Cystathionine gamma-lyase: Clinical, metabolic, genetic, and structural studies (Q24309290)

hydrogen sulfide biosynthetic process

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

Wuh-Liang Hwu

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Robert A. Hegele

object named as

Robert A Hegele

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S. Harvey Mudd

object named as

S Harvey Mudd

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author name string

Jan P Kraus

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Jindrich Hasek

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Viktor Kozich

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Renata Collard

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Sarah Venezia

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Bohumila Janosíková

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Jian Wang

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Sally P Stabler

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Robert H Allen

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Cornelis Jakobs

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Christine T Finn

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Yin-Hsiu Chien

Molecular Genetics and Metabolism

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language of work or name

English

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publication date

August 2009

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published in

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volume

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issue

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page(s)

250-9

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cites work

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Kinetics and inhibition of recombinant human cystathionine gamma-lyase. Toward the rational control of transsulfuration

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Cloning and nucleotide sequence of human liver cDNA encoding for cystathionine gamma-lyase

19 March 2017

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H2S as a physiologic vasorelaxant: hypertension in mice with deletion of cystathionine gamma-lyase

19 March 2017

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3-Mercaptopyruvate sulfurtransferase produces hydrogen sulfide and bound sulfane sulfur in the brain

19 March 2017

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Kinetic properties of polymorphic variants and pathogenic mutants in human cystathionine gamma-lyase

19 March 2017

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Genomic basis of cystathioninuria (MIM 219500) revealed by multiple mutations in cystathionine gamma-lyase (CTH).

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30 May 2018

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Primary cystathioninuria in an infant born out of incest

30 May 2018

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Relationship between cystathionine gamma-lyase gene polymorphism and essential hypertension in Northern Chinese Han population.

30 May 2018

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A functional transsulfuration pathway in the brain links to glutathione homeostasis

29 November 2018

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29 November 2018

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Single nucleotide polymorphism in CTH associated with variation in plasma homocysteine concentration

29 November 2018

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29 November 2018

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Measurement of homocysteine and other aminothiols in plasma: advantages of using tris(2-carboxyethyl)phosphine as reductant compared with tri-n-butylphosphine.

29 November 2018

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Biochemical basis for the dominant inheritance of hypermethioninemia associated with the R264H mutation of the MAT1A gene. A monomeric methionine adenosyltransferase with tripolyphosphatase activity

29 November 2018

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The possible role of hydrogen sulfide as an endogenous smooth muscle relaxant in synergy with nitric oxide.

29 November 2018

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Transsulfuration in mammals. Microassays and tissue distributions of three enzymes of the pathway

29 November 2018

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29 November 2018

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Quantitation of total homocysteine, total cysteine, and methionine in normal serum and urine using capillary gas chromatography-mass spectrometry

7 January 2021

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Large heterozygous deletion masquerading as homozygous missense mutation: a pitfall in diagnostic mutation analysis

7 January 2021

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Maternal gamma-cystathionase deficiency: absence of both teratogenic effects and pregnancy complications

7 January 2021

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