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One or more keywords matched the following items that are connected to Uitto, Jouni
Item TypeName
Concept Calcinosis
Academic Article Overexpression of fetuin-a counteracts ectopic mineralization in a mouse model of pseudoxanthoma elasticum (abcc6(-/-)).
Academic Article Parabiotic heterogenetic pairing of Abcc6-/-/Rag1-/- mice and their wild-type counterparts halts ectopic mineralization in a murine model of pseudoxanthoma elasticum.
Academic Article Functional characterization of SAMD9, a protein deficient in normophosphatemic familial tumoral calcinosis.
Academic Article Administration of vitamin K does not counteract the ectopic mineralization of connective tissues in Abcc6 (-/-) mice, a model for pseudoxanthoma elasticum.
Academic Article The Samd9L gene: transcriptional regulation and tissue-specific expression in mouse development.
Academic Article Connective tissue mineralization in Abcc6-/- mice, a model for pseudoxanthoma elasticum.
Academic Article Mouse Samd9l is not a functional paralogue of the human SAMD9, the gene mutated in normophosphataemic familial tumoral calcinosis.
Academic Article Targeted ablation of the abcc6 gene results in ectopic mineralization of connective tissues.
Academic Article A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis.
Academic Article Aberrant mineralization of connective tissues in a mouse model of pseudoxanthoma elasticum: systemic and local regulatory factors.
Academic Article Targeted ablation of Abcc1 or Abcc3 in Abcc6(-/-) mice does not modify the ectopic mineralization process.
Academic Article Pseudoxanthoma elasticum: reduced gamma-glutamyl carboxylation of matrix gla protein in a mouse model (Abcc6-/-).
Academic Article Ectopic mineralization of connective tissue in Abcc6-/- mice: effects of dietary modifications and a phosphate binder--a preliminary study.
Academic Article Normophosphatemic familial tumoral calcinosis is caused by deleterious mutations in SAMD9, encoding a TNF-alpha responsive protein.
Academic Article GALNT3, a gene associated with hyperphosphatemic familial tumoral calcinosis, is transcriptionally regulated by extracellular phosphate and modulates matrix metalloproteinase activity.
Academic Article Mutation update: Variants of the ENPP1 gene in pathologic calcification, hypophosphatemic rickets, and cutaneous hypopigmentation with punctate keratoderma.
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  • Calcinosis