Mundlos S - Search Results

1

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. Hum Mol Genet. 1995 Jan;4(1):71-5. doi: 10.1093/hmg/4.1.71. Hum Mol Genet. 1995. PMID: 7711736

2

Alternative splicing as the result of a type II procollagen gene (COL2A1) mutation in a patient with Kniest dysplasia.

Winterpacht A, Schwarze U, Mundlos S, Menger H, Spranger J, Zabel B. Winterpacht A, et al. Among authors: mundlos s. Hum Mol Genet. 1994 Oct;3(10):1891-3. doi: 10.1093/hmg/3.10.1891. Hum Mol Genet. 1994. PMID: 7849719 No abstract available.

3

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: mundlos s. Science. 1996 Apr 26;272(5261):548-51. doi: 10.1126/science.272.5261.548. Science. 1996. PMID: 8614804

4

Cleidocranial dysplasia in mice.

Mundlos S, Huang LF, Selby P, Olsen BR. Mundlos S, et al. 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.

5

Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity.

Ramesar RS, Greenberg J, Martin R, Goliath R, Bardien S, Mundlos S, Beighton P. Ramesar RS, et al. Among authors: mundlos s. J Med Genet. 1996 Jun;33(6):511-4. doi: 10.1136/jmg.33.6.511. J Med Genet. 1996. PMID: 8782054 Free PMC article.

6

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. FASEB J. 1997 Feb;11(2):125-32. doi: 10.1096/fasebj.11.2.9039954. FASEB J. 1997. PMID: 9039954 Review.

7

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. FASEB J. 1997 Mar;11(4):227-33. FASEB J. 1997. PMID: 9068611 Review.

8

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: mundlos s. Cell. 1997 May 30;89(5):765-71. doi: 10.1016/s0092-8674(00)80259-7. Cell. 1997. PMID: 9182764 Free article.

9

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.

Mundlos S, Otto F, Mundlos C, Mulliken JB, Aylsworth AS, Albright S, Lindhout D, Cole WG, Henn W, Knoll JH, Owen MJ, Mertelsmann R, Zabel BU, Olsen BR. Mundlos S, et al. Among authors: mundlos c. Cell. 1997 May 30;89(5):773-9. doi: 10.1016/s0092-8674(00)80260-3. Cell. 1997. PMID: 9182765 Free article.

10

The role of sonic hedgehog in vertebrate development.

Weed M, Mundlos S, Olsen BR. Weed M, et al. Among authors: mundlos s. Matrix Biol. 1997 May;16(2):53-8. doi: 10.1016/s0945-053x(97)90072-x. Matrix Biol. 1997. PMID: 9205942 Review.

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