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Results: 1-20 |
Results: 20
Genome screen for quantitative trait loci underlying normal variation in femoral structure
Authors: Koller, DL Liu, GD Econs, MJ Hui, SL Morin, PA Joslyn, G Rodriguez, LA Conneally, PM Christian, JC Johnston, CC Foroud, T Peacock, M
Citation: Dl. Koller et al., Genome screen for quantitative trait loci underlying normal variation in femoral structure, J BONE MIN, 16(6), 2001, pp. 985-991
Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23
Authors: White, KE Carn, G Lorenz-Depiereux, B Benet-Pages, A Strom, TM Econs, MJ
Citation: Ke. White et al., Autosomal-dominant hypophosphatemic rickets (ADHR) mutations stabilize FGF-23, KIDNEY INT, 60(6), 2001, pp. 2079-2086
The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting
Authors: White, KE Jonsson, KB Carn, G Hampson, G Spector, TD Mannstadt, M Lorenz-Depiereux, B Miyauchi, A Yang, IM Ljunggren, O Meitinger, T Strom, TM Juppner, H Econs, MJ
Citation: Ke. White et al., The autosomal dominant hypophosphatemic rickets (ADHR) gene is a secreted polypeptide overexpressed by tumors that cause phosphate wasting, J CLIN END, 86(2), 2001, pp. 497-500
Sib pair linkage and association studies between bone mineral density and the interleukim-6 gene locus
Authors: Takacs, I Koller, DL Peacock, M Christian, JC Evans, WE Hui, SL Conneally, PM Johnston, CC Foroud, T Econs, MJ
Citation: I. Takacs et al., Sib pair linkage and association studies between bone mineral density and the interleukim-6 gene locus, BONE, 27(1), 2000, pp. 169-173
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
Authors: White, KE Evans, WE O'Riordan, JLH Speer, MC Econs, MJ Lorenz-Depiereux, B Grabowski, M Meitinger, T Strom, TM
Citation: Ke. White et al., Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23, NAT GENET, 26(3), 2000, pp. 345-348
Disorders of phosphate metabolism
Authors: DiMeglio, LA White, KE Econs, MJ
Citation: La. Dimeglio et al., Disorders of phosphate metabolism, END METAB C, 29(3), 2000, pp. 591
MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia
Authors: Rowe, PSN de Zoysa, PA Dong, R Wang, HR White, KE Econs, MJ Oudet, CL
Citation: Psn. Rowe et al., MEPE, a new gene expressed in bone marrow and tumors causing osteomalacia, GENOMICS, 67(1), 2000, pp. 54-68
Molecular cloning of a novel human UDP-GalNAc : polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene
Authors: White, KE Lorenz, B Evans, WE Meitinger, T Strom, TM Econs, MJ
Citation: Ke. White et al., Molecular cloning of a novel human UDP-GalNAc : polypeptide N-acetylgalactosaminyltransferase, GalNAc-T8, and analysis as a candidate autosomal dominant hypophosphatemic rickets (ADHR) gene, GENE, 246(1-2), 2000, pp. 347-356
Heterogeneity in Paget disease of the bone
Authors: Nance, MA Nuttall, FQ Econs, MJ Lyles, KW Viles, KD Vance, JM Pericak-Vance, MA Speer, MC
Citation: Ma. Nance et al., Heterogeneity in Paget disease of the bone, AM J MED G, 92(5), 2000, pp. 303-307
Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis
Authors: Koller, DL Econs, MJ Morin, PA Christian, JC Hui, SL Parry, P Curran, ME Rodriguez, LA Conneally, PM Joslyn, G Peacock, M Johnston, CC Foroud, T
Citation: Dl. Koller et al., Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis, J CLIN END, 85(9), 2000, pp. 3116-3120
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus (vol 84, pg 4467, 1999)
Authors: Takacs, I Koller, DL Peacock, M Christian, JC Hui, SL Conneally, PM Johnston, CC Foroud, T Econs, MJ
Citation: I. Takacs et al., Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus (vol 84, pg 4467, 1999), J CLIN END, 85(1), 2000, pp. 138-138
Inherited phosphate wasting disorders
Authors: Econs, MJ White, KE
Citation: Mj. Econs et Ke. White, Inherited phosphate wasting disorders, GENETICS OF OSTEOPOROSIS AND METABOLIC BONE DISEASE, 2000, pp. 111-132
New insights into the pathogenesis of inherited phosphate wasting disorders
Authors: Econs, MJ
Citation: Mj. Econs, New insights into the pathogenesis of inherited phosphate wasting disorders, BONE, 25(1), 1999, pp. 131-135
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues
Authors: Filisetti, D Ostermann, G von Bredow, M Strom, T Filler, G Ehrich, J Pannetier, S Garnier, JM Rowe, P Francis, F Julienne, A Hanauer, A Econs, MJ Oudet, C
Citation: D. Filisetti et al., Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues, EUR J HUM G, 7(5), 1999, pp. 615-619
Osteopathia striata with cranial sclerosis
Authors: Lazar, CM Braunstein, EM Econs, MJ
Citation: Cm. Lazar et al., Osteopathia striata with cranial sclerosis, J BONE MIN, 14(1), 1999, pp. 152-153
Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrier
Authors: Takacs, I Cooper, H Weaver, DD Econs, MJ
Citation: I. Takacs et al., Bone mineral density and laboratory evaluation of a type II autosomal dominant osteopetrosis carrier, AM J MED G, 85(1), 1999, pp. 9-12
Locus heterogeneity of autosomal dominant osteopetrosis (ADO)
Authors: White, KE Koller, DL Takacs, I Buckwalter, EA Foroud, T Econs, MJ
Citation: Ke. White et al., Locus heterogeneity of autosomal dominant osteopetrosis (ADO), J CLIN END, 84(3), 1999, pp. 1047-1051
Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus
Authors: Takacs, I Koller, DL Peacock, M Christian, JC Hui, SL Conneally, PM Johnston, CC Foroud, T Econs, MJ
Citation: I. Takacs et al., Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus, J CLIN END, 84(12), 1999, pp. 4467-4471
The molecular basis of hypophosphatemic rickets
Authors: Econs, MJ Strom, TM
Citation: Mj. Econs et Tm. Strom, The molecular basis of hypophosphatemic rickets, CONT ENDOC, 10, 1999, pp. 39-55
A PDZ domain-containing protein with homology to Diphor-1 maps to human chromosome 1q21
Authors: White, KE Biber, J Murer, H Econs, MJ
Citation: Ke. White et al., A PDZ domain-containing protein with homology to Diphor-1 maps to human chromosome 1q21, ANN HUM GEN, 62, 1998, pp. 287-290
Risultati: 1-20 |