Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8

Molecular and Cellular Biology

Volumn 21, Issue 20, 2001, Pages 6951-6959

  Sock, E ^a   Schmidt, K ^a   Hermanns Borgmeyer, I ^a   Bosl M R ^a   Wegner, M ^a  

^a UNIVERSITY OF ERLANGEN NUREMBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHONDROGENESIS; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; GENE EXPRESSION; GENE MUTATION; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; WEIGHT REDUCTION;

ANIMALS; BETA-GALACTOSIDASE; BODY WEIGHT; CROSSES, GENETIC; DNA, COMPLEMENTARY; DNA-BINDING PROTEINS; EMBRYO; GENETIC VECTORS; GENOTYPE; MICE; MICE, TRANSGENIC; MODELS, GENETIC; MUTAGENESIS; MUTATION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; TIME FACTORS; TISSUE DISTRIBUTION; TRANSCRIPTION FACTORS;

EID: 0034807930     PISSN: 02707306     EISSN: None     Source Type: Journal    
DOI: 10.1128/MCB.21.20.6951-6959.2001     Document Type: Article

References (34)

1. Sox9 directly regulates the type-II collagen gene
2. Sox8 expression during chick embryogenesis
3. Muscle differentiation is antagonized by SOX15, a new member of the SOX protein family
4. Sox9 is required for cartilage formation
5. Phylogeny of the SOX family of developmental transcription factors based on sequence and structural indicators
6. The transcription factor Sox10 is a key regulator of peripheral glial development
7. Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene
8. An SRY-related sequence on the marsupial X chromosome: Implications for the evolution of the mammalian testis-determining gene
9. Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease
10. Myelin deficiencies in both the central and peripheral nervous system associated with a SOX10 mutation
11. Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos
12. A male-specific role for SOX9 in vertebrate sex determination
13. Sox10, a novel transcriptional modulator in glial cells
14. Sox9 is a potent activator of the chondrocyte-specific enhancer of the proα1(II) collagen gene
15. Identification of an enhancer sequence within the first intron required for cartilage-specific transcription of the alpha2(XI) collagen gene
16. SOX9 binds DNA, activates transcription, and coexpresses with type II collagen during chondrogenesis in the mouse
17. Sox1 directly regulates the γ-crystallin genes and is essential for lens development in mice
18. Expression and interactions of the two closely related homeobox genes Phox2a and Phox2b during neurogenesis
19. The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives
20. Protein zero expression is regulated by the glial transcription factor Sox10
21. Sox genes find their feet
22. The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome
23. Sox10 mutations in patients with Waardenburg-Hirschsprung disease
24. Cloning and characterisation of the sry-related transcription factor gene sox8
25. SOX9 enhances aggrecan gene promoter/enhancer activity and is up-regulated by retinoic acid in a cartilage-derived cell line, TC6
26. The Sox10(Dom) mouse: Modeling the genetic variation of Waardenburg-Shah (WS4) syndrome
27. Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
28. Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain
29. Neonatal lethality, and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene
30. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene Sox9
31. From head to toes: The multiple facets of Sox proteins
32. The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos
33. Trans-activation of the mouse cartilage-derived retinoic acid-sensitive protein gene by Sox9