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Propionyl-CoA carboxylase – A review

Molecular genetics and metabolism, 2017-12, Vol.122 (4), p.145-152

2017

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Vitamin K-dependent carboxylation of coagulation factors: insights from a cell-based functional study

Haematologica (Roma), 2020-08, Vol.105 (8), p.2164-2173

2020

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γ-Glutamyl carboxylase mutations differentially affect the biological function of vitamin K–dependent proteins

Blood, 2021-01, Vol.137 (4), p.533-543

2021

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GGCX mutants that impair hemostasis reveal the importance of processivity and full carboxylation to VKD protein function

Blood, 2022-10, Vol.140 (15), p.1710-1722

2022

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Structural and functional insights into enzymes of the vitamin K cycle

Journal of thrombosis and haemostasis, 2016-02, Vol.14 (2), p.236-247

2016

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Carboxylases in Natural and Synthetic Microbial Pathways

Applied and Environmental Microbiology, 2011-12, Vol.77 (24), p.8466-8477

ERB, Tobias J

2011

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GGCX variants leading to biallelic deficiency to γ‐carboxylate GRP cause skin laxity in VKCFD1 patients

Human mutation, 2022-01, Vol.43 (1), p.42-55

2022

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Monoterpene phenolic compound thymol promotes browning of 3T3-L1 adipocytes

European journal of nutrition, 2017-10, Vol.56 (7), p.2329-2341

2017

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Human forebrain organoid-based multi-omics analyses of PCCB as a schizophrenia associated gene linked to GABAergic pathways

Nature communications, 2023-08, Vol.14 (1), p.5176-13, Article 5176

2023

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Impaired vitamin K recycling in uremia is rescued by vitamin K supplementation

Kidney international, 2014-08, Vol.86 (2), p.286-293

2014

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Prediction of function for the polyprenyl transferase subgroup in the isoprenoid synthase superfamily

Proceedings of the National Academy of Sciences - PNAS, 2013-03, Vol.110 (13), p.E1196-E1202

2013

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Novel variants of the PCCB gene in Chinese patients with propionic acidemia

Clinica chimica acta, 2021-08, Vol.519, p.18-25

2021

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Characterization of vitamin K–dependent carboxylase mutations that cause bleeding and nonbleeding disorders

Blood, 2016-04, Vol.127 (15), p.1847-1855

2016

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A novel multidomain acyl-CoA carboxylase in Saccharopolyspora erythraea provides malonyl-CoA for de novo fatty acid biosynthesis

Scientific reports, 2019-04, Vol.9 (1), p.6725-6725, Article 6725

2019

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Analysis of MCCC2 gene variant in a pedigree affected with 3-methylcrotonyl coenzyme A carboxylase deficiency

Zhonghua yi xue yi chuan xue za zhi, 2021-01, Vol.38 (1), p.74

2021

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GGCX-Associated Phenotypes: An Overview in Search of Genotype-Phenotype Correlations

International journal of molecular sciences, 2017-02, Vol.18 (2), p.240-240

2017

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Functional Analysis of the PCCA and PCCB Gene Variants Predicted to Affect Splicing

International journal of molecular sciences, 2021-04, Vol.22 (8), p.4154

2021

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Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian

Medicine (Baltimore), 2021-03, Vol.100 (10), p.e24161-e24161

2021

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6,6′-Bieckol inhibits adipocyte differentiation through downregulation of adipogenesis and lipogenesis in 3T3-L1 cells

Journal of the science of food and agriculture, 2015-07, Vol.95 (9), p.1830-1837

2015

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Pseudoxanthoma elasticum‐like syndrome with coagulation deficiency associated with carotid artery hypoplasia and a novel gamma‐glutamyl carboxylase gene mutation

International journal of dermatology, 2021-01, Vol.60 (1), p.e13-e15

2021

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SNPs in SNCA, MCCC1, DLG2, GBF1 and MBNL2 are associated with Parkinson's disease in southern Chinese population

Journal of cellular and molecular medicine, 2020-08, Vol.24 (15), p.8744-8752

2020

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Splice-Site Mutation of Exon 3 Deletion in the Gamma-Glutamyl Carboxylase Gene Causes Inactivation of the Enzyme

Journal of investigative dermatology, 2016-11, Vol.136 (11), p.2314-2317

2016

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Leucine metabolism regulates TRI6 expression and affects deoxynivalenol production and virulence in Fusarium graminearum

Molecular microbiology, 2015-11, Vol.98 (4), p.760-769

2015

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Gamma-glutamyl carboxylase (GGCX) microsatellite and warfarin dosing

Blood, 2005-11, Vol.106 (10), p.3673-3674

2005

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A 3-methylcrotonyl-CoA carboxylase deficient human skin fibroblast transcriptome reveals underlying mitochondrial dysfunction and oxidative stress

The international journal of biochemistry & cell biology, 2016-09, Vol.78, p.116-129

2016

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Propionyl-CoA carboxylase – A review

Vitamin K-dependent carboxylation of coagulation factors: insights from a cell-based functional study

γ-Glutamyl carboxylase mutations differentially affect the biological function of vitamin K–dependent proteins

GGCX mutants that impair hemostasis reveal the importance of processivity and full carboxylation to VKD protein function

Structural and functional insights into enzymes of the vitamin K cycle

Carboxylases in Natural and Synthetic Microbial Pathways

GGCX variants leading to biallelic deficiency to γ‐carboxylate GRP cause skin laxity in VKCFD1 patients

Monoterpene phenolic compound thymol promotes browning of 3T3-L1 adipocytes

Human forebrain organoid-based multi-omics analyses of PCCB as a schizophrenia associated gene linked to GABAergic pathways

Impaired vitamin K recycling in uremia is rescued by vitamin K supplementation

Prediction of function for the polyprenyl transferase subgroup in the isoprenoid synthase superfamily

Novel variants of the PCCB gene in Chinese patients with propionic acidemia

Characterization of vitamin K–dependent carboxylase mutations that cause bleeding and nonbleeding disorders

A novel multidomain acyl-CoA carboxylase in Saccharopolyspora erythraea provides malonyl-CoA for de novo fatty acid biosynthesis

Analysis of MCCC2 gene variant in a pedigree affected with 3-methylcrotonyl coenzyme A carboxylase deficiency

GGCX-Associated Phenotypes: An Overview in Search of Genotype-Phenotype Correlations

Functional Analysis of the PCCA and PCCB Gene Variants Predicted to Affect Splicing

Gene diagnosis and pedigree analysis of two Han ethnicity families with propionic acidemia in Fujian

6,6′-Bieckol inhibits adipocyte differentiation through downregulation of adipogenesis and lipogenesis in 3T3-L1 cells

Pseudoxanthoma elasticum‐like syndrome with coagulation deficiency associated with carotid artery hypoplasia and a novel gamma‐glutamyl carboxylase gene mutation

SNPs in SNCA, MCCC1, DLG2, GBF1 and MBNL2 are associated with Parkinson's disease in southern Chinese population

Splice-Site Mutation of Exon 3 Deletion in the Gamma-Glutamyl Carboxylase Gene Causes Inactivation of the Enzyme

Leucine metabolism regulates TRI6 expression and affects deoxynivalenol production and virulence in Fusarium graminearum

Gamma-glutamyl carboxylase (GGCX) microsatellite and warfarin dosing

A 3-methylcrotonyl-CoA carboxylase deficient human skin fibroblast transcriptome reveals underlying mitochondrial dysfunction and oxidative stress

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