GO_REF:0000002
Gene Ontology annotation through association of InterPro records with GO terms
GO_REF:0000024
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
GO_REF:0000033
Annotation inferences using phylogenetic trees
GO_REF:0000107
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
GO_REF:0000116
Automatic Gene Ontology annotation based on Rhea mapping
GO_REF:0000120
Combined Automated Annotation using Multiple IEA Methods
PMID:11395499
Structural evidence for a functional role of human tissue nonspecific alkaline phosphatase in bone mineralization.
PMID:12162492
Kinetic characterization of hypophosphatasia mutations with physiological substrates.
PMID:16210410
Differential expression profiling of membrane proteins by quantitative proteomics in a human mesenchymal stem cell line undergoing osteoblast differentiation.
PMID:17023519
Evidence for auto/paracrine actions of vitamin D in bone: 1alpha-hydroxylase expression and activity in human bone cells.
PMID:19056867
Large-scale proteomics and phosphoproteomics of urinary exosomes.
PMID:19874193
Kinetic analysis of substrate utilization by native and TNAP-, NPP1-, or PHOSPHO1-deficient matrix vesicles.
PMID:2220817
Alkaline phosphatase (tissue-nonspecific isoenzyme) is a phosphoethanolamine and pyridoxal-5'-phosphate ectophosphatase: normal and hypophosphatasia fibroblast study.
PMID:23533145
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
PMID:23688511
An asparagine at position 417 of tissue-nonspecific alkaline phosphatase is essential for its structure and function as revealed by analysis of the N417S mutation associated with severe hypophosphatasia.
PMID:25982064
Molecular phenotype of tissue-nonspecific alkaline phosphatase with a proline (108) to leucine substitution associated with dominant odontohypophosphatasia.
PMID:28592560
Ectopic calcification in pseudoxanthoma elasticum responds to inhibition of tissue-nonspecific alkaline phosphatase.
PMID:33821301
Novel mutation in the ALPL gene with a dominant negative effect in a Japanese family.
PMID:41145834
TNAP dephosphorylates phosphocholine and phosphoethanolamine and participates in triglyceride transport from the liver to the bloodstream.
PMID:9781036
Identification of fifteen novel mutations in the tissue-nonspecific alkaline phosphatase (TNSALP) gene in European patients with severe hypophosphatasia.
file:human/ALPL/ALPL-deep-research-falcon.md
Deep research report: human ALPL / tissue-nonspecific alkaline phosphatase (TNAP)
Reactome:R-HSA-8940388
GPLD1 hydrolyses GPI-anchors from proteins
PMID:2153284
Selectivity of the cleavage/attachment site of phosphatidylinositol-glycan-anchored membrane proteins determined by site-specific mutagenesis at Asp-484 of placental alkaline phosphatase.
PMID:2162249
Expression of a Nagao-type, phosphatidylinositol-glycan anchored alkaline phosphatase in human choriocarcinomas.
PMID:29567797
Human ALPI deficiency causes inflammatory bowel disease and highlights a key mechanism of gut homeostasis.
PMID:21490328
Extracellular pyrophosphate metabolism and calcification in vascular smooth muscle.
PMID:33981039
Mitochondrial TNAP controls thermogenesis by hydrolysis of phosphocreatine.
PMID:12082181
Tissue-nonspecific alkaline phosphatase and plasma cell membrane glycoprotein-1 are central antagonistic regulators of bone mineralization.
PMID:23523568
A protective role for FGF-23 in local defence against disrupted arterial wall integrity?
PMID:7550313
Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6.
PMID:39728440
Structural and Functional Integration of Tissue-Nonspecific Alkaline Phosphatase Within the Alkaline Phosphatase Superfamily: Evolutionary Insights and Functional Implications.
PMID:33919113
Hypophosphatasia: A Unique Disorder of Bone Mineralization.
PMID:33477631
TNAP as a New Player in Chronic Inflammatory Conditions and Metabolism.
PMID:31413732
Update on the management of hypophosphatasia.
PMID:37982855
Proposed diagnostic criteria for the diagnosis of hypophosphatasia in children and adolescents: results from the HPP International Working Group.
PMID:40100438
Medical Management of Hypophosphatasia: Review of Data on Asfotase Alfa.
PMID:36699639
Gene Therapy Using Recombinant AAV Type 8 Vector Encoding TNAP-D(10) Improves the Skeletal Phenotypes in Murine Models of Osteomalacia.
PMID:39872235
Dental manifestations of hypophosphatasia: translational and clinical advances.
PMID:42020733
Glycerol-driven TNAP activation in thermogenesis and mineralization.
PMID:17043865
Mineralization process during acellular cementogenesis in rat molars: a histochemical and immunohistochemical study using fresh-frozen sections.
PMID:2039500
Tissue-specific and dexamethasone-inducible expression of alkaline phosphatase from alternative promoters of the rat bone/liver/kidney/placenta gene.
PMID:20818503
Increased expression of the receptor for activation of NF-kappaB and decreased runt-related transcription factor 2 expression in bone of rats with streptozotocin-induced diabetes.
PMID:11810315
Identification of pulmonary surfactant that bears intestinal-type and tissue-nonspecific-type alkaline phosphatase in endotoxin-induced rat bronchoalveolar fluid.
PMID:7669437
Administration of colony stimulating factor-1 to toothless osteopetrotic rats normalizes osteoblast, but not osteoclast, gene expression.