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Publications starting with "M", page 15
Mutation analysis of the CHK2 gene in breast carcinoma and other cancers
Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography
Mutation analysis of the Gadd45 gene at exon 4 in atypical fibroxanthoma
Mutation analysis of the MDM4 gene in German breast cancer patients
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly
Mutation and evolutionary analyses identify NR2E1- candidate-regulatory mutations in humans with severe cortical malformations
Mutation and Evolutionary Rates in Adélie Penguins from the Antarctic
Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype–phenotype relationships
Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media
Mutation at the position 2058 of the 23S rRNA as a cause of macrolide resistance in Streptococcus pyogenes
Mutation at Tyrosine in AMLRY (GILRY Like) Motif of Yeast eRF1 on Nonsense Codons Suppression and Binding Affinity to eRF3
Mutation Detection
Mutation detection analysis of a region of 16S-like ribosomal RNA gene of Entamoeba histolytica , Entamoeba dispar and Entamoeba moshkovskii
Mutation Detection by Real-Time PCR: A Simple, Robust and Highly Selective Method
Mutation detection using a novel plant endonuclease.
Mutation detection using ENDO1: Application to disease diagnostics in humans and TILLING and Eco-TILLING in plants
Mutation detection using immobilized mismatch binding protein (MutS).
Mutation detection using nucleotide analogs that alter electrophoretic mobility.
Mutation frequencies at codon 248 of the p53 tumour suppressor gene are not increased in colon cancer cell lines with the RER+ phenotype.
Mutation frequency and spectrum resulting from a single abasic site in a single-stranded vector.
Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts
Mutation I136V alters electrophysiological properties of the Na V 1.7 channel in a family with onset of erythromelalgia in the second decade
Mutation in mitochondrial complex I ND6 subunit is associated with defective response to hypoxia in human glioma cells
Mutation in Mouse Hei10, an E3 Ubiquitin Ligase, Disrupts Meiotic Crossing Over
Mutation in the loop C-terminal to the cyclophilin A binding site of HIV-1 capsid protein disrupts proper virus assembly and infectivity
Mutation of a Critical Arginine in Microsomal Prostaglandin E Synthase-1 Shifts the Isomerase Activity to a Reductase Activity That Converts Prostaglandin H 2 into Prostaglandin F 2α *
Mutation of a single lysine residue severely impairs the DNA recognition and regulatory functions of the VZV gene 62 transactivator protein.
Mutation of a single residue, β-glutamate-20, alters protein–lipid interactions of light harvesting complex II
Mutation of exposed hydrophobic amino acids to arginine to increase protein stability
Mutation of RNA Pol III Subunit rpc2/polr3b Leads to Deficiency of Subunit Rpc11 and Disrupts Zebrafish Digestive Development
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
Mutation of the casein kinase II phosphorylation site abolishes the anti-proliferative activity of p53.
Mutation of the Mouse Syce1 Gene Disrupts Synapsis and Suggests a Link between Synaptonemal Complex Structural Components and DNA Repair
Mutation of the Oct-1 POU-specific recognition helix leads to altered DNA binding and influences enhancement of adenovirus DNA replication.
Mutation of the Zebrafish Nucleoporin elys Sensitizes Tissue Progenitors to Replication Stress
Mutation of von Hippel–Lindau Tumour Suppressor and Human Cardiopulmonary Physiology
Mutation Patterns in the Human Genome: More Variable Than Expected
Mutation patterns of amino acid tandem repeats in the human proteome
Mutation patterns of mtDNA: Empirical inferences for the coding region
Mutation Rates and Gene Location: Some Like It Hot
Mutation Rates of TGFBR2 and ACVR2 Coding Microsatellites in Human Cells with Defective DNA Mismatch Repair
Mutation screen and association studies in the Diacylglycerol O-acyltransferase homolog 2 gene ( DGAT2 ), a positional candidate gene for early onset obesity on chromosome 11q13
Mutation screening of CHD5 in melanoma-prone families linked to 1p36 revealed no deleterious coding or splice site changes
Mutation screening of HSF4 in 150 age-related cataract patients
Mutation screening of two candidate genes from 13q32 in families affected with Bipolar disorder: human peptide transporter (SLC15A1) and human glypican5 (GPC5)
Mutation spectra of TA*, the major photoproduct of thymidylyl-(3'5')-deoxyadenosine, in Escherichia coli under SOS conditions.
Mutation spectrum in Escherichia coli DNA mismatch repair deficient (mutH) strain.
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
Mutation studies with human fibroblasts.
Mutation study of Spanish patients with Hereditary Hemorrhagic Telangiectasia
Mutational analyses of dinucleotide and tetranucleotide microsatellites in Escherichia coli : influence of sequence on expansion mutagenesis
Mutational analyses of the signals involved in the subcellular location of DSCR1
Mutational analysis defines the 5′-kinase and 3′-phosphatase active sites of T4 polynucleotide kinase
Mutational analysis of a conserved motif of Agrobacterium tumefaciens VirD2.
Mutational analysis of a function of xeroderma pigmentosum group A (XPA) protein in strand-specific DNA repair.
Mutational analysis of a transcriptional activation region of the VP16 protein of herpes simplex virus.
Mutational analysis of an essential binding site for the U3 snoRNA in the 5' external transcribed spacer of yeast pre-rRNA.
Mutational analysis of an essential binding site for the U3 snoRNA in the 5' external transcribed spacer of yeast pre-rRNA.
Mutational analysis of an essential binding site for the U3 snoRNA in the 5' external transcribed spacer of yeast pre-rRNA
Mutational analysis of BTAF1–TBP interaction: BTAF1 can rescue DNA-binding defective TBP mutants
Mutational analysis of Chlorella virus DNA ligase: catalytic roles of domain I and motif VI.
Mutational analysis of conserved residues in Hha I DNA methyltransferase
Mutational analysis of βCOP (Sec26p) identifies an appendage domain critical for function
Mutational Analysis of EGFR and Related Signaling Pathway Genes in Lung Adenocarcinomas Identifies a Novel Somatic Kinase Domain Mutation in FGFR4
Mutational analysis of Epstein-Barr virus nuclear antigen 1 (EBNA 1).
Mutational analysis of Escherichia coli DNA ligase identifies amino acids required for nick-ligation in vitro and for in vivo complementation of the growth of yeast cells deleted for CDC9 and LIG4.
Mutational analysis of exoribonuclease I from Saccharomyces cerevisiae.
Mutational analysis of highly conserved aspartate residues essential to the catalytic core of the piggyBac transposase
Mutational analysis of HIV-1 gp41 mediated apoptosis and its correlation with fusion/hemifusion
Mutational analysis of human CEACAM1: the potential of receptor polymorphism in increasing host susceptibility to bacterial infection
Mutational analysis of human profilin I reveals a second PI(4,5)-P 2 binding site neighbouring the poly(L-proline) binding site
Mutational analysis of molecular requirements for the actions of general anaesthetics at the γ-aminobutyric acid A receptor subtype, α1β2γ2
Mutational analysis of p50E4F suggests that DNA binding activity is mediated through an alternative structure in a zinc finger domain that is regulated by phosphorylation.
Mutational analysis of Peroxiredoxin IV: exclusion of a positional candidate for multinodular goitre
Mutational analysis of the 3'-->5' proofreading exonuclease of Escherichia coli DNA polymerase III.
Mutational analysis of the antigenomic trans-acting delta ribozyme: the alterations of the middle nucleotides located on the P1 stem.
Mutational analysis of the att DNA-binding domain of phage Mu transposase.
Mutational analysis of the Chlamydia trachomatis dnaK promoter defines the optimal –35 promoter element
Mutational analysis of the contribution of sequence motifs within the IgH enhancer to tissue specific transcriptional activation.
Mutational analysis of the core and modulator sequences of the BMV RNA3 subgenomic promoter.
Mutational analysis of the damage-recognition and catalytic mechanism of human SMUG1 DNA glycosylase
Mutational analysis of the DNA binding domain A of chromosomal protein HMG1.
Mutational analysis of the engrailed homeodomain recognition helix by phage display.
Mutational analysis of the human nucleotide excision repair gene ERCC1.
Mutational analysis of the L1 binding site of 23S rRNA in Escherichia coli.
Mutational analysis of the lac regulatory region: second-site changes that activate mutant promoters.
Mutational analysis of the nucleotide sequence at the FNR-dependent nirB promoter in Escherichia coli.
Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA)
Mutational analysis of the potential catalytic residues of the VV G1L metalloproteinase
Mutational analysis of the PRP4 protein of Saccharomyces cerevisiae suggests domain structure and snRNP interactions.
Mutational analysis of the regulatory region of the Mycobacterium plasmid pAL5000.
Mutational analysis of the reverse transcriptase and ribonuclease H domains of the human foamy virus.
Mutational analysis of the RNA pseudoknot involved in efficient ribosomal frameshifting in simian retrovirus-1.
Mutational analysis of the Saccharomyces cerevisiae general regulatory factor CP1.
Mutational analysis of the Tetrahymena telomerase RNA: identification of residues affecting telomerase activity in vitro.
Mutational analysis of the tobacco mosaic virus 5'-leader for altered ability to enhance translation.
Mutational analysis of the transcription start site of the yeast tRNA(Leu3) gene.
Mutational analysis of the tRNA3Lys/HIV-1 RNA (primer/template) complex.
Mutational analysis of upstream sequences required for transcriptional activation of the Klebsiella pneumoniae nifH promoter.
Mutational analysis of vaccinia virus topoisomerase identifies residues involved in DNA binding.
Mutational analysis of varicella-zoster virus major immediate-early protein IE62.
Mutational and transcriptional analyses of an avian pathogenic Escherichia coli ColV plasmid
Mutational comparison of the single-domained APOBEC3C and double-domained APOBEC3F/G anti-retroviral cytidine deaminases provides insight into their DNA target site specificities
Mutational dissection of the 21 bp repeat region of the SV40 early promoter reveals that it contains overlapping elements of the early-early and late-early promoters.
Mutational dynamics of the SARS coronavirus in cell culture and human populations isolated in 2003
Mutational evidence for competition between the P1 and the P10 helices of a mitochondrial group I intron.
Mutational fingerprints of aging
Mutational hotspots in the TP53 gene and, possibly, other tumor suppressors evolve by positive selection
Mutational optimization of the coelenterazine-dependent luciferase from Renilla
Mutational pattern and frequency of induced nucleotide changes in mouse ENU mutagenesis
Mutational sensitivity patterns define critical residues in the palm subdomain of the reverse transcriptase of human immunodeficiency virus type 1.
Mutational spectrometry without phenotypic selection: human mitochondrial DNA.
Mutational spectrum analysis of RNase H(35) deficient Saccharomyces cerevisiae using fluorescence-based directed termination PCR
Mutational study of sapovirus expression in insect cells
Mutational study of the rRNA in yeast mitochondria: functional importance of T1696 in the large rRNA gene.
Mutations affecting cleavage at the p10-capsid protease cleavage site block Rous sarcoma virus replication
Mutations affecting the biosynthesis of S-adenosylmethionine cause reduction of DNA methylation in Neurospora crassa.
Mutations altering the cleavage specificity of a homing endonuclease
Mutations and homologous recombination induced in mammalian cells by metabolites of benzo[a]pyrene and 1-nitropyrene.
Mutations at arginine residues in two Asian hemophilia B patients.
Mutations at the guanosine-binding site of the Tetrahymena ribozyme also affect site-specific hydrolysis.
Mutations Change the Boolean Logic of Gene Regulation
Mutations dissociating the inhibitory activity of the pokeweed antiviral protein on eukaryote translation and Escherichia coli growth.
Mutations in 16S rRNA in Escherichia coli at methyl-modified sites: G966, C967, and G1207.
Mutations in a Novel, Cryptic Exon of the Luteinizing Hormone/Chorionic Gonadotropin Receptor Gene Cause Male Pseudohermaphroditism
Mutations in a plastid-localized elongation factor G alter early stages of plastid development in Arabidopsis thaliana
Mutations in APC , CTNNB1 and K-ras genes and expression of hMLH1 in sporadic colorectal carcinomas from the Netherlands Cohort Study
Mutations in AtPS1 ( Arabidopsis thaliana Parallel Spindle 1 ) Lead to the Production of Diploid Pollen Grains
Mutations in domain V of the 23S ribosomal RNA of Bacillus subtilis that inactivate its protein folding property in vitro
Mutations in Drosophila Greatwall/Scant Reveal Its Roles in Mitosis and Meiosis and Interdependence with Polo Kinase
Mutations in E.coli 16s rRNA that enhance and decrease the activity of a suppressor tRNA.
Mutations in genes of Saccharomyces cerevisiae encoding pre-mRNA splicing factors cause cell cycle arrest through activation of the spindle checkpoint
Mutations in gfpt1 and skiv2l2 Cause Distinct Stage-Specific Defects in Larval Melanocyte Regeneration in Zebrafish
Mutations in hamster single-strand break repair gene XRCC1 causing defective DNA repair.
Mutations in Influenza A Virus (H5N1) and Possible Limited Spread, Turkey, 2006
Mutations in mitochondrial DNA accumulate differentially in three different human tissues during ageing.
Mutations in mitochondrial tRNA genes: a frequent cause of neuromuscular diseases.
Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia.
Mutations in normal breast tissue and breast tumours
Mutations in NYX of individuals with high myopia, but without night blindness
Mutations in PIK3CA are infrequent in neuroblastoma
Mutations in STAT3 and IL12RB1 impair the development of human IL-17–producing T cells
Mutations in target DNA elements of yeast HAP1 modulate its transcriptional activity without affecting DNA binding.
Mutations in the 23S rRNA gene are associated with clarithromycin resistance in Helicobacter pylori isolates in Brazil
Mutations in the 3'-untranslated region of GATA4 as molecular hotspots for congenital heart disease (CHD)
Mutations in the 915 region of Escherichia coli 16S ribosomal RNA reduce the binding of streptomycin to the ribosome.
Mutations in the C-terminus of the X protein of hepatitis B virus regulate Wnt-5a expression in hepatoma Huh7 cells: cDNA microarray and proteomic analyses
Mutations in the herpes simplex virus DNA polymerase gene conferring hypersensitivity to aphidicolin.
Mutations in the histone fold domain of the TAF12 gene show synthetic lethality with the TAF1 gene lacking the TAF N-terminal domain (TAND) by different mechanisms from those in the SPT15 gene encoding the TATA box-binding protein (TBP)
Mutations in the IGF-II pathway that confer resistance to lytic reovirus infection
Mutations in the Lactococcus lactis Ll.LtrB group II intron that retain mobility in vivo
Mutations in the mitochondrial DNA D-loop region are frequent in cervical cancer
Mutations in the mitochondrial oli1 gene of Saccharomyces cerevisiae affecting subunit 9 of the mitochondrial ATPase complex.
Mutations in the MutSα interaction interface of MLH1 can abolish DNA mismatch repair
Mutations in the peptidyl transferase region of E. coli 23S rRNA affecting translational accuracy.
Mutations in the Plasmodium falciparum cytochrome b gene are associated with delayed parasite recrudescence in malaria patients treated with atovaquone-proguanil
Mutations in the RNA polymerase recognition sequence of the Klebsiella pneumoniae nifH promoter permitting transcriptional activation in the absence of NifA binding to upstream activator sequences.
Mutations in the SLC2A9 Gene Cause Hyperuricosuria and Hyperuricemia in the Dog
Mutations in the TΨC Loop of E. coli tRNA Lys,3 Have Varied Effects on In Trans Complementation of HIV-1 Replication
Mutations in the TAR hairpin affect the equilibrium between alternative conformations of the HIV-1 leader RNA
Mutations in the TOPORS gene cause 1% of autosomal dominant retinitis pigmentosa
Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy
Mutations in the yeast Myb-like protein Bas1p resulting in discrimination between promoters in vivo but notin vitro.
Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans
Mutations in two global regulators lower individual mortality in Escherichia coli
Mutations in two regions upstream of the A gamma globin gene canonical promoter affect gene expression.
Mutations in U5 snRNA loop 1 influence the splicing of different genes in vivo
Mutations in UCP2 in Congenital Hyperinsulinism Reveal a Role for Regulation of Insulin Secretion
Mutations induced by DNA polymerase alpha upon in vitro replication of M13mp8(+) DNA.
Mutations induced in the hypoxanthine phosphoribosyl transferase gene by three urban air pollutants: acetaldehyde, benzo[a]pyrene diolepoxide, and ethylene oxide.
Mutations of acetylcholinesterase which confer insecticide resistance in Drosophila melanogaster populations
Mutations of Different Molecular Origins Exhibit Contrasting Patterns of Regional Substitution Rate Variation
Mutations of genes in synthesis of the carotenoid precursors of ABA lead to pre-harvest sprouting and photo-oxidation in rice
Mutations of Nonconserved Residues within the Calcium Channel α 1 -interaction Domain Inhibit β-Subunit Potentiation
Mutations of PIK3CA in gastric adenocarcinoma
Mutations on the Switch III region and the alpha3 helix of Galpha 16 differentially affect receptor coupling and regulation of downstream effectors
Mutations that alter the ability of the Escherichia coli cyclic AMP receptor protein to activate transcription.
Mutations that increase the affinity of a translational repressor for RNA.
Mutations to nonsense codons in human genetic disease: implications for gene therapy by nonsense suppressor tRNAs.
Mutations underlying 3-Hydroxy-3-Methylglutaryl CoA Lyase deficiency in the Saudi population
Mutations which alter splicing in the human hypoxanthine-guanine phosphoribosyltransferase gene.
Mutations within the decoding site of Escherichia coli 16S rRNA: growth rate impairment, lethality and intragenic suppression.
MutDB services: interactive structural analysis of mutation data
MutDB: update on development of tools for the biochemical analysis of genetic variation
MutL homologs in restriction-modification systems and the origin of eukaryotic MORC ATPases
MutM, a protein that prevents G.C----T.A transversions, is formamidopyrimidine-DNA glycosylase.
MuTrack: a genome analysis system for large-scale mutagenesis in the mouse
MutS binding protects heteroduplex DNA from exonuclease digestion in vitro: a simple method for detecting mutations.
MutS inhibits RecA-mediated strand transfer with methylated DNA substrates
MutScreener: primer design tool for PCR-direct sequencing
Mutual friends: Charles Dickens and Great Ormond Street Children's Hospital
Mutual information estimation reveals global associations between stimuli and biological processes
Mutual Information for Testing Gene-Environment Interaction
Mutual Inhibition between Kaposi's Sarcoma-Associated Herpesvirus and Epstein-Barr Virus Lytic Replication Initiators in Dually-Infected Primary Effusion Lymphoma
Mutual interactions between subunits of the human RNase MRP ribonucleoprotein complex
Mutual Mate Choice: When it Pays Both Sexes to Avoid Inbreeding
Mutual obligation, shared responsibility agreements & indigenous health strategy
Mutualistic Interactions Drive Ecological Niche Convergence in a Diverse Butterfly Community
Mutually Exclusive Expression of Virulence Genes by Malaria Parasites Is Regulated Independently of Antigen Production
Mutually exclusive recombination of wild-type and mutant loxP sites in vivo facilitates transposon-mediated deletions from both ends of genomic DNA in PACs
MutY, an adenine glycosylase active on G-A mispairs, has homology to endonuclease III.
MUTYH prevents OGG1 or APEX1 from inappropriately processing its substrate or reaction product with its C-terminal domain
Muybridge. Man in motion
MVB-12, a Fourth Subunit of Metazoan ESCRT-I, Functions in Receptor Downregulation
MvirDB—a microbial database of protein toxins, virulence factors and antibiotic resistance genes for bio-defence applications
My 2,000 best films: parallel phenotyping of Dictyostelium development
My continuing adventure with 21 CFR Part 11 - the evolution of Zymark's compliance
My first time: initiation into injecting drug use in Manipur and Nagaland, north-east India
My impossible health, or the case of James Joyce, catalogue of an exhibition
My life before penicillin
My own private Germany: Daniel Paul Schreber's secret history of modernity
My sister's keeper?: genomic research and the identifiability of siblings
My worries are no longer behind me
Myasthenia gravis
Myasthenia gravis and pregnancy: clinical implications and neonatal outcome
Myasthenia Gravis. Annals of the New York Academy of Sciences
Myb proteins inhibit fibroblast transformation by v-Rel
myb-specific probes.
MYBS: a comprehensive web server for mining transcription factor binding sites in yeast
Myc Dynamically and Preferentially Relocates to a Transcription Factory Occupied by Igh
“Myc’ed Messages”: Myc Induces Transcription of E2F1 while Inhibiting Its Translation via a microRNA Polycistron
Myc induces the nucleolin and BN51 genes: possible implications in ribosome biogenesis
Myc Oncogene-Induced Genomic Instability: DNA Palindromes in Bursal Lymphomagenesis
Mycelium development in Streptomyces antibioticus ATCC11891 occurs in an orderly pattern which determines multiphase growth curves
Mycobacteria: from genomes to disease control
Mycobacterial and nonbacterial pulmonary complications in hospitalized patients with human immunodeficiency virus infection: A prospective, cohort study
Mycobacterial immune reconstitution inflammatory syndrome in HIV-1 infection after antiretroviral therapy is associated with deregulated specific T-cell responses: Beneficial effect of IL-2 and GM-CSF immunotherapy
Mycobacterial Mutants with Defective Control of Phagosomal Acidification
Mycobacterial transcriptional signals: requirements for recognition by RNA polymerase and optimal transcriptional activity
Mycobacterium avium complex immune reconstitution inflammatory syndrome: Long term outcomes
Mycobacterium avium-intracellulare cellulitis occurring with septic arthritis after joint injection: a case report
Mycobacterium avium Lymphadenopathy among Children, Sweden
Mycobacterium avium subsp. hominissuis Infection in 2 Pet Dogs, Germany
Mycobacterium avium subspecies paratuberculosis is not associated with Type-2 Diabetes Mellitus
Mycobacterium bohemicum and Cervical Lymphadenitis in Children
Mycobacterium bovis Infection in Holstein Friesian Cattle, Iran
Mycobacterium bovis Strains Causing Smear-Positive Human Tuberculosis, Southwest Ireland
Mycobacterium celatum pulmonary infection.
Mycobacterium chelonei Breast Abscess Associated With Nipple Piercing
Mycobacterium haemophilum and Lymphadenitis in Immunocompetent Children, Israel
Mycobacterium haemophilum Infection after Alemtuzumab Treatment
Mycobacterium haemophilum osteomyelitis: case report and review of the literature
Mycobacterium setense Infection in Humans
Mycobacterium terrae isolated from indoor air of a moisture-damaged building induces sustained biphasic inflammatory response in mouse lungs.
Mycobacterium tuberculosis 6-kDa Early Secreted Antigenic Target (ESAT-6) protein downregulates Lipopolysaccharide induced c-myc expression by modulating the Extracellular Signal Regulated Kinases 1/2
Mycobacterium tuberculosis aortic graft infection with recurrent hemoptysis: a case report
Mycobacterium tuberculosis complex genetic diversity: mining the fourth international spoligotyping database (SpolDB4) for classification, population genetics and epidemiology
Mycobacterium tuberculosis from chronic murine infections that grows in liquid but not on solid medium
Mycobacterium tuberculosis Glucosyl-3-Phosphoglycerate Synthase: Structure of a Key Enzyme in Methylglucose Lipopolysaccharide Biosynthesis
Mycobacterium tuberculosis Induces Interleukin-32 Production through a Caspase- 1/IL-18/Interferon-γ-Dependent Mechanism
Mycobacterium tuberculosis interactome analysis unravels potential pathways to drug resistance
Mycobacterium tuberculosis monoarthritis in a child
Mycobacterium tuberculosis NAD + -dependent DNA ligase is selectively inhibited by glycosylamines compared with human DNA ligase I
Mycobacterium tuberculosis nuoG Is a Virulence Gene That Inhibits Apoptosis of Infected Host Cells
Mycobacterium tuberculosis RecA intein, a LAGLIDADG homing endonuclease, displays Mn 2+ and DNA-dependent ATPase activity
Mycobacterium tuberculosis Rv2118c codes for a single-component homotetrameric m 1 A58 tRNA methyltransferase
Mycobacterium tuberculosis Rv3802c Encodes a Phospholipase/Thioesterase and Is Inhibited by the Antimycobacterial Agent Tetrahydrolipstatin
Mycobacterium tuberculosis spoligotypes and drug susceptibility pattern of isolates from tuberculosis patients in peri-urban Kampala, Uganda
Mycobacterium ulcerans Disease, Peru
Mycobacterium xenopi Clinical Relevance and Determinants, the Netherlands
Mycolactone Diffuses from Mycobacterium ulcerans –Infected Tissues and Targets Mononuclear Cells in Peripheral Blood and Lymphoid Organs
Mycolic Acid Modification by the mmaA4 Gene of M. tuberculosis Modulates IL-12 Production
MycoperonDB: a database of computationally identified operons and transcriptional units in Mycobacteria
Mycophenolate mofetil inhibits the development of Coxsackie B3-virus-induced myocarditis in mice
Mycophenolate mofetil modulates adhesion receptors of the beta1 integrin family on tumor cells: impact on tumor recurrence and malignancy
Mycophenolate sodium treatment in patients with primary Sjögren syndrome: a pilot trial
Mycoplasma alkalescens demonstrated in bronchoalveolar lavage of cattle in Denmark
Mycoplasma and bacterial proteins resembling contractile proteins: a review.
Mycoplasma attachment to solid surfaces: a review.
Mycoplasma evolution: a review of the use of ribosomal and transfer RNA nucleotide sequences in the determination of phylogenetic relationships.
Mycoplasma Genitalium Among Women With Nongonococcal, Nonchlamydial Pelvic Inflammatory Disease
Mycoplasma genitalium : an efficient strategy to generate genetic variation from a minimal genome
Mycoplasma genitalium Lipoproteins Induce Human Monocytic Cell Expression of Proinflammatory Cytokines and Apoptosis by Activating Nuclear Factor κ B
Mycoplasma hyopharyngis Isolation From Swine
Mycoplasma Infection of Cell Cultures
Mycoplasma interaction with lymphocytes and phagocytes: role of hydrogen peroxide released from M. pneumoniae.
Mycoplasma Interactions with Lymphocytes and Phagocytes: Comments on Present Status
Mycoplasma pneumoniae attachment to WiDr cell cultures: competitive inhibition assays.
Mycoplasma pneumoniae respiratory disease symposium: summation and significance.
Mycoplasmal PID: a review of natural and experimental infections.
Mycoplasmas and bovine respiratory disease: studies related to pathogenicity and the immune response--a selective review.
Mycoplasmas as pathogens.
Mycorrhizal and non-mycorrhizal Lactuca sativa plants exhibit contrasting responses to exogenous ABA during drought stress and recovery
Mycosin-1, a subtilisin-like serine protease of Mycobacterium tuberculosis , is cell wall-associated and expressed during infection of macrophages
Mycosphaerella is polyphyletic
Mycosporine-Like Amino Acids and Marine Toxins - The Common and the Different
Mycothiol biosynthesis is essential for ethionamide susceptibility in Mycobacterium tuberculosis
Mycotic aneurysm of the posterior tibial artery – a rare complication of bacterial endocarditis: a case report
Mycotic Endocarditis and Meningitis
Mycotoxin Adducts on Human Serum Albumin: Biomarkers of Exposure to Stachybotrys chartarum
Mycotoxins: of molds and maladies.
Mycotoxins: toxicity, carcinogenicity, and the influence of various nutritional conditions *
Mycotrophy in Plants
Mycoviruses: a new dimension in microbiology.
MyD88 Dependent Signaling Contributes to Protective Host Defense against Burkholderia pseudomallei
Myd88 Is Required for an Antibody Response to Retroviral Infection
MyD88 Is Required for Protection from Lethal Infection with a Mouse-Adapted SARS-CoV
MyD88 predicts chemoresistance to paclitaxel in epithelial ovarian cancer
Myelin contributes to the parallel orientation of axonal growth on white matter in vitro
Myelin-mediated inhibition of oligodendrocyte precursor differentiation can be overcome by pharmacological modulation of Fyn-RhoA and protein kinase C signalling
Myelography for clinically atypical prolapsed lumbar intervertebral discs.
Myeloid antigens in childhood lymphoblastic leukemia:clinical data point to regulation of CD66c distinct from other myeloid antigens
Myeloid dendritic cells display downregulation of C-type lectin receptors and aberrant lectin uptake in systemic lupus erythematosus
Myeloid ecotropic viral integration site 1 (MEIS) 1 involvement in embryonic implantation
Myeloid hyperplasia in the SENCAR mouse: differentiation from granulocytic leukemia.
Myeloid leukemia after hematotoxins.
Myeloid sarcomas: a histologic, immunohistochemical, and cytogenetic study
MYELOMA AND RELATED DISORDERS: CLINICS IN HAEMATOLOGY
Myeloma--results of treatment 1986-1990.
Myeloma with multiple rearranged immunoglobulin kappa genes: only one kappa gene codes for kappa chains.
Myelomeningocele: neglected aspects
Myeloperoxidase: A New Biomarker of Inflammation in Ischemic Heart Disease and Acute Coronary Syndromes
Myeloperoxidase and adenosine-deaminase levels in the pleural fluid leakage induced by carrageenan in the mouse model of pleurisy.
Myeloperoxidase and eosinophil cationic protein in serum and sputum during antibiotic treatment in cystic fibrosis patients with Pseudomonas aeruginosa infection
Myeloperoxidase Promoter Polymorphism −463G Is Associated With More Severe Clinical Expression of Cystic Fibrosis Pulmonary Disease
Myeloproliferative disorder FOP-FGFR1 fusion kinase recruits phosphoinositide-3 kinase and phospholipase Cγ at the centrosome
Myelotoxicity induced in female B6C3F1 mice by inhalation of methyl isocyanate.
MyHits: a new interactive resource for protein annotation and domain identification
MyHits: improvements to an interactive resource for analyzing protein sequences
Myocardial bridging as a cause of acute myocardial infarction: a case report
Myocardial contractility in the echo lab: molecular, cellular and pathophysiological basis
Myocardial Doppler velocities as a marker of prognosis in the ICU
Myocardial dysfunction in rheumatoid arthritis: epidemiology and pathogenesis
Myocardial dysfunction in the periinfarct and remote regions following anterior infarction in rats quantified by 2D radial strain echocardiography: An observational cohort study
Myocardial first-pass perfusion cardiovascular magnetic resonance: history, theory, and current state of the art
Myocardial Hypertrophy Overrides the Angiogenic Response to Hypoxia
Myocardial infarction after taking zolmitriptan.
Myocardial infarction complicating critical illness
Myocardial infarction in association with misuse of anabolic steroids.
Myocardial infarction with normal coronary arteries: a case report and review of the literature
Myocardial injury associated with hyperinflation of the lung
Myocardial injury in infants ventilated on the paediatric intensive care unit: a case control study
Myocardial involvement during the early course of type 2 diabetes mellitus: usefulness of Myocardial Performance Index
Myocardial ischemia--association with perioperative cardiac morbidity.
Myocardial ischemia in the absence of epicardial coronary artery disease in Friedreich's ataxia
Myocardial Lesions Resulting from Dietary Deficiency *
Myocardial metabolism for the toxicologist.
Myocardial Metabolism—Therapeutic Aspects
Myocardial performance in conscious streptozotocin diabetic rats
Myocardial perfusion scintigraphy: the evidence
Myocardial Revascularization By Off Pump Coronary Bypass Surgery (OPCABG): A Ten Year Review
Myocardial segment-specific model generation for simulating the electrical action of the heart
Myocardial tissue Doppler echocardiography and N-terminal B-type natriuretic peptide (NT-proBNP) in diastolic and systolic heart failure
Myocarditis related to Campylobacter jejuni infection: A case report
Myochrysine Solution Structure and Reactivity
Myocilin mutations among primary open angle glaucoma patients of Kanyakumari district, South India
Myocilin polymorphisms and high myopia in subjects of European origin
Myocilin variations and familial glaucoma in Taxiarchis, a small Greek village
Myoclonia in Papio papio : Are they all “Epileptic” ?
Myocontrol in Aging
MYOCRISIN
MyoD- and nerve-dependent maintenance of MyoD expression in mature muscle fibres acts through the DRR/PRR element
MyoD uses overlapping but distinct elements to bind E-box and tetraplex structures of regulatory sequences of muscle-specific genes
MyoD1 promoter autoregulation is mediated by two proximal E-boxes.
Myoepithelial Cells: Any role in aspiration cytology smears of breast tumors?
Myoepithelial cells: good fences make good neighbors
MYOFACTION
Myofascial trigger points in cluster headache patients: a case series
Myofiber integrity depends on desmin network targeting to Z-disks and costameres via distinct plectin isoforms
Myogenesis in the basal bilaterian Symsagittifera roscoffensis (Acoela)
Myogenic Akt signaling upregulates the utrophin–glycoprotein complex and promotes sarcolemma stability in muscular dystrophy
Myoglobin clearance by super high-flux hemofiltration in a case of severe rhabdomyolysis: a case report
Myomectomy at time of cesarean delivery: a retrospective cohort study
Myonecrosis secondary to Clostridium Septicum in a patient with Occult Colon Malignancy: a case report
Myopathy, hypokalaemia and pica (geophagia) in pregnancy
Myosin-10 and actin filaments are essential for mitotic spindle function
Myosin Binding Protein C Positioned to Play a Key Role in Regulation of Muscle Contraction: Structure and Interactions of Domain C1
Myosin heavy chain and physiological adaptation of the rat diaphragm in elastase-induced emphysema
Myosin light chain 1 atrial isoform (MLC1A) is expressed in pre-B cells under control of the BOB.1/OBF.1 coactivator
Myosin-Vb functions as a dynamic tether for peripheral endocytic compartments during transferrin trafficking
Myosin VIIA, Important for Human Auditory Function, Is Necessary for Drosophila Auditory Organ Development
Myotatic, Kinesthetic and Vestibular Mechanisms
Myotonic dystrophy
Myotonic dystrophy: molecular windows on a complex etiology.
Myotonic dystrophy: relative sensitivity of symptoms signs and abnormal investigations.
MYRbase: analysis of genome-wide glycine myristoylation enlarges the functional spectrum of eukaryotic myristoylated proteins
Myriads of protein families, and still counting
Mys retrotransposons in Peromyscus leucopus and transgenic Mus musculus.
Mystat: A Personal Version of Systat
Mysteries of Science
Mystical Bedlam. Madness, anxiety, and healing in seventeenth-century England
Myxedema Heart Disease
Myxoid Malignant Fibrous Histiocytoma with Multiple Primary Sites
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