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Cited by in F6Publishing
For: 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]
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 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]
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 Lofaro FD, Mucciolo DP, Murro V, Pavese L, Quaglino D, Boraldi F. From Clinical Diagnosis to the Discovery of Multigene Rare Sequence Variants in Pseudoxanthoma elasticum: A Case Report. Front Med (Lausanne) 2021;8:726856. [PMID: 34513887 DOI: 10.3389/fmed.2021.726856] [Reference Citation Analysis]