12 Evaluation of two live, cold-passaged, temperature-sensitive respiratory syncytial virus vaccines in chimpanzees and in human adults, infants, and children

13 Effects of hypergravity on the photosynthetic flagellate, Euglena gracilis

14 Initial sequencing and analysis of the human genome

15 Emergence of teicoplanin resistance during therapy of Staphylococcus aureus endocarditis

16 TCTE1 is a conserved component of the dynein regulatory complex and is required for motility and metabolism in mouse spermatozoa

17 Investigation into the selection frequency of resistant mutants and the bacterial kill rate by levofloxacin and ciprofloxacin in non-mucoid Pseudomonas aeruginosa isolates from cystic fibrosis patients

18 Heterogeneity in the substitution process of amino acid sites of proteins coded for by mitochondrial DNA

19 a comparative study of the evolution of real incomes of pensioners and unemployed using genetic algorithms

20 Enhancement of Peroxidase Activity in Artificial Mimochrome VI Catalysts through Rational Design

21 Sterol-dependent repression of low density lipoprotein receptor promoter mediated by 16-base pair sequence adjacent to binding site for transcription factor Sp1

22 Transcription factor-specific requirements for coactivators and their acetyltransferase functions

23 A role for the Smc3 hinge domain in the maintenance of sister chromatid cohesion

24 Characterization of gtf, a glucosyltransferase gene in the genomes of Pediococcus parvulus and Oenococcus oeni, two bacterial species commonly found in wine

25 Pseudomonas aeruginosa defends against phages through type IV pilus glycosylation

26 Evolution, population structure, and phylogeography of genetically monomorphic bacterial pathogens

27 Signature-tagged mutagenesis in a chicken infection model leads to the identification of a novel avian pathogenic Escherichia coli fimbrial adhesin

28 Myc signaling via the ARF tumor suppressor regulates p53-dependent apoptosis and immortalization

29 Positional cloning of the nude locus: genetic, physical, and transcription maps of the region and mutations in the mouse and rat

30 Genetic analysis of T-DNA transcripts in nopaline crown galls

31 MAPK interacts with XGef and is required for CPEB activation during meiosis in Xenopus oocytes

32 A xenograft model for venous malformation

33 Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage

34 Disruption of the ARF-Mdm2-p53 tumor suppressor pathway in Myc-induced lymphomagenesis

35 Oseltamivir-resistant influenza A pandemic (H1N1) 2009 virus, Hong Kong, China

36 Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

37 Regulation of p53 stability by Mdm2

38 In vivo analysis of chromosome condensation in Saccharomyces cerevisiae

39 Establishment of left-right asymmetry in vertebrate development: the node in mouse embryos

40 The real life of pseudogenes

41 Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity

42 Physical Association of Saccharomyces cerevisiae Polo-like Kinase Cdc5 with Chromosomal Cohesin Facilitates DNA Damage Response

43 Genetic interaction between Wnt/beta-catenin and BMP receptor signaling during formation of the AER and the dorsal-ventral axis in the limb

44 Enforced proximity in the function of a famous scaffold

45 Eco1-dependent cohesin acetylation during establishment of sister chromatid cohesion

46 A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae

47 Cdkn2a encodes functional variation of p16INK4a but not p19ARF, which confers selection in mouse lung tumorigenesis

48 Genetic, biochemical, and clinical features of chronic granulomatous disease

49 Functional diversity and mutational analysis of Agrobacterium 6B oncoproteins

50 Effect of fasting and leptin deficiency on hypothalamic neuropeptide Y gene transcription in vivo revealed by expression of a lacZ reporter gene

51 The nature and character of the transition state for the ADP-ribosyltransferase reaction

52 Cohesins: chromosomal proteins that prevent premature separation of sister chromatids

53 Group A streptococcal infections in injection drug users in Barcelona, Spain: epidemiologic, clinical, and microbiologic analysis of 3 clusters of cases from 2000 to 2003

54 p53 and microRNA-34 are suppressors of canonical Wnt signaling

55 Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin

56 Genetic incorporation of histidine derivatives using an engineered pyrrolysyl-tRNA synthetase

57 Novel mutations associated with inherited human calcium-sensing receptor disorders: a clinical genetic study.

58 Robustness of coalescent estimators to between-lineage mutation rate variation.

59 PRISMOID: a comprehensive 3D structure database for post-translational modifications and mutations with functional impact.

60 Security mutation testing of the FileZilla FTP server

61 Improving test adequacy assessment by novel JavaScript mutation operators

62 The creation and selection of mutations resistant to a gene drive over multiple generations in the malaria mosquito.

63 High BRAFV600E mutation frequency in Chinese patients with papillary thyroid carcinoma increases diagnostic efficacy in cytologically indeterminate thyroid nodules.

64 Acute pulmonary thromboembolism caused by factor V Leiden mutation in South Korea: A case report.

65 In search for genetic explanation for LDLc variabily in an FH family: Common SNPs and a rare mutation in microsomal triglyceride transfer protein explain only part of LDL variability in an FH family.

66 Frequent mutations in EGFR, KRAS and TP53 genes in human lung cancer tumors detected by ion torrent DNA sequencing.

67 Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.

68 Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH.

69 Antiretroviral drug resistance mutations among patients failing first-line treatment in Hanoi, Vietnam

70 Characterization of the most common embCAB gene mutations associated with ethambutol resistance in Mycobacterium tuberculosis isolates from Iran

71 Evaluation of the accuracy of molecular assays targeting the mutation A2059G for detecting high-level azithromycin resistance in Neisseria gonorrhoeae: a systematic review and meta-analysis

72 Characterization of hepatitis C virus resistance to grazoprevir reveals complex patterns of mutations following on-treatment breakthrough that are not observed at relapse

73 Patterns of emergent resistance-associated mutations after initiation of non-nucleoside reverse-transcriptase inhibitor-containing antiretroviral regimens in Taiwan: a multicenter cohort study

74 The clinical significance of silent mutations with respect to ciprofloxacin resistance in MRSA

75 Interaction between rpsL and gyrA mutations affects the fitness and dual resistance of Mycobacterium tuberculosis clinical isolates against streptomycin and fluoroquinolones

76 Enriched whole genome sequencing identified compensatory mutations in the RNA polymerase gene of rifampicin-resistant Mycobacterium leprae strains

77 Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

78 Naturally occurring genotypic drug-resistant mutations of HBV in Huzhou, China: a single-center study

79 Genotyping of HBV and tracking of resistance mutations in treatment-naïve patients with chronic hepatitis B

80 Mycoplasma genitalium infection: current treatment options, therapeutic failure, and resistance-associated mutations

81 Detection of epidermal growth factor receptor mutation in lung cancer by droplet digital polymerase chain reaction

82 First Report of Diabetes Phenotype due to a Loss-of-Function ABCC8 Mutation Previously Known to Cause Congenital Hyperinsulinism

83 Acute Myeloid Leukemia with Concomitant BCR-ABL and NPM1 Mutations

84 Antiretroviral drug resistance mutations among patients failing first-line treatment in Hanoi, Vietnam

85 Characterization of the most common embCAB gene mutations associated with ethambutol resistance in Mycobacterium tuberculosis isolates from Iran

86 Evaluation of the accuracy of molecular assays targeting the mutation A2059G for detecting high-level azithromycin resistance in Neisseria gonorrhoeae: a systematic review and meta-analysis

87 Characterization of hepatitis C virus resistance to grazoprevir reveals complex patterns of mutations following on-treatment breakthrough that are not observed at relapse

88 Patterns of emergent resistance-associated mutations after initiation of non-nucleoside reverse-transcriptase inhibitor-containing antiretroviral regimens in Taiwan: a multicenter cohort study

89 The clinical significance of silent mutations with respect to ciprofloxacin resistance in MRSA

90 Interaction between rpsL and gyrA mutations affects the fitness and dual resistance of Mycobacterium tuberculosis clinical isolates against streptomycin and fluoroquinolones

91 Enriched whole genome sequencing identified compensatory mutations in the RNA polymerase gene of rifampicin-resistant Mycobacterium leprae strains

92 Molecular analysis of multidrug resistance in clinical isolates of Shigella spp. from 2001–2010 in Kolkata, India: role of integrons, plasmids, and topoisomerase mutations

93 Naturally occurring genotypic drug-resistant mutations of HBV in Huzhou, China: a single-center study

94 Genotyping of HBV and tracking of resistance mutations in treatment-naïve patients with chronic hepatitis B

95 Mycoplasma genitalium infection: current treatment options, therapeutic failure, and resistance-associated mutations

96 Detection of epidermal growth factor receptor mutation in lung cancer by droplet digital polymerase chain reaction

97 Proof of Principle that Molecular Modeling Followed by a Biophysical Experiment Can Develop Small Molecules that Restore Function to the Cardiac Thin Filament in the Presence of Cardiomyopathic Mutations.

98 Detection of genetic mutations associated with macrolide resistance of Mycoplasma pneumoniae

99 Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.

100 Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.

101 Where phonology meets morphology in the context of rapid language change and universal bilingualism: Irish initial mutations in child language

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