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Identification of putative genetic modifying factors that influence the development of Papillon–Lefévre or Haim–Munk syndrome phenotypes

Clinical and experimental dermatology, 2020-07, Vol.45 (5), p.555-559

2020

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HuCOP1 contributes to the regulation of DNA repair in keratinocytes

Molecular and cellular biochemistry, 2017-03, Vol.427 (1-2), p.103-109

2017

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Halogen bonding as a supramolecular dynamics catalyst

Nature communications, 2019-02, Vol.10 (1), p.916-916, Article 916

2019

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Abnormal regulation of fibronectin production by fibroblasts in psoriasis

British journal of dermatology (1951), 2016-03, Vol.174 (3), p.533-541

2016

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Detection of a rare CDKN2A intronic mutation in a Hungarian melanoma-prone family and its role in splicing regulation

British journal of dermatology (1951), 2012-07, Vol.167 (1), p.131-133

2012

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Scaling Law of Urban Ride Sharing

Scientific reports, 2017-03, Vol.7 (1), p.42868-42868, Article 42868

2017

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372 Mechanism of cytosolic nucleic acid-induced CX3CL1 expression of human keratinocytes

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S244-S244

2022

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177 Identification of putative genetic modifying factors that influence the development of Papillon-Lefévre or Haim-Munk syndrome phenotypes

Journal of investigative dermatology, 2021-10, Vol.141 (10), p.S178-S178

2021

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481 Functional studies on the pathogenic truncating mutations of CYLD

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S263-S263

2022

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The management and genetic background of pityriasis rubra pilaris: a single‐centre experience

Journal of the European Academy of Dermatology and Venereology, 2019-05, Vol.33 (5), p.944-949

2019

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A curious case of dynamic disorder in pyrrolidine rings elucidated by NMR crystallography

Chemical communications (Cambridge, England), 2020-11, Vol.56 (9), p.1439-1442

2020

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Characterization of human chymotrypsinogen activation

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2012-11, Vol.12 (6), p.544-544

2012

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176 Identification of putative phenotype-modifying genetic factors associated with phenotypic diversity in Brooke-Spiegler syndrome

Journal of investigative dermatology, 2021-10, Vol.141 (10), p.S178-S178

2021

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173 TRAF3 and NBR1 both influence the effect of CYLD(Arg936X) mutation on NF-κB activity

Journal of investigative dermatology, 2021-10, Vol.141 (10), p.S178-S178

2021

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373 Abnormal type VII collagen expression in non-lesional psoriatic skin

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S244-S244

2022

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Thrombosis and risk factors in female patients with a rare acquired thrombophilia: chronic myeloproliferative disorder - polycythaemia vera and essential thrombocythaemia

European review for medical and pharmacological sciences, 2014-12, Vol.18 (24), p.3810

2014

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One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes

Clinical and experimental dermatology, 2016-03, Vol.41 (2), p.190-195

2016

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Taming the dynamics in a pharmaceutical by cocrystallization: investigating the impact of the coformer by solid-state NMR

CrystEngComm, 2021-10, Vol.23 (39), p.6859-687

2021

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Highlights from the Faraday Discussion: Halogen Bonding in Supramolecular and Solid State Chemistry, July 10-12th 2017, Ottawa, Canada

Chemical communications (Cambridge, England), 2017-10, Vol.53 (85), p.11615-11621

2017

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BRAFV600E mutation in cutaneous lesions of patients with adult Langerhans cell histiocytosis

Journal of the European Academy of Dermatology and Venereology, 2015-06, Vol.29 (6), p.1205-1211

2015

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207 PRINS long non-coding RNA regulates IL-23 expression of keratinocytes

Journal of investigative dermatology, 2021-10, Vol.141 (10), p.S184-S184

2021

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Single Nucleotide Polymorphisms of the Fibroblast Growth Factor Receptor 2 Gene in Patients with Chronic Venous Insufficiency with Leg Ulcer

Journal of investigative dermatology, 2005-05, Vol.124 (5), p.1085-1088

2005

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Atypical neurofibromatosis type 1 with unilateral limb hypertrophy mimicking overgrowth syndrome

Clinical and experimental dermatology, 2017-10, Vol.42 (7), p.763-766

2017

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Rapid Identification of Halogen Bonds in Co‐Crystalline Powders via 127I Nuclear Quadrupole Resonance Spectroscopy

Angewandte Chemie International Edition, 2019-09, Vol.58 (38), p.13479-13485

International ed. in English, 2019

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233 Identification of genetic modifying factors responsible for the development of the distinct Papillon-Lefévre syndrome and Haim-Munk syndrome clinical phenotypes

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.S232-S232

2017

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Identification of putative genetic modifying factors that influence the development of Papillon–Lefévre or Haim–Munk syndrome phenotypes

HuCOP1 contributes to the regulation of DNA repair in keratinocytes

Halogen bonding as a supramolecular dynamics catalyst

Abnormal regulation of fibronectin production by fibroblasts in psoriasis

Detection of a rare CDKN2A intronic mutation in a Hungarian melanoma-prone family and its role in splicing regulation

Scaling Law of Urban Ride Sharing

372 Mechanism of cytosolic nucleic acid-induced CX3CL1 expression of human keratinocytes

177 Identification of putative genetic modifying factors that influence the development of Papillon-Lefévre or Haim-Munk syndrome phenotypes

481 Functional studies on the pathogenic truncating mutations of CYLD

The management and genetic background of pityriasis rubra pilaris: a single‐centre experience

A curious case of dynamic disorder in pyrrolidine rings elucidated by NMR crystallography

Characterization of human chymotrypsinogen activation

176 Identification of putative phenotype-modifying genetic factors associated with phenotypic diversity in Brooke-Spiegler syndrome

173 TRAF3 and NBR1 both influence the effect of CYLD(Arg936X) mutation on NF-κB activity

373 Abnormal type VII collagen expression in non-lesional psoriatic skin

Thrombosis and risk factors in female patients with a rare acquired thrombophilia: chronic myeloproliferative disorder - polycythaemia vera and essential thrombocythaemia

One mutation, two phenotypes: a single nonsense mutation of the CTSC gene causes two clinically distinct phenotypes

Taming the dynamics in a pharmaceutical by cocrystallization: investigating the impact of the coformer by solid-state NMR

Highlights from the Faraday Discussion: Halogen Bonding in Supramolecular and Solid State Chemistry, July 10-12th 2017, Ottawa, Canada

BRAFV600E mutation in cutaneous lesions of patients with adult Langerhans cell histiocytosis

207 PRINS long non-coding RNA regulates IL-23 expression of keratinocytes

Single Nucleotide Polymorphisms of the Fibroblast Growth Factor Receptor 2 Gene in Patients with Chronic Venous Insufficiency with Leg Ulcer

Atypical neurofibromatosis type 1 with unilateral limb hypertrophy mimicking overgrowth syndrome

Rapid Identification of Halogen Bonds in Co‐Crystalline Powders via 127I Nuclear Quadrupole Resonance Spectroscopy

233 Identification of genetic modifying factors responsible for the development of the distinct Papillon-Lefévre syndrome and Haim-Munk syndrome clinical phenotypes

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