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Program
- Plenary Speakers |
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280 elite scientists will address
the Genetics Congress.
We are proud to announce that the following individuals will be
among them.
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Leif
ANDERSSON
08:30 Tuesday July 8
Leif Andersson received his Ph.D. 1984 from the Swedish University
of Agricultural Sciences.
He has been associated with the Swedish University of Agricultural
Sciences since then and is now Professor in Animal Genetics.
The work in his group focuses on unravelling the molecular
basis for phenotypic diversity in domestic animals, from coat
colour to metabolic traits. The group has generated several
highly informative intercrosses in pigs and chicken. A particular
interest has been to make crosses between the wild ancestors
(wild boar and red junglefowl, respectively) and domestic
breeds in order to study the genetic basis for phenotypic
changes that has occurred due to domestication and selective
breeding.
Major contributions from the group include molecular dissection
of coat colour variation in the pig, mapping and characterisation
of major Qunatitative Trait Loci (QTLs) affecting fatness
and muscle development in the pig and positional cloning of
PRKAG3 encoding a new isoform of the -chain of AMP-activated
protein kinase (AMPK) controlling variation in glycogen content
in pig skeletal muscle. |
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| David
Botstein
17:30 Tuesday July 8
David Botstein, Professor of Genomics at Princeton University,
has made
numerous fundamental contributions to modern genetics. Throughout
his career he has been a powerhouse of innovation, and his
concepts and strategies have repeatedly opened new
avenues for modern genetic research. His contributions cover
much of the field of genetics, from the development of methods
of mutagenesis of bacteria and yeast, to the analysis of
the
problems of bacteriophage assembly and of eukaryotic cell
biology (such as the cytoskeleton and secretion), to the
development
of the basic principles of the application of genetic polymorphisms
for the mapping of the human genome. Most recently his strategy
to use DNA-arrays to characterize normal cellular processes
and disease-associated changes in these processes has paved
the way towards genome-wide diagnostics. David Botstein is
the winner of the Peter Gruber Foundation Genetics Prize
for
2003. This Prize will be presented at the Congress on Thursday
July 10.
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Sponsored By:
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Francis
COLLINS
08:30 Monday July 7
Francis S. Collins, M.D., Ph.D., is the Director of the National
Human Genome Research Institute at the National Institutes
of Health. He oversees the Human Genome Project, a complex
multidisciplinary scientific enterprise directed at mapping
and sequencing all of the human DNA, and determining aspects
of its function. A working draft of the human genome sequence
was announced in June of 2000, an initial analysis was published
in February of 2001, and the completed sequence is anticipated
in the spring of 2003. From the outset, the project has run
ahead of schedule and under budget, and all data has been
made immediately available to the scientific community, without
restrictions on access or use.
He received a B.S. from the University of Virginia, a Ph.D.
in Physical Chemistry from Yale, and an M.D. from the University
of North Carolina. Following a fellowship in Human Genetics
at Yale, he joined the faculty at the University of Michigan,
where he remained until moving to NIH in 1993. His research
led to the identification of genes responsible for cystic
fibrosis, neurofibromatosis, and Huntington's disease. He
is a member of the Institute of Medicine and the National
Academy of Sciences.
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| Jenny
GRAVES
17:00 Thursday July 10
Jenny Graves received degrees from Adelaide University in
1964 and 1967, then a PhD in Molecular Genetics at the University
of California at Berkeley in 1971. She returned to Australia
in 1971 to a lecturer position at La Trobe University, where
she remained until 2001, becoming Professor in 1992. She is
now Professor and Head of the Comparative Genomics Research
Group in the Research School of Biological Science at the
Australian National University in Canberra.
Jenny uses evolutionary variation between distantly related
mammals (humans, mice and Australian mammals such as kangaroos
and platypus) to deduce how gene arrangment, function, and
large-scale control evolved and how it works. Her work has
delivered many surprises about how sex is determined in all
mammals, and how sex chromosomes and the genes on them evolved.
Jenny has been President of GSA, co-Chair of the Comparative
Genetics Committee of the International Human Gene Mapping
Workshops, and Foundation President of the Cell Biology Society
of Australia and New Zealand. She was elected Fellow of the
Australian Academy of Sciences in 1999. |
Sponsored By:
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Yoshihide
HAYASHIZAKI
16:30 Monday July 7
Dr. Yoshihide Hayashizaki was awarded M.D. and Ph.D. from
Osaka University Medical School in 1982 and 1986 respectively
and the research work regarding human thyroid stimulating
hormone subunit gene was continued until 1990.
He worked in National Cardiovascular Center Research Institute
from 1990 to 1992 and achieved the development of the new
technology, restriction landmark genome scanning (RLGS) system.
From 1992, he started working in The Institute of Physical
and Chemical Research (RIKEN), and in 1995, he was appointed
as Project Director to start Mouse Encyclopedia Project in
Genome Science Laboratory, RIKEN Tsukuba Life Science Center,
which was transferred to Yokohama Campus.
Also he started activities for professorship in Basic Medical
Sciences, University of Tsukuba from 1995 and in Graduate
School of Integrated Sciences, Yokohama City University from
2001. Tokyo Techno-forum Gold Medal Prize and Tsukuba Prize
were awarded in 1995 and 2001 respectively. His research interest
is in application of Mouse Encyclopedia for analysis of gene
transcriptional network. |
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Robert HORVITZ
16:30 Friday July 11
Dr. H. Robert Horvitz received S.B. degrees in Mathematics
and in Economics from MIT in 1968 and a Ph.D. in Biology from
Harvard University in 1974. He was a postdoctoral fellow at
the MRC Laboratory of Molecular Biology in Cambridge, England
from 1974-1977 and joined the MIT Department of Biology as
a faculty member in 1978. Dr. Horvitz became an Investigator
of the Howard Hughes Medical Institute in 1988 and of the
McGovern Institute for Brain Research in 2001. Dr. Horvitz
has served on many editorial boards, visiting committees and
advisory committees. Dr. Horvitz was President of the Genetics
Society of America in 1995. Dr. Horvitz was elected to the
U.S. National Academy of Sciences in 1991, a Fellow of the
American Academy of Arts and Sciences in 1994, and a Fellow
of the American Academy of Microbiology in 1997.
Dr. Horvitz has received numerous awards for his accomplishments,
including the Charles A. Dana Award for Pioneering Achievements
in Health (1995); the General Motors Cancer Research Foundation
Alfred P. Sloan, Jr. Prize (1998);the Gairdner Foundation
International Award (Toronto, Canada, 1999); the Bristol-Myers
Squibb Award for Distinguished Achievement in Neuroscience,
2001; and the Nobel Prize in Physiology or Medicine, 2002.
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Sponsored By:
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Maria
JASIN
08:30 Wednesday July 9
Maria Jasin was a graduate student with Paul Schimmel at
the Massachusetts Intitute of Technology and received her
PhD in 1984.
She pursued post doctoral studies at the University of Zurich
with Walter Schaffner and at Stanford University in the Biochemistry
Department with Paul Berg. Dr. Jasin has been at Memorial
Sloan Kettering Cancer Center since 1990 where she is a full
member and holds the William E. Snee Chair.
She also has an appointment at the Cornell University Graduate
School of Medical Sciences. The research in her laboratory
focuses on understanding how genomic integrity is maintained
in mammalian cells, in particular how cells repair DNA double
strand breaks. These studies encompass DNA break repair during
meiosis in the formation of gametes, as well as a major interest
in understading how aberrant break repair can lead to genomic
rearrangements and promote tumorigenesis. |
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| Michael
LYNCH
08:30 Friday July 11
Michael Lynch, Department of Biology, Indiana University,
Bloomington, IN 47405, USA
Michael Lynch obtained his Ph. D. in ecology from the University
of Minnesota in 1977. After working in the fields of population
and community ecology for a few years, his research moved
into the area of evolutionary and quantitative genetics, and
from there his interests have expanded to include a focus
on the mechanisms responsible for the evolution of eukaryotic
genome complexity. Ongoing work also concerns the role of
mutation in evolution and extinction, with various applications
in genetic conservation. Attempts to address these issues
involve the integration of empirical work with two model organisms
(the nematode Caenorhabditis and the microcrustacean Daphnia),
computational analyses of whole-genome sequences, and mathematical
applications of population-genetic theory. Lynch is coauthor
(with Bruce Walsh) of Genetics and Analysis of Quantitative
Traits; past president of the Society for the Study of Evolution;
a fellow of the American Academy of Arts and Sciences and
the American Association for the Advancement of Science; and
the member of various NSF, NIH, and NRC panels.
Lynch, M., and J. C. Conery. 2000. The evolutionary fate
and consequences of duplicate genes. Science 290: 1151-1154.
Lynch, M. 2002. Intron evolution as a population-genetic
process. Proc. Natl. Acad. Sci. USA 99: 6118-6123. |
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Elliot
MEYEROWITZ
08:30 Thursday July 10
A member of the Caltech faculty since 1980, Meyerowitz studies
the genetics of flowering plants. Specifically, he is interested
in the genes that control the formation and development of
flowers, that regulate growth at the shoot apical meristem,
and that act in plant hormone responses. His laboratory has
identified and cloned homeotic flower development genes,
leading
to the "ABC Model" of floral organ specification;
was the first to clone plant hormone receptors (those for
ethylene); and has demonstrated a mechanism for cell-cell
communication in shoot apical meristems that involves an
extracellular
ligand and a transmembrane receptor kinase.
Meyerowitz received the Pelton Award from the Botanical Society
of America and the Conservation Research Foundation in 1994,
the Gibbs Medal from the American Society of Plant Physiologists
in 1995, won the Genetics Society of America Medal and shared
the LVMH "Science pour l'Art" Science Prize in 1996.
He was awarded the International Prize for Biology by the
Japan Society for the Promotion of Science in 1997, the Richard
Lounsbery Award of the U.S. National Academy of Sciences in
1999, and the Wilbur Cross Medal of Yale University in 2001.
He is a member of the U.S. National Academy of Sciences, the
American Academy of Arts and Sciences, and the American Philosophical
Society, and is a foreign associate of the Académie
des Sciences of France.
Bowman, J.L., Smyth, D.R. and Meyerowitz, E.M. (1989)
Genes directing flower development in Arabidopsis. Plant Cell
1, 37-52.
Meyerowitz, E.M. (2002) Plants compared to animals: the
broadest comparative study of development. Science 295, 1482-1485. |
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| Miroslav
RADMAN
16:30 Tuesday July 8
Miroslav Radman has been Professor at the Université Paris
V (Faculté de médécine Necker-Enfants Malades) since
1998. He studied biology and physical chemistry at the University
of Zagreb, and then obtained a Doctor of Science from the
Université libre de Bruxelles, Belgium, in 1969. After post-doctoral
study in France (with Professor Raymond Devoret at CNRS, Gif-sur-Yvette)
and the USA (with Dr Matthew Meselson at Harvard University),
he was Professor in the Université libre de Bruxelles (1973-1983),
and then Director of Research at the CNRS Laboratory of Mutagenesis,
Institut Jacques Monod, Paris (1983-1998). Professor Radman's
research is centred on the molecular mechanisms of DNA repair,
and their role in the appearance of cancers, and the evolution
of species. He proposed the general class of response of the
cell to genotoxic shock known as SOS repair. He also showed
the existence of endonuclease III, a repair enzyme that specifically
repairs mutagenic lesions caused by the oxidation of thymine.
He was involved in obtaining evidence for repair of mis-matched
bases, and showed that it was involved in the precocious development
of cancers in a mouse DNA repair mutant. Recently, Professor
Radman's work has highlighted the role of mismatch repair
in speciation, showing that it prevents recombination between
similar chromosomal sequences, and thus assures the stability
of genomes carrying repeated sequences, and the establishment
of genetic barriers between closely related species. Professor
Radman received the Spiridion Brusina Medal (Croatia) in 1998,
the Richard Lounsbery Prize in 2000, and was elected to l'Académie
des sciences, Paris in 2002.
Denamur E et al., 2000 Evolutionary implications of
the frequent horizontal transfer of mismatch repair genes.
Cell 103, 711-721
Giraud A et al., 2001 Costs and benefits of high
mutation rates: adaptive evolution of bacteria in the mouse
gut. Science 291, 2606-2608
Friedberg E C, Wagner R & Radman M 2002 Specialized DNA
polymerases, cellular survival and the genesis of mutations.
Science 296, 1627-1630 |

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Robert
SAINT
17:15 Friday July 11
Professor Saint graduated from Adelaide University, where
he studied keratin gene structure in the earliest days of
recombinant DNA technology. He then spent three years in Dr.
David Hogness's laboratory at Stanford University, where he
studied the structure and expression of the Bithorax Complex
of Drosophila melanogaster. On returning to Australia, he
worked at the Walter and Eliza Hall Institute and the CSIRO
Division of Entomology. In 1989 he moved back to Adelaide
University, where he was one of the pioneers of research into
cell cycle control in development, using D. melanogaster as
a model.
In 1994 he was appointed Professor of Genetics at Adelaide
University. He was an Australian Research Council (ARC) Special
Investigator, from 1997-1999. He then led a successful bid
for an ARC Special Research Centre, becoming Director of the
Centre for the Molecular Genetics of Development, in 2000.
At the start of 2002, he moved to the Research School of
Biological Sciences at the Australian National University
as Professor of Molecular Genetics and Evolution. His research
interests continue to be in the molecular genetics of cell
division and gene expression during Drosophila development,
with additional recent interests in the genetics and development
of coral.
L. O'Keefe, W.G. Somers, A. Harley, and R. SAINT (2001)
The Pebble GTP Exchange Factor and the Control of Cytokinesis.
Cell Struct. Function 26:619-626
T. Shandala, R.D. Kortschak, S. Gregory and R. SAINT.
(1999) The Drosophila dead ringer gene is required for normal
embryonic patterning through regulation of argos and buttonhead
expression. Development 126:4341-4349. |
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