2011 - Fellow of the American Association for the Advancement of Science (AAAS)
Heidi E. Hamm mostly deals with G protein, Heterotrimeric G protein, Biochemistry, Receptor and Cell biology. In most of her G protein studies, her work intersects topics such as Biophysics. Heidi E. Hamm interconnects Protein structure, GTPase, G protein-coupled receptor and G alpha subunit in the investigation of issues within Heterotrimeric G protein.
Her Receptor research is multidisciplinary, relying on both Guanosine triphosphate, Binding site and Effector. Her Cell biology research is multidisciplinary, incorporating elements of Exocytosis and Cell membrane. Her GTP-Binding Protein gamma Subunits research focuses on GTP-Binding Protein beta Subunits and how it relates to Beta-propeller.
Her primary areas of study are G protein, Cell biology, Biochemistry, Heterotrimeric G protein and Receptor. Particularly relevant to Transducin is her body of work in G protein. Her Transducin research incorporates themes from Phosphodiesterase and GTPase.
The various areas that Heidi E. Hamm examines in her Cell biology study include Exocytosis and Platelet, Thrombin. Her research investigates the connection with Biochemistry and areas like Biophysics which intersect with concerns in Nucleotide and Allosteric regulation. Her research on Heterotrimeric G protein frequently links to adjacent areas such as Effector.
Her primary scientific interests are in Receptor, Cell biology, G protein, G protein-coupled receptor and Biochemistry. Her work carried out in the field of Receptor brings together such families of science as Platelet activation, Platelet, Exocytosis and Effector. The concepts of her Cell biology study are interwoven with issues in SNARE complex, Thrombin and Synaptotagmin 1.
She has included themes like Biophysics and Allosteric regulation in her G protein study. Her research in Biophysics intersects with topics in Protein structure, Rhodopsin, GTP' and Binding site. Her work focuses on many connections between Biochemistry and other disciplines, such as PROTEASE-ACTIVATED RECEPTOR 4, that overlap with her field of interest in Stereochemistry and Potency.
Cell biology, G protein, Receptor, G protein-coupled receptor and Biochemistry are her primary areas of study. Her Cell biology study incorporates themes from Exocytosis, SNARE complex and Synaptotagmin 1. Her research integrates issues of Helix and Allosteric regulation in her study of G protein.
The Receptor study combines topics in areas such as Platelet activation and Pharmacology. As part of her studies on Biochemistry, Heidi E. Hamm frequently links adjacent subjects like Biophysics. Her studies in Heterotrimeric G protein integrate themes in fields like Neurotransmitter, Voltage-dependent calcium channel, Ternary complex, Presynaptic active zone and GTP'.
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The many faces of G protein signaling.
Heidi E. Hamm.
Journal of Biological Chemistry (1998)
The 2.0 Å crystal structure of a heterotrimeric G protein
David G. Lambright;John Sondek;Andrew Bohm;Nikolai P. Skiba.
Nature (1996)
Heterotrimeric G protein activation by G-protein-coupled receptors
William M. Oldham;Heidi E. Hamm.
Nature Reviews Molecular Cell Biology (2008)
The 2.2 A crystal structure of transducin-alpha complexed with GTP gamma S.
Joseph P. Noel;Heidi E. Hamm;Heidi E. Hamm;Paul B. Sigler.
Nature (1993)
Crystal structure of a G-protein beta gamma dimer at 2.1A resolution
John Sondek;Andrew Bohm;David G. Lambright;David G. Lambright;Heidi E. Hamm.
Nature (1996)
The 2.2 Å crystal structure of transducin-α complexed with GTP γ S
Joseph P. Noel;Heidi E. Hamm;Heidi E. Hamm;Paul B. Sigler.
Nature (1993)
Insights into G protein structure, function, and regulation
Theresa M. Cabrera-Vera;Jurgen Vanhauwe;Tarita O. Thomas;Martina Medkova.
Endocrine Reviews (2003)
Structural determinants for activation of the alpha-subunit of a heterotrimeric G protein.
David G. Lambright;Joseph P. Noel;Joseph P. Noel;Heidi E. Hamm;Paul B. Sigler.
Nature (1994)
GTPase Mechanism of Gproteins From the 1.7-A Crystal Structure of Transducin alpha-GDP-AIF-4
John Sondek;David G. Lambright;Joseph P. Noel;Heidi E. Hamm;Heidi E. Hamm.
Nature (1994)
D2 Dopamine Receptors in Striatal Medium Spiny Neurons Reduce L-Type Ca2+ Currents and Excitability via a Novel PLCβ1–IP3–Calcineurin-Signaling Cascade
Salvador Hernández-López;Tatiana Tkatch;Enrique Perez-Garci;Elvira Galarraga.
The Journal of Neuroscience (2000)
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