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Results: 1-17 |
Results: 17

Authors: Skvortsova, VI Limborska, SA Slominsky, PA Levitskaya, NI Levitsky, GN Shadrina, MI Kondratyeva, EA
Citation: Vi. Skvortsova et al., Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia, EUR J NEUR, 8(2), 2001, pp. 167-172

Authors: Miloserdova, OV Slominsky, PA Tarskaya, LA Sorensen, M Spitsyn, VA Limborskaya, SA
Citation: Ov. Miloserdova et al., Polymorphic markers of the angiotensin and angiotensin-converting enzyme genes in Yakuts: A lack of association with blood pressure, RUSS J GEN, 37(5), 2001, pp. 584-586

Authors: Miloserdova, OV Perova, NV Balabolkin, MI Slominsky, PA Limborskaya, SA
Citation: Ov. Miloserdova et al., Polymorphic variants of the renin-angiotensin system genes in the polymetabolic syndrome and non-insulin-dependent diabetes mellitus, RUSS J GEN, 37(10), 2001, pp. 1172-1176

Authors: Miloserdova, OV Slominsky, PA Mauyanov, IV Markov, DS Balabolkin, MI Limborska, SA
Citation: Ov. Miloserdova et al., Association between the insertion/deletion polymorphism of the angiotensin-converting enzyme gene and angiopathy in patients with non-insulin dependent diabetes mellitus in Chuvash Republic, RUSS J GEN, 37(1), 2001, pp. 98-101

Authors: Shadrina, MI Dolotov, OV Grivennikov, IA Slominsky, PA Andreeva, LA Inozemtseva, LS Limborska, SA Myasoedov, NF
Citation: Mi. Shadrina et al., Rapid induction of neurotrophin mRNAs in rat glial cell cultures by Semax,an adrenocorticotropic hormone analog, NEUROSCI L, 308(2), 2001, pp. 115-118

Authors: Karabanov, AV Ovchinnikov, IV Illarioshkin, SN Poleschuk, VV Slominsky, PA Markova, ED Rebrova, OY Limborskaya, SA Ivanova-Smolenskaya, IA
Citation: Av. Karabanov et al., Analysis of mutations in ATP7B gene and experience of the direct DNA-diagnosis in hepatolenticular degeneration, ZH NEVR PS, 101(4), 2001, pp. 44-47

Authors: Markova, ED Slominsky, PA Illarioshkin, SN Miklina, NI Shadrina, MI Popova, SN Limborska, SA Ivanova-Smolenskaya, IA
Citation: Ed. Markova et al., Molecular genetic analysis of torsion dystonia in Russia, RUSS J GEN, 36(7), 2000, pp. 785-790

Authors: Slominsky, PA Popova, SN Shadrina, MI Pomazanova, MA Lomova, TY Fatkhlislamova, RI Khusnutdinova, EK Guseva, IA Erdes, S Mikulich, AI Spitsyn, VA Limborska, SA
Citation: Pa. Slominsky et al., Normal polymorphism of the (CTG)(n) repeat in the myotonin protein kinase (DM) gene on chromosome 19q13.3 in Eastern European populations, RUSS J GEN, 36(7), 2000, pp. 809-813

Authors: Slominsky, PA Popova, SN Fatkhlislamova, RI Akhmadeeva, LR Magzhanov, RV Khusnutdinova, EK Limborska, SA
Citation: Pa. Slominsky et al., Analysis of (CTG)(n) triplet repeat expansion in patients with myotonic dystrophy from Bashkiria, RUSS J GEN, 36(6), 2000, pp. 695-698

Authors: Shadrina, MI Kopilov, VM Miloserdova, OV Slominsky, PA Limborska, SA
Citation: Mi. Shadrina et al., Analysis of a 32-base-pair deletion in the CCR5 chemokine receptor gene inHIV-1-infected individuals from Moscow, RUSS J GEN, 36(5), 2000, pp. 586-587

Authors: Slominsky, PA Metelskaya, VA Miloserdova, OV Perova, NV Limborska, SA
Citation: Pa. Slominsky et al., Analysis of the possible role of genetic factors in determination of the concentration of high-density-lipoprotein cholesterol in the Moscow population, RUSS J GEN, 36(10), 2000, pp. 1177-1180

Authors: Khidiyatova, IM Fatkhlislamova, RI Magzhanov, RV Popova, SN Slominsky, PA Limborska, SA Khusnutdinova, EK
Citation: Im. Khidiyatova et al., A study of expansion and mutation rate of the CTG repeat in the myotonic dystrophy gene, RUSS J GEN, 36(10), 2000, pp. 1185-1187

Authors: Skvortsova, VI Limborskaya, SA Slominsky, PA Levitskaya, NI Levitsky, GN Shadrina, MI Kondratyeva, EA
Citation: Vi. Skvortsova et al., Sporadic amyotrophic lateral sclerosis associated with Asp90Ala CuZn-superoxide dismutase mutations in Russia, ZH NEVR PS, 100(1), 2000, pp. 44-47

Authors: Spitsyn, VA Khorte, MV Pogoda, TV Slominsky, PA Nurbaev, SD Agapova, RK Limborska, SA
Citation: Va. Spitsyn et al., Apolipoprotein B 3'-VNTR polymorphism in the Udmurt population, HUMAN HERED, 50(4), 2000, pp. 224-226

Authors: Markova, ED Slominsky, PA Illarioshkin, SN Miklina, NI Popova, SN Limborska, SA Ivanova-Smolenskaya, IA
Citation: Ed. Markova et al., A novel mutation in the GTP cyclohydrolase I gene associated with a broad range of clinical presentations in a family with autosomal dominant dopa-responsive dystonia, EUR J NEUR, 6(5), 1999, pp. 605-608

Authors: Fatkhlislamova, RI Khidiyatova, IM Khusnutdinova, EK Popova, SN Slominsky, PA Limborska, SA
Citation: Ri. Fatkhlislamova et al., Analysis of polymorphism of CTG repetitive sequences in the gene of myotonic dystrophy in human populations of the Volga-Ural region, RUSS J GEN, 35(7), 1999, pp. 848-853

Authors: Popova, SN Mikulich, AI Slominsky, PA Shadrina, MI Pomazanova, MA Limborska, SA
Citation: Sn. Popova et al., Polymorphism of the (CTG)(n) repeat in the myotonin protein kinase (DM) gene in Belarussian populations: Analysis of interethnic heterogeneity, RUSS J GEN, 35(7), 1999, pp. 854-856
Risultati: 1-17 |