Stanford University
Showing 31-40 of 96 Results
-
James Ferrell
Professor of Chemical and Systems Biology and of Biochemistry
Current Research and Scholarly InterestsMy lab has two main goals: to understand the regulation of mitosis and to understand the systems-level logic of simple signaling circuits. We often make use of Xenopus laevis oocytes, eggs, and cell-free extracts for both sorts of study. We also carry out single-cell fluorescence imaging studies on mammalian cell lines. Our experimental work is complemented by computational and theoretical studies aimed at understanding the design principles and recurring themes of regulatory circuits.
-
Nathanael S. Gray
Krishnan-Shah Family Professor
BioNathanael Gray is the Krishnan-Shah Family Professor of Chemical and Systems Biology at Stanford, Co-Director of Cancer Drug Discovery Co-Leader of the Cancer Therapeutics Research Program, Member of Chem-H, and Program Leader for Small Molecule Drug Discovery for the Innovative Medicines Accelerator (IMA). His research utilizes the tools of synthetic chemistry, protein biochemistry, and cancer biology to discover and validate new strategies for the inhibition of anti-cancer targets. Dr. Gray’s research has had broad impact in the areas of kinase inhibitor design and in circumventing drug resistance.
Dr. Gray received his PhD in organic chemistry from the University of California at Berkeley in 1999 after receiving his BS degree with the highest honor award from the same institution in 1995. After completing his PhD, Dr. Gray was recruited to the newly established Genomics Institute of the Novartis Research Foundation (GNF) in San Diego, California. During his six year stay at GNF, Dr. Gray became the director of biological chemistry where he supervised a group of over fifty researchers integrating chemical, biological and pharmacological approaches towards the development of new experimental drugs. Some of the notable accomplishments of Dr. Gray’s team at GNF include: discovery of the first allosteric inhibitors of wild-type and mutant forms of BCR-ABL which resulted in clinical development of ABL001; discovery of the first selective inhibitors of the Anaplastic Lymphoma Kinase (ALK), an achievement that led to the development of now FDA-approved drugs such as ceritinib (LDK378) for the treatment of EML4-ALK expressing non-small cell lung cancer (NSCLC); and discovery that sphingosine-1-phosphate receptor-1 (S1P1) is the pharmacologically relevant target of the immunosuppressant drug Fingomilod (FTY720) followed by the development of Siponimod (BAF312), which is currently used for the treatment of multiple sclerosis.
In 2006, Dr. Gray returned to academia as a faculty member at the Dana Farber Cancer Institute and Harvard Medical School in Boston. There, he has established a discovery chemistry group that focuses on developing first-in-class inhibitors for newly emerging biological targets, including resistant alleles of existing targets, as well as inhibitors of well-validated targets, such as Her3 and RAS, that have previously been considered recalcitrant to small molecule drug development. Dr. Gray’s team developed covalent inhibitors of the T790M mutant of EGFR inspired the development of Osimertinib (AZD9291), now FDA approved for treatment of patients with relapsed lung cancer due to resistance to first generation EGFR inhibitors. Dr. Gray has also developed structure-based, generalized approaches for designing drugs to overcome one of the most common mechanisms of resistance observed against most kinase inhibitor drugs, mutation of the so-called "gatekeeper" residue, which has been observed in resistance to drugs targeting BCR-ABL, c-KIT and PDGFR.
In 2021, Dr. Gray joined Stanford University where he has joined the Stanford Cancer Institute, Chem-H and the Innovative Medicines Accelerator (IMA) to spur the development of prototype drugs.
These contributions have been recognized through numerous awards including the National Science Foundation’s Career award in 2007, the Damon Runyon Foundation Innovator award in 2008, the American Association for Cancer Research for Team Science in 2010 and for Outstanding Achievement in 2011 and the American Chemical Society award for Biological Chemistry in 2011, and the Nancy Lurie Marks endowed professorship in 2015 and the Paul Marks Prize in 2019, and the Hope Funds for Cancer Research in 2023. -
Wouter Huiting
Postdoctoral Scholar, Chemical and Systems Biology
BioWouter received his training at the University of Groningen, the Netherlands. Here he obtained a B.Sc.and M.Sc. in Human Movement Sciences (2008-2015), followed by a M.Sc. in Clinical and Molecular Neurosciences (2014-2016). He performed his doctoral research at the University of Groningen, obtaining his PhD degree in Molecular Cell Biology in 2021. Wouter continued his research in 2022 with a position as postdoctoral scholar at the Jarosz lab, at the department of Chemical and Systems Biology. Here he pursues his interest in the molecular forces underlying proteomic adaptation of cells and systems in development and disease. Outside of Stanford, Wouter is an avid sportsman, and likes cooking, hiking, birding, and in general loves to enjoy nature and wildlife with his wife and son.
-
Daniel Jarosz
Senior Associate Dean, Basic Science, Professor of Chemical and Systems Biology and of Developmental Biology
Current Research and Scholarly InterestsMy laboratory studies conformational switches in evolution, disease, and development. We focus on how molecular chaperones, proteins that help other biomolecules to fold, affect the phenotypic output of genetic variation. To do so we combine classical biochemistry and genetics with systems-level approaches. Ultimately we seek to understand how homeostatic mechanisms influence the acquisition of biological novelty and identify means of manipulating them for therapeutic and biosynthetic benefit.
-
Patrick Jurney
Affiliate, Chemical and Systems Biology Operations
Visiting Scholar, Chemical and Systems Biology OperationsBioPatrick Jurney is the Kordestani Endowed Chair and an Associate Professor of Biomedical Engineering at San Jose State University. A Fellow of the American Heart Association (FAHA), his research focuses on the intersection of fluid dynamics and cellular mechanics, with a particular emphasis on cardiovascular health and disease..
Dr. Jurney completed his Ph.D. in Thermal Fluid Systems at the University of Texas at Austin, where he designed and built microphysiological systems to investigate the role of nanoparticle properties in targeted drug delivery. Following his doctoral studies, he was a T-32 Fellow in Translational Engineering at Oregon Health & Science University (OHSU). During his fellowship, he worked with cardiovascular biomaterials and characterized how biomaterial properties influence endothelialization and thrombogenesis.
Currently, his research laboratory at SJSU investigates the role of fluid shear stress mechanotransduction on endothelial metabolic structure and function. Dr. Jurney is a pioneer in using holotomographic microscopy to study sub-cellular organelles in cardiovascular disease. He is also collaborating in the laboratory of Dr. Daria Mochly-Rosen to characterize the role of mitochondrial structure and dynamics in metabolic function in response to ischemia/reperfusion and other models of cardiovascular health and disease.
Website: https://www.jurneylab.org/
Email: patrick.jurney@sjsu.edu or pjurney@stanford.edu
