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UnknownABCA1, TCF7, NFATC1, PRKCZ, and PDGFA DNA methylation as potential epigenetic-sensitive targets in acute coronary syndrome via network analysis.
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S-EPMC9067513 | biostudies-literature
UnknownIn chronic myeloid leukemia patients on second-line tyrosine kinase inhibitor therapy, deep sequencing of BCR-ABL1 at the time of warning may allow sensitive detection of emerging drug-resistant mutants.
Not available
S-EPMC4970247 | biostudies-literature
UnknownExploring the Effects of Probiotic Treatment on Urinary and Serum Metabolic Profiles in Healthy Individuals.
Not available
S-EPMC10696601 | biostudies-literature
UnknownIncidence of second primary malignancies and related mortality in patients with imatinib-treated chronic myeloid leukemia.
Not available
S-EPMC5685244 | biostudies-literature
UnknownUpper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study.
Not available
S-EPMC10136754 | biostudies-literature
UnknownInterpreting Genetic Variants in Titin in Patients With Muscle Disorders.
Not available
S-EPMC5885217 | biostudies-literature
UnknownAge, corticosteroid treatment and site of mutations affect motor functional changes in young boys with Duchenne Muscular Dystrophy.
Not available
S-EPMC9337636 | biostudies-literature
UnknownThe Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.
Not available
S-EPMC7063120 | biostudies-literature
UnknownLandscape Analysis of <i>COL6A1</i>, <i>COL6A2</i>, and <i>COL6A3</i> Pathogenic Variants in a Large Italian Cohort Presenting with Collagen VI-Related Myopathies: A Nationwide Report.
Not available
S-EPMC12564197 | biostudies-literature
UnknownExpanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study.
Not available
S-EPMC9013059 | biostudies-literature
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