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Real-time quantitative polymerase chain reaction: A potential tool for genetic analysis in neuropathology
BRAIN PATHOLOGY
Alterations of K-ras and p53 mutations in colorectal cancer patients in Central Europe
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A
The molecular interactions of pyrethroid insecticides with insect and mammalian sodium channels
PEST MANAGEMENT SCIENCE
Nonnucleoside reverse transcriptase inhibitor resistance
JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
Of mice and malaria mutants: unravelling the genetics of drug resistance using rodent malaria models
TRENDS IN PARASITOLOGY
Accessing genetic variation: Genotyping single nucleotide polymorphisms
NATURE REVIEWS GENETICS
A 'hot-spot' mutation alters the mechanical properties of keratin filamentnetworks
NATURE CELL BIOLOGY
Conditions for single-strand conformation polymorphism (SSCP) analysis of BRCA1 gene using an automated electrophoresis unit
CLINICAL CHEMISTRY AND LABORATORY MEDICINE
Development of genetic hypotheses in essential hypertension
JOURNAL OF HUMAN GENETICS
Melanocortin receptors: their functions and regulation by physiological agonists and antagonists
CELLULAR AND MOLECULAR LIFE SCIENCES
Quantitation of heteroplasmy in mitochondrial DNA mutations by primer extension using Vent(R)(R)(exo-) DNA polymerase and RFLP analysis
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
Mitochondrial genome instability in human cancers
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH
Adaptive mutations, mutator DNA polymerases and genetic change strategies of pathogens
CURRENT OPINION IN MICROBIOLOGY
Resistance of Helicobacter pylori to antibiotics and its impact on treatment options
DRUG RESISTANCE UPDATES
SNPing in the human genome
CURRENT OPINION IN CHEMICAL BIOLOGY
What we could do now: molecular pathology of colorectal cancer
JOURNAL OF CLINICAL PATHOLOGY-MOLECULAR PATHOLOGY
Prevalence of polymorphisms in the dihydrofolate reductase and dihydropteroate synthetase genes of Plasmodium falciparum isolates from southern Mauritania
TROPICAL MEDICINE & INTERNATIONAL HEALTH
Resistance profiles to antiretroviral drugs in HIV-1 drug-naive patients in Argentina
ANTIVIRAL THERAPY
The other, forgotten genome: mitochondrial DNA and mental disorders
MOLECULAR PSYCHIATRY
Mutational spectrum of N-hydroxy-N-acetyl-4-aminobiphenyl at exon 3 of theHPRT gene
BIOMARKERS
Friedreich's ataxia and frataxin: Molecular genetics, evolution and pathogenesis (Review)
INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE
Protein mobility and GABA-induced conformational changes in GABA(A) receptor pore-lining M2 segment
NATURE NEUROSCIENCE
Presence of a major WFS1 mutation in Spanish wolfram syndrome pedigrees
MOLECULAR GENETICS AND METABOLISM
Clustering mutational spectra via classification likelihood and Markov chain Monte Carlo algorithms
JOURNAL OF AGRICULTURAL BIOLOGICAL AND ENVIRONMENTAL STATISTICS
A study of parameters that influence the HPLC and CE separation of double stranded DNA fragments and DNA mutants
JOURNAL OF LIQUID CHROMATOGRAPHY & RELATED TECHNOLOGIES
Hematologically important mutations: X-linked chronic granulomatous disease (Second update)
BLOOD CELLS MOLECULES AND DISEASES
The leukemia-associated AML1 (Runx1)-CBF beta complex functions as a DNA-induced molecular clamp
NATURE STRUCTURAL BIOLOGY
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases
JOURNAL OF NUCLEAR CARDIOLOGY
Clinical significance of K-ras mutations in intraoperative tumor drainage blood from patients with colorectal carcinoma
ANNALS OF SURGICAL ONCOLOGY
alpha-adducin gene and essential hypertension in China
CLINICAL AND EXPERIMENTAL HYPERTENSION
High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection
NATURE GENETICS
Identification of 12 novel mutations in the SLC3A1 gene in Swedish cystinuria patients
HUMAN MUTATION
Improved detection of CFTR mutations in southern California Hispanic CF patients
HUMAN MUTATION
RNase cleavage-based methods for mutation/SNP detection, past and present
HUMAN MUTATION
High incidence of N and K-Ras activating mutations in multiple myeloma andprimary plasma cell leukemia at diagnosis
HUMAN MUTATION
Automation in genotyping of single nucleotide polymorphisms
HUMAN MUTATION
Chromosome 21 abnormalities with AMLI amplification in acute lymphoblasticleukemia
GENES CHROMOSOMES & CANCER
Lack of association between N-ras gene mutations and clinical prognosis inBrazilian children with acute lymphoblastic leukemia
LEUKEMIA & LYMPHOMA
Plant plasma membrane H+-ATPases: Powerhouses for nutrient uptake
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY
Sarcolemmopathy: Muscular dystrophies with cell membrane defects
BRAIN PATHOLOGY
APEX disease gene resequencing: Mutations in exon 7 of the p53 tumor suppressor gene
BIOORGANIC & MEDICINAL CHEMISTRY
The V410M mutation associated with pyrethroid resistance in Heliothis virescens reduces the pyrethroid sensitivity of house fly sodium channels expressed in Xenopus oocytes
INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY
WBSCR14, a gene mapping to the Williams-Beuren syndrome deleted region, isa new member of the Mlx transcription factor network
HUMAN MOLECULAR GENETICS
Cryptic splicing involving the splice site mutation in the canine model ofDuchenne muscular dystrophy
NEUROMUSCULAR DISORDERS
Immunohistochemical detection of 8-hydroxy-2 '-deoxyguanosine in gallbladder epithelium of patients with pancreaticobiliary maljunction
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
Does detection of K-ras mutations in pancreatic juice influence clinical decision making?
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
Identification of a genetic determinant responsible for host specificity in Streptococcus thermophilus bacteriophages
MOLECULAR MICROBIOLOGY
Loss of CD95 expression is linked to most but not all p53 mutants in European hepatocellular carcinoma
JOURNAL OF MOLECULAR MEDICINE-JMM
Detection of thyroid-stimulating hormone receptor and G(s)alpha mutations:in 75 toxic thyroid nodules by denaturing gradient gel electrophoresis
JOURNAL OF MOLECULAR MEDICINE-JMM
Primary resistance to clarithromycin in clinical strains of Helicobacter pylori isolated from children in Poland
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS
Large-scale analysis of mutations in RET exon 16 in sporadic medullary thyroid carcinomas in Japan
JAPANESE JOURNAL OF CANCER RESEARCH
Successful induction of immune responses against mutant ras in melanoma patients using intradermal injection of peptides and GM-CSF as adjuvant
EXPERIMENTAL DERMATOLOGY
Comparative analysis of ras proto-oncogene mutations in selected mammaliantumors
MOLECULAR CARCINOGENESIS
Somatic INK4a-ARF locus mutations: A significant mechanism of gene inactivation in squamous cell carcinomas of the head and neck
MOLECULAR CARCINOGENESIS
XPA protein alters the specificity of ultraviolet light-induced mutagenesis in vitro
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
Age-related mitochondrial genotypic and phenotypic alterations in human skeletal muscle
FREE RADICAL BIOLOGY AND MEDICINE
Prevalence and rapid identification of clarithromycin-resistant Helicobacter pylori isolates in children
PEDIATRIC INFECTIOUS DISEASE JOURNAL
A modified mutagenic PCR-RFLP method for K-ras codon 12 and 13 mutations detection in NSCLC patients
MOLECULAR AND CELLULAR PROBES
A methodological strategy for PAH genotyping in populations with a marked molecular heterogeneity of hyperphenylalaninemia
MOLECULAR AND CELLULAR PROBES
Low mutational burden of individual acquired mitochondrial DNA mutations in brain
GENOMICS
Mutations of the transcription factor AML1/CBFA2 are uncommon in blastic transformation of chronic myeloid leukaemia
LEUKEMIA
Three-dimensional model of the SHBG-like region of anticoagulant protein S: New structure-function insights
PROTEINS-STRUCTURE FUNCTION AND GENETICS
Usefulness of supernatant of pancreatic juice for genetic analysis of K-ras in diagnosis of pancreatic carcinoma
PANCREAS
Differential distribution of simple sequence repeats in eukaryotic genome sequences
MOLECULAR BIOLOGY AND EVOLUTION
Evolutionary history of microsatellites in the obscure group of Drosophila
MOLECULAR BIOLOGY AND EVOLUTION
A maximum-likelihood approach to fitting equilibrium models of microsatellite evolution
MOLECULAR BIOLOGY AND EVOLUTION
High-throughput methods for detection of genetic variation
BIOTECHNIQUES
Three-dimensional structural analysis of fibronectin heparin-binding domain mutations
JOURNAL OF CELLULAR BIOCHEMISTRY
The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY
Oxidative damage to mitochondria and aging
EXPERIMENTAL GERONTOLOGY
Rapid mutational analysis of N-ras proto-oncogene in hematologic malignancies: a study of 77 Greek patients
HAEMATOLOGICA
Genotype and phenotype correlation in glucose-6-phosphate dehydrogenase deficiency
HAEMATOLOGICA
Compensating for central nervous system dysmyelination: Females with a proteolipid protein gene duplication and sustained clinical improvement
ANNALS OF NEUROLOGY
Long mutant dystrophins and variable phenotypes: evasion of nonsense-mediated decay?
HUMAN GENETICS
Abnormal propeptide processing resulting in the presence of two abnormal species of protein C in plasma - Characterization of the dysfunctional protein C Padua(3) (Protein CR-1L/propeptide)
THROMBOSIS AND HAEMOSTASIS
Roles of platelets and factor XI in the initiation of blood coagulation bythrombin
THROMBOSIS AND HAEMOSTASIS
High prevalence of K-ras-2 mutations in hepatocellular carcinomas in workers exposed to vinyl chloride
INTERNATIONAL ARCHIVES OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH
Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES
A unique basal pattern of p53 expression in ulcerative colitis is associated with mutation in the p53 gene
HISTOPATHOLOGY
Quantitative detection of single nucleotide polymorphisms for a pooled sample by a bioluminometric assay coupled with modified primer extension reactions (BAMPER)
NUCLEIC ACIDS RESEARCH
Combined SSCP/duplex analysis by capillary electrophoresis for more efficient mutation detection
NUCLEIC ACIDS RESEARCH
Analysis of a donor gene region for a variant surface glycoprotein and itsexpression site in African trypanosomes
NUCLEIC ACIDS RESEARCH
Genomic heterogeneity in Pea seed-borne mosaic virus isolates from Pakistan, the centre of diversity of the host species, Pisum sativum
ARCHIVES OF VIROLOGY
A novel Cys212Tyr founder mutation in parkin and allelic heterogeneity of juvenile Parkinsonism in a population from North West Colombia
NEUROSCIENCE LETTERS
Fabry disease (alpha-galactosidase A deficiency): Renal involvement and enzyme replacement therapy
RARE KIDNEY DISEASES
A new phenotype of Fabry disease with intermediate severity between the classical form and the cardiac variant
RARE KIDNEY DISEASES
Molecular biological diagnostics of metabolic myopathies
AKTUELLE NEUROLOGIE
Homology modeling of wild type and pyrimethamine/cycloguanil-cross resistant mutant type Plasmodium falciparum dihydrofolate reductase. A model for antimalarial chemotherapy resistance
BIOPHYSICAL CHEMISTRY
Treatment of acute myeloblastic leukaemia in a patient with Bombay blood type: a case report
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH
Androgen receptor gene mutation associated with complete androgen insensitivity syndrome and Sertoli cell adenoma
INTERNATIONAL JOURNAL OF GYNECOLOGICAL PATHOLOGY
Structural and evolutionary relationships among protein tyrosine phosphatase domains
MOLECULAR AND CELLULAR BIOLOGY
Selective inactivation of p53 facilitates mouse epithelial tumor progression without chromosomal instability
MOLECULAR AND CELLULAR BIOLOGY
Identification of domains and amino acids involved in GluR7 ion channel function
JOURNAL OF NEUROSCIENCE
Spontaneous mutation spectra in supF: comparative analysis of mammalian cell line base substitution spectra
MUTAGENESIS
Site-directed mutations in the mitochondrially encoded subunits I and III of yeast cytochrome oxidase
BIOCHEMICAL JOURNAL
Identification of post-translationally modified proteins in proteome studies
ELECTROPHORESIS
Multitemperature single-strand conformation polymorphism
ELECTROPHORESIS
From proteomics to genomics
ELECTROPHORESIS
Surgical treatment for non-dilated biliary tract with pancreaticobiliary maljunction should include excision of the extrahepatic bile duct
HEPATO-GASTROENTEROLOGY
Surgical treatment for congenital biliary dilatation, with or without intrahepatic bile duct dilatation
HEPATO-GASTROENTEROLOGY