Cargando…

A reverse genetic screen for genes involved in ciliary formation and function

Detalles Bibliográficos
Autores principales:	Moore, D, zur Lage, P, Gallone, G, Rodger, FE, Jarman, AP
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2012
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555953/ http://dx.doi.org/10.1186/2046-2530-1-S1-P35

Ejemplares similares

Screening for genes involved in cilia formation
por: Hall, EA, et al.
Publicado: (2012)

CG31320 (Heatr2) - ciliopathy candidate gene, functional analysis in fly and mouse models
por: Mali, G, et al.
Publicado: (2012)

The transcriptional regulation of ciliogenesis in differentiating Drosophila sensory neurons
por: Jarman, A, et al.
Publicado: (2012)

Characterisation of homologues of known and putative dynein assembly factors in a Drosophila model
por: Lage, P zur, et al.
Publicado: (2015)

The regulation of mechanosensory motile cilium formation
por: Jarman, A, et al.
Publicado: (2015)

The role of cilia and ciliary motility in otolith formation in the zebrafish embryo
por: Stooke-Vaughan, G, et al.
Publicado: (2012)

Towards gene therapy for primary ciliary dyskinesia
por: Munye, M, et al.
Publicado: (2012)

Body axis elongation and ciliary function in zebrafish require Noni a novel ciliary protein
por: Jerber, J, et al.
Publicado: (2012)

The evolution of ciliary signaling mechanisms
por: Abedin, M, et al.
Publicado: (2012)

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

Survey of the Ciliary Motility Machinery of Drosophila Sperm and Ciliated Mechanosensory Neurons Reveals Unexpected Cell-Type Specific Variations: A Model for Motile Ciliopathies
por: zur Lage, Petra, et al.
Publicado: (2019)

Transgenic tools for proteomic analysis of ciliary transport
por: Fang, X, et al.
Publicado: (2015)

Longitudinal lung function and structural changes in children with primary ciliary dyskinesia
por: Blanchon, S, et al.
Publicado: (2012)

High throughput high content reverse genetics visual screens of ciliogenesis and cilia maintenance
por: Szymanska, K, et al.
Publicado: (2012)

The Drosophila orthologue of the primary ciliary dyskinesia-associated gene, DNAAF3, is required for axonemal dynein assembly
por: zur Lage, Petra, et al.
Publicado: (2021)

Network model for visually mediated ciliary locomotion in Hermissenda
por: Baxter, Douglas A, et al.
Publicado: (2010)

Photoreceptor degeneration caused by defects of a ciliary kinase
por: Omori, Y, et al.
Publicado: (2012)

chemfp - fast and portable fingerprint formats and tools
por: Dalke, AP
Publicado: (2011)

Investigation into the Importance of genes encoding ciliary proteins in congenital heart disease using whole exome sequencing
por: Hartill, V, et al.
Publicado: (2015)

A three-step process of Nphp3 ciliary localization
por: Shiba, D, et al.
Publicado: (2012)

Primary ciliary dyskinesia and humoral immunodeficiency - what is the missing link?
por: Boon, Mieke, et al.
Publicado: (2013)

Biochemical characterization of transmembrane proteins (TMEMs) in the ciliary transition zone
por: Shoaib, E, et al.
Publicado: (2015)

Strongly Truncated Dnaaf4 Plays a Conserved Role in Drosophila Ciliary Dynein Assembly as Part of an R2TP-Like Co-Chaperone Complex With Dnaaf6
por: Lennon, Jennifer, et al.
Publicado: (2022)

Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151
por: Onoufriadis, A, et al.
Publicado: (2015)

Nasal nitric oxide is useful in an Australian Primary Ciliary Dyskinesia clinic
por: Morgan, L, et al.
Publicado: (2012)

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

Forebrain development in the Inpp5e ciliary mouse mutant is severely disrupted
por: Theil, T, et al.
Publicado: (2012)

Diagnostic of Primary Ciliary Dyskinesia: guidelines to obtain appropriate ciliate cell samples
por: Blanchon, S, et al.
Publicado: (2012)

C2 domains as protein-protein interaction modules in the ciliary transition zone
por: Remans, K, et al.
Publicado: (2015)

Ciliary beat pattern analysis below 37°C may risk PCD misdiagnosis
por: Jackson, C, et al.
Publicado: (2012)

Role of CSPP-L in recruitment of ciliopathy proteins to centriolar satellites and the ciliary transition zone
por: Patzke, S, et al.
Publicado: (2012)

Alteration of nephrocystins and IFT-A proteins causes similar ciliary phenotypes leading to Nephronophthisis
por: Saunier, S, et al.
Publicado: (2012)

Characterization of upper airway ciliary beat by coupling isolated and collective cilia motion analysis
por: Bottier, M, et al.
Publicado: (2015)

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

The function and regulation of the bHLH gene, cato, in Drosophila neurogenesis
por: zur Lage, Petra I, et al.
Publicado: (2010)

Novel MDR-reversing inhibitors of MRP subtypes related to antiretroviral drug resistance and CD4 cell counts
por: Hilgeroth, Andreas, et al.
Publicado: (2014)

Transition zone: the sequential assembly of its components parallels its dual role in basal body anchoring and ciliary function
por: Aubusson-Fleury, A, et al.
Publicado: (2015)

The Drosophila homologue of Rootletin is required for mechanosensory function and ciliary rootlet formation in chordotonal sensory neurons
por: Styczynska-Soczka, Katarzyna, et al.
Publicado: (2015)

Diagnostic algorithm for Primary Ciliary Dyskinesia: recommendations of the French National Centre for Rare Respiratory Diseases
por: Blanchon, S, et al.
Publicado: (2012)

Delineation of CCDC39/CCDC40 mutation spectrum and associated phenotypes in primary ciliary dyskinesia
por: Legendre, M, et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_pkk6okbf40l59oqqn5rbn1kacj