Glutathione S-transferase gene deletions in myelodysplasia.

Glutathione S-transferase gene deletions in myelodysplasia.

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Atoyebi, W, Kusec, R, Fidler, C, Peto, T, Boultwood, J, Wainscoat, J
التنسيق:	Journal article
اللغة:	English
منشور في:	1997

مواد مشابهة

Glutathione S-transferase theta 1 (GSTT1) gene defect in myelodysplasia and acute myeloid leukaemia
حسب: Atoyebi, W, وآخرون
منشور في: (1997)

Chromosomal deletions in myelodysplasia.
حسب: Boultwood, J, وآخرون
منشور في: (1995)

BRCA2 gene deletion is rare in chronic lymphocytic leukemia.
حسب: Pilozzi, E, وآخرون
منشور في: (1998)

Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
حسب: Boultwood, J, وآخرون
منشور في: (1991)

Gene deletions of glutathione S-transferase and iron status in sickle cell patients
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Prevalence of glutathione S-transferase gene deletions and their effect on sickle cell patients
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High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridisation (CGH)
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High-resolution genomic profiling of myelodysplasia (MDS) by microarray comparative genomic hybridization (CGH).
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Ha-ras hypervariable alleles in myelodysplasia.
حسب: Thein, S, وآخرون
منشور في: (1986)

Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.
حسب: Boultwood, J, وآخرون
منشور في: (1993)

Glutathione S-transferase variants and hypertension.
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Identification of acquired somatic mutations in the gene encoding chromatin-remodeling factor ATRX in the alpha-thalassemia myelodysplasia syndrome (ATMDS).
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Detection of glutathione S-transferases M1, T1 gene deletions among cancer patients in Mongolia
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Molecular characterization of the 7q deletion in myeloid disorders.
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Analysis of the glutathione <it>S</it>-transferase (<it>GST</it>) gene family
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Telomere length in myelodysplastic syndromes.
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MOLECULAR MAPPING OF THE 7Q-DELETION IN MYELOID DISORDERS
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DELETIONAL POLYMORPHISM OF GLUTATHIONE TRANSFERASE T1 AND M1 GENES IN PATIENTS WITH MYOCARDIAL INFARCTION AND METABOLIC SYNDROME
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Reduction of MTT by Glutathione S-Transferase
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Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the a thalassaemia myelodysplasia syndrome (ATMDS)
حسب: Gibbons, R, وآخرون
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Identification of acquired somatic mutations in the chromatin remodelling factor ATRX in the alpha thalassemia myelodysplasia syndrome (ATMDS).
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Gene expression and risk of leukemic transformation in myelodysplasia
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The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.
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Hidden Glutathione Transferases in the Human Genome
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Versatility of Glutathione Transferase Proteins
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Structure and functions of glutathione transferases
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Gene expression profiling in the myelodysplastic syndromes.
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Physical and transcriptional characterization of the commonly deleted region in del(9q) AML.
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Relationship between Glutathione S-transferase gene deletions (GSTT1 and GSTM1) and coronary artery disease/acute myocardial infarction.
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Linkage disequilibrium between two high-frequency deletion polymorphisms: implications for association studies involving the glutathione-S transferase (GST) genes.
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