Wnt, activin, and BMP signaling regulate distinct stages in the developmental pathway from embryonic stem cells to blood.

Canonical Wnt signaling is required for development of embryonic stem cell-derived mesoderm.

A hierarchical order of factors in the generation of FLK1- and SCL-expressing hematopoietic and endothelial progenitors from embryonic stem cells.

Development of erythroid and myeloid progenitors in the yolk sac and embryo proper of the mouse.

Deletion of the selection cassette, but not cis-acting elements, in targeted Flk1-lacZ allele reveals Flk1 expression in multipotent mesodermal progenitors.

Evidence for novel fate of Flk1+ progenitor: contribution to muscle lineage.

BMP type II receptor is required for gastrulation and early development of mouse embryos.

Bmpr encodes a type I bone morphogenetic protein receptor that is essential for gastrulation during mouse embryogenesis.

Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse.

Ontogeny of the haemopoietic system: yolk sac origin of in vivo and in vitro colony forming cells in the developing mouse embryo.

BMP signaling in the epiblast is required for proper recruitment of the prospective paraxial mesoderm and development of the somites.

Wnt, activin, and BMP signaling regulate distinct stages in the developmental pathway from embryonic stem cells to blood.

Dissecting hematopoietic differentiation using the embryonic stem cell differentiation model.

A crucial role for the ubiquitously expressed transcription factor Sp1 at early stages of hematopoietic specification

Dev106054 1..11

Dev106054 2391..2401

T lymphocyte potential marks the emergence of definitive hematopoietic progenitors in human pluripotent stem cell differentiation cultures.

Lineage Regulators Direct BMP and Wnt Pathways to Cell-Specific Programs during Differentiation and Regeneration

Differentiating Embryonic Stem Cells Pass through ‘Temporal Windows’ That Mark Responsiveness to Exogenous and Paracrine Mesendoderm Inducing Signals

BMP inhibition stimulates WNT-dependent generation of chondrogenic mesoderm from embryonic stem cells.

Spatio-temporal regulation of Wnt and retinoic acid signaling by tbx16/spadetail during zebrafish mesoderm differentiation

Differentiation of Embryonic Stem Cells to Clinically Relevant Populations: Lessons from Embryonic Development

Canonical Wnt signaling is required for development of embryonic stem cell-derived mesoderm.

A hierarchical order of factors in the generation of FLK1- and SCL-expressing hematopoietic and endothelial progenitors from embryonic stem cells.

Development of erythroid and myeloid progenitors in the yolk sac and embryo proper of the mouse.

Deletion of the selection cassette, but not cis-acting elements, in targeted Flk1-lacZ allele reveals Flk1 expression in multipotent mesodermal progenitors.

Evidence for novel fate of Flk1+ progenitor: contribution to muscle lineage.

BMP type II receptor is required for gastrulation and early development of mouse embryos.

Bmpr encodes a type I bone morphogenetic protein receptor that is essential for gastrulation during mouse embryogenesis.

Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse.

Ontogeny of the haemopoietic system: yolk sac origin of in vivo and in vitro colony forming cells in the developing mouse embryo.

BMP signaling in the epiblast is required for proper recruitment of the prospective paraxial mesoderm and development of the somites.

Wnt, activin, and BMP signaling regulate distinct stages in the developmental pathway from embryonic stem cells to blood.

Dissecting hematopoietic differentiation using the embryonic stem cell differentiation model.

A crucial role for the ubiquitously expressed transcription factor Sp1 at early stages of hematopoietic specification

Dev106054 1..11

Dev106054 2391..2401

T lymphocyte potential marks the emergence of definitive hematopoietic progenitors in human pluripotent stem cell differentiation cultures.

Lineage Regulators Direct BMP and Wnt Pathways to Cell-Specific Programs during Differentiation and Regeneration

Differentiating Embryonic Stem Cells Pass through ‘Temporal Windows’ That Mark Responsiveness to Exogenous and Paracrine Mesendoderm Inducing Signals

BMP inhibition stimulates WNT-dependent generation of chondrogenic mesoderm from embryonic stem cells.

Spatio-temporal regulation of Wnt and retinoic acid signaling by tbx16/spadetail during zebrafish mesoderm differentiation

Differentiation of Embryonic Stem Cells to Clinically Relevant Populations: Lessons from Embryonic Development

Canonical Wnt signaling is required for development of embryonic stem cell-derived mesoderm.

A hierarchical order of factors in the generation of FLK1- and SCL-expressing hematopoietic and endothelial progenitors from embryonic stem cells.

Development of erythroid and myeloid progenitors in the yolk sac and embryo proper of the mouse.

Deletion of the selection cassette, but not cis-acting elements, in targeted Flk1-lacZ allele reveals Flk1 expression in multipotent mesodermal progenitors.

Evidence for novel fate of Flk1+ progenitor: contribution to muscle lineage.

BMP type II receptor is required for gastrulation and early development of mouse embryos.

Bmpr encodes a type I bone morphogenetic protein receptor that is essential for gastrulation during mouse embryogenesis.

Bone morphogenetic protein-4 is required for mesoderm formation and patterning in the mouse.

Ontogeny of the haemopoietic system: yolk sac origin of in vivo and in vitro colony forming cells in the developing mouse embryo.

BMP signaling in the epiblast is required for proper recruitment of the prospective paraxial mesoderm and development of the somites.