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Radiation Hybrid Mapping

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Disease relevance of Radiation Hybrid Mapping


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Biological context of Radiation Hybrid Mapping


Anatomical context of Radiation Hybrid Mapping


Associations of Radiation Hybrid Mapping with chemical compounds


Gene context of Radiation Hybrid Mapping


Analytical, diagnostic and therapeutic context of Radiation Hybrid Mapping


  1. A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci. Richard, C.W., Withers, D.A., Meeker, T.C., Maurer, S., Evans, G.A., Myers, R.M., Cox, D.R. Am. J. Hum. Genet. (1991) [Pubmed]
  2. A radiation hybrid map of 15 loci on the distal long arm of chromosome 4, the region containing the gene responsible for facioscapulohumeral muscular dystrophy (FSHD). Winokur, S.T., Schutte, B., Weiffenbach, B., Washington, S.S., McElligott, D., Chakravarti, A., Wasmuth, J.H., Altherr, M.R. Am. J. Hum. Genet. (1993) [Pubmed]
  3. Indication for linkage of the human OB gene region with extreme obesity. Clement, K., Garner, C., Hager, J., Philippi, A., LeDuc, C., Carey, A., Harris, T.J., Jury, C., Cardon, L.R., Basdevant, A., Demenais, F., Guy-Grand, B., North, M., Froguel, P. Diabetes (1996) [Pubmed]
  4. Characterization of mouse Frizzled-3 expression in hair follicle development and identification of the human homolog in keratinocytes. Hung, B.S., Wang, X.Q., Cam, G.R., Rothnagel, J.A. J. Invest. Dermatol. (2001) [Pubmed]
  5. Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes. Maiti, A.K., Mattéi, M.G., Jorissen, M., Volz, A., Zeigler, A., Bouvagnet, P. Eur. J. Hum. Genet. (2000) [Pubmed]
  6. Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats. Aitman, T.J., Glazier, A.M., Wallace, C.A., Cooper, L.D., Norsworthy, P.J., Wahid, F.N., Al-Majali, K.M., Trembling, P.M., Mann, C.J., Shoulders, C.C., Graf, D., St Lezin, E., Kurtz, T.W., Kren, V., Pravenec, M., Ibrahimi, A., Abumrad, N.A., Stanton, L.W., Scott, J. Nat. Genet. (1999) [Pubmed]
  7. A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Semina, E.V., Ferrell, R.E., Mintz-Hittner, H.A., Bitoun, P., Alward, W.L., Reiter, R.S., Funkhauser, C., Daack-Hirsch, S., Murray, J.C. Nat. Genet. (1998) [Pubmed]
  8. A 1-Mb resolution radiation hybrid map of the canine genome. Guyon, R., Lorentzen, T.D., Hitte, C., Kim, L., Cadieu, E., Parker, H.G., Quignon, P., Lowe, J.K., Renier, C., Gelfenbeyn, B., Vignaux, F., DeFrance, H.B., Gloux, S., Mahairas, G.G., André, C., Galibert, F., Ostrander, E.A. Proc. Natl. Acad. Sci. U.S.A. (2003) [Pubmed]
  9. A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies). Kalaydjieva, L., Perez-Lezaun, A., Angelicheva, D., Onengut, S., Dye, D., Bosshard, N.U., Jordanova, A., Savov, A., Yanakiev, P., Kremensky, I., Radeva, B., Hallmayer, J., Markov, A., Nedkova, V., Tournev, I., Aneva, L., Gitzelmann, R. Am. J. Hum. Genet. (1999) [Pubmed]
  10. A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32. Varret, M., Rabès, J.P., Saint-Jore, B., Cenarro, A., Marinoni, J.C., Civeira, F., Devillers, M., Krempf, M., Coulon, M., Thiart, R., Kotze, M.J., Schmidt, H., Buzzi, J.C., Kostner, G.M., Bertolini, S., Pocovi, M., Rosa, A., Farnier, M., Martinez, M., Junien, C., Boileau, C. Am. J. Hum. Genet. (1999) [Pubmed]
  11. Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome. Wassif, C.A., Maslen, C., Kachilele-Linjewile, S., Lin, D., Linck, L.M., Connor, W.E., Steiner, R.D., Porter, F.D. Am. J. Hum. Genet. (1998) [Pubmed]
  12. Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype. Cerosaletti, K.M., Lange, E., Stringham, H.M., Weemaes, C.M., Smeets, D., Sölder, B., Belohradsky, B.H., Taylor, A.M., Karnes, P., Elliott, A., Komatsu, K., Gatti, R.A., Boehnke, M., Concannon, P. Am. J. Hum. Genet. (1998) [Pubmed]
  13. An ordered comparative map of the cattle and human genomes. Band, M.R., Larson, J.H., Rebeiz, M., Green, C.A., Heyen, D.W., Donovan, J., Windish, R., Steining, C., Mahyuddin, P., Womack, J.E., Lewin, H.A. Genome Res. (2000) [Pubmed]
  14. cDNA cloning and characterization of sciellin, a LIM domain protein of the keratinocyte cornified envelope. Champliaud, M.F., Burgeson, R.E., Jin, W., Baden, H.P., Olson, P.F. J. Biol. Chem. (1998) [Pubmed]
  15. ARHI is the center of allelic deletion on chromosome 1p31 in ovarian and breast cancers. Peng, H., Xu, F., Pershad, R., Hunt, K.K., Frazier, M.L., Berchuck, A., Gray, J.W., Hogg, D., Bast, R.C., Yu, Y. Int. J. Cancer (2000) [Pubmed]
  16. Construction of a BAC contig map of chromosome 16q by two-dimensional overgo hybridization. Han, C.S., Sutherland, R.D., Jewett, P.B., Campbell, M.L., Meincke, L.J., Tesmer, J.G., Mundt, M.O., Fawcett, J.J., Kim, U.J., Deaven, L.L., Doggett, N.A. Genome Res. (2000) [Pubmed]
  17. Localization of the fast skeletal muscle troponin I gene (TNNI2) to 11p15.5: genes for troponin I and T are organized in pairs. Barton, P.J., Townsend, P.J., Brand, N.J., Yacoub, M.H. Ann. Hum. Genet. (1997) [Pubmed]
  18. Molecular cloning and chromosomal mapping of olfactory receptor genes expressed in the male germ line: evidence for their wide distribution in the human genome. Vanderhaeghen, P., Schurmans, S., Vassart, G., Parmentier, M. Biochem. Biophys. Res. Commun. (1997) [Pubmed]
  19. Sequence characterization, polymorphism and chromosomal localizations of the porcine PSME1 and PSME2 genes. Wang, Y.F., Yu, M., te Pas, M.F., Yerle, M., Liu, B., Fan, B., Xiong, T.A., Li, K. Anim. Genet. (2004) [Pubmed]
  20. Cloning, expression, and characterization of a human inosine triphosphate pyrophosphatase encoded by the itpa gene. Lin, S., McLennan, A.G., Ying, K., Wang, Z., Gu, S., Jin, H., Wu, C., Liu, W., Yuan, Y., Tang, R., Xie, Y., Mao, Y. J. Biol. Chem. (2001) [Pubmed]
  21. Radiation hybrid mapping of genes in the lithium-sensitive wnt signaling pathway. Rhoads, A.R., Karkera, J.D., Detera-Wadleigh, S.D. Mol. Psychiatry (1999) [Pubmed]
  22. Mapping of 228 ESTs and 26 genes into an integrated physical and genetic map of human chromosome 17. Plummer, S.J., Simmons, J.A., Adams, L., Casey, G. Genomics (1997) [Pubmed]
  23. Evolution and expression of D2 and D3 dopamine receptor genes in zebrafish. Boehmler, W., Obrecht-Pflumio, S., Canfield, V., Thisse, C., Thisse, B., Levenson, R. Dev. Dyn. (2004) [Pubmed]
  24. Refined localisation of the genes for nebulin and titin on chromosome 2q allows the assignment of nebulin as a candidate gene for autosomal recessive nemaline myopathy. Pelin, K., Ridanpää, M., Donner, K., Wilton, S., Krishnarajah, J., Laing, N., Kolmerer, B., Millevoi, S., Labeit, S., de la Chapelle, A., Wallgren-Petterson, C. Eur. J. Hum. Genet. (1997) [Pubmed]
  25. A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32. Dixon, J., Gladwin, A.J., Loftus, S.K., Riley, J.H., Perveen, R., Wasmuth, J.J., Anand, R., Dixon, M.J. Am. J. Hum. Genet. (1994) [Pubmed]
  26. A candidate mammalian DNA methyltransferase related to pmt1p of fission yeast. Yoder, J.A., Bestor, T.H. Hum. Mol. Genet. (1998) [Pubmed]
  27. Cloning and characterization of a novel human histone deacetylase, HDAC8. Buggy, J.J., Sideris, M.L., Mak, P., Lorimer, D.D., McIntosh, B., Clark, J.M. Biochem. J. (2000) [Pubmed]
  28. Structure, chromosomal location, and tissue-specific expression of the mouse opticin gene. Takanosu, M., Boyd, T.C., Le Goff, M., Henry, S.P., Zhang, Y., Bishop, P.N., Mayne, R. Invest. Ophthalmol. Vis. Sci. (2001) [Pubmed]
  29. Cloning and mapping of human PKIB and PKIG, and comparison of tissue expression patterns of three members of the protein kinase inhibitor family, including PKIA. Zheng, L., Yu, L., Tu, Q., Zhang, M., He, H., Chen, W., Gao, J., Yu, J., Wu, Q., Zhao, S. Biochem. J. (2000) [Pubmed]
  30. Refined chromosomal localization of the mismatch repair and hereditary nonpolyposis colorectal cancer genes hMSH2 and hMSH6. Schmutte, C., Marinescu, R.C., Copeland, N.G., Jenkins, N.A., Overhauser, J., Fishel, R. Cancer Res. (1998) [Pubmed]
  31. The human vitamin D receptor gene (VDR) is localized to region 12cen-q12 by fluorescent in situ hybridization and radiation hybrid mapping: genetic and physical VDR map. Taymans, S.E., Pack, S., Pak, E., Orban, Z., Barsony, J., Zhuang, Z., Stratakis, C.A. J. Bone Miner. Res. (1999) [Pubmed]
  32. Cloning of STK13, a third human protein kinase related to Drosophila aurora and budding yeast Ipl1 that maps on chromosome 19q13.3-ter. Bernard, M., Sanseau, P., Henry, C., Couturier, A., Prigent, C. Genomics (1998) [Pubmed]
  33. Molecular cloning, expression and radiation hybrid mapping of the bovine deiodinase type II (DIO2) and deiodinase type III (DIO3) genes. Connor, E.E., Laiakis, E.C., Fernandes, V.M., Williams, J.L., Capuco, A.V. Anim. Genet. (2005) [Pubmed]
  34. Comparative sequence analysis and radiation hybrid mapping of the canine keratin 10 gene. Minor, J., Dunstan, R., Guyon, R., André, C., Barnhart, K., Credille, K. DNA Seq. (2005) [Pubmed]
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