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DOUGLAS IVEY, Ph.D.
San Francisco, CA

                     MOLECULAR DISCOVERY / GENETICS / BIOCHEMISTRY


My expertise is in molecular discovery. Prior accomplishments include the development and implementation of
a live cell-based high-throughput drug screening platform, vaccine candidate discovery in mice and the
identification and characterization of genetic mutations (created through random and site-directed mutagenesis)
and proteins (both structural and enzymatic) on multiple platforms including bacteria, yeast, filamentous fungi,
the protozoan parasite, Toxoplasma, and in mice.

My technical savvy, strong work ethic, creativity and dogged determination make me an ideal, hit-the-ground-
running candidate for championing high value projects.

                         RELEVANT EXPERTISE AND ACCOMPLISHMENTS

 ◆      Discovered, characterized and investigated protein targets in the parasite Toxoplasma through
 yeast two-hybrid screening, genomic and protein database mining, and mass spec analysis of affinity-
 purified multi-protein complexes.

 ◆      Developed and implemented a live yeast-based high-throughput screening platform, and
 multiple secondary assays (cytokine-detecting ELISA’s / kinetic analysis) to identify and develop
 isoform-specific inhibitors and activators of human cAMP and cGMP phosphodiesterases for
 therapeutic use.

 ◆     Generated, designed, managed, and mined large chemical compound datasets for lead
 generation and development. Developed chemical inventory procedures and protocols.

 ◆      Routinely performed detailed molecular analysis of proteins, post-translational modifications,
 protein-protein binding motifs, drug interaction mechanisms (kinetic analysis), and small molecules
 using a combination of immunoassays, molecular biology, genetic and biochemical tools.

 ◆       Developed and implemented an expression library DNA immunization protocol and procedure
 to isolate and characterize fungal vaccine candidates in mice.



EDUCATION
UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON
Ph.D., Microbiology and Molecular Genetics, 1999

UNIVERSITY OF HOUSTON-DOWNTOWN
B.S., Applied Microbiology, 1993

FELLOWSHIPS AND AWARDS
NIH Kirschstein National Research Service Award, 2003-2006
Ewing Halsell Foundation Grant, 2000
Graduate School of Biomedical Sciences Travel Awards, 1995-1998
18th and 19th International Fungal Genetics Conference Travel Awards, 1995 and 1997
Excellence in Microbiology Award, University of Houston-Downtown, 1993
F. Douglas Ivey, Ph.D.                                                      Curriculum vitae

RESEARCH EXPERIENCE
BOSTON COLLEGE
Molecular architecture and mechanisms of Toxoplasma gondii cellular division. Laboratory of Professor Marc-
Jan Gubbels, May 2009-Sept 2010.
      The obligate intracellular parasite Toxoplasma gondii divides by an internal budding process wherein
      two daughter cells form within the mother. The cytoskeleton of the parasite is complex, and serves as a
      scaffold for daughter cell assembly. Using a combination of genetics (i.e., yeast two-hybrid screens) and
      proteomics, I identified enzymes and proteins that interact with an essential and dynamic component of
      the contractile ring that is required during daughter cell maturation. My recent work focused on a family
      of phosphatases that participate with, and modify MORN1 during cytokinesis.

BOSTON COLLEGE
Discover, develop and commercialize small molecule regulators of cyclic nucleotide phosphodiesterases. Co-
Founder of Fission Pharmaceuticals, LLC with Prof. Charles S. Hoffman, 2006-2009.
      Developed fission yeast-based high throughput screen for mammalian and Trypanosomal
      PDE inhibitors and validated this screening platform on over 400,000 compound-enzyme
      combinations at the Broad Institute. Designed and implemented a versatile compound
      database through a collaboration with BC bioinformaticians.            Developed novel
      techniques to allow working with cGMP-specific PDEs, despite the apparent absence of
      cGMP signaling in fission yeast. Discovered the first small molecule activators of cAMP
      PDEs. Demonstrated that PDE7A/B and PDE4A/B subtype selective inhibitors retain
      therapeutic anti-inflammatory effects in tissue culture models. Played a central role
      initiating collaborations with academic laboratories interested in testing PDE
      inhibitors/activators in animal models for tumor metastasis, diffuse large B cell
      lymphomas, HIV/SIV infection and replication, apoptosis of human lymphoma cell lines,
      and compound-protein co-crystallization studies. Co-Founded Fission Pharmaceuticals,
      LLC and acted as CSO.

BOSTON COLLEGE
Genetic analysis of G protein signaling in Schizosaccharomyces pombe. Ruth L. Kirschstein National Research
Service Award, Laboratory of Prof. Charles S. Hoffman, 2002-2006.
       Defined protein-protein interactions, and structure-function relationships that govern G
       protein-mediated signal transduction of the glucose signaling pathway. This work led to
       the identification of a Gα (Gpa2) binding site on the Schizosaccharomyces pombe
       adenylate cyclase enzyme and was the first work to describe a direct physical interaction
       between a Gα subunit and adenylate cyclase in any fungal system.

        In a parallel project, a genetic screen was conducted to isolate mutant Gα alleles that
        promoted Gβγ-independent activation of the glucose/cAMP signaling pathway. Thirteen
        novel, constitutively activated Gα variants were identified and characterized by in vivo
        and in vitro assays. These experiments provide details into the mechanism of Gα
        activation and define critical residues within Gα proteins that were previously unrealized.

UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER-SAN ANTONIO
Valley Fever vaccine development. Postdoctoral Fellow, Laboratory of Prof. Rebecca A. Cox, 1999-2002.
       At the South Texas Center for Biotechnology in Medicine, with Profs. Rebecca Cox and
       Mitch Magee, I focused on vaccine development against the highly pathogenic fungus,
       Coccidioides immitis, the agent of Valley Fever. I championed a procedure called
       Expression Library Immunization and isolated a gene, ELI-Ag1, that protected mice
F. Douglas Ivey, Ph.D.                                                   Curriculum vitae
        against a lethal challenge with C. immitis spores when administered as a DNA-based
        vaccine.

UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON
“Functional analysis of GNA-1, a Gαi superfamily member found in the filamentous fungus Neurospora
crassa.” Ph.D. Dissertation, Laboratory of Prof. Katherine A. Borkovich, 1993-1999.
       My dissertation focused on G protein-mediated sensing in fungi. I provided the first
       biochemical evidence, in any fungal system, for positive regulation of adenylate cyclase
       by GNA-1. Discovered a mechanism by which intracellular cAMP levels are maintained
       by compensatory mechanisms involving a balance between PDE and adenylate cyclase
       activities. Reconstituted G protein-regulated adenylate cyclase activity through mixing
       experiments between G protein and adenylate cyclase mutant membrane extracts.
UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON
Study of the expression of the early genes, E2 and E4, of Human Papilloma Virus 2a. Laboratory of A.J.
Bednarz-Prashad, MD, Ph.D., Undergraduate Senior Honors Elective, 1992-1993
       My first research experience focused on restriction mapping, DNA subcloning, tissue
       culture, and performing Northern analyses to determine the order of expression of HPV
       2a early genes.
F. Douglas Ivey, Ph.D.                                                     Curriculum vitae
PUBLICATIONS
Demirbas, D., Ceyhan, O., Wyman, A., Ivey, F.D., Allain, C., Wang, L., Sharuk, M.N., Francis, S.H., and
Hoffman, C.S. “Use of a Schizosaccharomyces pombe PKA-repressible reporter to study cGMP metabolising
phosphodiesterases.” Cellular Signalling (23):594-601, 2011.

Anderson-White, B.R., Ivey, F.D., Cheng, K., Szatanek, T., Lorestani, A., Beckers, C.J., Ferguson, D.J.P.,
Sahoo, N. and Gubbels, M.J. “A family of intermediate filament-like proteins is sequentially assembled into the
cytoskeleton of Toxoplasma gondii.” Cellular Microbiology, 13(1):18-31, 2011.

Ivey, F.D., Taglia, F.X., Yang, F., Lander, M.M., Kelly, D.A., Hoffman, C.S. “Activated Alleles of the
Schizosaccharomyces pombe gpa2+ Gα Gene Identify Residues Involved in GDP-GTP Exchange.” Eukaryotic
Cell. 9(4):626-33, 2010.

Alaamery, M.A. Wyman, A.R., Ivey, F.D., Allain, C., Demirbas, D., Wang, L., Ceyhan, O., Hoffman, C.S.
“New classes of PDE7 inhibitors identified by a fission yeast-based HTS.” Journal of Biomolecular Screening
15(4):359-67, 2010.

Ivey, F.D. *, Wang, L. *, Demirbas, D., Allain, C.A., and Hoffman, C.S. “Development of a fission yeast-based
high throughput screen to identify chemical regulators of cAMP phosphodiesterases.” Journal of Biomolecular
Screening, 13(1):62-71, 2008.

Kao, R.S., Morreale, E., Wang, L., Ivey, F.D., and Hoffman, C.S. “Schizosaccharomyces pombe Git1 is a C2-
domain protein required for glucose activation of adenylate cyclase.” Genetics, 173:49-61, 2006.

Wang, L., Griffiths Jr., K., Zhang, Y.H., Ivey, F.D., and Hoffman, C.S. “Schizosaccharomyces pombe adenylate
cyclase suppressor mutations suggest a role for cAMP phosphodiesterase regulation in feedback control of
glucose/cAMP signaling.” Genetics, 171:1523-33, 2005.

Ivey, F.D. and Hoffman, C.S. “Direct activation of fission yeast adenylate cyclase by the Gpa2 Gα of the
glucose signaling pathway.” Proc Natl Acad Sci USA. 102(17):6108-13, 2005.

Wang, L., Kao, R., Ivey, F.D., and Hoffman, C.S. “Strategies for gene disruptions and plasmid constructions in
fission yeast.” Methods 33(3):199-205, 2004.

Ivey, F.D., Magee, D.M., Woitaske, M.D., Johnston, S.A., and Cox, R.A. “Identification of a protective antigen
of Coccidioides immitis by expression library immunization.” Vaccine 21:4359-4367, 2003.

Ivey, F.D. and Hoffman, C.S. “Pseudostructural inhibitors of G protein signaling during development.”
Developmental Cell (Preview) 3(2):154-5, 2002.

Jiang, C., Magee, D.M., Ivey, F.D., and Cox, R.A. “Role of signal sequence in vaccine-induced protection
against experimental coccidioidomycosis.” Infection and Immunity 70(7):3539-45, 2002.

Ivey, F.D., Kays, A.M., and Borkovich, K.A. “Shared and independent roles for a Gαi protein and adenylyl
cyclase in regulating development and stress responses in Neurospora crassa." Eukaryotic Cell. 1(4):634-642,
2002.

Ivey, F.D., Yang, Q., and Borkovich, K.A. “Positive regulation of adenylyl cyclase activity by a Gαi
homologue in Neurospora crassa.” Fungal Genetics and Biology 26:48-61, 1999.
F. Douglas Ivey, Ph.D.                                                  Curriculum vitae
Ivey, F.D. *, Hodge, P.N. *, Turner, G.E., and Borkovich, K.A. “The Gαi homologue gna-1 controls multiple
differentiation pathways in Neurospora crassa.” Molecular Biology of the Cell 7:1283-1297, 1996. * equal
contributions


PATENTS
United States Patent No. 7,342.101 B1 “Compositions and Methods Comprising a Protective Antigen of
Coccidioides immitis.” R.A. Cox, D.M. Magee, F.D. Ivey, and M.D. Woitaske. Issued March 11, 2008.

Application no. 12/426,171 “Inhibitors of cyclic AMP Phosphodiesterases.” Charles S. Hoffman, F. Douglas
Ivey and Arlene Wyman Petri. Filed April 17, 2009.


TEACHING EXPERIENCE
BOSTON COLLEGE
Advanced Molecular Biology Laboratory Course. Spring 2006
Trained and supervised laboratory personnel. 2002-present
UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON
Teaching Assistant in Medical Microbiology. 1993-1996
UNIVERSTY OF HOUSTON-DOWNTOWN
Teaching Assistant in Microbiology, Medical Microbiology, Techniques in Recombinant DNA, and
Biochemistry. 1991-1993


INVITED TALKS
“Mining G protein structure-function via genetic analysis in Schizosaccharomyces pombe.” The Second East
Coast Regional Fission Yeast Meeting, Miami, FL, 2005.

“Glucose signaling in Schizosaccharomyces pombe: The Gpa2-adenylyl cyclase connection.” Platform
presentation. 2004 Yeast Genetics and Molecular Biology Meeting, University of Washington, Seattle.

“Vaccine development against Coccidioides immitis," San Antonio Microbiologist Conference, Kerrville, TX,
2001.

“Heterotrimeric G proteins in Neurospora crassa," Neurospora 1998, Pacific Grove, CA.

“Properties of a Neurospora crassa gna-1 Gαi deletion mutant," Developmental control of gene expression and
protein modulation meeting, Stanford University, Palo Alto, CA, 1996.
F. Douglas Ivey, Ph.D.   Curriculum vitae
REFERENCES

Available on Request

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Ivey Ss

  • 1. DOUGLAS IVEY, Ph.D. San Francisco, CA MOLECULAR DISCOVERY / GENETICS / BIOCHEMISTRY My expertise is in molecular discovery. Prior accomplishments include the development and implementation of a live cell-based high-throughput drug screening platform, vaccine candidate discovery in mice and the identification and characterization of genetic mutations (created through random and site-directed mutagenesis) and proteins (both structural and enzymatic) on multiple platforms including bacteria, yeast, filamentous fungi, the protozoan parasite, Toxoplasma, and in mice. My technical savvy, strong work ethic, creativity and dogged determination make me an ideal, hit-the-ground- running candidate for championing high value projects. RELEVANT EXPERTISE AND ACCOMPLISHMENTS ◆ Discovered, characterized and investigated protein targets in the parasite Toxoplasma through yeast two-hybrid screening, genomic and protein database mining, and mass spec analysis of affinity- purified multi-protein complexes. ◆ Developed and implemented a live yeast-based high-throughput screening platform, and multiple secondary assays (cytokine-detecting ELISA’s / kinetic analysis) to identify and develop isoform-specific inhibitors and activators of human cAMP and cGMP phosphodiesterases for therapeutic use. ◆ Generated, designed, managed, and mined large chemical compound datasets for lead generation and development. Developed chemical inventory procedures and protocols. ◆ Routinely performed detailed molecular analysis of proteins, post-translational modifications, protein-protein binding motifs, drug interaction mechanisms (kinetic analysis), and small molecules using a combination of immunoassays, molecular biology, genetic and biochemical tools. ◆ Developed and implemented an expression library DNA immunization protocol and procedure to isolate and characterize fungal vaccine candidates in mice. EDUCATION UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON Ph.D., Microbiology and Molecular Genetics, 1999 UNIVERSITY OF HOUSTON-DOWNTOWN B.S., Applied Microbiology, 1993 FELLOWSHIPS AND AWARDS NIH Kirschstein National Research Service Award, 2003-2006 Ewing Halsell Foundation Grant, 2000 Graduate School of Biomedical Sciences Travel Awards, 1995-1998 18th and 19th International Fungal Genetics Conference Travel Awards, 1995 and 1997 Excellence in Microbiology Award, University of Houston-Downtown, 1993
  • 2. F. Douglas Ivey, Ph.D. Curriculum vitae RESEARCH EXPERIENCE BOSTON COLLEGE Molecular architecture and mechanisms of Toxoplasma gondii cellular division. Laboratory of Professor Marc- Jan Gubbels, May 2009-Sept 2010. The obligate intracellular parasite Toxoplasma gondii divides by an internal budding process wherein two daughter cells form within the mother. The cytoskeleton of the parasite is complex, and serves as a scaffold for daughter cell assembly. Using a combination of genetics (i.e., yeast two-hybrid screens) and proteomics, I identified enzymes and proteins that interact with an essential and dynamic component of the contractile ring that is required during daughter cell maturation. My recent work focused on a family of phosphatases that participate with, and modify MORN1 during cytokinesis. BOSTON COLLEGE Discover, develop and commercialize small molecule regulators of cyclic nucleotide phosphodiesterases. Co- Founder of Fission Pharmaceuticals, LLC with Prof. Charles S. Hoffman, 2006-2009. Developed fission yeast-based high throughput screen for mammalian and Trypanosomal PDE inhibitors and validated this screening platform on over 400,000 compound-enzyme combinations at the Broad Institute. Designed and implemented a versatile compound database through a collaboration with BC bioinformaticians. Developed novel techniques to allow working with cGMP-specific PDEs, despite the apparent absence of cGMP signaling in fission yeast. Discovered the first small molecule activators of cAMP PDEs. Demonstrated that PDE7A/B and PDE4A/B subtype selective inhibitors retain therapeutic anti-inflammatory effects in tissue culture models. Played a central role initiating collaborations with academic laboratories interested in testing PDE inhibitors/activators in animal models for tumor metastasis, diffuse large B cell lymphomas, HIV/SIV infection and replication, apoptosis of human lymphoma cell lines, and compound-protein co-crystallization studies. Co-Founded Fission Pharmaceuticals, LLC and acted as CSO. BOSTON COLLEGE Genetic analysis of G protein signaling in Schizosaccharomyces pombe. Ruth L. Kirschstein National Research Service Award, Laboratory of Prof. Charles S. Hoffman, 2002-2006. Defined protein-protein interactions, and structure-function relationships that govern G protein-mediated signal transduction of the glucose signaling pathway. This work led to the identification of a Gα (Gpa2) binding site on the Schizosaccharomyces pombe adenylate cyclase enzyme and was the first work to describe a direct physical interaction between a Gα subunit and adenylate cyclase in any fungal system. In a parallel project, a genetic screen was conducted to isolate mutant Gα alleles that promoted Gβγ-independent activation of the glucose/cAMP signaling pathway. Thirteen novel, constitutively activated Gα variants were identified and characterized by in vivo and in vitro assays. These experiments provide details into the mechanism of Gα activation and define critical residues within Gα proteins that were previously unrealized. UNIVERSITY OF TEXAS HEALTH SCIENCE CENTER-SAN ANTONIO Valley Fever vaccine development. Postdoctoral Fellow, Laboratory of Prof. Rebecca A. Cox, 1999-2002. At the South Texas Center for Biotechnology in Medicine, with Profs. Rebecca Cox and Mitch Magee, I focused on vaccine development against the highly pathogenic fungus, Coccidioides immitis, the agent of Valley Fever. I championed a procedure called Expression Library Immunization and isolated a gene, ELI-Ag1, that protected mice
  • 3. F. Douglas Ivey, Ph.D. Curriculum vitae against a lethal challenge with C. immitis spores when administered as a DNA-based vaccine. UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON “Functional analysis of GNA-1, a Gαi superfamily member found in the filamentous fungus Neurospora crassa.” Ph.D. Dissertation, Laboratory of Prof. Katherine A. Borkovich, 1993-1999. My dissertation focused on G protein-mediated sensing in fungi. I provided the first biochemical evidence, in any fungal system, for positive regulation of adenylate cyclase by GNA-1. Discovered a mechanism by which intracellular cAMP levels are maintained by compensatory mechanisms involving a balance between PDE and adenylate cyclase activities. Reconstituted G protein-regulated adenylate cyclase activity through mixing experiments between G protein and adenylate cyclase mutant membrane extracts. UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON Study of the expression of the early genes, E2 and E4, of Human Papilloma Virus 2a. Laboratory of A.J. Bednarz-Prashad, MD, Ph.D., Undergraduate Senior Honors Elective, 1992-1993 My first research experience focused on restriction mapping, DNA subcloning, tissue culture, and performing Northern analyses to determine the order of expression of HPV 2a early genes.
  • 4. F. Douglas Ivey, Ph.D. Curriculum vitae PUBLICATIONS Demirbas, D., Ceyhan, O., Wyman, A., Ivey, F.D., Allain, C., Wang, L., Sharuk, M.N., Francis, S.H., and Hoffman, C.S. “Use of a Schizosaccharomyces pombe PKA-repressible reporter to study cGMP metabolising phosphodiesterases.” Cellular Signalling (23):594-601, 2011. Anderson-White, B.R., Ivey, F.D., Cheng, K., Szatanek, T., Lorestani, A., Beckers, C.J., Ferguson, D.J.P., Sahoo, N. and Gubbels, M.J. “A family of intermediate filament-like proteins is sequentially assembled into the cytoskeleton of Toxoplasma gondii.” Cellular Microbiology, 13(1):18-31, 2011. Ivey, F.D., Taglia, F.X., Yang, F., Lander, M.M., Kelly, D.A., Hoffman, C.S. “Activated Alleles of the Schizosaccharomyces pombe gpa2+ Gα Gene Identify Residues Involved in GDP-GTP Exchange.” Eukaryotic Cell. 9(4):626-33, 2010. Alaamery, M.A. Wyman, A.R., Ivey, F.D., Allain, C., Demirbas, D., Wang, L., Ceyhan, O., Hoffman, C.S. “New classes of PDE7 inhibitors identified by a fission yeast-based HTS.” Journal of Biomolecular Screening 15(4):359-67, 2010. Ivey, F.D. *, Wang, L. *, Demirbas, D., Allain, C.A., and Hoffman, C.S. “Development of a fission yeast-based high throughput screen to identify chemical regulators of cAMP phosphodiesterases.” Journal of Biomolecular Screening, 13(1):62-71, 2008. Kao, R.S., Morreale, E., Wang, L., Ivey, F.D., and Hoffman, C.S. “Schizosaccharomyces pombe Git1 is a C2- domain protein required for glucose activation of adenylate cyclase.” Genetics, 173:49-61, 2006. Wang, L., Griffiths Jr., K., Zhang, Y.H., Ivey, F.D., and Hoffman, C.S. “Schizosaccharomyces pombe adenylate cyclase suppressor mutations suggest a role for cAMP phosphodiesterase regulation in feedback control of glucose/cAMP signaling.” Genetics, 171:1523-33, 2005. Ivey, F.D. and Hoffman, C.S. “Direct activation of fission yeast adenylate cyclase by the Gpa2 Gα of the glucose signaling pathway.” Proc Natl Acad Sci USA. 102(17):6108-13, 2005. Wang, L., Kao, R., Ivey, F.D., and Hoffman, C.S. “Strategies for gene disruptions and plasmid constructions in fission yeast.” Methods 33(3):199-205, 2004. Ivey, F.D., Magee, D.M., Woitaske, M.D., Johnston, S.A., and Cox, R.A. “Identification of a protective antigen of Coccidioides immitis by expression library immunization.” Vaccine 21:4359-4367, 2003. Ivey, F.D. and Hoffman, C.S. “Pseudostructural inhibitors of G protein signaling during development.” Developmental Cell (Preview) 3(2):154-5, 2002. Jiang, C., Magee, D.M., Ivey, F.D., and Cox, R.A. “Role of signal sequence in vaccine-induced protection against experimental coccidioidomycosis.” Infection and Immunity 70(7):3539-45, 2002. Ivey, F.D., Kays, A.M., and Borkovich, K.A. “Shared and independent roles for a Gαi protein and adenylyl cyclase in regulating development and stress responses in Neurospora crassa." Eukaryotic Cell. 1(4):634-642, 2002. Ivey, F.D., Yang, Q., and Borkovich, K.A. “Positive regulation of adenylyl cyclase activity by a Gαi homologue in Neurospora crassa.” Fungal Genetics and Biology 26:48-61, 1999.
  • 5. F. Douglas Ivey, Ph.D. Curriculum vitae Ivey, F.D. *, Hodge, P.N. *, Turner, G.E., and Borkovich, K.A. “The Gαi homologue gna-1 controls multiple differentiation pathways in Neurospora crassa.” Molecular Biology of the Cell 7:1283-1297, 1996. * equal contributions PATENTS United States Patent No. 7,342.101 B1 “Compositions and Methods Comprising a Protective Antigen of Coccidioides immitis.” R.A. Cox, D.M. Magee, F.D. Ivey, and M.D. Woitaske. Issued March 11, 2008. Application no. 12/426,171 “Inhibitors of cyclic AMP Phosphodiesterases.” Charles S. Hoffman, F. Douglas Ivey and Arlene Wyman Petri. Filed April 17, 2009. TEACHING EXPERIENCE BOSTON COLLEGE Advanced Molecular Biology Laboratory Course. Spring 2006 Trained and supervised laboratory personnel. 2002-present UNIVERSITY OF TEXAS MEDICAL SCHOOL-HOUSTON Teaching Assistant in Medical Microbiology. 1993-1996 UNIVERSTY OF HOUSTON-DOWNTOWN Teaching Assistant in Microbiology, Medical Microbiology, Techniques in Recombinant DNA, and Biochemistry. 1991-1993 INVITED TALKS “Mining G protein structure-function via genetic analysis in Schizosaccharomyces pombe.” The Second East Coast Regional Fission Yeast Meeting, Miami, FL, 2005. “Glucose signaling in Schizosaccharomyces pombe: The Gpa2-adenylyl cyclase connection.” Platform presentation. 2004 Yeast Genetics and Molecular Biology Meeting, University of Washington, Seattle. “Vaccine development against Coccidioides immitis," San Antonio Microbiologist Conference, Kerrville, TX, 2001. “Heterotrimeric G proteins in Neurospora crassa," Neurospora 1998, Pacific Grove, CA. “Properties of a Neurospora crassa gna-1 Gαi deletion mutant," Developmental control of gene expression and protein modulation meeting, Stanford University, Palo Alto, CA, 1996.
  • 6. F. Douglas Ivey, Ph.D. Curriculum vitae REFERENCES Available on Request