H. Douglas Braymer

Pennington Biomedical Research Center

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Stefany D. Primeaux

Louisiana State University Health Sciences Center New Orleans

George A. Bray

Pennington Biomedical Research Center

Maria J. Barnes

Des Moines University

A. D. Larson

Louisiana State University Agricultural Center

David A. York

Wayne State University

Jonquil M. Poret

Louisiana State University Health Sciences Center New Orleans

T K Ross

University of Wisconsin–Madison

Darryl A. Gaudet

Louisiana State University Health Sciences Center New Orleans

Simon H. Wender

University of Oklahoma

E C Achberger

Louisiana State University

Cooperative Institutions

Louisiana State University

Pennington Biomedical Research Center

Louisiana State University Agricultural Center

Louisiana State University Health Sciences Center New Orleans

Louisiana State University System

New England Biolabs (United States)

University of Pennsylvania

Université Laval

National Institutes of Health

University of Georgia

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The metabolic fate of some phenolic compounds in the rat

Dissertation Absts (1961)

H. Douglas Braymer

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Citations (1)

Procolipase gene expression in the rat brain: Source of endogenous enterostatin production in the brain

Brain Research (2006)

David A. York Ling Lin Sonjya R. Thomas H. Douglas Braymer MieJung Park

10.1016/j.brainres.2006.03.013

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Citations (24)

Purification and N-terminal amino acid sequences of two polypeptides encoded by the mcrB gene from Escherichia coli K-12

Gene (1992)

Ling Zheng Xuenin Wang H. Douglas Braymer

10.1016/0378-1119(92)90308-c

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Citations (4)

Notes- Methyl Ethers of Quercetin in Tobacco Flowers

The Journal of Organic Chemistry (1960)

Chia‐Chen Yang H. Douglas Braymer E. Angela Murphy W. Chorney Norma M. Scully

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTNotes- Methyl Ethers of Quercetin in Tobacco FlowersC Yang, H Braymer, E Murphy, W Chorney, N Scully, and S WenderCite this: J. Org. Chem. 1960, 25, 11, 2063–2064Publication Date (Print):November 1, 1960Publication History Published online19 March 2003Published inissue 1 November 1960https://pubs.acs.org/doi/10.1021/jo01081a624https://doi.org/10.1021/jo01081a624research-articleACS PublicationsRequest reuse permissionsArticle Views154Altmetric-Citations20LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts

10.1021/jo01081a624

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Citations (21)

Selection of intramural-enzyme mutants

Fungal Genetics Reports (1969)

Malcolm Sargent H. Douglas Braymer

Selection for mutants with altered enzymes in Neurosporo i s cx formidable tork Selection of intromurol-enzyme mutants.if the enzyme is normally located outside the cell membrane, whether within the wall (intramural) or outside of it (extrocellulor).Thir difficulty i s due to coca-

10.4148/1941-4765.2047

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Citations (3)

Sensitivity to the satiating effects of exendin 4 is decreased in obesity-prone Osborne–Mendel rats compared to obesity-resistant S5B/Pl rats

International Journal of Obesity (2010)

Stefany D. Primeaux Maria J. Barnes H. Douglas Braymer George A. Bray

Diet-induced obese

10.1038/ijo.2010.78

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Citations (23)

Purification of the Protein Employed in an Immunodiffusion Test to Diagnose Infectious Bovine Rhinotracheitis

Preparative Biochemistry (1979)

D. J. Brister L. T. Hart A. D. Larson H. Douglas Braymer

Abstract The antigen used in an immunodiffusion test to diagnose infectious bovine rhinotracheitis has been purified by affinity chromotography. The homogeneity of the antigen was indicated by sedimentation rate and sedimentation equilibrium experiments. A S˚20,w of 0.749 was determined and a molecular weight of 8900 was calculated from sedimentation equilibrium analysis. The purified antigen formed precipitin lines of identity with crude diagnostic antigen. Purified antigen remained serologically active in the immunodiffusion test after lyophilization and subsequent reconstitution.

Infectious bovine rhinotracheitis

Immunodiffusion

10.1080/00327487908061687

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Citations (1)

Effects of a High‐Fat Diet and Strain on Hypothalamic Gene Expression in Rats

Obesity Research (2002)

Andrea O. Schaffhauser Abram M. Madiehe H. Douglas Braymer George A. Bray David A. York

Abstract Objective: This study was designed to investigate whether dietary fat and genetic background might differentially alter the expression of hypothalamic genes involved in food intake. Research Methods and Procedures: Three‐month‐old Osborne‐Mendel (OM) and S5B/Pl rats were fed either a high‐fat or a low‐fat diet for 14 days. mRNA for neuropeptide Y (NPY), corticotrophin‐releasing hormone, NPY Y‐1 receptor and Y‐5 receptor, and serotonin 2c (5‐HT2c) receptors were measured using Northern blotting or ribonuclease protection assays. Results: OM rats showed an increased expression of NPY and corticotrophin‐releasing hormone compared with S5B/Pl rats. The expression of NPY‐Y1 and ‐Y5 receptor mRNA was significantly higher in the hypothalamus of OM rats compared with S5B/Pl rats. The expression of 5HT‐2c receptor mRNA was significantly reduced in both strains of rats eating a high‐fat diet when compared with the animals eating the low‐fat diet. Discussion: These data suggest that over activity of the NPY system may contribute to the development of obesity in OM rats and that expression of the 5HT‐2c receptor gene may be modulated by dietary fat.

10.1038/oby.2002.161

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Citations (46)

Nucleotide sequence of the McrB region of Escherichia coli K-12 and evidence for two independent translational initiation sites at the mcrB locus

Journal of Bacteriology (1989)

T K Ross E C Achberger H. Douglas Braymer

The McrB restriction system of Escherichia coli K-12 is responsible for the biological inactivation of foreign DNA that contains 5-methylcytosine residues (E. A. Raleigh and G. Wilson, Proc. Natl. Acad. Sci. USA 83:9070-9074, 1986). Within the McrB region of the chromosome is the mcrB gene, which encodes a protein of 51 kilodaltons (kDa) (T. K. Ross, E. C. Achberger, and H. D. Braymer, Gene 61:277-289, 1987), and the mcrC gene, the product of which is 39 kDa (T. K. Ross, E. C. Achberger, and H. D. Braymer, Mol. Gen. Genet., in press). The nucleotide sequence of a 2,695-base-pair segment encompassing the McrB region was determined. The deduced amino acid sequence was used to identify two open reading frames specifying peptides of 455 and 348 amino acids, corresponding to the products of the mcrB and mcrC genes, respectively. A single-nucleotide overlap was found to exist between the termination codon of the mcrB gene and the proposed initiation codon of the mcrC gene. The presence of an additional peptide of 33 kDa in strains containing various recombinant plasmids with portions of the McrB region has been reported by Ross et al. (Gene 61:277-289, 1987). The analysis of frameshift and deletion mutants of one such hybrid plasmid, pRAB-13, provided evidence for a second translational initiation site within the McrB open reading frame. The proposed start codon for translation of the 33-kDa peptide lies 481 nucleotides downstream from the initiation codon for the 51-kDa mcrB gene product. The 33-kDa peptide may play a regulatory role in the McrB restriction of DNA containing 5-methylcytosine.

Stop codon

10.1128/jb.171.4.1974-1981.1989

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Citations (44)

Characterization of the Escherichia coli modified cytosine restriction (mcrB) gene

Gene (1987)

T K Ross E C Achberger H. Douglas Braymer

Cytosine

10.1016/0378-1119(87)90191-0

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Citations (30)