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Journal Articles

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

Mark A. Rishavy, Kevin W. Hallgren, Lee A. Wilson, James M. Hiznay, Kurt W. Runge, Kathleen L. Berkner

Blood (2022) 140 (15): 1710–1722.

https://doi.org/10.1182/blood.2021014275

Published: 2022

Includes: Supplemental data

Journal Articles

Warfarin alters vitamin K metabolism: a surprising mechanism of VKORC1 uncoupling necessitates an additional reductase

Mark A. Rishavy, Kevin W. Hallgren, Lee Wilson, Savita Singh, Kurt W. Runge, Kathleen L. Berkner

Blood (2018) 131 (25): 2826–2835.

https://doi.org/10.1182/blood-2017-09-804666

Published: 2018

Includes: Supplemental data

Journal Articles

Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family.

Dhouha Darghouth, PhD, Kevin W Hallgren, Odile Issertial, Amine Bazaa, PhD, Kathleen L Berkner, PhD, Jean-Philippe Rosa, MD, PhD, Rémi Favier, MD

Blood (2009) 114 (22): 1302.

https://doi.org/10.1182/blood.V114.22.1302.1302

Published: 2009

Journal Articles

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

Dhouha Darghouth, Kevin W. Hallgren, Rebecca L. Shtofman, Amel Mrad, Youssef Gharbi, Ahmed Maherzi, Radhia Kastally, Sophie LeRicousse, Kathleen L. Berkner, Jean-Philippe Rosa

Blood (2006) 108 (6): 1925–1931.

https://doi.org/10.1182/blood-2005-12-010660

Published: 2006

Includes: Supplemental data

Journal Articles

Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family.

Dhouha Darghouth, Kevin W. Hallgren, PhD, Rebecca L. Hain, PhD, Amel Mrad, PhD, Youssef Gharbi, MD, Ahmed Maherzi, MD, Sophie LeRicousse, PhD, Radhia Kastally, PhD, Kathleen L. Berkner, PhD, Jean-Philippe Rosa, MD, PhD

Blood (2005) 106 (11): 2147.

https://doi.org/10.1182/blood.V106.11.2147.2147

Published: 2005

NARROW

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

Warfarin alters vitamin K metabolism: a surprising mechanism of VKORC1 uncoupling necessitates an additional reductase

Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family.

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family.

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ASH Publications

American Society of Hematology

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

Warfarin alters vitamin K metabolism: a surprising mechanism of VKORC1 uncoupling necessitates an additional reductase

Compound Heterozygosity of a W493C Substitution and R704/Premature Stop Codon within the γ-Glutamyl Carboxylase in Combined Vitamin K-Dependent Coagulation Factor Deficiency in a French Family.

Compound heterozygosity of novel missense mutations in the gamma-glutamyl-carboxylase gene causes hereditary combined vitamin K–dependent coagulation factor deficiency

Compound Heterozygosity in the Novel Mutations W157R and T591K in the γ-Glutamyl Carboxylase Gene Causes Hereditary Combined Vitamin K-Dependent Coagulation Factor Deficiency in a Tunisian Family.

Email alerts

ASH Publications

American Society of Hematology

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