Search Results - "Bruinsma, Paul"

Mesoporous Silica Synthesized by Solvent Evaporation:  Spun Fibers and Spray-Dried Hollow Spheres by Bruinsma, Paul J, Kim, Anthony Y, Liu, Jun, Baskaran, Suresh

“…Simple synthesis methods for mesoporous fibers and powders by rapid evaporation of hydrolyzed silicon alkoxide−surfactant solutions are described. Mesoporous…”
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Retrograde Transport of the Mannosyltransferase Och1p to the Early Golgi Requires a Component of the COG Transport Complex by Bruinsma, Paul, Spelbrink, Robert G., Nothwehr, Steven F.

“…The yeast COG complex has been proposed to function as a vesicle-tethering complex on an early Golgi compartment, but its role is not fully understood. COG…”
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Distinct domains within Vps35p mediate the retrieval of two different cargo proteins from the yeast prevacuolar/endosomal compartment by Nothwehr, S F, Bruinsma, P, Strawn, L A

“…Resident membrane proteins of the trans-Golgi network (TGN) of Saccharomyces cerevisiae are selectively retrieved from a prevacuolar/late endosomal…”
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Dynamic Mobility Spectra of Multicomponent Colloidal Suspensions by Bruinsma, Paul J, Smith, Peter A, Bunker, Bruce C

“…Recently, the electrokinetic sonic amplitude (ESA) signal has been measured over a range of frequencies (collectively termed the dynamic mobility spectrum) for…”
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Sorting of Yeast Membrane Proteins into an Endosome-to-Golgi Pathway Involves Direct Interaction of Their Cytosolic Domains with Vps35p by Nothwehr, Steven F., Ha, Seon-Ah, Bruinsma, Paul

“…Resident late-Golgi membrane proteins in Saccharomyces cerevisiae are selectively retrieved from a prevacuolar-endosomal compartment, a process dependent on…”
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Identification of a novel missense mutation of the SMNT gene in two siblings with spinal muscular atrophy by Wang, C H, Papendick, Brett D, Bruinsma, Paul, Day, J Kevin

“…Spinal muscular atrophy (SMA) is a motor neuron disease caused by mutations in the telomeric copy of the survival motor neuron ( SMN^sup T^ ) gene. Over 90% of…”
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The role of the yeast COG3, VPS35, and YDR141C proteins in membrane trafficking by Bruinsma, Paul

“…Localization mechanisms for resident trans-Golgi network (TGN) proteins have been shown to involve retrieval from the prevacuolar compartment (PVC) and “slow…”
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Identification of a novel missense mutation of the SMN(T) gene in two siblings with spinal muscular atrophy by Wang, C H, Papendick, B D, Bruinsma, P, Day, J K

“…Spinal muscular atrophy (SMA) is a motor neuron disease caused by mutations in the telomeric copy of the survival motor neuron (SMN(T)) gene. Over 90% of SMA…”
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Structure and permeation in gegenion complex Langmuir-Blodgett films by Bruinsma, Paul J., Stroeve, Pieter, Hoffmann, Catherine L., Rabolt, John F.

“…Polyion complexes of arachidic acid and poly (ethyleneimine) were deposited onto Celgard 2400 microporous support membranes and the permeabilities of carbon…”
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Identification of a novel missense mutation of the SMN T gene in two siblings with spinal muscular atrophy by Day, J. Kevin, Wang, C. H., Papendick, Brett D., Bruinsma, Paul

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Identification of a novel missense mutation of the SMN super(T) gene in two siblings with spinal muscular atrophy by Wang, CH, Papendick, Brett D, Bruinsma, Paul, Day, JKevin

“…Spinal muscular atrophy (SMA) is a motor neuron disease caused by mutations in the telomeric copy of the survival motor neuron ( SMN super( T ) ) gene. Over…”
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Rheological and Solid–Liquid Separation Properties of Bimodal Suspensions of Colloidal Gibbsite and Boehmite by Bruinsma, Paul J., Wang, Yong, Li, X.Shari, Liu, Jun, Smith, Peter A., Bunker, Bruce C.

“…Bimodal suspensions of nanometer-sized boehmite particles and micron-sized gibbsite particles in 0.10MNaNO3are used as models to gain insight into the physical…”
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Langmuir-Blodgett, gas-separation membranes by Bruinsma, Paul Joseph

“…Novel asymmetric composite membranes were fabricated by transferring monolayers onto porous support membranes. Langmuir-Blodgett (LB) films are attractive for…”
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Modulation of MAP kinase signaling by the chimaerin Rac GAPs by Bruinsma, Stephen Paul

“…The chimaerins are a family of Rac GTPase-activating proteins (GAPs) characterized by a phorbol ester-binding C1 domain. Chimaerins have been implicated in…”
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