(Q44244385)

1 December 2017

title

Investigating cellular metabolism of synthetic azidosugars with the Staudinger ligation (English)

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1 December 2017

6

Carolyn R Bertozzi

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1 December 2017

Eliana Saxon

1

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1 December 2017

Sarah J Luchansky

2

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1 December 2017

Howard C Hang

3

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1 December 2017

Chong Yu

4

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1 December 2017

Sandy C Lee

5

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1 December 2017

language of work or name

English

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publication date

1 December 2002

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Journal of the American Chemical Society

1 December 2017

published in

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1 December 2017

volume

124

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1 December 2017

issue

50

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1 December 2017

page(s)

14893-14902

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Chemical and biological strategies for engineering cell surface glycosylation

1 December 2017

cites work

2 references

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Incorporation of azides into recombinant proteins for chemoselective modification by the Staudinger ligation

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Metabolic delivery of ketone groups to sialic acid residues. Application To cell surface glycoform engineering

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Biosynthetic incorporation of unnatural sialic acids into polysialic acid on neural cells

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A small-molecule modulator of poly-alpha 2,8-sialic acid expression on cultured neurons and tumor cells

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5 October 2022

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Engineering novel cell surface receptors for virus-mediated gene transfer

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5 October 2022

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Substrate specificity of the sialic acid biosynthetic pathway

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Metabolic labeling of glycoproteins with chemical tags through unnatural sialic acid biosynthesis

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5 October 2022

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The azidonitration of tri-O-acetyl-D-galactal

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5 October 2022

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Human renin-binding protein is the enzyme N-acetyl-D-glucosamine 2-epimerase

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5 October 2022

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Elongation of the N-acyl side chain of sialic acids in MDCK II cells inhibits influenza A virus infection

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5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

Catabolic disposition of 3'-azido-2',3'-dideoxyuridine in hepatocytes with evidence of azido reduction being a general catabolic pathway of 3'-azido-2',3'-dideoxynucleosides

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5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

Biochemical engineering of the N-acyl side chain of sialic acid: biological implications

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5 October 2022

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Glycosylation inhibitors in biology and medicine

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5 October 2022

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5 October 2022

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Azides: their preparation and synthetic uses

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5 October 2022

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Engineering chemical reactivity on cell surfaces through oligosaccharide biosynthesis

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Versatile biosynthetic engineering of sialic acid in living cells using synthetic sialic acid analogues

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5 October 2022

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Reduction of aryl azides by thiols: Implications for the use of photoaffinity reagents

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

Cell surface engineering by a modified Staudinger reaction

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

Biosynthetic modulation of sialic acid-dependent virus-receptor interactions of two primate polyoma viruses

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Molecular cloning and functional expression of UDP-N-acetyl-glucosamine 2-epimerase/N-acetylmannosamine kinase

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

The reaction between thiols and 8-azidoadenosine derivatives

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

A bifunctional enzyme catalyzes the first two steps in N-acetylneuraminic acid biosynthesis of rat liver. Purification and characterization of UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

Inhibitors of the biosynthesis and processing of N-linked oligosaccharide chains

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

A procedure for quantitative determination of tris(2-carboxyethyl)phosphine, an odorless reducing agent more stable and effective than dithiothreitol

1 reference

5 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA027748X

Identifiers

DOI

10.1021/JA027748X

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1 December 2017

1 reference