Library

Tags: adapter molecules, Aminoacyl t RNA, Aminoacyl' site, Inhibitors of protein synthesis, polysome, Ribosomes, Shine-Dalgarno sequence, translation,

Tags: Alternative polyadenylation, Alternative splicing, Class switching, drug resistance, Enhancers and Repressors, Gene rearrangement, helix-turn-helix, Insulators, leucine zipper, Locus control regions, mRNA stability, nucleosomal structure, zinc finger,

Tags: CAP-cAMP complex, constitutive expression, double negative regulation, galactoside permease, lac repressor, negative control, rna polymerase, thiogalactoside transacetylase, β -galactosidase,

Tags: Adaptation, Gene expression i, Negative regulation, Positive regulation, repressor, Tissue-specific differentiation, Type A response, Type B response, Type C response,

Tags: codon, Degenerate, genetic code, Non-Overlapping, Non-Punctuated, Non-Sense codons, Reading frame, Redundant, Specificity, termination codons, Universal, Wobbling phenomenon,

Tags: 5' Capping, Alternative polyadenylation sites, Alternative splicing, CCA attachment, guanine-7-methyl transferase, hn RNA, introns, poly-A tail, S-Adenosyl methionine, snRNPs,

Tags: bbasal transcription complex, Enhancers and Repressors, eukaryotic RNA, Hormone response elements, promoter identification, TATA-binding protein (TBP), termination of transcription, TFIID,

Tags: -35 Sequence, hairpin, Pribnow box, Primary transcript, Rho-dependent termination, Rho-independent termination, rna polymerase, sigma subunit, superhelical complexes, TATA box, Topoisomerase, Transcription,

Tags: Aminoacyl t-RNA synthetase, Choramphenicol, Initiation factor (IF)-2, Peptidyl transferase, Tetracyclin, translation, Translocase,

Tags: Ataxia telangiectasia, B-cell leukemia, base excision repair, Bloom syndrome, Burkitt's lymphoma, Cockayne's syndrome, direct joining, DNA repair, double-strand break repair, Homologous Recombination, mismatch repair, Nonhomologous End-Joining (NHEJ, nucleotide excision repair, Philadelphia chromosome, Progeria (Hutchinson-Gilford Progeria syndrome), Rothmund-Thomson syndrome, Single-Strand Breaks (SSBs), Transcription-Coupled NER, Trichothiodystrophy, Werner syndrome, xeroderma pigmentosum,