Search Results - "Loo, Melinda A."
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Perturbation of Hsp90 interaction with nascent CFTR prevents its maturation and accelerates its degradation by the proteasome
Published in The EMBO journal (01-12-1998)“…Maturation of wild‐type CFTR nascent chains at the endoplasmic reticulum (ER) occurs inefficiently; many disease‐associated mutant forms do not mature but…”
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Dichotomy of astrocytoma migration and proliferation
Published in International journal of cancer (17-07-1996)“…Astrocytomas often show high rates of local invasion that lead to local recurrence of the disease. Histologically, the most highly invasive astrocytoma cells…”
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Determinants of human astrocytoma migration
Published in Cancer research (Chicago, Ill.) (15-07-1994)“…A unique characteristic of astrocytic malignancies is their frequent dissemination through the brain. Cellular determinants of migration include adhesion to…”
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4
Multiple proteolytic systems, including the proteasome, contribute to CFTR processing
Published in Cell (06-10-1995)“…The molecular components of the quality control system that rapidly degrades abnormal membrane and secretory proteins have not been identified. The cystic…”
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Substrates for Astrocytoma Invasion
Published in Neurosurgery (01-08-1995)Get full text
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Contrasting migratory response of astrocytoma cells to tenascin mediated by different integrins
Published in Journal of cell science (01-08-1996)“…Tenascin, an extracellular matrix protein, is expressed in human gliomas in vitro and in vivo. The distribution of tenascin at the invasive edge of these…”
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7
The role of extracellular matrix in human astrocytoma migration and proliferation studied in a microliter scale assay
Published in Clinical & experimental metastasis (01-11-1994)“…Ligands in the extracellular matrix (ECM) are known to mediate migration of normal as well as tumor cells via adhesion molecules such as the integrin receptor…”
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Substrates for astrocytoma invasion
Published in Neurosurgery (01-08-1995)“…A better understanding of the influences of specific extracellular substrates, including proteins, glycosaminoglycans, and parenchymal cells, on the invasive…”
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