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Saskia Letz

Showing results (1-10 of 4) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|February 13, 2014
A homozygous CaSR mutation causing a FHH phenotype completely masked by vitamin D deficiency presenting as ricketsDorothea Szczawinska, Dirk Schnabel, Saskia Letz, et al.
Plos One|December 16, 2014
Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemiaSaskia Letz, Christine Haag, Egbert Schulze, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Novel activating mutations of the calcium-sensing receptor: the calcilytic NPS-2143 mitigates excessive signal transduction of mutant receptorsSaskia Letz, Ramona Rus, Christine Haag, et al.
European Journal of Endocrinology|September 27, 2016
Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotypeMarkus Glaudo, Saskia Letz, Marcus Quinkler, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
The Journal of Clinical Endocrinology and Metabolism|February 13, 2014
A homozygous CaSR mutation causing a FHH phenotype completely masked by vitamin D deficiency presenting as ricketsDorothea Szczawinska, Dirk Schnabel, Saskia Letz, et al.
Plos One|December 16, 2014
Amino alcohol- (NPS-2143) and quinazolinone-derived calcilytics (ATF936 and AXT914) differentially mitigate excessive signalling of calcium-sensing receptor mutants causing Bartter syndrome Type 5 and autosomal dominant hypocalcemiaSaskia Letz, Christine Haag, Egbert Schulze, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Novel activating mutations of the calcium-sensing receptor: the calcilytic NPS-2143 mitigates excessive signal transduction of mutant receptorsSaskia Letz, Ramona Rus, Christine Haag, et al.
European Journal of Endocrinology|September 27, 2016
Heterozygous inactivating CaSR mutations causing neonatal hyperparathyroidism: function, inheritance and phenotypeMarkus Glaudo, Saskia Letz, Marcus Quinkler, et al.
Pageof 1