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Taxonomic bias in AMP prediction of invertebrate peptides

Scientific reports, 2021-09, Vol.11 (1), p.17924-17924, Article 17924

2021

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MicroRNA-146a alleviates chronic skin inflammation in atopic dermatitis through suppression of innate immune responses in keratinocytes

Journal of allergy and clinical immunology, 2014-10, Vol.134 (4), p.836-847.e11

2014

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MiR-125b, a MicroRNA Downregulated in Psoriasis, Modulates Keratinocyte Proliferation by Targeting FGFR2

Journal of investigative dermatology, 2011-07, Vol.131 (7), p.1521-1529

2011

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State and physiology behind personality in arthropods: a review

Behavioral ecology and sociobiology, 2022-11, Vol.76 (11), Article 150

2022

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Draft genome of a biparental beetle species, Lethrus apterus

BMC genomics, 2021-04, Vol.22 (1), p.301-301, Article 301

2021

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Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients

International journal of molecular sciences, 2023-04, Vol.24 (8), p.7401

2023

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A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder

BMC pediatrics, 2024-01, Vol.24 (1), p.47-47, Article 47

2024

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Inotocin, a potential modulator of reproductive behaviours in a biparental beetle, Lethrus apterus

Journal of insect physiology, 2021-07, Vol.132, p.104253-104253, Article 104253

2021

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Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the PTCH1 Gene in BCNS

Current issues in molecular biology, 2023-06, Vol.45 (7), p.5293-5304

2023

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Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease

International journal of molecular sciences, 2024-01, Vol.25 (2), p.1271

2024

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Mechanisms of IFN-γ–induced apoptosis of human skin keratinocytes in patients with atopic dermatitis

Journal of allergy and clinical immunology, 2012-05, Vol.129 (5), p.1297-1306

2012

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Phenotype–genotype correlations for clinical variants caused by CYLD mutations

European journal of medical genetics, 2015-05, Vol.58 (5), p.271-278

2015

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The updated genome of the Hungarian population of Aedes koreicus

Scientific reports, 2024-03, Vol.14 (1), p.7545-7545, Article 7545

2024

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An overlooked phenomenon: complex interactions of potential error sources on the quality of bacterial de novo genome assemblies

BMC genomics, 2024-01, Vol.25 (1), p.45-45, Article 45

2024

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Evaluation of potential reference genes for real-time qPCR analysis in a biparental beetle, Lethrus apterus (Coleoptera: Geotrupidae)

PeerJ (San Francisco, CA), 2017-11, Vol.5, p.e4047-e4047, Article e4047

2017

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Pharmacological Targeting of the Epidermal Barrier

Current pharmaceutical design, 2016-01, Vol.22 (35), p.5373

2016

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HB-EGF Induces COL7A1 Expression in Keratinocytes and Fibroblasts: Possible Mechanism Underlying Allogeneic Fibroblast Therapy in Recessive Dystrophic Epidermolysis Bullosa

Journal of investigative dermatology, 2011-08, Vol.131 (8), p.1771-1774

2011

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The anti-apoptotic protein G1P3 is overexpressed in psoriasis and regulated by the non-coding RNA, PRINS

Experimental dermatology, 2010-03, Vol.19 (3), p.269-278

2010

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Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: a case report

BMC pediatrics, 2019-01, Vol.19 (1), p.16-16, Article 16

2019

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Revertant Mosaicism in Recessive Dystrophic Epidermolysis Bullosa

Journal of investigative dermatology, 2010-07, Vol.130 (7), p.1937-1940

2010

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Electrochemotherapy for Non-melanoma Skin Cancer in a Child with Xeroderma Pigmentosum

Acta dermato-venereologica, 2017-09, Vol.97 (8), p.962-964

2017

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Report of a Novel ALOX12B Mutation in Self-Improving Collodion Ichthyosis with an Overview of the Genetic Background of the Collodion Baby Phenotype

Life (Basel, Switzerland), 2021-06, Vol.11 (7), p.624

2021

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The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson’s Disease in the Hungarian Population

Parkinson's disease, 2018, Vol.2018, p.9351598-7

2018

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Nuclear Factor κB Activation in a Type V Pityriasis Rubra Pilaris Patient Harboring Multiple CARD14 Variants

Frontiers in immunology, 2018-07, Vol.9, p.1564-1564

2018

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Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A

Journal of dermatological science, 2010-06, Vol.58 (3), p.220-222

2010

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Taxonomic bias in AMP prediction of invertebrate peptides

MicroRNA-146a alleviates chronic skin inflammation in atopic dermatitis through suppression of innate immune responses in keratinocytes

MiR-125b, a MicroRNA Downregulated in Psoriasis, Modulates Keratinocyte Proliferation by Targeting FGFR2

State and physiology behind personality in arthropods: a review

Draft genome of a biparental beetle species, Lethrus apterus

Genetic Etiology of Nonsyndromic Hearing Loss in Hungarian Patients

A novel de novo truncating variant in a Hungarian patient with CTNNB1 neurodevelopmental disorder

Inotocin, a potential modulator of reproductive behaviours in a biparental beetle, Lethrus apterus

Whole-Exome Sequencing Identified Two Novel Pathogenic Mutations in the PTCH1 Gene in BCNS

Missing Heritability in Albinism: Deep Characterization of a Hungarian Albinism Cohort Raises the Possibility of the Digenic Genetic Background of the Disease

Mechanisms of IFN-γ–induced apoptosis of human skin keratinocytes in patients with atopic dermatitis

Phenotype–genotype correlations for clinical variants caused by CYLD mutations

The updated genome of the Hungarian population of Aedes koreicus

An overlooked phenomenon: complex interactions of potential error sources on the quality of bacterial de novo genome assemblies

Evaluation of potential reference genes for real-time qPCR analysis in a biparental beetle, Lethrus apterus (Coleoptera: Geotrupidae)

Pharmacological Targeting of the Epidermal Barrier

HB-EGF Induces COL7A1 Expression in Keratinocytes and Fibroblasts: Possible Mechanism Underlying Allogeneic Fibroblast Therapy in Recessive Dystrophic Epidermolysis Bullosa

The anti-apoptotic protein G1P3 is overexpressed in psoriasis and regulated by the non-coding RNA, PRINS

Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: a case report

Revertant Mosaicism in Recessive Dystrophic Epidermolysis Bullosa

Electrochemotherapy for Non-melanoma Skin Cancer in a Child with Xeroderma Pigmentosum

Report of a Novel ALOX12B Mutation in Self-Improving Collodion Ichthyosis with an Overview of the Genetic Background of the Collodion Baby Phenotype

The rs13388259 Intergenic Polymorphism in the Genomic Context of the BCYRN1 Gene Is Associated with Parkinson’s Disease in the Hungarian Population

Nuclear Factor κB Activation in a Type V Pityriasis Rubra Pilaris Patient Harboring Multiple CARD14 Variants

Schöpf-Schulz-Passarge syndrome resulting from a homozygous nonsense mutation in WNT10A

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