Abstracts: Multiple nuclear pseudogenes of mitochondrial cytochrome b in Ctenomys (Caviomorpha, Rodentia) with either great similarity to or high divergence from the true mitochondrial sequence
Abstracts: Multiple paralogous genes related to the Streptomyces coelicolor developmental regulatory gene whiB are present in Streptomyces and other actinomycetes
Abstracts: Multiple paternity in Atlantic salmon: a way to maintain genetic variability in relicted populations. Interaction of Rearing Environment and Reproductive Tactic on Gene Expression Profiles in Atlantic Salmon
Abstracts: Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae. A super new twist on the initiation of meiotic recombination
Abstracts: Multiple phase variation in haemolytic, adhesive and antigenic properties of Streptococcus gordonii. In vitro phagocytosis and survival of Streptococcus suis capsular type 2 inside murine macrophages
Abstracts: Multiple Ras-dependent phosphorylation pathways regulate Myc protein stability. Inhibition of Wnt signaling by ICAT, a novel beta-catenin-interacting protein
Abstracts: Multiple reductive-dehalogenase-homologous genes are simultaneously transcribed during dechlorination by Dehalococcoides-containing cultures
Abstracts: Multiple sclerosis: a coordinated immunological attack against myelin in the central nervous system. A central role for microvillous receptor presentation in leukocyte adhesion under flow
Abstracts: Multiple small RNAs act additively to integrate sensory information and control quorum sensing in Vibrio harveyi
Abstracts: Multiple sulfatase deficiency is caused by mutations in the gene encoding the human C (sub)alpha -formylglycine generating enzyme
Abstracts: Multiple trait analysis of genetic mapping for quantitative trait loci. Maximum likelihood mapping of quantitative trait loci using full-sib families
Abstracts: Multiplex nucleic acid sequence-based amplification for simultaneous detection of several enteric viruses in model ready-to-eat foods
Abstracts: Multiplex PCR assay for detection of Vibrio vulnificus biotype 2 and simultaneous discrimination of serovar E strains
Abstracts: Multiplication of different Legionella species in Mono Mac 6 cells and in Acanthamoeba castellanii. Influence of Acanthamoeba castellanii on intracellular growth of different Legionella species in human monocytes
Abstracts: Multiplicative vs. arbitrary gene action in heterosis. Interval mapping of viability loci causing heterosis in Arabidopsis
Abstracts: Multiply antibiotic-resistant Streptococcus pneumoniae recovered from Spanish hospitals (1988-1994): novel major clones of serotypes 14, 19F and 15F
Abstracts: Multipoint approximations of identity-by-descent probabilities for accurate linkage analysis of distantly related individuals
Abstracts: Multipoint linkage-disequilibrium mapping with haplotype-block structure. Correlation of intergenerational family sizes suggests a genetic component of reproductive fitness
Abstracts: Multipoint oligogenic analysis of age-at-onset data with applications to Alzheimer disease pedigrees. Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting
Abstracts: Multipoint quantitative-trait linkage analysis in general pedigrees. Online system for faster multipoint linkage analysis via parallel execution on thousands of personal computers
Abstracts: Multispecies seabird feeding flocks in the Galapagos Islands. Molecular genetic status of Aleutian Canada Gees from Buldir and the Semidi Islands, Alaska
Abstracts: Multiubiquitin chain receptors define a layer of substrate selectivity in the ubiquitin-proteasome system. A proteasome howdunit: the case of the missing signal
Abstracts: Multivariate analyses of Burkholderia species in soil: Effect of crop and land use history. Multivariate analyses of Burkholderia species in soil: effect of crop and land use history
Abstracts: Multivariate analysis of male mating success on morphometric traits and chromosome dosage in the grasshopper Sinipta dalmani
Abstracts: Mumps in seat 21C! The RNA conductome. Wanted: Owl killers
Abstracts: Mur-LH, the broad-spectrum endolysin of Lactobacillus helveticus temperature bacteriophage phi-0303. Hydrolysis of sequenced beta-casein peptides provides new insight into peptidase activity from thermophilic lactic acid bacteria and highlights intrinsic resistance of phosphopeptides
Abstracts: Muscle stem cells in development, regeneration, and disease. WUSCHEL induces shoot stem cell activity and developmental plasticity in the root meristem
Abstracts: Mutagenesis of three surface-exposed loops of a Bacillus thuringiensis insecticidal toxin reveals residues important for toxicity, receptor recognition and possibly membrane insertion
Abstracts: Mutant lambda repressors with increased operator affinities reveal new, specific protein-DNA contacts. The effects of central asymmetry on the propagation of palindromic DNA in bacteriophage lambda are consistent with cruciform extrusion in vivo
Abstracts: Mutants and intersexual heterokaryons of Blakeslea trispora for production of beta-carotene and lycopene. Modification of sexual development and carotene production by acetate and other small carboxylic acids in Blakeslea trispora and Phycomyces blakesleeanus
Abstracts: Mutants of Streptomyces roseosporus that express enhanced recombination within partially homologous genes. A gene cloning system for 'Streptomyces toyocaensis.'
Abstracts: Mutant studies of phosphofructo-2-kinases do not reveal an essential role of fructose-2,6-bisphosphate in the regulation of carbon fluxes in yeast cells
Abstracts: Mutational analyses of fs(1)Ya, an essential, developmentally regulated, nuclear envelope protein in Drosophila
Abstracts: Mutational analysis and chemical modification of Cys24 of lactococcin B, a bacteriocin produced by Lactococcus lactis
Abstracts: Mutational analysis of mesentericin Y105, an anti-Listeria bactriocin, for determination of impact on bactericidal activity, in vitro secondary structure, and membrane interaction
Abstracts: Mutational analysis of pcpA and its role in pentachlorophenol degradation by Sphingomonas (Flavobacterium) chlorophenolica ATCC 39723
Abstracts: Mutational analysis of pre-mRNA splicing in Saccharomyces cerevisiae using a sensitive new reporter gene, CUP1
Abstracts: Mutational analysis of the Paracoccus denitrificans c-type cytochrome biosynthetic genes ccmABCDG: disruption of ccmC has distinct effects suggesting a role for CcmC independent of CcmAB
Abstracts: Mutational analysis of the role of HPr in Listeria monocytogenes. Collapse of the proton motive force in Listeria monocytogenes caused by a bacteriocin produced by Pediococcus acidilacti
Abstracts: Mutational and functional analysis of the [beta]-carotene ketolase involved in the production of canthaxanthin and astaxanthin
Abstracts: Mutational disruption of the biosynthesis genes coding for the antifungal metabolite 2,4-diacetylphloroglucinol does not influence the ecological fitness of Pseudomonas fluorescens F113 in the rhizosphere of sugarbeets
Abstracts: Mutational mechanisms for generating microsatellite allele-frequency distributions: an analysis of 4,558 markers
Abstracts: Mutation analysis of patients with Hermansky-Pudlak syndrome: a frameshift hot spot in the HPS (ital) gene and apparent locus heterogeneity
Abstracts: Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations
Abstracts: Mutation hot spots in the 5p31-linked corneal dystrophies. Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease
Abstracts: Mutation hot spots in the 5p31-linked corneal dystrophies. A note on power approximations for the transmission/disequilibrium test
Abstracts: Mutation in CUL4B, which encodes a member of cullin-RING ubiquitin ligase complex, causes X-linked mental retardation
Abstracts: Mutation in the follicle-stimulating hormone receptor gene causes hereditary hypergonadotropic ovarian failure
Abstracts: Mutation in the mismatch repair gene Msh6 causes cancer susceptibility. TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome
Abstracts: Mutation of the axonal transport motor kinesin enhances paralytic and suppresses shaker in drosophila. Identification of homeotic target genes in Drosophila melanogaster including nervy, a proto-oncogene homologue
Abstracts: Mutation of the ptsG gene results in increased production of succinate in fermentation of glucose by Escherichia coli
Abstracts: Mutation of the type X collagen gene (COL10A1(ital)) causes spondylometaphyseal dysplasia. Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p
Abstracts: Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes
Abstracts: Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Simultaneouly correcting for population stratification and for genotyping error in case-control association studies
Abstracts: Mutations at the murine motheaten locus are within the hematopoietic cell protein-tyrosine phosphatase (Hcph) gene
Abstracts: Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation
Abstracts: Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromes
Abstracts: Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development
Abstracts: Mutations in FGD4 encoding the Rho GDP/GTP exchange factor FRABIN cause autosomal recessive Charcot-Marie-Tooth type 4H
Abstracts: Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia
Abstracts: Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome. part 2 Amyotropic lateral sclerosis: unfolding the toxicity of the misfolded
Abstracts: Mutations in POL1 increase the mitotic instability of tandem inverted repeats in Saccharomyces cerevisiae. HTS1 encodes both the cytoplasmic and mitochondrial histidyl-tRNA synthetase of Saccharomyces cerevisiae: mutations alter the specificity of compartmentation
Abstracts: Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction
Abstracts: Mutations in the Anopheles gambiae pink-eye and white genes define distinct, tightly linked eye-color loci. Mosaic: A position-effect variegation eye-color mutant in the mosquito anopheles gambiae
Abstracts: Mutations in the Drosophila dTAK1 gene reveal a conserved function for MAPKKKs in the control of rel/NF-kappaB-dependent innate immune responses
Abstracts: Mutations in the embryonal subunit of the acetylcholine receptor (CHRNG) cause lethal and Escobar variants of multiple pterygium syndrome
Abstracts: Mutations in the ER-Golgi intermediate compartment protein ERGIC-53 cause combined deficiency of coagulation factors V and VIII
Abstracts: Mutations in the EXT1 and EXT2 genes in hereditary multiple exostoses. Recurrent mutation in the first zinc finger of the orphan nuclear receptor NR2E3 causes autosomal dominant retinitis pigmentosa
Abstracts: Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause 'cone dystrophy with supernormal rod electroretinogram' in humans
Abstracts: Mutations in the gene KCNV2 encoding a voltage-gated potassium channel subunit cause 'cone dystrophy with supernormal rod electroretinogram' in humans. part 2
Abstracts: Mutations in the human UDP-N-acetylglucosamine 2-epimerase gene define the disease sialuria and the allosteric site of the enzyme
Abstracts: Mutations in the myosin VIIA gene cause a wide phenotypic spectrum , including atypical Usher syndrome. Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls
Abstracts: Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia
Abstracts: Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A. Alzheimer presenilins in the nuclear membrane, interphase kinetochores, and centrosomes suggest a role in chromosome segregation
Abstracts: Mutations in the second-largest subunit of Drosophila RNA polymerase II interact with Ubx. Reverse genetics of Drosophila RNA polymerase II: identification and characterization of RpII140, the genomic locus for the second-largest subunit
Abstracts: Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement
Abstracts: Mutations in the tight-junction gene claudin 19 (CLDN19) are associated with renal magnesium wasting, renal failure, and severe ocular involvement. part 2
Abstracts: Mutations in the trpD gene of Corynebacterium glutamicum confer 5-methyltryptophan resistance by encoding a feedback-resistant anthranilate phosphoribosyltransferase
Abstracts: Mutations involving the transcription factor Cbfa1 cause cleidocranial dysplasia. Osf2/Cbfa1: a transcriptional activator of osteoblast differentiation
Abstracts: Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome
Abstracts: Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause x-linked mental retardation associated with a marfanoid habitus
Abstracts: Mutations modulating Raf signaling in Drosophila eye development. The 3' regulatory region of the Abdominal-B gene: genetic analysis supports a model of reiterated and interchangeable regulatory elements
Abstracts: Mutations showing specificity for normal growth or Mn(II)-dependent post-exponential phase cell division in Deinococcus radiodurans
Abstracts: Mutator-induced cytoplasmic mutants in barley: genetic evidence of activation of a putative chloroplast transposon
Abstracts: Mutator specificity and disease: looking over the FENce. Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis
Abstracts: Mutualistic associations of aphids and prokaryotes: biology of the genus Buchnera. Horizontal transfer of bacterial symbionts: Heritability and fitness effects in a novel aphid host
Abstracts: Mutually exclusive splicing of the insect Dscam Pre-mRNA directed by competing intronic RNA secondary structures
Abstracts: Myc activates telomerase. Regulation of homologous recombination: Chi inactivates RecBCD enzyme by disassembly of the three subunits
Abstracts: Myc activates telomerase. Telomere-mediated chromosome pairing during meiosis in budding yeast. Modulation of telomerase activity by telomere DNA-binding proteins in Oxytricha
Abstracts: Myc: A weapon of mass destruction. The trithorax group protein lid is a trimethyl histone H3K4 demethylase required for dMyc-induced cell growth
Abstracts: Myc-enhanced expression of Cul1 promotes ubiquitin-dependent proteolysis and cell cycle progression. Essential role of Max in early embyronic growth and development
Abstracts: Mycobacteria in water and loose deposits of drinking water distribution systems in Finland. Mycobacteria and fungi in moisture-damaged building materials
Abstracts: Mycobacterial ecology of the Rio Grande. Molecular cloning and expression of genes encoding a novel dioxygenase involved in low- and high-molecular-weight polycyclic aromatic hydrocarbon degradation in Mycobacterium vanbaalenii PYR-1
Abstracts: Mycobacterium avium subspecies paratuberculosis cultured from locally and commercially pasteurized cow's milk in the Czech Republic
Abstracts: Mycobacterium avium subsp. paratuberculosis in lake catchments, in river water abstracted for domestic use, and in effluent from domestic sewage treatment works: Diverse opportunities for environmental cycling and human exposure
Abstracts: Mycobacterium xenopi IS1395, a novel insertion sequence expanding the IS256 family. Recombinant BCG expressing the leishmania surface antigen Gp63 induces protective immunity against Leishmania major infection in BALB/C mice
Abstracts: Mycolic acid composition of Corynebacterium glutamicum and its cell surface mutants: effects of growth with glycine and isonicotinic acid hydrazide
Abstracts: Mycoplasma penetrans infection of Molt-3 lymphocytes induces changes in the lipid composition of host cells. Lymphocytic infiltration in the chicken trachea in response to Mycoplasma gallisepticum infection
Abstracts: Mycosubtilin overproduction by Bacillus subtilis BBG100 enhances the organism's antagonistic and biocontrol activities
Abstracts: Mycotoxins in crude building materials from water-damaged buildings. Effect of chlorine dioxide gas on fungi and mycotoxins associated with sick building syndrome
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