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Molecular Genetic

The Molecular Genetic Study of Genetic Markers of Predisposition to Physical Loading

The Molecular Genetic Study of Genetic Markers of Predisposition to Physical Loading

... of molecular genetic approaches that make it possible to determine a person’s predisposition to various activities, including the search for molecular genetic markers that determine a person’s ...

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Molecular genetic imaging: current and future perspectives

Molecular genetic imaging: current and future perspectives

... for molecular imaging. Molecular-genetic imaging provides visualization in space and time of normal as well as abnormal cellular processes at a molecular or genetic ...image ...

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Molecular genetic approaches to plant development

Molecular genetic approaches to plant development

... Int J De" Riolo 36 59 66 (1992) 59 Molecular genetic approaches to plant development WOUT BOERJAN, BART DEN BOER and MARC VAN MONTAGU' Laboratorium voor Genetica, Universiteit Gent Gent Belgium ABSTRA[.] ...

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Important molecular genetic markers of colorectal cancer

Important molecular genetic markers of colorectal cancer

... unique molecular profile, which is characterized by various genetic and epigenetic ...Several molecular genetic markers, which are currently used for CRC diagnosis, prognosis and treatment ...

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Molecular genetic control of leaf lifespan in plants - A review

Molecular genetic control of leaf lifespan in plants - A review

... specific action of age-related genes (Schippers et al., 2007). As expected, the gene expression profiles of ageing leaves are distinctively different from young leaves. Many of the genes expressed in green leaves are ...

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A molecular genetic study of inherited movements disorders

A molecular genetic study of inherited movements disorders

... individuals of whom 14 had been diagnosed as having dystonia. Initial studies typed the family for genetic systems, including red cell enzymes, serum proteins, and human leucocyte antigens (HLA) (Falk et al, ...

218

Molecular genetic analysis of primary ciliary dyskinesia

Molecular genetic analysis of primary ciliary dyskinesia

... disease locus when the affected individuals have all descended from a common ancestor in whom the mutation occurred. The concept of linkage disequilibrium can be explained by observing the effect of meiosis on a single ...

302

Recent Molecular Genetic Explorations of Caenorhabditis elegans MicroRNAs

Recent Molecular Genetic Explorations of Caenorhabditis elegans MicroRNAs

... One explanation for the apparent lack of visible phenotypes for microRNA gene deletion mutants, besides the functional redundancy among microRNAs of the same family discussed above, emerged from studies designed to ...

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Mitochondrial ATPase : biochemical and molecular genetic analysis

Mitochondrial ATPase : biochemical and molecular genetic analysis

... use molecular oxygen as the electron acceptor for the reoxidation of NADH and FADHj enormously increase their ability to generate ATP, compared with anaerobic cells, which transfer these electrons to an organic ...

199

Hemangioblastomas. Studies on the molecular genetic background.

Hemangioblastomas. Studies on the molecular genetic background.

... They occur as sporadic tumors and as a manifestation of von Hippel-Lindau (VHL) disease, a hereditary tumor syndrome that results from a germline mutation in the VHL tumor suppressor ge[r] ...

169

A molecular genetic analysis of human chromosome 13

A molecular genetic analysis of human chromosome 13

... number of murine chromosomes into intact mouse, hamster and human cell recipients. The first step in microcell fusion is mitotic arrest of the cell. Colchicine prevents microtubule assembly and induces prolonged mitotic ...

361

Clinical and molecular genetic study of movement disorders

Clinical and molecular genetic study of movement disorders

... microsatellite markers for mapping. Genotyping large numbers of microsatellite markers for linkage analysis is both costly and time-consuming. Unlike microsatellites which require gel-based methods to distinguish between ...

255

Molecular genetic basis of sudden cardiac death

Molecular genetic basis of sudden cardiac death

... Additionally, molecular interactions with such molecules as calcineurin, sex hormones, growth factors, among others, are probably involved in development of clinical signs, symptoms and age of ...

13

Molecular genetic study of hereditary retinoblastoma

Molecular genetic study of hereditary retinoblastoma

... One of the aims of localising and cloning any disease related gene is to establish diagnostic (predictive) DNA tests. These tests could be direct identifying the actual causative defects, or indirect as in the case of ...

397

Spinocerebellar ataxia: A clinical and molecular genetic study

Spinocerebellar ataxia: A clinical and molecular genetic study

... The high degree o f meiotic instability that was observed, in association with the finding of the SCA7 mutation in a patient with the typical phenotype of ADCA type II but with no family history, raised the possibility ...

188

Software and Methods for Analyzing Molecular Genetic Marker Data

Software and Methods for Analyzing Molecular Genetic Marker Data

... While this iterative search appears to be effective and provides an approximate solution to the core set selection problem, it does not guarantee an optimal solution. In fact, the nature of the algorithm’s swapping is ...

170

Optimal Sequencing Strategies for Surveying Molecular Genetic Diversity

Optimal Sequencing Strategies for Surveying Molecular Genetic Diversity

... The precision of estimation is an increasing function of the number of bases sequenced, for any fixed sequencing strategy and hence also when comparing the optimal strategi[r] ...

16

Molecular genetic studies of deafness

Molecular genetic studies of deafness

... However, molecular analysis of a large consanguineous family from India segregating congenital profound non-syndromic autosomal recessive deafness has now confirmed that mutations in the gene PDS result in a ...

314

Silver-Russell syndrome: genetic basis and molecular genetic testing

Silver-Russell syndrome: genetic basis and molecular genetic testing

... that copy number variation and aberrant methylation at different loci in 11p15 can be detected in one tube. Thus, methylation defects at both ICRs in 11p15 as well as duplications and UPDs of this region will be identi- ...

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A molecular genetic toolbox for Yarrowia lipolytica

A molecular genetic toolbox for Yarrowia lipolytica

... Construction of a multipurpose vector for rapid expression of fluorescently tagged proteins in Yarrowia lipolytica We constructed a multipurpose expression vector pYL15 (GenBank accession: KU378202) containing a codon ...

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