Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome von Kim, Hyung-Goo, Kurth, Ingo, Lan, Fei, Meliciani, Irene, Wenzel, Wolfgang, Eom, Soo Hyun, Kang, Gil Bu, Rosenberger, Georg, Tekin, Mustafa, Ozata, Metin, Bick, David P., Sherins, Richard J., Walker, Steven L., Shi, Yang, Gusella, James F., Layman, Lawrence C.

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Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome von Xu, Ning, Ph.D, Kim, Hyung-Goo, Ph.D, Bhagavath, Balasubramanian, M.D, Cho, Sung-Gyu, M.S, Lee, Jae Ho, Ph.D, Ha, Kyungsoo, M.S, Meliciani, Irene, M.S, Wenzel, Wolfgang, Ph.D, Podolsky, Robert H., Ph.D, Chorich, Lynn P., M.S, Stackhouse, Kathryn A., B.S, Grove, Anna M.H., B.S, Odom, Lawrence N., M.D, Ozata, Metin, M.D, Bick, David P., M.D, Sherins, Richard J., M.D, Kim, Soo-Hyun, Ph.D, Cameron, Richard S., Ph.D, Layman, Lawrence C., M.D

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WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome von Kim, Hyung-Goo, Ahn, Jang-Won, Kurth, Ingo, Ullmann, Reinhard, Kim, Hyun-Taek, Kulharya, Anita, Ha, Kyung-Soo, Itokawa, Yasuhide, Meliciani, Irene, Wenzel, Wolfgang, Lee, Deresa, Rosenberger, Georg, Ozata, Metin, Bick, David P., Sherins, Richard J., Nagase, Takahiro, Tekin, Mustafa, Kim, Soo-Hyun, Kim, Cheol-Hee, Ropers, Hans-Hilger, Gusella, James F., Kalscheuer, Vera, Choi, Cheol Yong, Layman, Lawrence C.

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7‑Alkyl-3-benzylcoumarins: A Versatile Scaffold for the Development of Potent and Selective Cannabinoid Receptor Agonists and Antagonists von Rempel, Viktor, Volz, Nicole, Hinz, Sonja, Karcz, Tadeusz, Meliciani, Irene, Nieger, Martin, Wenzel, Wolfgang, Bräse, Stefan, Müller, Christa E

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Probing hot spots on protein-protein interfaces with all-atom free-energy simulation von Meliciani, Irene, Klenin, Konstantin, Strunk, Timo, Schmitz, Katja, Wenzel, Wolfgang

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A fluorescence polarization assay for the experimental validation of an in silico model of the chemokine CXCL8 binding to receptor-derived peptides von Girrbach, Maria, Meliciani, Irene, Waterkotte, Björn, Berthold, Susann, Oster, Alisha, Brurein, Fiona, Strunk, Timo, Wadhwani, Parvesh, Berensmeier, Sonja, Wenzel, Wolfgang, Schmitz, Katja

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A fluorescence polarization assay for the experimental validation of an in silico model of the chemokine CXCL8 binding to receptor-derived peptidesElectronic supplementary informat... von Girrbach, Maria, Meliciani, Irene, Waterkotte, Björn, Berthold, Susann, Oster, Alisha, Brurein, Fiona, Strunk, Timo, Wadhwani, Parvesh, Berensmeier, Sonja, Wenzel, Wolfgang, Schmitz, Katja

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A fluorescence polarization assay for the experimental validation of an in silicomodel of the chemokine CXCL8 binding to receptor-derived peptides von Girrbach, Maria, Meliciani, Irene, Waterkotte, Bjorn, Berthold, Susann, Oster, Alisha, Brurein, Fiona, Strunk, Timo, Wadhwani, Parvesh, Berensmeier, Sonja, Wenzel, Wolfgang, Schmitz, Katja

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Performance of An All-Atom Free Energy Approach For Protein Structure Prediction von Anand, Priya, Strunk, Timo, Brieg, Martin, Meliciani, Irene, Wolf, Moritz, Klenin, Konstantin, Wenzel, Wolfgang

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A Combined Experimental and Simulation Approach to Develop Selective High-Affinity Small-Molecule Inhibitors of Cannabinoid Receptors CB1/CB2 von Meliciani, Irene, Volz, Nicole, Rempel, Viktor, Hinz, Sonja, Karcz, Tadeusz, Müller, Christa E., Bräse, Stefan, Wenzel, Wolfgang

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Oligogalacturonide-induced changes in the nuclear proteome of Arabidopsis thaliana von Casasoli, Manuela, Meliciani, Irene, Cervone, Felice, De Lorenzo, Giulia, Mattei, Benedetta

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Mutations in CHD7, Encoding a Chronatin-Remodeling Protein. Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome von Kim, Hyung-Goo, Kurth, Ingo, Lan, Fei, Meliciani, Irene, Wenzel, Wolfgang, Eom, Soo Hyun, Kang, Gil Bu, Rosenberger, Georg, Tekin, Mustafa, Ozata, Metin, Bick, David P, Sherins, Richard J, Walker, Steven L, Shi, Yang, Gusella, James F, Layman, Lawrence C

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Unique phenotype in a patient with CHARGE syndrome von Jain, Shobhit, Kim, Hyung-Goo, Lacbawan, Felicitas, Meliciani, Irene, Wenzel, Wolfgang, Kurth, Ingo, Sharma, Josefina, Schoeneman, Morris, Ten, Svetlana, Layman, Lawrence C, Jacobson-Dickman, Elka

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Application of Models for Biomolecular Structure and Interactions to Understand and Influence Biological Function von Meliciani, Irene

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A MOLECULAR SCAFFOLD TO MODULATE THROMBIN/ANTITHROMBIN ACTIVITY BY HEPARIN BINDING von PEREZ-SANCHEZ, HORACIO, MELICIANI, IRENE, CORRAL DE LA CALLE, JAVIER, GARCIA, VICENTE VICENTE, MARTINEZ-MARTINEZ, IRENE, NAVARRO-FERNANDEZ, JOSE, WENZEL, WOLFGANG

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D-myo-inositol 3,4,5,6-tetrakisphosphate to modulate thrombin/antithrombin activity by heparin binding von PEREZ-SANCHEZ, HORACIO, MELICIANI, IRENE, DE LA CALLE, JAVIER CORRAL, GARCIA, VICENTE VICENTE, MARTINEZ-MARTINEZ, IRENE, NAVARRO-FERNANDEZ, JOSE, WENZEL, WOLFGANG

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