Critical steps in the early evolution of the isocortex. Reduced expression of a distal gene of the prn gene cluster in deletion mutants of Aspergillus nidulans: Glycolytic gene expression in Saccharomyces cerevisiae: The mitochondrial alcohol dehydrogenase Adh3p is involved in a redox shuttle in Saccharomyces cerevisiae II J. Mutations in the pho80 gene confer permeability to 5-mononucleotides in Saccharomyces cerevisiae II Genetics. Further studies on mechanism of actionof an acid phosphatase from baker's yeast.ВИДЕО ПО ТЕМЕ: Здоровье. Генетический анализ. Алика Смехова. (06.05.2018)
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The role of pathogenic DJ-1 mutations in Parkinson's disease. Selective neurodegeneration in Huntington's disease. Ann Neurol , 38, Receissive amyotrophic lateral sclerosis with the D90A SOD1 mutation shares a common founder,evidence for a linked protective factor.
Hum Mol Genet , 13, Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis. Hum Mol Genet , 8, Neurofilaments and neurological disease. BioEssays , 24, Inducible nitric oxide synthase up- regulation in transgenic mouse model of familial amyotrophic lateral sclerosis.
J Neurochem , 72, Cigarette smoking, N-acetyltransferase 2 genetic polymorphisms, and breast cancer risk. Amiel J, Trochet JJ. Polyalanine expansions in human. A clinical and genealogical study of 36 patients. A clinical, genetic and enzymatic study. Doctoral thesis Umea University, Umea, Sweden Partial deficiency of manganese superoxide dismutase excacerbates a transgenic mouse model in a myotrophic lateral sclerosis.
The relationship between trinucleotide CAG repeat length and clinical features of Huntington's disease. Nat Genet , 4, CAG expansion affects the expression of mutant Huntingtin in the Huntington's disease brain. Neuron, , 15, Ethnic distribution of myotonic dystrophy gene. Lancet, , , Science, , , ATP7B gene mutation database, http: Ann Neurol , 46, Expression of the early-onset torsion dystonia gene DYT1 in human brain.
Ann Neurol ,43, Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 NAT2 and familial Parkinson's disease. Glutatione S-transferase Ml gene polimorphism and susceptibility to endometriosis in a French population.
Intergenerational stability of the myotonic dystrophy protomutation. Increased 3-nitrotyrosine nitration in both sporadic and familial amyotrophic lateral sclerosis. Ann Neurol ,42, Nature , , J Neurochem , 79, Saccharomyces cerevisiae Srs2 DNA helicase selectively blocks expansions of trinucleotide repeats.
Neurosci Lett , , Elevated hydroxyl radical generation in vivo in animal model of amyotrophic lateral sclerosis. J Neurichem , 71, Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Early-onset parkinsonism associated with PINK1 mutations: Neurology, , 65, Evidence for linkage between Wilson disease and esterase D in three kindreds: Genet Epidemiol , 3, A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonicdystrophy unstable CTG n repeat.
Hum Mol Genet, , 4, A contiguous linkage map of chromosome 13q with 39 distinct loci separated on average by 5. Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis.
J Neurochem , 64, Superoxide dismutase activity, oxidative damage, and mitochondrial energy metabolism in familial and sporadic amyotrophic lateral sclerosis. Frequency of the DYT1 mutation in primary torsion dystonia without family history. Idiopathic dystonia among Ashkenazi Jews, evidence for autosomal-dominant inheritance.
Ann Neurol , 26, The D YT1 phenotype and guidelines for diagnostic testing. Hereditary late-onset chorea without significant dementia, genetic evidence for substantial phenotypic variation in Huntington's disease.
Neurology , 45, Alanine tracts, the expanding story of human illness and trinucleotide repeats. Metabolic dysfunction in familial, but not sporadic, amyotrophic lateral sclerosis. J Neurochem , 1, Nat Gene, , V. Analysi of the clinical course of non-Jewish, autosomal dominant torsion dystonia.
Mov Disord , 1, Cell , 82, Neurofilament homeostasis and motoneurone degeneration. Parkinson's disease, schizophrenia, and personality traits. Arylamine N-acetyltransferase NAT2 mutations and their allelic linkage in unrelated Caucasian individuals: Am J Hum Genet.
Linkage of the gene for an autosomal dominant form of juvenile amuotrophic lateral sclerosis to chromosome 9q Am J Hum Genet , 3, Deux cas atrophie musculaire progressive avec lesions de la substance grise et des faisceaux antero-lateraux de la moele epinere.
Arch Physiol Norm Path. Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing. Am J Hum Genet ,74, Evidence for amechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type 1.
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutations. The contribution of cis-elements to disease-associated repeat instability, clinical and experimental evidence. Neuron , 24, Evolution of the Friedreich's ataxia trinucleotide repeat expansion, founder effect and premutations.
USA, , 94, Cox DW Molecular advances in Wilson disease. Prog Liver Dis, , 14, Superoxide dismutase catalyzes nitration of tyrosines by peroxynitrite in the rod and head domains of neurofilament-L. Ann Neurol , 6, A study of Wilson disease mutations in Britain.
Hum Mutat, , 14, Genotyping for polymorphisms in xenobiotic metabolism as a predictor of disease susceptibility. A point mutation in the FMR-1 gene associated with fragile X mental retardation. Nature Genet, , 3, Distribution of evolution of CTG repeats in the myotonin protein kinase gene in human populations.
Ann Neurol , 57, Amyotrophic lateral sclerosis and structural defects of CuZn-superoxide dismutase. Science , , Hairpin structure-forming propensity of the CCTG: CAGG tetranucleotide repeats contributes to the genetic instability associated with myotonicdystrophy type 2.
Lancet , , Excitotoxic injury of the neostriatum, a model for Huntington's disease. Trends Neurosci , 13, Mutational processes of simple-sequence repeat loci in human populations.
Population-based studies on incidence, survival rates, and genetic alterations in astrocytic and oligodendroglial gliomas. Glioblastoma multiforme oncogenomics and signaling pathways. Molecular pathogenesis of malignant glial tumors. Detailed characterization of alterations of chromosomes 7, 9, and 10 in glioblastomas as assessed by single-nucleotide polymorphism arrays.
The lac operon of Lactobacillus casei contains lacT, a gene coding for a protein of the BglG family of transcriptional antiterminators. Characterization of the sacQ genes from Bacillus licheniformis and Bacillus subtilis. Protein phosphorylation regulates transcription of the 3-glucoside utilization operon in E. In vitro reconstitution of transcriptional antitermination by the SacT and SacY proteins of Bacillus subtilis. Nucleotide sequences and operon structure of plasmid-borne genes mediating uptake and utilization of raffmose in Escherichia coli.
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Isolation and culture of rice protoplasts. The mechanism of chloroplast triazine resistance: Herbicide resistance in plants. Selection of dihaploid potato callus for resistance to the culture filtra te of Fusarium oxysporum. Fusion de protoplas-tes Nicotiana tabacum a cytoplasmes differents: Para-Fluorophenylalanine resistant cell lines of tobacco. Selektion in Kalluskulturen mit haploiden Zellen.
AND Capra hircus L. It was shown the high similarity of gene orders of homeological chromosomes in compared species, with the exception of 9th and 14th chromosome pairs. Today, phylogenetic research is supported by achievements of modern biology, such as the knowledge of structure and functioning of chromosome apparatus. Cytogenetic techniques are an important tool in systematics and phylogeny of mammals