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1. Sestrin2 drives ER-phagy in response to protein misfolding

2. The novel missense mutation Met48Lys in FKBP22 changes its structure and functions.

3. 3D-bioprinted patient-specific organotypic bone model mimicking mineralization dysregulation in FKBP10-related osteogenesis imperfecta

4. Physiological cell bioprinting density in human bone-derived cell-laden scaffolds enhances matrix mineralization rate and stiffness under dynamic loading

5. Physiological cell bioprinting density in human bone-derived cell-laden scaffolds enhances matrix mineralization rate and stiffness under dynamic loading

6. The phenotype of the musculocontractural type of Ehlers‐Danlos syndrome due to CHST14 mutations

9. Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta

10. Physiological Cell Bioprinting Density in Personalized 3d Bone Organoids Enhances Matrix Mineralization Rate and Stiffness Under Dynamic Loading Conditions

12. The 2017 international classification of the Ehlers–Danlos syndromes

13. The Ehlers–Danlos syndromes, rare types

14. Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta.

17. Omics Profiling of S2P Mutant Fibroblasts as a Mean to Unravel the Pathomechanism and Molecular Signatures of X-Linked MBTPS2 Osteogenesis Imperfecta

18. Loss-of-function variants in exon 4 of TAB2 cause a recognizable multisystem disorder with cardiovascular, facial, cutaneous, and musculoskeletal involvement

20. List of Contributors

22. Kyphoscoliotic type of Ehlers-Danlos Syndrome (EDS VIA) in six Egyptian patients presenting with a homogeneous clinical phenotype

23. COL1-Related Disorders: Case Report and Review of Overlapping Syndromes

24. Understanding pyrroline-5-carboxylate synthetase deficiency: clinical, molecular, functional, and expression studies, structure-based analysis, and novel therapy with arginine

28. Spondylocheiro dysplastic form of the Ehlers-Danlos syndrome-an autosomal-recessive entity caused by mutations in the zinc transporter gene SLC39A13

29. The novel missense mutation Met48Lys in FKBP22 changes its structure and functions

34. Clinical features, molecular results, and management of 12 individuals with the rare arthrochalasia Ehlers‐Danlos syndrome

35. FKBP14 Kyphoscoliotic Ehlers-Danlos Syndrome

36. Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications

39. Large expert-curated database for benchmarking document similarity detection in biomedical literature search

40. Large expert-curated database for benchmarking document similarity detection in biomedical literature search

41. FKBP14 Kyphoscoliotic Ehlers-Danlos Syndrome

43. Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency

45. COL1‐related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers‐Danlos syndrome overlap

47. Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta

48. Mutations in PLOD3, encoding lysyl hydroxylase 3, cause a complex connective tissue disorder including recessive dystrophic epidermolysis bullosa-like blistering phenotype with abnormal anchoring fibrils and type VII collagen deficiency

49. Pathogenic variants in PLOD3 result in a Stickler syndrome-like connective tissue disorder with vascular complications

50. Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

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