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Fetal and postnatal mouse bone tissue contains more calcium than is present in hydroxyapatite
Authors: Lange, C.; Li, C.; Manjubala, I.; Wagermaier, W.; Kuhnisch, J.; Kolanczyk, M.; Mundlos, S.; Knaus, P.; Fratzl, P.
Date of Publication (YYYY-MM-DD): 2011-11
Title of Journal: Journal of Structural Biology
Volume: 176
Issue / Number: 2
Start Page: 159
End Page: 167
Document Type: Article
ID: 573791.0


The organization of the osteocyte network in bone and potential mechanisms of passive mineral dissolution
Authors: Kerschnitzki, M.; Wagermaier, W.; Roschger, P.; Seto, J.; Shahar, R.; Duda, G.; Mundlos, S.; Fratzl, P.
Date of Publication (YYYY-MM-DD): 2011-05-07
Title of Journal: Bone
Volume: 48
Issue / Number: Suppl. Suppl. 2
Start Page: S139
End Page: S139
Document Type: Article
ID: 564574.0


The organization of the osteocyte network mirrors the extracellular matrix orientation in bone
Authors: Kerschnitzki, M.; Wagermaier, W.; Roschger, P.; Seto, J.; Shahar, R.; Duda, G. N.; Mundlos, S.; Fratzl, P.
Date of Publication (YYYY-MM-DD): 2011-02
Title of Journal: Journal of Structural Biology
Volume: 173
Issue / Number: 2
Start Page: 303
End Page: 311
Document Type: Article
ID: 564013.0


Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis.
Authors: Klopocki, E.; Lohan, S.; Brancati, F.; Koll, R.; Brehm, A.; Seemann, P.; Dathe, K.; Stricker, S.; Hecht, J.; Bosse, K.; Betz, R. C.; Garaci, F. G.; Dallapiccola, B.; Jain, M.; Muenke, M.; Ng, V. C.; Chan, W.; Chan, D.; Mundlos, S.
Date of Publication (YYYY-MM-DD): 2011-01-07
Title of Journal: American Journal of Human Genetics
Volume: 88
Issue / Number: 1
Start Page: 70
End Page: 75
Document Type: Article
ID: 538366.0


NOA1 is an essential GTPase required for mitochondrial protein synthesis
Authors: Kolanczyk, M.; Pech, M.; Zemojtel, T.; Yamamoto, H.; Mikula, I.; Calvaruso, M. A.; van den Brand, M.; Richter, R.; Fischer, B.; Ritz, A.; Kossler, N.; Thurisch, B.; Spoerle, R.; Smeitink, J.; Kornak, U.; Chan, D.; Vingron, M.; Martasek, P.; Lightowlers, R. N.; Nijtmans, L.; Schuelke, M.; Nierhaus, K. H.; Mundlos, S.
Date of Publication (YYYY-MM-DD): 2011-01-01
Title of Journal: Mol Biol Cell
Volume: 22
Issue / Number: 1
Start Page: 1
End Page: 11
Document Type: Article
ID: 538378.0


A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Authors: Diez-Roux, G.; Banfi, S.; Sultan, M.; Geffers, L.; Anand, S.; Rozado, D.; Magen, A.; Canidio, E.; Pagani, M.; Peluso, I.; Lin-Marq, N.; Koch, M.; Bilio, M.; Cantiello, I.; Verde, R.; De Masi, C.; Bianchi, S. A.; Cicchini, J.; Perroud, E.; Mehmeti, S.; Dagand, E.; Schrinner, S.; Nuernberger, A.; Schmidt, K.; Metz, K.; Zwingmann, C.; Brieske, N.; Springer, C.; Hernandez, A. M.; Herzog, S.; Grabbe, F.; Sieverding, C.; Fischer, B.; Schrader, K.; Brockmeyer, M.; Dettmer, S.; Helbig, C.; Alunni, V.; Battaini, M. A.; Mura, C.; Henrichsen, C. N.; Garcia-Lopez, R.; Echevarria, D.; Puelles, E.; Garcia-Calero, E.; Kruse, S.; Uhr, M.; Kauck, C.; Feng, G.; Milyaev, N.; Ong, C. K.; Kumar, L.; Lam, M.; Semple, C. A.; Gyenesei, A.; Mundlos, S.; Radelof, U.; Lehrach, H.; Sarmientos, P.; Reymond, A.; Davidson, D. R.; Dolle, P.; Antonarakis, S. E.; Yaspo, M. L.; Martinez, S.; Baldock, R. A.; Eichele, G.; Ballabio, A.
Date of Publication (YYYY-MM-DD): 2011-01
Title of Journal: PLoS Biology
Volume: 9
Issue / Number: 1
Sequence Number of Article: e1000582
Document Type: Article
ID: 546515.0


Brachydactyly type A1 with short humerus and associated skeletal features.
Authors: Lacombe, D.; Delrue, M. A.; Rooryck, C.; Morice-Picard, F.; Arveiler, B.; Maugey-Laulom, B.; Mundlos, S.; Toutain, A.; Chateil, J. F.
Date of Publication (YYYY-MM-DD): 2010-12-01
Title of Journal: American Journal of Medical Genetics Part A
Volume: 152A
Issue / Number: 12
Start Page: 3016
End Page: 3021
Document Type: Article
ID: 538386.0


Monozygotic twins with neurofibromatosis type 1 (NF1) display differences in methylation of NF1 gene promoter elements, 5' untranslated region, exon and intron 1.
Authors: Harder, A.; Titze, S.; Herbst, L.; Harder, T.; Guse, K.; Tinschert, S.; Kaufmann, D.; Rosenbaum, T.; Mautner, V. F.; Windt, E.; Wahlländer-Danek, U.; Wimmer, K.; Mundlos, S.; Peters, H.
Date of Publication (YYYY-MM-DD): 2010-12-01
Title of Journal: Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies.
Volume: 13
Issue / Number: 6
Start Page: 582
End Page: 594
Document Type: Article
ID: 538734.0


A novel homozygous Arg222Trp missense mutation in WNT7A in two sisters with severe Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.
Authors: Kantaputra, P. N.; Mundlos, S.; Sripathomsawat, W.
Date of Publication (YYYY-MM-DD): 2010-10-14
Title of Journal: American Journal of Medical Genetics Part A
Volume: 152A
Issue / Number: 11
Start Page: 2832
End Page: 2837
Document Type: Article
ID: 539471.0


Identity-by-descent filtering of exome sequence data identifies PIGV mutations in hyperphosphatasia mental retardation syndrome.
Authors: Krawitz, P. M.; Schweiger, M. R.; Rödelsperger, C.; Marcelis, C.; Kölsch, U.; Meisel, C.; Stephani, F.; Kinoshita, T.; Murakami, Y.; Bauer, S.; Isau, M.; Fischer, A.; Dahl, A.; Kerick, M.; Hecht, J.; Köhler, S.; Jager, M.; Grünhagen, J.; de Condor, B. J.; Doelken, S.; Brunner, H. G.; Meinecke, P.; Passarge, E.; Thompson, M. D.; Cole, D. E.; Horn, D.; Roscioli, T.; Mundlos, S.; Robinson, P. N.
Date of Publication (YYYY-MM-DD): 2010-08-29
Title of Journal: Nature Genetics
Volume: 42
Issue / Number: 10
Start Page: 827
End Page: 829
Document Type: Article
ID: 539693.0