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Проблемы и перспективы молекулярной генетики. Том 1 - Свердлов Е.Д.

Свердлов Е.Д. Проблемы и перспективы молекулярной генетики. Том 1 — М.: Наука, 2003. — 372 c.
ISBN 5-02-002753-7
Скачать (прямая ссылка): perspektivimoleculyargenetiki2003.djvu
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Ranum L.P.W., Rasmusen P.F., Benzow K.A. Genetic mapping of a second myotonic dystrophy locus // Nat. Genet. 1998. Vol. 19. P. 196-198.
Renges H.H., Peacock R., Dunning A.M. et al. Genetic relationship between the З'-VNTR and diallelic apolipoprotein В gene polymorphisms: haplotype analysis in individuals of European and south Asian origin // Ann. Human Genet. 1992. Vol. 56. P. 11-33.
Rich N. et al. Electromyography of rapid forearm flexion and extension and aging // Intern. J. Aging, and Hum. Develop. 1990. Vol. 31. P. 11-29.
Richards R.I. Simple repeat DNA is not replicated simply // Nat. Genet. 1994. Vol. 6. P. 114-116.
Richards R.I., Sutherland G.R. Dynamic mutation: possible mechanisms and significance in human disease // Trends Biochem Sci. 1997. Vol. 22. P. 432^-36.
Rosen D.R., Siddique Т., Patterson D. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis // Nature. 1993. Vol. 362. P. 59-62.
Rothstein J.D., Bristol L.A., Hosier B. et al. Chronic inhibition of superoxide dismutase produces apoptotic death of spinal neurons //Proc. Nat. Acad. Sci. USA. 1994. Vol. 91. P. 4155— 4159.
Rutledge D.R., Browe C.S., Kubilis P.S., Ross E.A. Analysis of two variants of the angiotensino-gen gene in essential hypertensive African-Americans // Amer. J. Hypertens. 1994. Vol. 7. P. 651-654.
369
Sajantila A., Lukka М., Syvanen A.-C. Experimentally observed germline mutations at human micro- and mini-satellite loci // Europ. J. Hum. Genet. 1999. Vol. 7, N 2. P. 263-266.
Sajantila A., Salem A-H., Savolainen P. et al. Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population // Proc. Nat. Acad. Sci. USA. 1996. Vol. 93, N21. P. 12035-12039 .
Semino ()., Passarino G., Oefner PJ. et al. The genetic legacy of Paleolithic Homo sapiens sapiens in extant europcans: A Y chromosome perspective // Science. 2000. Vol. 290, N 5494. P. 1155-1159.
Siddique Т., Nijhawan D., Hentati A. Molecular genetic basis of familial ALS // Neurology. 1996. Vol. 47. P. 27-34.
Siddique Т., Pericak-Vance M.A., Brooks B.R. et al. Genetic linkage analysis in familial amyotrophic lateral sclerosis // Abstr. Cytogenet. and Cell Genet 1989. Vol. 51. P. 1080.
Silveira I., Countinho P., Maciel P. Analysis of SCA1, DRPLA, MJD, SCA2 and SCA6 CAG repeats in 48 Portuguese ataxia families // Amer. J. Med. Genet. 1998. Vol. 81. P. 134-138
Skvortsova V.I.. Lumhorska S.A., Slominsky P.A. et al. Sporadic ALS associated with the D90A Cu, Zn superoxide dismutase mutation in Russia // Europ. J. Neurol. 2001. Vol. 8. P. 167-172.
Slominsky P.A., Markova E.D., Shadrina M.I. et al. A common 3-bp deletion in the DYT1 gene in Russian families with early-onset torsion dystonia // Hum. Mutat. 1999. Vol. 14, N 3. P. 269-272.
Slominsky P.A., Shadrina M.I., Kondratyeva E.A. et al. Cu, Zn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala(D90A) mutation and novel rare polymorphism IVS3+35 A > С // Ibid. 2000. Vol. 16, N 3. P. 227-228.
Spenser P.S., Kisby G., Smith R. // Handbook of ALS. N.Y.: Acad, press, 1992. P. 575-587.
Spitsyn V.A., Khorte M.V., Pogoda T.V. et al. Apolipoprotein В З’-VNTR polymorphism in the Udmurt population // Hum. Hered. 2000. Vol. 50, N 4. P. 224-226.
Steinberger D. High penetrance and pronounsed variation in expressivity of GCH-1 mutations in five families with DOPA-responsive dystonia // Ann. Neurol. 1998. Vol. 43. P. 634-639.
Summers K.M. Relationship between genotype and phenotype in monogenic diseases, revelance to polygenic diseases // Hum. Mutation. 1996. Vol. 7. P. 283-293.
Tanaka H. The gene for hereditary progressive dystonia with marked fluctuation maps to chromosome 14q // Am. Neurol. 1995. Vol. 37. P. 405^-08.
Tarnow L., Cambien Г., Rossing P. et al. Angiotensinogen gene polymorphisms in IDDM patients with diabetic nephropathy // Diabetes. 1996. Vol. 45. P. 367-369.
Thony B., Blau N. Mutations in the GTP cyclohydrolase I and 6-pyruvoyl-tetrahydropterin synthase genes // Hum. Mutat. 1997. Vol. 10. P. 11-20.
Tiret L., Bomwrdeaux A., Poirier O. et al. Synergistic effects of angiotensin-converting enzyme and angiotensin-II type 1 receptor gene polymorphisms on risk of myocardial infarction // Lancet. 1994. Vol. 344. P. 910-991.
Tiret L., Rigat B., Visvikis S. et al. Evidence from combined segregation and linkage analysis that a variant of the angiotensin-I-converting enzyme (ACE) gene controls plasma ACE level // Amer. J. Hum Genet. 1992. Vol. 51. P. 197-205.
Tishkoff S.A., Goldman A., Calafell F. et al. A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of moder humans and for the origin of myctonic dystrophy mutations // Amer. J. Hum. Genet. 1998. Vol. 62. P. 1389-1402.
Togari A., Ichinose 11., Matsumoto S. et al. Multiple mRNA forms of human GTP cyclohydrolase I // Biochem. and Biophys. Res. Commun. 1992. Vol. 187, N 1. P. 359-365.
Trocoso J.C., Gilbert M.R.. Muma N.A., Smith R. // Handbook of ALS. N.Y.: Acad, press, 1992. P. 543-554.
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