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Journal of Molecular Endocrinology
|
June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophy
Rene 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 profile
Ellen 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 system
Thomas 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 biome
Mike 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 neonates
Thomas 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 infants
Emma 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 newborn
Janine 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 morbidity
Annica 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 HGPS
Jonas Denecke, Thomas Brune, Tobias Feldhaus, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 37) with videos related to
Sort By:
Page
of 4
Journal of Molecular Endocrinology
|
June 9, 2007
The retinol acid receptor B gene is hypermethylated in patients with familial partial lipodystrophy
Rene 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 profile
Ellen 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 system
Thomas 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 biome
Mike 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 neonates
Thomas 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 infants
Emma 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 newborn
Janine 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 morbidity
Annica 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 HGPS
Jonas Denecke, Thomas Brune, Tobias Feldhaus, et al.
Page
of 4