204 results on '"Klausegger, Alfred"'
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2. Wundtherapie mit kaltem Plasma bei Epidermolysis bullosa dystrophica: Eine Pilotuntersuchung
3. A non-viral and selection-free COL7A1 HDR approach with improved safety profile for dystrophic epidermolysis bullosa
4. Predictable CRISPR/Cas9-Mediated COL7A1 Reframing for Dystrophic Epidermolysis Bullosa
5. Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial
6. Improved Double-Nicking Strategies for COL7A1-Editing by Homologous Recombination
7. Gene Editing–Mediated Disruption of Epidermolytic Ichthyosis–Associated KRT10 Alleles Restores Filament Stability in Keratinocytes
8. Splicing Modulation via Antisense Oligonucleotides in Recessive Dystrophic Epidermolysis Bullosa
9. Orofacial Anomalies in Kindler Epidermolysis Bullosa.
10. Cut and Paste: Efficient Homology-Directed Repair of a Dominant Negative KRT14 Mutation via CRISPR/Cas9 Nickases
11. COL7A1 Editing via CRISPR/Cas9 in Recessive Dystrophic Epidermolysis Bullosa
12. Cells from discarded dressings differentiate chronic from acute wounds in patients with Epidermolysis Bullosa
13. Plectin in Epidermolysis Bullosa and Autoimmune, Bullous Diseases
14. The power of next‐generation‐sequencing: A game‐changer with limitations.
15. General Aspects
16. Low-dose calcipotriol can elicit wound closure, anti-microbial, and anti-neoplastic effects in epidermolysis bullosa keratinocytes
17. Recessive Dystrophic Epidermolysis bullosa due to Hemizygous 40 kb Deletion of COL7A1 and the Proximate PFKFB4 Gene Focusing on the Mutation c.425A>G Mimicking Homozygous Status
18. Regeneration of the entire human epidermis using transgenic stem cells
19. Functional Correction of Type VII Collagen Expression in Dystrophic Epidermolysis Bullosa
20. 5′RNA Trans-Splicing Repair of COL7A1 Mutant Transcripts in Epidermolysis Bullosa
21. Pseudosyndaktylie – eine entzündliche und fibrotische Wundheilungsstörung bei rezessiver Epidermolysis bullosa dystrophica
22. Pseudosyndactyly – an inflammatory and fibrotic wound healing disorder in recessive dystrophic epidermolysis bullosa
23. Wundtherapie mit kaltem Plasma bei Epidermolysis bullosa dystrophica
24. 5′ Trans-Splicing Repair of the PLEC1 Gene
25. Additional file 4 of Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial
26. Additional file 3 of Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial
27. Additional file 1 of Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial
28. Additional file 2 of Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial
29. Haploinsufficiency due to deletion within the 3′-UTR of C1-INH-gene associated with hereditary angioedema
30. Personalized Development of Antisense Oligonucleotides for Exon Skipping Restores Type XVII Collagen Expression in Junctional Epidermolysis Bullosa
31. Founder mutation c.676insC in three unrelated Kindler syndrome families belonging to a particular clan from Pakistan
32. Compound heterozygous mutations p.Q1530X and 6103delG in COL7A1 causing recessive dystrophic epidermolysis bullosa in a Pakistani family
33. The international dystrophic epidermolysis bullosa patient registry: An online database of dystrophic epidermolysis bullosa patients and their COL7A1 mutations
34. A novel screening system improves genetic correction by internal exon replacement
35. EPIDERMOLYSIS BULLOSA WITH LATE-ONSET MUSCULAR DYSTROPHY AND PLECTIN DEFICIENCY
36. A NOVEL GLYCINE MUTATION IN THE COL7A1 GENE LEADING TO DOMINANT DYSTROPHIC EPIDERMOLYSIS BULLOSA WITH INTRA-FAMILIAL PHENOTYPICAL HETEROGENEITY
37. Novel KIND1 Gene Mutation in Kindler Syndrome With Severe Gastrointestinal Tract Involvement
38. Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay
39. Zahnveränderungen bei junktionaler Epidermolysis bullosa - Bericht uber eine Patientin mit einer Mutation im LAMB3-Gen
40. Identification of vitamin D target genes in human keratinocytes by subtractive screening
41. Expression of Neuropeptide Galanin and Galanin Receptors in Human Skin
42. Pathogenic Mechanisms in Epidermolysis Bullosa Naevi
43. Is Screening of the Candidate Gene Necessary in Unrelated Partners of Members of Families with Herlitz Junctional Epidermolysis Bullosa?
44. A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency
45. Epidermolysis bullosa Associated with Type 1 Diabetes Mellitus - Case Report of a Lethal Disease
46. A defect in the inner kinetochore protein CENPT causes a new syndrome of severe growth failure
47. Aging / Transcriptome and ultrastructural changes in dystrophic Epidermolysis bullosa resemble skin aging
48. PLoS ONE / Specialized yeast ribosomes : a customized tool for selective mRNA translation
49. Specialized yeast ribosomes: a customized tool for selective mRNA translation
50. Pseudosyndactyly - an inflammatory and fibrotic wound healing disorder in recessive dystrophic epidermolysis bullosa
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