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The detection of minimal residual disease (MRD) using immunoglobulin and T-cell receptor (TCR) rearrangements as PCR targets… Expand Gsα mutations and histopathology have been analysed in a series of 13 patients with fibrous dysplasia (FD) of bone, including 12… Expand Drugs and carcinogens are excreted from the body after metabolic conversion involving enzymes mediating oxidative metabolism and… Expand CONTEXT
Infertile men with obstructive azoospermia may have mutations in the cystic fibrosis transmembrane conductance regulator… Expand Mitochondrial defects can be caused by mutations in nuclear or mitochondrial DNA. Large deletion/duplication and point mutations… Expand Isolation of the gene for cystic fibrosis (CF), the cystic fibrosis transmembrane conductance regulator (CFTR), provided a basis… Expand BACKGROUND: The technique of allele‐specific polymerase chain reaction (PCR) amplification has been adapted for DNA‐based human… Expand Mutation detection is important in all areas of biology. Detection of unknown mutations can involve sequencing of kilobases of… Expand The prediction of neonatal alloimmune thrombocytopenia (NATP) in affected families has, in the past, been based on information… Expand A membrane-bound cytochrome b, a heterodimer formed by a 91-kD glycoprotein and a 22-kD polypeptide, is a critical component of… Expand