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Gene Section GPHN (Gephyrin) Atlas of Genetics and Cytogenetics in Oncology and Haematology
Gene Section GPHN (Gephyrin) Atlas of Genetics and Cytogenetics in Oncology and Haematology

... Disruption of the gephyrin gene is lethal at birth in the mouse. The mutant phenotype resembles that of humans with hereditary deficiency of molybdenum cofactor and hyperhekplexia, a disease which is associated with defects in glycinergic inhibition in many patients suggesting that gephyrin function ...
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Advanced Molecular and Cell Biology (Dorn, Holton)

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... Normaly, the TAL genes are not expressed in the thymus. The TAL genes become activated and expressed in the thymus upon chromosomal translocation which ultimately leads to the development of T-ALL. The (7;9) translocation express a TAL2 gene product of 108 amino acids. In leukemic cells this product ...
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Exam Handout for PHAR2811 students, 2009

... A wild type colony of E. coli was selected and cultured in a medium which did not contain either glucose or lactose as carbon source. After sufficient growth was achieved IPTG was added to the culture to a final concentration of 0.5 mM. This time was denoted as time zero. At 2, 4, 8, 16 and 32 min a ...
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NEDD9

Neural precursor cell expressed developmentally down-regulated protein 9 (NEDD-9) is a protein that in humans is encoded by the NEDD9 gene. NEDD-9 is also known as enhancer of filamentation 1 (EF1), CRK-associated substrate-related protein (CAS-L), and Cas scaffolding protein family member 2 (CASS2). An important paralog of this gene is BCAR1.
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