X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (6867) 6867
Book Chapter (25) 25
Book / eBook (6) 6
Dissertation (3) 3
Magazine Article (2) 2
Web Resource (2) 2
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (5191) 5191
humans (3036) 3036
cilia - metabolism (2758) 2758
cilia (2692) 2692
cell biology (2167) 2167
mice (1855) 1855
cilia - physiology (1414) 1414
male (1184) 1184
biochemistry & molecular biology (1124) 1124
proteins (1023) 1023
signal transduction (1019) 1019
female (1009) 1009
cilia - ultrastructure (988) 988
mutation (833) 833
primary cilia (755) 755
cells (748) 748
research (742) 742
intraflagellar transport (705) 705
protein (698) 698
cells, cultured (695) 695
developmental biology (658) 658
multidisciplinary sciences (622) 622
cilia - drug effects (613) 613
primary cilium (612) 612
physiological aspects (596) 596
expression (578) 578
genetics & heredity (521) 521
research article (515) 515
cilia - genetics (511) 511
cell line (508) 508
ciliogenesis (501) 501
biology (478) 478
cilia - pathology (470) 470
gene (460) 460
models, biological (459) 459
molecular sequence data (456) 456
gene expression (453) 453
genetic aspects (449) 449
localization (449) 449
rats (446) 446
analysis (433) 433
hedgehog proteins - metabolism (422) 422
microtubules - metabolism (412) 412
phenotype (409) 409
microscopy, electron (408) 408
neurosciences (406) 406
protein transport (406) 406
amino acid sequence (396) 396
mutations (393) 393
mice, knockout (392) 392
calcium - metabolism (387) 387
epithelial cells - metabolism (387) 387
flagella (386) 386
mouse (384) 384
immunohistochemistry (383) 383
flagella - metabolism (376) 376
polycystic kidney-disease (375) 375
disease (367) 367
epithelial cells (360) 360
mice, inbred c57bl (354) 354
respiratory system (352) 352
neurons (348) 348
microtubules (341) 341
cilia and ciliary motion (337) 337
physiology (337) 337
sense organs (335) 335
dyneins - metabolism (333) 333
protein binding (328) 328
left-right asymmetry (317) 317
phosphorylation (315) 315
zebrafish (309) 309
genes (308) 308
medicine (308) 308
adult (307) 307
identification (305) 305
complex (298) 298
epithelium (295) 295
activation (291) 291
disease models, animal (291) 291
dynein (290) 290
signal transduction - physiology (290) 290
gene expression regulation, developmental (289) 289
genetics (282) 282
time factors (277) 277
calcium (276) 276
cell differentiation (275) 275
science (271) 271
transport (271) 271
tubulin - metabolism (270) 270
life sciences (267) 267
biological transport (264) 264
membrane proteins - metabolism (261) 261
motility (261) 261
cell cycle (251) 251
differentiation (247) 247
proteins - metabolism (246) 246
morphogenesis (242) 242
bardet-biedl-syndrome (240) 240
cell proliferation (240) 240
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (6807) 6807
Japanese (58) 58
German (28) 28
Russian (25) 25
French (21) 21
Chinese (13) 13
Italian (8) 8
Spanish (5) 5
Polish (4) 4
Norwegian (3) 3
Czech (2) 2
Korean (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature genetics, ISSN 1546-1718, 2009, Volume 41, Issue 9, pp. 1027 - 1031
The primary cilium is an antenna-like structure that protrudes from the cell surface of quiescent/ differentiated cells and participates in extracellular... 
NETWORK | INOSITOL-POLYPHOSPHATE 5-PHOSPHATASE | POLYCYSTIC KIDNEY-DISEASE | BIOLOGY | GENETICS & HEREDITY | DISORDERS | PROTEINS | FIBROBLASTS | Humans | Fluorescent Dyes - metabolism | Culture Media, Serum-Free | Male | Phosphatidylinositol 3-Kinases - metabolism | Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Fibroblasts - ultrastructure | Obesity - genetics | Embryo, Mammalian - metabolism | Intellectual Disability - genetics | Indoles - metabolism | Tubulin - metabolism | Cell Nucleus - metabolism | Transfection | Mice, Mutant Strains | Cilia - ultrastructure | Bardet-Biedl Syndrome - genetics | Chromones - pharmacology | Microsatellite Repeats | Fibroblasts - metabolism | Genetic Linkage | Cell Line | Green Fluorescent Proteins - metabolism | Phosphoric Monoester Hydrolases - genetics | Cilia - pathology | Receptor, Platelet-Derived Growth Factor alpha - metabolism | Fluorescent Antibody Technique, Direct | Retinal Degeneration - genetics | Cells, Cultured | Enzyme Inhibitors - pharmacology | Morpholines - pharmacology | Mice, Transgenic | Genetic Markers | Cilia - metabolism | Cilia - genetics | Pigment Epithelium of Eye - metabolism | Animals | Embryo, Mammalian - cytology | Signal Transduction - physiology | Fibroblasts - cytology | Mice | Polymorphism, Single Nucleotide | Mutation | Pigment Epithelium of Eye - cytology | Penis - abnormalities | Gene mutations | Genetic aspects | Cellular signal transduction | Research | Health aspects | Risk factors | Brain diseases | Proteins | Tissue | Scanning electron microscopy | Transmission electron microscopy | Cysts | Rodents | Cell division
Journal Article
Journal Article
Annual review of cell and developmental biology, ISSN 1081-0706, 11/2011, Volume 27, Issue 1, pp. 513 - 537
Journal Article
Journal Article
The EMBO journal, ISSN 1460-2075, 2009, Volume 28, Issue 3, pp. 183 - 192
Journal Article
PLoS genetics, ISSN 1553-7404, 2015, Volume 11, Issue 10, p. e1005575
Ciliopathies are a group of human disorders caused by dysfunction of primary cilia, ubiquitous microtubule-based organelles involved in transduction of... 
COMPLEX | TRANSITION ZONE | CILIARY MEMBRANE | USHER-SYNDROME | GENES | GENETICS & HEREDITY | MUTATIONS | JOUBERT SYNDROME | OUTER SEGMENT | INTRAFLAGELLAR TRANSPORT | PRIMARY CILIUM | Abnormalities, Multiple - metabolism | Abnormalities, Multiple - pathology | Polycystic Kidney Diseases - genetics | Retina - metabolism | Microtubule-Associated Proteins - genetics | Microtubule-Associated Proteins - metabolism | Humans | Mixed Function Oxygenases - metabolism | rab GTP-Binding Proteins - genetics | Cerebellum - abnormalities | Encephalocele - metabolism | Gene Knockdown Techniques | Polycystic Kidney Diseases - pathology | Retinitis Pigmentosa | Kidney Diseases, Cystic - genetics | Nuclear Proteins - genetics | Eye Abnormalities - metabolism | Abnormalities, Multiple - genetics | Encephalocele - genetics | rab GTP-Binding Proteins - metabolism | Polycystic Kidney Diseases - metabolism | Cilia - pathology | Signal Transduction | Cerebellum - metabolism | Nuclear Proteins - metabolism | Zebrafish | Eye Abnormalities - genetics | Cilia - metabolism | Protein Transport - genetics | Cerebellum - pathology | Cilia - genetics | Kidney Diseases, Cystic - pathology | Proteins - genetics | Kidney Diseases, Cystic - metabolism | Animals | Ciliary Motility Disorders - pathology | Proteins - metabolism | Encephalocele - pathology | Eye Abnormalities - pathology | Retina - abnormalities | Ciliary Motility Disorders - metabolism | Mutation | Mixed Function Oxygenases - genetics | Retina - pathology | Ciliary Motility Disorders - genetics | Physiological aspects | Phenotype | Cell organelles | Cilia and ciliary motion | Analysis | Research & development | Proteins | R&D | Signal transduction | Genotype & phenotype | Photoreceptors | Grants | Localization | Experiments | Defects
Journal Article