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Alterations of epigenetic marks have an important role in myeloid malignancies.1 Mutations have been found in several epigenetic… Expand Chromosome 17q11-q21 is a region of the genome likely to harbor susceptibility to autism (MIM(209850)) based on earlier evidence… Expand We analyzed a cohort of 61 follicular lymphomas (FL) with an abnormal G-banded karyotype by spectral karyotyping (SKY) to better… Expand Gastric adenocarcinoma is a malignant tumor with a high incidence and a low survival rate. In order to identify genetic… Expand Gastric adenocarcinoma is a malignant tumor with a high incidence and a low survival rate. In order to identify genetic… Expand Chromosomal segment 17q11-q21 is a commonly amplified region in human breast carcinomas. Several lines of evidence suggest that… Expand A lymphoid-specific member of the G-protein-coupled receptor family has been identified by PCR with degenerate oligonucleotides… Expand The human estradiol 17 beta-hydroxysteroid dehydrogenase II (17 beta-HSD II) gene has been assigned by somatic cell hybridization… Expand Nineteen patients with acute promyelocytic leukemia (APL) and one with promyelocytic blast crisis were studied by a methotrexate… Expand Through the use of a cDNA probe, the human erbB-2 gene was localized by in situ hybridization of normal human chromosomes at… Expand