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Human, vii

Drugs which Independently have little effect on laboratory tests may Interact to produce a significant alteration of test values. Table VII presents several drug Interactions In diabetic human subjects which can affect an apparent test result (15). [Pg.277]

Strancar, A., Barut, M., Podgomik, A., Koselj, P, Schwinn, H., Raspor, P, and Josic, D., Application of compact porous tubes from preparative isolation of clotting factor VII from human plasma, /. Chromatogr. A, 760, 117, 1997. [Pg.309]

Factor IX Replacement Hemophilia B therapy may include recombinant (produced via transfection of mammalian cells with the human factor IX gene) or plasma-derived (concentrate from pooled plasma) factor IX (see Table 64-2). Guidelines for choosing the factor-concentrate formulation for hemophilia B are similar to the guidelines for hemophilia A. However, older-generation factor IX concentrates containing other vitamin K-dependent proteins (e.g., factors II, VII, and IX), called prothrombin complex concentrates (PCCs), have been associated with thrombogenic side effects. Consequently, these products are not first-line treatment for hemophilia B.11... [Pg.990]

PCCs contain the vitamin K-dependent factors II, VII, IX, and X. These agents represent another attempt to bypass the factor at which the antibody is directed (see Fig. 64-2). However, PCCs carry the risk of serious thrombotic complications. Porcine factor VIII is most useful when the inhibitor titer is less than 50 BU (see Fig. 64-2 for dose and frequency). Owing to its similarity to human factor VIII, porcine factor VIII participates in the coagulation cascade. However, most inhibitors have very weak neutralizing activity against it. Porcine factor VIII is a third-line agent (only after factor Vila and a PCC have failed) owing to a 15% incidence of cross-reactivity.15... [Pg.991]

Vitamin K is a fat-soluble vitamin cofactor for the activation of factors II, VII, IX, and X in the liver. Almost all neonates are vitamin K-deficient at as a result of (1) insignificant transplacental vitamin K crossover, (2) lack of colonization of the colon by vitamin K-producing bacteria, and (3) inadequate dietary vitamin K intake (especially in breast-fed infants because human milk contains less vitamin K than infant formula or cow s milk). Vitamin K-deficiency bleeding (VKDB) refers to bleeding attributable to vitamin K deficiency within first 6 months of life. It occurs in three general time frames early (0-24 hours), classic (1-7 days), and late (2-12 weeks). Early onset occurs rarely and usually is associated with maternal ingestion of anticonvulsants, rifampin, isoniazid, and warfarin. Classic vitamin K-dependent bleeding usually results from the lack of prophylactic vitamin K administration in... [Pg.997]

In chimpanzees, administration of Fab fragments of a monoclonal anti-F-VII antibody preceding an endotoxin bolus injection effectively blocked the activation of the coagulation pathway (B25). Administration of monoclonal anti-lL-6 under the same experimental conditions attenuated the activation of coagulation, while the fibrinolytic system remained unaltered. However, administration of monoclonal anti-TNF enhanced the tendency to microvascular thrombosis (P17,18). Monoclonal anti-TF antibodies administered to baboons as a pretreatment attenuated coagulopathy after induction of E. coli sepsis in these animals (T4). Primates pretreated with anti-C5a antibodies before infusion of E. coli developed less hypotension and had better survival rates than untreated animals, who developed ARDS and septic shock with a mortality rate of 75% (S35, Z6). No favorable treatment results have been published yet with one of these treatment modalities given to humans. [Pg.86]

Different tissues in the body have different types of collagen (there are 27 in total) classified as collagen types I, II, and so on. Type I collagen, for example, the most abundant collagen of the human body, makes up the tendons and the organic part of bone type II collagen makes up articular cartilage type IV makes up the eye lens type VII and type XI colla-... [Pg.352]

Anderberg, E. K., C. Nystrom, and P. Artursson. Epithelial transport of drugs in cell culture. VII Effects of pharmaceutical surfactant excipients and bile adds on transepithelial permeability in monolayers of human intestinal epithelial (Caco-2) cells,... [Pg.85]

Two other myosin types have been implicated in hearing and vestibular function [62]. The defect in the Snell s waltzer mouse was found to be a mutation in a myosin VI gene that produces degeneration of the cochlea and vestibular apparatus. Myosin VI is localized to the cuticular plate of the hair cell under stereocilia. Similarly, mutations in a myosin VII gene are responsible for the shaker-1 mouse and several human genetic deafness disorders. This myosin, myosin Vila, is found in a band near the base of the stereocilia distinct from distributions of myosin ip and myosin VI. [Pg.498]

Article 6(1) of the Sixth Amendment requires PMN s to contain information and data necessary for evaluating the potential risks of new substances to humans and the environment. This specifically includes certain exposure information listed in Annex VII, concerning proposed uses and estimated yearly production volumes (in ranges, and broken down by use categories). Further, Article 6(1) requires submission of "a declaration concerning the unfavourable effects of the substance in terms of the various uses envisaged," which appears to require statements of the risks that may be associated with the use categories provided under Annex VII.(26)... [Pg.44]

V, proximal anastomosis within the temporal component, and distal interconnection between the latter and the cervical component VI, two anastomotic rami sent from the buccal division of the cervical to the zygomatic part of the temporal VII, transverse ramus, from the trunk of the nerve, contributing to the buccal ramus formed by anastomosis between the two major divisions VIII, richly plexiform communications, especially within the temporal portion of the nerve. From Barry J. Anson, Atlas of Human Anatomy, p. 37. [Pg.67]

The NCI domain of type VII collagen binds to the /33 chain of laminin, " laminin-5 a3(33 2), and type IV collagen. The triple helical domain of type VII collagen functions to promote the migration of human keratinocytes. °... [Pg.488]

Human fibroblast Collagenase (HFC) 57.000 (glycosylated) 52.000 0.32 Type 1, II, III, VII and X collagens gelatins a-Ms casein fibroblasts keratinocytes macrophages U937 cells endothelial cells [27,34]... [Pg.280]

Compliance with the requirements relating to clinical investigations (AIMDD Annex VII MDD Annex X) is assisted by adoption of standard EN 540 on Clinical Investigation of Medical Devices for Human Subjects, which is very similar to pharmaceutical GCP. [Pg.547]


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See also in sourсe #XX -- [ Pg.2 ]

See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.9 , Pg.19 , Pg.21 , Pg.23 , Pg.28 , Pg.41 , Pg.74 , Pg.93 , Pg.102 ]




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Human factor VII

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