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Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease

Scientific reports, 2021-03, Vol.11 (1), p.6332-6332, Article 6332

2021

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De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination

The Journal of cell biology, 2018-04, Vol.217 (4), p.1353-1368

2018

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Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice

Neuron (Cambridge, Mass.), 2008-02, Vol.57 (3), p.393-405

2008

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Author Correction: Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease

Scientific reports, 2021-07, Vol.11 (1), p.14198-14198, Article 14198

2021

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Dynamin 2 mutations in Charcot―Marie―Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination

Brain (London, England : 1878), 2012-05, Vol.135 (Pt 5), p.1395-1411

2012

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MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B

Brain (London, England : 1878), 2012-07, Vol.135 (Pt 7), p.2032-2047

2012

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Muscle-specific function of the centronuclear myopathy and Charcot-Marie-Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism, mitochondria, muscle fibers, neuromuscular junctions and peripheral nerves

Human molecular genetics, 2013-11, Vol.22 (21), p.4417-4429

2013

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L’illusione della conoscenza nei Paradossi di Ortensio Lando

Italies : culture, civilisation, société, 2021-05, p.63-73

Tinelli, Elisa

2021

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L’illusione della conoscenza nei Paradossi di Ortensio Lando

Italies : culture, civilisation, société, 2021-02, Vol.24, p.63-73

Elisa Tinelli

2021

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Author Correction: Global network analysis in Schizosaccharomycespombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease

Scientific reports, 2021-07, Vol.11 (1)

2021

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L’illusione della conoscenza nei Paradossi di Ortensio Lando

Italies : culture, civilisation, société, 2020-12 (24), p.63-73

Tinelli, Elisa

2020

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RENATO RICCO, Sulle tracce di Didone. Fra Età Classica e Rinascimento, l’evoluzione letteraria di un mito, Napoli, Guida Editori, 2015

Studi giraldiani, 2017-07, Vol.3, p.297-304

Elisa Tinelli

2017

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NCLs and ER: A stressful relationship

Biochimica et biophysica acta. Molecular basis of disease, 2017-06, Vol.1863 (6), p.1273-1281

2017

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Antagonists of transient receptor potential-mucolipin 1: A new therapeutic strategy for cancer therapy

Biophysical journal, 2024-02, Vol.123 (3), p.260a-260a

2024

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Reuse of building components – Assessment system to support decisions in indoor re-layout interventions

Agathón (Online), 2024-06, Vol.15

2024

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Mice carrying an analogous heterozygous dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy

Human molecular genetics, 2020-05, Vol.29 (8), p.1253-1273

2020

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Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice

The Journal of neuroscience, 2006-02, Vol.26 (8), p.2358-2368

2006

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P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice

Human molecular genetics, 2011-06, Vol.20 (11), p.2081-2090

2011

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P0S63del impedes the arrival of wild-type PO glycoprotein to myelin in CMT1 B mice

Human molecular genetics, 2011, Vol.20 (11), p.2081-2090

2011

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Illusions et chimères

Italies : culture, civilisation, société, 2020

2020

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Pathogenic P0 mutations are blocked at various quality control check points

The FASEB journal, 2009-04, Vol.23 (S1)

2009

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MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot―Marie―Tooth disease type 1 B

Brain (London, England : 1878), 2012, Vol.135, p.2032-2047

2012

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Article: Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice

Neuron (Cambridge, Mass.), 2008-02, Vol.57 (3), p.393-405

2008

Volltextzugriff (PDF)

Highly tumorigenic lung cancer CD133⁺ cells display stem-like features and are spared by cisplatin treatment

Proceedings of the National Academy of Sciences - PNAS, 2009-09, Vol.106 (38), p.16281-16286

2009

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Auditory time perception impairment in children with developmental dyscalculia

Research in developmental disabilities, 2024-06, Vol.149, p.104733, Article 104733

2024

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Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease

De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination

Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice

Author Correction: Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease

Dynamin 2 mutations in Charcot―Marie―Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination

MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot-Marie-Tooth disease type 1B

Muscle-specific function of the centronuclear myopathy and Charcot-Marie-Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism, mitochondria, muscle fibers, neuromuscular junctions and peripheral nerves

L’illusione della conoscenza nei Paradossi di Ortensio Lando

L’illusione della conoscenza nei Paradossi di Ortensio Lando

Author Correction: Global network analysis in Schizosaccharomycespombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease

L’illusione della conoscenza nei Paradossi di Ortensio Lando

RENATO RICCO, Sulle tracce di Didone. Fra Età Classica e Rinascimento, l’evoluzione letteraria di un mito, Napoli, Guida Editori, 2015

NCLs and ER: A stressful relationship

Antagonists of transient receptor potential-mucolipin 1: A new therapeutic strategy for cancer therapy

Reuse of building components – Assessment system to support decisions in indoor re-layout interventions

Mice carrying an analogous heterozygous dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy

Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice

P0S63del impedes the arrival of wild-type P0 glycoprotein to myelin in CMT1B mice

P0S63del impedes the arrival of wild-type PO glycoprotein to myelin in CMT1 B mice

Illusions et chimères

Pathogenic P0 mutations are blocked at various quality control check points

MpzR98C arrests Schwann cell development in a mouse model of early-onset Charcot―Marie―Tooth disease type 1 B

Article: Ablation of the UPR-Mediator CHOP Restores Motor Function and Reduces Demyelination in Charcot-Marie-Tooth 1B Mice

Highly tumorigenic lung cancer CD133⁺ cells display stem-like features and are spared by cisplatin treatment

Auditory time perception impairment in children with developmental dyscalculia

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