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Synaptojanin 1 Mutation in Parkinson’s Disease Brings Further Insight into the Neuropathological Mechanisms

BioMed research international, 2014-01, Vol.2014, p.289728-9

2014

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Trans-synaptic spread of tau pathology in vivo

PloS one, 2012-02, Vol.7 (2), p.e31302-e31302

2012

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Sustained effects of nonallele-specific Huntingtin silencing

Annals of neurology, 2009-03, Vol.65 (3), p.276-285

2009

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A new F-box protein 7 gene mutation causing typical Parkinson's disease

Movement disorders, 2015-07, Vol.30 (8), p.1130-1133

2015

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A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease

Annals of neurology, 2016-02, Vol.79 (2), p.335-337

2016

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Allele-specific silencing of mutant huntingtin in rodent brain and human stem cells

PloS one, 2014-06, Vol.9 (6), p.e99341-e99341

2014

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LKB1 and Notch Pathways Interact and Control Biliary Morphogenesis

PloS one, 2015-12, Vol.10 (12), p.e0145400-e0145400

2015

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Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel

Frontiers in neurology, 2017-10, Vol.8, p.567-567

2017

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Vitamin D insufficiency and schizophrenia risk: Evaluation of hyperprolinemia as a mediator of association

Schizophrenia research, 2014-06, Vol.156 (1), p.15-22

2014

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AXIN deficiency in human and mouse hepatocytes induces hepatocellular carcinoma in the absence of β-catenin activation

Journal of hepatology, 2018-06, Vol.68 (6), p.1203-1213

2018

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Optimal antagonism of GPIIb/IIIa favors platelet adhesion by inhibiting thrombus growth. An ex vivo capillary perfusion chamber study in the guinea pig

Arteriosclerosis, thrombosis, and vascular biology, 1996-01, Vol.16 (1), p.56

1996

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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

American journal of human genetics, 2016-03, Vol.98 (3), p.500-513

2016

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NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

Neurobiology of aging, 2017-09, Vol.57, p.247.e9-247.e13

2017

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Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

JAMA neurology, 2018-11, Vol.75 (11), p.1416

2018

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Poster #125 ASSOCIATION OF HYPERPROLINEMIA WITH SCHIZOPHRENIA: IMPLICATIONS FOR THE ETIOLOGY, CLINICAL MANAGEMENT AND TREATMENT OF SCHIZOPHRENIA PATIENTS

Schizophrenia research, 2012-04, Vol.136, p.S136-S137

2012

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The tetrapeptide AcSDKP reduces the sensitivity of murine CFU-MK and CFU-GM progenitors to aracytine in vitro and in vivo

International journal of hematology, 1998-08, Vol.68 (2), p.145-155

1998

Volltextzugriff (PDF)

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease

Neurobiology of aging, 2018-04, Vol.64, p.159.e5-159.e8

2018

Volltextzugriff (PDF)

LKB1 and Notch Pathways Interact and Control Biliary Morphogenesis

PloS one, 2015-12

2015

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A N ovel N onsense M utation in DNAJC 6 E xpands the P henotype of A utosomal‐ R ecessive J uvenile‐ O nset P arkinson's D isease

Annals of neurology, 2016-02, Vol.79 (2), p.335-337

2016

Volltextzugriff (PDF)

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

American journal of human genetics, 2016-03, Vol.98 (3), p.1

2016

Volltextzugriff (PDF)

Haemophore‐mediated signalling in Serratia marcescens: a new mode of regulation for an extra cytoplasmic function (ECF) sigma factor involved in haem acquisition

Molecular microbiology, 2004-08, Vol.53 (4), p.1267-1277

2004

Volltextzugriff (PDF)

SYNJ1

Encyclopedia of Signaling Molecules, p.5287-5294

Volltextzugriff (PDF)

Fecal microbiota transplantation to maintain remission in Crohn's disease: a pilot randomized controlled study

Microbiome, 2020-02, Vol.8 (1), p.12-12, Article 12

2020

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Relation between Mechanical Hardening and Nitrogen Profile of PBII Nitrided Titanium Alloy

Materials, 2022-12, Vol.15 (24), p.9028

2022

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Synaptojanin 1 Mutation in Parkinson’s Disease Brings Further Insight into the Neuropathological Mechanisms

Trans-synaptic spread of tau pathology in vivo

Sustained effects of nonallele-specific Huntingtin silencing

A new F-box protein 7 gene mutation causing typical Parkinson's disease

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease

Allele-specific silencing of mutant huntingtin in rodent brain and human stem cells

LKB1 and Notch Pathways Interact and Control Biliary Morphogenesis

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel

Vitamin D insufficiency and schizophrenia risk: Evaluation of hyperprolinemia as a mediator of association

AXIN deficiency in human and mouse hepatocytes induces hepatocellular carcinoma in the absence of β-catenin activation

Optimal antagonism of GPIIb/IIIa favors platelet adhesion by inhibiting thrombus growth. An ex vivo capillary perfusion chamber study in the guinea pig

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing

Poster #125 ASSOCIATION OF HYPERPROLINEMIA WITH SCHIZOPHRENIA: IMPLICATIONS FOR THE ETIOLOGY, CLINICAL MANAGEMENT AND TREATMENT OF SCHIZOPHRENIA PATIENTS

The tetrapeptide AcSDKP reduces the sensitivity of murine CFU-MK and CFU-GM progenitors to aracytine in vitro and in vivo

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease

LKB1 and Notch Pathways Interact and Control Biliary Morphogenesis

A N ovel N onsense M utation in DNAJC 6 E xpands the P henotype of A utosomal‐ R ecessive J uvenile‐ O nset P arkinson's D isease

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

Haemophore‐mediated signalling in Serratia marcescens: a new mode of regulation for an extra cytoplasmic function (ECF) sigma factor involved in haem acquisition

SYNJ1

Fecal microbiota transplantation to maintain remission in Crohn's disease: a pilot randomized controlled study

Relation between Mechanical Hardening and Nitrogen Profile of PBII Nitrided Titanium Alloy

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