MeSH Review:
Genetic Research
Alda,
Paclt,
Koudelová,
Krepelová,
Uhlíková,
Gazdíková,
Bauer,
Neumeister,
Young,
Stastny,
Stiller,
Hall,
Nosaka,
Tachi,
Shimpuku,
Kawamura,
Ohura,
Patkar,
Berrettini,
Hoehe,
Hill,
Gottheil,
Thornton,
Weinstein,
Lessov,
Martin,
Statham,
Todorov,
Slutske,
Bucholz,
Heath,
Madden,
Mahan,
Ardlie,
Krenitsky,
Walsh,
Clough,
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- Molecular biology as a tool for genetic research in hypertension: application to the renin gene. Soubrier, F., Houot, A.M., Jeunemaitre, X., Plouin, P.F., Corvol, P. J. Cardiovasc. Pharmacol. (1988)
- Evaluation of newborns with skeletal dysplasias. Macpherson, R.I., Pai, G.S. Indian journal of pediatrics. (2000)
- Pharmacogenetics of lithium response in bipolar disorder. Alda, M. Journal of psychiatry & neuroscience : JPN. (1999)
- Individual differences in sensitivity to nicotine: implications for genetic research on nicotine dependence. Pomerleau, O.F. Behav. Genet. (1995)
- AAAS conference explores ethical aspects of large pedigree genetic research. Glass, R.M. JAMA (1992)
- Evolution of the RNA polymerase II C-terminal domain. Stiller, J.W., Hall, B.D. Proc. Natl. Acad. Sci. U.S.A. (2002)
- Quantitative trait loci analysis of structural and material skeletal phenotypes in C57BL/6J and DBA/2 second-generation and recombinant inbred mice. Lang, D.H., Sharkey, N.A., Mack, H.A., Vogler, G.P., Vandenbergh, D.J., Blizard, D.A., Stout, J.T., McClearn, G.E. J. Bone Miner. Res. (2005)
- Fetal programming of polycystic ovary syndrome by androgen excess: evidence from experimental, clinical, and genetic association studies. Xita, N., Tsatsoulis, A. J. Clin. Endocrinol. Metab. (2006)
- The neoplastic pathogenesis of solitary and multiple osteochondromas. Porter, D.E., Simpson, A.H. J. Pathol. (1999)
- Myotonic muscular dystrophy. Alberts, M.J., Roses, A.D. Neurologic clinics. (1989)
- Collaborative design for automated DNA storage that allows for rapid, accurate, large-scale studies. Mahan, S., Ardlie, K.G., Krenitsky, K.F., Walsh, G., Clough, G. Assay and drug development technologies. (2004)
- A genetic investigation of E2A function in lymphocyte development. Hanrahan, J., Pan, L., Greenbaum, S., Bradney, C., Hjelmeland, M., Dai, M., Zhuang, Y. Immunol. Res. (2000)
- Defining nicotine dependence for genetic research: evidence from Australian twins. Lessov, C.N., Martin, N.G., Statham, D.J., Todorov, A.A., Slutske, W.S., Bucholz, K.K., Heath, A.C., Madden, P.A. Psychological medicine. (2004)
- Implications of genetic research on the role of the serotonin in depression: emphasis on the serotonin type 1A receptor and the serotonin transporter. Neumeister, A., Young, T., Stastny, J. Psychopharmacology (Berl.) (2004)
- Genetics of proteinases of lactic acid bacteria. Kok, J., Venema, G. Biochimie (1988)
- No association found between 158 Val/Met polymorphism of the COMT gene and schizophrenia with minor physical anomalies. Joo, E.J., Jeong, S.H., Ahn, Y.M., Lee, K.Y., Chang Yoon, S., Kim, E.J., Kim, S.U., Cho, S.C., Sik Kim, Y. Psychiatry research. (2005)
- No association between polymorphisms in the serotonin transporter gene and susceptibility to cocaine dependence among African-American individuals. Patkar, A.A., Berrettini, W.H., Hoehe, M., Hill, K.P., Gottheil, E., Thornton, C.C., Weinstein, S.P. Psychiatr. Genet. (2002)
- Association of calcitonin receptor gene polymorphism with early marginal bone loss around endosseous implants. Nosaka, Y., Tachi, Y., Shimpuku, H., Kawamura, T., Ohura, K. The International journal of oral & maxillofacial implants. (2002)
- Biochemical markers and genetic research of ADHD. Paclt, I., Koudelová, J., Krepelová, A., Uhlíková, P., Gazdíková, M., Bauer, P. Neuro Endocrinol. Lett. (2005)
- Dissecting the genetics of type 1 diabetes: relevance for familial clustering and differences in incidence. Buzzetti, R., Quattrocchi, C.C., Nisticò, L. Diabetes/metabolism reviews. (1998)
- A radioenzymatic assay of catechol-O-methyltransferase in hair root cells: comparison with erythrocyte activity. Hoo, J.J., Strohmeyer, T., Beckermann, W.J., Agarwal, D.P., Goedde, H.W. Hum. Genet. (1981)
- Association of a polymorphism of the serotonin 1B receptor gene and alcohol dependence with inactive aldehyde dehydrogenase-2. Hasegawa, Y., Higuchi, S., Matsushita, S., Miyaoka, H. Journal of neural transmission (Vienna, Austria : 1996) (2002)