378 results on '"Olsen, B R"'
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2. Monoculodes bousfieldi sp. n. from the Arctic hydrothermal vent Loki’s Castle
3. Synpolydactyly Phenotypes Correlate with Size of Expansions in HOXD13 Polyalanine Tract
4. Preparation of Antisera Specific for the Amino and Carboxyl Propeptides of Type I and Type II Procollagens
5. The Cell Biology of Collagen Secretion
6. Regulation of adipogenesis and osteogenesis in mesenchymal stem cells by vascular endothelial growth factor A
7. Immunoidentification of Type XII Collagen in Embryonic Tissues
8. The mouse palate and its cellular responses to midpalatal suture expansion forces
9. Regulation of the bone vascular network is sexually dimorphic
10. Pathogenesis of Osteoarthritis-Like Changes in the Joints of Mice Deficient in Type Ix Collagen
11. Osteoarthritis-Like Changes and Decreased Mechanical Function of Articular Cartilage in the Joints of Mice With the Chondrodysplasia Gene (cho)
12. Overexpression of the NC4 domain of type IX collagen induces osteoarthritis in mice
13. The roles of collagen genes in skeletal development and morphogenesis
14. Synthetic Membranes: Volume II
15. Seasonal variation in wax ester concentration and gut content in a Baltic Sea copepod [Limnocalanus macrurus (Sars 1863)]
16. PCR-DHPLC assay for the identification of predator-prey interactions
17. Of mice and men: heritable skeletal disorders
18. Tissue specific expression of Type XIV collagen- a member of the FACIT class of collagen
19. "A rare disorder, yes; an unimportant one, never".
20. Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development‐matrix components and their homeostasis
21. Heritable diseases of the skeleton. Part I: Molecular insights into skeletal development‐transcription factors and signaling pathways 1
22. Polyalanine Expansion in Synpolydactyly Might Result from Unequal Crossing-Over of HOXD13
23. Cleidocranial Dysplasia in Mice
24. Skeletal and Hematopoietic Defects in Mice Transgenic for Collagen Xa
25. Structure of the human TIMP-3 gene and its cell cycle-regulated promoter
26. Mouse Col18a1 is expressed in a tissue-specific manner as three alternative variants and is localized in basement membrane zones.
27. FACIT Collagens and Their Biological Roles.
28. Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family
29. Mice lacking alpha 1 (IX) collagen develop noninflammatory degenerative joint disease.
30. Isolation and sequencing of cDNAs for proteins with multiple domains of Gly-Xaa-Yaa repeats identify a distinct family of collagenous proteins.
31. Alpha 1-VIII collagen is expressed in the rat glomerulus and in resident glomerular cells
32. Multiple negative elements in a gene that codes for an extracellular matrix protein, collagen X, restrict expression to hypertrophic chondrocytes.
33. Expression of simian virus 40 large T (tumor) oncogene in mouse chondrocytes induces cell proliferation without loss of the differentiated phenotype.
34. Osteoarthritis associated with mild chondrodysplasia in transgenic mice expressing alpha 1(IX) collagen chains with a central deletion.
35. The alpha 2(VIII) collagen gene. A novel member of the short chain collagen family located on the human chromosome 1.
36. Non-fibrillar collagenous proteins synthesized by rat mesangial cells.
37. The alpha 1 (IX) collagen gene gives rise to two different transcripts in both mouse embryonic and human fetal RNA.
38. Tissue-Specific Expression of Type IX Collagen
39. The Structure of Type XII Collagen
40. Gene for the human transmembrane-type protein tyrosine phosphatase H (PTPRH): genomic structure, fine-mapping and its exclusion as a candidate for Peutz-Jeghers syndrome.
41. Collagen XII Mutation Disrupts Matrix Structure of Periodontal Ligament and Skin.
42. The Structure of Type XII Collagena.
43. Tissue-Specific Expression of Type IX Collagena.
44. Medullary carcinoma of the thyroid. Diagnostic problems.
45. The role of collagen-derived proteolytic fragments in angiogenesis
46. Expression of frizzled genes in mouse costochondral chondrocytes
47. Mouse models of abnormal skeletal development and homeostasis
48. The mechanism of palatal clefting in the Col11a1 mutant mouse
49. Tissue specific regulation of VEGF expression during bone development requires Cbfa1/Runx2
50. Exon skipping mutation in the COL9A2 gene in a family with multiple epiphyseal dysplasia
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