-
1
-
-
0042166167
-
Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification
-
Rutsch F., Ruf N., Vaingankar S., Toliat M.R., Suk A., Hohne W., et al. Mutations in ENPP1 are associated with 'idiopathic' infantile arterial calcification. Nat Genet 2003, 34:379-381.
-
(2003)
Nat Genet
, vol.34
, pp. 379-381
-
-
Rutsch, F.1
Ruf, N.2
Vaingankar, S.3
Toliat, M.R.4
Suk, A.5
Hohne, W.6
-
2
-
-
0035135119
-
PC-1 nucleoside triphosphate pyrophosphohydrolase deficiency in idiopathic infantile arterial calcification
-
Rutsch F., Vaingankar S., Johnson K., Goldfine I., Maddux B., Schauerte P., et al. PC-1 nucleoside triphosphate pyrophosphohydrolase deficiency in idiopathic infantile arterial calcification. Am J Pathol 2001, 158:543-554.
-
(2001)
Am J Pathol
, vol.158
, pp. 543-554
-
-
Rutsch, F.1
Vaingankar, S.2
Johnson, K.3
Goldfine, I.4
Maddux, B.5
Schauerte, P.6
-
3
-
-
76049121613
-
Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene
-
Levy-Litan V., Hershkovitz E., Avizov L., Leventhal N., Bercovich D., Chalifa-Caspi V., et al. Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene. Am J Hum Genet 2010, 86:273-278.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 273-278
-
-
Levy-Litan, V.1
Hershkovitz, E.2
Avizov, L.3
Leventhal, N.4
Bercovich, D.5
Chalifa-Caspi, V.6
-
4
-
-
76049105171
-
Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic rickets
-
Lorenz-Depiereux B., Schnabel D., Tiosano D., Hausler G., Strom T.M. Loss-of-function ENPP1 mutations cause both generalized arterial calcification of infancy and autosomal-recessive hypophosphatemic rickets. Am J Hum Genet 2010, 86:267-272.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 267-272
-
-
Lorenz-Depiereux, B.1
Schnabel, D.2
Tiosano, D.3
Hausler, G.4
Strom, T.M.5
-
5
-
-
77951258759
-
Association of ALPL and ENPP1 gene polymorphisms with bone strength related skeletal traits in a Chuvashian population
-
Ermakov S., Toliat M.R., Cohen Z., Malkin I., Altmueller J., Livshits G., et al. Association of ALPL and ENPP1 gene polymorphisms with bone strength related skeletal traits in a Chuvashian population. Bone 2010, 46:1244-1250.
-
(2010)
Bone
, vol.46
, pp. 1244-1250
-
-
Ermakov, S.1
Toliat, M.R.2
Cohen, Z.3
Malkin, I.4
Altmueller, J.5
Livshits, G.6
-
6
-
-
0028795761
-
Membrane glycoprotein PC-1 and insulin-resistance in non-insulin-dependent diabetes-mellitus
-
Maddux B.A., Sbraccia P., Kumakura S., Sasson S., Youngren J., Fisher A., et al. Membrane glycoprotein PC-1 and insulin-resistance in non-insulin-dependent diabetes-mellitus. Nature 1995, 373:448-451.
-
(1995)
Nature
, vol.373
, pp. 448-451
-
-
Maddux, B.A.1
Sbraccia, P.2
Kumakura, S.3
Sasson, S.4
Youngren, J.5
Fisher, A.6
-
7
-
-
0029759418
-
PC-1 content in skeletal muscle of non-obese, non-diabetic subjects: relationship to insulin receptor tyrosine kinase and whole body insulin sensitivity
-
Frittitta L., Youngren J., Vigneri R., Maddux B.A., Trischitta V., Goldfine I.D. PC-1 content in skeletal muscle of non-obese, non-diabetic subjects: relationship to insulin receptor tyrosine kinase and whole body insulin sensitivity. Diabetologia 1996, 39:1190-1195.
-
(1996)
Diabetologia
, vol.39
, pp. 1190-1195
-
-
Frittitta, L.1
Youngren, J.2
Vigneri, R.3
Maddux, B.A.4
Trischitta, V.5
Goldfine, I.D.6
-
8
-
-
23044493861
-
Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes
-
Meyre D., Bouatia-Naji N., Tounian A., Samson C., Lecoeur C., Vatin V., et al. Variants of ENPP1 are associated with childhood and adult obesity and increase the risk of glucose intolerance and type 2 diabetes. Nat Genet 2005, 37:863-867.
-
(2005)
Nat Genet
, vol.37
, pp. 863-867
-
-
Meyre, D.1
Bouatia-Naji, N.2
Tounian, A.3
Samson, C.4
Lecoeur, C.5
Vatin, V.6
-
9
-
-
0028228997
-
Arthritis and ankylosis in TWY mice with hereditary multiple osteochondral lesions - with special reference to calcium deposition
-
Sakamoto M., Hosoda Y., Kojimahara K., Yamazaki T., Yoshimura Y. Arthritis and ankylosis in TWY mice with hereditary multiple osteochondral lesions - with special reference to calcium deposition. Pathol Int 1994, 44:420-427.
-
(1994)
Pathol Int
, vol.44
, pp. 420-427
-
-
Sakamoto, M.1
Hosoda, Y.2
Kojimahara, K.3
Yamazaki, T.4
Yoshimura, Y.5
-
10
-
-
0028969463
-
Elevation of alkaline-phosphatase activity induced by parathyroid-hormone in osteoblast like cells from the spinal hyperostotic mouse TWY (twy/twy)
-
Terakado A., Tagawa M., Goto S., Yamazaki M., Moriya H., Fujimura S. Elevation of alkaline-phosphatase activity induced by parathyroid-hormone in osteoblast like cells from the spinal hyperostotic mouse TWY (twy/twy). Calcif Tissue Int 1995, 56:135-139.
-
(1995)
Calcif Tissue Int
, vol.56
, pp. 135-139
-
-
Terakado, A.1
Tagawa, M.2
Goto, S.3
Yamazaki, M.4
Moriya, H.5
Fujimura, S.6
-
11
-
-
0030733501
-
Potential role of streptozotocin in enhancing ossification of the posterior longitudinal ligament of the cervical spine in the hereditary spinal hyperostotic mouse (twy/twy)
-
Baba H., Furusawa N., Fukuda M., Maezawa Y., Imura S., Kawahara N., et al. Potential role of streptozotocin in enhancing ossification of the posterior longitudinal ligament of the cervical spine in the hereditary spinal hyperostotic mouse (twy/twy). Eur J Histochem 1997, 41:191-202.
-
(1997)
Eur J Histochem
, vol.41
, pp. 191-202
-
-
Baba, H.1
Furusawa, N.2
Fukuda, M.3
Maezawa, Y.4
Imura, S.5
Kawahara, N.6
-
12
-
-
0030457803
-
Characteristics and mechanism of the ossification of posterior longitudinal ligament in the tip-toe walking Yoshimura (twy) mouse
-
Furusawa N., Baba H., Imura S., Fukuda M. Characteristics and mechanism of the ossification of posterior longitudinal ligament in the tip-toe walking Yoshimura (twy) mouse. Eur J Histochem 1996, 40:199-210.
-
(1996)
Eur J Histochem
, vol.40
, pp. 199-210
-
-
Furusawa, N.1
Baba, H.2
Imura, S.3
Fukuda, M.4
-
13
-
-
0031859977
-
Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine
-
Okawa A., Nakamura I., Goto S., Moriya H., Nakamura Y., Ikegawa S. Mutation in Npps in a mouse model of ossification of the posterior longitudinal ligament of the spine. Nat Genet 1998, 19:271-273.
-
(1998)
Nat Genet
, vol.19
, pp. 271-273
-
-
Okawa, A.1
Nakamura, I.2
Goto, S.3
Moriya, H.4
Nakamura, Y.5
Ikegawa, S.6
-
14
-
-
0033011551
-
Calcitonin simultaneously regulates both periosteal hyperostosis and trabecular osteopenia in the spinal hyperostotic mouse (twy/twy) in vivo
-
Okawa A., Goto S., Moriya H. Calcitonin simultaneously regulates both periosteal hyperostosis and trabecular osteopenia in the spinal hyperostotic mouse (twy/twy) in vivo. Calcif Tissue Int 1999, 64:239-247.
-
(1999)
Calcif Tissue Int
, vol.64
, pp. 239-247
-
-
Okawa, A.1
Goto, S.2
Moriya, H.3
-
15
-
-
0002113093
-
Germline deletion of the nucleoside triphosphate pyrophosphohydrolase (NTPPPH) plasma cell membrane glycoprotein-1 (PC-1) produces abnormal calcification of periarticular tissues
-
Shaker Publishing, L. Vanduffel, R. Lemmems (Eds.)
-
Sali A., Favaloro J., Terkeltaub R., Goding J. Germline deletion of the nucleoside triphosphate pyrophosphohydrolase (NTPPPH) plasma cell membrane glycoprotein-1 (PC-1) produces abnormal calcification of periarticular tissues. Ecto-ATPases and related ectoenzymes 1999, 267-282. Shaker Publishing. L. Vanduffel, R. Lemmems (Eds.).
-
(1999)
Ecto-ATPases and related ectoenzymes
, pp. 267-282
-
-
Sali, A.1
Favaloro, J.2
Terkeltaub, R.3
Goding, J.4
-
16
-
-
21144434783
-
Sustained osteomalacia of long bones despite major improvement in other hypophosphatasia-related mineral deficits in tissue nonspecific alkaline phosphatase/nucleotide pyrophosphatase phosphodiesterase 1 double-deficient mice
-
Anderson H.C., Harmey D., Camacho N.P., Garimella R., Sipe J.B., Tague S., et al. Sustained osteomalacia of long bones despite major improvement in other hypophosphatasia-related mineral deficits in tissue nonspecific alkaline phosphatase/nucleotide pyrophosphatase phosphodiesterase 1 double-deficient mice. Am J Pathol 2005, 166:1711-1720.
-
(2005)
Am J Pathol
, vol.166
, pp. 1711-1720
-
-
Anderson, H.C.1
Harmey, D.2
Camacho, N.P.3
Garimella, R.4
Sipe, J.B.5
Tague, S.6
-
17
-
-
0025144935
-
Plasma-cell membrane glycoprotein PC-1 - cDNA cloning of the human molecule, amino acid sequence, and chromosomal location
-
Buckley M.F., Loveland K.A., McKinstry W.J., Garson O.M., Goding J.W. Plasma-cell membrane glycoprotein PC-1 - cDNA cloning of the human molecule, amino acid sequence, and chromosomal location. J Biol Chem 1990, 265:17506-17511.
-
(1990)
J Biol Chem
, vol.265
, pp. 17506-17511
-
-
Buckley, M.F.1
Loveland, K.A.2
McKinstry, W.J.3
Garson, O.M.4
Goding, J.W.5
-
18
-
-
0026718793
-
Molecular-cloning of cDNAs for human fibroblast nucleotide pyrophosphatase
-
Funakoshi I., Kato H., Horie K., Yano T., Hori Y., Kobayashi H., et al. Molecular-cloning of cDNAs for human fibroblast nucleotide pyrophosphatase. Arch Biochem Biophys 1992, 295:180-187.
-
(1992)
Arch Biochem Biophys
, vol.295
, pp. 180-187
-
-
Funakoshi, I.1
Kato, H.2
Horie, K.3
Yano, T.4
Hori, Y.5
Kobayashi, H.6
-
19
-
-
0034490045
-
Nucleotide pyrophosphatases/phosphodiesterases on the move
-
Bollen M., Gijsbers R., Ceulemans H., Stalmans W., Stefan C. Nucleotide pyrophosphatases/phosphodiesterases on the move. Crit Rev Biochem Mol Biol 2000, 35:393-432.
-
(2000)
Crit Rev Biochem Mol Biol
, vol.35
, pp. 393-432
-
-
Bollen, M.1
Gijsbers, R.2
Ceulemans, H.3
Stalmans, W.4
Stefan, C.5
-
20
-
-
80052142300
-
Npp1 promotes atherosclerosis in ApoE knockout mice
-
Nitschke Y., Weissen-Plenz G., Terkeltaub R., Rutsch F. Npp1 promotes atherosclerosis in ApoE knockout mice. J Cell Mol Med 2011, 15:2273-2283.
-
(2011)
J Cell Mol Med
, vol.15
, pp. 2273-2283
-
-
Nitschke, Y.1
Weissen-Plenz, G.2
Terkeltaub, R.3
Rutsch, F.4
-
21
-
-
0034813884
-
Inorganic pyrophosphate generation and disposition in pathophysiology
-
Terkeltaub R.A. Inorganic pyrophosphate generation and disposition in pathophysiology. Am J Physiol Cell Physiol 2001, 281:C1-C11.
-
(2001)
Am J Physiol Cell Physiol
, vol.281
-
-
Terkeltaub, R.A.1
-
22
-
-
27744451970
-
I) in pathologic calcification of articular cartilage
-
I) in pathologic calcification of articular cartilage. Front Biosci 2005, 10:988-997.
-
(2005)
Front Biosci
, vol.10
, pp. 988-997
-
-
Johnson, K.1
Terkeltaub, R.2
-
23
-
-
0031885056
-
Ecto-phosphodiesterase/pyrophosphatase of lymphocytes and non-lymphoid cells: structure and function of the PC-1 family
-
Goding J.W., Terkeltaub R., Maurice M., Deterre P., Sali A., Belli S.I. Ecto-phosphodiesterase/pyrophosphatase of lymphocytes and non-lymphoid cells: structure and function of the PC-1 family. Immunol Rev 1998, 161:11-26.
-
(1998)
Immunol Rev
, vol.161
, pp. 11-26
-
-
Goding, J.W.1
Terkeltaub, R.2
Maurice, M.3
Deterre, P.4
Sali, A.5
Belli, S.I.6
-
24
-
-
34548012770
-
Modulation of purinergic signaling by NPP-type ectophosphodiesterases
-
Stefan C., Jansen S., Bollen M. Modulation of purinergic signaling by NPP-type ectophosphodiesterases. Purinergic Signal 2006, 2:361-370.
-
(2006)
Purinergic Signal
, vol.2
, pp. 361-370
-
-
Stefan, C.1
Jansen, S.2
Bollen, M.3
-
25
-
-
0031021476
-
Autotaxin is an exoenzyme possessing 5'-nucleotide phosphodiesterase/ATP pyrophosphatase and ATPase activities
-
Clair T., Lee H.Y., Liotta L.A., Stracke M.L. Autotaxin is an exoenzyme possessing 5'-nucleotide phosphodiesterase/ATP pyrophosphatase and ATPase activities. J Biol Chem 1997, 272:996-1001.
-
(1997)
J Biol Chem
, vol.272
, pp. 996-1001
-
-
Clair, T.1
Lee, H.Y.2
Liotta, L.A.3
Stracke, M.L.4
-
26
-
-
0027296082
-
Phosphorylation and nucleotide-dependent dephosphorylation of hepatic polypeptides related to the plasma-cell differentiation antigen PC-1
-
Uriarte M., Stalmans W., Hickman S., Bollen M. Phosphorylation and nucleotide-dependent dephosphorylation of hepatic polypeptides related to the plasma-cell differentiation antigen PC-1. Biochem J 1993, 293:93-100.
-
(1993)
Biochem J
, vol.293
, pp. 93-100
-
-
Uriarte, M.1
Stalmans, W.2
Hickman, S.3
Bollen, M.4
-
27
-
-
0018084369
-
5'-Nucleotide phosphodiesterase - isolation of covalently bound 5'-monophosphate, an intermediate in catalytic mechanism
-
Landt M., Butler L.G. 5'-Nucleotide phosphodiesterase - isolation of covalently bound 5'-monophosphate, an intermediate in catalytic mechanism. Biochemistry 1978, 17:4130-4135.
-
(1978)
Biochemistry
, vol.17
, pp. 4130-4135
-
-
Landt, M.1
Butler, L.G.2
-
28
-
-
0141560730
-
Matrix vesicles and calcification
-
Anderson H.C. Matrix vesicles and calcification. Curr Rheumatol Rep 2003, 5:222-226.
-
(2003)
Curr Rheumatol Rep
, vol.5
, pp. 222-226
-
-
Anderson, H.C.1
-
29
-
-
0033695669
-
Osteoblast tissue-nonspecific alkaline phosphatase antagonizes and regulates PC-1
-
Johnson K.A., Hessle L., Vaingankar S., Wennberg C., Mauro S., Narisawa S., et al. Osteoblast tissue-nonspecific alkaline phosphatase antagonizes and regulates PC-1. Am J Physiol Regul Integr Comp Physiol 2000, 279:R1365-R1377.
-
(2000)
Am J Physiol Regul Integr Comp Physiol
, vol.279
-
-
Johnson, K.A.1
Hessle, L.2
Vaingankar, S.3
Wennberg, C.4
Mauro, S.5
Narisawa, S.6
-
31
-
-
0037047051
-
Tissue-nonspecific alkaline phosphatase and plasma cell membrane glycoprotein-1 are central antagonistic regulators of bone mineralization
-
Hessle L., Johnson K.A., Anderson H.C., Narisawa S., Sali A., Goding J.W., et al. Tissue-nonspecific alkaline phosphatase and plasma cell membrane glycoprotein-1 are central antagonistic regulators of bone mineralization. Proc Natl Acad Sci U S A 2002, 99:9445-9449.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 9445-9449
-
-
Hessle, L.1
Johnson, K.A.2
Anderson, H.C.3
Narisawa, S.4
Sali, A.5
Goding, J.W.6
-
32
-
-
1642313676
-
Concerted regulation of inorganic pyrophosphate and osteopontin by Akp2, Enpp1, and Ank - an integrated model of the pathogenesis of mineralization disorders
-
Harmey D., Hessle L., Narisawa S., Johnson K.A., Terkeltaub R., Millan J.L. Concerted regulation of inorganic pyrophosphate and osteopontin by Akp2, Enpp1, and Ank - an integrated model of the pathogenesis of mineralization disorders. Am J Pathol 2004, 164:1199-1209.
-
(2004)
Am J Pathol
, vol.164
, pp. 1199-1209
-
-
Harmey, D.1
Hessle, L.2
Narisawa, S.3
Johnson, K.A.4
Terkeltaub, R.5
Millan, J.L.6
-
33
-
-
33748082636
-
Elevated skeletal osteopontin levels contribute to the hypophosphatasia phenotype in Akp2(-/-) mice
-
Harmey D., Johnson K.A., Zelken J., Camacho N.P., Hoylaerts M.F., Noda M., et al. Elevated skeletal osteopontin levels contribute to the hypophosphatasia phenotype in Akp2(-/-) mice. J Bone Miner Res 2006, 21:1377-1386.
-
(2006)
J Bone Miner Res
, vol.21
, pp. 1377-1386
-
-
Harmey, D.1
Johnson, K.A.2
Zelken, J.3
Camacho, N.P.4
Hoylaerts, M.F.5
Noda, M.6
-
34
-
-
78951478417
-
Cellular ATP synthesis mediated by type III sodium-dependent phosphate transporter Pit-1 is critical to chondrogenesis
-
Sugita A., Kawai S., Hayashibara T., Amano A., Ooshima T., Michigami T., et al. Cellular ATP synthesis mediated by type III sodium-dependent phosphate transporter Pit-1 is critical to chondrogenesis. J Biol Chem 2011, 286:3094-3103.
-
(2011)
J Biol Chem
, vol.286
, pp. 3094-3103
-
-
Sugita, A.1
Kawai, S.2
Hayashibara, T.3
Amano, A.4
Ooshima, T.5
Michigami, T.6
-
35
-
-
79251482785
-
Loss of skeletal mineralization by the simultaneous ablation of PHOSPHO1 and alkaline phosphatase function: a unified model of the mechanisms of initiation of skeletal calcification
-
Yadav M.C., Simao A.M.S., Narisawa S., Huesa C., McKee M.D., Farquharson C., et al. Loss of skeletal mineralization by the simultaneous ablation of PHOSPHO1 and alkaline phosphatase function: a unified model of the mechanisms of initiation of skeletal calcification. J Bone Miner Res 2011, 26:286-297.
-
(2011)
J Bone Miner Res
, vol.26
, pp. 286-297
-
-
Yadav, M.C.1
Simao, A.M.S.2
Narisawa, S.3
Huesa, C.4
McKee, M.D.5
Farquharson, C.6
-
36
-
-
0028233939
-
Causal link between nucleotide pyrophosphohydrolase overactivity and increased intracellular inorganic pyrophosphate generation demonstrated by transfection of cultured fibroblasts and osteoblasts with plasma-cell membrane glycoprotein-1 - relevance to calcium pyrophosphate dihydrate deposition disease
-
Terkeltaub R., Rosenbach M., Fong F., Goding J. Causal link between nucleotide pyrophosphohydrolase overactivity and increased intracellular inorganic pyrophosphate generation demonstrated by transfection of cultured fibroblasts and osteoblasts with plasma-cell membrane glycoprotein-1 - relevance to calcium pyrophosphate dihydrate deposition disease. Arthritis Rheum 1994, 37:934-941.
-
(1994)
Arthritis Rheum
, vol.37
, pp. 934-941
-
-
Terkeltaub, R.1
Rosenbach, M.2
Fong, F.3
Goding, J.4
-
37
-
-
0034647482
-
Role of the mouse ank gene in control of tissue calcification and arthritis
-
Ho A.M., Johnson M.D., Kingsley D.M. Role of the mouse ank gene in control of tissue calcification and arthritis. Science 2000, 289:265-270.
-
(2000)
Science
, vol.289
, pp. 265-270
-
-
Ho, A.M.1
Johnson, M.D.2
Kingsley, D.M.3
-
38
-
-
0021733794
-
Hereditary joint disorder in progressive ankylosis (ank/ank) mice. I. Association of calcium hydroxyapatite deposition with inflammatory arthropathy
-
Hakim F.T., Cranley R., Brown K.S., Eanes E.D., Harne L., Oppenheim J.J. Hereditary joint disorder in progressive ankylosis (ank/ank) mice. I. Association of calcium hydroxyapatite deposition with inflammatory arthropathy. Arthritis Rheum 1984, 27:1411-1420.
-
(1984)
Arthritis Rheum
, vol.27
, pp. 1411-1420
-
-
Hakim, F.T.1
Cranley, R.2
Brown, K.S.3
Eanes, E.D.4
Harne, L.5
Oppenheim, J.J.6
-
39
-
-
34447538396
-
Pyrophosphate inhibits mineralization of osteoblast cultures by binding to mineral, up-regulating osteopontin, and inhibiting alkaline phosphatase activity
-
Addison W.N., Azari F., Sorensen E.S., Kaartinen M.T., McKee M.D. Pyrophosphate inhibits mineralization of osteoblast cultures by binding to mineral, up-regulating osteopontin, and inhibiting alkaline phosphatase activity. J Biol Chem 2007, 282:15872-15883.
-
(2007)
J Biol Chem
, vol.282
, pp. 15872-15883
-
-
Addison, W.N.1
Azari, F.2
Sorensen, E.S.3
Kaartinen, M.T.4
McKee, M.D.5
-
41
-
-
80655149476
-
Ectonucleotide pyrophosphatase/phosphodiesterase-1 (ENPP1) protein regulates osteoblast differentiation
-
Nam H.K., Liu J., Li Y., Kragor A., Hatch N.E. Ectonucleotide pyrophosphatase/phosphodiesterase-1 (ENPP1) protein regulates osteoblast differentiation. J Biol Chem 2011, 286:39059-39071.
-
(2011)
J Biol Chem
, vol.286
, pp. 39059-39071
-
-
Nam, H.K.1
Liu, J.2
Li, Y.3
Kragor, A.4
Hatch, N.E.5
-
42
-
-
84855860969
-
Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6
-
Nitschke Y., Baujat G., Botschen U., Wittkampf T., du Moulin M., Stella J., et al. Generalized arterial calcification of infancy and pseudoxanthoma elasticum can be caused by mutations in either ENPP1 or ABCC6. Am J Hum Genet 2012, 90:25-39.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 25-39
-
-
Nitschke, Y.1
Baujat, G.2
Botschen, U.3
Wittkampf, T.4
du Moulin, M.5
Stella, J.6
-
43
-
-
80052153431
-
Genetics in arterial calcification: pieces of a puzzle and cogs in a wheel
-
Rutsch F., Nitschke Y., Terkeltaub R. Genetics in arterial calcification: pieces of a puzzle and cogs in a wheel. Circ Res 2011, 109:578-592.
-
(2011)
Circ Res
, vol.109
, pp. 578-592
-
-
Rutsch, F.1
Nitschke, Y.2
Terkeltaub, R.3
-
44
-
-
0016416418
-
Idiopathic arterial calcification of infancy: a clinicopathologic study
-
Moran J.J. Idiopathic arterial calcification of infancy: a clinicopathologic study. Pathol Annu 1975, 10:393-417.
-
(1975)
Pathol Annu
, vol.10
, pp. 393-417
-
-
Moran, J.J.1
-
45
-
-
0033752990
-
Low levels of urinary inorganic pyrophosphate indicating systemic pyrophosphate deficiency in a boy with idiopathic infantile arterial calcification
-
Rutsch F., Schauerte P., Kalhoff H., Petrarulo M., August C., Diekmann L. Low levels of urinary inorganic pyrophosphate indicating systemic pyrophosphate deficiency in a boy with idiopathic infantile arterial calcification. Acta Paediatr 2000, 89:1265-1269.
-
(2000)
Acta Paediatr
, vol.89
, pp. 1265-1269
-
-
Rutsch, F.1
Schauerte, P.2
Kalhoff, H.3
Petrarulo, M.4
August, C.5
Diekmann, L.6
-
46
-
-
68149120891
-
Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy
-
Rutsch F., Boeyer P., Nitschke Y., Ruf N., Lorenz-Depierieux B., Wittkampf T., et al. Hypophosphatemia, hyperphosphaturia, and bisphosphonate treatment are associated with survival beyond infancy in generalized arterial calcification of infancy. Circ Cardiovasc Genet 2008, 1:133-140.
-
(2008)
Circ Cardiovasc Genet
, vol.1
, pp. 133-140
-
-
Rutsch, F.1
Boeyer, P.2
Nitschke, Y.3
Ruf, N.4
Lorenz-Depierieux, B.5
Wittkampf, T.6
-
47
-
-
60749131707
-
Generalized arterial calcification of infancy: treatment with bisphosphonates
-
Ramjan K.A., Roscioli T., Rutsch F., Sillence D., Munns C.F.J. Generalized arterial calcification of infancy: treatment with bisphosphonates. Nat Clin Pract Endocrinol Metab 2009, 5:167-172.
-
(2009)
Nat Clin Pract Endocrinol Metab
, vol.5
, pp. 167-172
-
-
Ramjan, K.A.1
Roscioli, T.2
Rutsch, F.3
Sillence, D.4
Munns, C.F.J.5
-
48
-
-
0021224880
-
Generalized arterial calcification of infancy - 3 case reports, including spontaneous regression with long-term survival
-
Sholler G.F., Yu J.S., Bale P.M., Hawker R.E., Celermajer J.M., Kozlowski K. Generalized arterial calcification of infancy - 3 case reports, including spontaneous regression with long-term survival. J Pediatr 1984, 105:257-260.
-
(1984)
J Pediatr
, vol.105
, pp. 257-260
-
-
Sholler, G.F.1
Yu, J.S.2
Bale, P.M.3
Hawker, R.E.4
Celermajer, J.M.5
Kozlowski, K.6
-
49
-
-
33344454730
-
Generalized arterial calcification of infancy: two siblings with prolonged survival
-
Ciana G., Trappan A., Bembi B., Benettoni A., Maso G., Zennaro F., et al. Generalized arterial calcification of infancy: two siblings with prolonged survival. Eur J Pediatr 2006, 165:258-263.
-
(2006)
Eur J Pediatr
, vol.165
, pp. 258-263
-
-
Ciana, G.1
Trappan, A.2
Bembi, B.3
Benettoni, A.4
Maso, G.5
Zennaro, F.6
-
50
-
-
84860321632
-
Cutaneous features of pseudoxanthoma elasticum in a patient with generalized arterial calcification of infancy due to a homozygous missense mutation in the ENPP1 gene
-
Li Q., Schumacher W., Jablonski D., Siegel D., Uitto J. Cutaneous features of pseudoxanthoma elasticum in a patient with generalized arterial calcification of infancy due to a homozygous missense mutation in the ENPP1 gene. Br J Dermatol 2012, 166:1107-1111.
-
(2012)
Br J Dermatol
, vol.166
, pp. 1107-1111
-
-
Li, Q.1
Schumacher, W.2
Jablonski, D.3
Siegel, D.4
Uitto, J.5
-
51
-
-
18844465976
-
Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum
-
Le Saux O., Urban Z., Tschuch C., Csiszar K., Bacchelli B., Quaglino D., et al. Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticum. Nat Genet 2000, 25:223-227.
-
(2000)
Nat Genet
, vol.25
, pp. 223-227
-
-
Le Saux, O.1
Urban, Z.2
Tschuch, C.3
Csiszar, K.4
Bacchelli, B.5
Quaglino, D.6
-
52
-
-
0034705145
-
Pseudoxanthoma elasticum: mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter
-
Ringpfeil F., Lebwohl M.G., Christiano A.M., Uitto J. Pseudoxanthoma elasticum: mutations in the MRP6 gene encoding a transmembrane ATP-binding cassette (ABC) transporter. Proc Natl Acad Sci U S A 2000, 97:6001-6006.
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 6001-6006
-
-
Ringpfeil, F.1
Lebwohl, M.G.2
Christiano, A.M.3
Uitto, J.4
-
54
-
-
0032806520
-
Association of the human NPPS gene with ossification of the posterior longitudinal ligament of the spine (OPLL)
-
Nakamura I., Ikegawa S., Okawa A., Okuda S., Koshizuka Y., Kawaguchi H., et al. Association of the human NPPS gene with ossification of the posterior longitudinal ligament of the spine (OPLL). Hum Genet 1999, 104:492-497.
-
(1999)
Hum Genet
, vol.104
, pp. 492-497
-
-
Nakamura, I.1
Ikegawa, S.2
Okawa, A.3
Okuda, S.4
Koshizuka, Y.5
Kawaguchi, H.6
-
55
-
-
0036133540
-
Nucleotide pyrophosphatase gene polymorphism associated with ossification of the posterior longitudinal ligament of the spine
-
Koshizuka Y., Kawaguchi H., Ogata N., Ikeda T., Mabuchi A., Seichi A., et al. Nucleotide pyrophosphatase gene polymorphism associated with ossification of the posterior longitudinal ligament of the spine. J Bone Miner Res 2002, 17:138-144.
-
(2002)
J Bone Miner Res
, vol.17
, pp. 138-144
-
-
Koshizuka, Y.1
Kawaguchi, H.2
Ogata, N.3
Ikeda, T.4
Mabuchi, A.5
Seichi, A.6
-
56
-
-
18244378248
-
The extent of ossification of posterior longitudinal ligament of the spine associated with nucleotide pyrophosphatase gene and leptin receptor gene polymorphisms
-
Tahara M., Aiba A., Yamazaki M., Ikeda Y., Goto S., Moriya H., et al. The extent of ossification of posterior longitudinal ligament of the spine associated with nucleotide pyrophosphatase gene and leptin receptor gene polymorphisms. Spine 2005, 30:877-880.
-
(2005)
Spine
, vol.30
, pp. 877-880
-
-
Tahara, M.1
Aiba, A.2
Yamazaki, M.3
Ikeda, Y.4
Goto, S.5
Moriya, H.6
-
57
-
-
79956073084
-
The appearance and modulation of osteocyte marker expression during calcification of vascular smooth muscle cells
-
Zhu D., Mackenzie N.C.W., Millan J.L., Farquharson C., MacRae V.E. The appearance and modulation of osteocyte marker expression during calcification of vascular smooth muscle cells. PLoS One 2011, 6:e19595.
-
(2011)
PLoS One
, vol.6
-
-
Zhu, D.1
Mackenzie, N.C.W.2
Millan, J.L.3
Farquharson, C.4
MacRae, V.E.5
-
59
-
-
74049140470
-
S100A12 mediates aortic wall remodeling and aortic aneurysm
-
Bowman M.H., Wilk J., Heydemann A., Kim G., Rehman J., Lodato J.A., et al. S100A12 mediates aortic wall remodeling and aortic aneurysm. Circ Res 2010, 106:145-U291.
-
(2010)
Circ Res
, vol.106
-
-
Bowman, M.H.1
Wilk, J.2
Heydemann, A.3
Kim, G.4
Rehman, J.5
Lodato, J.A.6
-
60
-
-
77953232228
-
Circulating soluble receptor for advanced glycation end-product levels are decreased in patients with calcific aortic valve stenosis
-
Basta G., Corciu A.I., Vianello A., Del Turco S., Foffa I., Navarra T., et al. Circulating soluble receptor for advanced glycation end-product levels are decreased in patients with calcific aortic valve stenosis. Atherosclerosis 2010, 210:614-618.
-
(2010)
Atherosclerosis
, vol.210
, pp. 614-618
-
-
Basta, G.1
Corciu, A.I.2
Vianello, A.3
Del Turco, S.4
Foffa, I.5
Navarra, T.6
-
61
-
-
0028301910
-
Modulation of crystal-formation by bone phosphoproteins - structural specificity of the osteopontin-mediated inhibition of hydroxyapatite formation
-
Hunter G.K., Kyle C.L., Goldberg H.A. Modulation of crystal-formation by bone phosphoproteins - structural specificity of the osteopontin-mediated inhibition of hydroxyapatite formation. Biochem J 1994, 300:723-728.
-
(1994)
Biochem J
, vol.300
, pp. 723-728
-
-
Hunter, G.K.1
Kyle, C.L.2
Goldberg, H.A.3
-
62
-
-
0027249892
-
Osteopontin-hydroxyapatite interactions in-vitro - inhibition of hydroxyapatite formation and growth in a gelatin-gel
-
Boskey A.L., Maresca M., Ullrich W., Doty S.B., Butler W.T., Prince C.W. Osteopontin-hydroxyapatite interactions in-vitro - inhibition of hydroxyapatite formation and growth in a gelatin-gel. Bone Miner 1993, 22:147-159.
-
(1993)
Bone Miner
, vol.22
, pp. 147-159
-
-
Boskey, A.L.1
Maresca, M.2
Ullrich, W.3
Doty, S.B.4
Butler, W.T.5
Prince, C.W.6
-
63
-
-
0037152187
-
Inactivation of the osteopontin gene enhances vascular calcification of matrix Gla protein-deficient mice: evidence for osteopontin as an inducible inhibitor of vascular calcification in vivo
-
Speer M.Y., McKee M.D., Guldberg R.E., Liaw L., Yang H.Y., Tung E., et al. Inactivation of the osteopontin gene enhances vascular calcification of matrix Gla protein-deficient mice: evidence for osteopontin as an inducible inhibitor of vascular calcification in vivo. J Exp Med 2002, 196:1047-1055.
-
(2002)
J Exp Med
, vol.196
, pp. 1047-1055
-
-
Speer, M.Y.1
McKee, M.D.2
Guldberg, R.E.3
Liaw, L.4
Yang, H.Y.5
Tung, E.6
-
64
-
-
0036900001
-
Osteopontin inhibits mineral deposition and promotes regression of ectopic calcification
-
Steitz S.A., Speer M.Y., McKee M.D., Liaw L., Almeida M., Yang H., et al. Osteopontin inhibits mineral deposition and promotes regression of ectopic calcification. Am J Pathol 2002, 161:2035-2046.
-
(2002)
Am J Pathol
, vol.161
, pp. 2035-2046
-
-
Steitz, S.A.1
Speer, M.Y.2
McKee, M.D.3
Liaw, L.4
Almeida, M.5
Yang, H.6
-
65
-
-
12444251079
-
Osteopontin deficiency attenuates atherosclerosis in female apolipoprotein E-deficient mice
-
Matsui Y., Rittling S.R., Okamoto H., Inobe M., Jia N., Shimizu T., et al. Osteopontin deficiency attenuates atherosclerosis in female apolipoprotein E-deficient mice. Arterioscler Thromb Vasc Biol 2003, 23:1029-1034.
-
(2003)
Arterioscler Thromb Vasc Biol
, vol.23
, pp. 1029-1034
-
-
Matsui, Y.1
Rittling, S.R.2
Okamoto, H.3
Inobe, M.4
Jia, N.5
Shimizu, T.6
-
66
-
-
0347986784
-
Angiotensin II-accelerated atherosclerosis and aneurysm formation is attenuated in osteopontin-deficient mice
-
Bruemmer D., Collins A.R., Noh G., Wang W., Territo M., Arias-Magallona S., et al. Angiotensin II-accelerated atherosclerosis and aneurysm formation is attenuated in osteopontin-deficient mice. J Clin Invest 2003, 112:1318-1331.
-
(2003)
J Clin Invest
, vol.112
, pp. 1318-1331
-
-
Bruemmer, D.1
Collins, A.R.2
Noh, G.3
Wang, W.4
Territo, M.5
Arias-Magallona, S.6
-
67
-
-
84874242004
-
ATP release acts as survival signal and prevents the mineralization of aortic valve by P2Y(2) and PI3K/AKT signaling
-
Cote N., El Husseini D., Pepin A., Bosse Y., Bouvet C., Audet A., et al. ATP release acts as survival signal and prevents the mineralization of aortic valve by P2Y(2) and PI3K/AKT signaling. Circulation 2011, 124:A11911.
-
(2011)
Circulation
, vol.124
-
-
Cote, N.1
El Husseini, D.2
Pepin, A.3
Bosse, Y.4
Bouvet, C.5
Audet, A.6
-
68
-
-
57449105957
-
Endocrine functions of bone in mineral metabolism regulation
-
Quarles L.D. Endocrine functions of bone in mineral metabolism regulation. J Clin Invest 2008, 118:3820-3828.
-
(2008)
J Clin Invest
, vol.118
, pp. 3820-3828
-
-
Quarles, L.D.1
-
69
-
-
52649142085
-
Pathogenic role of Fgf23 in Dmp1-null mice
-
Liu S., Zhou J., Tang W., Menard R., Feng J.Q., Quarles L.D. Pathogenic role of Fgf23 in Dmp1-null mice. Am J Physiol Endocrinol Metab 2008, 295:E254-E261.
-
(2008)
Am J Physiol Endocrinol Metab
, vol.295
-
-
Liu, S.1
Zhou, J.2
Tang, W.3
Menard, R.4
Feng, J.Q.5
Quarles, L.D.6
-
70
-
-
33745850756
-
Pathogenic role of Fgf23 in Hyp mice
-
Liu S.G., Zhou J.P., Tang W., Jiang X., Rowe D.W., Quarles L.D. Pathogenic role of Fgf23 in Hyp mice. Am J Physiol Endocrinol Metab 2006, 291:E38-E49.
-
(2006)
Am J Physiol Endocrinol Metab
, vol.291
-
-
Liu, S.G.1
Zhou, J.P.2
Tang, W.3
Jiang, X.4
Rowe, D.W.5
Quarles, L.D.6
-
71
-
-
36849017126
-
The parathyroid is a target organ for FGF23 in rats
-
Ben-Dov I.Z., Galitzer H., Lavi-Moshayoff V., Goetz R., Kuro-o M., Mohammadi M., et al. The parathyroid is a target organ for FGF23 in rats. J Clin Invest 2007, 117:4003-4008.
-
(2007)
J Clin Invest
, vol.117
, pp. 4003-4008
-
-
Ben-Dov, I.Z.1
Galitzer, H.2
Lavi-Moshayoff, V.3
Goetz, R.4
Kuro-o, M.5
Mohammadi, M.6
-
72
-
-
33646578195
-
Regulation of fibroblast growth factor-23 signaling by Klotho
-
Kurosu H., Ogawa Y., Miyoshi M., Yamamoto M., Nandi A., Rosenblatt K.P., et al. Regulation of fibroblast growth factor-23 signaling by Klotho. J Biol Chem 2006, 281:6120-6123.
-
(2006)
J Biol Chem
, vol.281
, pp. 6120-6123
-
-
Kurosu, H.1
Ogawa, Y.2
Miyoshi, M.3
Yamamoto, M.4
Nandi, A.5
Rosenblatt, K.P.6
-
73
-
-
80051687775
-
Bone proteins PHEX and DMP1 regulate fibroblastic growth factor Fgf23 expression in osteocytes through a common pathway involving FGF receptor (FGFR) signaling
-
Martin A., Liu S., David V., Li H., Karydis A., Feng J.Q., et al. Bone proteins PHEX and DMP1 regulate fibroblastic growth factor Fgf23 expression in osteocytes through a common pathway involving FGF receptor (FGFR) signaling. FASEB J 2011, 25:2551-2562.
-
(2011)
FASEB J
, vol.25
, pp. 2551-2562
-
-
Martin, A.1
Liu, S.2
David, V.3
Li, H.4
Karydis, A.5
Feng, J.Q.6
-
74
-
-
50849104780
-
Genetic evidence of serum phosphate-independent functions of FGF-23 on bone
-
Sitara D., Kim S., Razzaque M.S., Bergwitz C., Taguchi T., Schuler C., et al. Genetic evidence of serum phosphate-independent functions of FGF-23 on bone. PLoS Genet 2008, 4:10.
-
(2008)
PLoS Genet
, vol.4
, pp. 10
-
-
Sitara, D.1
Kim, S.2
Razzaque, M.S.3
Bergwitz, C.4
Taguchi, T.5
Schuler, C.6
-
75
-
-
79959991101
-
Elevated FGF 23 and phosphorus are associated with coronary calcification in hemodialysis patients
-
Srivaths P.R., Goldstein S.L., Silverstein D.M., Krishnamurthy R., Brewer E.D. Elevated FGF 23 and phosphorus are associated with coronary calcification in hemodialysis patients. Pediatr Nephrol 2011, 26:945-951.
-
(2011)
Pediatr Nephrol
, vol.26
, pp. 945-951
-
-
Srivaths, P.R.1
Goldstein, S.L.2
Silverstein, D.M.3
Krishnamurthy, R.4
Brewer, E.D.5
-
76
-
-
77954090037
-
Fibroblast growth factor-23 (FGF-23) is independently correlated to aortic calcification in haemodialysis patients
-
Nasrallah M.M., El-Shehaby A.R., Salem M.M., Osman N.A., El Sheikh E., El Din U.A.A.S. Fibroblast growth factor-23 (FGF-23) is independently correlated to aortic calcification in haemodialysis patients. Nephrol Dial Transplant 2010, 25:2679-2685.
-
(2010)
Nephrol Dial Transplant
, vol.25
, pp. 2679-2685
-
-
Nasrallah, M.M.1
El-Shehaby, A.R.2
Salem, M.M.3
Osman, N.A.4
El Sheikh, E.5
El Din, U.A.A.S.6
-
77
-
-
67650892239
-
Circulating fibroblast growth factor-23 is associated with vascular dysfunction in the community
-
Mirza M.A.I., Larsson A., Lind L., Larsson T.E. Circulating fibroblast growth factor-23 is associated with vascular dysfunction in the community. Atherosclerosis 2009, 205:385-390.
-
(2009)
Atherosclerosis
, vol.205
, pp. 385-390
-
-
Mirza, M.A.I.1
Larsson, A.2
Lind, L.3
Larsson, T.E.4
-
78
-
-
70349656941
-
Relationship between circulating FGF23 and total body atherosclerosis in the community
-
Mirza M.A.I., Hansen T., Johansson L., Ahlstrom H., Larsson A., Lind L., et al. Relationship between circulating FGF23 and total body atherosclerosis in the community. Nephrol Dial Transplant 2009, 24:3125-3131.
-
(2009)
Nephrol Dial Transplant
, vol.24
, pp. 3125-3131
-
-
Mirza, M.A.I.1
Hansen, T.2
Johansson, L.3
Ahlstrom, H.4
Larsson, A.5
Lind, L.6
-
79
-
-
70450230670
-
Serum intact FGF23 associate with left ventricular mass, hypertrophy and geometry in an elderly population
-
Mirza M.A.I., Larsson A., Melhus H., Lind L., Larsson T.E. Serum intact FGF23 associate with left ventricular mass, hypertrophy and geometry in an elderly population. Atherosclerosis 2009, 207:546-551.
-
(2009)
Atherosclerosis
, vol.207
, pp. 546-551
-
-
Mirza, M.A.I.1
Larsson, A.2
Melhus, H.3
Lind, L.4
Larsson, T.E.5
-
80
-
-
66349097180
-
Fibroblast growth factor 23 and left ventricular hypertrophy in chronic kidney disease
-
Gutierrez O.M., Januzzi J.L., Isakova T., Laliberte K., Smith K., Collerone G., et al. Fibroblast growth factor 23 and left ventricular hypertrophy in chronic kidney disease. Circulation 2009, 119:2545-2552.
-
(2009)
Circulation
, vol.119
, pp. 2545-2552
-
-
Gutierrez, O.M.1
Januzzi, J.L.2
Isakova, T.3
Laliberte, K.4
Smith, K.5
Collerone, G.6
-
81
-
-
9644303231
-
Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice
-
Sitara D., Razzaque M.S., Hesse M., Yoganathan S., Taguchi T., Erben R.G., et al. Homozygous ablation of fibroblast growth factor-23 results in hyperphosphatemia and impaired skeletogenesis, and reverses hypophosphatemia in Phex-deficient mice. Matrix Biol 2004, 23:421-432.
-
(2004)
Matrix Biol
, vol.23
, pp. 421-432
-
-
Sitara, D.1
Razzaque, M.S.2
Hesse, M.3
Yoganathan, S.4
Taguchi, T.5
Erben, R.G.6
-
82
-
-
34250667000
-
Role of hyperphosphatemia and 1,25-dihydroxyvitamin D in vascular calcification and mortality in fibroblastic growth factor 23 null mice
-
Stubbs J.R., Liu S., Tang W., Zhou J., Wang Y., Yao X., et al. Role of hyperphosphatemia and 1,25-dihydroxyvitamin D in vascular calcification and mortality in fibroblastic growth factor 23 null mice. J Am Soc Nephrol 2007, 18:2116-2124.
-
(2007)
J Am Soc Nephrol
, vol.18
, pp. 2116-2124
-
-
Stubbs, J.R.1
Liu, S.2
Tang, W.3
Zhou, J.4
Wang, Y.5
Yao, X.6
-
83
-
-
9244240970
-
Transgenic mice overexpressing human fibroblast growth factor 23 (R176Q) delineate a putative role for parathyroid hormone in renal phosphate wasting disorders
-
Bai X.Y., Miao D.S., Li J.R., Goltzman D., Karaplis A.C. Transgenic mice overexpressing human fibroblast growth factor 23 (R176Q) delineate a putative role for parathyroid hormone in renal phosphate wasting disorders. Endocrinology 2004, 145:5269-5279.
-
(2004)
Endocrinology
, vol.145
, pp. 5269-5279
-
-
Bai, X.Y.1
Miao, D.S.2
Li, J.R.3
Goltzman, D.4
Karaplis, A.C.5
-
84
-
-
9144248333
-
FGF-23 transgenic mice demonstrate hypophosphatemic rickets with reduced expression of sodium phosphate cotransporter type IIa
-
Shimada T., Urakawa I., Yamazaki Y., Hasegawa H., Hino R., Yoneya T., et al. FGF-23 transgenic mice demonstrate hypophosphatemic rickets with reduced expression of sodium phosphate cotransporter type IIa. Biochem Biophys Res Commun 2004, 314:409-414.
-
(2004)
Biochem Biophys Res Commun
, vol.314
, pp. 409-414
-
-
Shimada, T.1
Urakawa, I.2
Yamazaki, Y.3
Hasegawa, H.4
Hino, R.5
Yoneya, T.6
-
85
-
-
3042634460
-
Transgenic mice expressing fibroblast growth factor 23 under the control of the alpha 1(I) collagen promoter exhibit growth retardation, osteomalacia, and disturbed phosphate homeostasis
-
Larsson T., Marsell R., Schipani E., Ohlsson C., Ljunggren O., Tenenhouse H.S., et al. Transgenic mice expressing fibroblast growth factor 23 under the control of the alpha 1(I) collagen promoter exhibit growth retardation, osteomalacia, and disturbed phosphate homeostasis. Endocrinology 2004, 145:3087-3094.
-
(2004)
Endocrinology
, vol.145
, pp. 3087-3094
-
-
Larsson, T.1
Marsell, R.2
Schipani, E.3
Ohlsson, C.4
Ljunggren, O.5
Tenenhouse, H.S.6
-
86
-
-
84860778116
-
Vascular Klotho deficiency potentiates the development of human artery calcification and mediates resistance to FGF-23
-
Lim K.L.T., Molostvov G., Lee C., Lam F., Zehnder D., Hsiao L.L. Vascular Klotho deficiency potentiates the development of human artery calcification and mediates resistance to FGF-23. Circulation 2012, 125(18):2243-2255.
-
(2012)
Circulation
, vol.125
, Issue.18
, pp. 2243-2255
-
-
Lim, K.L.T.1
Molostvov, G.2
Lee, C.3
Lam, F.4
Zehnder, D.5
Hsiao, L.L.6
-
87
-
-
0031747108
-
Elevated PC-1 content in cultured skin fibroblasts correlates with decreased in vivo and in vitro insulin action in nondiabetic subjects - evidence that PC-1 may be an intrinsic factor in impaired insulin receptor signaling
-
Frittitta L., Spampinato D., Solini A., Nosadini R., Goldfine I.D., Vigneri R., et al. Elevated PC-1 content in cultured skin fibroblasts correlates with decreased in vivo and in vitro insulin action in nondiabetic subjects - evidence that PC-1 may be an intrinsic factor in impaired insulin receptor signaling. Diabetes 1998, 47:1095-1100.
-
(1998)
Diabetes
, vol.47
, pp. 1095-1100
-
-
Frittitta, L.1
Spampinato, D.2
Solini, A.3
Nosadini, R.4
Goldfine, I.D.5
Vigneri, R.6
-
88
-
-
0033957339
-
Membrane glycoprotein PC-1 inhibition of insulin receptor function occurs via direct interaction with the receptor alpha-subunit
-
Maddux B.A., Goldfine I.D. Membrane glycoprotein PC-1 inhibition of insulin receptor function occurs via direct interaction with the receptor alpha-subunit. Diabetes 2000, 49:13-19.
-
(2000)
Diabetes
, vol.49
, pp. 13-19
-
-
Maddux, B.A.1
Goldfine, I.D.2
-
89
-
-
0029742448
-
Skeletal muscle content of membrane glycoprotein PC-1 in obesity - relationship to muscle glucose transport
-
Youngren J.F., Maddux B.A., Sasson S., Sbraccia P., Tapscott E.B., Swanson M.S., et al. Skeletal muscle content of membrane glycoprotein PC-1 in obesity - relationship to muscle glucose transport. Diabetes 1996, 45:1324-1328.
-
(1996)
Diabetes
, vol.45
, pp. 1324-1328
-
-
Youngren, J.F.1
Maddux, B.A.2
Sasson, S.3
Sbraccia, P.4
Tapscott, E.B.5
Swanson, M.S.6
-
90
-
-
33646078811
-
Overexpression of the insulin receptor inhibitor PC-1/ENPP1 induces insulin resistance and hyperglycemia
-
Maddux B.A., Chang Y.N., Accili D., McGuinness O.P., Youngren J.F., Goldfine I.D. Overexpression of the insulin receptor inhibitor PC-1/ENPP1 induces insulin resistance and hyperglycemia. Am J Physiol Endocrinol Metab 2006, 290:E746-E749.
-
(2006)
Am J Physiol Endocrinol Metab
, vol.290
-
-
Maddux, B.A.1
Chang, Y.N.2
Accili, D.3
McGuinness, O.P.4
Youngren, J.F.5
Goldfine, I.D.6
-
91
-
-
80054949735
-
Metabolic consequences of ENPP1 overexpression in adipose tissue
-
Pan W., Ciociola E., Saraf M., Tumurbaatar B., Tuvdendorj D., Prasad S., et al. Metabolic consequences of ENPP1 overexpression in adipose tissue. Am J Physiol Endocrinol Metab 2011, 301:E901-E911.
-
(2011)
Am J Physiol Endocrinol Metab
, vol.301
-
-
Pan, W.1
Ciociola, E.2
Saraf, M.3
Tumurbaatar, B.4
Tuvdendorj, D.5
Prasad, S.6
-
92
-
-
67651085620
-
Suppression of PC-1/ENPP-1 expression improves insulin sensitivity in vitro and in vivo
-
Zhou H.H., Chin C.-N., Wu M., Ni W., Quan S., Liu F., et al. Suppression of PC-1/ENPP-1 expression improves insulin sensitivity in vitro and in vivo. Eur J Pharmacol 2009, 616:346-352.
-
(2009)
Eur J Pharmacol
, vol.616
, pp. 346-352
-
-
Zhou, H.H.1
Chin, C.-N.2
Wu, M.3
Ni, W.4
Quan, S.5
Liu, F.6
-
93
-
-
79955872917
-
ENPP1 affects insulin action and secretion: evidences from in vitro studies
-
Di Paola R., Caporarello N., Marucci A., Dimatteo C., Iadicicco C., Del Guerra S., et al. ENPP1 affects insulin action and secretion: evidences from in vitro studies. PLoS One 2011, 6:e19462.
-
(2011)
PLoS One
, vol.6
-
-
Di Paola, R.1
Caporarello, N.2
Marucci, A.3
Dimatteo, C.4
Iadicicco, C.5
Del Guerra, S.6
-
94
-
-
0031894737
-
Membrane glycoprotein PC-1 and insulin resistance
-
Goldfine I.D., Maddux B.A., Youngren J.F., Frittitta L., Trischitta V., Dohm G.L. Membrane glycoprotein PC-1 and insulin resistance. Mol Cell Biochem 1998, 182:177-184.
-
(1998)
Mol Cell Biochem
, vol.182
, pp. 177-184
-
-
Goldfine, I.D.1
Maddux, B.A.2
Youngren, J.F.3
Frittitta, L.4
Trischitta, V.5
Dohm, G.L.6
-
95
-
-
73649116744
-
-
Genetic variants of the ENPP1/PC-1 gene are associated with hypertriglyceridemia in male subjects. 7
-
Tanyolaç S., Bremer A.A., Hodoglugil U., Movsesyan I., Pullinger C.R., Heiner S.W., Malloy M.J., Kane J.P., Goldfine I.D. Genetic variants of the ENPP1/PC-1 gene are associated with hypertriglyceridemia in male subjects. 2009;7: 543-548.
-
(2009)
, pp. 543-548
-
-
Tanyolaç, S.1
Bremer, A.A.2
Hodoglugil, U.3
Movsesyan, I.4
Pullinger, C.R.5
Heiner, S.W.6
Malloy, M.J.7
Kane, J.P.8
Goldfine, I.D.9
-
96
-
-
0032857338
-
A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance
-
Pizzuti A., Frittitta L., Argiolas A., Baratta R., Goldfine I.D., Bozzali M., et al. A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistance. Diabetes 1999, 48:1881-1884.
-
(1999)
Diabetes
, vol.48
, pp. 1881-1884
-
-
Pizzuti, A.1
Frittitta, L.2
Argiolas, A.3
Baratta, R.4
Goldfine, I.D.5
Bozzali, M.6
-
97
-
-
39149099952
-
The role of membrane glycoprotein plasma cell antigen 1 ectonucleotide pyrophosphatase phosphodiesterase 1 in the pathogenesis of insulin resistance and related abnormalities
-
Goldfine I.D., Maddux B.A., Youngren J.F., Reaven G., Accili D., Trischitta V., et al. The role of membrane glycoprotein plasma cell antigen 1 ectonucleotide pyrophosphatase phosphodiesterase 1 in the pathogenesis of insulin resistance and related abnormalities. Endocr Rev 2008, 29:62-75.
-
(2008)
Endocr Rev
, vol.29
, pp. 62-75
-
-
Goldfine, I.D.1
Maddux, B.A.2
Youngren, J.F.3
Reaven, G.4
Accili, D.5
Trischitta, V.6
-
98
-
-
33847022334
-
Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes
-
Willer C.J., Bonnycastle L.L., Conneely K.N., Duren W.L., Jackson A.U., Scott L.J., et al. Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes. Diabetes 2007, 56:256-264.
-
(2007)
Diabetes
, vol.56
, pp. 256-264
-
-
Willer, C.J.1
Bonnycastle, L.L.2
Conneely, K.N.3
Duren, W.L.4
Jackson, A.U.5
Scott, L.J.6
-
99
-
-
42449116149
-
The EBPP1 K121Q polymorphism is associated with type 2 diabetes in European populations: evidence from an updated meta-analysis in 42,042 subjects
-
McAteer J.B., Prudente S., Bacci S., Lyon H.N., Hirschhorn J.N., Trischitta V., et al. The EBPP1 K121Q polymorphism is associated with type 2 diabetes in European populations: evidence from an updated meta-analysis in 42,042 subjects. Diabetes 2008, 57:1125-1130.
-
(2008)
Diabetes
, vol.57
, pp. 1125-1130
-
-
McAteer, J.B.1
Prudente, S.2
Bacci, S.3
Lyon, H.N.4
Hirschhorn, J.N.5
Trischitta, V.6
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