Literature DB >> 15042841

[Genomic and molecular medicine].

V S Baranov1.   

Abstract

Molecular medicine is a new research field underlain by achievements of the Human Genome Project. The review considers the contribution of the Laboratory of Prenatal Diagnostics of the Ott Institute of Obstetrics and Gynecology to the development of molecular medicine in Russia. Special emphasis is placed on molecular diagnostics, predictive medicine, and gene therapy. The lab obtained priority results in devising and promoting methods of molecular diagnostics of the most common severe hereditary disorders such as cystic fibrosis, Duchenne muscular dystrophy, hemophilia A, and fragile X syndrome. Owing to the Russian program Human Genome, St. Petersburg researchers laid the foundations for theoretical and applied predictive medicine, which is aimed at identifying and analyzing the genes associated with predisposition to high-incidence multifactorial disorders. Experiments with mdx mice providing a model of Duchenne muscular dystrophy were carried out to select the optimal way of delivering a transgene (cDNA of the dystrophin gene) contained in various constructs for the purpose of gene therapy.

Entities:  

Mesh:

Year:  2004        PMID: 15042841     DOI: 10.1023/b:mbil.0000015146.27286.ec

Source DB:  PubMed          Journal:  Mol Biol (Mosk)        ISSN: 0026-8984


  23 in total

1.  [Analysis of allele frequency of seven microsatellite loci of Y chromosome in three Tuva populations].

Authors:  V A Stepanov; V P Puzyrev
Journal:  Genetika       Date:  2000-02

2.  [Microsatellite haplotypes of the Y-chromosome demonstrate the absence of subdivisions and presence of several components in the Tuvinian male gene pool].

Authors:  V A Stepanov; V P Puzyrev
Journal:  Genetika       Date:  2000-03

Review 3.  [Genomic investigations in genetic cardiology: status and prospects].

Authors:  V P Puzyrev
Journal:  Vestn Ross Akad Med Nauk       Date:  2000

Review 4.  [Genetics of arterial hypertension (current research paradigms)].

Authors:  V P Puzyrev
Journal:  Klin Med (Mosk)       Date:  2003

5.  Regional assignment of the human cell cycle control gene CDC2 to chromosome 10q21 by in situ hybridization.

Authors:  S A Nazarenko; N V Ostroverhova; N K Spurr
Journal:  Hum Genet       Date:  1991-09       Impact factor: 4.132

Review 6.  Genomics: structural and functional studies of genomes.

Authors:  V A McKusick
Journal:  Genomics       Date:  1997-10-15       Impact factor: 5.736

7.  Genetic markers in coronary artery disease in a Russian population.

Authors:  V A Stepanov; V P Puzyrev; R S Karpov; A I Kutmin
Journal:  Hum Biol       Date:  1998-02       Impact factor: 0.553

Review 8.  Recent advances in the genetics of allergy and asthma.

Authors:  G G Anderson; W O Cookson
Journal:  Mol Med Today       Date:  1999-06

9.  Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.

Authors:  Pascale Richard; Philippe Charron; Lucie Carrier; Céline Ledeuil; Theary Cheav; Claire Pichereau; Abdelaziz Benaiche; Richard Isnard; Olivier Dubourg; Marc Burban; Jean-Pierre Gueffet; Alain Millaire; Michel Desnos; Ketty Schwartz; Bernard Hainque; Michel Komajda
Journal:  Circulation       Date:  2003-04-21       Impact factor: 29.690

10.  Structure of the regulatory domain of scallop myosin at 2 A resolution: implications for regulation.

Authors:  A Houdusse; C Cohen
Journal:  Structure       Date:  1996-01-15       Impact factor: 5.006

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