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P Wonerow

Showing results (1-10 of 13) with videos related to

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Oncogene|October 19, 2001
The transmembrane adapter LAT plays a central role in immune receptor signallingP Wonerow, S P Watson
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidismD Führer, P Wonerow, H Willgerodt, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 28, 2002
Thyrotropin receptor mutations as a tool to understand thyrotropin receptor actionP Wonerow, S Neumann, T Gudermann, et al.
European Journal of Medical Research|July 25, 1996
Constitutively activating mutations of the thyrotropin receptor and thyroid diseaseD Führer, H P Holzapfel, P Wonerow, et al.
The Journal of Biological Chemistry|May 9, 1998
Deletions in the third intracellular loop of the thyrotropin receptor. A new mechanism for constitutive activationP Wonerow, T Schöneberg, G Schultz, et al.
Clinical Endocrinology|September 30, 2000
Functional characterization of five constitutively activating thyrotrophin receptor mutationsP Wonerow, S Chey, D Führer, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Somatic mutations in the thyrotropin receptor gene and not in the Gs alpha protein gene in 31 toxic thyroid nodulesD Führer, H P Holzapfel, P Wonerow, et al.
Thyroid : Official Journal of the American Thyroid Association|September 11, 1999
Variable phenotype associated with Ser505Asn-activating thyrotropin-receptor germline mutationD Führer, M Mix, P Wonerow, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Identification of constitutively activating somatic thyrotropin receptor mutations in a subset of toxic multinodular goitersH P Holzapfel, D Führer, P Wonerow, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor geneH P Holzapfel, P Wonerow, W von Petrykowski, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Oncogene|October 19, 2001
The transmembrane adapter LAT plays a central role in immune receptor signallingP Wonerow, S P Watson
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Identification of a new thyrotropin receptor germline mutation (Leu629Phe) in a family with neonatal onset of autosomal dominant nonautoimmune hyperthyroidismD Führer, P Wonerow, H Willgerodt, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 28, 2002
Thyrotropin receptor mutations as a tool to understand thyrotropin receptor actionP Wonerow, S Neumann, T Gudermann, et al.
European Journal of Medical Research|July 25, 1996
Constitutively activating mutations of the thyrotropin receptor and thyroid diseaseD Führer, H P Holzapfel, P Wonerow, et al.
The Journal of Biological Chemistry|May 9, 1998
Deletions in the third intracellular loop of the thyrotropin receptor. A new mechanism for constitutive activationP Wonerow, T Schöneberg, G Schultz, et al.
Clinical Endocrinology|September 30, 2000
Functional characterization of five constitutively activating thyrotrophin receptor mutationsP Wonerow, S Chey, D Führer, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Somatic mutations in the thyrotropin receptor gene and not in the Gs alpha protein gene in 31 toxic thyroid nodulesD Führer, H P Holzapfel, P Wonerow, et al.
Thyroid : Official Journal of the American Thyroid Association|September 11, 1999
Variable phenotype associated with Ser505Asn-activating thyrotropin-receptor germline mutationD Führer, M Mix, P Wonerow, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Identification of constitutively activating somatic thyrotropin receptor mutations in a subset of toxic multinodular goitersH P Holzapfel, D Führer, P Wonerow, et al.
The Journal of Clinical Endocrinology and Metabolism|November 14, 1997
Sporadic congenital hyperthyroidism due to a spontaneous germline mutation in the thyrotropin receptor geneH P Holzapfel, P Wonerow, W von Petrykowski, et al.
Pageof 2