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Related to erythroblastosis: erythroblastosis fetalis
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  • noun

Words related to erythroblastosis

a blood disease characterized by the abnormal presence of erythroblasts in the blood

References in periodicals archive ?
Cellular and molecular mechanisms of renal carcinogenesis induced by avian erythroblastosis virus.
Furthermore, the avian erythroblastosis virus oncogene, mentioned above, actually represents a form of EGFR that is missing its complete ECD, rather than just a portion of it.
Kim Gun-shik of Tokyo Korean Christian Church in Japan and his wife was born with this same incompatibility of the Rh-negative blood group, or erythroblastosis fetalis.
Neoplasms that have been reported in hyacinth macaws are bronchogenic adenocarcinoma with spinal invasion, (6) hepatic adenocarcinoma, (7) erythroblastosis of the spleen, (7) subcutaneous myelolipoma, (8) and cloacal papilloma.
Of fetal hypoxic lesions, mild erythroblastosis of fetal blood (Figure 6, A) is regarded as the only reliable (and, therefore, the best) evidence of chronic, in utero hypoxia; however, fetal erythroblasts can also be released from their stores in response to acute hypoxia.
The discovery of fusion transcripts for the TMPRSS2 [4] (transmembrane protease, serine 2) and ERG [v-ets erythroblastosis virus E26 oncogene homolog (avian)] genes (i.
Barbara Brown, his mother, alleges that your laboratory was negligent in performing tests before and at the time of the baby's birth that led to his mental retardation because of erythroblastosis.
In obstetrics, a major advancement occurred with the almost complete elimination of a disease state called erythroblastosis fetalis, or the Rhesis (Rh) disease.
b) SOP, standard operating procedure; PCA, prostate cancer; TMA, transcription-mediated amplification; ERG, v-ets erythroblastosis Virus E26 oncogene homolog; FISH, fluorescence in-situ hybridization; ROMA, risk of ovarian malignancy algorithm; APE1, apurinic endonuclease 1.
Gene fusion between erythroblastosis virus E26 transforming sequence (ETS) genes, particularly the ETS-related gene (ERG), and transmembrane protease serine 2 (TMPRSS2) has recently been identified in prostatic malignancies.
11,12,18,19) Hemolymphatic tumors reported include lymphoma, lymphoid leukosis, erythroblastosis, Marek's disease, and myeloproliferative disease.
His mother, Barbara Brown, alleges that your laboratory's negligence in performing tests before and at the time of the baby's birth led to his mental retardation due to erythroblastosis.
Recurrent genetic aberrations, most commonly caused by chromosomal rearrangements and copy number gains and losses [such as fusions in the v-ets erythroblastosis virus E26 oncogene homolog 1 (avian) (ETS) [3] gene family and phosphatase and tensin homolog (PTEN) loss] have been identified in many patients (33, 34).
In 2005, chromosomal rearrangements were identified in prostate cancer that fuse the 5' untranslated region of the androgen-regulated gene transmembrane protease, serine 2 (TMPRSS2), with v-ets erythroblastosis virus E26 oncogene homolog (avian) (ERG) or ets variant 1 (ETV1), 2 members of the ETS transcription factor family.