Genetic modulation of nephrocalcinosis in mouse models of ectopic mineralization: the Abcc6(tm1Jfk) and Enpp1(asj) mutant mice

scientific article

Genetic modulation of nephrocalcinosis in mouse models of ectopic mineralization: the Abcc6(tm1Jfk) and Enpp1(asj) mutant mice is …
instance of (P31):
scholarly articleQ13442814

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P6179Dimensions Publication ID1019109736
P356DOI10.1038/LABINVEST.2014.52
P932PMC publication ID4039617
P698PubMed publication ID24732453
P5875ResearchGate publication ID261734764

P50authorQiaoli LiQ89706920
Jouni UittoQ26985339
P2093author name stringJohn P Sundberg
Thea P Price
David W Chou
P2860cites workMOAT-E (ARA) is a full-length MRP/cMOAT subfamily transporter expressed in kidney and liverQ42053609
Connective tissue mineralization in Abcc6-/- mice, a model for pseudoxanthoma elasticumQ42141765
Tamm-Horsfall protein knockout mice are more prone to urinary tract infection: rapid communicationQ44376514
Sonographic detection of renal changes in pseudoxanthoma elasticum.Q45081291
Pseudoxanthoma elasticum: progress in research toward treatment: summary of the 2012 PXE international research meetingQ45324816
Apatite plaque particles in inner medulla of kidneys of calcium oxalate stone formers: osteopontin localizationQ46545480
Reduced plasma pyrophosphate levels in hemodialysis patientsQ46549194
Quantification of the calcification phenotype of Abcc6-deficient mice with microcomputed tomographyQ47100496
Identification of proteins extracted from calcium oxalate and calcium phosphate crystals induced in the urine of healthy and stone forming subjectsQ47725972
Regulatory T cells improve nephrocalcinosis but not dystrophic cardiac calcinosis in DBA/2 mice.Q50489999
Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatmentQ63441478
A stable animal model of diet-induced calcium oxalate crystalluriaQ74429063
The mutational spectrum of ENPP1 as arising after the analysis of 23 unrelated patients with generalized arterial calcification of infancy (GACI)Q81159927
Extracutaneous ultrastructural alterations in pseudoxanthoma elasticumQ28189764
Disruption of Abcc6 in the mouse: novel insight in the pathogenesis of pseudoxanthoma elasticumQ28250100
Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spineQ28505453
Targeted inactivation of Npt2 in mice leads to severe renal phosphate wasting, hypercalciuria, and skeletal abnormalitiesQ28587985
Analysis of urinary calculi using an infrared microspectroscopic surface reflectance imaging techniqueQ33268310
Genetics in arterial calcification: pieces of a puzzle and cogs in a wheelQ33352008
Dietary magnesium, not calcium, prevents vascular calcification in a mouse model for pseudoxanthoma elasticumQ33808444
Elevated dietary magnesium prevents connective tissue mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6(-/-)).Q33889808
Mutations in the GGCX and ABCC6 genes in a family with pseudoxanthoma elasticum-like phenotypesQ33979143
Targeted ablation of the abcc6 gene results in ectopic mineralization of connective tissuesQ34042814
Nephrocalcinosis in animal models with and without stonesQ34351298
Magnesium carbonate-containing phosphate binder prevents connective tissue mineralization in Abcc6(-/-) mice-potential for treatment of pseudoxanthoma elasticumQ34421007
Plasma pyrophosphate and vascular calcification in chronic kidney diseaseQ35078539
Biomineralization and matrix vesicles in biology and pathologyQ35115937
Diagnostic and therapeutic approaches in patients with secondary hyperoxaluriaQ35212760
Renal epithelial cells rapidly bind and internalize calcium oxalate monohydrate crystalsQ35608154
Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6Q35671719
Pseudoxanthoma elasticum: molecular genetics and putative pathomechanismsQ35950515
Restricting dietary magnesium accelerates ectopic connective tissue mineralization in a mouse model of pseudoxanthoma elasticum (Abcc6(-/-) ).Q36174964
Mineralization/anti-mineralization networks in the skin and vascular connective tissuesQ36986492
Nephrocalcinosis: new insights into mechanisms and consequencesQ37417881
Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: genotypic overlap with pseudoxanthoma elasticumQ37623356
Genetics in arterial calcification: lessons learned from rare diseasesQ38057485
The mineralization phenotype in Abcc6 ( -/- ) mice is affected by Ggcx gene deficiency and genetic background--a model for pseudoxanthoma elasticumQ40847416
Adhesion, internalization and metabolism of calcium oxalate monohydrate crystals by renal epithelial cellsQ41082752
Mutant Enpp1asj mice as a model for generalized arterial calcification of infancyQ41823162
P433issue6
P304page(s)623-632
P577publication date2014-04-14
P1433published inLaboratory InvestigationQ6467260
P1476titleGenetic modulation of nephrocalcinosis in mouse models of ectopic mineralization: the Abcc6(tm1Jfk) and Enpp1(asj) mutant mice
P478volume94

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cites work (P2860)
Q89506746ABCC6 Deficiency Promotes Development of Randall Plaque
Q27343503ENPP1-Fc prevents mortality and vascular calcifications in rodent model of generalized arterial calcification of infancy
Q46414748How do stones form? Is unification of theories on stone formation possible?
Q40136215Intraperitoneal pyrophosphate treatment reduces renal calcifications in Npt2a null mice.
Q36187569Juxta-articular joint-capsule mineralization in CD73 deficient mice: similarities to patients with NT5E mutations
Q37585811Mouse genome-wide association study identifies polymorphisms on chromosomes 4, 11, and 15 for age-related cardiac fibrosis
Q92151959Pseudoxanthoma Elasticum, Kidney Stones and Pyrophosphate: From a Rare Disease to Urolithiasis and Vascular Calcifications
Q33610690Response of Npt2a knockout mice to dietary calcium and phosphorus.
Q26739933Show and tell: disclosure and data sharing in experimental pathology
Q28542530Spontaneous asj-2J mutant mouse as a model for generalized arterial calcification of infancy: a large deletion/insertion mutation in the Enpp1 gene
Q26781908The ABCC6 Transporter as a Paradigm for Networking from an Orphan Disease to Complex Disorders
Q38390378What is nephrocalcinosis?

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