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1.
Phys Rev Lett ; 97(6): 062502, 2006 Aug 11.
Article in English | MEDLINE | ID: mdl-17026166

ABSTRACT

A new experimental approach to the famous problem of the anomalously slow Gamow-Teller (GT) transitions in the beta decay of the A=14 multiplet is presented. The GT strength distributions to excited states in 14C and 14O were studied in high-resolution (d,2He) and (3He,t) charge-exchange reactions on 14N. No-core shell-model calculations capable of reproducing the suppression of the beta decays predict a selective excitation of Jpi=2+ states. The experimental confirmation represents a validation of the assumptions about the underlying structure of the 14N ground state wave function. However, the fragmentation of the GT strength over three 2+ final states remains a fundamental issue not explained by the present no-core shell model using a 6homega model space, suggesting possibly the need to include cluster structure in these light nuclei in a consistent way.

2.
Science ; 258(5090): 1944-6, 1992 Dec 18.
Article in English | MEDLINE | ID: mdl-1335166

ABSTRACT

Retinoids have a broad spectrum of biological activities and are useful therapeutic agents. Their physiological activities are mediated by two types of receptors, the retinoic acid receptors (RARs) and the retinoid X receptors (RXRs). RARs, as well as several related receptors, require heterodimerization with RXRs for effective DNA binding and function. However, in the presence of 9-cis-retinoic acid, a ligand for both RARs and RXRs, RXRs can also form homodimers. A series of retinoids is reported that selectively activates RXR homodimers but does not affect RAR-RXR heterodimers and thus demonstrates that both retinoid response pathways can be independently activated.


Subject(s)
Receptors, Cell Surface/metabolism , Receptors, Retinoic Acid , Retinoids/metabolism , Transcription Factors , Animals , Cell Line , Chloramphenicol O-Acetyltransferase/genetics , Chloramphenicol O-Acetyltransferase/metabolism , Kinetics , Macromolecular Substances , Molecular Structure , Receptors, Cell Surface/drug effects , Receptors, Cell Surface/genetics , Recombinant Fusion Proteins/metabolism , Retinoid X Receptors , Retinoids/chemistry , Retinoids/pharmacology , Structure-Activity Relationship , Transcription, Genetic , Transfection , Tretinoin/metabolism , Tretinoin/pharmacology
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