[HTML][HTML] Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - eLife, 2015 - zora.uzh.ch
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
[PDF][PDF] Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - idekerlab.ucsd.edu
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - eLife, 2015 - experts.umn.edu
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
[PDF][PDF] Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - 2015 - Citeseer
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
[PDF][PDF] Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
JL Silhavy - eLife - core.ac.uk
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
[PDF][PDF] Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - openaccessrepository.it
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - Elife, 2015 - europepmc.org
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - ELIFE, 2015 - koasas.kaist.ac.kr
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
[PDF][PDF] Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
S Roosing, M Hofree, S Kim, E Scott, B Copeland… - academia.edu
Defective primary ciliogenesis or cilium stability forms the basis of human ciliopathies,
including Joubert syndrome (JS), with defective cerebellar vermis development. We …
including Joubert syndrome (JS), with defective cerebellar vermis development. We …