Possible roles of Runx1 and Sox9 in incipient intramembranous ossification.
T Yamashiro, XP Wang, Z Li, S Oya, T Aberg, T … - J Bone Miner Res, 2004 - ncbi.nlm.nih.gov
Click here to read Possible roles of Runx1 and Sox9 in incipient
intramembranous ossification. Yamashiro T, Wang XP, Li Z, Oya S ...
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Dysregulation of Chondrogenesis in Human Cleidocranial Dysplasia. - Full text - MIT Libraries
Q Zheng, E Sebald, G Zhou, Y Chen, W Wilcox, B Lee … - Am. J. Hum. Genet, 2005 - journals.uchicago.edu
... the relative expression levels of known RUNX2 targets VEGF, MMP13, and COL10A1,
as well as for the transcription factor genes RUNX1, RUNX2, RUNX3, and SOX9. ...
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Requisite roles of Runx2 and Cbfb in skeletal development - Full text - MIT Libraries
T Komori - J Bone Miner Metab, 2003 - springerlink.com
... the following roles of these genes in different cell lineages: Runx1 is essential ...
Sry-type HMG box 9 (Sox9) is essential for mesenchymal condensa- tion, which ...
Cited by 4 - Web Search - springerlink.com - ncbi.nlm.nih.gov

Regulation of skeletal development by the Runx family of transcription factors - Full text - MIT Libraries
T Komori - Journal of Cellular Biochemistry, 2005 - doi.wiley.com
... The transcription factor Sox9 plays an essential role in mesenchymal condensation
leading to ... Runx FAMILY IS COMPOSED OF THREE GENES, Runx1/Cbfa2/Pebp2aB, Runx2 ...
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Overlapping expression of Runx 1 (Cbfa 2) and Runx 2 (Cbfa 1) transcription factors supports … - Full text - MIT Libraries
N Smith, Y Dong, JB Lian, J Pratap, PD Kingsley, … - Journal of Cellular Physiology, 2005 - doi.wiley.com
... The expres- sion of Runx1 and Runx2 at early embryonic stages coincides with initial
cartilage formation reflected by Sox9 and type II collagen mRNA expression ...
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Runx 2, A multifunctional transcription factor in skeletal development - Full text - MIT Libraries
T Komori - Journal of Cellular Biochemistry, 2002 - doi.wiley.com
... Runx1 and Runx3 also seem to contribute to these processes. Runx proteins may be
involved in the process of mesenchymal condensation at an early step. Sox9, ...
Cited by 19 - Web Search - ncbi.nlm.nih.gov

Runx 2 and Runx 3 are essential for chondrocyte maturation, and Runx 2 regulates limb growth through … - Full text - MIT Libraries
CA Yoshida, H Yamamoto, T Fujita, T Furuichi, K … - Genes & Development, 2004 - genesdev.org
... 3 –/– cartilage were released from the inhibitory effect of Sox9 on maturation ... The
Runx family consists of three genes, Runx1, Runx2, and Runx3 (Komori 2002 ...
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Runx 1/AML 1 hematopoietic transcription factor contributes to skeletal development in vivo - Full text - MIT Libraries
JB Lian, E Balint, A Javed, H Drissi, R Vitti, EJ … - Journal of Cellular Physiology, 2003 - doi.wiley.com
... Runx1/AML1 Hematopoietic Transcription Factor ... lz/þ ). The resulting fusion protein
reflects Runx1 promoter activity in its native context. ...
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Control of RUNX 2 isoform expression: The role of promoters and enhancers - Full text - MIT Libraries
M Stock, F Otto - Journal of Cellular Biochemistry, 2005 - doi.wiley.com
... reported to be a crucial checkpoint in the expression of RUNX1 protein [Pozner et ...
Furthermore increased levels of Sox9, Coll II and Coll X indicate an enhanced ...
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Runx2/Cbfa1: A Multifunctional Regulator of Bone Formation
JB Lian, GS Stein - Curr Pharm Design, 2003 - ingentaconnect.com
... through PPARδ and CEβPα [20, 21], or to chondrocytes through Sox9 [22] and ... Runx1
(AML1/Cbfa2/ PEBP2αB) is essential for definitive hematopoiesis [45, 46]. ...
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Runx3 is involved in hair shape determination. - Full text - MIT Libraries
E Raveh, S Cohen, D Levanon, Y Groner, U Gat - DEVELOPMENTAL DYNAMICS, 2005 - doi.wiley.com
... In light of the major phenotypes observed in mice null for Runx1 and Runx2 ... the
above-described sim- ilarities between the phenotypes, and because Sox9 was found ...
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Transcriptional Dysregulation in Skeletal Malformation Syndromes
PIA HERMANNS, B LEE - American Journal of Medical Genetics (Semin. Med. Genet.), 2001 - doi.wiley.com
... similar to the critical role for Sox9 during chondrogenesis. ... in the mouse show that
it directly regulates the activity of the homologous RUNX1 protein during ...
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A RUNX2/PEBP2 alpha A/CBFA1 mutation displaying impaired transactivation and Smad interaction in … - Full text - MIT Libraries
YW Zhang, N Yasui, K Ito, G Huang, M Fujii, J … - Cancer Res, 2005 - dx.doi.org
... and H. Asahara Smad3 Induces Chondrogenesis through the Activation of SOX9 via CREB ...
Yokomizo, and Y. Ito Dimerization with PEBP2{beta} protects RUNX1/AML1 from ...
Cited by 88 - Web Search - pnas.org - pubmedcentral.nih.gov - ncbi.nlm.nih.gov - all 6 versions »

The State of the Art of the Zebrafish Model for Toxicology and Toxicologic Pathology Research-- …
JM Spitsbergen, ML Kent - Toxicologic Pathology, 2003 - dx.doi.org
... A transgenic zebrafish expressing a RUNX1-CBF2T1 translocation shows a preleukemic
syndrome (257 ... Chiang et al (92, 93) reveal the role of sox9 genes in gonadal ...
Cited by 13 - Web Search - taylorandfrancis.metapress.com - ingentaconnect.com - ncbi.nlm.nih.gov - all 6 versions » - Get it from MIT Libraries

Abstracts from the 4th Annual Conference on Mesenchymal and Non-Hematopoietic Stem Cells: Focus on …
S II, P SESSION - Cytotherapy, 2005 - taylorandfrancis.metapress.com
... The MSC nature of purified cells was further confirmed by real-time measurements
of transcription factors cbfa-1, Sox9 and PPARγ that were 10–100-fold ...
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Isolierung, Sequenzierung und Charakterisierung der genomischen Region von Frunx2, dem Fugu-rubripes …
JH Eggers - freidok.ub.uni-freiburg.de
... Im Unterschied zu Runx1 und Runx3, die vor allem in hämatopoetischen ... vermutet, die
durch Haploinsuffizienz von Sox9 verursacht wird (Sox9 kodiert einen ...
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Phenotype discovery by gene expression profiling: Mapping of biological processes linked to BMP-2- … - Full text - MIT Libraries
E Balint, D Lapointe, H Drissi, C van der Meijden, … - Journal of Cellular Biochemistry, 2003 - doi.wiley.com
... Transcription factors that have been identified as BMP-2 responsive for skeletogen-
esis include Sox9, which is crucial for chondro- genesis and Cbfa1/Runx2 ...
Cited by 16 - Web Search - ncbi.nlm.nih.gov - ncbi.nlm.nih.gov

Cloning of the breakpoints of a de novo inversion of chromosome 8, inv(8)(p 11. 2 q 23. 1) in a … - Full text - MIT Libraries
M Tadin-Strapps, D Warburton, FAM Baumeister, SG … - Cytogenetic and Genome Research, 2004 - content.karger.com
... with campomelic dysplasia and autosomal sex reversal map more than 130 kb from SOX9. ...
MM, Larson RA, Rowley JD: Genomic DNA breakpoints in AML/RUNX1 and ETO ...
Cited by 1 - Web Search - dx.doi.org - karger.com - ncbi.nlm.nih.gov - all 5 versions »

3 rdAnnual Conference on Mesenchymal and Nonhematopoietic Stem Cells: Focus on adult stem cells
I Pierre Charbord, F Villejuif, UK London - Cytotherapy, 2004 - taylorandfrancis.metapress.com
Page 1. 3 rd Annual Conference on Mesenchymal and Nonhematopoietic Stem Cells: Focus
on adult stem cells October 9 Á / 11, 2003 New Orleans, LA, USA Program ...
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Autoreferate des Symposiums¹ Molekulargenetische Aspekte der Destruktion, Regeneration und von … - Full text - MIT Libraries
W Leitung - Z Rheumatol, 2000 - springerlink.com
Page 1. Z Rheumatol 59:389–421 (2000) © Steinkopff Verlag 2000 ABSTRACTS
Autoreferate des Symposiums ¹Molekulargenetische Aspekte ...
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