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239. KMENT, M.; PYTLK, R.; JIRSEK, J.E.; JANDA, J.; ZELNCEK, P.; DRBAL, K.: Mezinrodn etick smrnice CIOMS pro biomedicnsk vzkum. Zdravotnick noviny, 1995, roc. 44, 32 ; , s. 2-3. 240. KNIGOV, R.: Prix Femmes d' Europe - Cena 'zena Evropy'. Vita Nostra Revue, 1995, 1-2 ; , s. 64-66. 241. KORYCH, B.; POKORN, M.: Geografick medicna. Zdrav, 1995, roc. 43, 7 ; , s. 8-9. 242. KZOV, E.: Jak jsou moznosti a postaven v soucasnosti ceskch zen. Zdrav. noviny, Lk. listy, 1995, roc. 14, 45 ; , s. 9. 243. KZOV, E.: Program Svtov zdravotnick organizace ke zdrav zen. Zdrav. noviny, Lk. listy, 1995, roc. 14, 10 ; , s. 3-4. 244. KZOV, E.: Zdrav nemocnice nebo uzdravovna? Zpravodaj FNKV, 1995, 5 ; , s. 13-14. 245. KZOV, E.: Zprva o zdrav zen v Cesk republice. Zdravotnick noviny, Lk. listy, 1995, roc. 14, 12 ; , s. 3-5. 246. KUCHYNKA, P.; KEPELKOV, J.: Ndory oka - diagnostika a terapie. Zdrav. noviny, Lk. listy, 1995, roc. 44, 20 ; , s. 4. 247. KUCHYNKA, P.; NOVK, P.: Ultrasonick fakoemulzifikace jdra ocn cocky. Zdrav. noviny, Lk. listy, 1995, roc. 44, 20 ; , s. 11. 248. LEZAL, D.; KONK, K.; TRKAL, V.; HORK, L.: Vyuzit optickch vlken v medicn. Skl a keramika, 1995, roc. 1, ; , s. 45. 249. LIKOVSK, Z.; TUREK, B.: Zamyslen nad stedn dobou zivota ceskch sldk. Kvasn prmysl, 1995, roc. 41, s. 313316. 250. MALINA, L.: Dermatovenerologie 1995 - soucasn stav oboru a nkter odborn otzky. Zdravotnick noviny, Lkask listy, 1995, roc. 44, 43 ; , s. 1. 251. MALINA, L.: Solrn dermatitida a chronick polymorfn fotodermatza. Zdravotnick noviny, Lkask listy, 1995, roc. 44, 45 ; , s. 3-4. 252. PAVELKA, K.; VENCOVSK, J.; HRBA, J.: K problematice vzkumu v Revmatologickm stavu v Praze. Cesk revmatologie, 1995, roc. 3, ; , s. 142-144. 253. POVSIL, C.; STTESK, J.: Zprva vboru Spolecnosti patolog Cesk lkask spolecnosti J. E. Purkyn za rok 1994. Cesko-slovensk patologie a Soudn lkastv, 1995, roc. 31, 2 ; , s. 65-66. 254. PROVAZNKOV, H.: Zdrav vysokoskolskch student a jeho determinanty. Alma Mater, 1995, roc. 5, 1-2 ; , s. 60-66. 255. RDL, P.: Deratizace msta Hradec Krlov. Zpravodaj DDD, 1995, roc. 4, ; , s. 18-21. 256. RDL, P.: Kurs k udlen odborn zpsobilosti pracovnk pro odchyt toulavch, zdivocelch a vybranch synantropnch zvat . Zpravodaj DDD, 1995, roc. 4, 2 ; , s. 28-29. 257. RDL, P.: Problematika toulavch kocek. Zpravodaj DDD, 1995, roc. 4, ; , s. 13-18. 258. SCHINDLER, J.: Enterokoky jako nosokomiln a infekcn agens. Zprvy CEM, 1995, roc. 4, 3 ; , s. 5. 259. SCHINDLER, J.: Scientific Working Group on Monitoring and Management of Bacterial Resistance to Antimicrobial Agents. Zprva ze sluzebn cesty. Zprvy Centra epidemiologie a mikrobiologie, 1995, roc. 4, 2 ; , s. 25-26. 260. SCHINDLER, J.: Stafylokoky rezistentn k methicilinu - MRS. Zprvy CEM, 1995, roc. 4, 5 ; , s. 4-5. 261. SCHINDLER, J.: Zmny v klasifikaci a nomenklatue. Zprvy Centra epidemiologie a mikrobiologie, 1995, roc. 4, 5 ; , s. 5. 262. SCHNEIDROV, D.: Breastfeeding Basic for Babies Says ANIMA. Central European Journal of Occupational and Environmental Medicine, 1995, Spring Summer ; , s. 4. 263. STRNSK, J.: Zprva ze VI. mezinrodnho symposia o virovch hepatitidch. Madrid, 3.-5. nora 1994. Casopis lka ceskch, 1995, roc. 134, 3 ; , s. 90. 264. SIMEK, J.: Soucasn problmy zdravotnictv z pohledu ucitele lkask etiky. Vita Nostra Revue, 1995, 1-2 ; , s. 42-45. 265. SPALEK, V.; STREJCEK, J.: Eutanazie v poped zjmu tm na celm svt. Zdravotnick noviny, Lkask listy, 1995, roc. 44, 50 ; , s. 4. 266. URBSKOV, P.: Prkaz stafylokok rezistentnch k oxacilinu methicilinu MRS ; . Zprvy Centra epidemiologie a mikrobiologie, 1995, roc. 4, 3 ; , s. 5. 267. URBSKOV, P.: Referencn kmeny pro vyseten citlivosti hemofil a pneumokok. Zprvy Centra epidemiologie a mikrobiologie, 1995, roc. 4, 1 ; , s. 5-6. 268. VANCKOV, E.: III. semin Cesk spolecnosti na ochranu dt. Hygiena, 1995, roc. 40, 1 ; , s. 52. 269. VANCKOV, E.: Ohldnut za mezinrodnm rokem rodiny. Otec, dt, rodina, 1995, roc. 1, 4 ; , s. 12-13. 270. VANCKOV, E.: Zprva o IV. semini Cesk spolecnosti na ochranu dt. Hygiena, 1995, roc. 40, 2 ; , s. 186. 271. VENCOVSK, J.: Autoprotiltky u systmovch revmatoickch onemocnn. Zdravotnick noviny, Lkask listy, 1995, roc. 44, 28 ; , s. 6-7. 272. VENCOVSK JI: Nov smry v soucasn terapii revmatoidn artritidy. Zdrav.noviny, Lk. listy, 1995, roc. 44, 28 ; , s. 6-7. 273. VOJTCHOVSK, M.: Klinick problmy a diagnostika demenc. Zdrav. noviny, Lkask listy, 1995, roc. 44, 13 ; , s. 11. 274. VOJTCHOVSK, M.: Psychiatrie budoucnosti bude zejm gerontopsychiatrie. Regena, 1995, roc. 5, 7 ; , s. 2-3. 275. ZICHA, J.: Interpretace srologie EBV. Farmakoterapeutick informace, 1995, 8-9 ; , s. 6-7. 276. AKSELRODOV, Z.: 9congres Mondial des Professeurs de Franais Tokyo, du 25 au 31 aout 1996 ; . Bulletin de LAssociation des Professeurs de Franais, 1996, 21 ; , s.23-25 and xalatan.
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METHYLENETETRAHYDROFOLATE REDUCTASE MTHFR ; MOLECULAR PHARMACOGENETICS: ISOFORM CHARACTERIZATION AND HUMAN LIVER EXPRESSION. Y. N. Martin, BS, T. V. Nguyen, PhD, N. Hernandez-Alvarado, BS, J. S. Leeder, PharmD, PhD, R. M. Weinshilboum, MD, Mayo Clinic College of Medicine, Children's Mercy Hospital, Kansas City, MO, Rochester, MN. BACKGROUND: MTHFR genetic variation is a risk factor for cardiovascular disease and fetal neural tube defects. In fetal liver, MTHFR exists as 70 and 77 kDa isoforms. Gene resequencing studies revealed a nonsynonymous cSNP in the 77 kDa isoform, an isoform which has never been successfully expressed or characterized. We expressed the 77kDa isoform with the E2 and V222 polymorphisms and performed functional genomic studies. We also studied patterns of isoform expression during fetal growth and development. METHODS: The two isoforms and the variant allozymes were expressed using bacterial and mammalian systems and their biochemical properties were studied. Expression of both isoforms in 73 human fetal livers was measured using Western blots. RESULTS: Recombinant wild-type WT ; 77 kDa isoform and the D2E allozyme showed no significant differences in activity or substrate kinetics as compared to the recombinant 70 kDa isoform. However, the V222 77 kDa allozyme had 26% of WT activity. 77 kDa isoform expression decreased during fetal development, while this trend was less evident for the 70 kDa isoform. Both isoforms showed large individual variation in expression at comparable gestational age. CONCLUSIONS: These studies represent the first successful expression and characterization of the 77 kDa MTHFR isoform and variant allozymes and provide insight into MTHFR pharmacogenetics as well as variation in expression during fetal growth and development and xenical, for example, wellbutrin and breast feeding.
Blanger A, Martel L, Berthelot J-M, Wilkins R. Gender differences in disability-free life expectancies for selected risk factors and chronic conditions in Canada. In Laditka S, ed., Health Expectations for Older Women: International Perspectives. Special edition Journal of Women and Aging 2002; 14 1 ; in press ; . Mayer F, Ross N, Berthelot J-M, Wilkins R. Disability-free life expectancy by health region. Health Reports Statistics Canada, Catalogue 82-003 ; 2002; 13 4 ; : 49-61. Sanmartin C and Berthelot J-M. Regional differences in self-reported unmet health needs. Health Reports Statistics Canada, Catalogue 82-003 ; 2002; S13 in press ; . Shields M and Tremblay S. The health of Canada's communities. Health Reports Statistics Canada, Catalogue 82-003 ; 2002; S13. Tremblay S, Ross N and Berthelot J-M. Ontario Grade 3 student achievement. Canadian Social Trends. Statistics Canada Catalogue 11-008 ; Summer 2002, pp. 15-19. Tremblay S, Ross N and Berthelot J-M. Regional socio-economic context and health. Health Reports Statistics Canada, Catalogue 82003 ; 2002; S13. Wilkins R, Berthelot J-M, Ng E. Trends in mortality by neighbourhood income in urban Canada from 1971 to 1996. Health Reports Statistics Canada, Catalogue 82-003 ; 2002; S13. Yang H, Kramer MS, Platt R, Blondel B, Grart G, Morin I, Wilkins R, Usher R. How does early ultrasound estimation of gestational age lead to higher rates of preterm birth? American Journal of Obstetrics and Gynecology 2002; 186 3 ; : 433-7.
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Novo Nordisk uses gene technology and genetically modified organisms GMOs ; in biomedical research and the production of pharmaceuticals. We believe gene technology can help solve many of today's health issues and allow us to provide products in sufficient quantity or quality. Yet we recognise that use of this technology causes concerns. We take every precaution to ensure the safe use of GMOs. The GMOs we use for production are in the lowest risk category with no known risks to humans or the environment. All GMOs are handled under closed or contained conditions. The final products do not contain GMOs. We recognise the concern about the level of antibiotic resistance among microorganisms in the environment. Therefore, new production strains will be without antibiotic resistance genes whenever technically possible and practically feasible. No damage to human health or the environment has ever been recorded in our use of GMOs for research and production.
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