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Results: 1-23 |
Results: 23
2 NOVEL SLAVIC POINT MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN PATIENTS WITH FAMILIAR HYPERCHOLESTEROLEMIA FROM ST. PETERSBURG, RUSSIA
Authors: KH C SKOBELEVA NA SHEVTSOV SP KONSTANTINOV VO DENISENKO AD SCHWARTZ EI
Citation: C. Kh et al., 2 NOVEL SLAVIC POINT MUTATIONS IN THE LOW-DENSITY-LIPOPROTEIN RECEPTOR GENE IN PATIENTS WITH FAMILIAR HYPERCHOLESTEROLEMIA FROM ST. PETERSBURG, RUSSIA, MOLECULAR GENETICS AND METABOLISM, 63(1), 1998, pp. 31-34
PREVALENCE OF THE METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) C677T MUTATION IN PATIENTS WITH VARICOSE-VEINS OF LOWER-LIMBS
Authors: SVERDLOVA AM BUBNOVA NA BARANOVSKAYA SS VASINA VI AVITISJAN AO SCHWARTZ EI
Citation: Am. Sverdlova et al., PREVALENCE OF THE METHYLENETETRAHYDROFOLATE REDUCTASE (MTHFR) C677T MUTATION IN PATIENTS WITH VARICOSE-VEINS OF LOWER-LIMBS, MOLECULAR GENETICS AND METABOLISM, 63(1), 1998, pp. 35-36
COMPARATIVE-ANALYSIS OF APO(A) GENE ALLELES - DISTRIBUTION OF PENTANUCLEOTIDE REPEATS IN POSITION-1373 AND C T TRANSITION IN POSITION+93 AMONG PATIENTS WITH MYOCARDIAL-INFARCTION AND A CONTROL-GROUP IN ST-PETERSBURG, RUSSIA/
Authors: VOLKOVA MV VASINA VI FOMICHEVA EV SCHWARTZ EI
Citation: Mv. Volkova et al., COMPARATIVE-ANALYSIS OF APO(A) GENE ALLELES - DISTRIBUTION OF PENTANUCLEOTIDE REPEATS IN POSITION-1373 AND C T TRANSITION IN POSITION+93 AMONG PATIENTS WITH MYOCARDIAL-INFARCTION AND A CONTROL-GROUP IN ST-PETERSBURG, RUSSIA/, Biochemical and molecular medicine, 61(2), 1997, pp. 208-213
INDUCER-DEPENDENT AND TIME-DEPENDENT ACTIVATION OF CYP2B1 2 GENE-TRANSCRIPTION IN LIVER OF WISTAR RATS/
Authors: SCHWARTZ EI DUZHAK TG GULYAEVA LF LYAKHOVICH VV
Citation: Ei. Schwartz et al., INDUCER-DEPENDENT AND TIME-DEPENDENT ACTIVATION OF CYP2B1 2 GENE-TRANSCRIPTION IN LIVER OF WISTAR RATS/, The FASEB journal, 11(9), 1997, pp. 262-262
AGE-DEPENDENT INFLUENCE OF SOME GENES POLYMORPHISMS ON PREDISPOSITIONTO MYOCARDIAL-INFARCTION IN ST. PETERSBURG, RUSSIA
Authors: SCHWARTZ EI VOLKOVA MV SVERDLOVA AM BARANOVSKAYA SS VASINA VI FOMICHEVA EV
Citation: Ei. Schwartz et al., AGE-DEPENDENT INFLUENCE OF SOME GENES POLYMORPHISMS ON PREDISPOSITIONTO MYOCARDIAL-INFARCTION IN ST. PETERSBURG, RUSSIA, Atherosclerosis, 134(1-2), 1997, pp. 82-82
THE EFFECT OF HLA-B ALLELE ON THE IDDM RISK DEFINED BY DRB1-ASTERISK-04 SUBTYPES AND DQB1-ASTERISK-0302
Authors: NEJENTSEV S REIJONEN H ADOJAAN B KOVALCHUK L SOCHNEVS A SCHWARTZ EI AKERBLOM HK ILONEN J
Citation: S. Nejentsev et al., THE EFFECT OF HLA-B ALLELE ON THE IDDM RISK DEFINED BY DRB1-ASTERISK-04 SUBTYPES AND DQB1-ASTERISK-0302, Diabetes, 46(11), 1997, pp. 1888-1892
HLA-DQB1-ASTERISK-0304-DRB1-ASTERISK-0408 HAPLOTYPE ASSOCIATED WITH INSULIN-DEPENDENT DIABETES-MELLITUS IN POPULATIONS IN THE EASTERN BALTIC REGION
Authors: ILONEN J KOSKINEN S NEJENTSEV S SJOROOS M KNIP M SCHWARTZ EI ADOJAAN B KOVALCHUK L SOCHNEVS A
Citation: J. Ilonen et al., HLA-DQB1-ASTERISK-0304-DRB1-ASTERISK-0408 HAPLOTYPE ASSOCIATED WITH INSULIN-DEPENDENT DIABETES-MELLITUS IN POPULATIONS IN THE EASTERN BALTIC REGION, Tissue antigens, 49(5), 1997, pp. 532-534
IDENTIFICATION OF THE C-]T POLYMORPHISM IN THE -POSITION OF THE APO(A) GENE BY MISMATCH PCR-MEDIATED SITE-DIRECTED MUTAGENESIS AND RESTRICTION ENZYME DIGESTION(93)
Authors: VOLKOVA MV VASINA VI OBRAZTSOVA GI SCHWARTZ EI
Citation: Mv. Volkova et al., IDENTIFICATION OF THE C-]T POLYMORPHISM IN THE -POSITION OF THE APO(A) GENE BY MISMATCH PCR-MEDIATED SITE-DIRECTED MUTAGENESIS AND RESTRICTION ENZYME DIGESTION(93), Biochemical and molecular medicine, 59(1), 1996, pp. 91-92
CYP2D6 GENOTYPING IN A RUSSIAN POPULATION USING A NOVEL-APPROACH FOR IDENTIFICATION OF THE CYP2D6A MUTATION
Authors: AKHMEDOVA SN PUSHNOVA EA ANISIMOV S BOGDANOVA LA BOVA LK SCHWARTZ EI
Citation: Sn. Akhmedova et al., CYP2D6 GENOTYPING IN A RUSSIAN POPULATION USING A NOVEL-APPROACH FOR IDENTIFICATION OF THE CYP2D6A MUTATION, Biochemical and molecular medicine, 58(2), 1996, pp. 234-236
FREQUENCY OF A SPECIFIC CYTOCHROME P4502D6B (CYP2D6B) MUTANT ALLELE IN CLINICALLY DIFFERENTIATED GROUPS OF PATIENTS WITH PARKINSON DISEASE
Authors: AKHMEDOVA SN PUSHNOVA EA YAKIMOVSKY AF AVTONOMOV VV SCHWARTZ EI
Citation: Sn. Akhmedova et al., FREQUENCY OF A SPECIFIC CYTOCHROME P4502D6B (CYP2D6B) MUTANT ALLELE IN CLINICALLY DIFFERENTIATED GROUPS OF PATIENTS WITH PARKINSON DISEASE, Biochemical and molecular medicine, 54(2), 1995, pp. 88-90
COMPLETE SPECTRUM OF PAH MUTATIONS IN TATARIA - PRESENCE OF SLAVIC, TURKIC AND SCANDINAVIAN MUTATIONS
Authors: KUZMIN AI EISENSMITH RC GOLTSOV AA SERGEEVA NA SCHWARTZ EI WOO SLC
Citation: Ai. Kuzmin et al., COMPLETE SPECTRUM OF PAH MUTATIONS IN TATARIA - PRESENCE OF SLAVIC, TURKIC AND SCANDINAVIAN MUTATIONS, European journal of human genetics, 3(4), 1995, pp. 246-255
SPECTRUM OF PHENYLKETONURIA MUTATIONS OF PHENYLALANIN HYDROXYLASE GENE IN ST-PETERSBURG POPULATION
Authors: BARANOVSKAYA SS SHEVTSOV SP MAKSIMOVA SP KUZMIN AI SCHWARTZ EI
Citation: Ss. Baranovskaya et al., SPECTRUM OF PHENYLKETONURIA MUTATIONS OF PHENYLALANIN HYDROXYLASE GENE IN ST-PETERSBURG POPULATION, Doklady Akademii nauk. Rossijskaa akademia nauk, 340(5), 1995, pp. 709-711
THE FREQUENCY OF MCAD MUTATION (K329E) IN THE FINNISH POPULATION
Authors: SCHWARTZ EI ILONEN J SKOBELEVA NA AKERBLOM HK
Citation: Ei. Schwartz et al., THE FREQUENCY OF MCAD MUTATION (K329E) IN THE FINNISH POPULATION, European journal of pediatrics, 154(6), 1995, pp. 501-501
THE MISDIRECTION INTERACTIVE
Authors: SCHWARTZ EI
Citation: Ei. Schwartz, THE MISDIRECTION INTERACTIVE, Technology review, 98(8), 1995, pp. 26-27
SHORT-TERM CHANGES IN CALCIUM BUT NOT PROTEIN-INTAKE ALTER THE RATE OF BONE-RESORPTION IN HEALTHY-SUBJECTS AS ASSESSED BY URINARY PYRIDINIUM CROSS-LINK EXCRETION
Authors: SHAPSES SA ROBINS SP SCHWARTZ EI CHOWDHURY H
Citation: Sa. Shapses et al., SHORT-TERM CHANGES IN CALCIUM BUT NOT PROTEIN-INTAKE ALTER THE RATE OF BONE-RESORPTION IN HEALTHY-SUBJECTS AS ASSESSED BY URINARY PYRIDINIUM CROSS-LINK EXCRETION, The Journal of nutrition, 125(11), 1995, pp. 2814-2821
RECURRENCE OF THE R408W MUTATION IN THE PHENYLALANINE-HYDROXYLASE LOCUS IN EUROPEANS
Authors: EISENSMITH RC GOLTSOV AA ONEILL C TYFIELD LA SCHWARTZ EI KUZMIN AI BARANOVSKAYA SS TSUKERMAN GL TREACY E SCRIVER CR GUTTLER F GULDBERG P EIKEN HG APOLD J SVENSSON E NAUGHTEN E CAHALANE SF CROKE DT COCKBURN F WOO SLC
Citation: Rc. Eisensmith et al., RECURRENCE OF THE R408W MUTATION IN THE PHENYLALANINE-HYDROXYLASE LOCUS IN EUROPEANS, American journal of human genetics, 56(1), 1995, pp. 278-286
A RAPID AND SIMPLE DNA-FINGERPRINTING METHOD USING RLFP AND SSCP ANALYSIS OF THE HYPERVARIABLE NONCODING REGION OF HUMAN MITOCHONDRIAL-DNA
Authors: PUSHNOVA EA AKHMEDOVA SN SHEVTSOV SP SCHWARTZ EI
Citation: Ea. Pushnova et al., A RAPID AND SIMPLE DNA-FINGERPRINTING METHOD USING RLFP AND SSCP ANALYSIS OF THE HYPERVARIABLE NONCODING REGION OF HUMAN MITOCHONDRIAL-DNA, Human mutation, 3(3), 1994, pp. 292-296
NONISOTOPIC IDENTIFICATION OF 2 POINT MUTATIONS IN THE CYP21 GENE RESPONSIBLE FOR NONCLASSIC 21-HYDROXYLASE DEFICIENCY
Authors: SHEVTSOV SP RECHITSKY S VERLINSKY O SCHWARTZ EI
Citation: Sp. Shevtsov et al., NONISOTOPIC IDENTIFICATION OF 2 POINT MUTATIONS IN THE CYP21 GENE RESPONSIBLE FOR NONCLASSIC 21-HYDROXYLASE DEFICIENCY, Biochemical medicine and metabolic biology, 52(2), 1994, pp. 85-88
IDENTIFICATION OF THE LINKAGE OF MUTATIONS CAUSING CYSTIC-FIBROSIS TODIFFERENT ALLELES OF A TETRANUCLEOTIDE REPEAT IN INTRON 6A OF THE CFTR GENE
Authors: POTAPOVA OY VORONINA OV GAITSKHOKI VS BOGACHEVA EV UEMBITSKAYA TE KUPRINA EA KAPRANOV NI BERLIN YA SCHWARTZ EI
Citation: Oy. Potapova et al., IDENTIFICATION OF THE LINKAGE OF MUTATIONS CAUSING CYSTIC-FIBROSIS TODIFFERENT ALLELES OF A TETRANUCLEOTIDE REPEAT IN INTRON 6A OF THE CFTR GENE, Biochemical medicine and metabolic biology, 51(2), 1994, pp. 185-187
THE SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN AZERBAIJAN
Authors: TAGIEV AF SURIN VL GOLTSOV AA LUKIANENKO AV SOLOVYEV GY GULIEVA EA PLUTALOV OV KABOEV OK MAMEDOVA TA DADASHEVA TS RUSTAMOV RS SCHWARTZ EI BERLIN YA
Citation: Af. Tagiev et al., THE SPECTRUM OF BETA-THALASSEMIA MUTATIONS IN AZERBAIJAN, Human mutation, 2(2), 1993, pp. 152-154
LINKAGE DISEQUILIBRIUM BETWEEN CYSTIC-FIBROSIS MUTATIONS AND POLYMORPHIC 4-BP REPEAT WITHIN CFTR GENE
Authors: GAITSKHOKI VS VORONINA OV POTAPOVA OY KIRJUKHINA LV GEMBITSKAYA TE KAPRANOV NI PETROVA NV KHAFIZOVA ZA SCHWARTZ EI
Citation: Vs. Gaitskhoki et al., LINKAGE DISEQUILIBRIUM BETWEEN CYSTIC-FIBROSIS MUTATIONS AND POLYMORPHIC 4-BP REPEAT WITHIN CFTR GENE, Biochemical medicine and metabolic biology, 50(2), 1993, pp. 186-189
DISTRIBUTION OF THE PHENYLALANINE-HYDROXYLASE MUTATION R408W IN THE COMMONWEALTH-OF-INDEPENDENT-STATES (CIS)
Authors: GOLTSOV AA EISENSMITH RC SCHWARTZ EI WOO SLC
Citation: Aa. Goltsov et al., DISTRIBUTION OF THE PHENYLALANINE-HYDROXYLASE MUTATION R408W IN THE COMMONWEALTH-OF-INDEPENDENT-STATES (CIS), American journal of human genetics, 53(3), 1993, pp. 809-809
DISTRIBUTION OF SOME POINT MUTATIONS IN THE PHENYLALANINE-HYDROXYLASEGENE OF PHENYLKETONURIA PATIENTS FROM THE MOSCOW REGION
Authors: CHARIKOVA EV KHALCHITSKII SE ANTOSHECHKIN AG SCHWARTZ EI
Citation: Ev. Charikova et al., DISTRIBUTION OF SOME POINT MUTATIONS IN THE PHENYLALANINE-HYDROXYLASEGENE OF PHENYLKETONURIA PATIENTS FROM THE MOSCOW REGION, Human heredity, 43(4), 1993, pp. 244-249
Risultati: 1-23 |