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Mitochondrial dynamics in Parkinson's disease: a role for α-synuclein?

Disease models & mechanisms, 2017-09, Vol.10 (9), p.1075-1087

2017

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Influence of micro– and macrostructure when determining the contact resistivity of interconnects based on electrically conductive adhesives

Solar energy materials and solar cells, 2023-09, Vol.260, p.112490, Article 112490

2023

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Mitochondrial behavior when things go wrong in the axon

Frontiers in cellular neuroscience, 2022-08, Vol.16, p.959598-959598

2022

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Contact resistivity of ECA bonded joints: How to extrapolate it?

AIP Conference Proceedings, 2022, Vol.2709 (1)

2022

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Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

Molecular psychiatry, 2010-06, Vol.15 (6), p.637-646

2010

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Contact resistivity of ECA bonded joints

AIP Conference Proceedings, 2021, Vol.2367 (1)

2021

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Unraveling axonal mechanisms of traumatic brain injury

Acta neuropathologica communications, 2022-09, Vol.10 (1), p.140-140, Article 140

2022

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Developmental and hypoxia-induced cell death share common ultrastructural and biochemical apoptotic features in the central nervous system

Neuroscience, 2013-11, Vol.252, p.190-200

2013

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NGF, TrkA-P and neuroprotection after a hypoxic event in the developing central nervous system

International journal of developmental neuroscience, 2018-12, Vol.71 (1), p.111-121

2018

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Treatment of thyroid associated ophthalmopathy with periocular injections of triamcinolone

British journal of ophthalmology, 2004-11, Vol.88 (11), p.1380-1386

2004

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Intramuscular cavernous venous malformation of extraocular muscles. Fractionated stereotactic radiotherapy as a therapeutic alternative

Archivos de la Sociedad Española de Oftalmología (English ed.), 2020-06, Vol.95 (6), p.293-296

2020

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Swedish Alzheimer’s disease variant perturbs activity of retrograde molecular motors and causes widespread derangement of axonal transport pathways

The Journal of biological chemistry, 2024-04, Vol.300 (4), p.107137-107137, Article 107137

2024

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Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36

Human molecular genetics, 2001-10, Vol.10 (21), p.2447-2452

2001

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Acute hypoxia and programmed cell death in developing CNS: Differential vulnerability of chick optic tectum layers

Neuroscience, 2006-10, Vol.142 (3), p.645-653

2006

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Information retrieved from specimens at Natural History Collections can improve the quality of field-based ecological networks

Community ecology, 2014-12, Vol.15 (2), p.187-193

2014

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Kinesin-1-mediated axonal transport of CB1 receptors is required for cannabinoid-dependent axonal growth and guidance

Development (Cambridge), 2020-04, Vol.147 (8)

2020

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Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function

Journal of cell science, 2014-04, Vol.127 (Pt 7), p.1537-1549

2014

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Multidrug resistance 1 gene polymorphisms are not associated with inflammatory bowel disease and response to therapy in Italian patients

Alimentary pharmacology & therapeutics, 2005-12, Vol.22 (11‐12), p.1129-1138

2005

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Validation of methodology to determine the contact resistivity of ECA-based bonds grounded on end–contact resistance measurements using redundant and modified TLM test structures

Solar energy materials and solar cells, 2023-10, Vol.262, p.112518, Article 112518

2023

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Variants of OCTN1–2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis

Alimentary pharmacology & therapeutics, 2006-02, Vol.23 (4), p.497-506

2006

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First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q

European journal of human genetics : EJHG, 1998-03, Vol.6 (2), p.151-157

1998

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Association of T‐786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease

British journal of haematology, 2004-01, Vol.124 (2), p.240-243

2004

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Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

Nature genetics, 1993-12, Vol.5 (4), p.338-343

1993

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High resolution linkage and linkage disequilibrium analyses of chromosome 1p36 SNPs identify new positional candidate genes for low bone mineral density

Osteoporosis international, 2009-02, Vol.20 (2), p.341-346

2009

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The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Nature genetics, 1993-12, Vol.5 (4), p.344-350

1993

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Mitochondrial dynamics in Parkinson's disease: a role for α-synuclein?

Influence of micro– and macrostructure when determining the contact resistivity of interconnects based on electrically conductive adhesives

Mitochondrial behavior when things go wrong in the axon

Contact resistivity of ECA bonded joints: How to extrapolate it?

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

Contact resistivity of ECA bonded joints

Unraveling axonal mechanisms of traumatic brain injury

Developmental and hypoxia-induced cell death share common ultrastructural and biochemical apoptotic features in the central nervous system

NGF, TrkA-P and neuroprotection after a hypoxic event in the developing central nervous system

Treatment of thyroid associated ophthalmopathy with periocular injections of triamcinolone

Intramuscular cavernous venous malformation of extraocular muscles. Fractionated stereotactic radiotherapy as a therapeutic alternative

Swedish Alzheimer’s disease variant perturbs activity of retrograde molecular motors and causes widespread derangement of axonal transport pathways

Variance component linkage analysis indicates a QTL for femoral neck bone mineral density on chromosome 1p36

Acute hypoxia and programmed cell death in developing CNS: Differential vulnerability of chick optic tectum layers

Information retrieved from specimens at Natural History Collections can improve the quality of field-based ecological networks

Kinesin-1-mediated axonal transport of CB1 receptors is required for cannabinoid-dependent axonal growth and guidance

Fast axonal transport of the proteasome complex depends on membrane interaction and molecular motor function

Multidrug resistance 1 gene polymorphisms are not associated with inflammatory bowel disease and response to therapy in Italian patients

Validation of methodology to determine the contact resistivity of ECA-based bonds grounded on end–contact resistance measurements using redundant and modified TLM test structures

Variants of OCTN1–2 cation transporter genes are associated with both Crohn's disease and ulcerative colitis

First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q

Association of T‐786C eNOS gene polymorphism with increased susceptibility to acute chest syndrome in females with sickle cell disease

Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

High resolution linkage and linkage disequilibrium analyses of chromosome 1p36 SNPs identify new positional candidate genes for low bone mineral density

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

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