Journal Article
RDF
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Must the Past Have a Beginning?
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Must We All Have a Vast, Flowing Qi? Revisiting Mengzi 2A2
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Mutagenesis and comparative sequence analysis of a base triple joining the two domains of group I ribozymes
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Mutagenesis of a stacking contact in the MS2 coat protein-RNA complex
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MUTANT EXPRESSION OF MALE COPULATORY BURSA SURFACE-MARKERS IN CAENORHABDITIS-ELEGANS
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MUTANTS OF THE BACTERIOPHAGE-MS2 COAT PROTEIN THAT ALTER ITS COOPERATIVE BINDING TO RNA
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MUTANTS OF THE LAC PROMOTER WITH LARGE INSERTIONS AND DELETIONS BETWEEN THE CAP BINDING-SITE AND THE -35 REGION
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Mutation Carriers with Reduced C-Afferent Density Reveal Cortical Dynamics of Pain-Action Relationship during Acute Pain
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Mutation in TERT separates processivity from anchor-site function
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Mutation of the TERT promoter, switch to active chromatin, and monoallelic TERT expression in multiple cancers
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Mutation of the arginine finger in the active site of Escherichia coli DbpA abolishes ATPase and helicase activity and confers a dominant slow growth phenotype.
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Mutation of the IIB myosin heavy chain gene results in muscle fiber loss and compensatory hypertrophy
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Mutation of the?5 nicotinic acetylcholine receptor subunit increases ethanol and nicotine consumption in adolescence and impacts adult drug consumption
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Mutation screening of the SynGAP gene in patients with dyslexia.
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MUTATION THAT CONFERS TEMPERATURE SENSITIVITY ON TRANSLATION OF RIIB IN BACTERIOPHAGE-T4
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Mutation-order divergence by sexual selection: diversification of sexual signals in similar environments as a first step in speciation
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Mutational analysis of the purine riboswitch aptamer domain
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Mutational load analysis of unrelated individuals.
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Mutations affecting stability and deadenylation of the yeast MFA2 transcript.
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MUTATIONS AFFECTING TRANSLATION OF THE BACTERIOPHAGE-T4 RIIB GENE CLONED IN ESCHERICHIA-COLI
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MUTATIONS AT THE GUANOSINE-BINDING SITE OF THE TETRAHYMENA RIBOZYME ALSO AFFECT SITE-SPECIFIC HYDROLYSIS
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Mutations at the same amino acid in myosin that cause either skeletal or cardiac myopathy have distinct molecular phenotypes
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Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 Are Identified in Individuals with Congenital Hypogonadotropic Hypogonadism
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Mutations in KIF7 implicated in idiopathic scoliosis in humans and axial curvatures in zebrafish
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Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly
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Mutations in a newly identified Drosophila melanogaster gene, mago nashi, disrupt germ cell formation and result in the formation of mirror-image symmetrical double abdomen embryos.
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MUTATIONS IN A NONCONSERVED SEQUENCE OF THE TETRAHYMENA RIBOZYME INCREASE ACTIVITY AND SPECIFICITY
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Mutations in concserved intron sequences affect multiple steps in the yeast splicing pathways, particularly assembly of the spliceosome
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Mutations in cye-1, a Caenorhabditis elegans cyclin E homolog, reveal coordination between cell-cycle control and vulval development
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Mutations in heparan sulfate 60-sulfotransferase 1 (HS6ST1) contribute to human GnRH deficiency
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