Limborskaia Sa

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Limborska Sa
Publication record
57 papers · 97 citations · H-index 5

PAPERS

Analysis of a GSTM1 gene deletion in the context of the GSTM genomic cluster diversity in three Russian populations
20140 citationsauthor #3
[Association study of polymorphic markers of F12, PON1, PON2, NOS2, PDE4D, HIF1a, GPIba, CYP11B2 genes with ischemic stroke in Russian patients].
201212 citationsauthor #8
[Fourth international school on molecular genetics for young scientists "GENOMICS and cell biology"].
20110 citationsauthor #1
[The effect of semax and its C-end peptide PGP on expression of the neurotrophins and their receptors in the rat brain during incomplete global ischemia].
20118 citationsauthor #5
Analysis of polymorphic variants of PDE4D gene in patients with acute stroke from Moldavian population
20112 citationsauthor #10
[Association of cerebral stroke with a phosphodiesterase 4D (PDE4D) gene polymorphism in the Moscow population].
20113 citationsauthor #2
[Analysis of single nucleotide polymorphism rs415430 in the WNT3 gene in the Russian population with the Parkinson disease].
20112 citationsauthor #7
[Human minisatellite markers: D1S80 locus in population studies].
20084 citationsauthor #2
[Expression peculiarities of EGR1, neurotrophins and their receptor genes in human lung cancer and in normal lung tissue].
20072 citationsauthor #4
[Human molecular genetics: study in the area of medical and ethnic genomics].
20041 citationsauthor #1
[Clinical and genetic analysis of juvenile parkinsonism in Russia].
20047 citationsauthor #6
Analysis of the Glutathione S-Transferase P1 Gene Ile105Val Polymorphism in the Patients with Sporadic Motor Neuron Disease from Russia
20048 citationsauthor #8
[Changes in the frequency of alleles and genotypes of insertional-deletional polymorphism of the angiotensin-converting enzyme gene, dependent on age].
20021 citationsauthor #3
[A simple and rapid method for detection of the 106Gln mutation in Wilson-Konovalov disease].
20021 citationsauthor #5
Polymorphism of the Angiotensin-Converting Enzyme Gene in Patients with Coronary Heart Disease from the Moscow Population
20015 citationsauthor #5
The possible role of genetic factors in the cholesterol high density lipoprotein level in the Moscow population
20000 citationsauthor #5
Analysis of expansion of the triplet repeat (CTG)n in myotonic dystrophy patients from Bashkir
20002 citationsauthor #7
Expansion and mutation rate in CTG repeats in the myotonic dystrophy gene
20001 citationsauthor #6
[Sporadic amyotrophic lateral sclerosis associated with Asp90Ala CuZn-superoxide dismutase mutations in Russia].
20002 citationsauthor #2
[Analysis of polymorphism of CTG repetitive sequences in the gene of myotonic dystrophy in human populations of the Volga-Ural region].
19990 citationsauthor #6
[Human molecular genetics: medico-genetic and population studies].
19994 citationsauthor #1
[Distribution of the 32 bp deletion in the CCR5 chemokine receptor gene in populations of the Volga-Ural region].
19980 citationsauthor #4
[Isolation of a protein, specifically binding with a triplet repeat of the (CTG)n type].
19971 citationsauthor #3
The apolipoprotein AII gene is not a risk factor for development ischemic heart disease in the Moscow population
19974 citationsauthor #4
[Analysis of polymorphism of the 5'-terminal region of apolipoprotein B gene in patients with ischemic heard disease].
19962 citationsauthor #5
Analysis of allelic variants of the hypervariable locus of apolipoprotein B in Bashkir and Komi populations
19951 citationsauthor #6
[Isolation of a new nuclear protein specifically binding with M13-type minisatellite].
19950 citationsauthor #2
[Analysis of DNA polymorphism detected by genomic fingerprinting based on phage M13 DNA, in populations of Bashkir and Komi].
19941 citationsauthor #5
[Analysis of genetic distances between populations using human DNA "fingerprints" detected by a phage M13 DNA probe].
19911 citationsauthor #3
Use of DNA polymorphism detected by M13 phage DNA in population studies
19914 citationsauthor #4
Nonisotope variant of genomic fingerprinting based on the phage M13 DNA in kinship studies in man
19900 citationsauthor #4
Analysis of sequences from human brain cDNA gene bank which are functionally active in nervous tissue and tumor cells
19890 citationsauthor #7
The use of DNA from phage M13 for the analysis of interindividual polymorphism of human DNA as demonstrated by a population study in Krasnodar city
19892 citationsauthor #6
[Heterogeneity of globin protein synthesis in bone marrow cells of patients with homozygous beta-thalassemia from Tadzhikistan].
19880 citationsauthor #5
[Genomic fingerprints of organisms from different taxonomic groups: the use of phage M13 DNA as a hybridization probe].
19884 citationsauthor #5
Importance and outlook of research in the field of human molecular genetics
19870 citationsauthor #1
Globin synthesis in patients with low reticulocyte levels in the peripheral blood
19840 citationsauthor #1
[Molecular genetic studies of beta-thalassemia heterogeneity].
19830 citationsauthor #1
[Moleculo-genetic study of beta-thalassemia heterogenity in the USSR].
19830 citationsauthor #4
[Construction of a clone bank of human fibroblast cDNA: determination of the collagen sequences and copies of the repetitive genome elements].
19839 citationsauthor #4
[Synthesis of full-length complementary DNA on a matrix of partially purified human procollagen mRNA in the presence of a ribonuclease inhibitor].
19820 citationsauthor #4
[Various forms of beta-thalassemia among children of Azerbaĭjan].
19810 citationsauthor #3
Enzymatic DNA synthesis on a procollagen mRNA matrix from human fibroblasts
19811 citationsauthor #4
Collagen and globin genes in healthy subjects and hereditary disease
19810 citationsauthor #1
[Study of the molecular causes of thalassemia. II. Deletion of alpha-globin genes in hemoglobinopathy H].
19800 citationsauthor #5
Disorder of globin chain synthesis in patients without signs of thalassemia
19800 citationsauthor #1
[Heterogeneity in the synthesis of globin protein chains in homozygous (major) beta-thalassemia].
19790 citationsauthor #1
Method of studying globin protein synthesis in thalassemia
19790 citationsauthor #1
Molecular biological studies of hereditary diseases
19790 citationsauthor #2
[Etiology of beta-thalassemia in children (molecular studies)].
19780 citationsauthor #1
[Molecular causes of thalassemia. I. Identification of globin mRNA in homozygous beta-thalassemia using complementary human globin DNA].
19780 citationsauthor #1
Isolation of human globin mRNA and synthesis of complementary DNA.
19770 citationsauthor #1
Use of molecular biology approaches in studying hereditary diseases
19760 citationsauthor #1
Isolation of human globin mRNA and synthesis of its complementary DNA by the reverse transcription route
19761 citationsauthor #1
Study of the structure and activity of the genome using the methods of nucleic acid renaturation and hybridization
19750 citationsauthor #1
The effect of chromatin proteins on transcription of repeating portions of the genome
19740 citationsauthor #1
[Regulation of the biosynthesis of messenger RNA in the animal cell. IV. The role of F-1 histone in inhibiting the transcription of repeating DNA nucleotide sequences].
19731 citationsauthor #1

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1983 9 citations

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2004 16 citations

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2011 15 citations

2012 12 citations

2014 0 citations

Limborskaia Sa

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