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Nature, ISSN 0028-0836, 2013, Volume 504, Issue 7480, pp. 456 - 459
Journal Article
Current Biology, ISSN 0960-9822, 05/2018, Volume 28, Issue 9, pp. R567 - R569
While a ciliated organizer generates vertebrate left–right asymmetry, most invertebrates lack an organizer and instead utilize a myosin-based mechanism. A... 
EMBRYO | LATERALITY | FLUID | NODAL CILIA | ELEGANS | BIOCHEMISTRY & MOLECULAR BIOLOGY | UNCONVENTIONAL MYOSIN | HANDEDNESS | FLOW | DROSOPHILA | CELL BIOLOGY | Vertebrates | Myosins | Animals | Cilia | Muscle proteins | Myosin
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2016, Volume 1454, pp. 123 - 147
Cilia play a key role in the determination of the left-right axis in vertebrates by generating and sensing flow of extraembryonic fluid at the left-right... 
Nodal cilia | Kupffer’s vesicle | Cilium | GECI | Phenotype | Animals | Biological Transport | Microscopy | Calcium - metabolism | Zebrafish - metabolism | Embryo, Nonmammalian | Calcium Signaling | Cilia - metabolism | Microscopy, Fluorescence
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 2/2012, Volume 109, Issue 6, pp. 2021 - 2026
Journal Article
Journal Article
Annual Review of Genetics, ISSN 0066-4197, 11/2013, Volume 47, Issue 1, pp. 353 - 376
Once obscure, the cilium has come into the spotlight during the past decade. It is now clear that aside from generating locomotion by motile cilia, both motile... 
left-right asymmetry | zebrafish | polycystic kidney disease | intraflagellar transport | Joubert syndrome | heterotaxy | Heterotaxy | Zebrafish | Intraflagellar transport | Left-right asymmetry | Polycystic kidney disease | INTRAFLAGELLAR TRANSPORT PROTEINS | EXOME CAPTURE | POLYCYSTIC KIDNEY-DISEASE | PLANAR CELL POLARITY | OF-FUNCTION MUTATIONS | ZINC-FINGER NUCLEASES | JOUBERT-SYNDROME | GENETICS & HEREDITY | BARDET-BIEDL-SYNDROME | INNER DYNEIN ARMS | MOTILE CILIA | Cilia - physiology | Polycystic Kidney Diseases - genetics | Flagella - physiology | Ciliary Motility Disorders - physiopathology | Heterotaxy Syndrome - genetics | Heterotaxy Syndrome - physiopathology | Humans | Homeostasis | Polycystic Kidney, Autosomal Recessive - physiopathology | Cerebellum - abnormalities | Polycystic Kidney, Autosomal Recessive - genetics | Cerebellar Diseases - physiopathology | Polycystic Kidney Diseases - physiopathology | Retinitis Pigmentosa | Polycystic Kidney, Autosomal Dominant - genetics | Cilia - ultrastructure | Kidney Diseases, Cystic - genetics | Bardet-Biedl Syndrome - genetics | Disease Models, Animal | Encephalocele - genetics | Kidney Diseases, Cystic - physiopathology | Nervous System - cytology | Flagella - ultrastructure | Retina - physiopathology | Abnormalities, Multiple | Bardet-Biedl Syndrome - physiopathology | Eye Abnormalities - genetics | Encephalocele - physiopathology | Molecular Motor Proteins - physiology | Animals | Cerebellar Diseases - genetics | DNA Repair | Retina - abnormalities | Eye Abnormalities - physiopathology | Polycystic Kidney, Autosomal Dominant - physiopathology | DNA Damage | Kidney Diseases, Cystic - congenital | Cell Movement | Ciliary Motility Disorders - genetics | Physiological aspects | Amino acid sequence | Genetic aspects | Research | Cilia and ciliary motion
Journal Article
Annual Review of Genetics, ISSN 0066-4197, 01/2013, Volume 47, pp. 353 - 353
Once obscure, the cilium has come into the spotlight during the past decade. It is now clear that aside from generating locomotion by motile cilia, both motile... 
Journal Article
Annual Review of Genetics, ISSN 0066-4197, 01/2013, Volume 47, p. 353
  Once obscure, the cilium has come into the spotlight during the past decade. It is now clear that aside from generating locomotion by motile cilia, both... 
Proteins | Homeostasis | Genetics | Biology | Cells
Journal Article