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Results: 1-22 |
Results: 22
Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes
Authors: Bernard, MA Hall, CE Hogu, DA Cole, WG Scott, A Snuggs, MB Clines, GA Ludecke, HJ Lovett, M Van Winkle, WB Hecht, JT
Citation: Ma. Bernard et al., Diminished levels of the putative tumor suppressor proteins EXT1 and EXT2 in exostosis chondrocytes, CELL MOTIL, 48(2), 2001, pp. 149-162
A crown model for simulating long-term stand and gap dynamics in northern hardwood forests
Authors: Choi, J Lorimer, CG Vanderwerker, J Cole, WG Martin, GL
Citation: J. Choi et al., A crown model for simulating long-term stand and gap dynamics in northern hardwood forests, FOREST ECOL, 152(1-3), 2001, pp. 235-258
Three weeks of Kirschner wire fixation for displaced lateral condylar fractures of the humerus in children
Authors: Thomas, DP Howard, AW Cole, WG Hedden, DM
Citation: Dp. Thomas et al., Three weeks of Kirschner wire fixation for displaced lateral condylar fractures of the humerus in children, J PED ORTH, 21(5), 2001, pp. 565-569
Potential treatment for clubfeet based on growth factor blockade
Authors: Li, C Nguyen, Q Cole, WG Alman, BA
Citation: C. Li et al., Potential treatment for clubfeet based on growth factor blockade, J PED ORTH, 21(3), 2001, pp. 372-377
Separation of amniotic membranes after amniocentesis in an individual withthe classic form of EDS and haploinsufficiency for COL5A1 expression
Authors: Stoler, JM Bromley, B Castro, MA Cole, WG Florer, J Wenstrup, RJ
Citation: Jm. Stoler et al., Separation of amniotic membranes after amniocentesis in an individual withthe classic form of EDS and haploinsufficiency for COL5A1 expression, AM J MED G, 101(2), 2001, pp. 174-177
COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II
Authors: Bouma, P Cabral, WA Cole, WG Marini, JC
Citation: P. Bouma et al., COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II, J BIOL CHEM, 276(16), 2001, pp. 13356-13364
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda
Authors: Gedeon, AK Tiller, GE Le Merrer, M Heuertz, S Tranebjaerg, L Chitayat, D Robertson, S Glass, IA Savarirayan, R Cole, WG Rimoin, DL Kousseff, BG Ohashi, H Zabel, B Munnich, A Gecz, J Mulley, JC
Citation: Ak. Gedeon et al., The molecular basis of X-linked spondyloepiphyseal dysplasia tarda, AM J HU GEN, 68(6), 2001, pp. 1386-1397
Idiopathic toe-walking: Does treatment alter the natural history?
Authors: Eastwood, DM Menelaus, MB Dickens, DRV Broughton, NS Cole, WG
Citation: Dm. Eastwood et al., Idiopathic toe-walking: Does treatment alter the natural history?, J PED ORT B, 9(1), 2000, pp. 47-49
Cytoskeletal abnormalities in chondrocytes with EXT1 and EXT2 mutations
Authors: Bernard, MA Hogue, DA Cole, WG Sanford, T Snuggs, MB Montufar-Solis, D Duke, PJ Carson, DD Scott, A Van Winkle, WB Hecht, JT
Citation: Ma. Bernard et al., Cytoskeletal abnormalities in chondrocytes with EXT1 and EXT2 mutations, J BONE MIN, 15(3), 2000, pp. 442-450
A shortened course of parenteral antibiotic therapy in the management of acute septic arthritis of the hip
Authors: Kim, HKW Alman, B Cole, WG
Citation: Hkw. Kim et al., A shortened course of parenteral antibiotic therapy in the management of acute septic arthritis of the hip, J PED ORTH, 20(1), 2000, pp. 44-47
Rapid determination of COL2A1 mutations in individuals with Stickler syndrome: Analysis of potential premature termination codons
Authors: Wilkin, DJ Liberfarb, R Davis, J Levy, HP Cole, WG Francomano, CA Cohn, DH
Citation: Dj. Wilkin et al., Rapid determination of COL2A1 mutations in individuals with Stickler syndrome: Analysis of potential premature termination codons, AM J MED G, 94(2), 2000, pp. 141-148
COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDS
Authors: Wenstrup, RJ Florer, JB Willing, MC Giunta, C Steinmann, B Young, F Susic, M Cole, WG
Citation: Rj. Wenstrup et al., COL5A1 haploinsufficiency is a common molecular mechanism underlying the classical form of EDS, AM J HU GEN, 66(6), 2000, pp. 1766-1776
Age characteristics of coarse woody debris (Pinus strobus) in a lake littoral zone
Authors: Guyette, RP Cole, WG
Citation: Rp. Guyette et Wg. Cole, Age characteristics of coarse woody debris (Pinus strobus) in a lake littoral zone, CAN J FISH, 56(3), 1999, pp. 496-505
Genes and orthopaedics
Authors: Cole, WG
Citation: Wg. Cole, Genes and orthopaedics, J BONE-BR V, 81B(2), 1999, pp. 190-192
Tardy displacement of traumatic radial head dislocation in childhood
Authors: Weisman, DS Rang, M Cole, WG
Citation: Ds. Weisman et al., Tardy displacement of traumatic radial head dislocation in childhood, J PED ORTH, 19(4), 1999, pp. 523-526
Treatment of aneurysmal bone cysts with saucerization and bone marrow injection in children
Authors: Hemmadi, SS Cole, WG
Citation: Ss. Hemmadi et Wg. Cole, Treatment of aneurysmal bone cysts with saucerization and bone marrow injection in children, J PED ORTH, 19(4), 1999, pp. 540-542
Genetics and pediatric orthopaedics
Authors: Cole, WG
Citation: Wg. Cole, Genetics and pediatric orthopaedics, J PED ORTH, 19(3), 1999, pp. 281-282
Ehlers-Danlos syndrome type VII: Clinical features and molecular defects
Authors: Giunta, C Superti-Furga, A Spranger, S Cole, WG Steinmann, B
Citation: C. Giunta et al., Ehlers-Danlos syndrome type VII: Clinical features and molecular defects, J BONE-AM V, 81A(2), 1999, pp. 225-238
Alternative splicing of exon 37 of FBN1 deletes part of an 'eight-cysteine' domain resulting in the Marfan syndrome
Authors: McGrory, J Cole, WG
Citation: J. Mcgrory et Wg. Cole, Alternative splicing of exon 37 of FBN1 deletes part of an 'eight-cysteine' domain resulting in the Marfan syndrome, CLIN GENET, 55(2), 1999, pp. 118-121
Pseudo-Volkmann's contracture due to tethering of flexor digitorum profundus to fractures of the ulna in children
Authors: Deeney, VF Kaye, JJ Geary, SP Cole, WG
Citation: Vf. Deeney et al., Pseudo-Volkmann's contracture due to tethering of flexor digitorum profundus to fractures of the ulna in children, J PED ORTH, 18(4), 1998, pp. 437-440
Metaphrase: An aid to the clinical conceptualization and formalization of patient problems in healthcare enterprises
Authors: Tuttle, MS Olson, NE Keck, KD Cole, WG Erlbaum, MS Sherertz, DD Chute, CG Elkin, PL Atkin, GE Kaihoi, BH Safran, C Rind, D Law, V
Citation: Ms. Tuttle et al., Metaphrase: An aid to the clinical conceptualization and formalization of patient problems in healthcare enterprises, METH INF M, 37(4-5), 1998, pp. 373-383
Mutation analysis of LMX1B gene in nail-patella syndrome patients
Authors: McIntosh, I Dreyer, SD Clough, MV Dunston, JA Eyaid, W Roig, CM Montgomery, T Ala-Mello, S Kaitila, I Winterpacht, A Zabel, B Frydman, M Cole, WG Francomano, CA Lee, B
Citation: I. Mcintosh et al., Mutation analysis of LMX1B gene in nail-patella syndrome patients, AM J HU GEN, 63(6), 1998, pp. 1651-1658
Risultati: 1-22 |