These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. Alkaline phosphatase: placental and tissue-nonspecific isoenzymes hydrolyze phosphoethanolamine, inorganic pyrophosphate, and pyridoxal 5'-phosphate. Substrate accumulation in carriers of hypophosphatasia corrects during pregnancy. Whyte MP; Landt M; Ryan LM; Mulivor RA; Henthorn PS; Fedde KN; Mahuren JD; Coburn SP J Clin Invest; 1995 Apr; 95(4):1440-5. PubMed ID: 7706447 [TBL] [Abstract][Full Text] [Related]
4. Tissue-Nonspecific Alkaline Phosphatase-A Gatekeeper of Physiological Conditions in Health and a Modulator of Biological Environments in Disease. Liedtke D; Hofmann C; Jakob F; Klopocki E; Graser S Biomolecules; 2020 Dec; 10(12):. PubMed ID: 33302551 [TBL] [Abstract][Full Text] [Related]
5. Normal activity of nucleoside triphosphate pyrophosphatase in alkaline phosphatase-deficient fibroblasts from patients with infantile hypophosphatasia. Caswell AM; Whyte MP; Russell RG J Clin Endocrinol Metab; 1986 Nov; 63(5):1237-41. PubMed ID: 3020080 [TBL] [Abstract][Full Text] [Related]
6. Perinatal hypophosphatasia: tissue levels of vitamin B6 are unremarkable despite markedly increased circulating concentrations of pyridoxal-5'-phosphate. Evidence for an ectoenzyme role for tissue-nonspecific alkaline phosphatase. Whyte MP; Mahuren JD; Fedde KN; Cole FS; McCabe ER; Coburn SP J Clin Invest; 1988 Apr; 81(4):1234-9. PubMed ID: 3350970 [TBL] [Abstract][Full Text] [Related]
7. The mechanism of mineralization and the role of alkaline phosphatase in health and disease. Orimo H J Nippon Med Sch; 2010 Feb; 77(1):4-12. PubMed ID: 20154452 [TBL] [Abstract][Full Text] [Related]
8. Physiological role of alkaline phosphatase explored in hypophosphatasia. Whyte MP Ann N Y Acad Sci; 2010 Mar; 1192():190-200. PubMed ID: 20392236 [TBL] [Abstract][Full Text] [Related]
9. Hypophosphatasia: biochemical screening of a Dutch kindred and evidence that urinary excretion of inorganic pyrophosphate is a marker for the disease. Macfarlane JD; Poorthuis BJ; van de Kamp JJ; Russell RG; Caswell AM Clin Chem; 1988 Sep; 34(9):1937-41. PubMed ID: 2843309 [TBL] [Abstract][Full Text] [Related]
10. Perinatal hypophosphatasia: radiology, pathology and molecular biology studies in a family harboring a splicing mutation (648+1A) and a novel missense mutation (N400S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene. Sergi C; Mornet E; Troeger J; Voigtlaender T Am J Med Genet; 2001 Oct; 103(3):235-40. PubMed ID: 11745997 [TBL] [Abstract][Full Text] [Related]
11. Alkaline phosphatase: Structure, expression and its function in bone mineralization. Vimalraj S Gene; 2020 Sep; 754():144855. PubMed ID: 32522695 [TBL] [Abstract][Full Text] [Related]
12. Alkaline phosphatase knock-out mice recapitulate the metabolic and skeletal defects of infantile hypophosphatasia. Fedde KN; Blair L; Silverstein J; Coburn SP; Ryan LM; Weinstein RS; Waymire K; Narisawa S; Millán JL; MacGregor GR; Whyte MP J Bone Miner Res; 1999 Dec; 14(12):2015-26. PubMed ID: 10620060 [TBL] [Abstract][Full Text] [Related]
13. Hypophosphatasia: phenotypic variability and possible Croatian origin of the c.1402g>A mutation of TNSALP gene. Petković Ramadza D; Stipoljev F; Sarnavka V; Begović D; Potocki K; Fumić K; Mornet E; Barić I Coll Antropol; 2009 Dec; 33(4):1255-8. PubMed ID: 20102078 [TBL] [Abstract][Full Text] [Related]
15. Serum alkaline phosphatase, serum pyrophosphatase, phosphorylethanolamine and inorganic pyrophosphate in plasma and urine. A genetic and clinical study of hypophosphatasia. Sørensen SA; Flodgaard H; Sørensen E Monogr Hum Genet; 1978; 10():66-9. PubMed ID: 214699 [No Abstract] [Full Text] [Related]
16. Hypophosphatasia: Enzyme Replacement Therapy Brings New Opportunities and New Challenges. Whyte MP J Bone Miner Res; 2017 Apr; 32(4):667-675. PubMed ID: 28084648 [TBL] [Abstract][Full Text] [Related]
17. Pyridoxine-responsive seizures as the first symptom of infantile hypophosphatasia caused by two novel missense mutations (c.677T>C, p.M226T; c.1112C>T, p.T371I) of the tissue-nonspecific alkaline phosphatase gene. Baumgartner-Sigl S; Haberlandt E; Mumm S; Scholl-Bürgi S; Sergi C; Ryan L; Ericson KL; Whyte MP; Högler W Bone; 2007 Jun; 40(6):1655-61. PubMed ID: 17395561 [TBL] [Abstract][Full Text] [Related]
18. Hypophosphatasia: clinicopathologic comparison of the infantile, childhood, and adult forms. Fallon MD; Teitelbaum SL; Weinstein RS; Goldfischer S; Brown DM; Whyte MP Medicine (Baltimore); 1984 Jan; 63(1):12-24. PubMed ID: 6690884 [TBL] [Abstract][Full Text] [Related]
19. Adult hypophosphatasia. Current aspects. Wendling D; Jeannin-Louys L; Kremer P; Fellmann F; Toussirot E; Mornet E Joint Bone Spine; 2001 Mar; 68(2):120-4. PubMed ID: 11324927 [TBL] [Abstract][Full Text] [Related]
20. [Childhood hypophosphatasia]. Mulder AL; van den Bos SN; Gerrits GP; Theunissen PM Ned Tijdschr Geneeskd; 1997 Jul; 141(27):1345-8. PubMed ID: 9380189 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]