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N-SREBP2 Provides a Mechanism for Dynamic Control of Cellular Cholesterol Homeostasis

Cells (Basel, Switzerland), 2024-08, Vol.13 (15), p.1255

2024

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

European Cells and Materials, 2017-09, Vol.34, p.128-141

2017

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The Majority of Adrenocorticotropin Receptor (Melanocortin 2 Receptor) 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, 2008-12, Vol.93 (12), p.4948-4954

2008

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Mechanical loading inhibits cartilage inflammatory signalling via an HDAC6 and IFT-dependent mechanism regulating primary cilia elongation

Osteoarthritis and cartilage, 2019-07, Vol.27 (7), p.1064-1074

2019

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Primary cilia disassembly down-regulates mechanosensitive hedgehog signalling: a feedback mechanism controlling ADAMTS-5 expression in chondrocytes

Osteoarthritis and cartilage, 2014-03, Vol.22 (3), p.490-498

2014

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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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The immune cell infiltrate in the tumour microenvironment of phaeochromocytomas and paragangliomas

Endocrine-related cancer, 2022-11, Vol.29 (11), p.589-598

2022

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The primary cilium influences interleukin-1β-induced NFκB signalling by regulating IKK activity

Cellular signalling, 2014-08, Vol.26 (8), p.1735-1742

2014

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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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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

2007

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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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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.640-642

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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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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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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Expression, localization and tau exon 10 splicing activity of the brain RNA-binding protein TNRC4

Human molecular genetics, 2007-11, Vol.16 (22), p.2760-2769

2007

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Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaK

The international journal of biochemistry & cell biology, 2007, Vol.39 (4), p.736-751

2007

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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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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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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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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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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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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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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 in paediatrics, 2009, Vol.71 (1), p.149-150

2009

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Thermal-Hydraulic Performance Prediction in Fluid Power Systems

Proceedings of the Institution of Mechanical Engineers. Part I, Journal of systems and control engineering, 1996-11, Vol.210 (4), p.231-242

1996

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N-SREBP2 Provides a Mechanism for Dynamic Control of Cellular Cholesterol Homeostasis

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

The Majority of Adrenocorticotropin Receptor (Melanocortin 2 Receptor) Mutations Found in Familial Glucocorticoid Deficiency Type 1 Lead to Defective Trafficking of the Receptor to the Cell Surface

Mechanical loading inhibits cartilage inflammatory signalling via an HDAC6 and IFT-dependent mechanism regulating primary cilia elongation

Primary cilia disassembly down-regulates mechanosensitive hedgehog signalling: a feedback mechanism controlling ADAMTS-5 expression in chondrocytes

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

The immune cell infiltrate in the tumour microenvironment of phaeochromocytomas and paragangliomas

The primary cilium influences interleukin-1β-induced NFκB signalling by regulating IKK activity

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

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

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

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

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

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

Expression, localization and tau exon 10 splicing activity of the brain RNA-binding protein TNRC4

Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaK

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

Unfolding retinal dystrophies: a role for molecular chaperones?

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

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

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

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

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

Thermal-Hydraulic Performance Prediction in Fluid Power Systems

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