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Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signalling

European cells & materials, 2017-09, Vol.34, p.128-141

2017

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Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

Trends in molecular medicine, 2005-04, Vol.11 (4), p.177-185

2005

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Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Nature genetics, 2005-02, Vol.37 (2), p.166-170

2005

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

Nature genetics, 2005-10, Vol.37 (10), p.1135-1140

2005

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HSJ1 Is a Neuronal Shuttling Factor for the Sorting of Chaperone Clients to the Proteasome

Current biology, 2005-06, Vol.15 (11), p.1058-1064

2005

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The Chaperone Environment at the Cytoplasmic Face of the Endoplasmic Reticulum Can Modulate Rhodopsin Processing and Inclusion Formation

The Journal of biological chemistry, 2003-05, Vol.278 (21), p.19087-19094

2003

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Nuclear translocation of the Hsp70/Hsp90 organizing protein mSTI1 is regulated by cell cycle kinases

Journal of cell science, 2004-02, Vol.117 (Pt 5), p.701-710

2004

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Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease

Molecular therapy, 2007-06, Vol.15 (6), p.1100-1105

2007

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Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3

Human molecular genetics, 2002-11, Vol.11 (24), p.3065-3074

2002

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Unfolding retinal dystrophies: a role for molecular chaperones?

Trends in Molecular Medicine, 2001-09, Vol.7 (9), p.414-421

2001

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Isolation and characterization of murine Cds ( CDP-diacylglycerol synthase) 1 and 2

Gene, 2005-08, Vol.356, p.19-31

2005

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Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane

Human molecular genetics, 2000-08, Vol.9 (13), p.1919-1926

2000

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The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retina

Human molecular genetics, 2002-04, Vol.11 (7), p.823-831

2002

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Mechanical strain disrupts primary cilia structure and modulates hedgehog signalling in adult chondrocytes

Cilia (London), 2012-11, Vol.1 (S1), p.P53-P53, Article P53

2012

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Neuronal DnaJ proteins HSJ1a and HSJ1b: a role in linking the Hsp70 chaperone machine to the ubiquitin-proteasome system?

Biochemical Society transactions, 2004-08, Vol.32 (Pt 4), p.640

2004

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Seasonal changes in stress-70 protein levels reflect thermal tolerance in the marine bivalve Mytilus edulis L

Journal of experimental marine biology and ecology, 1998-10, Vol.229 (1), p.53-68

1998

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Delineation of the Plasma Membrane Targeting Domain of the X-Linked Retinitis Pigmentosa Protein RP2

Investigative ophthalmology & visual science, 2002-06, Vol.43 (6), p.2015-2020

2002

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Heat-shock induces rapid resorption of primary cilia

Cilia (London), 2012-11, Vol.1 (S1), p.P52-P52, Article P52

2012

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An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene

British journal of ophthalmology, 2004-04, Vol.88 (4), p.528-532

2004

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Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sorting

Biochemical journal, 2003-06, Vol.372 (Pt 2), p.427-433

2003

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AIP, a Protein Mutated in Familial Acromegaly, Plays a Role in the Regulation of Cell Proliferation and Shows Cell-Type Specific Subcellular Localisation

Hormone research, 2009-01, Vol.71 (1), p.149

2009

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Stress-70 protein induction in Mytilus edulis: Tissue-specific responses to elevated temperature reflect relative vulnerability and physiological function

Journal of experimental marine biology and ecology, 1997-10, Vol.217 (2), p.225-235

1997

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Assay and Functional Analysis of the ARL3 Effector RP2 Involved in X‐Linked Retinitis Pigmentosa

Methods in Enzymology, 2005, Vol.404, p.468-480

2005

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Identification and characterization of a human mitochondrial homologue of the bacterial co-chaperone GrpE

Gene, 2001-04, Vol.267 (1), p.125-134

2001

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The majority of ACTH receptor (MC2R) mutations found in Familial Glucocorticoid Deficiency type 1 lead to defective trafficking of the receptor to the cell surface

The journal of clinical endocrinology and metabolism, 2008-10, Vol.93 (12), p.4948-4954

2008

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Chondrocyte expansion is associated with loss of primary cilia and disrupted hedgehog signalling

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

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

HSJ1 Is a Neuronal Shuttling Factor for the Sorting of Chaperone Clients to the Proteasome

The Chaperone Environment at the Cytoplasmic Face of the Endoplasmic Reticulum Can Modulate Rhodopsin Processing and Inclusion Formation

Nuclear translocation of the Hsp70/Hsp90 organizing protein mSTI1 is regulated by cell cycle kinases

Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease

Localization in the human retina of the X-linked retinitis pigmentosa protein RP2, its homologue cofactor C and the RP2 interacting protein Arl3

Unfolding retinal dystrophies: a role for molecular chaperones?

Isolation and characterization of murine Cds ( CDP-diacylglycerol synthase) 1 and 2

Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane

The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retina

Mechanical strain disrupts primary cilia structure and modulates hedgehog signalling in adult chondrocytes

Neuronal DnaJ proteins HSJ1a and HSJ1b: a role in linking the Hsp70 chaperone machine to the ubiquitin-proteasome system?

Seasonal changes in stress-70 protein levels reflect thermal tolerance in the marine bivalve Mytilus edulis L

Delineation of the Plasma Membrane Targeting Domain of the X-Linked Retinitis Pigmentosa Protein RP2

Heat-shock induces rapid resorption of primary cilia

An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene

Organization on the plasma membrane of the retinitis pigmentosa protein RP2: investigation of association with detergent-resistant membranes and polarized sorting

AIP, a Protein Mutated in Familial Acromegaly, Plays a Role in the Regulation of Cell Proliferation and Shows Cell-Type Specific Subcellular Localisation

Stress-70 protein induction in Mytilus edulis: Tissue-specific responses to elevated temperature reflect relative vulnerability and physiological function

Assay and Functional Analysis of the ARL3 Effector RP2 Involved in X‐Linked Retinitis Pigmentosa

Identification and characterization of a human mitochondrial homologue of the bacterial co-chaperone GrpE

The majority of ACTH receptor (MC2R) mutations found in Familial Glucocorticoid Deficiency type 1 lead to defective trafficking of the receptor to the cell surface

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