X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (12) 12
animals (10) 10
mutation (8) 8
genetic structures (7) 7
humans (7) 7
mice (7) 7
proteins (7) 7
sense organs (7) 7
mice, inbred c57bl (6) 6
article (5) 5
gene (5) 5
mice, knockout (5) 5
photoreceptors (5) 5
retina (5) 5
amino acid sequence (4) 4
blindness (4) 4
cells (4) 4
gene mutations (4) 4
genetic aspects (4) 4
genetics (4) 4
genetics & heredity (4) 4
heterozygote (4) 4
mouse model (4) 4
physiological aspects (4) 4
protein (4) 4
retinal degeneration (4) 4
signal transduction (4) 4
causes of (3) 3
cell biology (3) 3
cilia (3) 3
dominant retinitis-pigmentosa (3) 3
exons (3) 3
expression (3) 3
genetic disorders (3) 3
in-vivo (3) 3
membranes (3) 3
mglur6 (3) 3
molecular sequence data (3) 3
mutations (3) 3
neurosciences (3) 3
night blindness - genetics (3) 3
photoreceptor (3) 3
photoreceptor cells - metabolism (3) 3
report (3) 3
stationary night blindness (3) 3
amino acids - pharmacology (2) 2
analysis (2) 2
animal models (2) 2
articles (2) 2
biochemistry (2) 2
c-terminus (2) 2
channel (2) 2
chromosome mapping (2) 2
complete form (2) 2
cone electroretinogram (2) 2
degeneration (2) 2
depolarizing bipolar cell (2) 2
disease models, animal (2) 2
dog breeds (2) 2
electroretinogram (2) 2
eye diseases (2) 2
female (2) 2
gene expression (2) 2
intraflagellar transport protein (2) 2
localization (2) 2
membrane (2) 2
membrane proteins - chemistry (2) 2
membrane proteins - metabolism (2) 2
mice, transgenic (2) 2
models, biological (2) 2
morphogenesis (2) 2
mouse (2) 2
multidisciplinary sciences (2) 2
mutation, missense (2) 2
myopia - genetics (2) 2
neuroscience (2) 2
night blindness (2) 2
night blindness - physiopathology (2) 2
nyctalopin (2) 2
outer segment (2) 2
pedigree (2) 2
point mutation (2) 2
protein transport (2) 2
rds mutant mice (2) 2
research (2) 2
research article (2) 2
retinal bipolar cells (2) 2
retinal bipolar cells - physiology (2) 2
retinal rod photoreceptor cells - physiology (2) 2
rhodopsin - genetics (2) 2
rhodopsin - metabolism (2) 2
rich repeat protein (2) 2
rod outer segment membranes (2) 2
rod outer segments (2) 2
rodents (2) 2
synaptic-transmission (2) 2
trafficking (2) 2
trpm cation channels - genetics (2) 2
trpm cation channels - metabolism (2) 2
xanthenes - pharmacology (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The American Journal of Human Genetics, ISSN 0002-9297, 02/2012, Volume 90, Issue 2, pp. 331 - 339
Complete congenital stationary night blindness (cCSNB) is a clinically and genetically heterogeneous group of retinal disorders characterized by nonprogressive... 
COMPLETE FORM | LIGHT RESPONSE | CHANNEL | MGLUR6 | SYNAPTIC-TRANSMISSION | MOUSE MODEL | GENETICS & HEREDITY | NYCTALOPIN | RICH REPEAT PROTEIN | MUTATIONS | CONE ELECTRORETINOGRAM | Electroretinography - methods | Night Blindness - metabolism | Humans | Dark Adaptation - genetics | Retinal Rod Photoreceptor Cells - metabolism | Gene Knockdown Techniques - methods | Myopia - metabolism | Receptors, Metabotropic Glutamate - genetics | Retinal Bipolar Cells - physiology | Chromosome Mapping - methods | Genetic Diseases, X-Linked | Night Blindness - genetics | Retinal Bipolar Cells - metabolism | Eye Diseases, Hereditary | Signal Transduction | Mice, Inbred C57BL | Zebrafish | Mice, Inbred C3H | Myopia - genetics | Animals | Myopia - physiopathology | Pedigree | Night Blindness - physiopathology | Retinal Rod Photoreceptor Cells - physiology | Heterozygote | Mice | Receptors, G-Protein-Coupled - genetics | Mutation | Chromosome mapping | Usage | Gene mutations | Retinal bipolar cells | Causes of | Physiological aspects | Night blindness | Genetic aspects | Research | Analysis | Genetic disorders | Proteins | Rodents | Blindness | Gene expression | Cells | Index Medicus | Animal models | Antibodies | Insertion | stationary night blindness | Retina | Guanine nucleotide-binding protein | Electroretinograms | Depolarization | Signal transduction | Vision | Bipolar cells | Gene mapping | DNA sequencing | Report
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 05/2017, Volume 216, Issue 5, pp. 1489 - 1499
Journal Article
JOURNAL OF CELL BIOLOGY, ISSN 0021-9525, 05/2017, Volume 216, Issue 5, pp. 1489 - 1499
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 05/2017, Volume 216, Issue 5, p. 1489
The primary cilium is a highly conserved organelle housing specialized molecules responsible for receiving and processing extracellular signals. A recently... 
Physiological aspects | Cell interaction | Photoreceptors | Observations | Cilia and ciliary motion
Journal Article
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 12/2015, Volume 97, Issue 6, pp. 904 - 913
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2017, Volume 13, Issue 4, pp. e1006740 - e1006740
Arf4 is proposed to be a critical regulator of membrane protein trafficking in early secretory pathway. More recently, Arf4 was also implicated in regulating... 
ADP-RIBOSYLATION FACTOR | ROD PHOTORECEPTORS | C-TERMINUS | TRANSGENIC MOUSE | GENETICS & HEREDITY | MITOTIC SPINDLE | TRAFFICKING | OUTER SEGMENT | INTRAFLAGELLAR TRANSPORT PROTEIN | DOMINANT RETINITIS-PIGMENTOSA | PRIMARY CILIA | Sequence Deletion | Cilia - pathology | Kidney - pathology | Nucleotide Motifs - genetics | Retinal Degeneration - genetics | Humans | Pancreas, Exocrine - pathology | Cilia - genetics | Kidney Diseases, Cystic - pathology | Mice, Knockout | Kidney - metabolism | Animals | Pancreas, Exocrine - growth & development | Photoreceptor Cells - metabolism | Kidney Diseases, Cystic - genetics | Mice | Photoreceptor Cells - pathology | Retinal Degeneration - pathology | ADP-Ribosylation Factors - genetics | Disease Models, Animal | Gene mutations | Retinal degeneration | Physiological aspects | Genetic aspects | Research | Risk factors | Membrane proteins | Funding | Colleges & universities | Retina | Biochemistry | Lethality | Assaying | Dehydrogenase | Proteins | Assembly | Obesity | Data acquisition | Abnormalities | Amino acid sequence | Electron microscopy | Organelles | Stem cells | Cytoskeleton | Mutation | Collecting duct | Kidney transplantation | Anomalies | Residues | Membranes | Retinitis pigmentosa | Amino acids | Cases (containers) | Rod outer segment membranes | Medical schools | Defects | Visual perception | Malfunctions | Specialization | Clonal deletion | Rodents | Degeneration | Pancreas | Cilia | Data processing | C-Terminus | Medicine | Vertebrates | Cell death | Hedgehog protein | Coiling | Blindness | Photoreceptors | Kidney diseases | Position (location) | Collapsin response mediator protein 2 | Index Medicus
Journal Article
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 06/2019, Volume 116, Issue 26, pp. 13087 - 13096
Journal Article
Journal of Neurophysiology, ISSN 0022-3077, 11/2012, Volume 108, Issue 9, pp. 2442 - 2451
Journal Article
The Journal of neuroscience : the official journal of the Society for Neuroscience, ISSN 0270-6474, 7/2011, Volume 31, Issue 27, pp. 10060 - 10066
Expression of channels to specific neuronal sites can critically impact their function and regulation. Currently, the molecular mechanisms underlying this... 
TRPM1 | depolarizing bipolar cell | retina | dendritic targeting | nyctalopin
Journal Article