Alain Hovnanian mainly focuses on Genetics, Netherton syndrome, LEKTI, KLK5 and KLK7. Netherton syndrome connects with themes related to Cell biology in his study. In his research, Filaggrin, Elastase and Skin erythema is intimately related to Proteases, which falls under the overarching field of LEKTI.
His KLK5 research is multidisciplinary, relying on both Cathelicidin, Antimicrobial peptides, Serine Peptidase Inhibitor Kazal-Type 5 and Kallikrein. He interconnects Gene polymorphism, Immunology and Atopy in the investigation of issues within Serine Peptidase Inhibitor Kazal-Type 5. His KLK7 research integrates issues from Molecular biology and Stratum corneum.
His primary areas of investigation include Genetics, Netherton syndrome, Gene, Dermatology and Molecular biology. His study in Netherton syndrome is interdisciplinary in nature, drawing from both Serine Peptidase Inhibitor Kazal-Type 5, Stratum corneum, LEKTI, Immunology and KLK5. His LEKTI research incorporates themes from Proteases and Kallikrein.
Alain Hovnanian combines subjects such as Proinflammatory cytokine, KLK7 and Cell biology with his study of KLK5. His biological study spans a wide range of topics, including Disease and Pathology. His Molecular biology study incorporates themes from Epidermolysis bullosa dystrophica and Mutant.
Alain Hovnanian spends much of his time researching Netherton syndrome, Dermatology, Cell biology, Kallikrein and Hidradenitis suppurativa. His Netherton syndrome study integrates concerns from other disciplines, such as Protease, KLK5, Stratum corneum and LEKTI. Many of his studies involve connections with topics such as KLK7 and KLK5.
The various areas that he examines in his LEKTI study include Proteases and Ichthyosis. His Cell biology research is multidisciplinary, incorporating elements of OLMSTED SYNDROME, Desmoglein 3 and Gene, Mendelian inheritance. His Kallikrein study which covers Pharmacology that intersects with Serine Peptidase Inhibitor Kazal-Type 5 and Transepidermal water loss.
Alain Hovnanian mostly deals with Pathology, Microbiome, Staphylococcus epidermidis, Microbiology and Hidradenitis suppurativa. His study in the field of Epidermolysis bullosa simplex and Anetoderma also crosses realms of Macular hyperpigmentation. His Microbiome research encompasses a variety of disciplines, including Actinomyces, Prevotella, Microbiological culture, Mobiluncus and Kocuria.
Along with Staphylococcus epidermidis, other disciplines of study including Staphopain, Protease inhibitor, Proteases, Human skin and Netherton syndrome are integrated into his research. He interconnects Cohort study, Oncology, Young adult, Mutation and Gene mutation in the investigation of issues within Hidradenitis suppurativa. His Genetic enhancement research includes elements of Phase i ii, Ex vivo, Transgene, Recombinant DNA and Recessive dystrophic epidermolysis bullosa.
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TLR3 deficiency in patients with herpes simplex encephalitis.
Shen Ying Zhang;Shen Ying Zhang;Emmanuelle Jouanguy;Emmanuelle Jouanguy;Sophie Ugolini;Asma Smahi.
Science (2007)
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.
Jo David Fine;Robin A J Eady;Eugene A. Bauer;Johann W. Bauer.
Journal of The American Academy of Dermatology (2008)
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndrome.
S Chavanas;C Bodemer;A Rochat;D Hamel-Teillac.
Nature Genetics (2000)
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease
A. Sakuntabhai;V. Ruiz-Perez;S. Carter;N. Jacobsen.
Nature Genetics (1999)
Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification
Jo David Fine;Leena Bruckner-Tuderman;Robin A.J. Eady;Eugene A. Bauer.
Journal of The American Academy of Dermatology (2014)
Increased serine protease activity and cathelicidin promotes skin inflammation in rosacea
Kenshi Yamasaki;Anna Di Nardo;Antonella Bardan;Masamoto Murakami.
Nature Medicine (2007)
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009
Vinzenz Oji;Gianluca Tadini;Masashi Akiyama;Claudine Blanchet Bardon.
Journal of The American Academy of Dermatology (2010)
A European study of HLA-B in Stevens-Johnson syndrome and toxic epidermal necrolysis related to five high-risk drugs.
Christine Lonjou;Nicolas Borot;Peggy Sekula;Neil Ledger.
Pharmacogenetics and Genomics (2008)
Kallikrein 5 induces atopic dermatitis–like lesions through PAR2-mediated thymic stromal lymphopoietin expression in Netherton syndrome
Anaïs Briot;Céline Deraison;Céline Deraison;Matthieu Lacroix;Matthieu Lacroix;Chrystelle Bonnart;Chrystelle Bonnart.
Journal of Experimental Medicine (2009)
Kallikrein-mediated proteolysis regulates the antimicrobial effects of cathelicidins in skin
Kenshi Yamasaki;Jürgen Schauber;Alvin Coda;Henry Lin.
The FASEB Journal (2006)
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