Search research articles
Contact Us
Filters
Showing results (11-20 of 27) with videos related to
Page
of 3
Sort By:
Plos One
|
May 3, 2014
Influence of oxygen tension on dopaminergic differentiation of human fetal stem cells of midbrain and forebrain origin
Christina Krabbe, Sara Thornby Bak, Pia Jensen, et al.
Journal of Molecular Neuroscience : MN
|
March 5, 2009
Characterization of Meteorin--an evolutionary conserved neurotrophic factor
Jesper Roland Jørgensen, Lachlan Thompson, Lone Fjord-Larsen, et al.
Antibiotics (Basel, Switzerland)
|
April 30, 2021
The Effect of Colistin Treatment on the Selection of Colistin-Resistant <i>Escherichia coli</i> in Weaner Pigs
Shahana Ahmed, Claus Hansen, Ane Laursen Dahlkilde, et al.
American Journal of Medical Genetics
|
July 13, 2002
HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg
Klaus Wilbrandt Kjaer, Jess Hedeboe, Merete Bugge, et al.
Genome Research
|
December 22, 2007
Comparative genomics beyond sequence-based alignments: RNA structures in the ENCODE regions
Elfar Torarinsson, Zizhen Yao, Eric D Wiklund, et al.
Experimental Neurology
|
February 14, 2006
Identification of novel genes regulated in the developing human ventral mesencephalon
Jesper Roland Jørgensen, Bengt Juliusson, Karen Friis Henriksen, et al.
Gene
|
May 30, 2002
Genomic structure, chromosome mapping and expression analysis of the human AVIL gene, and its exclusion as a candidate for locus for inflammatory bowel disease at 12q13-14 (IBD2)
Zeynep Tümer, Peter J P Croucher, Lars Riff Jensen, et al.
Nucleic Acids Research
|
April 19, 2012
Sequence and expression analysis of gaps in human chromosome 20
Sheroy Minocherhomji, Stefan Seemann, Yuan Mang, et al.
European Journal of Human Genetics : EJHG
|
July 18, 2013
The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2
Lusine Nazaryan, Eunice G Stefanou, Claus Hansen, et al.
Journal of Medical Genetics
|
June 7, 2007
Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2
Linda P Jakobsen, Reinhard Ullmann, Steen B Christensen, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Plos One
|
May 3, 2014
Influence of oxygen tension on dopaminergic differentiation of human fetal stem cells of midbrain and forebrain origin
Christina Krabbe, Sara Thornby Bak, Pia Jensen, et al.
Journal of Molecular Neuroscience : MN
|
March 5, 2009
Characterization of Meteorin--an evolutionary conserved neurotrophic factor
Jesper Roland Jørgensen, Lachlan Thompson, Lone Fjord-Larsen, et al.
Antibiotics (Basel, Switzerland)
|
April 30, 2021
The Effect of Colistin Treatment on the Selection of Colistin-Resistant <i>Escherichia coli</i> in Weaner Pigs
Shahana Ahmed, Claus Hansen, Ane Laursen Dahlkilde, et al.
American Journal of Medical Genetics
|
July 13, 2002
HOXD13 polyalanine tract expansion in classical synpolydactyly type Vordingborg
Klaus Wilbrandt Kjaer, Jess Hedeboe, Merete Bugge, et al.
Genome Research
|
December 22, 2007
Comparative genomics beyond sequence-based alignments: RNA structures in the ENCODE regions
Elfar Torarinsson, Zizhen Yao, Eric D Wiklund, et al.
Experimental Neurology
|
February 14, 2006
Identification of novel genes regulated in the developing human ventral mesencephalon
Jesper Roland Jørgensen, Bengt Juliusson, Karen Friis Henriksen, et al.
Gene
|
May 30, 2002
Genomic structure, chromosome mapping and expression analysis of the human AVIL gene, and its exclusion as a candidate for locus for inflammatory bowel disease at 12q13-14 (IBD2)
Zeynep Tümer, Peter J P Croucher, Lars Riff Jensen, et al.
Nucleic Acids Research
|
April 19, 2012
Sequence and expression analysis of gaps in human chromosome 20
Sheroy Minocherhomji, Stefan Seemann, Yuan Mang, et al.
European Journal of Human Genetics : EJHG
|
July 18, 2013
The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2
Lusine Nazaryan, Eunice G Stefanou, Claus Hansen, et al.
Journal of Medical Genetics
|
June 7, 2007
Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2
Linda P Jakobsen, Reinhard Ullmann, Steen B Christensen, et al.
Page
of 3