Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
5R01HD028460-05
Application #
2201120
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1991-08-01
Project End
1997-07-31
Budget Start
1995-08-01
Budget End
1997-07-31
Support Year
5
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Harvard University
Department
Physiology
Type
Schools of Medicine
DUNS #
082359691
City
Boston
State
MA
Country
United States
Zip Code
02115
Ataliotis, P; Mercola, M (1997) Distribution and functions of platelet-derived growth factors and their receptors during embryogenesis. Int Rev Cytol 172:95-127
Nascone, N; Mercola, M (1997) Organizer induction determines left-right asymmetry in Xenopus. Dev Biol 189:68-78
Payne, J; Shibasaki, F; Mercola, M (1997) Spina bifida occulta in homozygous Patch mouse embryos. Dev Dyn 209:105-16
Dunn, M K; Mercola, M (1996) Cloning and expression of Xenopus CCT gamma, a chaperonin subunit developmentally regulated in neural-derived and myogenic lineages. Dev Dyn 205:387-94
Symes, K; Mercola, M (1996) Embryonic mesoderm cells spread in response to platelet-derived growth factor and signaling by phosphatidylinositol 3-kinase. Proc Natl Acad Sci U S A 93:9641-4
Dunn, M K; Mercola, M; Moore, D D (1995) Cyclopamine, a steroidal alkaloid, disrupts development of cranial neural crest cells in Xenopus. Dev Dyn 202:255-70
Ataliotis, P; Symes, K; Chou, M M et al. (1995) PDGF signalling is required for gastrulation of Xenopus laevis. Development 121:3099-110
Nascone, N; Mercola, M (1995) An inductive role for the endoderm in Xenopus cardiogenesis. Development 121:515-23
Ho, L; Symes, K; Yordan, C et al. (1994) Localization of PDGF A and PDGFR alpha mRNA in Xenopus embryos suggests signalling from neural ectoderm and pharyngeal endoderm to neural crest cells. Mech Dev 48:165-74
Symes, K; Yordan, C; Mercola, M (1994) Morphological differences in Xenopus embryonic mesodermal cells are specified as an early response to distinct threshold concentrations of activin. Development 120:2339-46

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