Brain-specific Foxp1 deletion impairs neuronal development and causes autistic-like behaviour von Bacon, C, Schneider, M, Le Magueresse, C, Froehlich, H, Sticht, C, Gluch, C, Monyer, H, Rappold, G A

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The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome von CLEMENT-JONES, M, SCHILLER, S, LINDSAY, S, RAPPOLD, G. A, RAO, E, BLASCHKE, R. J, ZUNIGA, A, ZELLER, R, ROBSON, S. C, BINDER, G, GLASS, I, STRACHAN, T

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Molecular identification of the corticosterone-sensitive extraneuronal catecholamine transporter von Gründemann, Dirk, Schechinger, Birgit, Rappold, Gudrun, Schömig, Edgar

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Human Mesenchymal Stem Cells Derived from Bone Marrow Display a Better Chondrogenic Differentiation Compared with Other Sources von Bernardo, M. E., Emons, J. A. M., Karperien, M., Nauta, A. J., Willemze, R., Roelofs, H., Romeo, S., Marchini, A., Rappold, G. A., Vukicevic, S., Locatelli, F., Fibbe, W. E.

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Network-driven discovery yields new insight into Shox2-dependent cardiac rhythm control von Hoffmann, S., Schmitteckert, S., Raedecke, K., Rheinert, D., Diebold, S., Roeth, R., Weiss, B., Granzow, M., Niesler, B., Griesbeck, A., Eckstein, V., Zimmermann, W.-H., Just, S., Rappold, G.A.

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Smoke Sense Initiative Leverages Citizen Science to Address the Growing Wildfire‐Related Public Health Problem von Rappold, A.G., Hano, M.C., Prince, S., Wei, L., Huang, S.M., Baghdikian, C., Stearns, B., Gao, X., Hoshiko, S., Cascio, W.E., Diaz‐Sanchez, D., Hubbell, B.

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A Member of a Gene Family on Xp22.3, VCX-A, Is Deleted in Patients with X-Linked Nonspecific Mental Retardation von Fukami, Maki, Kirsch, Stefan, Schiller, Simone, Richter, Alexandra, Benes, Vladimir, Franco, Brunella, Muroya, Koji, Rao, Ercole, Merker, Sabine, Niesler, Beate, Ballabio, Andrea, Ansorge, Wilhelm, Ogata, Tsutomu, Rappold, Gudrun A.

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SHOX: Growth, Léri–Weill and Turner Syndromes von Blaschke, Rüdiger J, Rappold, Gudrun A

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Cloning, physical mapping and expression analysis of the human 5-HT3 serotonin receptor-like genes HTR3C, HTR3D and HTR3E von Niesler, Beate, Frank, Bernd, Kapeller, Johannes, Rappold, Gudrun A

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Evolutionary breakpoint analysis on Y chromosomes of higher primates provides insight into human Y evolution von Wimmer, R., Kirsch, S., Rappold, G.A., Schempp, W.

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The evolution of the azoospermia factor region AZFa in higher primates von Wimmer, R., Kirsch, S., Rappold, G.A., Schempp, W.

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Brachytelephalangic dwarfism due to the loss of ARSE and SHOX genes resulting from an X;Y translocation von Seidel, J, Schiller, S, Kelbova, C, Beensen, V, Orth, U, Vogt, S, Claussen, U, Zintl, F, Rappold, GA

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FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes von RAO, E, WEISS, B, FUKAMI, M, MERTZ, A, MEDER, J, OGATA, T, HEINRICH, U, GARCIA-HERAS, J, SCHIEBEL, K, RAPPOLD, G. A

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Transposition of SRY into the Ancestral Pseudoautosomal Region Creates a New Pseudoautosomal Boundary in a Progenitor of Simian Primates von Gläser, Birgitta, Myrtek, Daniel, Rumpler, Yves, Schiebel, Katrin, Hauwy, Marcel, Rappold, Gudrun A., Schempp, Werner

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5q31 Microdeletions: Definition of a Critical Region and Analysis of LRRTM2, a Candidate Gene for Intellectual Disability von Kleffmann, W., Zink, A.M., Lee, J.A., Senderek, J., Mangold, E., Moog, U., Rappold, G.A., Wohlleber, E., Engels, H.

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A Novel Murine PKA-Related Protein Kinase Involved in Neuronal Differentiation von Blaschke, Rüdiger J., Monaghan, A.Paula, Bock, Dagmar, Rappold, Gudrun A.

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The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator von Rao, E, Blaschke, R J, Marchini, A, Niesler, B, Burnett, M, Rappold, G A

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Elevated DNA sequence diversity in the genomic region of the phosphatase PPP2R3L gene in the human pseudoautosomal region von Schiebel, K., Meder, J., Rump, A., Rosenthal, A., Winkelmann, M., Fischer, C., Bonk, T., Humeny, A., Rappold, G.A.

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Hypervariable telomeric sequences from the human sex chromosomes are pseudoautosomal von Cooke, Howard J, Brown, William R. A, Rappold, Gudrun A

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Prevalence of mutations in the short stature homeobox containing gene (SHOX) in Madelung deformity of childhood von Flanagan, S F, Munns, C F J, Hayes, M, Williams, B, Berry, M, Vickers, D, Rao, E, Rappold, G A, Batch, J A, Hyland, V J, Glass, I A

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