Mundlos S - Search Results

1

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.

2

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.

3

Mouse clavicular development: analysis of wild-type and cleidocranial dysplasia mutant mice.

Huang LF, Fukai N, Selby PB, Olsen BR, Mundlos S. Huang LF, et al. Among authors: mundlos s. Dev Dyn. 1997 Sep;210(1):33-40. doi: 10.1002/(SICI)1097-0177(199709)210:1<33::AID-AJA4>3.0.CO;2-2. Dev Dyn. 1997. PMID: 9286593 Free article.

4

Regulation of chondrocyte differentiation by Cbfa1.

Kim IS, Otto F, Zabel B, Mundlos S. Kim IS, et al. Among authors: mundlos s. Mech Dev. 1999 Feb;80(2):159-70. doi: 10.1016/s0925-4773(98)00210-x. Mech Dev. 1999. PMID: 10072783 Free article.

5

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.

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

Mutations in the RUNX2 gene in patients with cleidocranial dysplasia.

Otto F, Kanegane H, Mundlos S. Otto F, et al. Among authors: mundlos s. Hum Mutat. 2002 Mar;19(3):209-16. doi: 10.1002/humu.10043. Hum Mutat. 2002. PMID: 11857736 Review.

8

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

9

Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia.

Quack I, Vonderstrass B, Stock M, Aylsworth AS, Becker A, Brueton L, Lee PJ, Majewski F, Mulliken JB, Suri M, Zenker M, Mundlos S, Otto F. Quack I, et al. Among authors: mundlos s. Am J Hum Genet. 1999 Nov;65(5):1268-78. doi: 10.1086/302622. Am J Hum Genet. 1999. PMID: 10521292 Free PMC article.

10

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.

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