22
results
for author:"Korn B."
in Literature Citations
| Ubc9 fusion-directed SUMOylation identifies constitutive and inducible SUMOylation. Jakobs A., Himstedt F., Funk M., Korn B., Gaestel M., Niedenthal R. Nucleic Acids Res. 35:E109-E109(2007) · UniProtKB (6) |
| An anthropoid-specific segmental duplication on human chromosome 1q22. Kuryshev V.Y., Vorobyov E., Zink D., Schmitz J., Rozhdestvensky T.S., Muenstermann E., Ernst U., Wellenreuther R., Moosmayer P., Bechtel S. et al. |
| A human protein-protein interaction network: a resource for annotating the proteome. Stelzl U., Worm U., Lalowski M., Haenig C., Brembeck F.H., Goehler H., Stroedicke M., Zenkner M., Schoenherr A., Koeppen S. et al. Cell 122:957-968(2005) · Mapped (14) |
| An endoribonuclease-prepared siRNA screen in human cells identifies genes essential for cell division. Kittler R., Putz G., Pelletier L., Poser I., Heninger A.-K., Drechsel D., Fischer S., Konstantinova I., Habermann B., Grabner H. et al. Nature 432:1036-1040(2004) · UniProtKB (1) |
| The oxidized subunit B8 from human complex I adopts a thioredoxin fold. Brockmann C., Diehl A., Rehbein K., Strauss H., Schmieder P., Korn B., Kuhne R., Oschkinat H. Structure 12:1645-1654(2004) · UniProtKB (1) |
| Analysis of CREM-dependent gene expression during mouse spermatogenesis. Beissbarth T., Borisevich I., Horlein A., Kenzelmann M., Hergenhahn M., Klewe-Nebenius A., Klaren R., Korn B., Schmid W., Vingron M. et al. Mol. Cell. Endocrinol. 212:29-39(2003) · Mapped (11) |
| SREBP cleavage-activating protein (SCAP) is required for increased lipid synthesis in liver induced by cholesterol deprivation and insulin elevation. Matsuda M., Korn B.S., Hammer R.E., Moon Y.-A., Komuro R., Horton J.D., Goldstein J.L., Brown M.S., Shimomura I. Genes Dev. 15:1206-1216(2001) · UniProtKB (1) |
| Pbx4, a new Pbx family member on mouse chromosome 8 is expressed during spermatogenesis. Wagner K., Mincheva A., Korn B., Lichter P., Poepperl H. |
| Characterization of a cluster of human high/ultrahigh sulfur keratin-associated protein genes embedded in the type I keratin gene domain on chromosome 17q12-21. Rogers M.A., Langbein L., Winter H., Ehmann C., Praetzel S., Korn B., Schweizer J. J. Biol. Chem. 276:19440-19451(2001) · UniProtKB (28) |
| Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. Wiemann S., Weil B., Wellenreuther R., Gassenhuber J., Glassl S., Ansorge W., Boecher M., Bloecker H., Bauersachs S., Blum H. et al. Genome Res. 11:422-435(2001) · UniProtKB (471) |
| Blunted feedback suppression of SREBP processing by dietary cholesterol in transgenic mice expressing sterol-resistant SCAP(D443N). Korn B.S., Shimomura I., Bashmakov Y., Hammer R.E., Horton J.D., Goldstein J.L., Brown M.S. J. Clin. Invest. 102:2050-2060(1998) · UniProtKB (1) |
| Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome. Dahmane N., Ait-Ghezala G., Gosset P., Chamoun Z., Dufresne-Zacharia M.-C., Lopes C., Rabatel N., Gassanova-Maugenre S., Chettouh Z., Abramowski V. et al. Genomics 48:12-23(1998) · UniProtKB (9) |
| APM-1, a novel human gene, identified by aberrant co-transcription with papillomavirus oncogenes in a cervical carcinoma cell line, encodes a BTB/POZ-zinc finger protein with growth inhibitory activity. Reuter S., Bartelmann M., Vogt M., Geisen C., Napierski I., Kahn T., Delius H., Lichter P., Weitz S., Korn B. et al. EMBO J. 17:215-222(1998) · UniProtKB (3) |
| A new inward rectifier potassium channel gene (KCNJ15) localized on chromosome 21 in the Down syndrome chromosome region 1 (DCR1). Gosset P., Ghezala G.A., Korn B., Yaspo M.-L., Poutska A., Lehrach H., Sinet P.-M., Creau N. |
| DMBT1, a new member of the SRCR superfamily on chromosome 10q25.3-q26.1 is deleted in malignant brain tumours. Mollenhauer J., Wiemann S., Scheurlen W., Korn B., Hayashi Y., Wilgenbus K.K., von Deimling A., Poustka A. Nat. Genet. 17:32-39(1997) · UniProtKB (1) |
| The genomic organization of a human creatine transporter (CRTR) gene located in Xq28. Sandoval N., Bauer D., Brenner V., Coy J.F., Drescher B., Kioschis P., Korn B., Nyakatura G., Poustka A., Reichwald K. et al. Genomics 35:383-385(1996) · UniProtKB (1) |
| Construction of a transcription map of a 300 kb region around the human G6PD locus by direct cDNA selection. Sedlacek Z., Korn B., Konecki D.S., Siebenhaar R., Coy J.F., Kioschis P., Poustka A. Hum. Mol. Genet. 2:1865-1869(1993) · UniProtKB (1) |
| MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. Vits L., van Camp G., Coucke P., Fransen E., de Boulle K., Reyniers E., Korn B., Poustka A., Wilson G., Schrander-Stumpel C. et al. Nat. Genet. 7:408-413(1994) · UniProtKB (1) |
| Evolutionary conservation and genomic organization of XAP-4, an Xq28 located gene coding for a human rab GDP-dissociation inhibitor (GDI). Sedlacek Z., Konecki D.S., Korn B., Klauck S.M., Poustka A. Mamm. Genome 5:633-639(1994) · UniProtKB (1) |
| The mouse homologue of the tuberin gene (TSC2) maps to a conserved synteny group between mouse chromosome 17 and human 16p13.3. Olsson P.G., Sutherland H.F., Nowicka U., Korn B., Poustka A., Frischauf A.M. Genomics 25:339-340(1995) · Mapped (11) |
| A gene (PEX) with homologies to endopeptidases is mutated in patients with X-linked hypophosphatemic rickets. The HYP consortium |
| Expression patterns of two human genes coding for different rab GDP-dissociation inhibitors (GDIs), extremely conserved proteins involved in cellular transport. Bachner D., Sedlacek Z., Korn B., Hameister H., Poustka A. Hum. Mol. Genet. 4:701-708(1995) · UniProtKB (2) · Mapped (10) |
