Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Eugene I Schwartz"'
Autor:
Olga V. Sirotkina, Eugene I. Schwartz, Alexander L. Shwarzman, S.N. Pchelina, Anastasiya E. Taraskina, Tatyana Vavilova
Publikováno v:
Thrombosis Research. 115:199-203
0049-3848/$ see front matter D 200 doi:10.1016/j.thromres.2004.08.020 Abbreviations: INR, international polymerase chain reaction; SNPs, sin phisms; DNA, deoxyribonucleic acid; S * Corresponding author. Saint-Pete ical University, L. Tolstogo Street,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::572325e13286908bb45316953533c8d3
https://doi.org/10.1016/j.thromres.2004.08.020
https://doi.org/10.1016/j.thromres.2004.08.020
Publikováno v:
Journal of Human Genetics. 46:188-191
Complications of insulin-dependent diabetes mellitus (IDDM) are a major cause of morbidity and mortality; however, the mechanisms of their development are still to be elucidated. Genetic susceptibility contributes to the pathogenesis of nephropathy i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38f7ac02c0c5e79bc5b5d96f09e10a2e
https://doi.org/10.1007/s100380170087
https://doi.org/10.1007/s100380170087
Publikováno v:
Journal of the Neurological Sciences. 184:179-182
Two up-to-date known paraoxonase 1 (PON1) polymorphisms (Gln--Arg 191 and Leu--Met 54) affect the hydrolysis of toxic oxons and might intensify effects of pollutants, organophosphates and other environmental chemicals in development of Parkinson's di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b82fbc6a93d34c3fce0b7e7d360ad8c
https://doi.org/10.1016/s0022-510x(01)00439-7
https://doi.org/10.1016/s0022-510x(01)00439-7
Complete Spectrum of PAH Mutations in Tataria: Presence of Slavic, Turkic and Scandinavian Mutations
Autor:
Alexei A. Goltsov, Alexei I. Kuzmin, Randy C. Eisensmith, Eugene I. Schwartz, Savio L. C. Woo, Naila A. Sergeeva
Publikováno v:
European Journal of Human Genetics. 3:246-255
Phenylketonuria (PKU) is an autosomal recessive disorder associated with a deficiency of hepatic phenylalanine hydroxylase (PAH). Although the molecular lesions present in the PAH genes of PKU patients have previously been determined in several Slavi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d08e6c72051cb5ac05a794f7504bb0bd
https://doi.org/10.1159/000472305
https://doi.org/10.1159/000472305
Autor:
Eugene I. Schwartz, Sergey V. Anisimov, Lilia V. Lenskaya, Maria V. Volkova, Dina V. Solovieva, Vladimir Kh Khavinson
Publikováno v:
The journals of gerontology. Series A, Biological sciences and medical sciences. 56(1)
Apolipoprotein C-III (apoC-III) is the major component of triglyceride-rich lipoproteins. One of six identified polymorphisms in the apoC-III 5 9 -untranslated region (T-455C) is located within a functional insulin-response element. In a group of 137
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7cb627b8bb5b94254d506623f7f71ae
https://pubmed.ncbi.nlm.nih.gov/11193221
https://pubmed.ncbi.nlm.nih.gov/11193221
Autor:
Helena Reijonen, Jorma Ilonen, Bela Adojaan, Hans K. Åkerblom, Liliya Kovalchuk, S Nejentsev, Eugene I Schwartz, Arthur Sochnevs
Publikováno v:
Diabetes, 46(11), 1888-92. American Diabetes Association Inc.
Nejentsev, S, Reijonen, H, Adojaan, B, Kovalchuk, L, Sochnevs, A, Schwartz, E I, Akerblom, H K & Ilonen, J 1997, ' The effect of HLA-B allele on the IDDM risk defined by DRB1*04 subtypes and DQB1*0302 ', Diabetes, vol. 46, no. 11, pp. 1888-92 .
Nejentsev, S, Reijonen, H, Adojaan, B, Kovalchuk, L, Sochnevs, A, Schwartz, E I, Akerblom, H K & Ilonen, J 1997, ' The effect of HLA-B allele on the IDDM risk defined by DRB1*04 subtypes and DQB1*0302 ', Diabetes, vol. 46, no. 11, pp. 1888-92 .
The genes encoding the HLA-DQ heterodimer molecules, DQB1 and DQA1, have been found to have the strongest association with IDDM risk, although there is cumulative evidence for the effect of other gene loci within the major histocompatibility complex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18cb3fb8c62218a5f7726f2f95016335
https://research.vumc.nl/en/publications/432a4221-6aab-45c0-b0f9-2e4538129a5a
https://research.vumc.nl/en/publications/432a4221-6aab-45c0-b0f9-2e4538129a5a
Publikováno v:
Biochemical and molecular medicine. 58(2)
The frequency of 29A and 29B mutations in the CYP2D6 gene, the most common mutations among Caucasoid PM (debrisoquine 4-hydroxylase defficient) individuals, has been analyzed in the Russian population. For the detection of the 29A mutation, a new one
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::515b12293fbb1d107ecb0ba752f9f58f
https://pubmed.ncbi.nlm.nih.gov/8812745
https://pubmed.ncbi.nlm.nih.gov/8812745
Publikováno v:
Biochemical and molecular medicine. 54(2)
The frequency of the cytochrome P4502D6B CYP2D6B (29B) mutant allele has been determined in three clinically distinct groups of patients with Parkinson disease. No differences in mutation frequency among the patients with the rigidity-akinetic and mo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7645530a69c5a2a8920b355daf6b9290
https://pubmed.ncbi.nlm.nih.gov/8581363
https://pubmed.ncbi.nlm.nih.gov/8581363
Publikováno v:
Biochemical and Molecular Medicine. 59:91-92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5af33d1ef1e3af1201c88a001eb200e
https://doi.org/10.1006/bmme.1996.0071
https://doi.org/10.1006/bmme.1996.0071