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E I Schwartz

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Journal of Human Genetics|April 27, 2001

The C825T polymorphism in the G-protein beta3 subunit gene and diabetic complications in IDDM patientsN S Shcherbak, E I Schwartz

Journal of the Neurological Sciences|March 10, 2001

Paraoxonase 1 Met--Leu 54 polymorphism is associated with Parkinson's diseaseS N Akhmedova, A K Yakimovsky, E I Schwartz

Biochemical Medicine and Metabolic Biology|August 1, 1994

Nonisotopic identification of two point mutations in the CYP21 gene responsible for nonclassic 21-hydroxylase deficiencyS P Shevtsov, S Rechitsky, O Verlinsky, et al.

The Journal of Nutrition|November 1, 1995

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 excretionS A Shapses, S P Robins, E I Schwartz, et al.

Biochemistry. Biokhimiia|October 22, 2002

Inducer effect on the complex formation between rat liver nuclear proteins and cytochrome P450 2B gene regulatory elementsT G Duzhak, E I Schwartz, L F Gulyaeva, et al.

Human Heredity|July 1, 1993

Distribution of some point mutations in the phenylalanine hydroxylase gene of phenylketonuria patients from the Moscow regionE V Charikova, S E Khalchitskii, A G Antoshechkin, et al.

Human Mutation|January 1, 1994

A rapid and simple DNA fingerprinting method using RFLP and SSCP analysis of the hypervariable noncoding region of human mitochondrial DNAE A Pushnova, S N Akhmedova, S P Shevtsov, et al.

Biochemical and Molecular Medicine|August 1, 1997

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, RussiaM V Volkova, V I Vasina, E V Fomicheva, et al.

Human Mutation|January 1, 1992

A modified approach to identification of the sickle cell anemia mutation by means of allele-specific polymerase chain reactionK R Birikh, O V Plutalov, E I Schwartz, et al.

Molecular Genetics and Metabolism|November 24, 1999

Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy in IDDM patientsN S Shcherbak, Z V Shutskaya, A M Sheidina, et al.

Pageof 3

Search research articles

Showing results (1-10 of 24) with videos related to

Sort By:

Pageof 3

Journal of Human Genetics|April 27, 2001

The C825T polymorphism in the G-protein beta3 subunit gene and diabetic complications in IDDM patientsN S Shcherbak, E I Schwartz

Journal of the Neurological Sciences|March 10, 2001

Paraoxonase 1 Met--Leu 54 polymorphism is associated with Parkinson's diseaseS N Akhmedova, A K Yakimovsky, E I Schwartz

Biochemical Medicine and Metabolic Biology|August 1, 1994

Nonisotopic identification of two point mutations in the CYP21 gene responsible for nonclassic 21-hydroxylase deficiencyS P Shevtsov, S Rechitsky, O Verlinsky, et al.

The Journal of Nutrition|November 1, 1995

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 excretionS A Shapses, S P Robins, E I Schwartz, et al.

Biochemistry. Biokhimiia|October 22, 2002

Inducer effect on the complex formation between rat liver nuclear proteins and cytochrome P450 2B gene regulatory elementsT G Duzhak, E I Schwartz, L F Gulyaeva, et al.

Human Heredity|July 1, 1993

Distribution of some point mutations in the phenylalanine hydroxylase gene of phenylketonuria patients from the Moscow regionE V Charikova, S E Khalchitskii, A G Antoshechkin, et al.

Human Mutation|January 1, 1994

A rapid and simple DNA fingerprinting method using RFLP and SSCP analysis of the hypervariable noncoding region of human mitochondrial DNAE A Pushnova, S N Akhmedova, S P Shevtsov, et al.

Biochemical and Molecular Medicine|August 1, 1997

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, RussiaM V Volkova, V I Vasina, E V Fomicheva, et al.

Human Mutation|January 1, 1992

A modified approach to identification of the sickle cell anemia mutation by means of allele-specific polymerase chain reactionK R Birikh, O V Plutalov, E I Schwartz, et al.

Molecular Genetics and Metabolism|November 24, 1999

Methylenetetrahydrofolate reductase gene polymorphism as a risk factor for diabetic nephropathy in IDDM patientsN S Shcherbak, Z V Shutskaya, A M Sheidina, et al.

Pageof 3