MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During Development-Reference-Cited by-同舟云学术

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MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During Development

Published:1999-08-01 Issue:8 Volume:8 Page:1397-1407
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Buchner G.,Montini E.,Andolfi G.,Quaderi N.,Cainarca S.,Messali S.,Bassi M. T.,Ballabio A.,Meroni G.,Franco B.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/8/8/1397/1647589/8-8-1397.pdf

Reference55 articles.

1. The nuclear-cytoplasmic distribution of the Xenopus nuclear factor, xnf7, coincides with its state of phosphorylation during early development

2. A putative zinc-binding protein on lampbrush chromosome loops.

3. The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR

4. Acute promyelocytic leukemia: from genetics to treatment

5. Developmentally regulated expression of a human "finger"-containing gene encoded by the 5' half of the ret transforming gene.

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