Lange, C., C. Li, I. Manjubala, W. Wagermaier, J. Kuhnisch, M. Kolanczyk, S. Mundlos, P. Knaus and P. Fratzl: Fetal and postnatal mouse bone tissue contains more calcium than is present in hydroxyapatite. In: Journal of Structural Biology 176, 2, 159-167 (2011).
Kerschnitzki, M., W. Wagermaier, P. Roschger, J. Seto, R. Shahar, G. Duda, S. Mundlos and P. Fratzl: The organization of the osteocyte network in bone and potential mechanisms of passive mineral dissolution. In: Bone 48, Suppl. Suppl. 2, S139-S139 (2011).
Kerschnitzki, M., W. Wagermaier, P. Roschger, J. Seto, R. Shahar, G. N. Duda, S. Mundlos and P. Fratzl: The organization of the osteocyte network mirrors the extracellular matrix orientation in bone. In: Journal of Structural Biology 173, 2, 303-311 (2011).
Klopocki, E., S. Lohan, F. Brancati, R. Koll, A. Brehm, P. Seemann, K. Dathe, S. Stricker, J. Hecht, K. Bosse, R. C. Betz, F. G. Garaci, B. Dallapiccola, M. Jain, M. Muenke, V. C. Ng, W. Chan, D. Chan and S. Mundlos: Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.. In: American Journal of Human Genetics 88, 1, 70-75 (2011).
url: http://www.ncbi.nlm.nih.gov/pubmed/21167467
doi: i:10.1016/j.ajhg.2010.11.006
Kolanczyk, M., M. Pech, T. Zemojtel, H. Yamamoto, I. Mikula, M. A. Calvaruso, M. van den Brand, R. Richter, B. Fischer, A. Ritz, N. Kossler, B. Thurisch, R. Spoerle, J. Smeitink, U. Kornak, D. Chan, M. Vingron, P. Martasek, R. N. Lightowlers, L. Nijtmans, M. Schuelke, K. H. Nierhaus and S. Mundlos: NOA1 is an essential GTPase required for mitochondrial protein synthesis. In: Mol Biol Cell 22, 1, 1-11 (2011).
url: http://www.ncbi.nlm.nih.gov/pubmed/21118999
Diez-Roux, G., S. Banfi, M. Sultan, L. Geffers, S. Anand, D. Rozado, A. Magen, E. Canidio, M. Pagani, I. Peluso, N. Lin-Marq, M. Koch, M. Bilio, I. Cantiello, R. Verde, C. De Masi, S. A. Bianchi, J. Cicchini, E. Perroud, S. Mehmeti, E. Dagand, S. Schrinner, A. Nuernberger, K. Schmidt, K. Metz, C. Zwingmann, N. Brieske, C. Springer, A. M. Hernandez, S. Herzog, F. Grabbe, C. Sieverding, B. Fischer, K. Schrader, M. Brockmeyer, S. Dettmer, C. Helbig, V. Alunni, M. A. Battaini, C. Mura, C. N. Henrichsen, R. Garcia-Lopez, D. Echevarria, E. Puelles, E. Garcia-Calero, S. Kruse, M. Uhr, C. Kauck, G. Feng, N. Milyaev, C. K. Ong, L. Kumar, M. Lam, C. A. Semple, A. Gyenesei, S. Mundlos, U. Radelof, H. Lehrach, P. Sarmientos, A. Reymond, D. R. Davidson, P. Dolle, S. E. Antonarakis, M. L. Yaspo, S. Martinez, R. A. Baldock, G. Eichele and A. Ballabio: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.. In: PLoS Biology 9, 1, Seq. No.: e1000582 (2011).
url: http://www.plosbiology.org/article/fetchObjectAttachment.action;jsessionid=77C6A9DC7F2FBC7152B12146E455F6A8.ambra02?uri=info%3Adoi%2F10.1371%2Fjournal.pbio.1000582&representation=PDF
Lacombe, D., M. A. Delrue, C. Rooryck, F. Morice-Picard, B. Arveiler, B. Maugey-Laulom, S. Mundlos, A. Toutain and J. F. Chateil: Brachydactyly type A1 with short humerus and associated skeletal features.. In: American Journal of Medical Genetics Part A 152A, 12, 3016-3021 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/21077205
doi: 10.1002/ajmg.a.33761
Harder, A., S. Titze, L. Herbst, T. Harder, K. Guse, S. Tinschert, D. Kaufmann, T. Rosenbaum, V. F. Mautner, E. Windt, U. Wahlländer-Danek, K. Wimmer, S. Mundlos and H. Peters: Monozygotic twins with neurofibromatosis type 1 (NF1) display differences in methylation of NF1 gene promoter elements, 5' untranslated region, exon and intron 1.. In: Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies. 13, 6, 582-594 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/21142935
doi: 10.1375/twin.13.6.582
Kantaputra, P. N., S. Mundlos and W. Sripathomsawat: A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.. In: American Journal of Medical Genetics Part A 152A, 11, 2832-2837 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20949531
doi: 10.1002/ajmg.a.33673
Krawitz, P. M., M. R. Schweiger, C. Rödelsperger, C. Marcelis, U. Kölsch, C. Meisel, F. Stephani, T. Kinoshita, Y. Murakami, S. Bauer, M. Isau, A. Fischer, A. Dahl, M. Kerick, J. Hecht, S. Köhler, M. Jager, J. Grünhagen, B. J. de Condor, S. Doelken, H. G. Brunner, P. Meinecke, E. Passarge, M. D. Thompson, D. E. Cole, D. Horn, T. Roscioli, S. Mundlos and P. N. Robinson: Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.. In: Nature Genetics 42, 10, 827-829 (2010).
url: http://www.ncbi.nlm.nih.gov/pubmed/20802478
doi: 10.1038/ng.653
http://edoc.mpg.de
The Max Planck Society does not take any responsibility for the content of this export.