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Human Mutation
|
March 25, 2010
EYS is a major gene for rod-cone dystrophies in France
Isabelle Audo, José-Alain Sahel, Saddek Mohand-Saïd, et al.
Investigative Ophthalmology & Visual Science
|
March 19, 2010
Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa
Mai M Abd El-Aziz, Ciara A O'Driscoll, Rebecca S Kaye, et al.
Stem Cells (Dayton, Ohio)
|
July 18, 2015
Cytostatic Effect of Repeated Exposure to Simvastatin: A Mechanism for Chronic Myotoxicity Revealed by the Use of Mesodermal Progenitors Derived from Human Pluripotent Stem Cells
Delphine Peric, Isabel Barragan, Karine Giraud-Triboult, et al.
Journal of Affective Disorders
|
October 2, 2012
Strong effects of environmental factors on prevalence and course of major depressive disorder are not moderated by 5-HTTLPR polymorphisms in a large Dutch sample
Wouter J Peyrot, Christel M Middeldorp, Rick Jansen, et al.
Nature Genetics
|
October 7, 2008
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
Mai M Abd El-Aziz, Isabel Barragan, Ciara A O'Driscoll, et al.
BMC Genomics
|
October 6, 2014
Genetic and epigenetic regulation of gene expression in fetal and adult human livers
Marc Jan Bonder, Silva Kasela, Mart Kals, et al.
The Journal of Clinical Investigation
|
May 1, 2026
Conventional type-1 DC density is associated with checkpoint inhibitor response across multiple types of cancer
Alvaro Lopez-Janeiro, José González-Gomariz, Fadi Issa, et al.
The Lancet. Respiratory Medicine
|
August 14, 2018
Epigenetic prediction of response to anti-PD-1 treatment in non-small-cell lung cancer: a multicentre, retrospective analysis
Michäel Duruisseaux, Anna Martínez-Cardús, Maria E Calleja-Cervantes, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Human Mutation
|
March 25, 2010
EYS is a major gene for rod-cone dystrophies in France
Isabelle Audo, José-Alain Sahel, Saddek Mohand-Saïd, et al.
Investigative Ophthalmology & Visual Science
|
March 19, 2010
Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa
Mai M Abd El-Aziz, Ciara A O'Driscoll, Rebecca S Kaye, et al.
Stem Cells (Dayton, Ohio)
|
July 18, 2015
Cytostatic Effect of Repeated Exposure to Simvastatin: A Mechanism for Chronic Myotoxicity Revealed by the Use of Mesodermal Progenitors Derived from Human Pluripotent Stem Cells
Delphine Peric, Isabel Barragan, Karine Giraud-Triboult, et al.
Journal of Affective Disorders
|
October 2, 2012
Strong effects of environmental factors on prevalence and course of major depressive disorder are not moderated by 5-HTTLPR polymorphisms in a large Dutch sample
Wouter J Peyrot, Christel M Middeldorp, Rick Jansen, et al.
Nature Genetics
|
October 7, 2008
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa
Mai M Abd El-Aziz, Isabel Barragan, Ciara A O'Driscoll, et al.
BMC Genomics
|
October 6, 2014
Genetic and epigenetic regulation of gene expression in fetal and adult human livers
Marc Jan Bonder, Silva Kasela, Mart Kals, et al.
The Journal of Clinical Investigation
|
May 1, 2026
Conventional type-1 DC density is associated with checkpoint inhibitor response across multiple types of cancer
Alvaro Lopez-Janeiro, José González-Gomariz, Fadi Issa, et al.
The Lancet. Respiratory Medicine
|
August 14, 2018
Epigenetic prediction of response to anti-PD-1 treatment in non-small-cell lung cancer: a multicentre, retrospective analysis
Michäel Duruisseaux, Anna Martínez-Cardús, Maria E Calleja-Cervantes, et al.
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of 3