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Clinical Rheumatology|August 5, 2004
Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patientsBernd Frank, Beate Niesler, Brigitta Bondy, et al.
BMC Medical Genetics|May 14, 2005
Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA)Nadja Muncke, Beate Niesler, Ralph Roeth, et al.
Experimental Cell Research|May 30, 2006
MEGAP impedes cell migration via regulating actin and microtubule dynamics and focal complex formationYing Yang, Marco Marcello, Volker Endris, et al.
Journal of Molecular Biology|December 6, 2005
Phosphorylation on Ser106 modulates the cellular functions of the SHOX homeodomain proteinAntonio Marchini, Laurent Daeffler, Tiina Marttila, et al.
American Journal of Human Genetics|June 3, 2005
Identification of a major recombination hotspot in patients with short stature and SHOX deficiencyKatja U Schneider, Nitin Sabherwal, Karin Jantz, et al.
The Journal of Comparative Neurology|December 31, 2010
Serotonin receptor diversity in the human colon: Expression of serotonin type 3 receptor subunits 5-HT3C, 5-HT3D, and 5-HT3EJohannes Kapeller, Dorothee Möller, Felix Lasitschka, et al.
The Journal of Biological Chemistry|June 5, 2010
RIC-3 exclusively enhances the surface expression of human homomeric 5-hydroxytryptamine type 3A (5-HT3A) receptors despite direct interactions with 5-HT3A, -C, -D, and -E subunitsJutta Walstab, Christian Hammer, Felix Lasitschka, et al.
Molecular Pharmacology|March 30, 2007
Characterization of the novel human serotonin receptor subunits 5-HT3C,5-HT3D, and 5-HT3EBeate Niesler, Jutta Walstab, Sandra Combrink, et al.
The Journal of Clinical Endocrinology and Metabolism|October 19, 2006
Growth hormone is effective in treatment of short stature associated with short stature homeobox-containing gene deficiency: Two-year results of a randomized, controlled, multicenter trialWerner F Blum, Brenda J Crowe, Charmian A Quigley, et al.
Journal of Medical Genetics|December 22, 2006
Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiencyGudrun Rappold, Werner F Blum, Elena P Shavrikova, et al.
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