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Nancy Y. Ip

Researcher at Hong Kong University of Science and Technology

Publications -  390
Citations -  37404

Nancy Y. Ip is an academic researcher from Hong Kong University of Science and Technology. The author has contributed to research in topics: Cyclin-dependent kinase 5 & Neurotrophin. The author has an hindex of 78, co-authored 381 publications receiving 34323 citations. Previous affiliations of Nancy Y. Ip include University of Cambridge & Chinese Academy of Sciences.

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Method of enhancing differentiation and survival of neuronal precursor cells

TL;DR: In this article, a method of enhancing the differentiation of neuronal precursor cells into NGF-dependent neuronal cells, which method includes treating precursor cells with a combination of a member of the FGF family and a members of the CTNF family to enhance their effectiveness and survival in transplantation therapy for the treatment of diseases such as Parkinson's disease.
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A DNA microarray for the authentication of toxic traditional Chinese medicinal plants.

TL;DR: Chip-based authentication of medicinal plants may be useful as inexpensive and rapid tool for quality control and safety monitoring of herbal pharmaceuticals and neutraceuticals.
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Neurotrophic factors and their receptors

TL;DR: These two distinct classes of neurotrophic factors, utilizing distinct signaling pathways, can interact to effect the growth and differentiation of neuronal progenitors during neuropoiesis in a way analogous to that exhibited by the cytokines during hematopoiesis.
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Ephrin-B1 Reverse Signaling Activates JNK through a Novel Mechanism That Is Independent of Tyrosine Phosphorylation

TL;DR: A novel reverse signaling pathway transduced by ephrin-B1 is identified, which is independent of tyrosine phosphorylation but involves the activation of JNK through TAK1 and MKK4/MKK7 and leads to changes in cell morphology.
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Cdk5-Dependent Mst3 Phosphorylation and Activity Regulate Neuronal Migration through RhoA Inhibition

TL;DR: The results show that Mst3 regulates neuronal migration through modulating the activity of RhoA, a Rho-GTPase critical for actin cytoskeletal reorganization, and collectively suggest that Cdk5–Mst3 signaling regulates neurons migration via RHoA-dependent actin dynamics.