4.7 Article

The ciliopathy protein TALPID3/KIAA0586 acts upstream of Rab8 activation in zebrafish photoreceptor outer segment formation and maintenance

Related references

Note: Only part of the references are listed.
Article Genetics & Heredity

KIAA0586 is Mutated in Joubert Syndrome

Ruxandra Bachmann-Gagescu et al.

HUMAN MUTATION (2015)

Article Genetics & Heredity

Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity

R. Bachmann-Gagescu et al.

JOURNAL OF MEDICAL GENETICS (2015)

Article Biochemistry & Molecular Biology

Recoverin depletion accelerates cone photoresponse recovery

Jingjing Zang et al.

OPEN BIOLOGY (2015)

Article Biochemistry & Molecular Biology

Spata7 is a retinal ciliopathy gene critical for correct RPGRIP1 localization and protein trafficking in the retina

Aiden Eblimit et al.

HUMAN MOLECULAR GENETICS (2015)

Article Anatomy & Morphology

Failure of centrosome migration causes a loss of motile cilia in talpid3 mutants

Louise A. Stephen et al.

DEVELOPMENTAL DYNAMICS (2013)

Review Clinical Neurology

joubert syndrome: congenital cerebellar ataxia with the molar tooth

Marta Romani et al.

LANCET NEUROLOGY (2013)

Article Pediatrics

The Molar Tooth Sign Is Pathognomonic for Joubert Syndrome!

Andrea Poretti et al.

PEDIATRIC NEUROLOGY (2013)

Article Ophthalmology

Protein sorting, targeting and trafficking in photoreceptor cells

Jillian N. Pearring et al.

PROGRESS IN RETINAL AND EYE RESEARCH (2013)

Article Biochemistry & Molecular Biology

The ciliopathy gene cc2d2a controls zebrafish photoreceptor outer segment development through a role in Rab8-dependent vesicle trafficking

Ruxandra Bachmann-Gagescu et al.

HUMAN MOLECULAR GENETICS (2011)

Review Medicine, General & Internal

Mechanisms of Disease: Ciliopathies

Friedhelm Hildebrandt et al.

NEW ENGLAND JOURNAL OF MEDICINE (2011)

Article Multidisciplinary Sciences

Primary cilia membrane assembly is initiated by Rab11 and transport protein particle II (TRAPPII) complex-dependent trafficking of Rabin8 to the centrosome

Christopher J. Westlake et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2011)

Review Genetics & Heredity

The primary cilium: a signalling centre during vertebrate development

Sarah C. Goetz et al.

NATURE REVIEWS GENETICS (2010)

Review Anatomy & Morphology

What Drives Cell Morphogenesis: A Look Inside the Vertebrate Photoreceptor

Breandan Kennedy et al.

DEVELOPMENTAL DYNAMICS (2009)

Review Anatomy & Morphology

Intraflagellar transport and the sensory outer segment of vertebrate photoreceptors

Christine Insinna et al.

DEVELOPMENTAL DYNAMICS (2008)

Article Anatomy & Morphology

The Tol2kit:: A multisite Gateway-based construction kit for Tol2 transposon transgenesis constructs

Kristen M. Kwan et al.

DEVELOPMENTAL DYNAMICS (2007)

Review Cell Biology

Mechanisms of disease - When cilia go bad: cilia defects and ciliopathies

Manfred Fliegauf et al.

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)

Article Cell Biology

Functional dissection of Rab GTPases involved in primary cilium formation

Shin-ichiro Yoshimura et al.

JOURNAL OF CELL BIOLOGY (2007)

Article Biochemistry & Molecular Biology

A core complex of BBS proteins cooperates with the GTPase Rab8 to promote ciliary membrane biogenesis

Maxence V. Nachury et al.

Review Biotechnology & Applied Microbiology

Tol2: a versatile gene transfer vector in vertebrates

Koichi Kawakami

GENOME BIOLOGY (2007)

Review Multidisciplinary Sciences

The primary cilium as the cell's antenna: Signaling at a sensory organelle

Veena Singla et al.

SCIENCE (2006)

Article Cell Biology

The chicken talpid3 gene encodes a novel protein essential for Hedgehog signaling

Megan G. Davey et al.

GENES & DEVELOPMENT (2006)

Article Cell Biology

Craniofacial development in the talpid3 chicken mutant

P Buxton et al.

DIFFERENTIATION (2004)

Article Multidisciplinary Sciences

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin

DY Nishimura et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)

Article Neurosciences

Retinal function and morphology in two zebrafish models of oculo-renal syndromes

R Bahadori et al.

EUROPEAN JOURNAL OF NEUROSCIENCE (2003)

Article Multidisciplinary Sciences

Activation of mislocalized opsin kills rod cells: A novel mechanism for rod cell death in retinal disease

PD Alfinito et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)

Article Multidisciplinary Sciences

Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) gene

JG Gao et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2002)