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Harald Brumm

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The Journal of Clinical Endocrinology and Metabolism|October 5, 2002
Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effectHarald Brumm, Arne Pfeufer, Heike Biebermann, et al.
Obesity (Silver Spring, Md.)|November 11, 2008
Lifestyle intervention in obese children with variations in the melanocortin 4 receptor geneThomas Reinehr, Johannes Hebebrand, Susann Friedel, et al.
Human Genetics|November 18, 2008
Increased constraints on MC4R during primate and human evolutionDavid A Hughes, Anke Hinney, Harald Brumm, et al.
Endocrine|February 14, 2009
A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesityChristian L Roth, Michael Ludwig, Joachim Woelfle, et al.
Endocrinology|July 14, 2007
Evolutionary aspects in evaluating mutations in the melanocortin 4 receptorClaudia Stäubert, Patrick Tarnow, Harald Brumm, et al.
Obesity (Silver Spring, Md.)|July 9, 2011
Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-throughHarald Brumm, Jessica Mühlhaus, Florian Bolze, et al.
Obesity Facts|January 8, 2010
A heterozygous mutation in the third transmembrane domain causes a dominant-negative effect on signalling capability of the MC4RPatrick Tarnow, Anne Rediger, Harald Brumm, et al.
BMC Genetics|May 5, 2007
Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13Susann Friedel, Kathrin Reichwald, André Scherag, et al.
The Journal of Clinical Endocrinology and Metabolism|February 24, 2006
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from GermanyAnke Hinney, Thomas Bettecken, Patrick Tarnow, et al.
Hormone Research in Paediatrics|June 13, 2012
Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatednessJessica Mühlhaus, Carolin Pütter, Harald Brumm, et al.
Pageof 1

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

Sort By:
Pageof 1
The Journal of Clinical Endocrinology and Metabolism|October 5, 2002
Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effectHarald Brumm, Arne Pfeufer, Heike Biebermann, et al.
Obesity (Silver Spring, Md.)|November 11, 2008
Lifestyle intervention in obese children with variations in the melanocortin 4 receptor geneThomas Reinehr, Johannes Hebebrand, Susann Friedel, et al.
Human Genetics|November 18, 2008
Increased constraints on MC4R during primate and human evolutionDavid A Hughes, Anke Hinney, Harald Brumm, et al.
Endocrine|February 14, 2009
A novel melanocortin-4 receptor gene mutation in a female patient with severe childhood obesityChristian L Roth, Michael Ludwig, Joachim Woelfle, et al.
Endocrinology|July 14, 2007
Evolutionary aspects in evaluating mutations in the melanocortin 4 receptorClaudia Stäubert, Patrick Tarnow, Harald Brumm, et al.
Obesity (Silver Spring, Md.)|July 9, 2011
Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-throughHarald Brumm, Jessica Mühlhaus, Florian Bolze, et al.
Obesity Facts|January 8, 2010
A heterozygous mutation in the third transmembrane domain causes a dominant-negative effect on signalling capability of the MC4RPatrick Tarnow, Anne Rediger, Harald Brumm, et al.
BMC Genetics|May 5, 2007
Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13Susann Friedel, Kathrin Reichwald, André Scherag, et al.
The Journal of Clinical Endocrinology and Metabolism|February 24, 2006
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from GermanyAnke Hinney, Thomas Bettecken, Patrick Tarnow, et al.
Hormone Research in Paediatrics|June 13, 2012
Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatednessJessica Mühlhaus, Carolin Pütter, Harald Brumm, et al.
Pageof 1