Antibodies to TSH‐receptor in thyroid autoimmune disease interact with monoclonal antibodies whose epitopes are broadly distributed on the receptor von MINICH, W. B., LENZNER, C., MORGENTHALER, N. G.

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Hepatocyte Nuclear Factor-4α Involved in Type 1 Maturity-Onset Diabetes of the Young Is a Novel Target of AMP-Activated Protein Kinase von LECLERC, Isabelle, LENZNER, Claudia, GOURDON, Laurence, VAULONT, Sophie, KAHN, Axel, VIOLLET, Benoit

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Cre-mediated germline mosaicism: a method allowing rapid generation of several alleles of a target gene von Holzenberger, M, Lenzner, C, Leneuve, P, Zaoui, R, Hamard, G, Vaulont, S, Bouc, Y L

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The Effect of Thyrotropin-Receptor Blocking Antibodies on Stimulating Autoantibodies from Patients with Graves' Disease von Lenzner, Cornelia, Morgenthaler, Nils G.

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Trinucleotide repeat polymorphism at the PKLR locus von Lenzner, C., Jacobasch, G., Reis, A., Thiele, B., Nürnberg, P.

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Affinity purification and diagnostic use of TSH receptor autoantibodies from human serum von Morgenthaler, Nils G., Minich, Waldemar B., Willnich, Marita, Bogusch, Thomas, Hollidt, Jörg M., Weglöhner, Wolfgang, Lenzner, Cornelia, Bergmann, Andreas

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A Coated Tube Assay for the Detection of Blocking Thyrotropin Receptor Autoantibodies von Minich, Waldemar B., Lenzner, Cornelia, Bergmann, Andreas, Morgenthaler, Nils G.

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Molecular Analysis of 29 Pyruvate Kinase–Deficient Patients From Central Europe With Hereditary Hemolytic Anemia von Lenzner, Claudia, Nürnberg, Peter, Jacobasch, Gisela, Gerth, Christa, Thiele, Bernd-Joachim

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Molecular analysis of 29 pyruvate kinase-deficient patients from Central Europe with hereditary hemolytic anemia von LENZNER, C, NÜRNBERG, P, JACOBASCH, G, GERTH, C, THIELE, B.-J

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Hepatocyte nuclear factor-4alpha involved in type 1 maturity-onset diabetes of the young is a novel target of AMP-activated protein kinase von Leclerc, I, Lenzner, C, Gourdon, L, Vaulont, S, Kahn, A, Viollet, B

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Mutations in the pyruvate kinase L gene in patients with hereditary hemolytic anemia von LENZNER, C, NÜRNBERG, P, THIELE, B.-J, REIS, A, BRABEC, V, SAKALOVA, A, JACOBASCH, G

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Structure of the promoter and complete sequence of the gene coding for the rabbit translationally controlled tumor protein (TCTP) P23 von Thiele, Holger, Berger, Mario, Lenzner, Claudia, Kühn, Hartmut, Thiele, Bernd‐Joachim

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Monitoring genomic alterations with a panel of oligonucleotide probes specific for various simple repeat motifs von Nürnberg, Peter, Barth, Ingrid, Fuhrmann, Eike, Lenzner, Claudia, Losanova, Tanka, Peters, Christian, Pöche, Hubert, Thiel, Gundula

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Monitoring genomic alterations with a panel of oligonucleotide probe specific for various simple repeat motifs von NUÊRMBERG, P, BARTH, I, FUHRMANN, E, LENZNER, C, LOSANOVA, T, PETERS, C, POÊCHE, H, THIEL, G

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Complete Genomic Sequence of the Human PK-L/R-Gene Includes Four Intragenic Polymorphisms Defining Different Haplotype Backgrounds of Normal and Mutant PK-Genes von Lenzner, Claudia, Nürnberg, Peter, Jacobasch, Gisela, Thiele, Bernd-Joachm

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Phosphorus acceptor doped ZnO nanowires prepared by pulsed-laser deposition von Cao, B Q, Lorenz, M, Rahm, A, von Wenckstern, H, Czekalla, C, Lenzner, J, Benndorf, G, Grundmann, M

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Drivers of future alien species impacts: An expert‐based assessment von Essl, Franz, Lenzner, Bernd, Bacher, Sven, Bailey, Sarah, Capinha, Cesar, Daehler, Curtis, Dullinger, Stefan, Genovesi, Piero, Hui, Cang, Hulme, Philip E., Jeschke, Jonathan M., Katsanevakis, Stelios, Kühn, Ingolf, Leung, Brian, Liebhold, Andrew, Liu, Chunlong, MacIsaac, Hugh J., Meyerson, Laura A., Nuñez, Martin A., Pauchard, Aníbal, Pyšek, Petr, Rabitsch, Wolfgang, Richardson, David M., Roy, Helen E., Ruiz, Gregory M., Russell, James C., Sanders, Nathan J., Sax, Dov F., Scalera, Riccardo, Seebens, Hanno, Springborn, Michael, Turbelin, Anna, Kleunen, Mark, Holle, Betsy, Winter, Marten, Zenni, Rafael D., Mattsson, Brady J., Roura‐Pascual, Nuria

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Non-linear optical deformation potentials in uniaxially strained ZnO microwires von Sturm, C., Wille, M., Lenzner, J., Khujanov, S., Grundmann, M.

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Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation von Jensen, Lars Riff, Amende, Marion, Gurok, Ulf, Moser, Bettina, Gimmel, Verena, Tzschach, Andreas, Janecke, Andreas R., Tariverdian, Gholamali, Chelly, Jamel, Fryns, Jean-Pierre, Van Esch, Hilde, Kleefstra, Tjitske, Hamel, Ben, Moraine, Claude, Gécz, Jozef, Turner, Gillian, Reinhardt, Richard, Kalscheuer, Vera M., Ropers, Hans-Hilger, Lenzner, Steffen

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METHOD FOR PRODUCING ALKYL ESTERS OF TETRONIC ACID von LENZNER,JOACHIM ,CH

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