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Thomas Langmann

Showing results (121-130 of 162) with videos related to

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Journal of Neuroinflammation|January 9, 2014
Translocator protein (18 kDa) (TSPO) is expressed in reactive retinal microglia and modulates microglial inflammation and phagocytosisMarcus Karlstetter, Caroline Nothdurfter, Alexander Aslanidis, et al.
Scientific Reports|February 19, 2016
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Kristof Van Schil, Marcus Karlstetter, Alexander Aslanidis, et al.
Atherosclerosis|February 5, 2013
Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locusChrista Zollbrecht, Martina Grassl, Sabine Fenk, et al.
Brain : a Journal of Neurology|March 15, 2013
Immune cells perturb axons and impair neuronal survival in a mouse model of infantile neuronal ceroid lipofuscinosisJanos Groh, Thomas G Kühl, Chi Wang Ip, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|March 16, 2020
Major Predictive Factors for Progression of Early to Late Age-Related Macular DegenerationVasilena Sitnilska, Eveline Kersten, Lebriz Altay, et al.
The Journal of Biological Chemistry|February 13, 2002
Identification of sterol-independent regulatory elements in the human ATP-binding cassette transporter A1 promoter: role of Sp1/3, E-box binding factors, and an oncostatin M-responsive elementThomas Langmann, Mustafa Porsch-Ozcürümez, Susanne Heimerl, et al.
Experimental Eye Research|September 26, 2017
Regulated efflux of photoreceptor outer segment-derived cholesterol by human RPE cellsFederica Storti, Gabriele Raphael, Vera Griesser, et al.
Frontiers in Cellular Neuroscience|October 26, 2019
Loss of IL-10 Promotes Differentiation of Microglia to a M1 PhenotypeBjörn Laffer, Dirk Bauer, Susanne Wasmuth, et al.
Frontiers in Immunology|August 15, 2018
The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 StatusMaren Kasper, Karoline Walscheid, Björn Laffer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 15, 2014
Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletionKristof Van Schil, Françoise Meire, Marcus Karlstetter, et al.
Pageof 17

Showing results (121-130 of 162) with videos related to

Sort By:
Pageof 17
Journal of Neuroinflammation|January 9, 2014
Translocator protein (18 kDa) (TSPO) is expressed in reactive retinal microglia and modulates microglial inflammation and phagocytosisMarcus Karlstetter, Caroline Nothdurfter, Alexander Aslanidis, et al.
Scientific Reports|February 19, 2016
Autosomal recessive retinitis pigmentosa with homozygous rhodopsin mutation E150K and non-coding cis-regulatory variants in CRX-binding regions of SAMD7Kristof Van Schil, Marcus Karlstetter, Alexander Aslanidis, et al.
Atherosclerosis|February 5, 2013
Expression pattern in human macrophages dependent on 9p21.3 coronary artery disease risk locusChrista Zollbrecht, Martina Grassl, Sabine Fenk, et al.
Brain : a Journal of Neurology|March 15, 2013
Immune cells perturb axons and impair neuronal survival in a mouse model of infantile neuronal ceroid lipofuscinosisJanos Groh, Thomas G Kühl, Chi Wang Ip, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|March 16, 2020
Major Predictive Factors for Progression of Early to Late Age-Related Macular DegenerationVasilena Sitnilska, Eveline Kersten, Lebriz Altay, et al.
The Journal of Biological Chemistry|February 13, 2002
Identification of sterol-independent regulatory elements in the human ATP-binding cassette transporter A1 promoter: role of Sp1/3, E-box binding factors, and an oncostatin M-responsive elementThomas Langmann, Mustafa Porsch-Ozcürümez, Susanne Heimerl, et al.
Experimental Eye Research|September 26, 2017
Regulated efflux of photoreceptor outer segment-derived cholesterol by human RPE cellsFederica Storti, Gabriele Raphael, Vera Griesser, et al.
Frontiers in Cellular Neuroscience|October 26, 2019
Loss of IL-10 Promotes Differentiation of Microglia to a M1 PhenotypeBjörn Laffer, Dirk Bauer, Susanne Wasmuth, et al.
Frontiers in Immunology|August 15, 2018
The Phenotype of Monocytes in Anterior Uveitis Depends on the HLA-B27 StatusMaren Kasper, Karoline Walscheid, Björn Laffer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 15, 2014
Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletionKristof Van Schil, Françoise Meire, Marcus Karlstetter, et al.
Pageof 17