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H Biebermann

Showing results (11-20 of 22) with videos related to

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European Journal of Endocrinology|June 21, 2001
Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidismP Ambrugger, I Stoeva, H Biebermann, et al.
Nature Genetics|June 10, 1998
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humansH Krude, H Biebermann, W Luck, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 2, 1999
Alterations of neonatal thyroid functionA Grüters, H Krude, H Biebermann, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 7, 1998
A conserved tyrosine residue (Y601) in transmembrane domain 5 of the human thyrotropin receptor serves as a molecular switch to determine G-protein couplingH Biebermann, T Schöneberg, A Schulz, et al.
The Journal of Clinical Endocrinology and Metabolism|May 20, 1998
Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptorA Grüters, T Schöneberg, H Biebermann, et al.
The Journal of Clinical Endocrinology and Metabolism|April 30, 2010
Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesisA Thorwarth, I Mueller, H Biebermann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1996
Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidismA Grüters, B Köhler, A Wolf, et al.
Human Mutation|August 26, 1998
V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanismsT Schöneberg, A Schulz, H Biebermann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|February 9, 2007
A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesityE Rettenbacher, P Tarnow, H Brumm, et al.
The Journal of Clinical Endocrinology and Metabolism|April 22, 2011
Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex developmentB Köhler, H Biebermann, V Friedsam, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
European Journal of Endocrinology|June 21, 2001
Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidismP Ambrugger, I Stoeva, H Biebermann, et al.
Nature Genetics|June 10, 1998
Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humansH Krude, H Biebermann, W Luck, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 2, 1999
Alterations of neonatal thyroid functionA Grüters, H Krude, H Biebermann, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|November 7, 1998
A conserved tyrosine residue (Y601) in transmembrane domain 5 of the human thyrotropin receptor serves as a molecular switch to determine G-protein couplingH Biebermann, T Schöneberg, A Schulz, et al.
The Journal of Clinical Endocrinology and Metabolism|May 20, 1998
Severe congenital hyperthyroidism caused by a germ-line neo mutation in the extracellular portion of the thyrotropin receptorA Grüters, T Schöneberg, H Biebermann, et al.
The Journal of Clinical Endocrinology and Metabolism|April 30, 2010
Screening chromosomal aberrations by array comparative genomic hybridization in 80 patients with congenital hypothyroidism and thyroid dysgenesisA Thorwarth, I Mueller, H Biebermann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|January 1, 1996
Screening for mutations of the human thyroid peroxidase gene in patients with congenital hypothyroidismA Grüters, B Köhler, A Wolf, et al.
Human Mutation|August 26, 1998
V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanismsT Schöneberg, A Schulz, H Biebermann, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|February 9, 2007
A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesityE Rettenbacher, P Tarnow, H Brumm, et al.
The Journal of Clinical Endocrinology and Metabolism|April 22, 2011
Analysis of the Wilms' tumor suppressor gene (WT1) in patients 46,XY disorders of sex developmentB Köhler, H Biebermann, V Friedsam, et al.
Pageof 3