47 results on '"Bonaventure J"'
Search Results
2. Increasing paddy yields and improving farm management: results from participatory experiments with good agricultural practices (GAP) in Tanzania
3. Glycosaminoglycans and Proteoglycans in Neoplastic Tissues and Their Role in Tumor Growth and Metastasis
4. ICAT (inhibitor of β-catenin and TCF4), un nouveau régulateur de la motilité et de l’invasion des cellules de mélanome
5. Melting dynamics of large ice balls in a turbulent swirling flow
6. Skeletal development in human
7. t(4;14)(p16;q32)
8. FGFR3 (fibroblast growth factor receptor 3)
9. Bypassing melanocyte senescence by β-catenin: A novel way to promote melanoma
10. Activation of NF-κB by Akt upregulates Snail expression and induces epithelium mesenchyme transition
11. Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasias
12. Monozygotic twins with Crouzon syndrome: Concordance for craniosynostosis and discordance for thumb duplication
13. Monozygotic twins with Crouzon syndrome: Concordance for craniosynostosis and discordance for thumb duplication
14. Absence of functional receptors for parathyroid hormone and parathyroid hormone-related peptide in Blomstrand chondrodysplasia.
15. Des mutations du gène H-Twist sont responsables du syndrome de Saethre-Chotzen
16. Abnormal FGFR 3 Expression in Cartilage of Thanatophoric Dysplasia Fetuses
17. Altered collagen of human pathological fibroblasts impairs the synthesis of fibronectin
18. Common Mutations in the Fibroblast Growth Factor Receptor 3 (FGFR 3) Gene Account for Achondroplasia, Hypochondroplasia and Thanatophoric Dwarfism
19. Récepteurs des facteurs de croissance fibroblastique et anomalies héréditaires de la croissance osseuse
20. Common mutations in the gene encoding fibroblast growth factor receptor 3 account for achondroplasia, hypochondroplasia and thanatophoric dysplasia
21. Clinical and genetic heterogeneity of hypochondroplasia.
22. Mutations within the gene encoding the alpha 1 (X) chain of type X collagen (COL10A1) cause metaphyseal chondrodysplasia type Schmid but not several other forms of metaphyseal chondrodysplasia.
23. L'odontochondrodysplasie
24. Common mutations in the fibroblast growth factor receptor 3 (FGFR3) gene account for achondroplasia, hypochondroplasia, and thanatophoric dwarfism
25. Type II collagenopathies: Are there additional family members?
26. Mutations in three subdomains of the carboxy-terminal region of collagen type X account for most of the Schmid metaphyseal dysplasias
27. Substitution of aspartic acid for glycine at position 310 in type II collagen produces achondrogenesis II, and substitution of serine at position 805 produces hypochondrogenesis: analysis of genotype-phenotype relationships
28. Des anomalies du récepteur 3 des facteurs de croissance fibroblastique sont responsables d'une chondrodysplasie létale : le nanisme thanatophore
29. Reexpression of Cartilage-Specific Genes by Dedifferentiated Human Articular Chondrocytes Cultured in Alginate Beads
30. Mutation in the COL2A1 gene in a patient with hypochondrogenesis. Expression of mutated COL2A1 gene is accompanied by expression of genes for type I procollagen in chondrocytes.
31. Achondrogenesis type IB (Fraccaro): Study of collagen in the tissue and in chondrocytes cultured in agarose
32. Dernière heure : l'achondroplasie est associée à une mutation dans le domaine transmembranaire du récepteur 3 des facteurs de croissance fibroblastiques (FGFR3)
33. Type II collagen defect in two sibs with the Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity
34. Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene
35. Organization and characterization of fibrillar collagens in fish scales in situ and in vitro
36. Morphological and biochemical studies of a mouse mutant (fro/fro) with bone fragility
37. Cellular control of the organization of an ordered three-dimensional collagen matrix
38. Modulation of sulfated proteoglycan synthesis and collagen gene expression by chondrocytes grown in the presence of bFGF alone or combined with IGF1
39. CHARACTERIZATION OF IGFI RECEPTORS ON IN VITRO DIFFERENTIATING GROWTH PLATE (GP) CHONDROCYTES GROWN IN CULTURE
40. Effect of relaxin on the phenotype of collagens synthesized by cultured rabbit chondrocytes
41. MODULATION DE L'EXPRESSION DE GENES DE COLLAGENE DANS DES CHONDROCYTES EPIPHYSAIRES DE LAPIN EN CULTURE
42. Effect of relaxin on the phenotype of collagens synthesized by cultured rabbit chondrocytes
43. Introduction
44. Interleukin-1 α modulates collagen gene expression in cultured synovial cells
45. In vitro spleen cell proliferation following in vivo treatment with a synthetic glycolipid or lipid A in three mouse strains
46. Effects of structural variations in synthetic glycolipids upon mitogenicity for spleen lymphocytes, adjuvancy for humoral immune response and on anti-tumour potential
47. Effet de GH sur la différenciation de chondrocytes de lapin prépubère en culture sans sérum et sur l'activité radioimmunologique Sm-C/IGF1 mesurable dans le milieu de culture
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.