R
R. Baer
Researcher at Laboratory of Molecular Biology
Publications - 21
Citations - 1674
R. Baer is an academic researcher from Laboratory of Molecular Biology. The author has contributed to research in topics: Chromosomal translocation & T cell. The author has an hindex of 16, co-authored 21 publications receiving 1656 citations.
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Diversity and rearrangement of the human T cell rearranging γ genes: nine germ-line variable genes belonging to two subgroups
TL;DR: Nine T cell gamma variable (V) gene segments isolated from human DNA show that major rearrangements can be observed that are attributable to the five active V gamma genes, and human cells with the phenotype of helper T cells can undergo productive V gamma-J gamma joining.
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Altered nucleotide sequences of a translocated c-myc gene in Burkitt lymphoma.
TL;DR: The nucleotide sequence of a translocated c-myc gene in a Burkitt lymphoma reveals multiple base changes in the coding region, probably the result of somatic mutations that occurred during and after translocation, and may contribute to oncogenesis by allowing synthesis of an altered c- myc gene product.
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Protein dimerization between Lmo2 (Rbtn2) and Tal1 alters thymocyte development and potentiates T cell tumorigenesis in transgenic mice.
R. C. Larson,Isabelle Lavenir,T. A. Larson,R. Baer,Alan J. Warren,Isobel Wadman,K. Nottage,Terence H. Rabbitts +7 more
TL;DR: Interaction between these two proteins can alter T cell development and potentiate tumorigenesis, and provide formal proof that TAL1 is an oncogene, apparently acting as a tumour promoter in this system.
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The LIM protein RBTN2 and the basic helix-loop-helix protein TAL1 are present in a complex in erythroid cells
TL;DR: It is demonstrated, using anti-RBTN2 and anti-TAL1 antisera, that the LIM protein RBTN2 is not phosphorylated and is complexed with the TAL1 phosphoprotein in the nucleus of erythroid cells, providing a direct link between proteins activated by chromosomal translocations in T-cell acute leukemia.
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Fusion of an immunoglobulin variable gene and a T cell receptor constant gene in the chromosome 14 inversion associated with T cell tumors
TL;DR: The structure of the alpha-chain genes in a T cell line harboring the chromosome 14 inversion is investigated and it is found that the VH-J alpha C alpha rearrangement is productive at the genomic level and therefore may encode a hybrid immunoglobulin/T cell receptor polypeptide.