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Thomas Brune

Showing results (21-30 of 37) with videos related to

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Journal of Molecular Endocrinology|June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophyRene Cortese, Florian Eckhardt, Marianne Volleth, et al.
FEMS Microbiology Ecology|February 18, 2009
Response of total and nitrate-dissimilating bacteria to reduced N deposition in a spruce forest soil profileEllen Kandeler, Thomas Brune, Esther Enowashu, et al.
Transfusion|August 24, 2007
Quality and stability of red cells derived from gravity-separated placental blood with a hollow-fiber systemThomas Brune, Sara Fill, Gerd Heim, et al.
Glycoconjugate Journal|January 2, 2008
Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS)Jonas Denecke, Christian Kranz, Manfred Nimtz, et al.
American Journal of Botany|May 27, 2011
Old-New World and trans-African disjunctions of Thamnosma (Rutaceae): intercontinental long-distance dispersal and local differentiation in the succulent biomeMike Thiv, Timotheüs van der Niet, Frank Rutschmann, et al.
Biology of the Neonate|May 16, 2002
Autologous placental blood transfusion for the therapy of anaemic neonatesThomas Brune, Henk Garritsen, Ralf Witteler, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 29, 2018
Harbouring group B streptococci in a neonatal intensive care unit led to an outbreak among preterm infantsEmma Åberg, Ann Ottosson, Margareta Granlund, et al.
European Journal of Human Genetics : EJHG|March 16, 2012
Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newbornJanine Reunert, Rüdiger Wentzell, Michael Walter, et al.
Pediatrics|January 27, 2010
The Stockholm Neonatal Family Centered Care Study: effects on length of stay and infant morbidityAnnica Ortenstrand, Björn Westrup, Eva Berggren Broström, et al.
Human Mutation|May 4, 2006
A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPSJonas Denecke, Thomas Brune, Tobias Feldhaus, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Journal of Molecular Endocrinology|June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophyRene Cortese, Florian Eckhardt, Marianne Volleth, et al.
FEMS Microbiology Ecology|February 18, 2009
Response of total and nitrate-dissimilating bacteria to reduced N deposition in a spruce forest soil profileEllen Kandeler, Thomas Brune, Esther Enowashu, et al.
Transfusion|August 24, 2007
Quality and stability of red cells derived from gravity-separated placental blood with a hollow-fiber systemThomas Brune, Sara Fill, Gerd Heim, et al.
Glycoconjugate Journal|January 2, 2008
Characterization of the N-glycosylation phenotype of erythrocyte membrane proteins in congenital dyserythropoietic anemia type II (CDA II/HEMPAS)Jonas Denecke, Christian Kranz, Manfred Nimtz, et al.
American Journal of Botany|May 27, 2011
Old-New World and trans-African disjunctions of Thamnosma (Rutaceae): intercontinental long-distance dispersal and local differentiation in the succulent biomeMike Thiv, Timotheüs van der Niet, Frank Rutschmann, et al.
Biology of the Neonate|May 16, 2002
Autologous placental blood transfusion for the therapy of anaemic neonatesThomas Brune, Henk Garritsen, Ralf Witteler, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 29, 2018
Harbouring group B streptococci in a neonatal intensive care unit led to an outbreak among preterm infantsEmma Åberg, Ann Ottosson, Margareta Granlund, et al.
European Journal of Human Genetics : EJHG|March 16, 2012
Neonatal progeria: increased ratio of progerin to lamin A leads to progeria of the newbornJanine Reunert, Rüdiger Wentzell, Michael Walter, et al.
Pediatrics|January 27, 2010
The Stockholm Neonatal Family Centered Care Study: effects on length of stay and infant morbidityAnnica Ortenstrand, Björn Westrup, Eva Berggren Broström, et al.
Human Mutation|May 4, 2006
A homozygous ZMPSTE24 null mutation in combination with a heterozygous mutation in the LMNA gene causes Hutchinson-Gilford progeria syndrome (HGPS): insights into the pathophysiology of HGPSJonas Denecke, Thomas Brune, Tobias Feldhaus, et al.
Pageof 4