Search Results - "Kühl, W"

Refine Results
  1. 1

    Adaptation of the Winkie Drill for subglacial bedrock sampling by Boeckmann, Grant V., Gibson, Chris J., Kuhl, Tanner W., Moravec, Elliot, Johnson, Jay A., Meulemans, Zack, Slawny, Kristina

    Published in Annals of glaciology (01-04-2021)
    “…The Winkie Drill is an agile, commercially available rock coring system. The U.S. Ice Drilling Program has modified a Winkie Drill for subglacial rock and…”
    Get full text
    Journal Article
  2. 2

    Core handling, transportation and processing for the South Pole ice core (SPICEcore) project by Souney, Joseph M., Twickler, Mark S., Aydin, Murat, Steig, Eric J., Fudge, T. J., Street, Leah V., Nicewonger, Melinda R., Kahle, Emma C., Johnson, Jay A., Kuhl, Tanner W., Casey, Kimberly A., Fegyveresi, John M., Nunn, Richard M., Hargreaves, Geoffrey M.

    Published in Annals of glaciology (01-04-2021)
    “…An intermediate-depth (1751 m) ice core was drilled at the South Pole between 2014 and 2016 using the newly designed US Intermediate Depth Drill. The South…”
    Get full text
    Journal Article
  3. 3
  4. 4

    Receptor-Agonist Interactions in Service-Theoretic Perspective, Effects of Molecular Timing on the Shape of Dose-Response Curves by Kühl, Peter W., Jobmann, Manfred

    “…Service-theoretic concepts and methods, widely used in other fields (e.g., telecommunication and operations research), are useful also in a biochemical setting…”
    Get full text
    Journal Article
  5. 5

    Solubility and Liquid Density of Binary Mixtures of n‑Hexane or 1‑Hexanol with Krypton, Sulfur Hexafluoride, or R143a by Jander, Julius H., Piszko, Maximilian, Kühl, Julius V. W., Rausch, Michael H., Fröba, Andreas P.

    Published in Journal of chemical and engineering data (13-04-2023)
    “…Within the present study, the solubility, phase behavior, and liquid density of binary systems consisting of n-hexane (C6H14) or 1-hexanol (C6H14O) and krypton…”
    Get full text
    Journal Article
  6. 6
  7. 7

    Identification of the Second Common Jewish Gaucher Disease Mutation Makes Possible Population-Based Screening for the Heterozygous State by Beutler, E., Gelbart, T., Kuhl, W., Sorge, J., West, C.

    “…Gaucher disease is an autosomal recessive glycolipid storage disease characterized by a deficiency of glucocerebrosidase. The disease is most common in persons…”
    Get full text
    Journal Article
  8. 8

    Excess-substrate inhibition in enzymology and high-dose inhibition in pharmacology: a reinterpretation [corrected] by Kühl, P W

    Published in Biochemical journal (15-02-1994)
    “…A kinetic model, called the Recovery Model, which incorporates an obligatory recovery phase of fixed duration (tr) in the operation cycle of a macromolecule…”
    Get full text
    Journal Article
  9. 9
  10. 10

    A redox cycling model for the action of beta-adrenoceptor agonists by Kühl, P W

    Published in Experientia (15-09-1985)
    “…A cyclic redox mechanism for the action of beta-adrenoceptor agonists is proposed. It has the following features: a) beta-adrenoceptor agonists act by…”
    Get full text
    Journal Article
  11. 11

    Molecular heterogeneity of glucose-6-phosphate dehydrogenase A by Beutler, E, Kuhl, W, Vives-Corrons, JL, Prchal, JT

    Published in Blood (15-11-1989)
    “…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is probably the most common disease-producing genetic polymorphism of humans. Virtually all G6PD-deficient…”
    Get full text
    Journal Article
  12. 12

    Molecular Heterogeneity of Glucose-6-Phosphate Dehydrogenase A by Beutler, E., Kuhl, W., Vives-Corrons, J.-L., Prchal, J.T.

    Published in Blood (15-11-1989)
    “…Glucose-6-phosphate dehydrogenase (G6PD) deficiency is probably the most common disease-producing genetic polymorphism of humans. Virtually all G6PD-deficient…”
    Get full text
    Journal Article
  13. 13

    DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants by BEUTLER, E, KUHL, W, GELABART, T, FORMAN, L

    Published in The Journal of biological chemistry (05-03-1991)
    “…Over 400 supposedly biochemically and genetically distinct variants of glucose-6-phosphate dehydrogenase (G6PD) have been described in the past. In order to…”
    Get full text
    Journal Article
  14. 14

    Identification of the Binding Domain for NADP+ of Human Glucose-6-phosphate Dehydrogenase by Sequence Analysis of Mutants by Hirono, Akira, Kuhl, Wanda, Gelbart, Terri, Forman, Linda, Fairbanks, Virgil F., Beutler, Ernest

    “…Human erythrocyte glucose-6-phosphate dehydrogenase is normally quite stable in the presence of 10 μ M NADP+. Certain glucose-6-phosphate dehydrogenase…”
    Get full text
    Journal Article
  15. 15
  16. 16

    Mechanical stress and deformation of SMT components during temperature cycling and PCB bending by Kuhl, Reiner W

    Published in Soldering & surface mount technology (01-08-1999)
    “…A very common method to predict the reliability of components soldered on printed circuit board (PCB) or substrates is by bending tests and temperature cycle…”
    Get full text
    Journal Article
  17. 17

    Complete Correction of the Enzymatic Defect of Type I Gaucher Disease Fibroblasts by Retroviral-Mediated Gene Transfer by Sorge, Joseph, Kuhl, Wanda, West, Carol, Beutler, Ernest

    “…Glucocerebrosidase cDNA and the neomycin-resistance gene (neo) were cloned into a retrovirus vector. Mouse fibroblasts infected with this vector expressed…”
    Get full text
    Journal Article
  18. 18

    Failure of alglucerase infused into Gaucher disease patients to localize in marrow macrophages by Beutler, E, Kuhl, W, Vaughan, L M

    Published in Molecular medicine (Cambridge, Mass.) (01-03-1995)
    “…Gaucher disease is a common glycolipid storage disease, caused by a deficiency of lysosomal beta-glucosidase (glucocerebrosidase). Alglucerase is a form of…”
    Get full text
    Journal Article
  19. 19

    Glucocerebrosidase Processing in Normal Fibroblasts and in Fibroblasts from Patients with Type I, Type II, and Type III Gaucher Disease by Beutler, Ernest, Kuhl, Wanda

    “…Fibroblasts from normal subjects and patients with the three types of Gaucher disease were labeled with [3H]leucine. Glucocerebrosidase antigen was…”
    Get full text
    Journal Article
  20. 20