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Page 1
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).
Rowe PS, Oudet CL, Francis F, Sinding C, Pannetier S, Econs MJ, Strom TM, Meitinger T, Garabedian M, David A, Macher MA, Questiaux E, Popowska E, Pronicka E, Read AP, Mokrzycki A, Glorieux FH, Drezner MK, Hanauer A, Lehrach H, Goulding JN, O'Riordan JL. Rowe PS, et al. Hum Mol Genet. 1997 Apr;6(4):539-49. doi: 10.1093/hmg/6.4.539. Hum Mol Genet. 1997. PMID: 9097956
MEPE has the properties of an osteoblastic phosphatonin and minhibin.
Rowe PS, Kumagai Y, Gutierrez G, Garrett IR, Blacher R, Rosen D, Cundy J, Navvab S, Chen D, Drezner MK, Quarles LD, Mundy GR. Rowe PS, et al. Bone. 2004 Feb;34(2):303-19. doi: 10.1016/j.bone.2003.10.005. Bone. 2004. PMID: 14962809 Free PMC article.
DMP1 and MEPE expression are elevated in osteocytes after mechanical loading in vivo: theoretical role in controlling mineral quality in the perilacunar matrix.
Harris SE, Gluhak-Heinrich J, Harris MA, Yang W, Bonewald LF, Riha D, Rowe PS, Robling AG, Turner CH, Feng JQ, McKee MD, Nicollela D. Harris SE, et al. Among authors: rowe ps. J Musculoskelet Neuronal Interact. 2007 Oct-Dec;7(4):313-5. J Musculoskelet Neuronal Interact. 2007. PMID: 18094489 Free PMC article. No abstract available.
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 hypophosphatemic rickets.
Econs MJ, Friedman NE, Rowe PS, Speer MC, Francis F, Strom TM, Oudet C, Smith JA, Ninomiya JT, Lee BE, Bergen H. Econs MJ, et al. Among authors: rowe ps. J Clin Endocrinol Metab. 1998 Oct;83(10):3459-62. doi: 10.1210/jcem.83.10.5167. J Clin Endocrinol Metab. 1998. PMID: 9768646
The wrickkened pathways of FGF23, MEPE and PHEX.
Rowe PS. Rowe PS. Crit Rev Oral Biol Med. 2004 Sep 1;15(5):264-81. doi: 10.1177/154411130401500503. Crit Rev Oral Biol Med. 2004. PMID: 15470265 Free PMC article. Review.
66 results