Olsen BR - Search Results

1

Heritable diseases of the skeleton. Part I: Molecular insights into skeletal development-transcription factors and signaling pathways.

Mundlos S, Olsen BR. Mundlos S, et al. Among authors: olsen br. FASEB J. 1997 Feb;11(2):125-32. doi: 10.1096/fasebj.11.2.9039954. FASEB J. 1997. PMID: 9039954 Review.

2

Genetic mapping of cleidocranial dysplasia and evidence of a microdeletion in one family.

Mundlos S, Mulliken JB, Abramson DL, Warman ML, Knoll JH, Olsen BR. Mundlos S, et al. Among authors: olsen br. Hum Mol Genet. 1995 Jan;4(1):71-5. doi: 10.1093/hmg/4.1.71. Hum Mol Genet. 1995. PMID: 7711736

3

Spondylometaphyseal dysplasia in mice carrying a dominant negative mutation in a matrix protein specific for cartilage-to-bone transition.

Jacenko O, LuValle PA, Olsen BR. Jacenko O, et al. Among authors: olsen br. Nature. 1993 Sep 2;365(6441):56-61. doi: 10.1038/365056a0. Nature. 1993. PMID: 8361538

4

Mutations in collagen genes resulting in metaphyseal and epiphyseal dysplasias.

Olsen BR. Olsen BR. Bone. 1995 Aug;17(2 Suppl):45S-49S. doi: 10.1016/8756-3282(95)00208-u. Bone. 1995. PMID: 8579897 Review.

5

Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13.

Muragaki Y, Mundlos S, Upton J, Olsen BR. Muragaki Y, et al. Among authors: olsen br. Science. 1996 Apr 26;272(5261):548-51. doi: 10.1126/science.272.5261.548. Science. 1996. PMID: 8614804

6

Role of cartilage collagens in formation of the skeleton.

Olsen BR. Olsen BR. Ann N Y Acad Sci. 1996 Jun 8;785:124-30. doi: 10.1111/j.1749-6632.1996.tb56250.x. Ann N Y Acad Sci. 1996. PMID: 8702118 Review. No abstract available.

7

Cleidocranial dysplasia in mice.

Mundlos S, Huang LF, Selby P, Olsen BR. Mundlos S, et al. Among authors: olsen br. Ann N Y Acad Sci. 1996 Jun 8;785:301-2. doi: 10.1111/j.1749-6632.1996.tb56290.x. Ann N Y Acad Sci. 1996. PMID: 8702161 No abstract available.

8

Unravelling the molecular genetics of osteoarthrosis.

Vikkula M, Olsen BR. Vikkula M, et al. Among authors: olsen br. Ann Med. 1996 Aug;28(4):301-4. doi: 10.3109/07853899608999084. Ann Med. 1996. PMID: 8862683 Free article. Review.

9

Heritable diseases of the skeleton. Part II: Molecular insights into skeletal development-matrix components and their homeostasis.

Mundlos S, Olsen BR. Mundlos S, et al. Among authors: olsen br. FASEB J. 1997 Mar;11(4):227-33. FASEB J. 1997. PMID: 9068611 Review.

10

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development.

Otto F, Thornell AP, Crompton T, Denzel A, Gilmour KC, Rosewell IR, Stamp GW, Beddington RS, Mundlos S, Olsen BR, Selby PB, Owen MJ. Otto F, et al. Among authors: olsen br. Cell. 1997 May 30;89(5):765-71. doi: 10.1016/s0092-8674(00)80259-7. Cell. 1997. PMID: 9182764 Free article.

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