607 results on '"Hausser, Ingrid"'
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2. Epidermal or Dermal Collagen VII Is Sufficient for Skin Integrity: Insights to Anchoring Fibril Homeostasis
3. Dermatologic manifestations and diagnostic assessments of the Ehlers-Danlos syndromes: A clinical review
4. Loss of glyoxalase 2 alters the glucose metabolism in zebrafish
5. Accumulation of acetaldehyde in aldh2.1−/− zebrafish causes increased retinal angiogenesis and impaired glucose metabolism
6. Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen
7. QR-313, an Antisense Oligonucleotide, Shows Therapeutic Efficacy for Treatment of Dominant and Recessive Dystrophic Epidermolysis Bullosa: A Preclinical Study
8. Regulation of Gluconeogenesis by Aldo-keto-reductase 1a1b in Zebrafish
9. ECM1 Prevents Activation of Transforming Growth Factor β, Hepatic Stellate Cells, and Fibrogenesis in Mice
10. Clinically Relevant Correction of Recessive Dystrophic Epidermolysis Bullosa by Dual sgRNA CRISPR/Cas9-Mediated Gene Editing
11. Impaired Detoxification of Trans, Trans‐2,4‐Decadienal, an Oxidation Product from Omega‐6 Fatty Acids, Alters Insulin Signaling, Gluconeogenesis and Promotes Microvascular Disease
12. Constitutional absence of epithelial integrin α3 impacts the composition of the cellular microenvironment of ILNEB keratinocytes
13. Deletion of a Pathogenic Mutation-Containing Exon of COL7A1 Allows Clonal Gene Editing Correction of RDEB Patient Epidermal Stem Cells
14. SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy
15. Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features
16. Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans
17. Mutations in ATP6V1E1 or ATP6V1A Cause Autosomal-Recessive Cutis Laxa
18. Prohibitin, STAT3 and SH2D4A physically and functionally interact in tumor cell mitochondria
19. Characterization of experimental diabetic neuropathy using multicontrast magnetic resonance neurography at ultra high field strength
20. Impaired Detoxification of Trans, Trans‐2,4‐Decadienal, an Oxidation Product from Omega‐6 Fatty Acids, Alters Insulin Signaling, Gluconeogenesis and Promotes Microvascular Disease.
21. Integra®-Dermal Regeneration Template and Split-Thickness Skin Grafting: A Therapy Approach to Correct Aplasia Cutis Congenita and Epidermolysis Bullosa in Carmi Syndrome
22. Collagen VII Half-Life at the Dermal-Epidermal Junction Zone: Implications for Mechanisms and Therapy of Genodermatoses
23. Gene Editing for the Efficient Correction of a Recurrent COL7A1 Mutation in Recessive Dystrophic Epidermolysis Bullosa Keratinocytes
24. The role of cutaneous manifestations in the diagnosis of the Ehlers-Danlos syndromes
25. Extracutaneous features and complications of the Ehlers-Danlos syndromes: A systematic review
26. High Local Concentrations of Intradermal MSCs Restore Skin Integrity and Facilitate Wound Healing in Dystrophic Epidermolysis Bullosa
27. Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis Imperfecta
28. Extracutaneous features and complications of the Ehlers-Danlos syndromes: A systematic review
29. 2. Morphologische Grundlagen erblicher Bindegewebserkrankungen
30. Cell tropism and viral clearance during SARS-CoV-2 lung infection
31. The role of cutaneous manifestations in the diagnosis of the Ehlers‐Danlos syndromes
32. Comparative Morphological, Metabolic and Transcriptome Analyses in elmo1−/−, elmo2−/−, and elmo3−/− Zebrafish Mutants Identified a Functional Non-Redundancy of the Elmo Proteins
33. Topical Enzyme-Replacement Therapy Restores Transglutaminase 1 Activity and Corrects Architecture of Transglutaminase-1-Deficient Skin Grafts
34. Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length
35. Aloxe3 Knockout Mice Reveal a Function of Epidermal Lipoxygenase-3 as Hepoxilin Synthase and Its Pivotal Role in Barrier Formation
36. S1 guidelines for the diagnosis and treatment of ichthyoses – update
37. S1‐Leitlinie zur Diagnostik und Therapie der Ichthyosen – Aktualisierung
38. Spiny Keratoderma der Hand‐ und Fußflächen – einmal gesehen, nie wieder vergessen
39. Spiny keratoderma of the palms and soles – once seen, never forgotten
40. Multiple Arterial Dissections and Connective Tissue Abnormalities
41. Methylglyoxal Induces Endothelial Dysfunction via a Stunning-like Phenotype
42. 12R-Lipoxygenase Deficiency Disrupts Epidermal Barrier Function
43. pdx1 Knockout Leads to a Diabetic Nephropathy-Like Phenotype in Zebrafish and Identifies Phosphatidylethanolamine as Metabolite Promoting Early Diabetic Kidney Damage
44. Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009
45. Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis
46. Methylglyoxal Induces Endothelial Dysfunction via Stunning
47. Mechanisms of Fibroblast Cell Therapy for Dystrophic Epidermolysis Bullosa: High Stability of Collagen VII Favors Long-term Skin Integrity
48. Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers–Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis
49. Development of an Ichthyosiform Phenotype in Alox12b-Deficient Mouse Skin Transplants
50. Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
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