699 results on '"Hovnanian, Alain"'
Search Results
2. Highly Efficient Ex Vivo Correction of COL7A1 through Ribonucleoprotein-Based CRISPR/Cas9 and Homology-Directed Repair to Treat Recessive Dystrophic Epidermolysis Bullosa
3. Pachyonychia Congenita: A Research Agenda Leading to New Therapeutic Approaches
4. Comparative analyses of Netherton syndrome patients and Spink5 conditional knock-out mice uncover disease-relevant pathways
5. Successful treatment of JAK1-associated inflammatory disease
6. Interplay of Staphylococcal and Host Proteases Promotes Skin Barrier Disruption in Netherton Syndrome
7. EGFR Signaling Is Overactive in Pachyonychia Congenita: Effective Treatment with Oral Erlotinib
8. Citrullinated Histone H3, a Marker for Neutrophil Extracellular Traps, Is Associated with Poor Prognosis in Cutaneous Squamous Cell Carcinoma Developing in Patients with Recessive Dystrophic Epidermolysis Bullosa.
9. A Potent and Selective Kallikrein-5 Inhibitor Delivers High Pharmacological Activity in Skin from Patients with Netherton Syndrome
10. Inborn Errors of Immunity in Hidradenitis Suppurativa: a New Lead for HS Genetics?
11. Large-scale functional inference for skin-expressing lncRNAs using expression and sequence information
12. The Whey Acidic Protein WFDC12 Is Specifically Expressed in Terminally Differentiated Keratinocytes and Regulates Epidermal Serine Protease Activity
13. Glucosylated cholesterol in skin: Synthetic role of extracellular glucocerebrosidase
14. The Surface Microbiome of Clinically Unaffected Skinfolds in Hidradenitis Suppurativa: A Cross-Sectional Culture-Based and 16S rRNA Gene Amplicon Sequencing Study in 60 Patients
15. Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
16. A cross-sectional study of erythromelalgia in patients with pachyonychia congenita.
17. Mutations in PERP Cause Dominant and Recessive Keratoderma
18. Generation and characterization of induced pluripotent stem cell lines from two patients with recessive dystrophic epidermolysis Bullosa
19. Efficacy of Dupilumab for Controlling Severe Atopic Dermatitis in a Patient with Hyper-IgE Syndrome
20. The Microbiological Landscape of Anaerobic Infections in Hidradenitis Suppurativa: A Prospective Metagenomic Study
21. Supplementary Data from Identification of Rigosertib for the Treatment of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
22. The Molecular Revolution in Cutaneous Biology: Emerging Landscape in Genomic Dermatology: New Mechanistic Ideas, Gene Editing, and Therapeutic Breakthroughs
23. Selective Substrates and Inhibitors for Kallikrein-Related Peptidase 7 (KLK7) Shed Light on KLK Proteolytic Activity in the Stratum Corneum
24. ISID0852 - Olmsted syndrome due to PERP mutations shows activation of the EGFR pathway and is improved by oral erlotinib
25. Prenatal Diagnosis of Epidermolysis Bullosa: Current Aspects and Perspectives
26. Type I IFNs link skin-associated dysbiotic commensal bacteria to pathogenic inflammation and angiogenesis in rosacea
27. Biological treatments for pediatric Netherton syndrome
28. AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer
29. Antisense-Mediated Splice Modulation to Reframe Transcripts
30. Correction to: Antisense-Mediated Splice Modulation to Reframe Transcripts
31. ESDR290 - Strategies to improve in vivo survival of Mesenchymal Stromal Cells after injection in immunodeficient mice
32. ESDR304 - Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
33. ESDR263 - EGFR signalling is overactive in Pachyonychia congenita: effective treatment with oral erlotinib
34. ESDR213 - Genetic study of the largest Tunisian cohort of 15 patients with Netherton syndrome: Two new SPINK5 mutations and founder effect
35. ESDR290 - Strategies to improve in vivo survival of Mesenchymal Stromal Cells after injection in immunodeficient mice
36. ESDR304 - Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
37. ESDR263 - EGFR signalling is overactive in Pachyonychia congenita: effective treatment with oral erlotinib
38. Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin
39. Type I interferons link skin-associated dysbiotic commensal bacteria to pathogenic inflammation and angiogenesis in rosacea
40. Phage Display Selected Cyclic Peptide Inhibitors of Kallikrein-Related Peptidases 5 and 7 and Their In Vivo Delivery to the Skin
41. Proteases: common culprits in human skin disorders
42. AXIN2 germline testing in a French cohort validates pathogenic variants as a rare cause of predisposition to colorectal polyposis and cancer.
43. Identification by in silico and in vitro screenings of small organic molecules acting as reversible inhibitors of kallikreins
44. Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
45. Drug Repurposing Reveals mTOR Inhibition as a Promising Strategy for Epidermolysis Bullosa Simplex
46. Bacterial pathogens associated with Hidradenitis Suppurativa, France
47. Ichtyose congénitale autosomique récessive et psoriasis : association fortuite ou lien physiopathologique ?
48. Transcription factor E4F1 is essential for epidermal stem cell maintenance and skin homeostasis
49. Netherton syndrome subtypes share IL-17/IL-36 signature with distinct IFN-α and allergic responses
50. TLR3 Deficiency in Patients with Herpes Simplex Encephalitis
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