D E Heinrichs
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Explore the profile of D E Heinrichs including associated specialties, affiliations and a list of published articles.
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15
Citations
981
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Recent Articles
1.
Hayworth J, Kasper K, Leon-Ponte M, Herfst C, Yue D, Brintnell W, et al.
Clin Exp Immunol
. 2009 Aug;
157(1):60-70.
PMID: 19659771
Staphylococcal enterotoxin B (SEB) is a pyrogenic exotoxin and a potent superantigen which causes massive T cell activation and cytokine secretion, leading to profound immunosuppression and morbidity. The inhibition of...
2.
Sebulsky M, Heinrichs D
J Bacteriol
. 2001 Aug;
183(17):4994-5000.
PMID: 11489851
Staphylococcus aureus can utilize several hydroxamate siderophores for growth under iron-restricted conditions. Previous findings have shown that S. aureus possesses a cytoplasmic membrane-associated traffic ATPase that is involved in the...
3.
Sebulsky M, Hohnstein D, Hunter M, Heinrichs D
J Bacteriol
. 2000 Jul;
182(16):4394-400.
PMID: 10913070
Staphylococcus aureus was shown to transport iron complexed to a variety of hydroxamate type siderophores, including ferrichrome, aerobactin, and desferrioxamine. An S. aureus mutant defective in the ability to transport...
4.
Amor K, Heinrichs D, Frirdich E, Ziebell K, Johnson R, Whitfield C
Infect Immun
. 2000 Feb;
68(3):1116-24.
PMID: 10678915
In the lipopolysaccharides of Escherichia coli there are five distinct core oligosaccharide (core OS) structures, designated K-12 and R1 to R4. The objective of this work was to determine the...
5.
Graninger M, Nidetzky B, Heinrichs D, Whitfield C, Messner P
J Biol Chem
. 1999 Aug;
274(35):25069-77.
PMID: 10455186
The thymidine diphosphate-L-rhamnose biosynthesis pathway is required for assembly of surface glycoconjugates in a growing list of bacterial pathogens, making this pathway a potential therapeutic target. However, the terminal reactions...
6.
Heinrichs D, Yethon J, Amor P, Whitfield C
J Biol Chem
. 1998 Oct;
273(45):29497-505.
PMID: 9792656
The major core oligosaccharide biosynthesis operons from prototype Escherichia coli strains displaying R1 and R4 lipopolysaccharide core types were polymerase chain reaction-amplified and analyzed. Comparison of deduced products of the...
7.
Heinrichs D, Yethon J, Whitfield C
Mol Microbiol
. 1998 Oct;
30(2):221-32.
PMID: 9791168
Bacterial lipopolysaccharides (LPS) are unique and complex glycolipids that provide characteristic components of the outer membranes of Gram-negative bacteria. In LPS of the Enterobacteriaceae, the core oligosaccharide links a highly...
8.
Yethon J, Heinrichs D, Monteiro M, Perry M, Whitfield C
J Biol Chem
. 1998 Oct;
273(41):26310-6.
PMID: 9756860
The waaY, waaQ, and waaP genes are located in the central operon of the waa (formerly rfa) locus on the chromosome of Escherichia coli. This locus contains genes whose products...
9.
Heinrichs D, Monteiro M, Perry M, Whitfield C
J Biol Chem
. 1998 May;
273(15):8849-59.
PMID: 9535865
In Escherichia coli F632, the 14-kilobase pair chromosomal region located between waaC (formerly rfaC) and waaA (kdtA) contains genes encoding enzymes required for the synthesis of the type R2 core...
10.
Poole K, Tetro K, Zhao Q, Neshat S, Heinrichs D, Bianco N
Antimicrob Agents Chemother
. 1996 Sep;
40(9):2021-8.
PMID: 8878574
The region upstream of the multiple antibiotic resistance efflux operon mexA-mexB-oprM in Pseudomonas aeruginosa was sequenced, and a gene, mexR, was identified. The predicted MexR product contains 147 amino acids...