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Journal Article
Combustion and Flame, ISSN 0010-2180, 2011, Volume 158, Issue 8, pp. 1542 - 1552
Oxyfuel combustion is a technology for Carbon Capture & Storage from coal fired power plants. One drawback is the large necessary amount of recirculation of... 
Recirculation rate | CSNB | Oxyfuel | Experiments | Natural gas | ENGINEERING, CHEMICAL | THERMODYNAMICS | ENGINEERING, MULTIDISCIPLINARY | ENERGY & FUELS | TECHNOLOGY | ENGINEERING, MECHANICAL | Reduction | Furnaces | Flame temperature | Controlled atmospheres | Fuel consumption | Combustion | Flue gases
Journal Article
Advances in Experimental Medicine and Biology, ISSN 0065-2598, 2018, Volume 1085, pp. 61 - 64
In congenital stationary night blindness (CSNB), there is a defect in rod photoreceptor signal transmission. This disorder of night vision is non-progressive.... 
X-linked | Congenital stationary night blindness | CSNB | MEDICINE, RESEARCH & EXPERIMENTAL | OPHTHALMOLOGY | GENETICS & HEREDITY | CELL BIOLOGY
Journal Article
Progress in Retinal and Eye Research, ISSN 1350-9462, 03/2015, Volume 45, pp. 58 - 110
Congenital stationary night blindness (CSNB) refers to a group of genetically and clinically heterogeneous retinal disorders. Seventeen different genes with... 
Animal models | Prevalence | Fundus albipunctatus | Oguchi disease | Molecular genetics | Diagnostics | Pathophysiology | Protein function | Schubert-Bornschein | Congenital stationary night blindness (CSNB) | MELANOMA-ASSOCIATED RETINOPATHY | CALCIUM-DEPENDENT INACTIVATION | COMPOUND HETEROZYGOUS MUTATION | MIZUO-NAKAMURA PHENOMENON | ON-BIPOLAR CELLS | LEUCINE-RICH REPEAT | PRIMATE PHOTOPIC ELECTRORETINOGRAM | SCANNING LASER OPHTHALMOSCOPY | OPHTHALMOLOGY | 11-CIS-RETINOL DEHYDROGENASE GENE | RETINITIS PUNCTATA ALBESCENS | Humans | Eye Diseases, Hereditary - diagnosis | Myopia - diagnosis | Genetic Diseases, X-Linked - genetics | Myopia - therapy | Eye Proteins - genetics | Night Blindness - genetics | Night Blindness - therapy | Genetic Diseases, X-Linked - physiopathology | Disease Models, Animal | Electroretinography | Eye Diseases, Hereditary - physiopathology | Genetic Association Studies | Night Blindness - diagnosis | Genotype | Genetic Diseases, X-Linked - diagnosis | Eye Diseases, Hereditary - genetics | Myopia - genetics | Phenotype | Animals | Myopia - physiopathology | Night Blindness - physiopathology | Eye Diseases, Hereditary - therapy | Mutation | Genetic Diseases, X-Linked - therapy | Genetic Therapy - methods | Proteins | Genetic research | Genetic aspects | Genetic disorders | Analysis | Prevalence studies (Epidemiology)
Journal Article
Documenta Ophthalmologica, ISSN 0012-4486, 8/2018, Volume 137, Issue 1, pp. 57 - 62
Journal Article
ZDRAVNISKI VESTNIK-SLOVENIAN MEDICAL JOURNAL, ISSN 1318-0347, 06/2012, Volume 81, pp. I16 - I28
Purpose: Congenital stationary night blindness (CSNB) is a group of retinal disorders with diverse clinical characteristics. The most common types are complete... 
incomplete CSNB | PHOTOPIC ELECTRORETINOGRAM | FORM | CLINICAL ELECTRORETINOGRAPHY | RESPONSES | MEDICINE, GENERAL & INTERNAL | complete CSNB | FUNDUS-ALBIPUNCTATUS | GENE | ELECTROPHYSIOLOGY | children | electroretinogram | ON-OFF ERG | ELECTRODE | MUTATIONS | CSNB | night blindness
Journal Article
International Journal of Developmental Neuroscience, ISSN 0736-5748, 12/2006, Volume 24, Issue 8, pp. 524 - 525
Journal Article
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, ISSN 0721-832X, 04/2019, Volume 257, Issue 6, pp. 1207 - 1215
To assess the pupil light response (PLR) to chromatic stimulation in patients with different types of X-linked congenital stationary night blindness (CSNB).... 
PUPILLARY CONSTRICTION | RESPONSES DRIVEN | LIGHT RESPONSES | Pupillography | MELANOPSIN | MOUSE | Night blindness | NYCTALOPIN | CACNA1F | NYX | CHANNEL | GENE | Retinal degeneration | OPHTHALMOLOGY | CSNB | MUTATIONS | Care and treatment | Genetic disorders | Ophthalmology | Ganglion | Analysis | Retinal ganglion cells | Blindness | Bipolar cells | Retina | Nyctalopia | Ganglion cells | Stationary night blindness
Journal Article
Journal Article
Methods in molecular biology (Clifton, N.J.), ISSN 1064-3745, 2013, Volume 963, pp. 319 - 326
Arrayed primer extension (APEX) is a microarray-based genotyping method that enables to simultaneously analyze hundreds of known mutations in the genome.... 
Night blindness | Mutation analysis | CSNB | Calcium | APEX | Microarray | DNA Primers - genetics | DNA Mutational Analysis | Oligonucleotide Array Sequence Analysis - methods | Night Blindness - genetics | Humans | Polymerase Chain Reaction
Journal Article