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The European Respiratory Journal
|
December 25, 2009
Effects of pentobarbital on upper airway patency during sleep
M Eikermann, D J Eckert, N L Chamberlin, et al.
Human Molecular Genetics
|
August 17, 2005
ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies
Wojciech Wiszniewski, Charles M Zaremba, Alexander N Yatsenko, et al.
Journal of Applied Genetics
|
May 11, 2010
Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic features
J Bogdanowicz, B Pawłowska, A Ilnicka, et al.
International Immunopharmacology
|
March 17, 2009
Decreased inflammation and augmented expression of trophic factors correlate with MOG-induced neuroprotection of the injured nigrostriatal system in the murine MPTP model of Parkinson's disease
I Kurkowska-Jastrzebska, E Bałkowiec-Iskra, A Ciesielska, et al.
Nucleic Acids Research
|
January 1, 2017
Restriction endonuclease AgeI is a monomer which dimerizes to cleave DNA
Giedre Tamulaitiene, Virginija Jovaisaite, Gintautas Tamulaitis, et al.
The International Journal of Medical Robotics + Computer Assisted Surgery : MRCAS
|
May 13, 2017
Robotic guided waterjet cutting technique for high tibial dome osteotomy: A pilot study
Eduardo M Suero, Ralph Westphal, David Zaremba, et al.
Nucleic Acids Research
|
October 3, 2008
Central base pair flipping and discrimination by PspGI
Roman H Szczepanowski, Michael A Carpenter, Honorata Czapinska, et al.
Nature Neuroscience
|
May 22, 2012
Hepatocyte growth factor mediates mesenchymal stem cell–induced recovery in multiple sclerosis models
Lianhua Bai, Donald P Lennon, Arnold I Caplan, et al.
Environmental Microbiology
|
October 15, 2013
Productivity and salinity structuring of the microplankton revealed by comparative freshwater metagenomics
Alexander Eiler, Katarzyna Zaremba-Niedzwiedzka, Manuel Martínez-García, et al.
Journal of Applied Genetics
|
March 2, 2017
A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene
Janusz G Zimowski, Jacek Pilch, Magdalena Pawelec, et al.
Page
of 97
Search research articles
Search
Showing results (561-570 of 967) with videos related to
Sort By:
Page
of 97
The European Respiratory Journal
|
December 25, 2009
Effects of pentobarbital on upper airway patency during sleep
M Eikermann, D J Eckert, N L Chamberlin, et al.
Human Molecular Genetics
|
August 17, 2005
ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies
Wojciech Wiszniewski, Charles M Zaremba, Alexander N Yatsenko, et al.
Journal of Applied Genetics
|
May 11, 2010
Subtelomeric rearrangements in Polish subjects with intellectual disability and dysmorphic features
J Bogdanowicz, B Pawłowska, A Ilnicka, et al.
International Immunopharmacology
|
March 17, 2009
Decreased inflammation and augmented expression of trophic factors correlate with MOG-induced neuroprotection of the injured nigrostriatal system in the murine MPTP model of Parkinson's disease
I Kurkowska-Jastrzebska, E Bałkowiec-Iskra, A Ciesielska, et al.
Nucleic Acids Research
|
January 1, 2017
Restriction endonuclease AgeI is a monomer which dimerizes to cleave DNA
Giedre Tamulaitiene, Virginija Jovaisaite, Gintautas Tamulaitis, et al.
The International Journal of Medical Robotics + Computer Assisted Surgery : MRCAS
|
May 13, 2017
Robotic guided waterjet cutting technique for high tibial dome osteotomy: A pilot study
Eduardo M Suero, Ralph Westphal, David Zaremba, et al.
Nucleic Acids Research
|
October 3, 2008
Central base pair flipping and discrimination by PspGI
Roman H Szczepanowski, Michael A Carpenter, Honorata Czapinska, et al.
Nature Neuroscience
|
May 22, 2012
Hepatocyte growth factor mediates mesenchymal stem cell–induced recovery in multiple sclerosis models
Lianhua Bai, Donald P Lennon, Arnold I Caplan, et al.
Environmental Microbiology
|
October 15, 2013
Productivity and salinity structuring of the microplankton revealed by comparative freshwater metagenomics
Alexander Eiler, Katarzyna Zaremba-Niedzwiedzka, Manuel Martínez-García, et al.
Journal of Applied Genetics
|
March 2, 2017
A rare subclinical or mild type of Becker muscular dystrophy caused by a single exon 48 deletion of the dystrophin gene
Janusz G Zimowski, Jacek Pilch, Magdalena Pawelec, et al.
Page
of 97