Human Molecular Genetics, 0964-6906

Tidskrift

Fler filtreringsmöjligheter
  1. 2007
  2. 2006
  3. Cholinergic neuronal defect without cell loss in Huntington's disease.

    Ruben Smith, Chung, H., Rundquist, S., Maat-Schieman, M. L. C., Colgan, L., Elisabet Englund, Liu, Y-J., Roos, R. A. C., Faull, R. L. M., Brundin, P. & Jia-Yi Li, 2006, I : Human Molecular Genetics. 15, 21, s. 3119-3131

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  4. MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene

    Storlazzi, CT., Fioretos, T., Surace, C., Lonoce, A., Mastrorilli, A., Strömbeck, B., D'Addabbo, P., Iacovelli, F., Minervini, C., Aventin, A., Dastugue, N., Fonatsch, C., Hagemeijer, A., Jotterand, M., Muhlematter, D., Lafage-Pochitaloff, M., Nguyen-Khac, F., Schoch, C., Slovak, ML., Smith, A. & 4 andra, Sole, F., Van Roy, N., Bertil Johansson & Rocchi, M., 2006, I : Human Molecular Genetics. 15, 6, s. 933-942

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  5. Progressive alterations in the hypothalamic-pituitary-adrenal axis in the R6/2 transgenic mouse model of Huntington's disease

    Maria Björkqvist, Åsa Petersén, Karl Bacos, Isaacs, J., Norlén, P., Gil, J., Popovic, N., Sundler, F., Bates, GP., Tabrizi, SJ., Brundin, P. & Hindrik Mulder, 2006, I : Human Molecular Genetics. 15, 10, s. 1713-1721

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  6. 2005
  7. Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22

    Parsons, C. A., Mroczkowski, H. J., Fiona E A McGuigan, Albagha, O. M. E., Manolagas, S., Reid, D. M., Ralston, S. H. & Shmookler Reis, R. J., 2005 nov 1, I : Human Molecular Genetics. 14, 21, s. 3141-8 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  8. Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophy

    Baker, N. L., Mörgelin, M., Peat, R., Goemans, N., North, K. N., Bateman, J. F. & Lamande, S. R., 2005, I : Human Molecular Genetics. 14, 2, s. 279-293

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  9. Orexin loss in Huntington's disease.

    Åsa Petersén, Gil, J., Maat-Schieman, M. L. C., Maria Björkqvist, Tanila, H., Araújo, I. M., Ruben Smith, Popovic, N., Nils Wierup, Norlén, P., Jia-Yi Li, Roos, R. A., Sundler, F., Hindrik Mulder & Brundin, P., 2005, I : Human Molecular Genetics. 14, 1, s. 39-47

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  10. The R6/2 transgenic mouse model of Huntington's disease develops diabetes due to deficient {beta}-cell mass and exocytosis.

    Maria Björkqvist, Malin Fex, Erik Renström, Nils Wierup, Åsa Petersén, Gil, J., Karl Bacos, Popovic, N., Jia-Yi Li, Sundler, F., Brundin, P. & Hindrik Mulder, 2005, I : Human Molecular Genetics. 14, 5, s. 565-574

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  11. Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome

    Nuber, U., Kriaucionis, S., Roloff, T. C., Guy, J., Selfridge, J., Steinhoff, C., Schulz, R., Lipkowitz, B., Ropers, H. H., Holmes, M. C. & Bird, A., 2005, I : Human Molecular Genetics. 14, 15, s. 2247-2256

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  12. 2004
  13. Laminin {alpha}1 chain reduces muscular dystrophy in laminin {alpha}2 chain deficient mice.

    Kinga Gawlik, Miyagoe-Suzuki, Y., Ekblom, P., Takeda, S. & Madeleine Durbeej-Hjalt, 2004, I : Human Molecular Genetics. 13, 16, s. 1775-1784

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  14. Meta-analysis of genome-wide scans for hypertension and blood pressure in Caucasians shows evidence of susceptibility regions on chromosomes 2 and 3.

    Koivukoski, L., Fisher, S. A., Kanninen, T., Lewis, C. M., Wowern, F., Hunt, S., Kardia, S. L. R., Levy, D., Perola, M., Rankinen, T., Rao, D. C., Rice, T., Thiel, B. A. & Olle Melander, 2004, I : Human Molecular Genetics. 13, 19, s. 2325-2332

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  15. 2003
  16. Fusion of the FUS and BBF2H7 genes in low grade fibromyxoid sarcoma

    Storlazzi, T., Fredrik Mertens, Nascimento, A., Isaksson, M., Wejde, J., Brosjo, O., Nils Mandahl & Panagopoulos, I., 2003 sep 15, I : Human Molecular Genetics. 12, 18, s. 2349-2358 10 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  17. A genome wide scan for early onset primary hypertension in Scandinavians.

    von Wowern, F., Kristina Bengtsson Boström, Lindgren, C., Marju Orho-Melander, Fyhrquist, F., Lindblad, U., Lennart Råstam, Forsblom, C., Kanninen, T., Almgren, P., Burri, P., Katzman, P., Leif Groop, Hulthén, U. L. & Olle Melander, 2003, I : Human Molecular Genetics. 12, 16, s. 2077-2081

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  18. A meta-analysis of four European genome screens (GIFT Consortium) shows evidence for a novel region on chromosome 17p11.2-q22 linked to type 2 diabetes.

    Demenais, F., Kanninen, T., Lindgren, C., Wiltshire, S., Gaget, S., Dandrieux, C., Almgren, P., Marketa Sjögren, Hattersley, A., Dina, C., Tuomi, T., McCarthy, M. I., Froguel, P. & Leif Groop, 2003, I : Human Molecular Genetics. 12, 15, s. 1865-1873

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  19. Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to disease

    Bomprezzi, R., Markus Ringnér, Kim, S., Bittner, ML., Khan, J., Chen, YD., Elkahloun, A., Yu, AM., Bielekova, B., Meltzer, PS., Martin, R., McFarland, HF. & Trent, JM., 2003, I : Human Molecular Genetics. 12, 17, s. 2191-2199

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  20. High resolution mapping of an arthritis susceptibility locus on rat chromosome 4, and characterization of regulated phenotypes

    Ribbhammar, U., Flornes, L., Backdahl, L., Holger Luthman, Fossum, S. & Lorentzen, JC., 2003, I : Human Molecular Genetics. 12, 17, s. 2087-2096

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  21. 2002
  22. Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women

    Albagha, O. M. E., Tasker, P. N., Fiona E A McGuigan, Reid, D. M. & Ralston, S. H., 2002 sep 15, I : Human Molecular Genetics. 11, 19, s. 2289-95

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  23. A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.

    Buckley, P. G., Mantripragada, K. K., Benetkiewicz, M., Tapia-Páez, I., Diaz De Ståhl, T., Rosenquist, M., Ali, H., Jarbo, C., De Bustos, C., Hirvelä, C., Sinder Wilén, B., Fransson, I., Thyr, C., Johnsson, B-I., Bruder, C. E. G., Menzel, U., Hergersberg, M., Mandahl, N., Blennow, E., Wedell, A. & 11 andra, Beare, D. M., Collins, J. E., Dunham, I., Albertson, D., Pinkel, D., Bastian, B. C., Faruqi, A. F., Lasken, R. S., Ichimura, K., Collins, V. P. & Dumanski, J. P., 2002, I : Human Molecular Genetics. 11, 25, s. 3221-3229

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  24. Impaired dopamine storage resulting from alpha-synuclein mutations may contribute to the pathogenesis of Parkinson's disease.

    Lotharius, J. & Brundin, P., 2002, I : Human Molecular Genetics. 11, 20, s. 2395-2407

    Forskningsoutput: TidskriftsbidragÖversiktsartikel

  25. 2001
  26. Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families

    J Vallon-Christersson, Cayanan, C., Haraldsson, K., N Loman, Bergthorsson, J. T., Brøndum-Nielsen, K., Gerdes, A. M., Møller, P., U Kristoffersson, Håkan Olsson, Åke Borg & Monteiro, A. N., 2001 feb 15, I : Human Molecular Genetics. 10, 4, s. 353-60 8 s.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  27. DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis

    Esteller, M., Fraga, M. F., Guo, M., Garcia-Foncillas, J., Hedenfalk, I., Godwin, A. K., Trojan, J., Vaurs-Barriere, C., Bignon, Y-J., Ramus, S., Benitez, J., Caldes, T., Akiyama, Y., Yuasa, Y., Launonen, V., Canal, M. J., Rodriguez, R., Capella, G., Peinado, M. A., Borg, Å. & 4 andra, Aaltonen, L. A., Ponder, B. A., Baylin, S. B. & Herman, J. G., 2001, I : Human Molecular Genetics. 10, 26, s. 3001-3007

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  28. Expanded CAG repeats in exon 1 of the Huntington's disease gene stimulate dopamine-mediated striatal neuron autophagy and degeneration

    Åsa Petersén, Larsen, K. E., Behr, G. G., Romero, N., Przedborski, S., Brundin, P. & Sulzer, D., 2001, I : Human Molecular Genetics. 10, 12, s. 1243-1254

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  29. Fusion of the MORF and CBP genes in acute myeloid leukemia with the t(10;16)(q22;p13)

    Panagopoulos, I., Thoas Fioretos, Isaksson, M., Samuelsson, U., Billström, R., Strömbeck, B., Felix Mitelman & Bertil Johansson, 2001, I : Human Molecular Genetics. 10, 4, s. 395-404

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift