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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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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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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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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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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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Improper Trafficking of Melanocyte-Specific Proteins in Hermansky–Pudlak Syndrome Type-5

Journal of investigative dermatology, 2007-06, Vol.127 (6), p.1471-1478

2007

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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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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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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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Rab27B-Mediated Metabolic Reprogramming Induces Secretome Acidification and Chemoresistance in Breast Cancer Cells

Exosomes and microvesicles, 2013, p.1

2013

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

Expert review of proteomics, 2016-04, Vol.13 (5), p.471-479

2016

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Potential for urban agriculture to support accessible and impactful undergraduate biology education

Ecology and evolution, 2022-03, Vol.12 (3), p.e8721-n/a

2022

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Evaluation of Quinazoline Analogues as Glucocerebrosidase Inhibitors with Chaperone Activity

Journal of medicinal chemistry, 2011-02, Vol.54 (4), p.1033-1058

2011

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Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma

Nature genetics, 2009-05, Vol.41 (5), p.518-520

2009

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Critical role of N-cadherin in myofibroblast invasion and migration in vitro stimulated by colon-cancer-cell-derived TGF-beta or wounding

Journal of cell science, 2004-09, Vol.117 (Pt 20), p.4691-4703

2004

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Discovery of a Novel Noniminosugar Acid α Glucosidase Chaperone Series

Journal of medicinal chemistry, 2012-09, Vol.55 (17), p.7546-7559

2012

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A New Glucocerebrosidase Chaperone Reduces -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

Volltextzugriff (PDF)

Cellular Defects in Chediak–Higashi Syndrome Correlate with the Molecular Genotype and Clinical Phenotype

Journal of investigative dermatology, 2007-11, Vol.127 (11), p.2674-2677

2007

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Discovery, SAR, and Biological evaluation of Non-Inhibitory Small Molecule Chaperones of Glucocerebrosidase

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

2012

Volltextzugriff (PDF)

Discovery of a novel non-iminosugar acid alpha glucosidase chaperone series

Journal of medicinal chemistry, 2012-08, Vol.55 (17), p.7546-7559

2012

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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

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

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

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

An immunohistochemical analysis of Rab27B distribution in fetal and adult tissue

An Ex(o)citing Machinery for Invasive Tumor Growth

Improper Trafficking of Melanocyte-Specific Proteins in Hermansky–Pudlak Syndrome Type-5

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

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

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

Rab27B-Mediated Metabolic Reprogramming Induces Secretome Acidification and Chemoresistance in Breast Cancer Cells

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

Potential for urban agriculture to support accessible and impactful undergraduate biology education

Evaluation of Quinazoline Analogues as Glucocerebrosidase Inhibitors with Chaperone Activity

Analysis of the matrix metalloproteinase family reveals that MMP8 is often mutated in melanoma

Critical role of N-cadherin in myofibroblast invasion and migration in vitro stimulated by colon-cancer-cell-derived TGF-beta or wounding

Discovery of a Novel Noniminosugar Acid α Glucosidase Chaperone Series

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

Cellular Defects in Chediak–Higashi Syndrome Correlate with the Molecular Genotype and Clinical Phenotype

Discovery, SAR, and Biological evaluation of Non-Inhibitory Small Molecule Chaperones of Glucocerebrosidase

Discovery of a novel non-iminosugar acid alpha glucosidase chaperone series

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