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K Brusgaard

Showing results (21-30 of 31) with videos related to

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Clinical Genetics|May 29, 2009
The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancyT Sandal, L B Laborie, K Brusgaard, et al.
Diabetologia|August 23, 2008
Transcriptional profiling of myotubes from patients with type 2 diabetes: no evidence for a primary defect in oxidative phosphorylation genesC M Frederiksen, K Højlund, L Hansen, et al.
BJS Open|March 10, 2021
Intraoperative ultrasound imaging in the surgical treatment of congenital hyperinsulinism: prospective, blinded studyA P Bjarnesen, P Dahlin, E Globa, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 10, 2012
Unraveling the effects of 1,25OH2D3 on global gene expression in pancreatic isletsH Wolden-Kirk, L Overbergh, C Gysemans, et al.
Clinical Genetics|November 18, 2015
JP-HHT phenotype in Danish patients with SMAD4 mutationsA M Jelsig, P M Tørring, A D Kjeldsen, et al.
International Journal of Colorectal Disease|March 17, 2016
Disease pattern in Danish patients with Peutz-Jeghers syndromeA M Jelsig, N Qvist, L Sunde, et al.
Hereditas|January 1, 1996
Chromosome localization of the gene for growth hormone in the common shrew (Sorex araneus)S N Malchenko, I V Koroleva, K Brusgaard, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 1, 1995
Chromosomal and regional localization of the loci for IGKC, IGGC, ALDB, HOXB, GPT, and PRNP in the American mink (Mustela vison): comparisons with human and mouseT M Khlebodarova, S N Malchenko, N M Matveeva, et al.
Journal of Medical Genetics|July 7, 2000
Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemiaR Thiart, C L Scholtz, J Vergotine, et al.
Endocrinology|January 16, 2014
Discovery of molecular pathways mediating 1,25-dihydroxyvitamin D3 protection against cytokine-induced inflammation and damage of human and male mouse islets of LangerhansH Wolden-Kirk, D Rondas, M Bugliani, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Clinical Genetics|May 29, 2009
The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancyT Sandal, L B Laborie, K Brusgaard, et al.
Diabetologia|August 23, 2008
Transcriptional profiling of myotubes from patients with type 2 diabetes: no evidence for a primary defect in oxidative phosphorylation genesC M Frederiksen, K Højlund, L Hansen, et al.
BJS Open|March 10, 2021
Intraoperative ultrasound imaging in the surgical treatment of congenital hyperinsulinism: prospective, blinded studyA P Bjarnesen, P Dahlin, E Globa, et al.
The Journal of Steroid Biochemistry and Molecular Biology|November 10, 2012
Unraveling the effects of 1,25OH2D3 on global gene expression in pancreatic isletsH Wolden-Kirk, L Overbergh, C Gysemans, et al.
Clinical Genetics|November 18, 2015
JP-HHT phenotype in Danish patients with SMAD4 mutationsA M Jelsig, P M Tørring, A D Kjeldsen, et al.
International Journal of Colorectal Disease|March 17, 2016
Disease pattern in Danish patients with Peutz-Jeghers syndromeA M Jelsig, N Qvist, L Sunde, et al.
Hereditas|January 1, 1996
Chromosome localization of the gene for growth hormone in the common shrew (Sorex araneus)S N Malchenko, I V Koroleva, K Brusgaard, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|October 1, 1995
Chromosomal and regional localization of the loci for IGKC, IGGC, ALDB, HOXB, GPT, and PRNP in the American mink (Mustela vison): comparisons with human and mouseT M Khlebodarova, S N Malchenko, N M Matveeva, et al.
Journal of Medical Genetics|July 7, 2000
Predominance of a 6 bp deletion in exon 2 of the LDL receptor gene in Africans with familial hypercholesterolaemiaR Thiart, C L Scholtz, J Vergotine, et al.
Endocrinology|January 16, 2014
Discovery of molecular pathways mediating 1,25-dihydroxyvitamin D3 protection against cytokine-induced inflammation and damage of human and male mouse islets of LangerhansH Wolden-Kirk, D Rondas, M Bugliani, et al.
Pageof 4