Chondrodysplasia and neurological abnormalities in ATF-2-deficient mice (Q28271799)

2

object named as

M J Grusby

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author name string

A M Reimold

1

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B Kosaras

3

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J W Fries

4

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R Mori

5

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S Maniwa

6

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I M Clauss

7

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T Collins

8

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R L Sidman

9

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M J Glimcher

The murine gene encoding secreted phosphoprotein 1 (osteopontin): promoter structure, activity, and induction in vivo by estrogen and progesterone

10

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language of work or name

English

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publication date

18 January 1996

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published in

Nature

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volume

379

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issue

6562

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page(s)

262-5

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cites work

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Characterization of a 5'-flanking region of the human liver/bone/kidney alkaline phosphatase gene: two kinds of mRNA from a single gene

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Jun-Fos and receptors for vitamins A and D recognize a common response element in the human osteocalcin gene

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A gene for achondroplasia–hypochondroplasia maps to chromosome 4p

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Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia

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Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

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A cDNA for a human cyclic AMP response element-binding protein which is distinct from CREB and expressed preferentially in brain

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Cyclic AMP-Independent ATF Family Members Interact with NF-κB and Function in the Activation of the E-Selectin Promoter in Response to Cytokines

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Three NF-kappa B binding sites in the human E-selectin gene required for maximal tumor necrosis factor alpha-induced expression

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mXBP/CRE-BP2 and c-Jun form a complex which binds to the cyclic AMP, but not to the 12-O-tetradecanoylphorbol-13-acetate, response element

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Mechanisms of transcriptional synergism between distinct virus-inducible enhancer elements

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Retinoblastoma gene product activates expression of the human TGF-β2 gene through transcription factor ATF-2

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A specific member of the ATF transcription factor family can mediate transcription activation by the adenovirus E1a protein

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HBV X protein alters the DNA binding specificity of CREB and ATF-2 by protein-protein interactions

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Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein.

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Targeted mutation of the CREB gene: compensation within the CREB/ATF family of transcription factors.

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Pleiotropic effects of a null mutation in the c-fos proto-oncogene

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Bone and haematopoietic defects in mice lacking c-fos

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Transcription factor ATF2 regulation by the JNK signal transduction pathway

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In situ hybridization studies suggest a role for the basic region‐leucine zipper protein hXBP‐1 in exocrine gland and skeletal development during mouse embryogenesis

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