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Didier Lochmatter

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

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Hormone Research in Paediatrics|January 22, 2011
RNA interference in mammalian cell systemsDidier Lochmatter, Primus-E Mullis
Endocrine Development|November 28, 2012
Isolated growth hormone deficiency type 2: from gene to therapyMaria Consolata Miletta, Didier Lochmatter, Vibor Pektovic, et al.
European Journal of Endocrinology|October 11, 2007
GH mutant (R77C) in a pedigree presenting with the delay of growth and pubertal development: structural analysis of the mutant and evaluation of the biological activityVibor Petkovic, Mario Thevis, Didier Lochmatter, et al.
The Journal of Clinical Endocrinology and Metabolism|May 24, 2007
Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and statureVibor Petkovic, Amélie Besson, Mario Thevis, et al.
Endocrinology|March 31, 2010
Growth hormone (GH)-releasing hormone increases the expression of the dominant-negative GH isoform in cases of isolated GH deficiency due to GH splice-site mutationsVibor Petkovic, Michela Godi, Didier Lochmatter, et al.
Endocrinology|July 2, 2010
Isolated GH deficiency type II: knockdown of the harmful Delta3GH recovers wt-GH secretion in rat tumor pituitary cellsDidier Lochmatter, Molly Strom, André Eblé, et al.
Endocrinology|October 14, 2006
Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosisSouzan Salemi, Shida Yousefi, Didier Lochmatter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2007
Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiencyBarbara Räz, Marco Janner, Vibor Petkovic, et al.
The Journal of Clinical Endocrinology and Metabolism|December 3, 2009
Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and actionVibor Petkovic, Michela Godi, Amit V Pandey, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2007
Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiencyVibor Petkovic, Didier Lochmatter, James Turton, et al.
Pageof 1

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

Sort By:
Pageof 1
Hormone Research in Paediatrics|January 22, 2011
RNA interference in mammalian cell systemsDidier Lochmatter, Primus-E Mullis
Endocrine Development|November 28, 2012
Isolated growth hormone deficiency type 2: from gene to therapyMaria Consolata Miletta, Didier Lochmatter, Vibor Pektovic, et al.
European Journal of Endocrinology|October 11, 2007
GH mutant (R77C) in a pedigree presenting with the delay of growth and pubertal development: structural analysis of the mutant and evaluation of the biological activityVibor Petkovic, Mario Thevis, Didier Lochmatter, et al.
The Journal of Clinical Endocrinology and Metabolism|May 24, 2007
Evaluation of the biological activity of a growth hormone (GH) mutant (R77C) and its impact on GH responsiveness and statureVibor Petkovic, Amélie Besson, Mario Thevis, et al.
Endocrinology|March 31, 2010
Growth hormone (GH)-releasing hormone increases the expression of the dominant-negative GH isoform in cases of isolated GH deficiency due to GH splice-site mutationsVibor Petkovic, Michela Godi, Didier Lochmatter, et al.
Endocrinology|July 2, 2010
Isolated GH deficiency type II: knockdown of the harmful Delta3GH recovers wt-GH secretion in rat tumor pituitary cellsDidier Lochmatter, Molly Strom, André Eblé, et al.
Endocrinology|October 14, 2006
Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosisSouzan Salemi, Shida Yousefi, Didier Lochmatter, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2007
Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiencyBarbara Räz, Marco Janner, Vibor Petkovic, et al.
The Journal of Clinical Endocrinology and Metabolism|December 3, 2009
Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and actionVibor Petkovic, Michela Godi, Amit V Pandey, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2007
Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiencyVibor Petkovic, Didier Lochmatter, James Turton, et al.
Pageof 1