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Books on the topic 'Outer membrane protein'

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Author: Grafiati

Published: 4 June 2021

Last updated: 9 March 2023

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1

Shand, Geoffrey Harold. Antibiotic resistance and outer membrane protein antigens of Pseudomonas aeruginasa. Birmingham: University of Aston. Department of Pharmaceutical Sciences, 1985.

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2

Kraak, Wilma A. G. Outer membrane protein typing of Haemophilus influenzae: An epidemiological tool in type b and non-encapsulated strains. Oxford: Oxford Polytechnic, 1990.

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3

Sun, Frank. Identification of Porphyromonas (Bacteroides) Gingivalis outer membrane proteins that bind to and degrade human matrix proteins. [Toronto: Faculty of Dentistry, University of Toronto, 1992.

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4

Mortimer, Peter G. S. The role of Esherichia coli outer membrane proteins in determining the accumulation of and susceptibility to antibiotics. Birmingham: University of Birmingham, 1991.

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5

Maciver, Isobel. The effect of haem limitation and iron restriction on outer membrane proteins and on respiratory systems of non typable Haemophilus influenzae. Birmingham: Aston University. Department of Pharmaceutical Sciences, 1989.

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6

Characterization of the maltose regulon of Vibrio cholerae: Involvement of maltose in production of outer membrane proteins and secretion of virulence factors. Uppsala: Swedish University of Agricultural Sciences, Dept. of Molecular Genetics, Uppsala Genetic Center, 1993.

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7

Kania, Stephen Anthony. Isolation and characterization of a 78,000 dalton outer membrane protein of Haemophilus somnus. 1987.

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8

The 2.05 Å crystal structure of LptB, an essential protein in gram-negative bacterial outer membrane biogenesis. 2011.

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9

Structural and Functional Relationships in Prokaryotes. Springer, 2004.

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10

Barton, Larry L. Structural and Functional Relationships in Prokaryotes. Springer London, Limited, 2005.

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11

Bacterial outer membranes as model systems. New York: Wiley, 1987.

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12

The Periplasm. ASM Press, 2006.

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13

Bacterial and eukaryotic porins: Structure, function, mechanism. Weinheim [Germany]: Wiley-VCH, 2004.

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14

Lennon, Rachel, and Neil Turner. The molecular basis of glomerular basement membrane disorders. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0320_update_001.

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Abstract:

The glomerular basement membrane (GBM) is a condensed network of extracellular matrix molecules which provides a scaffold and niche to support the function of the overlying glomerular cells. Within the glomerulus, the GBM separates the fenestrated endothelial cells, which line capillary walls from the epithelial cells or podocytes, which cover the outer aspect of the capillaries. In common with basement membranes throughout the body, the GBM contains core components including collagen IV, laminins, nidogens, and heparan sulphate proteoglycans. However, specific isoforms of these proteins are required to maintain the integrity of the glomerular filtration barrier.Across the spectrum of glomerular disease there is alteration in glomerular extracellular matrix (ECM) and a number of histological patterns are recognized. The GBM can be thickened, expanded, split, and irregular; the mesangial matrix may be expanded and glomerulosclerosis represents a widespread accumulation of ECM proteins associated with loss of glomerular function. Whilst histological patterns may follow a sequence or provide diagnostic clues, there remains limited understanding about the mechanisms of ECM regulation and how this tight control is lost in glomerular disease. Monogenic disorders of the GBM including Alport and Pierson syndromes have highlighted the importance of both collagen IV and laminin isoforms and these observations provide important insights into mechanisms of glomerular disease.

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15

Bacterial and Eukaryotic Porins: Structure, Function, Mechanism. Wiley-VCH, 2004.

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