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A high-throughput genome-wide siRNA screen for ciliogenesis identifies new ciliary functional components and ciliopathy genes

Cilia (London), 2015-07, Vol.4 (S1), p.O12-O12, Article O12

2015

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P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S13-S13

2014

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[S2.3]: Defects in non‐canonical Wnt signalling and actin cytoskeleton remodelling as pathogenic mechanisms in Meckel–Gruber syndrome

International journal of developmental neuroscience, 2010-12, Vol.28 (8), p.644-645

2010

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MKS1 interacts with components of the ubiquitin-proteasome pathway to regulate ciliogenesis and multiple signalling pathways

Cilia (London), 2012-11, Vol.1 (S1), p.P108-P108, Article P108

2012

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High throughput high content reverse genetics visual screens of ciliogenesis and cilia maintenance

Cilia (London), 2012-11, Vol.1 (S1), p.P49-P49, Article P49

2012

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Reach distances between two horizontal photoelectric beams

Ergonomics, 1986-01, Vol.29 (1), p.87-97

1986

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Research distances between two horizontal photoelectric beams

Ergonomics, 1986-01, Vol.29, p.87-97

1986

Volltextzugriff (PDF)

Inflammation activation and resolution in human tendon disease

Science translational medicine, 2015-10, Vol.7 (311), p.311ra173

2015

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Spectroscopic studies of some semiquinone radical ions

Wheway, Ashley G

1974

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Spectroscopic studies of some semiquinone radical ions

Wheway, Ashley G

1974

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Rotator cuff repair with biological graft augmentation causes adverse tissue outcomes

Acta orthopaedica, 2020-12, Vol.91 (6), p.782-788

2020

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Comparison of Cellular Responses to TGF-β1 and BMP-2 Between Healthy and Torn Tendons

The American journal of sports medicine, 2021-06, Vol.49 (7), p.1892-1903

2021

Volltextzugriff (PDF)

Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project

Frontiers in genetics, 2019-03, Vol.10, p.127

2019

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Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

Genome medicine, 2021-02, Vol.13 (1), p.34-34, Article 34

2021

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Platelet-Rich Plasma Injection With Arthroscopic Acromioplasty for Chronic Rotator Cuff Tendinopathy: A Randomized Controlled Trial

The American journal of sports medicine, 2015-12, Vol.43 (12), p.2891-2897

2015

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B Cell-Activating Factor Belonging to the TNF Family (BAFF)-R Is the Principal BAFF Receptor Facilitating BAFF Costimulation of Circulating T and B Cells

The Journal of immunology (1950), 2004-07, Vol.173 (2), p.807-817

2004

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A single cell atlas of frozen shoulder capsule identifies features associated with inflammatory fibrosis resolution

Nature communications, 2024-02, Vol.15 (1), p.1394-1394, Article 1394

2024

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Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome

American journal of human genetics, 2022-07, Vol.109 (7), p.1217-1241

2022

Volltextzugriff (PDF)

Proresolving Mediators LXB4 and RvE1 Regulate Inflammation in Stromal Cells from Patients with Shoulder Tendon Tears

The American journal of pathology, 2019-11, Vol.189 (11), p.2258-2268

2019

Volltextzugriff (PDF)

TNF Deficiency Fails to Protect BAFF Transgenic Mice against Autoimmunity and Reveals a Predisposition to B Cell Lymphoma

The Journal of immunology (1950), 2004-01, Vol.172 (2), p.812-822

2004

Volltextzugriff (PDF)

ERK1/2 drives IL-1β-induced expression of TGF-β1 and BMP-2 in torn tendons

Scientific reports, 2019-12, Vol.9 (1), p.19005-10, Article 19005

2019

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15-Epi-LXA4 and MaR1 counter inflammation in stromal cells from patients with Achilles tendinopathy and rupture

The FASEB journal, 2019-07, Vol.33 (7), p.8043-8054

2019

Volltextzugriff (PDF)

15‐Epi‐Lxa 4 and MaR1 counter inflammation in stromal cells from patients with Achilles tendinopathy and rupture

The FASEB journal, 2019-07, Vol.33 (7), p.8043-8054

2019

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DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration

Genetics in medicine, 2020-12, Vol.22 (12), p.2041-2051

2020

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A high-throughput genome-wide siRNA screen for ciliogenesis identifies new ciliary functional components and ciliopathy genes

P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

[S2.3]: Defects in non‐canonical Wnt signalling and actin cytoskeleton remodelling as pathogenic mechanisms in Meckel–Gruber syndrome

MKS1 interacts with components of the ubiquitin-proteasome pathway to regulate ciliogenesis and multiple signalling pathways

High throughput high content reverse genetics visual screens of ciliogenesis and cilia maintenance

Reach distances between two horizontal photoelectric beams

Research distances between two horizontal photoelectric beams

Inflammation activation and resolution in human tendon disease

Spectroscopic studies of some semiquinone radical ions

Spectroscopic studies of some semiquinone radical ions

Rotator cuff repair with biological graft augmentation causes adverse tissue outcomes

Comparison of Cellular Responses to TGF-β1 and BMP-2 Between Healthy and Torn Tendons

Opportunities and Challenges for Molecular Understanding of Ciliopathies-The 100,000 Genomes Project

Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly

Platelet-Rich Plasma Injection With Arthroscopic Acromioplasty for Chronic Rotator Cuff Tendinopathy: A Randomized Controlled Trial

B Cell-Activating Factor Belonging to the TNF Family (BAFF)-R Is the Principal BAFF Receptor Facilitating BAFF Costimulation of Circulating T and B Cells

A single cell atlas of frozen shoulder capsule identifies features associated with inflammatory fibrosis resolution

Identification and functional evaluation of GRIA1 missense and truncation variants in individuals with ID: An emerging neurodevelopmental syndrome

Proresolving Mediators LXB4 and RvE1 Regulate Inflammation in Stromal Cells from Patients with Shoulder Tendon Tears

TNF Deficiency Fails to Protect BAFF Transgenic Mice against Autoimmunity and Reveals a Predisposition to B Cell Lymphoma

ERK1/2 drives IL-1β-induced expression of TGF-β1 and BMP-2 in torn tendons

Selective advantage of mutant stem cells in human clonal hematopoiesis is associated with attenuated response to inflammation and aging

15-Epi-LXA4 and MaR1 counter inflammation in stromal cells from patients with Achilles tendinopathy and rupture

15‐Epi‐Lxa 4 and MaR1 counter inflammation in stromal cells from patients with Achilles tendinopathy and rupture

DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration

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