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Barres, Ben
A.
Developmental Biology and Neurosciences
Our lab is interested in the neuronal-glial
interactions that underlie the development and function
of the mammlian central nervous system.
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Crabtree,
Gerald R.
Developmental
Biology and Pathology
Morphogenesis and axonal outgrowth in the nervous system. The role of
ATP-dependent chromatin remodeling complexes in development of the neurvous
and immune systems.
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Lab Web Page
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Fuller,
Margaret T.
Developmental Biology and Genetics
Transcriptional and post transcriptional regulation of spermatogenesis;
Cell morphogenesis and cell cycle control during differentiation; Genetic
control of stem cell behavior.
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Hogness,
David S.
Emeritus Professor of Developmental Biology and of Biochemistry
Temporal and hormonal
control of Drosophila development
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Kaiser,
A. Dale
Biochemistry, Cancer Biology and Developmental Biology
How are genes regulated to construct a developmental program? How do
signals received from other cells change the program and coordinate it
for multicellular development? The approach taken by our laboratory group
to answer these questions utilizes biochemistry and genetics; genetics
to isolate mutants that have particular defects in development and biochemistry
to determine the molecular basis of the defects. We study fruiting body
development in Myxococcus xanthus, a social bacterium.
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Kim,
Seung K.
Developmental Biology
We study morphogenesis and cell differentiation in the pancreas, an endoderm-derived
organ, using molecular, embryologic and genetic methods in mice, chicks
and human tissues. Our work suggests that critical epithelial-mesenchymal
cell interactions during pancreas ontogeny are regulated by Hedgehog,
FGF and TGF-ß signaling pathways. We wish to translate these basic
studies into novel diagnostic and therapeutic strategies for diabetes
mellitus and pancreas cancer.
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Kim, Stuart
K.
Developmental Biology and Genetics
We study cell polarity and MAP kinase signaling in C. elegans. We have
found that a complex of PDZ-containing proteins is required for basolateral
localization of the LET-23 receptor in epithelial cells. We have identified
genes regulated by MAP kinase signaling using DNA microarrays.
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Kingsley,
David M.
Developmental Biology
My laboratory uses a variety of genetic, cellular, and molecular approaches
to study skeletal development in humans, mice, and fish. Many of our
studies begin with classical genetic traits that disrupt normal skeletal
development. By isolating the genes responsible for these traits, it
should be possible to identify the key genetic pathways that underlie
skeletal patterning, skeletal disease, and skeletal evolution in higher
animals.
Lab
Summary
Recent
Publications
Lab Web Pages:
http://kingsley.stanford.edu
http://www.hhmi.org/research/investigators/kingsley.html
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McAdams,
Harley
Developmental Biology
We study the design and function of genetic regulatory networks from
a total system perspective. We are particularly focused on the overall
network that controls the cell cycle, asymmetric cell division, and metabolism
of the bacterium Caulobacter crescentus. Methods we use include application
of gene expression microarrays, bioinformatic analysis of genomic data,
and modeling studies.
Lab Web Pages:
http://caulo.stanford.edu/usr/hm/
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Nusse,
Roeland
Cancer Biology and
Developmental Biology
We are interested in the tole of the Wnt gene family in intercellular
signaling during embryogenesis and tumorigenesis. We work on two Drosophila
Wnt genes: wingless and DWnt-2. These genes have very specific phenotype
in the fly. We use Drosophila genetics and cell culture assays to understand
how these proteins work during embryogenesis. We have found that Frizzled
proteins act as receptors for Wnts.
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Porzig,
Ellen F.
Developmental Biology and Molecular Pharmacology
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Scott,
Matthew P.
Developmental Biology, Genetics,
Neurosciences and Cancer Biology
We study regulators of transcription and signaling that control animal
development and prevent cancerous growth. Particular areas include homeobox
genes, hedgehog/patched signaling and its links to skin and brain cancer,
chromatin gene regulation machines, and neural and heart development.
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Shapiro,
Lucille
Cancer Biology, Developmental Biology and Genetics
A basic question in developmental biology involves the mechanisms used
to generate the three-dimensional organization of a cell from a one-dimensional
genetic code. Our goal is to define these mechanisms using both molecular
genetics and biochemistry. The developmental program by which a single
cell proceeds to a fully-developed organism involves........... Shapiro
web page
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Spudich,
James A.
Biochemistry and Developmental
Biology
Biochemical, molecular genetic, and structural studies of actin, myosin,
and associated regulatory proteins from eukaryotic cells: Work focuses
on the design and development of in vitro assays for ATP dependent movement
of purified myosin on filaments reconstituted from purified actin. Myosin
gene cloning and expression of site directed mutagenized forms, which
are analyzed for altered functions, is also carried out. Emphasis is
on the molecular basis of energy transduction that leads to myosin movements
on actin filaments and on regulation of actin and myosin interactions
and of their assembly states, with particular interest in Dictyostelium
cytokinesis, and other forms of cell movement.
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Talbot,
William S.
Developmental Biology
We use genetic and genomic approaches to investigate the molecular basis
of cell fate specification and morphogenesis in the zebrafish embryo.
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Recent
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Villeneuve,
Anne M.
Developmental Biology and Genetics
Mechanisms underlying pairing and recombination between homologous chromosomes
during meiosis, using the nematode Caenorhabditis elegans as an experimental
system. High-resolution 3-D imaging of meiotic chromosomes. Transgene-mediated
cosuppression of germline gene expression.
Lab
Summary
Recent Publications
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Weissman,
Irving L.
Cancer Biology, Developmental Biology and Immunology Biological Sciences Development
of T and B lymphocytes; cell-surface receptors for oncornaviruses in leukemia.
Hematopoietic stem cells; Lymphocyte homing, lymphoma invasiveness and
metastasis.
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