MEPE has the properties of an osteoblastic phosphatonin and minhibin von Rowe, P.S.N, Kumagai, Y, Gutierrez, G, Garrett, I.R, Blacher, R, Rosen, D, Cundy, J, Navvab, S, Chen, D, Drezner, M.K, Quarles, L.D, Mundy, G.R

Volltext

Surface plasmon resonance (SPR) confirms that MEPE binds to PHEX via the MEPE–ASARM motif: a model for impaired mineralization in X-linked rickets (HYP) von Rowe, Peter S.N., Garrett, Ian R., Schwarz, Patricia M., Carnes, David L., Lafer, Eileen M., Mundy, Gregory R., Gutierrez, Gloria E.

Volltext

Serum MEPE-ASARM-peptides are elevated in X-linked rickets (HYP): implications for phosphaturia and rickets von Bresler, Doron, Bruder, Jan, Mohnike, Klaus, Fraser, William D, Rowe, Peter S N

Volltext

The wrickkened pathways of FGF23, MEPE and PHEX von Rowe, Peter S N

Volltext

MEPE, a New Gene Expressed in Bone Marrow and Tumors Causing Osteomalacia von Rowe, Peter S.N, de Zoysa, Priyal A, Dong, Rong, Wang, Huei Rong, White, Kenneth E, Econs, Michael J, Oudet, Claudine L

Volltext

Inhibition of MEPE cleavage by Phex von Guo, Rong, Rowe, Peter S.N, Liu, Shiguang, Simpson, Leigh G, Xiao, Zhou-Sheng, Darryl Quarles, L

Volltext

MEPE OF45 as a new target for sensitizing human tumour cells to DNA damage inducers von Zhang, P, Wang, H, Rowe, P S N, Hu, B, Wang, Y

Volltext

A gene ( PEX ) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets von Poustka, A, Davies, K.E, Lorenz, B, Korn, B, Drezner, M.K, O'Riordan, J.L.H, Pannetier, S, Rowe, P.S.N, Summerfield, T, Nesbitt, T, Meindl, A, Lehrach, H, Strom, T.M, Popowska, E, Mountford, R, Cagnoli, B, Mohnike, K.L, Hanauer, A, Reinhardt, R, Read, A.P, Econs, M.J, Murken, J, de Jong, P, Goulding, J.N, Hennig, S, Meitinger, T, Oudet, C, Francis, F, Pronicka, E

Volltext

Distribution of Mutations in the PEX Gene in Families with X-linked Hypophosphataemic Rickets (HYP) von Rowe, Peter S. N., Oudet, Claudine L., Francis, Fiona, Sinding, Christiane, Pannetier, Solange, Econs, Mike J., Strom, Tim M., Meitinger, Thomas, Garabedian, Michele, David, Albert, Macher, Marie-Alice, Questiaux, Elisabeth, Popowska, Ewa, Pronicka, Ewa, Read, Andrew P., Mokrzycki, Agnes, Glorieux, Francis H., Drezner, Marc K., Hanauer, Andre, Lehrach, Hans, Goulding, Johnathan N., O'Riordan, Jeffrey L. H.

Volltext

The molecular background to hypophosphataemic rickets von ROWE, P S N

Volltext

Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets von Francis, F, Strom, T M, Hennig, S, Böddrich, A, Lorenz, B, Brandau, O, Mohnike, K L, Cagnoli, M, Steffens, C, Klages, S, Borzym, K, Pohl, T, Oudet, C, Econs, M J, Rowe, P S, Reinhardt, R, Meitinger, T, Lehrach, H

Volltext

Analysis of the human hephaestin gene and protein: comparative modelling of the N-terminus ecto-domain based upon ceruloplasmin von Syed, Basharut A., Beaumont, Nick J., Patel, Alpesh, Naylor, Claire E., Bayele, Henry K., Joannou, Christopher L., Rowe, Peter S.N., Evans, Robert W., Srai, S. Kaila S.

Volltext

The role of the PHEX gene (PEX) in families with X-linked hypophosphataemic rickets von Rowe, Peter S.N

Volltext

A PHEX gene mutation is responsible for adult-onset vitamin D-resistant hypophosphatemic osteomalacia : Evidence that the disorder is not a distinct entity from X-linked hypophosph... von ECONS, M. J, FRIEDMAN, N. E, BERGEN, H, ROWE, P. S. N, SPEER, M. C, FRANCIS, F, STROM, T. M, OUDET, C, SMITH, J. A, NINOMIYA, J. T, LEE, B. E

Volltext

Candidate 56 and 58 kDa protein(s) responsible for mediating the renal defects in oncogenic hypophosphatemic osteomalacia von Rowe, P.S.N., Ong, A.C.M., Cockerill, F.J., Goulding, J.N., Hewison, M.

Volltext

DMP1 and MEPE expression are elevated in osteocytes after mechanical loading in vivo: theoretical role in controlling mineral quality in the perilacunar matrix von Harris, S E, Gluhak-Heinrich, J, Harris, M A, Yang, W, Bonewald, L F, Riha, D, Rowe, P S N, Robling, A G, Turner, C H, Feng, J Q, McKee, M D, Nicollela, D

Volltext

Rapid isolation of DNA sequences flanking microsatellite repeats von Rowe, P.S.N, Francis, F, Goulding, J

Volltext

The gene for X-linked hypophosphataemic rickets maps to a 200-300 kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE) von ROWE, P. S. N, GOULDING, J. N, WEISSENBACH, J, FRASER, W, DREZNER, M. K, DAVIES, K. E, O'RIORDAN, J. L. H, FRANCIS, F, OUDET, C, ECONS, M. J, HANAUER, A, LEHRACH, H, READ, A. P, MOUNTFORD, R. C, SUMMERFIELD, T

Volltext

An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome von BLAIR, H. J, UWECHUE, I. C, BARSH, G. S, ROWE, P. S. N, BOYD, Y

Volltext

Construction of a High-Resolution Linkage Map for Xp22.1-p22.2 and Refinement of the Genetic Localization of the Coffin-Lowry Syndrome Gene von Biancalana, Valerie, Trivier, Elisabeth, Weber, Chantal, Weissenbach, Jean, Rowe, Peter S.N., O'Riordan, Jeffrey L.H., Partington, Michael W., Heyberger, Sandra, Oudet, Claudine, Hanauer, Andre

Volltext