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H NEUMANN

Showing results (351-360 of 418) with videos related to

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Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Clinical Genetics|August 4, 2016
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paragangliomaA S Hoekstra, B van den Ende, X P Julià, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2011
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sitesHartmut P H Neumann, Maren Sullivan, Aurelia Winter, et al.
British Journal of Cancer|October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastomaD Astuti, M Morris, C Krona, et al.
Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1991
Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau diseaseB R Seizinger, D I Smith, M R Filling-Katz, et al.
Diabetologia|February 27, 2015
Leptin induces fasting hypoglycaemia in a mouse model of diabetes through the depletion of glycerolHeather C Denroche, Michelle M Kwon, Whitney L Quong, et al.
Annals of Human Genetics|January 12, 2010
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndromeMaren Sullivan, Zoran Erlic, Michael M Hoffmann, et al.
The British Journal of Dermatology|April 16, 1998
The effect of addition of calcipotriol ointment (50 micrograms/g) to acitretin therapy in psoriasisP C van de Kerkhof, F Cambazard, P E Hutchinson, et al.
Human Mutation|March 19, 2005
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry diseaseEllen Schäfer, Karin Baron, Urs Widmer, et al.
Pageof 42

Showing results (351-360 of 418) with videos related to

Sort By:
Pageof 42
Endocrine-Related Cancer|February 22, 2012
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3Angelica Malinoc, Maren Sullivan, Thorsten Wiech, et al.
Clinical Genetics|August 4, 2016
Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paragangliomaA S Hoekstra, B van den Ende, X P Julià, et al.
The Journal of Clinical Endocrinology and Metabolism|May 27, 2011
Germline mutations of the TMEM127 gene in patients with paraganglioma of head and neck and extraadrenal abdominal sitesHartmut P H Neumann, Maren Sullivan, Aurelia Winter, et al.
British Journal of Cancer|October 27, 2004
Investigation of the role of SDHB inactivation in sporadic phaeochromocytoma and neuroblastomaD Astuti, M Morris, C Krona, et al.
Endocrine-Related Cancer|May 24, 2008
Evaluation of a functional epigenetic approach to identify promoter region methylation in phaeochromocytoma and neuroblastomaCaroline D E Margetts, Mark Morris, Dewi Astuti, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1991
Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau diseaseB R Seizinger, D I Smith, M R Filling-Katz, et al.
Diabetologia|February 27, 2015
Leptin induces fasting hypoglycaemia in a mouse model of diabetes through the depletion of glycerolHeather C Denroche, Michelle M Kwon, Whitney L Quong, et al.
Annals of Human Genetics|January 12, 2010
Epidemiological approach to identifying genetic predispositions for atypical hemolytic uremic syndromeMaren Sullivan, Zoran Erlic, Michael M Hoffmann, et al.
The British Journal of Dermatology|April 16, 1998
The effect of addition of calcipotriol ointment (50 micrograms/g) to acitretin therapy in psoriasisP C van de Kerkhof, F Cambazard, P E Hutchinson, et al.
Human Mutation|March 19, 2005
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry diseaseEllen Schäfer, Karin Baron, Urs Widmer, et al.
Pageof 42