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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
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Molecular Biology

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  1. Molecular basis for membrane phospholipid diversity: why are there so many lipids? Dowhan, W. Annu. Rev. Biochem. (1997) [Pubmed]
  2. Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q. Compton, J.G., DiGiovanna, J.J., Santucci, S.K., Kearns, K.S., Amos, C.I., Abangan, D.L., Korge, B.P., McBride, O.W., Steinert, P.M., Bale, S.J. Nat. Genet. (1992) [Pubmed]
  3. The molecular biology of Laron dwarfism and medullary thyroid cancer. Jackson, C.E., Norum, R.A. N. Engl. J. Med. (1989) [Pubmed]
  4. The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity. Lee, W.H., Shew, J.Y., Hong, F.D., Sery, T.W., Donoso, L.A., Young, L.J., Bookstein, R., Lee, E.Y. Nature (1987) [Pubmed]
  5. The molecular biology of RU486. Is there a role for antiprogestins in the treatment of breast cancer? Horwitz, K.B. Endocr. Rev. (1992) [Pubmed]
  6. A cosmid contig and high resolution restriction map of the 2 megabase region containing the Huntington's disease gene. Baxendale, S., MacDonald, M.E., Mott, R., Francis, F., Lin, C., Kirby, S.F., James, M., Zehetner, G., Hummerich, H., Valdes, J. Nat. Genet. (1993) [Pubmed]
  7. Narcolepsy in orexin knockout mice: molecular genetics of sleep regulation. Chemelli, R.M., Willie, J.T., Sinton, C.M., Elmquist, J.K., Scammell, T., Lee, C., Richardson, J.A., Williams, S.C., Xiong, Y., Kisanuki, Y., Fitch, T.E., Nakazato, M., Hammer, R.E., Saper, C.B., Yanagisawa, M. Cell (1999) [Pubmed]
  8. Cell biology of the hippocampal formation in schizophrenia. Weinberger, D.R. Biol. Psychiatry (1999) [Pubmed]
  9. Molecular genetics of attention-deficit/hyperactivity disorder. Faraone, S.V., Perlis, R.H., Doyle, A.E., Smoller, J.W., Goralnick, J.J., Holmgren, M.A., Sklar, P. Biol. Psychiatry (2005) [Pubmed]
  10. Neurodegeneration caused by proteins with an aberrant carboxyl-terminus. Vidal, R., Delisle, M.B., Ghetti, B. J. Neuropathol. Exp. Neurol. (2004) [Pubmed]
  11. Molecular genetics of the T cell-receptor beta chain. Davis, M.M. Annu. Rev. Immunol. (1985) [Pubmed]
  12. Cellular and molecular biology of the aquaporin water channels. Borgnia, M., Nielsen, S., Engel, A., Agre, P. Annu. Rev. Biochem. (1999) [Pubmed]
  13. Acyl-coenzyme A:cholesterol acyltransferase. Chang, T.Y., Chang, C.C., Cheng, D. Annu. Rev. Biochem. (1997) [Pubmed]
  14. Molecular biology and genetics of tubulin. Cleveland, D.W., Sullivan, K.F. Annu. Rev. Biochem. (1985) [Pubmed]
  15. Molecular biology of mammalian plasma membrane amino acid transporters. Palacín, M., Estévez, R., Bertran, J., Zorzano, A. Physiol. Rev. (1998) [Pubmed]
  16. Multiple antibiotic-resistant Klebsiella and Escherichia coli in nursing homes. Wiener, J., Quinn, J.P., Bradford, P.A., Goering, R.V., Nathan, C., Bush, K., Weinstein, R.A. JAMA (1999) [Pubmed]
  17. MUNC-ing around with insulin action. James, D.E. J. Clin. Invest. (2005) [Pubmed]
  18. Mutation of the acetylcholine receptor alpha subunit causes a slow-channel myasthenic syndrome by enhancing agonist binding affinity. Sine, S.M., Ohno, K., Bouzat, C., Auerbach, A., Milone, M., Pruitt, J.N., Engel, A.G. Neuron (1995) [Pubmed]
  19. A single point mutation leading to loss of catalytic activity in human thiopurine S-methyltransferase. Krynetski, E.Y., Schuetz, J.D., Galpin, A.J., Pui, C.H., Relling, M.V., Evans, W.E. Proc. Natl. Acad. Sci. U.S.A. (1995) [Pubmed]
  20. Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7). Mariani, G., Herrmann, F.H., Bernardi, F., Schved, J.F., Auerswald, G., Ingerslev, J. Blood (2000) [Pubmed]
  21. Physiology and biochemistry of Drosophila learning mutants. Davis, R.L. Physiol. Rev. (1996) [Pubmed]
  22. Three-dimensional structure of beta-galactosidase from E. coli. Jacobson, R.H., Zhang, X.J., DuBose, R.F., Matthews, B.W. Nature (1994) [Pubmed]
  23. Clinical counterpoint: gonadotropin-releasing hormone deficiency: perspectives from clinical investigation. Crowley, W.F., Jameson, J.L. Endocr. Rev. (1992) [Pubmed]
  24. The ROOT HAIR DEFECTIVE3 gene encodes an evolutionarily conserved protein with GTP-binding motifs and is required for regulated cell enlargement in Arabidopsis. Wang, H., Lockwood, S.K., Hoeltzel, M.F., Schiefelbein, J.W. Genes Dev. (1997) [Pubmed]
  25. Senescence, aging, and malignant transformation mediated by p53 in mice lacking the Brca1 full-length isoform. Cao, L., Li, W., Kim, S., Brodie, S.G., Deng, C.X. Genes Dev. (2003) [Pubmed]
  26. Class I-like HLA genes map telomeric to the HLA-A2 locus in human cells. Orr, H.T., DeMars, R. Nature (1983) [Pubmed]
  27. The molecular biology of thyroid peroxidase: cloning, expression and role as autoantigen in autoimmune thyroid disease. McLachlan, S.M., Rapoport, B. Endocr. Rev. (1992) [Pubmed]
  28. BRCA2 germline mutations in familial pancreatic carcinoma. Hahn, S.A., Greenhalf, B., Ellis, I., Sina-Frey, M., Rieder, H., Korte, B., Gerdes, B., Kress, R., Ziegler, A., Raeburn, J.A., Campra, D., Grützmann, R., Rehder, H., Rothmund, M., Schmiegel, W., Neoptolemos, J.P., Bartsch, D.K. J. Natl. Cancer Inst. (2003) [Pubmed]
  29. Isolation of a murine Ly-6 cDNA reveals a new multigene family. LeClair, K.P., Palfree, R.G., Flood, P.M., Hammerling, U., Bothwell, A. EMBO J. (1986) [Pubmed]
  30. The desmoplakin carboxyl terminus coaligns with and specifically disrupts intermediate filament networks when expressed in cultured cells. Stappenbeck, T.S., Green, K.J. J. Cell Biol. (1992) [Pubmed]
  31. Feedback repression is required for mammalian circadian clock function. Sato, T.K., Yamada, R.G., Ukai, H., Baggs, J.E., Miraglia, L.J., Kobayashi, T.J., Welsh, D.K., Kay, S.A., Ueda, H.R., Hogenesch, J.B. Nat. Genet. (2006) [Pubmed]
  32. Recent advances in the molecular biology of dopamine receptors. Gingrich, J.A., Caron, M.G. Annu. Rev. Neurosci. (1993) [Pubmed]
  33. Molecular biology of serotonin receptors. Julius, D. Annu. Rev. Neurosci. (1991) [Pubmed]
  34. Humoral and cell-mediated immune responses to live recombinant BCG-HIV vaccines. Aldovini, A., Young, R.A. Nature (1991) [Pubmed]
  35. Molecular biology of steroid hormone synthesis. Miller, W.L. Endocr. Rev. (1988) [Pubmed]
  36. Molecular genetics of the achaete-scute gene complex of D. melanogaster. Campuzano, S., Carramolino, L., Cabrera, C.V., Ruíz-Gómez, M., Villares, R., Boronat, A., Modolell, J. Cell (1985) [Pubmed]
  37. The molecular genetics of the bithorax complex of Drosophila: characterization of the products of the Abdominal-B domain. Celniker, S.E., Keelan, D.J., Lewis, E.B. Genes Dev. (1989) [Pubmed]
  38. Emx2 patterns the neocortex by regulating FGF positional signaling. Fukuchi-Shimogori, T., Grove, E.A. Nat. Neurosci. (2003) [Pubmed]
  39. DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features. Paloneva, J., Mandelin, J., Kiialainen, A., Bohling, T., Prudlo, J., Hakola, P., Haltia, M., Konttinen, Y.T., Peltonen, L. J. Exp. Med. (2003) [Pubmed]
  40. Allelic loss at chromosomes 3p, 8p, 13q, and 17p associated with poor prognosis in head and neck cancer. Li, X., Lee, N.K., Ye, Y.W., Waber, P.G., Schweitzer, C., Cheng, Q.C., Nisen, P.D. J. Natl. Cancer Inst. (1994) [Pubmed]
  41. Innovative approaches to plasminogen activator therapy. Haber, E., Quertermous, T., Matsueda, G.R., Runge, M.S. Science (1989) [Pubmed]
  42. Molecular genetic approaches to understanding the actin cytoskeleton. Sutherland, J.D., Witke, W. Curr. Opin. Cell Biol. (1999) [Pubmed]
  43. Distinct narcolepsy syndromes in Orexin receptor-2 and Orexin null mice: molecular genetic dissection of Non-REM and REM sleep regulatory processes. Willie, J.T., Chemelli, R.M., Sinton, C.M., Tokita, S., Williams, S.C., Kisanuki, Y.Y., Marcus, J.N., Lee, C., Elmquist, J.K., Kohlmeier, K.A., Leonard, C.S., Richardson, J.A., Hammer, R.E., Yanagisawa, M. Neuron (2003) [Pubmed]
  44. Pancreatic triglyceride lipase and colipase: insights into dietary fat digestion. Lowe, M.E. Gastroenterology (1994) [Pubmed]
  45. Personal historical chronicle of six decades of basic and applied research in virology, immunology, and vaccinology. Hilleman, M.R. Immunol. Rev. (1999) [Pubmed]
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