Browse by Journal Title

2009

ASTD: The Alternative Splicing and Transcript Diversity database.
Koscielny, G., Texier, V.L., Gopalakrishnan, C., Kumanduri, V., Riethoven, J.J., Nardone, F., Stanley, E., Fallsehr, C., Hofmann, O., Kull, M., Harrington, E., Boue, S., Eyras, E., Plass, M., Lopez, F., Ritchie, W., Moucadel, V., Ara, T., Pospisil, H., Herrmann, A., Reich, J.G., Guigo, R., Bork, P., Doeberitz, M.V., Vilo, J., Hide, W., Apweiler, R., Thanaraj, T.A. and Gautheret, D.
Genomics 93 (3): 213-220. March 2009

2008

Combinatorial effects of four histone modifications in transcription and differentiation.
Fischer, J.J., Toedling, J., Krueger, T., Schueler, M., Huber, W. and Sperling, S.
Genomics 91 (1): 41-51. January 2008

2007

A cross-species comparison of X-chromosome inactivation in Eutheria.
Yen, Z.C., Meyer, I.M., Karalic, S. and Brown, C.J.
Genomics 90 (4): 453-463. October 2007

Genomic organization of transcriptomes in mammals: Coregulation and cofunctionality.
Purmann, A., Toedling, J., Schueler, M., Carninci, P., Lehrach, H., Hayashizaki, Y., Huber, W. and Sperling, S.
Genomics 89 (5): 580-587. May 2007

2006

Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes.
Ruf, N., Duenzinger, U., Brinckmann, A., Haaf, T., Nuernberg, P. and Zechner, U.
Genomics 87 (4): 509-519. April 2006

2003

High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases.
Herbon, N., Werner, M., Braig, C., Gohlke, H., Dütsch, G., Illig, T., Altmüller, J., Hampe, J., Lantermann, A., Schreiber, S., Bonifacio, E., Ziegler, A., Schwab, S., Wildenauer, D., van den Boom, D., Braun, A., Knapp, M., Reitmeir, P. and Wjst, M.
Genomics 81 (5): 510-8. May 2003

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia.
Ciccarelli, F.D., Proukakis, C., Patel, H., Cross, H., Azam, S., Patton, M.A., Bork, P. and Crosby, A.H.
Genomics 81 (4): 437-441. April 2003

2001

Identification and localization of a new human myotubularin-related protein gene, mtmr8, on 8p22-p23.
Appel, S., Reichwald, K., Zimmermann, W., Reis, A., Rosenthal, A. and Hennies, H.C.
Genomics 75 (1-3): 6-8. July 2001

Molecular characterization of a cDNA encoding functional human CLK4 kinase and localization to chromosome 5q35 [correction of 4q35].
Schultz, J., Jones, T., Bork, P., Sheer, D., Blencke, S., Steyrer, S., Wellbrock, U., Bevec, D., Ullrich, A. and Wallasch, C.
Genomics 71 : 368-370. 1 February 2001

Refinement of the gene locus for autosomal dominant medullary cystic kidney disease type 1 (MCKD1) and construction of a physical and partial transcriptional map of the region.
Fuchshuber, A., Kroiss, S., Karle, S., Berthold, S., Huck, K., Burton, C., Rahman, N., Koptides, M., Deltas, C., Otto, E., Rueschendorf, F., Feest, T. and Hildebrandt, F.
Genomics 72 (3): 278-284. 1 January 2001

2000

High-throughput scanning of the rat genome using interspersed repetitive sequence-PCR markers.
Gosele, C., Hong, L., Kreitler, T., Rossmann, M., Hieke, B., Gross, U., Kramer, M., Himmelbauer, H., Bihoreau, M.T., Kwitek-Black, A.E., Twigger, S., Tonellato, P.J., Jacob, H.J., Schalkwyk, L.C., Lindpaintner, K., Ganten, D., Lehrach, H. and Knoblauch, M.
Genomics 69 (3): 287-294. 1 November 2000

A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions.
Jenne, D.E., Tinschert, S., Stegmann, E., Reimann, H., Nuernberg, P., Horn, D., Naumann, I., Buske, A. and Thiel, G.
Genomics 66 : 93-97. 15 May 2000

1999

Mutation in the beta A3/A1-crystallin encoding geneCryba1 causes a dominant cataract in the mouse.
Graw, J., Jung, M., Loester, J., Klopp, N., Soewarto, D., Fella, C., Fuchs, H., Reis, A., Wolf, E., Balling, R. and de Angelis, M.H.
Genomics 62 (1): 67-73. 15 November 1999

Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): The integration of genetic and physical maps of the TOC region on 17q25.
Risk, J.M., Ruhrberg, C., Hennies, H.C., Mills, H.S., Di Colandrea, T., Evans, K.E., Ellis, A., Watt, F.M., Bishop, D.T., Spurr, N.K., Stevens, H.P., Leigh, I.M., Reis, A., Kelsell, D.P. and Field, J.K.
Genomics 59 : 234-242. 15 July 1999

A genome-wide search for linkage to asthma.
Wjst, M., Fischer, G., Immervoll, T., Jung, M., Saar, K., Rueschendorf, F., Reis, A., Ulbrecht, M., Gomolka, M., Weiss, E.H., Jaeger, L., Nickel, R., Richter, K., Kjellman, N.I.M., Griese, M., von Berg, A., Gappa, M., Riedel, F., Boehle, M., van Koningsbruggen, S., Schoberth, P., Szczepanski, R., Dorsch, W., Silbermann, M., Loesgen, S., Scholz, M., Bickeboller, H. and Wichmann, H.E.
Genomics 58 (1): 1-8. 15 May 1999

Fine-structure mapping of the hereditary inclusion body myopathy locus.
Eisenberg, I., Thiel, C., Levi, T., Tiram, E., Argov, Z., Sadeh, M., Jackson, C.L., Thierfelder, L. and Mitrani-Rosenbaum, S.
Genomics 55 : 43-48. 1 January 1999

1998

Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2.
Zechner, U., Scheel, S., Hemberger, M., Hopp, M., Haaf, T., Fundele, R., Wanker, E.E., Lehrach, H., Wedemeyer, N. and Himmelbauer, H.
Genomics 54 : 505-510. 15 December 1998

Genomic organization of a 225-kb region in Xq28 containing the gene for X-linked myotubular myopathy (MTM1) and a related gene (MTMR1).
Kioschis, P., Wiemann, S., Heiss, N.S., Francis, F., Goetz, C., Poustka, A., Taudien, S., Platzer, M., Wiehe, T., Beckmann, G., Weber, J., Nordsiek, G. and Rosenthal, A.
Genomics 54 : 256-266. 1 December 1998

EDG6, a novel G-protein-coupled receptor related to receptors for bioactive lysophospholipids, is specifically expressed in lymphoid tissue.
Graeler, M.H., Bernhardt, G. and Lipp, M.
Genomics 53 (2): 164-169. 15 October 1998

The linked human elongation initiation factor 4A1 (EIF4A1) and CD68 genes map to chromosome 17p13.
Jones, E., Quinn, C.M., See, C.G., Montgomery, D.S., Ford, M.J., Koelble, K., Gordon, S. and Greaves, D.R.
Genomics 53 : 248-250. 15 October 1998

Assignment of the gene encoding the core promoter element binding protein (COPEB) to human chromosome 10p15 by somatic hybrid analysis and fluorescence in situ hybridization.
Onyango, P., Koritschoner, N.P., Patrito, L.C., Zenke, M. and Weith, A.
Genomics 48 : 143-144. 1 January 1998

1997

Localization of the human HIP1 gene close to the elastin (ELN) locus on 7q11.23.
Wedemeyer, N., Peoples, R., Himmelbauer, H., Lehrach, H., Francke, U. and Wanker, E.E.
Genomics 46 : 313-315. 1 December 1997

Construction and characterization of a 10 genome equivalent yeast artificial chromosome library for the laboratory rat, rattus norvegicus.
Cai, L., Schalkwyk, L.C., Schoeberleinstehli, A., Zee, R.Y.L., Smith, A., Haaf, T., Georges, M., Lehrach, H. and Lindpaintner, K.
Genomics 39 : 385-392. 1 January 1997

The reticulocalbindin gene maps to the WAGR region in man and to the small eye Harwell deletion in mouse.
Kent, J., Lee, M., Schedl, A., Boyle, S., Fantes, J., Powell, N.M., Rushmere, N., Abbott, C., van Heyningen, V. and Bickmore, W.
Genomics 42 : 260-267. 1 January 1997

Similar organization of the lipopolysaccharide-binding protein (LBP) and phospholipid transfer protein (PLTP) genes suggests a common gene family of lipid-binding proteins.
Kirschning, C., Au-Young, J., Lamping, N., Reuter, D., Pfeil, D., Seilhamer, J.J. and Schumann, R.R.
Genomics 46 : 416-425. 1 January 1997

1996

Structure of the human CD97 gene: exon shuffling has generated a new type of seven-span transmembrane molecule related to the secretin receptor superfamily.
Hamann, J., Hartmann, E. and van Lier, R.
Genomics 32 : 144-147. 1 January 1996

1995

Palmoplantar keratoderma in association with carcinoma of the esophagus maps to chromosome 17q distal to the keratin gene cluster.
Hennies, H.C., Hagedorn, M. and Reis, A.
Genomics 29 : 537-540. 20 September 1995

Fructose-1,6-bisphosphatase: Genetic and physical mapping to human chromosome 9q22.3 and evaluation in non-insulin-dependent diabetes mellitus.
Rothschild, C.B., Freedman, B.I., Hodge, R., Rao, P.N., Pettenati, M.J., Anderson, R.A., Akots, G., Qadri, A., Roh, B., Fajans, S.S., Reis, A., Morris, D.J., Usala, A., Hayward, C., Brock, D., Colle, E., Spray, B.J., Rich, S.S. and Bowden, D.W.
Genomics 29 : 187-194. 1 September 1995

A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1.
Fantes, J.A., Oghene, K., Boyle, S., Danes, S., Fletcher, J.M., Bruford, E.A., Williamson, K., Seawright, A., Schedl, A., Hanson, I., Zehetner, G., Bhogal, R., Lehrach, H., Gregory, S., Williams, J., Little, P.F.R., Sellar, G.C., Hoovers, J., Mannens, M., Weissenbach, J., Junien, C., van Heyningen, V. and Bickmore, W.A.
Genomics 25 : 447-461. 1 January 1995

1994

Analysis of 133 meioses places the genes for nevoid basal cell carcinoma (Gorlin) syndrome and Fanconi anemia group C in a 2.6- cM interval and contributes to the fine map of 9q22.3.
Farndon, P.A., Morris, D.J., Hardy, C., McConville, C.M., Weissenbach, J., Kilpatrick, M.W. and Reis, A.
Genomics 23 : 486-489. 1 January 1994

Localization of the human beta-catenin gene (CTNNB1) to 3p21: A region implicated in tumor development.
Kraus, C., Liehr, T., Huelsken, J., Behrens, J., Birchmeier, W., Grzeschik, K.H. and Ballhausen, W.G.
Genomics 23 : 272-274. 1 January 1994

A YAC contig spanning the nevoid basal cell carcinoma syndrome, Fanconi anaemia group C, and xeroderma pigmentosum group A loci on chromosome 9q.
Morris, D.J. and Reis, A.
Genomics 23 : 23-29. 1 January 1994

Porcine (GT)n sequences: structure and association with dispersed and tandem repeats.
Wilke, K., Jung, M., Chen, Y. and Geldermann, H.
Genomics 21 : 63-70. 1 January 1994

1991

Sequences of junction fragments in the deletion-prone region of the dystrophin gene.
Love, D.R., England, S.B., Speer, A., Marsden, F.R., Bloomfield, J.F., Roche, A.L., Cross, G.S., Mountford, R.C., Smith, T.J. and Davies, K.E.
Genomics 10 : 57-67. 1 January 1991