Lista de obras -

An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes

artículo científico publicado en 2008

Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling

artículo científico publicado en 2010

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

artículo científico publicado en 2003

Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory cilia

artículo científico publicado en 2006

Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene

scientific journal article

Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling

artículo científico publicado en 2015

Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans

artículo científico publicado en 2013

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

scientific journal article

EFHC1, implicated in juvenile myoclonic epilepsy, functions at the cilium and synapse to modulate dopamine signaling

artículo científico publicado en 2019

Functional coordination of intraflagellar transport motors.

artículo científico publicado en 2005

Functional genomics of the cilium, a sensory organelle

scientific journal article

Functional interaction between phosducin-like protein 2 and cytosolic chaperonin is essential for cytoskeletal protein function and cell cycle progression

artículo científico publicado en 2007

Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins

artículo científico publicado en 2009

Identification of 526 conserved metazoan genetic innovations exposes a new role for cofactor E-like in neuronal microtubule homeostasis

artículo científico publicado en 2013

Identification of ciliary and ciliopathy genes in Caenorhabditis elegans through comparative genomics

artículo científico publicado en 2006

Localization of a Guanylyl Cyclase to Chemosensory Cilia Requires the Novel Ciliary MYND Domain Protein DAF-25 ⬇️

artículo científico publicado el 24 de noviembre de 2010

Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function

artículo científico publicado en 2007

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport

artículo científico publicado en 2004

MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis ⬇️

artículo científico publicado en 2011

MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone

artículo científico publicado en 2016

Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors

artículo científico publicado en 2006

Mutations in a Guanylate Cyclase GCY-35/GCY-36 Modify Bardet-Biedl Syndrome–Associated Phenotypes in Caenorhabditis elegans ⬇️

artículo científico publicado el 13 de octubre de 2011

Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome

artículo científico publicado en 2004

PhLP3 modulates CCT-mediated actin and tubulin folding via ternary complexes with substrates

artículo científico publicado en 2006

Role for intraflagellar transport in building a functional transition zone

scientific article published on 14 November 2018

Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components into distinct modules based on transport and phenotypic profiles

artículo científico publicado en 2007

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone

artículo científico publicado en 2011

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

artículo científico publicado en 2004

The WD repeat-containing protein IFTA-1 is required for retrograde intraflagellar transport.

artículo científico publicado en 2006

The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

artículo científico publicado en 2012

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

artículo científico publicado en 2006

The roles of evolutionarily conserved functional modules in cilia-related trafficking

artículo científico publicado en 2013

The sensory cilia of Caenorhabditis elegans

scientific article published on 08 March 2007

Lista de obras de

An essential role for DYF-11/MIP-T3 in assembling functional intraflagellar transport complexes

Bardet-Biedl syndrome-associated small GTPase ARL6 (BBS3) functions at or near the ciliary gate and modulates Wnt signaling

Basal body dysfunction is a likely cause of pleiotropic Bardet-Biedl syndrome

Caenorhabditis elegans DYF-2, an orthologue of human WDR19, is a component of the intraflagellar transport machinery in sensory cilia

Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease gene

Conserved Genetic Interactions between Ciliopathy Complexes Cooperatively Support Ciliogenesis and Ciliary Signaling

Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

EFHC1, implicated in juvenile myoclonic epilepsy, functions at the cilium and synapse to modulate dopamine signaling

Functional coordination of intraflagellar transport motors.

Functional genomics of the cilium, a sensory organelle

Functional interaction between phosducin-like protein 2 and cytosolic chaperonin is essential for cytoskeletal protein function and cell cycle progression

Functional interactions between the ciliopathy-associated Meckel syndrome 1 (MKS1) protein and two novel MKS1-related (MKSR) proteins

Identification of 526 conserved metazoan genetic innovations exposes a new role for cofactor E-like in neuronal microtubule homeostasis

Identification of ciliary and ciliopathy genes in Caenorhabditis elegans through comparative genomics

Localization of a Guanylyl Cyclase to Chemosensory Cilia Requires the Novel Ciliary MYND Domain Protein DAF-25 ⬇️

Loss of Bardet Biedl syndrome proteins causes defects in peripheral sensory innervation and function

Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport

MKS and NPHP modules cooperate to establish basal body/transition zone membrane associations and ciliary gate function during ciliogenesis ⬇️

MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone

Mechanism of transport of IFT particles in C. elegans cilia by the concerted action of kinesin-II and OSM-3 motors

Mutations in a Guanylate Cyclase GCY-35/GCY-36 Modify Bardet-Biedl Syndrome–Associated Phenotypes in Caenorhabditis elegans ⬇️

Mutations in a member of the Ras superfamily of small GTP-binding proteins causes Bardet-Biedl syndrome

PhLP3 modulates CCT-mediated actin and tubulin folding via ternary complexes with substrates

Role for intraflagellar transport in building a functional transition zone

Sensory ciliogenesis in Caenorhabditis elegans: assignment of IFT components into distinct modules based on transport and phenotypic profiles

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

The WD repeat-containing protein IFTA-1 is required for retrograde intraflagellar transport.

The base of the cilium: roles for transition fibres and the transition zone in ciliary formation, maintenance and compartmentalization

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

The roles of evolutionarily conserved functional modules in cilia-related trafficking

The sensory cilia of Caenorhabditis elegans