Cargando…

A systems biology approach towards the prediction of ciliopathy mechanisms

Detalles Bibliográficos
Autores principales:	Koutroumpas, K, Dam, J Van, Toedt, G, Lu, Q, Reeuwijk, J Van, Boldt, K, Gibson, T, Roepman, R, Ueffing, M, Russell, RB, Huynen, M, Elati, M, Képès, F
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2015
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518625/ http://dx.doi.org/10.1186/2046-2530-4-S1-P88

Ejemplares similares

From proteomic data to networks: statistics and methods reveal ciliary protein interaction landscape
por: Lu, Q, et al.
Publicado: (2015)

Scrutinizing ciliopathies by unravelling the ciliary interactome
por: van Reeuwijk, J, et al.
Publicado: (2012)

Systematic exploration of the ciliary protein landscape by large-scale affinity proteomics
por: Boldt, K, et al.
Publicado: (2015)

Differential requirements of ciliogenic/ciliopathy module components in restricting Joubert syndrome-associated Arl13b to a C. elegans Inv-like ciliary compartment
por: Blacque, O, et al.
Publicado: (2012)

Dissecting the sub-structure of the intraflagellar transport complex B
por: Texier, Y, et al.
Publicado: (2012)

Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice
por: Boldt, K, et al.
Publicado: (2012)

KOUNCIL: Kidney-Oriented Understanding of Correcting Ciliopathies
por: Stokman, M, et al.
Publicado: (2015)

SYSCILIA, “A systems biology approach to dissect cilia function and its disruption in human genetic disease”
por: Roepman, R, et al.
Publicado: (2012)

A reference to assess cilium phenotype in ciliopathy patients
por: Oud, M, et al.
Publicado: (2015)

A high-throughput genome-wide siRNA screen for ciliogenesis identifies new ciliary functional components and ciliopathy genes
por: Szymanska, K, et al.
Publicado: (2015)

PDZD7 connects the Usher protein complex to the intraflagellar transport machinery
por: Vrieze, E De, et al.
Publicado: (2015)

The lebercilin-like protein is embedded in a ciliary protein network and is preferentially expressed in motile cilia
por: Mans, DA, et al.
Publicado: (2012)

Identification of novel interaction partners for Vlgr1b/GPR98 - a key component of the periciliary Usher syndrome protein network in photoreceptor cells
por: Knapp, B, et al.
Publicado: (2012)

Pericentrin interacts with KASH domain-containing protein Syne-2
por: Falk, N, et al.
Publicado: (2015)

Combatting renal ciliopathies
por: Giles, RH
Publicado: (2012)

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
por: Wheway, Gabrielle, et al.
Publicado: (2015)

The Interaction of CCDC104/BARTL1 with Arl3 and Implications for Ciliary Function
por: Lokaj, Mandy, et al.
Publicado: (2015)

The more we know, the more we have to discover: an exciting future for understanding cilia and ciliopathies
por: Benmerah, Alexandre, et al.
Publicado: (2015)

Severe ciliopathy-related phenotypes in mice with dysregulation of tubulin polyglutamylation
por: Ikegami, K, et al.
Publicado: (2012)

DNA Methylation and Ciliopathies: a way to be explored
por: Alvarez-Satta, M, et al.
Publicado: (2015)

Identification of mutations in DYNC2LI1, a member of the mammalian cytoplasmic dynein 2 complex, expands the clinical spectrum of Jeune/ATD ciliopathies
por: Kessler, K, et al.
Publicado: (2015)

Screening ciliopathy genes in the model organism Trypanosoma brucei
por: Barry, S, et al.
Publicado: (2012)

3D renal modeling classifies BHD as a ciliopathy, possibly responsive to treatment with PTC124
por: Basten, S, et al.
Publicado: (2012)

Characterizing the morbid genome of ciliopathies
por: Shaheen, Ranad, et al.
Publicado: (2016)

Clinical and genetic analyses of a Dutch cohort of 40 patients with a nephronophthisis-related ciliopathy
por: Stokman, Marijn F., et al.
Publicado: (2018)

The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking
por: Bachmann-Gagescu, Ruxandra, et al.
Publicado: (2015)

Cell-based assay for ciliopathy patients to improve accurate diagnosis using ALPACA
por: Doornbos, Cenna, et al.
Publicado: (2021)

Origin and extension of the IFT complex in early eukaryotic evolution
por: van Dam, J, et al.
Publicado: (2012)

Defective airway intraflagellar transport underlies a combined motile and primary ciliopathy syndrome caused by IFT74 mutations
por: Fassad, Mahmoud R, et al.
Publicado: (2023)

Novel links between ciliopathies and FGF-related craniofacial syndromes
por: Liu, K, et al.
Publicado: (2012)

Function of the Ciliopathy gene RPGRIP1L in cortical neurogenesis
por: Pézeron, G, et al.
Publicado: (2015)

Evidence for a role of the ciliopathy protein MKS1 in cell polarity
por: Collado-Hilly, M, et al.
Publicado: (2015)

NINL and DZANK1 Co-function in Vesicle Transport and Are Essential for Photoreceptor Development in Zebrafish
por: Dona, Margo, et al.
Publicado: (2015)

Remodeling Cildb, a popular database for cilia and links for ciliopathies
por: Arnaiz, O, et al.
Publicado: (2015)

A transition zone complex of ciliopathy proteins regulates ciliary composition
por: Reiter, JF, et al.
Publicado: (2012)

X-box promoter motif searches: from C. elegans to humans to novel candidate ciliopathies
por: Lauter, G, et al.
Publicado: (2015)

Regulation of canonical Wnt signalling by the ciliopathy protein MKS1 and the E2 ubiquitin-conjugating enzyme UBE2E1
por: Szymanska, Katarzyna, et al.
Publicado: (2022)

Mainzer-Saldino syndrome is a ciliopathy caused by mutations in the IFT140 gene
por: Perrault, I, et al.
Publicado: (2012)

CiliaCarta: An integrated and validated compendium of ciliary genes
por: van Dam, Teunis J. P., et al.
Publicado: (2019)

Multidisciplinary nephrogenetic outpatient clinic combined with diagnostic exome sequencing for improved diagnostics and treatment
por: Lugtenberg, D, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_gkfs386fsv2a5hc0n37691039h