329 related articles for article (PubMed ID: 12783851)
1. Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia.
Sock E; Pagon RA; Keymolen K; Lissens W; Wegner M; Scherer G
Hum Mol Genet; 2003 Jun; 12(12):1439-47. PubMed ID: 12783851
[TBL] [Abstract][Full Text] [Related]
2. Dimerization of SOX9 is required for chondrogenesis, but not for sex determination.
Bernard P; Tang P; Liu S; Dewing P; Harley VR; Vilain E
Hum Mol Genet; 2003 Jul; 12(14):1755-65. PubMed ID: 12837698
[TBL] [Abstract][Full Text] [Related]
3. Sex reversal by loss of the C-terminal transactivation domain of human SOX9.
Südbeck P; Schmitz ML; Baeuerle PA; Scherer G
Nat Genet; 1996 Jun; 13(2):230-2. PubMed ID: 8640233
[TBL] [Abstract][Full Text] [Related]
4. Compound effects of point mutations causing campomelic dysplasia/autosomal sex reversal upon SOX9 structure, nuclear transport, DNA binding, and transcriptional activation.
Preiss S; Argentaro A; Clayton A; John A; Jans DA; Ogata T; Nagai T; Barroso I; Schafer AJ; Harley VR
J Biol Chem; 2001 Jul; 276(30):27864-72. PubMed ID: 11323423
[TBL] [Abstract][Full Text] [Related]
5. Functional and structural studies of wild type SOX9 and mutations causing campomelic dysplasia.
McDowall S; Argentaro A; Ranganathan S; Weller P; Mertin S; Mansour S; Tolmie J; Harley V
J Biol Chem; 1999 Aug; 274(34):24023-30. PubMed ID: 10446171
[TBL] [Abstract][Full Text] [Related]
6. Trans-activation of the mouse cartilage-derived retinoic acid-sensitive protein gene by Sox9.
Xie WF; Zhang X; Sakano S; Lefebvre V; Sandell LJ
J Bone Miner Res; 1999 May; 14(5):757-63. PubMed ID: 10320524
[TBL] [Abstract][Full Text] [Related]
7. Mutational analysis of the SOX9 gene in campomelic dysplasia and autosomal sex reversal: lack of genotype/phenotype correlations.
Meyer J; Südbeck P; Held M; Wagner T; Schmitz ML; Bricarelli FD; Eggermont E; Friedrich U; Haas OA; Kobelt A; Leroy JG; Van Maldergem L; Michel E; Mitulla B; Pfeiffer RA; Schinzel A; Schmidt H; Scherer G
Hum Mol Genet; 1997 Jan; 6(1):91-8. PubMed ID: 9002675
[TBL] [Abstract][Full Text] [Related]
8. SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse.
Ng LJ; Wheatley S; Muscat GE; Conway-Campbell J; Bowles J; Wright E; Bell DM; Tam PP; Cheah KS; Koopman P
Dev Biol; 1997 Mar; 183(1):108-21. PubMed ID: 9119111
[TBL] [Abstract][Full Text] [Related]
9. Cooperative binding of Sox10 to DNA: requirements and consequences.
Schlierf B; Ludwig A; Klenovsek K; Wegner M
Nucleic Acids Res; 2002 Dec; 30(24):5509-16. PubMed ID: 12490719
[TBL] [Abstract][Full Text] [Related]
10. Sox9-dependent transcriptional regulation of the proprotein convertase furin.
Guimont P; Grondin F; Dubois CM
Am J Physiol Cell Physiol; 2007 Jul; 293(1):C172-83. PubMed ID: 17360815
[TBL] [Abstract][Full Text] [Related]
11. Adjacent DNA sequences modulate Sox9 transcriptional activation at paired Sox sites in three chondrocyte-specific enhancer elements.
Bridgewater LC; Walker MD; Miller GC; Ellison TA; Holsinger LD; Potter JL; Jackson TL; Chen RK; Winkel VL; Zhang Z; McKinney S; de Crombrugghe B
Nucleic Acids Res; 2003 Mar; 31(5):1541-53. PubMed ID: 12595563
[TBL] [Abstract][Full Text] [Related]
12. A nuclear export signal within the high mobility group domain regulates the nucleocytoplasmic translocation of SOX9 during sexual determination.
Gasca S; Canizares J; De Santa Barbara P; Mejean C; Poulat F; Berta P; Boizet-Bonhoure B
Proc Natl Acad Sci U S A; 2002 Aug; 99(17):11199-204. PubMed ID: 12169669
[TBL] [Abstract][Full Text] [Related]
13. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9.
Wagner T; Wirth J; Meyer J; Zabel B; Held M; Zimmer J; Pasantes J; Bricarelli FD; Keutel J; Hustert E; Wolf U; Tommerup N; Schempp W; Scherer G
Cell; 1994 Dec; 79(6):1111-20. PubMed ID: 8001137
[TBL] [Abstract][Full Text] [Related]
14. Heterozygous SOX9 mutations allowing for residual DNA-binding and transcriptional activation lead to the acampomelic variant of campomelic dysplasia.
Staffler A; Hammel M; Wahlbuhl M; Bidlingmaier C; Flemmer AW; Pagel P; Nicolai T; Wegner M; Holzinger A
Hum Mutat; 2010 Jun; 31(6):E1436-44. PubMed ID: 20513132
[TBL] [Abstract][Full Text] [Related]
15. Structural and functional characterization of the mouse Sox9 promoter: implications for campomelic dysplasia.
Kanai Y; Koopman P
Hum Mol Genet; 1999 Apr; 8(4):691-6. PubMed ID: 10072439
[TBL] [Abstract][Full Text] [Related]
16. A SOX9 defect of calmodulin-dependent nuclear import in campomelic dysplasia/autosomal sex reversal.
Argentaro A; Sim H; Kelly S; Preiss S; Clayton A; Jans DA; Harley VR
J Biol Chem; 2003 Sep; 278(36):33839-47. PubMed ID: 12810722
[TBL] [Abstract][Full Text] [Related]
17. Two independent nuclear localization signals are present in the DNA-binding high-mobility group domains of SRY and SOX9.
Südbeck P; Scherer G
J Biol Chem; 1997 Oct; 272(44):27848-52. PubMed ID: 9346931
[TBL] [Abstract][Full Text] [Related]
18. The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences.
Peirano RI; Wegner M
Nucleic Acids Res; 2000 Aug; 28(16):3047-55. PubMed ID: 10931919
[TBL] [Abstract][Full Text] [Related]
19. Sox9, a key transcription factor of bone morphogenetic protein-2-induced chondrogenesis, is activated through BMP pathway and a CCAAT box in the proximal promoter.
Pan Q; Yu Y; Chen Q; Li C; Wu H; Wan Y; Ma J; Sun F
J Cell Physiol; 2008 Oct; 217(1):228-41. PubMed ID: 18506848
[TBL] [Abstract][Full Text] [Related]
20. Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.
Kwok C; Weller PA; Guioli S; Foster JW; Mansour S; Zuffardi O; Punnett HH; Dominguez-Steglich MA; Brook JD; Young ID
Am J Hum Genet; 1995 Nov; 57(5):1028-36. PubMed ID: 7485151
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]