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Postdoctoral position opportunities available in laboratories of Pew Scholars

Note: This list is provided as a service to potential applicants who may wish to apply to one of these well established labs. However, applicants to the Pew Latin American Fellows Program may select a mentor/sponsoring lab at an academic institution of their choice within the United States.

Please click on the research area below to read the job listing.

Posted 6/26/08

Research Area: Computational Biology, Gene networks and MicroRNAs

Project title: microRNA regulatory networks in vertebrate development

Description of project: A postdoctoral position is available immediately to study the microRNA gene regulatory network in zebrafish as a model system. My lab combines genetics with gene expression profile and computational biology to identify the miRNA targets in vivo and understand their functions during development.

Applicants require a strong background of computational biology, and perl programming, experience in molecular biology or developmental biology is preferred but not necessary.

Please e-mail CV and names of three references to:
Antonio J. Giraldez Ph.D.
Lois and Franklin Top Assistant Professor.
Pew Scholar
Yale University
School of Medicine
Genetics Department
Phone: 203 785 5423
Fax: 203 785 4415
Email: antonio.giraldez@yale.edu
Website: http://www.yale.edu/giraldezlab

Posted 5/9/08

Research Area: Synaptic transmission, synaptic plasticity, fusion pores, exocytosis, membrane fusion, fusion machine, synaptotagmin, SNARE, botulism, tetanus

Description of project: To use modern imaging and biophysical methods to study the modes of exocytosis at nerve terminals, and to relate changes in the mode of neurotransmitter release with synaptic plasticity. Also, to study the 'mechanics' of reconstituted fusion machines, and to study bacterial the toxins that cause botulism and tetanus.

A postdoctoral position is available immediately to study fusion pores that mediate the release of neurotransmitters from neurons using optical, biophysical and biochemical approaches and/or to study the structure and function of reconstituted membrane fusion machines.

Applicants with a strong background in: membrane biophysics, optical imaging, sub cellular fractionation, and membrane protein biochemistry are encouraged to apply.

Please forward CV and names of three references to:
Edwin R. Chapman, Ph.D.
University of Wisconsin
HHMI and Department of Physiology
1300 University Avenue, SMI 129
Madison, WI 53706

Phone: (608) 263-1762
Fax: (608) 265-5512
Email: chapman@physiology.wisc.edu
Websites: http://www.hhmi.org/research/investigators/chapman.html
http://www.physiology.wisc.edu/faculty/chapman.html
http://www.physiology.wisc.edu/chapman/

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Posted 5/9/08

Research Area: Structural Biology of Chromatin Factors and Enzymes

Description of project: A postdoctoral position is available to determine the structures of eukaryotic gene regulatory complexes including histone modificatione enzymes and transcription factors bound to nucleosomes. Crystals are available for some projects, while crystallization conditions need to be determined or optimized for others.

The Tan laboratory is fully equipped for biochemical, crystallization and crystallography work. Our efforts are also enhanced by techniques to reconstitute multicomponent complexes (Nature Struct. Biol., 8:695, 2001, Prot. Expr. Purif., 40:385, 2005, MCB, 25:5535, 2005) and crystallization design ideas developed during successful structural determination of the yeast TFIIA/TBP/DNA and MATalpha2/MCM1/DNA ternary complexes (Nature, 381:127, 1996; Nature, 391:660, 1998; JMB 297:947, 2000).

Crystallographers and molecular biologists/biochemists who would like to learn crystallography are encouraged to apply. Prior experience with macromolecular crystallography and protein expression/purification is preferred but not essential.

Please send curriculum vitae and the names of three references to:
Dr. Song Tan
Center for Gene Regulation
Dept. of Biochemistry and Molecular Biology
108 Althouse Laboratory
Penn State University
University Park, PA 16802
Phone: 814-865-3355
Fax: 814-863-7024
Email: sxt30@psu.edu,
Website: http://www.bmb.psu.edu/faculty/tan/lab/

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Posted 5/9/08

Research Area: Molecular Neuroscience of Behavior

Description of project: A postdoctoral position is available immediately to study the neural code that underlies innate behavior initiated by olfactory cues in the mouse. We have recently identified and purified a pheromone ligand that promotes aggression (Chamero et al Nature 450:899). This study revealed the existence of a second ligand which we now aim to identify. We will utilize calcium imaging, biophysical fractionation, molecular biology, mouse behavioral assays, and immunohistochemistry to purify and validate the pheromone ligand. We are skilled and able to train new postdocs in all necessary techniques; however the strongest candidates will already have expertise in one of these areas and an interest in olfactory neurobiology.

Please forward CV and names of three references to:
Lisa Stowers, Ph.D.
The Scripps Research Institute,
ICND 232, 10550 North Torrey Pines Road
La Jolla, CA 92037 USA
Phone: 858-784-7285
Fax: 858-784-7299
Email: stowers@scripps.edu
Website: http://www.scripps.edu/research/faculty.php?rec_id=10252

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Posted 5/9/08

Research Area: cell biology, genetics, imaging

Description of project: A postdoctoral position is available immediately to study the three-dimensional organization of the nuclear genome". We are using a set of biochemical, genetic, cell biological methods to understand the biogenesis and organization of the cell nucleus.

Applicants with a strong background in: Drosophila genetics and fluorescence microscopy preferred.

Please forward CV and names of three references to:
Martin W Hetzer, Ph.D.
Address: 10010 N. Torrey Pines Road
Phone: (858) 453-4100 x1419
Email: hetzer@salk.edu
Website: http://www.salk.edu/faculty/faculty_details.php?id=63

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Posted 5/9/08

Research Area: theory of evolvability

Description of project: A postdoctoral position is available to study evolutionary theory. The Masel group's main research interests are in evolvability, gene networks, canalization, and evolutionary capacitance, using a mixture of analytical theory, bioinformatic and simulation approaches. Funding is not tied to a specific project, but applications that do not demonstrate substantial familiarity with our work will not receive a reply. The position is renewable over multiple years, with a start date in mid-2008.

Ph.D. with strong quantitative background and computational and/or modeling experience is required. A background in evolutionary theory is preferred.

Please forward CV and names of three references to:
Joanna Masel, Ph.D.
Ecology & Evolutionary Biology
1041 E Lowell St
University of Arizona, Tucson AZ 85721, USA
Phone: 1 520 626 9888
Fax: 1 520 621 9190
Email: masel@u.arizona.edu
Website: http://eebweb.arizona.edu/faculty/masel

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Posted 5/9/08

Research Area: Membrane protein crystallography

Description of project: A postdoctoral position is available immediately to study the structure and mechanism of active transport (See Nature, 450: 515-521; PNAS,102:17969-17974; and Mol.Cell, 12:651-661). The lab is well-funded with access to the latest equipments for protein crystallization, cryoelectron microscopy, and other biophysical measurements. For more information please visit our website at http://chen.bio.purdue.edu.

Applicants with a strong background in biochemistry and crystallography are preferred.

Please forward CV and names of three references to:
Jue Chen, Ph.D.
Associate Professor
Department of Biological Sciences
Purdue University
West Lafayette, IN 47907
USA
Phone: 765-406-3113
Fax: 765-496-1189
Email: chenjue@purdue.edu
Website: http://chen.bio.purdue.edu

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Posted 5/9/08

Research Area: Transcription, Chromatin, Gene Regulation and Molecular Virology

Description of project: A postdoctoral position is available to study mechanisms of chromatin-dependent transcription and posttranslational modification of transcription factors, cofactors and the general transcription machinery. In vitro-reconstituted chromatin transcription systems are frequently used in the lab to identify the factors and pathways leading to gene activation and repression. Current studies include functional interplays between tumor suppressor proteins, such as p53, and various DNA tumor virus-encoded oncoproteins. Several cellular chromatin adaptors, including Brd4 and SMC5/SMC6, are also studied to define their roles in mediating cellular and viral gene expression.

Applicants with a strong background in protein biochemistry, molecular biology and virology are preferred.

Please forward CV and names of three references to:
Dr. Cheng-Ming Chiang
Simmons Comprehensive Cancer Center
UT Southwestern Medical Center
Building ND2.210H
5323 Harry Hines Blvd.
Dallas, Texas 75390
Phone: (214) 645-6128
Fax: (214) 645-6347
E-mail: Cheng-Ming.Chiang@UTSouthwestern.edu
Website: http://www.utsouthwestern.edu/findfac/research/0,2357,95126,00.html

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Posted 5/9/08

Research Area: Structural Biology of Dynein

Description of project: A postdoctoral position is available immediately to study the 3D structure and function of the molecular motor Dynein using cryo-electron tomography, sub-tomogram averaging and classification (Nicastro et al. 2006 Science 313:944).

Applicants with a strong background in: cryo-EM or with Dynein preferred.

Please forward CV and names of three references to:
Dr. Daniela Nicastro
MS 029 Rosenstiel Center, Brandeis University, 415 South Street
Waltham, MA 02454, USA
Phone: (781)-736-2408
Fax: (781)-736-2419
Email: nicastro@brandeis.edu
Website: http://www.bio.brandeis.edu/nicastrolab/

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Posted 5/9/08

Research Area: Cilia and Flagella

Description of project: A postdoctoral position is available immediately to study cilia and flagella in the model organism Chlamydomonas or Tetrahymena using molecular genetic approaches (KO, RNAi), biochemistry and imaging.
Applicants with a strong background in: molecular genetics (e.g. RNAi) in Chlamydomonas or Tetrahymena, and with cilia & flagella preferred.

Please forward CV and names of three references to:
Dr. Daniela Nicastro
MS 029 Rosenstiel Center, Brandeis University, 415 South Street
Waltham, MA 02454, USA
Phone: (781)-736-2408
Fax: (781)-736-2419
Email: nicastro@brandeis.edu
Website: http://www.bio.brandeis.edu/nicastrolab/

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Posted 5/9/08

Research Area: Proteomics of Cytoskeletal Assemblies

Description of project: A postdoctoral position is available immediately to study the proteomics of cytoskeletal assemblies, such as axonemes and MTOC, using biochemical approaches, mass spectrometry and imaging.

Applicants with a strong background in: biochemistry and mass. spec., cytoskeleton preferred.

Please forward CV and names of three references to:
Dr. Daniela Nicastro
MS 029 Rosenstiel Center, Brandeis University, 415 South Street
Waltham, MA 02454, USA
Phone: (781)-736-2408
Fax: (781)-736-2419
Email: nicastro@brandeis.edu
Website: http://www.bio.brandeis.edu/nicastrolab/

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Posted 5/9/08

Research Area: Correlative Light and Electron Microscopy

Description of project: A postdoctoral position is available immediately in our newly implemented cellular visualization facility for Correlative Light and Electron Microscopy (CLEM), to collaborate with cell and neurobiologists to perform state of the art cellular imaging.

Applicants with a strong background in: TEM specimen preparation, LM and TEM imaging preferred.

Please forward CV and names of three references to:
Dr. Daniela Nicastro
MS 029 Rosenstiel Center, Brandeis University, 415 South Street
Waltham, MA 02454, USA
Phone: (781)-736-2408
Fax: (781)-736-2419
Email: nicastro@brandeis.edu
Website: http://www.bio.brandeis.edu/nicastrolab/

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Posted 5/9/08

Research Area: Viral Vaccine Immunology

Description of project: A postdoctoral position is available immediately to study the cellular and molecular mechanisms regulating the development of long term antibody and memory B cell responses, including the roles of CD4 T cells, specific proteins of interest, and aspects of neutralizing antibody selection. The goal of the laboratory is to elucidate the immunobiology of successful vaccines and apply those principles/mechanisms to the development of future vaccines. The smallpox vaccine is the primary experimental model system used, both in mice and man, with addition viral and protein immunogen systems also utilized.

Applicants with a strong background in: immunology, molecular biology, or infectious diseases preferred.

Please forward CV and names of three references to:

Shane Crotty, Ph.D
The La Jolla Institute for Allergy and Immunology (LIAI)
9420 Athena Circle
La Jolla CA 92037
Phone: (858) 752-6816
Fax: (858) 752-6993
Email: shane@liai.org
Website: www.liai.org

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Posted 5/9/08

Research Area: Phosphorylation signaling in cancer, inflammation and Alzheimer's disease

Description of project: A postdoctoral position is available immediately to study phosphorylation signaling in cancer, inflammation and Alzheimer's disease (see review: Lu, K. P. and Zhou, X. Z., 2007, The prolyl isomerase Pin1: A pivotal new twist in phosphorylation signalling and disease. Nature Reviews Mol. Cell. Biol. 8: 904-916.)

Applicants with a strong background in: Cell biology, neurobiology or immunity preferred.

Please forward CV and names of three references to:
Kun Ping Lu, M.D., Ph.D.
New Research Building, Room 1030K
77 Avenue Louis Pasteur
Harvard Medical School
Boston, MA 02115
Phone: 617-667-4143
Fax: 617-667-0610
Email: klu@bidmc.harvard.edu
Website: http://research.bidmc.harvard.edu/HemOnc/PingLab/index.htm

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Posted 5/9/08

Research Area: Cell Motility and Actin Cytoskeleton
THREE-DIMENSIONAL STRUCTURE DETERMINATION OF MACROMOLECULAR MACHINES INVOLVED IN CELL MOTILITY

Description of project:
A postdoctoral position is available immediately to study molecular machines involved in the assembly and regulation of the actin cytoskeleton at the leading edge of motile cells. Structural characterization of these multimolecular protein complexes is likely to reveal potential mechanisms underlying cell growth, differentiation and migration as well as the role of these interactions in tumor invasion and metastasis. We combine various electron cryomicroscopy, image analysis and bioinformatics techniques to extract high-resolution structural information of these large dynamic assemblies in their fully hydrated state. In particular, we study the role of Arp2/3 complex in actin filament network assembly, the role of myosin in cell migration, and the role of actin binding proteins in providing a scaffold for cell protrusions and adhesion. We are also developing techniques and protocols that allows us to image whole cell, in their fully hydrate state, and to use bioinformatics tools, to correlate between the high-resolution structural information motives with the in situ characterization obtained from living cells. The Burnham Institute for Medical Research forms part of a vibrant scientific community situated next to the Pacific Ocean, including the Scripps and Salk Institutes, as well as UCSD. "

Applicants with a strong background in Biophysics, or Material Science or Bioengineering with some working knowledge of high resolution TEM

Please forward CV and names of three references to:
Dr. Dorit Hanein
Burnham Institute for Medical Research
Phone: 858 646 3134
Fax: 858 6464 3172
Email: dorit@burnham.org
Website: www.burnham.org

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Posted 5/9/08

Research Area: Herbal medicines/dietary supplements use in the prevention and treatment of prostate cancer

Description of project: A postdoctoral position is available immediately to study the role of herbal medicines/dietary supplements in the prevention and treatment of prostate cancer. My lab has a long term interest in finding novel estrogens and estrogen receptors as well as in finding novel functions for estrogens and their related receptors. We are currently working on role of phytoestrogens and their interactions with the hedgehog signaling pathway at the molecular level in prostate cancer.

Applicants with a strong background in Molecular biology and/or pathology preferred.

Please forward CV and names of three references to:
Dennis B Lubahn, PhD
University of Missouri
Biochemistry Department
110A ASRC 920 East Campus Drive
Columbia, Missouri 65211
Phone: 573-884-6781
Fax: 573-882-6827
Email: LubahnD@missouri.edu
Website: www.phyto-research.org

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Posted 5/9/08

Research Area: Stem Cell and Developmental Biology

Description of project: A postdoctoral position is available immediately to investigate the molecular mechanisms of stem cell differentiation.

Applicants with a strong background in: Stem cell biology preferred.

Please forward CV and names of three references to:
Juan Carlos Izpisua Belmonte
The Salk Institute for Biological Studies
10010 North Torrey Pines Road
La Jolla, CA 92037 USA
Phone: (858) 453-4100 x1130
Fax: (858) 453-2573
Email: belmonte@salk.edu

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Posted 5/9/08

Research Area: Regulation of human transcription by non-coding RNAs

Description of project: A postdoctoral position is available immediately to study the control of mRNA transcription by non-coding RNAs in human cells. Specifically, we are studying the mechanism of transcriptional repression by ncRNAs that bind directly to RNA polymerase II, including the repression of transcription by human Alu RNA in response to heat shock (Molecular Cell, 2008, 29: 499-509). We are also interested in engineering non-coding RNAs to control transcription and cell growth in model systems relevant to human disease. The experimental approaches encompass mechanistic biochemical studies in a reconstituted transcription system through genome-wide analysis of transcription and ncRNA occupancy in human cells.

Applicants with a strong background in biochemistry, mammalian cell culture, or microarrays preferred.

Please forward CV and names of three references to:
James A. Goodrich
Department of Chemistry and Biochemistry,
215 UCB, University of Colorado
Boulder, CO 80309-0215.
Phone: 303-492-3273
Fax: 303-492-5894
Email: james.goodrich@colorado.edu
Website: http://www.colorado.edu/chem/goodrichlab/

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Posted 5/9/08

Research Area: Directed Evolution and Mechanistic Analysis of Fluorescent Proteins

Description of project: A postdoctoral position is available immediately to study fluorescent proteins (FPs), including DsRed and its variants. One line of investigation involves using directed evolution to engineer specific structural and photophysical properties into existing FPs. This work involves creating truly monomeric FP variants, and optimizing them for brightness, spectral properties, and photostability. A complementary line of investigation focuses on the underlying chemical mechanisms that generate the FP chromophores. This work involves using a combination of crystallography, biophysical analysis, and biochemistry to dissect chromophore maturation pathways. Both approaches are integrated with cell biology experiments aimed at characterizing the behavior of FPs in living systems. This project will be jointly mentored by a cell biologist (Ben Glick) and a structural biologist (Bob Keenan), both of whom have expertise with directed evolution of FPs.

Applicants with a strong background in: biochemistry, structural biology, and/or cell biological imaging preferred.

Please forward CV and names of three references to:
Benjamin Glick
The University of Chicago
920 East 58th Street
Chicago, IL 60637
USA
Phone: 773-702-5315
Fax: 773-702-3172
Email: bsglick@uchicago.edu
Website: http://mgcb.uchicago.edu/faculty/glick/index.html

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Posted 5/9/08

Research Area: Chromatin and Epigenetics

Description of project: Applications are invited from highly ambitious and motivated scientists for a Postdoctoral Research Fellowship position in the Department of Biochemistry and Molecular Biology at the University of Southern California's Norris Comprehensive Cancer Center in sunny Los Angeles. The overall goals of the lab are to understand the role of chromatin and epigenetics in normal development and disease progression using a diverse array of model systems and cutting-edge technologies. The focus of the lab is on histone modifications. For more information on the lab and PI, visit http://www.histonecode.com.

Current available research projects include, but are not limited to:

1) Defining the epigenomic signatures of various human cells, especially stem cells, in terms of DNA methylation and histone modifications using available ultrahigh-throughput ChIP-Seq technology.

2) Implementing a novel method developed in the lab to isolate, identify and study post-translational modification-specific histone binding proteins in vivo.

3) Determining the function and biological significance of the methylation of histone H4K20 by PR-Set7 and Suv4-20 in transcription, the cell cycle, DNA replication, DNA damage/repair and genomic stability.

4) Studying the role of critical chromatin modifiers in C. elegans development and longevity.

A strong foundation in biochemistry and molecular biology are required. A high level of proficiency in speaking, writing and reading English are also required. Experience in computational bioinformatics, chromatin/epigenetics techniques, mouse models, C. elegans, human ES cells or primary mammalian cell culture are desired. The candidate must have obtained a Ph.D. or M.D. degree within the last five years. Salary will be determined by candidate experience using the current NIH scale. USC offers an outstanding benefits package including medical, dental and retirement.

For full consideration, please submit a cover letter that includes a brief statement of your future research and career goals, your detailed CV, and the names and contact information of three references electronically to:

Judd C. Rice, Ph.D.
Assistant Professor of Biochemistry and Molecular Biology
USC/Norris Comprehensive Cancer Center and the USC Epigenome Center
juddrice@usc.edu

Completed applications will be reviewed upon receipt, and selected candidates will be contacted for a personal interview.

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Posted 5/9/08

Research Area: Cell Cycle Checkpoints

Description of project: A postdoctoral position is available immediately to study cellular mechanisms that maintain genome integrity. We have recently completed two large-scale RNAi genetic screens along with two protein-protein interaction screens. These screens identified approximately 20 novel proteins that have functions in maintaining genome integrity during DNA replication. A position is open to study these proteins with the goal of defining their genome maintenance functions. Furthermore, we wish to test the hypothesis that several of these proteins are important tumor suppressors that are mutated in human cancers.
Applicants with a strong background in: molecular cell biology preferred.

Please forward CV and names of three references to:

David Cortez
Vanderbilt University School of Medicine
Department of Biochemistry
613 Light Hall, 23rd Pierce Avenue
Nashville, TN 37232
Phone: 615-322-8547
Fax: 615-343-0704
Email: david.cortez@vanderbilt.edu
Website: http://www.mc.vanderbilt.edu/root/vumc.php?site=cortezlab

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Posted 5/9/08

Research Area: Cell Migration, Infectious Diseases

Description of project: We are seeking a postdoctoral fellow to join an exciting interdisciplinary initiative to define the molecular machinery that drive cell migration (and used / hijacked by pathogens during infection). Work at the Hanein lab will focus on resolving the structure of these cellular assemblies through a novel use of correlative live-cell fluorescence imaging and electron tomography. Bioinformatic tools will be used to combine information derived by X-ray crystallography, and NMR, with the information generated electron microscopy imaging, to ultimately provide atomic resolutions models of these macromolecular machines. The Burnham Institute for Medical Research (www.burnham.org) forms part of a vibrant scientific community situated next to the Pacific Ocean, including the Scripps and Salk institutes, and UCSD.

Applicants should hold some experience in experimental and/or computation structural biology.

Please forward CV and names of three references to:
Dorit Hanein at dorit@burnham.org
Dorit Hanein, PhD
BIMR, 101901 North Torrey Pines Rd., La Jolla 92037 California, US
Phone: 858 646 3134
Fax: 858 646 3172
Email: dorit@burnham.org
Website: www.burnham.org,

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Posted 5/9/08

Research Area: Function and Assembly of the Vertebrate Nuclear Pore

Description of project: A postdoctoral position is available immediately to study multiple aspects of the following: The focus of our research is the eukaryotic nucleus: its structure and function. A primary area of interest is the nuclear pore, a large macromolecular complex of 120 million daltons which spans the nuclear envelope. All communication between the nucleus and cytoplasm occurs through the nuclear pore: the pore actively imports proteins needed for DNA replication, RNA transcription and gene control, while excluding cytoplasmic proteins. The pore also must export messenger RNA, tRNA, snRNAs, and ribosomal precursors. With respect to the nuclear pore, we are studying: (1) the assembly and function of the nuclear pore, (2) the structure and component proteins of the pore, and (3) reconstitution of the nuclear pore using an in vitro nuclear assembly system. (see website http://www.biology.ucsd.edu/labs/forbes/ for publications).

Applicants with a strong background in Molecular and Cellular Biology preferred.

Please forward CV and names of three references to:
Dr.Douglass Jane Forbes
Section of Cell and Developmental Biology
Division of Biological Sciences 0347
University of California-San Diego
9500 Gilman Drive
La Jolla, CA, USA
92093-0347

Phone: 858-534-3398
Fax: 858-534-0555
Email: dforbes@ucsd.edu
Website: http://www.biology.ucsd.edu/labs/forbes/

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Posted 5/9/08

Research Area: Immunology

Description of project: A postdoctoral position is available immediately to study the sensitivity of T-cells related to cancer. The goal of this project is to elucidate the basic mechanisms that lead to suboptimal T cell responses against tumor (self) antigens using novel imaging and biophysical techniques (Krogsgaard, Mol Cell, 2003; Krogsgaard et al., Nature, 2005; Krogsgaard and Davis, NI, 2005).

Applicants with a strong background in: immunology, molecular biology, biophysics, bioengineering or related fields preferred.

Please forward CV and names of three references to:
Michelle Krogsgaard
Krogsm01@nyumc.org
Michelle Krogsgaard, Ph.D
522 First Avenue, SRB 1311
Phone: 212 263 9266
Fax: 212 263 9250
Email: krogsm01@nyumc.org
Website: http://www.med.nyu.edu/research/krogsm01.html

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Posted 5/9/08

Research Area: Pain Circuitry Development

Description of project: A postdoctoral position is available immediately to study the development of the pain sensory circuitry, with the long-term goal of identifying new targets for pain treatment. Our approach was to systematically identify transcription factor (TF) genes expressed in developing pain sensory neurons, followed by performing genetic analysis to determine their functions. The human and mouse genomes encode about 1500 TF genes. From 2002-2004, we had used in situ hybridization to compile a genome-scale map of TFs expressed in the developing mouse nervous system (Science 2004; 306(5705): 2255-7). Subsequent genetic studies have led to identification of two master regulators, Runx1 and Tlx3. Runx1 is required for the expression of many ion channels and receptors in peripheral nociceptors, and is required for thermal and neuropathic pain (Neuron, 49, 365-77). Tlx3 operates in spinal pain relay nociceptors, and is required for specification of a cohort of glutamate and peptide transmitters (Nature Neuroscience 7: 510-7; Journal of Neuroscience 28:4037-46). Mice lacking Tlx3 also exhibit pain deficits. The new postdoc will continue to work on how these and other transcriptional regulators to control nociceptor cell diversity generation and specific pain circuit assembly.

Applicants with a strong background in: molecular biology, developmental biology and/or neuroscience will be preferred.

Please forward CV and names of three references to:
Qiufu Ma
Department of Neurobiology
Harvard Medical School
Department of Cancer Biology
Dana-Farber Cancer Institute
1 Jimmy Fund Way
Boston, MA 02115
Phone: 617 632-4594
Fax: 617 632-4595
Email: Qiufu_Ma@dfci.harvard.edu
Website: http://neuro.med.harvard.edu/faculty/ma.html

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Posted 5/9/08

Research Area: Normal and leukemogenic Notch signaling

Description of project: Two postdoctoral positions are available immediately in the Blacklow laboratory in the Department of Pathology at Brigham and Women's Hospital to develop inhibitors targeting the Notch pathway in T-cell acute lymphocytic leukemia. Successful candidates will join a multidisciplinary team investigating T-ALL pathogenesis and inhibition using structural, biochemical, cell culture, and in vivo approaches.

Applicants with a strong background in: structural and molecular biology, biochemistry, and/or cell and tissue culture are preferred.

Please forward CV and names of three references to:
Stephen Blacklow
Brigham and Women's Hospital
Phone: 617-525-4415
Fax: 617-525-4414
Email: sblacklow@rics.bwh.harvard.edu
Website: http://pathology.bwh.harvard.edu/blacklow/

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Posted 5/9/08

Research Area: Cancer Biology

Description of project:
A postdoctoral position is available immediately to study Wnt signaling in stem cell regulation and mammary tumorigenesis.

Applicants with a strong background in Cell or Developmental Biology preferred.

Please forward CV and names of three references to:
Anthony M.C. Brown, Ph.D.
Weill Cornell Cancer Research Lab
310 E. 67th Street, Rm 3-59
New York, NY 10065, USA

Phone: 212 734 0567 x2320
Fax: 212 249 0013
Email: amcbrown@med.cornell.edu
Website: http://www.med.cornell.edu/research/amcbrown/

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Posted 5/9/08

Research Areas: Rho GTPases, Wound Healing, & Transcriptional Repression

Description of Project: Our lab uses developmental, genetic, cellular, molecular, and biochemical approaches to look at different regulatory mechanisms and pathways required for proper Drosophila embryonic development. A postdoctoral position is available to join our research team. Our current efforts are divided between three areas of study.
(1) Mechanisms of Rho GTPase action. Rho GTPases play a central role in diverse biological processes such as actin dynamics, microtubule stability, control of gene expression, oncogenic transformation, cell-cell and cell-matrix adhesion, and epithelial wound repair. Our work currently focuses on the use of genetic and biochemical techniques to elucidate the molecular partners that act downstream or in concert with Rho1 to allow for distinct, spatio-temporally restricted responses at various stages of development.
(2) Wound Healing. The wound repair mechanisms are critical for cell (and organismal) survival and appear to have many parallels with the developmental processes required to form tissues in the first place. We are investigating the cellular and molecular mechanisms of single cell and multicellular wound repair and their ensuing biological manifestations within the context of a whole organism.
(3) Transcriptional Repression and Cofactor Recruitment. Transcriptional repression is an important feature of developmental processes where it is necessary for establishing complex patterns of gene expression. We have been using the bHLH transcriptional repressor Hairy as a canonical developmental repressor model system. Our current focus is on characterizing cofactors required for Hairy-mediated repression and the identification of its direct downstream targets.

**For additional information, please see our lab web site: http://www.fhcrc.org/science/labs/parkhurst/
The Hutchinson Center is highly interactive and provides an excellent intellectual environment for pursuing scientific research.

Please forward CV and the names of three references (with contact information) to:
Susan Parkhurst, Ph.D.
Member, Division of Basic Sciences
Fred Hutchinson Cancer Research Center
1100 Fairview Avenue North; A1-162
P.O. Box 19024
Seattle, WA 98109-1024

Tel: (206) 667-6466
Fax: (206) 667-6497
email: susanp@fhcrc.org
website: http://www.fhcrc.org/science/labs/parkhurst/

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Posted 5/9/08

Research Area: Structural virology

Description of project: A postdoctoral position is available immediately to study the structural mechanisms of how herpesviruses enter cells. We use a combination of x-ray crystallography, biochemistry, and functional assays to study the entry machinery of herpesviruses. Current available projects focus on the structure of various components of the viral entry machinery and how these proteins interact. The laboratory is fully equipped for all aspects of molecular biology and biochemistry and has access to X-ray crystallography facilities and the biophysical and imaging resources at Tufts University.

Applicants with a strong background in biochemistry and crystallography are preferred. Applicants should have a Ph.D. with 0-2 years postdoctoral research experience.

Please forward a cover letter, a CV, and names of three references to:
Katya Heldwein
Department of Molecular Biology and Microbiology
Tufts University School of Medicine
136 Harrison Avenue
Boston, MA 02155
Phone: (617) 636-0858
Fax: (617) 636-0337
Email: katya.heldwein@tufts.edu
Website: http://www.tufts.edu/sackler/microbiology/faculty/heldwein/index.html

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Posted 5/9/08

Research Area: Stem Cells

Description of project: A postdoctoral position is available immediately to study the biology of adult stem cells in Drosophila.

Applicants with a strong background in: Developmental Genetics preferred.

Please forward CV and names of three references to:

Craig Micchelli
Washington University School of Medicine
Dept. of Developmental Biology
660 S. Euclid Avenue,
St. Louis, MO 63110

Phone: 314.362.7036
Fax: 314.362.7058
Email: micchelli@wustl.edu

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Posted 5/9/08

Research Area: Neurobiology and Stem Cell Biology

Description of project: A postdoctoral position is available immediately to study the role of irreversible genetic and epigenetic changes in neuronal differentiation and disease. We aim to use new stem cell technologies such as cloning by nuclear transfer and viral induced pluripotency protocols to induce neurons to become pluripotent cell lines. These studies will enable us to dissect the steps involved in neuronal differentiation and cell cycle exit, and to perform whole genome analyses on individual neurons, which has not previously been possible. We ultimately wish to apply our new methods to neurons that have been affected by various neurological diseases including inherited developmental defects and late onset neurodegenerative disorders such as Parkinson’s and Alzheimer’s disease.

Applicants with a strong background in: Molecular biology, cell biology, developmental biology, molecular or cellular neurobiology are preferred. We are also interested in applicants with clinical expertise in human neurological diseases or mouse models of these diseases.

Please forward CV and names of three references to:
Dr. Kristin Baldwin, Ph.D.
10550 N. Torrey Pines Rd.
ICND 202
La Jolla, CA 92037

Phone: 858-784-9466
Fax: 858-784-9860
Email: kbaldwin@scripps.edu
Website: http://www.scripps.edu/research/faculty.php?rec_id=22025

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Posted 5/9/08

Research Area: Molecular Neurobiology

Description of project: A postdoctoral position is available immediately to study the formation and function of specific neural circuits in the brain, using the mouse olfactory system as a model. We take advantage of the unique organization and genetic tractability of the mouse olfactory system to label specific neural circuits in gene targeted mice, to manipulate them with genetically encoded neuronal activators or inhibitors, and to identify specific genes that may be involved in building circuits during development or in remodeling them in response to environmental stimuli. Projects in the lab include developing new genetic technologies to label and identify neurons that respond to specific odors, to understand how attractive and repulsive odors are differentially represented in the brain, and to identify genes responsible for linking sensory neurons to the cortical sites of odor perception.

Applicants with a strong background in: Molecular biology, cell biology, developmental biology, virology, molecular or cellular neurobiology are preferred, though any strong applicant with experience in biomedical research or chemistry will be considered.

Please forward CV and names of three references to:
Dr. Kristin Baldwin, Ph.D.
10550 N. Torrey Pines Rd
ICND 202
La Jolla, CA 92037

Phone: 858-784-9466
Fax: 858-784-9860
Email: kbaldwin@scripps.edu
Website: http://www.scripps.edu/research/faculty.php?rec_id=22025

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