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Comparative viscosimetric determination of cellulase activity

, : Comparative viscosimetric determination of cellulase activity. Pharmaceutica Acta Helvetiae 33(8-10): 571-582


PMID: 13601108

Other references

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Slotta, J.E.; Braun, O.O.; Menger, M.D.; Thorlacius, H., 2010: Capture of platelets to the endothelium of the femoral vein is mediated by CD62P and CD162. Platelets contribute to blood coagulation at sites of vascular injury and to the recruitment of leukocytes at sites of inflammation. Under pathological conditions, platelets are involved in numerous diseases and clinical complications, such as dee...

Tanaka, Y.; Hirano, N.; Kaneko, J.; Kamio, Y.; Yao, M.; Tanaka, I., 2011: 2-Methyl-2,4-pentanediol induces spontaneous assembly of staphylococcal α-hemolysin into heptameric pore structure. Staphylococcal α-hemolysin is expressed as a water-soluble monomeric protein and assembles on membranes to form a heptameric pore structure. The heptameric pore structure of α-hemolysin can be prepared from monomer in vitro only in the presence...

Raymond, H.Met, 1957: Direct vascular action of quebrachamine. Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales 151(1): 74-76

Sengupta, N.; Morris, C.G.; Kirwan, J.; Amdur, R.J.; Mendenhall, W.M., 2010: Definitive radiotherapy for carcinoma in situ of the true vocal cords. To report long-term rates of tumor control after radiotherapy (RT) for carcinoma in situ (CIS) of the true vocal cords (TVC). Thirty-seven patients with CIS of the TVC were treated curatively with megavoltage RT between July 1967 and December 2005...

Schönemann, W.; Gallienne, E.; Ikeda-Obatake, K.; Asano, N.; Nakagawa, S.; Kato, A.; Adachi, I.; Górecki, M.; Frelek, J.; Martin, O.R., 2014: Glucosylceramide mimics: highly potent GCase inhibitors and selective pharmacological chaperones for mutations associated with types 1 and 2 Gaucher disease. A series of iminoxylitol derivatives carrying a C-linked di-O-acyl or di-O-alkyl glyceryl substituent were prepared and characterized. All of these compounds, which were designed as glucosylceramide (GlcCer) mimics, were nanomolar inhibitors of ly...