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Uitto, Jouni
One or more keywords matched the following items that are connected to
Uitto, Jouni
Item Type
Name
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.
Search Criteria
Calcinosis