PubMed for id: 1519473748

Year	Number of Results
1993	2
1994	1
1995	1
1997	1
1998	1
2000	1
2006	1
2023	1
2024	3

1

METTL3 Promotes Osteogenic Differentiation of Human Periodontal Ligament Stem Cells through IGF2BP1-Mediated Regulation of Runx2 Stability.

Sun X, Meng X, Piao Y, Dong S, Dong Q. Sun X, et al. Int J Med Sci. 2024 Feb 4;21(4):664-673. doi: 10.7150/ijms.90485. eCollection 2024. Int J Med Sci. 2024. PMID: 38464837 Free PMC article.

2

A synthetic, closed-looped gene circuit for the autonomous regulation of RUNX2 activity during chondrogenesis.

Kaur G, Wu B, Murali S, Lanigan T, Coleman RM. Kaur G, et al. FASEB J. 2024 Feb 29;38(4):e23484. doi: 10.1096/fj.202300348RR. FASEB J. 2024. PMID: 38407380

3

Scopolamine regulates the osteogenic differentiation of human periodontal ligament stem cells through lactylation modification of RUNX2 protein.

Wu Y, Gong P. Wu Y, et al. Pharmacol Res Perspect. 2024 Feb;12(1):e1169. doi: 10.1002/prp2.1169. Pharmacol Res Perspect. 2024. PMID: 38258916 Free PMC article.

4

Cleidocranial Dysplasia Spectrum Disorder.

Machol K, Mendoza-Londono R, Lee B. Machol K, et al. 2006 Jan 3 [updated 2023 Apr 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2006 Jan 3 [updated 2023 Apr 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301686 Free Books & Documents. Review.

5

Transcriptional autoregulation of the bone related CBFA1/RUNX2 gene.

Drissi H, Luc Q, Shakoori R, Chuva De Sousa Lopes S, Choi JY, Terry A, Hu M, Jones S, Neil JC, Lian JB, Stein JL, Van Wijnen AJ, Stein GS. Drissi H, et al. J Cell Physiol. 2000 Sep;184(3):341-50. doi: 10.1002/1097-4652(200009)184:3<341::AID-JCP8>3.0.CO;2-Z. J Cell Physiol. 2000. PMID: 10911365

6

Genomic organization, expression of the human CBFA1 gene, and evidence for an alternative splicing event affecting protein function.

Geoffroy V, Corral DA, Zhou L, Lee B, Karsenty G. Geoffroy V, et al. Mamm Genome. 1998 Jan;9(1):54-7. doi: 10.1007/s003359900679. Mamm Genome. 1998. PMID: 9434946

7

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. Cell. 1997 May 30;89(5):773-9. doi: 10.1016/s0092-8674(00)80260-3. Cell. 1997. PMID: 9182765 Free article.

8

PEBP2/PEA2 represents a family of transcription factors homologous to the products of the Drosophila runt gene and the human AML1 gene.

Ogawa E, Maruyama M, Kagoshima H, Inuzuka M, Lu J, Satake M, Shigesada K, Ito Y. Ogawa E, et al. Proc Natl Acad Sci U S A. 1993 Jul 15;90(14):6859-63. doi: 10.1073/pnas.90.14.6859. Proc Natl Acad Sci U S A. 1993. PMID: 8341710 Free PMC article.

9

AML1, AML2, and AML3, the human members of the runt domain gene-family: cDNA structure, expression, and chromosomal localization.

Levanon D, Negreanu V, Bernstein Y, Bar-Am I, Avivi L, Groner Y. Levanon D, et al. Genomics. 1994 Sep 15;23(2):425-32. doi: 10.1006/geno.1994.1519. Genomics. 1994. PMID: 7835892

10

A gene for cleidocranial dysplasia maps to the short arm of chromosome 6.

Feldman GJ, Robin NH, Brueton LA, Robertson E, Thompson EM, Siegel-Bartelt J, Gasser DL, Bailey LC, Zackai EH, Muenke M. Feldman GJ, et al. Am J Hum Genet. 1995 Apr;56(4):938-43. Am J Hum Genet. 1995. PMID: 7717404 Free PMC article.

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