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Relative calibration of the LIGO and Virgo detectors using astrophysical events from their third observing run

Classical and quantum gravity, 2022-10, Vol.39 (19), p.195019

2022

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Did Mark make use of the Source Q? An analysis of the Beelzebul controversy (Mk 3,20-30 and Par.)

Syx, Raoul A. S

1994

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The Implication of Early Chromatin Changes in X Chromosome Inactivation

Cell, 2019-01, Vol.176 (1-2), p.182-197.e23

2019

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Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation

eLife, 2016-02, Vol.5

2016

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Locus specific epigenetic modalities of random allelic expression imbalance

Nature communications, 2021-09, Vol.12 (1), p.5330-5330, Article 5330

2021

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Xist-dependent imprinted X inactivation and the early developmental consequences of its failure

Nature structural & molecular biology, 2017-03, Vol.24 (3), p.226

2017

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Contribution of epigenetic landscapes and transcription factors to X-chromosome reactivation in the inner cell mass

Nature communications, 2017-11, Vol.8 (1), p.1297-14, Article 1297

2017

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Microarray analyses of the dorsal root ganglia support a role for innate neuro-immune pathways in persistent pain in experimental osteoarthritis

Osteoarthritis and cartilage, 2020-05, Vol.28 (5), p.581-592

2020

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The role of Xist‐mediated Polycomb recruitment in the initiation of X‐chromosome inactivation

EMBO reports, 2019-10, Vol.20 (10), p.e48019-n/a

2019

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Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria

Human mutation, 2012-10, Vol.33 (10), p.1485-1493

2012

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Kinetics of Xist -induced gene silencing can be predicted from combinations of epigenetic and genomic features

Genome research, 2019-07, Vol.29 (7), p.1087

2019

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Hypermobility, the Ehlers-Danlos syndromes and chronic pain

Clinical and experimental rheumatology, 2017-09, Vol.35 Suppl 107 (5), p.116

2017

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Editorial: Ehlers-Danlos syndrome: from bedside to bench

Frontiers in genetics, 2024, Vol.15, p.1399386-1399386

2024

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Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers-Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix

Genetics in medicine, 2020-01, Vol.22 (1), p.112-123

2020

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Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome

Matrix biology, 2020-07, Vol.89, p.59-75

2020

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756 - MATRISOME GENE CHANGES IN DORSAL ROOT GANGLIA IN MOUSE MODELS OF OSTEOARTHRITIS PAIN SUGGEST A ROLE FOR FIBROBLAST-NOCICEPTOR COMMUNICATION IN CHRONIC PAIN

Osteoarthritis and cartilage, 2024-04, Vol.32, p.S517-S517

2024

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Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers–Danlos syndrome

Human mutation, 2021-10, Vol.42 (10), p.1294-1306

2021

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Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen

Genetics in medicine, 2021-12, Vol.23 (12), p.2378-2385

2021

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The case of the electronic cigarette in the EU

European journal of health law, 2014-01, Vol.21 (2), p.161-175

Syx, Eugenie

2014

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Loss of TANGO1 Leads to Absence of Bone Mineralization

JBMR plus, 2021-03, Vol.5 (3), p.e10451-n/a

2021

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Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa

American journal of human genetics, 2017-02, Vol.100 (2), p.216-227

2017

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Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder

American journal of human genetics, 2013-06, Vol.92 (6), p.935-945

2013

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The Ehlers-Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism

Genes, 2022-01, Vol.13 (2), p.265

2022

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Bi-allelic AEBP1 mutations in two patients with Ehlers–Danlos syndrome

Human molecular genetics, 2019-06, Vol.28 (11), p.1853-1864

2019

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Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis

Human mutation, 2015-05, Vol.36 (5), p.535-547

2015

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Relative calibration of the LIGO and Virgo detectors using astrophysical events from their third observing run

Did Mark make use of the Source Q? An analysis of the Beelzebul controversy (Mk 3,20-30 and Par.)

The Implication of Early Chromatin Changes in X Chromosome Inactivation

Maternal LSD1/KDM1A is an essential regulator of chromatin and transcription landscapes during zygotic genome activation

Locus specific epigenetic modalities of random allelic expression imbalance

Xist-dependent imprinted X inactivation and the early developmental consequences of its failure

Contribution of epigenetic landscapes and transcription factors to X-chromosome reactivation in the inner cell mass

Microarray analyses of the dorsal root ganglia support a role for innate neuro-immune pathways in persistent pain in experimental osteoarthritis

The role of Xist‐mediated Polycomb recruitment in the initiation of X‐chromosome inactivation

Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteria

Kinetics of Xist -induced gene silencing can be predicted from combinations of epigenetic and genomic features

Hypermobility, the Ehlers-Danlos syndromes and chronic pain

Editorial: Ehlers-Danlos syndrome: from bedside to bench

Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers-Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix

Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome

756 - MATRISOME GENE CHANGES IN DORSAL ROOT GANGLIA IN MOUSE MODELS OF OSTEOARTHRITIS PAIN SUGGEST A ROLE FOR FIBROBLAST-NOCICEPTOR COMMUNICATION IN CHRONIC PAIN

Clinical and molecular characteristics of 168 probands and 65 relatives with a clinical presentation of classical Ehlers–Danlos syndrome

Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen

The case of the electronic cigarette in the EU

Loss of TANGO1 Leads to Absence of Bone Mineralization

Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa

Defective Initiation of Glycosaminoglycan Synthesis due to B3GALT6 Mutations Causes a Pleiotropic Ehlers-Danlos-Syndrome-like Connective Tissue Disorder

The Ehlers-Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism

Bi-allelic AEBP1 mutations in two patients with Ehlers–Danlos syndrome

Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis

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