D. Stone

发表

G protein mutations that alter the pheromone response in Saccharomyces cerevisiae

S. Reed, D. Stone, 1990, Molecular and cellular biology.

The yeast claudin Dcv1 is important for demarcating the front domain of pheromone-responding yeast cells

D. Stone, M. Sukumar, Reagan DeFlorio, 2022, bioRxiv.

Mating yeast cells use an intrinsic polarity site to assemble a pheromone-gradient tracking machine

Jie Liang, Wei Tian, Beth Statler, 2019, The Journal of cell biology.

Phosphorylation of G&bgr; is crucial for efficient chemotropism in yeast

D. Eddington, R. Arkowitz, D. Stone, 2013, Journal of Cell Science.

Phosphorylated Gβ is a directional cue during yeast gradient tracking

B. Kay, Leon A Venegas, R. Arkowitz, 2021, Science Signaling.

In Situ Assays of Chemotropism During Yeast Mating.

R. Arkowitz, D. Stone, 2016, Methods in molecular biology.

Self-regulation of 70-kilodalton heat shock proteins in Saccharomyces cerevisiae

E. Craig, D. Stone, 1990, Molecular and cellular biology.

The Mating-Speciﬁc G (cid:97) Protein of Saccharomyces cerevisiae Downregulates the Mating Signal by a Mechanism That Is Dependent on Pheromone and Independent of G (cid:98)(cid:103) Sequestration

S. Reed, D. Stone, H. F. Stratton, 1996 .

Stoichiometry of G protein subunits affects the Saccharomyces cerevisiae mating pheromone signal transduction pathway

S. Reed, D. Stone, G. M. Cole, 1990, Molecular and cellular biology.

Complex interactions among members of an essential subfamily of hsp70 genes in Saccharomyces cerevisiae

D E Stone, M. Werner-Washburne, E. Craig, 1987, Molecular and cellular biology.

N-myristoylation is required for function of the pheromone-responsive G alpha protein of yeast: conditional activation of the pheromone response by a temperature-sensitive N-myristoyl transferase.

M. Goebl, S. Reed, D. Stone, 1991, Genes & development.

Prion‐promoted phosphorylation of heterologous amyloid is coupled with ubiquitin‐proteasome system inhibition and toxicity

S. Liebman, D. Stone, Zi Yang, 2014, Molecular microbiology.

Polarization of the Yeast Pheromone Receptor Requires Its Internalization but Not Actin-dependent Secretion

David E. Stone, Amber Ismael, R. Arkowitz, 2010, Molecular biology of the cell.

The pheromone-induced nuclear accumulation of the Fus3 MAPK in yeast depends on its phosphorylation state and on Dig1 and Dig2

Hyenchol Kim, D. Stone, Ernest Blackwell, 2007, BMC Cell Biology.

Gβ promotes pheromone receptor polarization and yeast chemotropism by inhibiting receptor phosphorylation

Youfang Cao, Jie Liang, Wei Tian, 2016, Science Signaling.

Phosphorylation of the pheromone-responsive Gβ protein of Saccharomyces cerevisiae does not affect its mating-specific signaling function

M. Cismowski, D. Stone, E. Li, 1998, Molecular and General Genetics MGG.

Effect of the Pheromone-Responsive Gα and Phosphatase Proteins of Saccharomyces cerevisiae on the Subcellular Localization of the Fus3 Mitogen-Activated Protein Kinase

Hyenchol Kim, D. Stone, Ernest Blackwell, 2003, Molecular and Cellular Biology.

Differential phosphoproteome profiling by affinity capture and tandem matrix‐assisted laser desorption/ionization mass spectrometry

D. Stone, M. Metodiev, A. Timanova, 2004, Proteomics.

The yeast pheromone-responsive Gα protein stimulates recovery from chronic pheromone treatment by two mechanisms that are activated at distinct levels of stimulus

D. Stone, Jianlong Zhou, M. Arora, 2007, Cell Biochemistry and Biophysics.

A pathway in the yeast cell division cycle linking protein kinase C (Pkc1) to activation of Cdc28 at START.

S. Reed, A. Hubberstey, B. Buehrer, 1996, The EMBO journal.

The mating-specific Galpha interacts with a kinesin-14 and regulates pheromone-induced nuclear migration in budding yeast.

J. Cooper, S. Zaichick, S. Nelson, 2009, Molecular biology of the cell.

Pheromone-induced polarization is dependent on the Fus3p MAPK acting through the formin Bni1p

M. Rose, D. Matheos, D. Stone, 2004, The Journal of cell biology.

Biochemical Analysis of Yeast Gα Mutants That Enhance Adaptation to Pheromone

M. Cismowski, D. Stone, M. Metodiev, 2001 .

Pitfalls and Rewards of Setting Up a Liquid Biopsy Approach for the Detection of Driver Mutations in Circulating Tumor DNAs: Our Institutional Experience

M. Rowbotham, L. Soroceanu, A. Dar, 2022, Journal of personalized medicine.

Quantitative proteomics reveals a Gα/MAPK signaling hub that controls pheromone-induced cellular polarization in yeast.

D. Stone, Reagan DeFlorio, M. Metodiev, 2019, Journal of proteomics.

Gβγ Recruits Rho1 to the Site of Polarized Growth during Mating in Budding Yeast*

E. Bar, D. Stone, Eli E. Bar, 2003, Journal of Biological Chemistry.

Substitutions in the pheromone-responsive Gbeta protein of Saccharomyces cerevisiae confer a defect in recovery from pheromone treatment.

D. Stone, E. Meldrum, H. F. Stratton, 1998, Genetics.

The mating-specific G(alpha) protein of Saccharomyces cerevisiae downregulates the mating signal by a mechanism that is dependent on pheromone and independent of G(beta)(gamma) sequestration

S. Reed, D. Stone, J. Zhou, 1996, Molecular and cellular biology.

Gradient tracking in mating yeast depends on Bud1 inactivation and actin-independent vesicle delivery

D. Stone, Chih-Yu Pai, Xin Wang, 2022, The Journal of cell biology.

Roles of regulated internalization in the polarization of cell surface receptors

Wei Tian, Jie Liang, Youfang Cao, 2014, 2014 36th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.

Yeast chemotropism: A paradigm shift in chemical gradient sensing

D. Stone, Amber Ismael, 2017, Cellular logistics.

A microfluidic device that forms and redirects pheromone gradients to study chemotropism in yeast.

D. Eddington, D. Stone, Reagan DeFlorio, 2012, Lab on a chip.

Dse1 may control cross talk between the pheromone and filamentation pathways in yeast

D. Stone, Oleksii Dubrovskyi, Eli E. Bar, 2009, Current Genetics.

Regulation of MAPK Function by Direct Interaction with the Mating-Specific Gα in Yeast

M. Rose, D. Matheos, D. Stone, 2002, Science.