AAAAAA

   
Results: 1-10 |
Results: 10
Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia
Authors: Nurnberg, P Thiele, H Chandler, D Hohne, W Cunningham, ML Ritter, H Leschik, G Uhlmann, K Mischung, C Harrop, K Goldblatt, J Borochowitz, ZU Kotzot, D Westermann, F Mundlos, S Braun, HS Laing, N Tinschert, S
Citation: P. Nurnberg et al., Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia, NAT GENET, 28(1), 2001, pp. 37-41
Sonic hedgehog is a survival factor for hypaxial muscles during mouse development
Authors: Kruger, M Mennerich, D Fees, S Schafer, R Mundlos, S Braun, T
Citation: M. Kruger et al., Sonic hedgehog is a survival factor for hypaxial muscles during mouse development, DEVELOPMENT, 128(5), 2001, pp. 743-752
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda
Authors: Tiller, GE Hannig, VL Dozier, D Carrel, L Trevarthen, KC Wilcox, WR Mundlos, S Haines, JL Gedeon, AK Gecz, J
Citation: Ge. Tiller et al., A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda, AM J HU GEN, 68(6), 2001, pp. 1398-1407
Mouse mutant "rib-vertebrae" (rv): A defect in somite polarity
Authors: Nacke, S Schafer, R De Angelis, MH Mundlos, S
Citation: S. Nacke et al., Mouse mutant "rib-vertebrae" (rv): A defect in somite polarity, DEV DYNAM, 219(2), 2000, pp. 192-200
Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B
Authors: Schwabe, GC Tinschert, S Buschow, C Meinecke, P Wolff, G Gillessen-Kaesbach, G Oldridge, M Wilkie, AOM Komec, R Mundlos, S
Citation: Gc. Schwabe et al., Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B, AM J HU GEN, 67(4), 2000, pp. 822-831
Skeletal morphogenesis
Authors: Mundlos, S
Citation: S. Mundlos, Skeletal morphogenesis, METH MOL B, 136, 2000, pp. 61-70
Regulation of chondrocyte differentiation by Cbfa1
Authors: Kim, IS Otto, F Zabel, B Mundlos, S
Citation: Is. Kim et al., Regulation of chondrocyte differentiation by Cbfa1, MECH DEVEL, 80(2), 1999, pp. 159-170
Polytopic anomalies with agenesis of the lower vertebral column
Authors: Bohring, A Lewin, SO Reynolds, JF Voigtlander, T Rittinger, O Carey, JC Kopernik, M Smith, R Zackai, EH Leonard, NJ Gritter, HL Bamforth, JS Okun, N McLeod, DR Super, M Powell, P Mundlos, S Hennekam, RCM van Langen, IM Viskochil, DH Wiedemann, HR Opitz, JM
Citation: A. Bohring et al., Polytopic anomalies with agenesis of the lower vertebral column, AM J MED G, 87(2), 1999, pp. 99-114
Cleidocranial dysplasia: clinical and molecular genetics
Authors: Mundlos, S
Citation: S. Mundlos, Cleidocranial dysplasia: clinical and molecular genetics, J MED GENET, 36(3), 1999, pp. 177-182
Mutation analysis of cove binding factor A1 in patients with cleidocranialdysplasia
Authors: Quack, I Vonderstrass, B Stock, M Aylsworth, AS Becker, A Brueton, L Lee, PJ Majewski, F Mulliken, JB Suri, M Zenker, M Mundlos, S Otto, F
Citation: I. Quack et al., Mutation analysis of cove binding factor A1 in patients with cleidocranialdysplasia, AM J HU GEN, 65(5), 1999, pp. 1268-1278
Risultati: 1-10 |