Job Description

Postdoctoral & Staff Researcher Positions
- University of Wisconsin School of Medicine, Madison, Wisconsin, USA

Description: The Bresnick laboratory is expanding our research group to accompany our transition to the new cutting-edge research facility at the Wisconsin Institute of Medical Research (WIMR) in the University of Wisconsin School of Medicine and Public Health. We will relocate to this new space in the beginning of 2009, although the position(s) is available asap. The WIMR will provide a first-rate scholarly environment for conducting innovative basic and translational research. Madison, WI offers an outstanding living environment with considerable cultural opportunities, excellent schools, and abundant parks.

We use multidisciplinary approaches to understand important biological processes, including stem/progenitor cell function, blood cell development, and vascular biology. Such approaches include genomics, proteomics, chemical genetics, and computational analysis, as well as traditional molecular, cellular, and biochemical methodologies. In addition to elucidating biological principles, we aim to develop innovative therapeutic strategies based on targeting novel mechanisms. Projects include:

  1. Mechanisms of hematopoiesis. Defining such mechanisms has enormous importance, as deviations from hematopoietic programs yield leukemias, lymphomas and other blood disorders. We are analyzing the function and regulation of GATA transcription factors that control hematopoietic stem and progenitor cell function, hematopoiesis, and additional important processes. Transcriptional profiling and chromatin immunoprecipitation studies have identified a large cohort of novel GATA factor target genes, including genes encoding proteins that bear no obvious similarity to known proteins. Loss-of-function and gain-of-function studies are being conducted in mice, zebrafish, and cultured cells to elucidate new biological pathways, which will provide key insights into mechanisms of development, differentiation, and human disease.

  2. Transcriptional control of hemoglobin synthesis. These studies address fundamental mechanistic questions on how chromatin modification/remodeling regulates transcription of endogenous loci and also how hemoglobin synthesis is dysregulated in human hemoglobinopathies. Many questions remain unanswered regarding how dynamic changes in chromatin are orchestrated during development, differentiation, and pathophysiological processes.

  3. Linking GATA factor mechanisms to human disease. GATA-1 mutations cause human leukemias, while GATA-2 mutations occur in leukemia as well as coronary artery disease. We discovered a link between GATA-2 function and Parkinson’s disease and also a GATA-1-regulated endogenous suppressor of angiogenesis that functions via a novel mechanism. Studying GATA factors can yield important insights of considerable relevance to human disease.

Qualifications: The successful candidate will develop both independent and collaborative experiments in one or more of our focal areas

Application Details: Applications should be sent to Emery H. Bresnick, Ph.D via e-mail using the contact link below.

Contact: Emery H. Bresnick

Closing Date: Check with institute

© 2004-2009 Epigenome Network of Excellence
Printed from: