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For: Hao Z, Jin DY, Chen X, Schurgers LJ, Stafford DW, Tie JK. γ-Glutamyl carboxylase mutations differentially affect the biological function of vitamin K-dependent proteins. Blood 2021;137:533-43. [PMID: 33507293 DOI: 10.1182/blood.2020006329] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Berkner KL, Runge KW. Vitamin K-Dependent Protein Activation: Normal Gamma-Glutamyl Carboxylation and Disruption in Disease. Int J Mol Sci 2022;23:5759. [PMID: 35628569 DOI: 10.3390/ijms23105759] [Reference Citation Analysis]
2 Xu C, Cunqing Y, Chun GU, Min WU, Jun LI, Xueyun H, Jiaxin F, Li S, Cheng AN, Guijian L, Fengxiang S, Bo P. The relationship between serum vitamin K concentration and coronary artery calcification in middle-aged and elderly people. Clin Chim Acta 2022:S0009-8981(22)01130-5. [PMID: 35504322 DOI: 10.1016/j.cca.2022.04.1001] [Reference Citation Analysis]
3 Ghosh S, Oldenburg J, Czogalla-Nitsche KJ. The Role of GRP and MGP in the Development of Non-Hemorrhagic VKCFD1 Phenotypes. Int J Mol Sci 2022;23:798. [PMID: 35054981 DOI: 10.3390/ijms23020798] [Reference Citation Analysis]
4 Ghosh S, Kraus K, Biswas A, Müller J, Buhl AL, Forin F, Singer H, Höning K, Hornung V, Watzka M, Czogalla-Nitsche KJ, Oldenburg J. GGCX mutations show different responses to vitamin K thereby determining the severity of the hemorrhagic phenotype in VKCFD1 patients. J Thromb Haemost 2021;19:1412-24. [PMID: 33590680 DOI: 10.1111/jth.15238] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Mathonnet A, Cunat S, Allias F, Caillot S, Thonnon C, Till M, Attié-Bitach T, Touraine R, Meunier S, Cartellier C, Rossi M, Attia J, Putoux A. GGCX-related congenital combined vitamin K-dependent clotting factors deficiency-1: Description of a fetus with chondrodysplasia punctata. Am J Med Genet A 2021. [PMID: 34558179 DOI: 10.1002/ajmg.a.62503] [Reference Citation Analysis]
6 Ghosh S, Kraus K, Biswas A, Müller J, Forin F, Singer H, Höning K, Hornung V, Watzka M, Oldenburg J, Czogalla-Nitsche KJ. GGCX variants leading to biallelic deficiency to γ-carboxylate GRP cause skin laxity in VKCFD1 patients. Hum Mutat 2022;43:42-55. [PMID: 34816548 DOI: 10.1002/humu.24300] [Reference Citation Analysis]
7 Lin JH, Wu H, Zou WB, Masson E, Fichou Y, Le Gac G, Cooper DN, Férec C, Liao Z, Chen JM. Splicing Outcomes of 5' Splice Site GT>GC Variants That Generate Wild-Type Transcripts Differ Significantly Between Full-Length and Minigene Splicing Assays. Front Genet 2021;12:701652. [PMID: 34422003 DOI: 10.3389/fgene.2021.701652] [Reference Citation Analysis]
8 Lai Y, Masatoshi H, Ma Y, Guo Y, Zhang B. Role of Vitamin K in Intestinal Health. Front Immunol 2021;12:791565. [PMID: 35069573 DOI: 10.3389/fimmu.2021.791565] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Kaesler N, Schurgers LJ, Floege J. Vitamin K and cardiovascular complications in CKD patients. Kidney Int 2021:S0085-2538(21)00687-6. [PMID: 34310988 DOI: 10.1016/j.kint.2021.06.037] [Reference Citation Analysis]
10 Chen X, Furukawa N, Jin DY, Liu Y, Stafford DW, Williams CM, Suhara Y, Tie JK. Naturally occurring UBIAD1 mutations differentially affect menaquinone biosynthesis and vitamin K-dependent carboxylation. FEBS J 2021. [PMID: 34813684 DOI: 10.1111/febs.16291] [Reference Citation Analysis]