The scientist’s investigation covers issues in Cell biology, Endoplasmic reticulum, Reticulon, Membrane protein and Membrane contact site. His Cell biology study combines topics from a wide range of disciplines, such as Biochemistry and Sterol. William A. Prinz has included themes like ERMES and Translocase of the outer membrane in his Endoplasmic reticulum study.
His work in Reticulon addresses subjects such as Saccharomyces cerevisiae, which are connected to disciplines such as GTPase and Membrane topology. His research integrates issues of Sterol transport and Yeast in his study of Membrane protein. His work deals with themes such as TIM/TOM complex, Mitochondrial membrane transport protein, ER membrane protein complex, Signal transduction and Organelle, which intersect with Membrane contact site.
William A. Prinz focuses on Cell biology, Endoplasmic reticulum, Biochemistry, Organelle and Membrane. His studies deal with areas such as Biogenesis, Membrane contact site and Membrane protein as well as Cell biology. The study incorporates disciplines such as GTPase, Phosphatidylethanolamine and Cell membrane in addition to Endoplasmic reticulum.
The Organelle study combines topics in areas such as Lipid metabolism and Signal transduction. His Membrane research includes themes of Biophysics and Intracellular. His Reticulon study incorporates themes from Integral membrane protein, Saccharomyces cerevisiae and Organelle biogenesis.
William A. Prinz spends much of his time researching Cell biology, Lipid droplet, Biogenesis, Endoplasmic reticulum and Organelle. In general Cell biology, his work in Mitochondrion is often linked to Abnormal mitochondrial morphology linking many areas of study. His Endoplasmic reticulum research is mostly focused on the topic Reticulon.
The concepts of his Reticulon study are interwoven with issues in Protein domain, Transmembrane domain and Organelle biogenesis. His research in Organelle intersects with topics in Biophysics, Membrane and Yeast. His Membrane research is multidisciplinary, relying on both Lipid Transport and Signal transduction, Calcium signaling.
Cell biology, Biogenesis, Endoplasmic reticulum, Lipid droplet and Mitochondrion are his primary areas of study. His Cell biology study frequently links to related topics such as Organelle biogenesis. The various areas that he examines in his Organelle biogenesis study include Reticulon, Protein domain and C2 domain.
His Mitochondrion research incorporates elements of Phenotype and Transgene. His study in Signalling is interdisciplinary in nature, drawing from both Signal transduction, Calcium signaling, Membrane, Lipid metabolism and Organelle. The concepts of his Cytoplasm study are interwoven with issues in Membrane curvature, Phospholipid and Phosphatidylethanolamine.
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.
A Class of Membrane Proteins Shaping the Tubular Endoplasmic Reticulum
Gia K. Voeltz;William A. Prinz;Yoko Shibata;Julia M. Rist.
Cell (2006)
Mutations that allow disulfide bond formation in the cytoplasm of Escherichia coli
Alan I. Derman;William A. Prinz;Dominique Belin;Jon Beckwith.
Science (1993)
A class of dynamin-like GTPases involved in the generation of the tubular ER network.
Junjie Hu;Yoko Shibata;Peng-Peng Zhu;Christiane Voss.
Cell (2009)
Membrane expansion alleviates endoplasmic reticulum stress independently of the unfolded protein response
Sebastian Schuck;William A. Prinz;Kurt S. Thorn;Christiane Voss.
Journal of Cell Biology (2009)
Structural mechanism for sterol sensing and transport by OSBP-related proteins
Young Jun Im;Sumana Raychaudhuri;William A. Prinz;James H. Hurley.
Nature (2005)
Bridging the gap: Membrane contact sites in signaling, metabolism, and organelle dynamics
William A. Prinz.
Journal of Cell Biology (2014)
Mechanisms Determining the Morphology of the Peripheral ER
Yoko Shibata;Yoko Shibata;Tom Shemesh;William A. Prinz;Alexander F. Palazzo;Alexander F. Palazzo.
Cell (2010)
Membrane proteins of the endoplasmic reticulum induce high-curvature tubules.
Junjie Hu;Yoko Shibata;Christiane Voss;Tom Shemesh.
Science (2008)
The reticulon and DP1/Yop1p proteins form immobile oligomers in the tubular endoplasmic reticulum.
Yoko Shibata;Christiane Voss;Julia M. Rist;Junjie Hu.
Journal of Biological Chemistry (2008)
Nonvesicular sterol movement from plasma membrane to ER requires oxysterol-binding protein–related proteins and phosphoinositides
Sumana Raychaudhuri;Young Jun Im;James H. Hurley;William A. Prinz.
Journal of Cell Biology (2006)
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:
Howard Hughes Medical Institute
University College London
National Institutes of Health
University of Fribourg
University of California, Davis
Massachusetts General Hospital
National Institutes of Health
National University of Singapore
National Institutes of Health
University of California, Berkeley
Rockefeller University
Shanghai Jiao Tong University
George Mason University
ETH Zurich
Michigan State University
University of Nevada, Reno
Rio de Janeiro State University
University of Saskatchewan
Oulu University Hospital
Deakin University
German Aerospace Center
Yonsei University
University of Quebec at Montreal
University of Wisconsin–Madison
University of Amsterdam
University of Western Australia