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Rubicon: LC3‐associated phagocytosis and beyond

The FEBS journal, 2018-04, Vol.285 (8), p.1379-1388

2018

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Programmed Necrosis and Disease:We interrupt your regular programming to bring you necroinflammation

Cell death and differentiation, 2019-01, Vol.26 (1), p.25-40

2019

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Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis

Oral diseases, 2019-04, Vol.25 (3), p.646-651

2019

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Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR‐ and EDA‐associated nonsyndromic oligodontia

Human mutation, 2020-11, Vol.41 (11), p.1957-1966

2020

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Inflamm-Aging-Related Cytokines of IL-17 and IFN-γ Accelerate Osteoclastogenesis and Periodontal Destruction

Journal of Immunology Research, 2021-08, Vol.2021, p.9919024-12

2021

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More Than Skin Deep: Autophagy Is Vital for Skin Barrier Function

Frontiers in immunology, 2018-06, Vol.9, p.1376-1376

2018

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Global deletion of Optineurin results in altered type I IFN signaling and abnormal bone remodeling in a model of Paget's disease

Cell death and differentiation, 2020-01, Vol.27 (1), p.71-84

2020

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Distinct impacts of bi‐allelic WNT10A mutations on the permanent and primary dentitions in odonto‐onycho‐dermal dysplasia

American journal of medical genetics. Part A, 2019-01, Vol.179 (1), p.57-64

2019

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Novel PITX2 mutations identified in Axenfeld–Rieger syndrome and the pattern of PITX2‐related tooth agenesis

Oral diseases, 2019-11, Vol.25 (8), p.2010-2019

2019

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The Roles of FOXO1 in Periodontal Homeostasis and Disease

Journal of Immunology Research, 2021, Vol.2021, p.5557095-12

2021

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Dopaminergic effects on in vitro osteogenesis

Bone research, 2015-07, Vol.3 (3), p.130-139

2015

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Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype‐phenotype correlation analyses of TP63‐related disorders

Molecular genetics & genomic medicine, 2019-06, Vol.7 (6), p.e704-n/a

2019

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Mutations in WNT10B Are Identified in Individuals with Oligodontia

American journal of human genetics, 2016-07, Vol.99 (1), p.195-201

2016

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Dopamine suppresses osteoclast differentiation via cAMP/PKA/CREB pathway

Cellular signalling, 2021-02, Vol.78, p.109847-109847, Article 109847

2021

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BMP4 mutations in tooth agenesis and low bone mass

Archives of oral biology, 2019-07, Vol.103, p.40-46

2019

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Dramatic Improvement of the Mechanical Strength of Silane-Modified Hydroxyapatite–Gelatin Composites via Processing with Cosolvent

ACS omega, 2018-03, Vol.3 (3), p.3592-3598

2018

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Systemic Dietary Hesperidin Modulation of Osteoclastogenesis, Bone Homeostasis and Periodontal Disease in Mice

International journal of molecular sciences, 2022-06, Vol.23 (13), p.7100

2022

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A novel inhibitor of nuclear factor kappa-B kinase subunit gamma mutation identified in an incontinentia pigmenti patient with syndromic tooth agenesis

Archives of oral biology, 2019-05, Vol.101, p.100-107

2019

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Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome

Scientific reports, 2016-12, Vol.6 (1), p.38680-38680, Article 38680

2016

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Optineurin regulates NRF2-mediated antioxidant response in a mouse model of Paget's disease of bone

Science advances, 2023-01, Vol.9 (4), p.eade6998-eade6998

2023

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A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia

Mutagenesis, 2014-09, Vol.29 (5), p.319-323

2014

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Occlusal Rehabilitation in a Patient with Oligodontia and Microdontia using Implants and Full-Ceramic Restorations: A Clinical Report

The Chinese journal of dental research : the official journal of the Scientific Section of the Chinese Stomatological Association (CSA), 2019, Vol.22 (4), p.281

2019

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Rubicon: LC 3‐associated phagocytosis and beyond

The FEBS journal, 2018-04, Vol.285 (8), p.1379-1388

2018

Volltextzugriff (PDF)

Genetic analysis: Wnt and other pathways in non-syndromic tooth agenesis

Oral diseases, 2018-07, Vol.25 (3), p.646-651

2018

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Correction: Global deletion of optineurin results in altered type I IFN signaling and abnormal bone remodeling in a model of Paget's disease

Cell death and differentiation, 2023-03, Vol.30 (3), p.855-855

2023

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Rubicon: LC3‐associated phagocytosis and beyond

Programmed Necrosis and Disease:We interrupt your regular programming to bring you necroinflammation

Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR‐ and EDA‐associated nonsyndromic oligodontia

Inflamm-Aging-Related Cytokines of IL-17 and IFN-γ Accelerate Osteoclastogenesis and Periodontal Destruction

More Than Skin Deep: Autophagy Is Vital for Skin Barrier Function

Global deletion of Optineurin results in altered type I IFN signaling and abnormal bone remodeling in a model of Paget's disease

Distinct impacts of bi‐allelic WNT10A mutations on the permanent and primary dentitions in odonto‐onycho‐dermal dysplasia

Novel PITX2 mutations identified in Axenfeld–Rieger syndrome and the pattern of PITX2‐related tooth agenesis

The Roles of FOXO1 in Periodontal Homeostasis and Disease

Dopaminergic effects on in vitro osteogenesis

Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype‐phenotype correlation analyses of TP63‐related disorders

Mutations in WNT10B Are Identified in Individuals with Oligodontia

Dopamine suppresses osteoclast differentiation via cAMP/PKA/CREB pathway

BMP4 mutations in tooth agenesis and low bone mass

Dramatic Improvement of the Mechanical Strength of Silane-Modified Hydroxyapatite–Gelatin Composites via Processing with Cosolvent

Systemic Dietary Hesperidin Modulation of Osteoclastogenesis, Bone Homeostasis and Periodontal Disease in Mice

A novel inhibitor of nuclear factor kappa-B kinase subunit gamma mutation identified in an incontinentia pigmenti patient with syndromic tooth agenesis

Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome

Optineurin regulates NRF2-mediated antioxidant response in a mouse model of Paget's disease of bone

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia

Occlusal Rehabilitation in a Patient with Oligodontia and Microdontia using Implants and Full-Ceramic Restorations: A Clinical Report

Rubicon: LC 3‐associated phagocytosis and beyond

Genetic analysis: Wnt and other pathways in non-syndromic tooth agenesis

Correction: Global deletion of optineurin results in altered type I IFN signaling and abnormal bone remodeling in a model of Paget's disease

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