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Items: 5

1.
Identification of RUNX2 variants associated with cleidocranial dysplasia
Xueren Gao, Kunxia Li, Yanjie Fan, Yu Sun, Xiaomei Luo, Lili Wang, Huili Liu, Zhuwen Gong, Jianguo Wang, Yu Wang, Xuefan Gu, Yongguo Yu
Hereditas. 2019; 156: 31. Published online 2019 Sep 16. doi: 10.1186/s41065-019-0107-7
PMCID:
PMC6747736
AbstractArticlePDF–1.3M
2.
A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.
G J Feldman, N H Robin, L A Brueton, E Robertson, E M Thompson, J Siegel-Bartelt, D L Gasser, L C Bailey, E H Zackai, M Muenke
Am J Hum Genet. 1995 Apr; 56(4): 938–943.
PMCID:
PMC1801197
SummaryPage BrowsePDF–1.4M
3.
PEBP2/PEA2 represents a family of transcription factors homologous to the products of the Drosophila runt gene and the human AML1 gene.
E Ogawa, M Maruyama, H Kagoshima, M Inuzuka, J Lu, M Satake, K Shigesada, Y Ito
Proc Natl Acad Sci U S A. 1993 Jul 15; 90(14): 6859–6863. doi: 10.1073/pnas.90.14.6859
PMCID:
PMC47032
SummaryPage BrowsePDF–1.5M
4.
Is NO the Answer? The Nitric Oxide Pathway Can Support Bone Morphogenetic Protein 2 Mediated Signaling
Christopher Differ, Franka Klatte-Schulz, Nicole Bormann, Susann Minkwitz, Petra Knaus, Britt Wildemann
Cells. 2019 Oct; 8(10): 1273. Published online 2019 Oct 18. doi: 10.3390/cells8101273
PMCID:
PMC6830101
AbstractArticlePDF–5.4M
5.
An investigation of BMP-7 mediated alterations to BMP signalling components in human tenocyte-like cells
Franka Klatte-Schulz, Gerry Giese, Christopher Differ, Susann Minkwitz, Karen Ruschke, Regina Puts, Petra Knaus, Britt Wildemann
Sci Rep. 2016; 6: 29703. Published online 2016 Jul 11. doi: 10.1038/srep29703
PMCID:
PMC4942578
AbstractArticlePDF–1.0M

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