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Lars Hansen

Showing results (111-120 of 178) with videos related to

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American Journal of Human Genetics|February 12, 2013
Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinismKaren Grønskov, Christopher M Dooley, Elsebet Østergaard, et al.
Diabetes|January 24, 2003
The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetesEva-Maria D Nielsen, Lars Hansen, Bendix Carstensen, et al.
Nucleic Acids Research|May 5, 2017
Precise integration of inducible transcriptional elements (PrIITE) enables absolute control of gene expressionRita Pinto, Lars Hansen, John Hintze, et al.
Molecular Vision|March 2, 2019
A splice-site variant in the lncRNA gene <i>RP1-140A9.1</i> cosegregates in the large Volkmann cataract familyHans Eiberg, Annemette F Mikkelsen, Mads Bak, et al.
Social Psychiatry and Psychiatric Epidemiology|March 9, 2011
A semi-structured clinical interview for psychosis sub-groups (SCIPS): development and psychometric propertiesYoshihiro Kinoshita, David Kingdon, Kuni Kinoshita, et al.
BMC Medical Genetics|March 25, 2011
The PTPN22 C1858T gene variant is associated with proinsulin in new-onset type 1 diabetesLotte B Nielsen, Sven Pörksen, Marie Louise M Andersen, et al.
European Journal of Medical Genetics|August 6, 2017
A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani familyUzma Abdullah, Muhammad Farooq, Yuan Mang, et al.
Investigative Ophthalmology & Visual Science|February 1, 2008
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2Bernd Wissinger, Susann Dangel, Herbert Jägle, et al.
The Journal of Clinical Endocrinology and Metabolism|May 24, 2007
Meal-stimulated glucagon release is associated with postprandial blood glucose level and does not interfere with glycemic control in children and adolescents with new-onset type 1 diabetesSven Pörksen, Lotte B Nielsen, Anne Kaas, et al.
Plos One|August 7, 2008
Non-replication of genome-wide based associations between common variants in INSIG2 and PFKP and obesity in studies of 18,014 DanesCamilla H Andreasen, Mette S Mogensen, Knut Borch-Johnsen, et al.
Pageof 18

Showing results (111-120 of 178) with videos related to

Sort By:
Pageof 18
American Journal of Human Genetics|February 12, 2013
Mutations in c10orf11, a melanocyte-differentiation gene, cause autosomal-recessive albinismKaren Grønskov, Christopher M Dooley, Elsebet Østergaard, et al.
Diabetes|January 24, 2003
The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetesEva-Maria D Nielsen, Lars Hansen, Bendix Carstensen, et al.
Nucleic Acids Research|May 5, 2017
Precise integration of inducible transcriptional elements (PrIITE) enables absolute control of gene expressionRita Pinto, Lars Hansen, John Hintze, et al.
Molecular Vision|March 2, 2019
A splice-site variant in the lncRNA gene <i>RP1-140A9.1</i> cosegregates in the large Volkmann cataract familyHans Eiberg, Annemette F Mikkelsen, Mads Bak, et al.
Social Psychiatry and Psychiatric Epidemiology|March 9, 2011
A semi-structured clinical interview for psychosis sub-groups (SCIPS): development and psychometric propertiesYoshihiro Kinoshita, David Kingdon, Kuni Kinoshita, et al.
BMC Medical Genetics|March 25, 2011
The PTPN22 C1858T gene variant is associated with proinsulin in new-onset type 1 diabetesLotte B Nielsen, Sven Pörksen, Marie Louise M Andersen, et al.
European Journal of Medical Genetics|August 6, 2017
A novel mutation in CDK5RAP2 gene causes primary microcephaly with speech impairment and sparse eyebrows in a consanguineous Pakistani familyUzma Abdullah, Muhammad Farooq, Yuan Mang, et al.
Investigative Ophthalmology & Visual Science|February 1, 2008
Cone dystrophy with supernormal rod response is strictly associated with mutations in KCNV2Bernd Wissinger, Susann Dangel, Herbert Jägle, et al.
The Journal of Clinical Endocrinology and Metabolism|May 24, 2007
Meal-stimulated glucagon release is associated with postprandial blood glucose level and does not interfere with glycemic control in children and adolescents with new-onset type 1 diabetesSven Pörksen, Lotte B Nielsen, Anne Kaas, et al.
Plos One|August 7, 2008
Non-replication of genome-wide based associations between common variants in INSIG2 and PFKP and obesity in studies of 18,014 DanesCamilla H Andreasen, Mette S Mogensen, Knut Borch-Johnsen, et al.
Pageof 18