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Exosomes released from breast cancer carcinomas stimulate cell movement

PloS one, 2015-03, Vol.10 (3), p.e0117495-e0117495

2015

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Discovery, Structure–Activity Relationship, and Biological Evaluation of Noninhibitory Small Molecule Chaperones of Glucocerebrosidase

Journal of medicinal chemistry, 2012-06, Vol.55 (12), p.5734-5748

2012

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Progress and potential of non-inhibitory small molecule chaperones for the treatment of Gaucher disease and its implications for Parkinson disease

Expert review of proteomics, 2016-05, Vol.13 (5), p.471-479

2016

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Disorders of lysosome-related organelle biogenesis: clinical and molecular genetics

Annual review of genomics and human genetics, 2008-01, Vol.9 (1), p.359-386

2008

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Effect of the Secretory Small GTPase Rab27B on Breast Cancer Growth, Invasion, and Metastasis

JNCI : Journal of the National Cancer Institute, 2010-06, Vol.102 (12), p.866-880

2010

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Validation of anti-glucocerebrosidase antibodies for western blot analysis on protein lysates of murine and human cells

Biochemical journal, 2019-01, Vol.476 (2), p.261-274

2019

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Vacuolar H+ ATPase expression and activity is required for Rab27B‐dependent invasive growth and metastasis of breast cancer

International journal of cancer, 2013-08, Vol.133 (4), p.843-854

2013

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Glucocerebrosidase is shaking up the synucleinopathies

Brain (London, England : 1878), 2014-05, Vol.137 (5), p.1304-1322

2014

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Modeling and quantification of cancer cell invasion through collagen type I matrices

The International journal of developmental biology, 2010, Vol.54 (5), p.887

2010

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A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease

Disease models & mechanisms, 2016-07, Vol.9 (7), p.769-778

2016

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The secretory small GTPase Rab27B as a marker for breast cancer progression

Oncotarget, 2010-08, Vol.1 (4), p.304-308

2010

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Cellular and clinical report of new Griscelli syndrome type III cases

Pigment cell and melanoma research, 2012-01, Vol.25 (1), p.47-56

2012

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An immunohistochemical analysis of Rab27B distribution in fetal and adult tissue

The International journal of developmental biology, 2012, Vol.56 (5), p.363

2012

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An Ex(o)citing Machinery for Invasive Tumor Growth

Cancer research (Chicago, Ill.), 2010-12, Vol.70 (23), p.9533-9537

2010

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A New Glucocerebrosidase Chaperone Reduces α-Synuclein and Glycolipid Levels in iPSC-Derived Dopaminergic Neurons from Patients with Gaucher Disease and Parkinsonism

The Journal of neuroscience, 2016-07, Vol.36 (28), p.7441-7452

2016

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A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis

Journal of medical genetics, 2012-07, Vol.49 (7), p.462-472

2012

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Lysosomal storage and impaired autophagy lead to inflammasome activation in Gaucher macrophages

Aging cell, 2016-02, Vol.15 (1), p.77-88

2016

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α-Synuclein Interacts with Glucocerebrosidase Providing a Molecular Link between Parkinson and Gaucher Diseases

The Journal of biological chemistry, 2011-08, Vol.286 (32), p.28080-28088

2011

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Bone marrow-derived mesenchymal stem cells promote colorectal cancer progression through paracrine neuregulin 1/HER3 signalling

Gut, 2013-04, Vol.62 (4), p.550-560

2013

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Characterization of the Molecular Defects in Rab27a, Caused by RAB27A Missense Mutations Found in Patients with Griscelli Syndrome

The Journal of biological chemistry, 2003-03, Vol.278 (13), p.11386-11392

2003

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Interactions of Human Myosin Va Isoforms, Endogenously Expressed in Human Melanocytes, Are Tightly Regulated by the Tail Domain

Journal of investigative dermatology, 2003-03, Vol.120 (3), p.465-475

2003

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Critical lessons from a pragmatic randomized trial of home-based COVID-19 testing in rural Native American and Latino communities

The Journal of rural health, 2024-03

2024

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Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits

Human molecular genetics, 2013-05, Vol.22 (10), p.2067-2082

2013

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Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited [alpha]-synuclein accumulation and age-dependent sensorimotor deficits

Human molecular genetics, 2013-05, Vol.22 (10), p.2067-2082

2013

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A mutation in SCARB2 is a modifier in gaucher disease

Human mutation, 2011-11, Vol.32 (11), p.1232-1238

2011

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Exosomes released from breast cancer carcinomas stimulate cell movement

Discovery, Structure–Activity Relationship, and Biological Evaluation of Noninhibitory Small Molecule Chaperones of Glucocerebrosidase

Progress and potential of non-inhibitory small molecule chaperones for the treatment of Gaucher disease and its implications for Parkinson disease

Disorders of lysosome-related organelle biogenesis: clinical and molecular genetics

Effect of the Secretory Small GTPase Rab27B on Breast Cancer Growth, Invasion, and Metastasis

Validation of anti-glucocerebrosidase antibodies for western blot analysis on protein lysates of murine and human cells

Vacuolar H+ ATPase expression and activity is required for Rab27B‐dependent invasive growth and metastasis of breast cancer

Glucocerebrosidase is shaking up the synucleinopathies

Modeling and quantification of cancer cell invasion through collagen type I matrices

A new glucocerebrosidase-deficient neuronal cell model provides a tool to probe pathophysiology and therapeutics for Gaucher disease

The secretory small GTPase Rab27B as a marker for breast cancer progression

Cellular and clinical report of new Griscelli syndrome type III cases

An immunohistochemical analysis of Rab27B distribution in fetal and adult tissue

An Ex(o)citing Machinery for Invasive Tumor Growth

A New Glucocerebrosidase Chaperone Reduces α-Synuclein and Glycolipid Levels in iPSC-Derived Dopaminergic Neurons from Patients with Gaucher Disease and Parkinsonism

A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis

Lysosomal storage and impaired autophagy lead to inflammasome activation in Gaucher macrophages

α-Synuclein Interacts with Glucocerebrosidase Providing a Molecular Link between Parkinson and Gaucher Diseases

Bone marrow-derived mesenchymal stem cells promote colorectal cancer progression through paracrine neuregulin 1/HER3 signalling

Characterization of the Molecular Defects in Rab27a, Caused by RAB27A Missense Mutations Found in Patients with Griscelli Syndrome

Interactions of Human Myosin Va Isoforms, Endogenously Expressed in Human Melanocytes, Are Tightly Regulated by the Tail Domain

Critical lessons from a pragmatic randomized trial of home-based COVID-19 testing in rural Native American and Latino communities

Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited α-synuclein accumulation and age-dependent sensorimotor deficits

Atp13a2-deficient mice exhibit neuronal ceroid lipofuscinosis, limited [alpha]-synuclein accumulation and age-dependent sensorimotor deficits

A mutation in SCARB2 is a modifier in gaucher disease

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