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Neuromuscular Disorders : NMD
|
February 6, 2026
Preemptive immunotherapy for fetal acetylcholine receptor antibody disorder (FARAD): from recurrent pregnancy losses to a healthy infant - a case report
Stefan Verlohren, Christof Dame, Beate Mayer, et al.
Aorta (Stamford, Conn.)
|
January 23, 2016
Indomethacin Prevents the Progression of Thoracic Aortic Aneurysm in Marfan Syndrome Mice
Gao Guo, Claus-Eric Ott, Johannes Grünhagen, et al.
Journal of Vascular Surgery
|
January 9, 2013
The fibrillin-1 hypomorphic mgR/mgR murine model of Marfan syndrome shows severe elastolysis in all segments of the aorta
Simon Schwill, Philipp Seppelt, Johannes Grünhagen, et al.
BMC Genomics
|
March 26, 2011
Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing
Marten Jäger, Claus-Eric Ott, Johannes Grünhagen, et al.
Scientific Reports
|
December 10, 2017
BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
Isabelle Schreiber, Gina Dörpholz, Claus-Eric Ott, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 5, 2009
Promiscuous and depolarization-induced immediate-early response genes are induced by mechanical strain of osteoblasts
Claus-Eric Ott, Sebastian Bauer, Thomas Manke, et al.
Journal of Medical Genetics
|
June 22, 2012
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
Claus Eric Ott, Hendrikje Hein, Silke Lohan, et al.
Human Molecular Genetics
|
October 27, 2012
Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice
Gao Guo, Begoña Muñoz-García, Claus-Eric Ott, et al.
Bone
|
May 21, 2013
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1
Claus-Eric Ott, Björn Fischer, Phillipe Schröter, et al.
Scientific Reports
|
August 21, 2019
Evaluation of the role of STAP1 in Familial Hypercholesterolemia
Magdalena Danyel, Claus-Eric Ott, Thomas Grenkowitz, et al.
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of 5
Search research articles
Search
Showing results (11-20 of 42) with videos related to
Sort By:
Page
of 5
Neuromuscular Disorders : NMD
|
February 6, 2026
Preemptive immunotherapy for fetal acetylcholine receptor antibody disorder (FARAD): from recurrent pregnancy losses to a healthy infant - a case report
Stefan Verlohren, Christof Dame, Beate Mayer, et al.
Aorta (Stamford, Conn.)
|
January 23, 2016
Indomethacin Prevents the Progression of Thoracic Aortic Aneurysm in Marfan Syndrome Mice
Gao Guo, Claus-Eric Ott, Johannes Grünhagen, et al.
Journal of Vascular Surgery
|
January 9, 2013
The fibrillin-1 hypomorphic mgR/mgR murine model of Marfan syndrome shows severe elastolysis in all segments of the aorta
Simon Schwill, Philipp Seppelt, Johannes Grünhagen, et al.
BMC Genomics
|
March 26, 2011
Composite transcriptome assembly of RNA-seq data in a sheep model for delayed bone healing
Marten Jäger, Claus-Eric Ott, Johannes Grünhagen, et al.
Scientific Reports
|
December 10, 2017
BMPs as new insulin sensitizers: enhanced glucose uptake in mature 3T3-L1 adipocytes via PPARγ and GLUT4 upregulation
Isabelle Schreiber, Gina Dörpholz, Claus-Eric Ott, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
March 5, 2009
Promiscuous and depolarization-induced immediate-early response genes are induced by mechanical strain of osteoblasts
Claus-Eric Ott, Sebastian Bauer, Thomas Manke, et al.
Journal of Medical Genetics
|
June 22, 2012
Microduplications upstream of MSX2 are associated with a phenocopy of cleidocranial dysplasia
Claus Eric Ott, Hendrikje Hein, Silke Lohan, et al.
Human Molecular Genetics
|
October 27, 2012
Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice
Gao Guo, Begoña Muñoz-García, Claus-Eric Ott, et al.
Bone
|
May 21, 2013
Severe neuronopathic autosomal recessive osteopetrosis due to homozygous deletions affecting OSTM1
Claus-Eric Ott, Björn Fischer, Phillipe Schröter, et al.
Scientific Reports
|
August 21, 2019
Evaluation of the role of STAP1 in Familial Hypercholesterolemia
Magdalena Danyel, Claus-Eric Ott, Thomas Grenkowitz, et al.
Page
of 5