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


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


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

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


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


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


Identification and localization of a new human myotubularin-related protein gene, mtmr8, on 8p22-p23.
Appel, S. and Reichwald, K. and Zimmermann, W. and Reis, A. and 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. and Jones, T. and Bork, P. and Sheer, D. and Blencke, S. and Steyrer, S. and Wellbrock, U. and Bevec, D. and 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. and Kroiss, S. and Karle, S. and Berthold, S. and Huck, K. and Burton, C. and Rahman, N. and Koptides, M. and Deltas, C. and Otto, E. and Rueschendorf, F. and Feest, T. and Hildebrandt, F.
Genomics 72 (3): 278-284. 1 January 2001


High-throughput scanning of the rat genome using interspersed repetitive sequence-PCR markers.
Gosele, C. and Hong, L. and Kreitler, T. and Rossmann, M. and Hieke, B. and Gross, U. and Kramer, M. and Himmelbauer, H. and Bihoreau, M.T. and Kwitek-Black, A.E. and Twigger, S. and Tonellato, P.J. and Jacob, H.J. and Schalkwyk, L.C. and Lindpaintner, K. and Ganten, D. and 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. and Tinschert, S. and Stegmann, E. and Reimann, H. and Nuernberg, P. and Horn, D. and Naumann, I. and Buske, A. and Thiel, G.
Genomics 66 : 93-97. 15 May 2000


Mutation in the beta A3/A1-crystallin encoding geneCryba1 causes a dominant cataract in the mouse.
Graw, J. and Jung, M. and Loester, J. and Klopp, N. and Soewarto, D. and Fella, C. and Fuchs, H. and Reis, A. and Wolf, E. and 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. and Ruhrberg, C. and Hennies, H.C. and Mills, H.S. and Di Colandrea, T. and Evans, K.E. and Ellis, A. and Watt, F.M. and Bishop, D.T. and Spurr, N.K. and Stevens, H.P. and Leigh, I.M. and Reis, A. and Kelsell, D.P. and Field, J.K.
Genomics 59 : 234-242. 15 July 1999

A genome-wide search for linkage to asthma.
Wjst, M. and Fischer, G. and Immervoll, T. and Jung, M. and Saar, K. and Rueschendorf, F. and Reis, A. and Ulbrecht, M. and Gomolka, M. and Weiss, E.H. and Jaeger, L. and Nickel, R. and Richter, K. and Kjellman, N.I.M. and Griese, M. and von Berg, A. and Gappa, M. and Riedel, F. and Boehle, M. and van Koningsbruggen, S. and Schoberth, P. and Szczepanski, R. and Dorsch, W. and Silbermann, M. and Loesgen, S. and Scholz, M. and 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. and Thiel, C. and Levi, T. and Tiram, E. and Argov, Z. and Sadeh, M. and Jackson, C.L. and Thierfelder, L. and Mitrani-Rosenbaum, S.
Genomics 55 : 43-48. 1 January 1999


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. and Scheel, S. and Hemberger, M. and Hopp, M. and Haaf, T. and Fundele, R. and Wanker, E.E. and Lehrach, H. and 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. and Wiemann, S. and Heiss, N.S. and Francis, F. and Goetz, C. and Poustka, A. and Taudien, S. and Platzer, M. and Wiehe, T. and Beckmann, G. and Weber, J. and 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. and 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. and Quinn, C.M. and See, C.G. and Montgomery, D.S. and Ford, M.J. and Koelble, K. and 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. and Koritschoner, N.P. and Patrito, L.C. and Zenke, M. and Weith, A.
Genomics 48 : 143-144. 1 January 1998


Localization of the human HIP1 gene close to the elastin (ELN) locus on 7q11.23.
Wedemeyer, N. and Peoples, R. and Himmelbauer, H. and Lehrach, H. and 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. and Schalkwyk, L.C. and Schoeberleinstehli, A. and Zee, R.Y.L. and Smith, A. and Haaf, T. and Georges, M. and 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. and Lee, M. and Schedl, A. and Boyle, S. and Fantes, J. and Powell, N.M. and Rushmere, N. and Abbott, C. and 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. and Au-Young, J. and Lamping, N. and Reuter, D. and Pfeil, D. and Seilhamer, J.J. and Schumann, R.R.
Genomics 46 : 416-425. 1 January 1997


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. and Hartmann, E. and van Lier, R.
Genomics 32 : 144-147. 1 January 1996


Palmoplantar keratoderma in association with carcinoma of the esophagus maps to chromosome 17q distal to the keratin gene cluster.
Hennies, H.C. and 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. and Freedman, B.I. and Hodge, R. and Rao, P.N. and Pettenati, M.J. and Anderson, R.A. and Akots, G. and Qadri, A. and Roh, B. and Fajans, S.S. and Reis, A. and Morris, D.J. and Usala, A. and Hayward, C. and Brock, D. and Colle, E. and Spray, B.J. and 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. and Oghene, K. and Boyle, S. and Danes, S. and Fletcher, J.M. and Bruford, E.A. and Williamson, K. and Seawright, A. and Schedl, A. and Hanson, I. and Zehetner, G. and Bhogal, R. and Lehrach, H. and Gregory, S. and Williams, J. and Little, P.F.R. and Sellar, G.C. and Hoovers, J. and Mannens, M. and Weissenbach, J. and Junien, C. and van Heyningen, V. and Bickmore, W.A.
Genomics 25 : 447-461. 1 January 1995


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. and Morris, D.J. and Hardy, C. and McConville, C.M. and Weissenbach, J. and 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. and Liehr, T. and Huelsken, J. and Behrens, J. and Birchmeier, W. and 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. and Jung, M. and Chen, Y. and Geldermann, H.
Genomics 21 : 63-70. 1 January 1994


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

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