clemens D. Cohen.
American Journal of Pathology (2002)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Icahn School of Medicine at Mount Sinai
University of Michigan–Ann Arbor
RWTH Aachen University
Heidelberg University
European Bioinformatics Institute
German Cancer Research Center
Ludwig-Maximilians-Universität München
Goethe University Frankfurt
Leiden University Medical Center
Heidelberg University
Pontifical Catholic University of Rio Grande do Sul
Tsinghua University
Xidian University
Simon Fraser University
University of Maryland, College Park
Northeast Normal University
University of Florida
University of California, Davis
Johns Hopkins University School of Medicine
University of California, Davis
Carnegie Institution for Science
University of Santiago de Compostela
University of Oregon
University of Connecticut
University of Michigan–Ann Arbor
Lawrence Berkeley National Laboratory