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Andrew J.W. Furley

Researcher at University of Sheffield

Publications -  57
Citations -  4911

Andrew J.W. Furley is an academic researcher from University of Sheffield. The author has contributed to research in topics: Cellular differentiation & Cell adhesion molecule. The author has an hindex of 30, co-authored 56 publications receiving 4744 citations. Previous affiliations of Andrew J.W. Furley include National Institute for Medical Research & Columbia University.

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Lineage promiscuity in hemopoietic differentiation and leukemia.

TL;DR: It is suggested that verifiable and consistent examples of apparent lineage infidelity do not reflect genetic misprogramming but rather the existence of a transient phase of limited promiscuity of gene expression occurring in normal biopotential or multipotential progenitors and able to be preserved as a relic in leukemic blast cell populations that are in maturation arrest.
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The axonal glycoprotein TAG-1 is an immunoglobulin superfamily member with neurite outgrowth-promoting activity

TL;DR: A full-length cDNA clone encoding rat TAG-1, a 135 kd glycoprotein expressed transiently on the surface of subsets of neurons in the developing mammalian nervous system, is isolated and suggests that this protein plays a role in the initial growth and guidance of axons in vivo.
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Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

TL;DR: It is demonstrated that Caspr2 and TAG-1 form a scaffold that is necessary to maintain K+ channels at the juxtaparanodal region, suggesting that axon–glia interactions mediated by these proteins allow myelinating glial cells to organize ion channels in the underlying axonal membrane.
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Errors in corticospinal axon guidance in mice lacking the neural cell adhesion molecule L1

TL;DR: It is shown that mice that do not express L1 have defects in the guidance of axons of the corticospinal tract, a major motor control pathway projecting from the cortex to the spinal cord, and the presence of a ligand for L1, CD24, specifically at the point of decussation suggests a mechanism in which L1 functions to guide corticOSPinal axons across the midline.
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Cooperation of BMP7 and SHH in the Induction of Forebrain Ventral Midline Cells by Prechordal Mesoderm

TL;DR: A model whereby axial mesoderm both induces the differentiation of overlying neural cells and controls the rostrocaudal character of the ventral midline of the neural tube is suggested.