1 - 25 of
38
results
for author:"Wiemann S."
in Literature Citations
| Modeling ERBB receptor-regulated G1/S transition to find novel targets for de novo trastuzumab resistance. Sahin O., Frohlich H., Lobke C., Korf U., Burmester S., Majety M., Mattern J., Schupp I., Chaouiya C., Thieffry D. et al. BMC Syst Biol 3:1-1(2009) · Mapped (15) |
| Norepinephrine transporter and catecholamine-O-methyltransferase gene variants and attention-deficit/hyperactivity disorder symptoms in adults. Retz W., Rosler M., Kissling C., Wiemann S., Hunnerkopf R., Coogan A., Thome J., Freitag C. J Neural Transm 115:323-329(2008) · Mapped (15) |
| The full-ORF clone resource of the German cDNA consortium. Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H. et al. BMC Genomics 8:399-399(2007) · UniProtKB (2,241) |
| A polymorphism at the 3'-untranslated region of the CLOCK gene is associated with adult attention-deficit hyperactivity disorder. Kissling C., Retz W., Wiemann S., Coogan A.N., Clement R.M., Hunnerkopf R., Conner A.C., Freitag C.M., Rosler M., Thome J. Am. J. Med. Genet. B Neuropsychiatr. Genet. 147:333-338(2008) · Mapped (7) |
| Reduced expression of vacuole membrane protein 1 affects the invasion capacity of tumor cells. Sauermann M., Sahin O., Sultmann H., Hahne F., Blaszkiewicz S., Majety M., Zatloukal K., Fuzesi L., Poustka A., Wiemann S. et al. Oncogene 27:1320-1326(2008) · Mapped (5) |
| Genetic association of the human corticotropin releasing hormone receptor 1 (CRHR1) with binge drinking and alcohol intake patterns in two independent samples. Treutlein J., Kissling C., Frank J., Wiemann S., Dong L., Depner M., Saam C., Lascorz J., Soyka M., Preuss U.W. et al. Mol. Psychiatry 11:594-602(2006) · Mapped (7) |
| 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. |
| The systematic functional characterisation of Xq28 genes prioritises candidate disease genes. Kolb-Kokocinski A., Mehrle A., Bechtel S., Simpson J.C., Kioschis P., Wiemann S., Wellenreuther R., Poustka A. BMC Genomics 7:29-29(2006) · UniProtKB (2) |
| Alternative pre-mRNA processing regulates cell-type specific expression of the IL4l1 and NUP62 genes. Wiemann S., Kolb-Kokocinski A., Poustka A. BMC Biol. 3:16-16(2005) · UniProtKB (2) |
| Gamma-BAR, a novel AP-1-interacting protein involved in post-Golgi trafficking. Neubrand V.E., Will R.D., Moebius W., Poustka A., Wiemann S., Schu P., Dotti C.G., Pepperkok R., Simpson J.C. EMBO J. 24:1122-1133(2005) · UniProtKB (2) |
| The cellular level of telomere dysfunction determines induction of senescence or apoptosis in vivo. Lechel A., Satyanarayana A., Ju Z., Plentz R.R., Schaetzlein S., Rudolph C., Wilkens L., Wiemann S.U., Saretzki G., Malek N.P. et al. EMBO Rep. 6:275-281(2005) · Mapped (10) |
| SMART amplification combined with cDNA size fractionation in order to obtain large full-length clones. German cDNA Consortium BMC Genomics 5:36-36(2004) · UniProtKB (1) |
| Frequent downregulation of DMBT1 and galectin-3 in epithelial skin cancer. Mollenhauer J., Deichmann M., Helmke B., Muller H., Kollender G., Holmskov U., Ligtenberg T., Krebs I., Wiemann S., Bantel-Schaal U. et al. Int. J. Cancer 105:149-157(2003) · Mapped (10) |
| No association of alcohol dependence with a NMDA-receptor 2B gene variant. Schumann G., Rujescu D., Szegedi A., Singer P., Wiemann S., Wellek S., Giegling I., Klawe C., Anghelescu I., Heinz A. et al. Mol. Psychiatry 8:11-12(2003) · Mapped (2) |
| The SRCR/SID region of DMBT1 defines a complex multi-allele system representing the major basis for its variability in cancer. Mollenhauer J., Mueller H., Kollender G., Lyer S., Diedrichs L., Helmke B., Holmskov U., Ligtenberg T., Herbertz S., Krebs I. et al. Genes Chromosomes Cancer 35:242-255(2002) · UniProtKB (1) · Mapped (4) |
| Sequential changes of the DMBT1 expression and location in normal lung tissue and lung carcinomas. Mollenhauer J., Helmke B., Muller H., Kollender G., Lyer S., Diedrichs L., Holmskov U., Ligtenberg T., Herbertz S., Krebs I. et al. Genes Chromosomes Cancer 35:164-169(2002) · Mapped (5) |
| Pore membrane and/or filament interacting like protein 1 (POMFIL1) is predominantly expressed in the nervous system and encodes different protein isoforms. Coy J.F., Wiemann S., Bechmann I., Baechner D., Nitsch R., Kretz O., Christiansen H., Poustka A. |
| Deleted in malignant brain tumors 1 is a versatile mucin-like molecule likely to play a differential role in digestive tract cancer. Mollenhauer J., Herbertz S., Helmke B., Kollender G., Krebs I., Madsen J., Holmskov U., Sorger K., Schmitt L., Wiemann S. et al. |
| Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. Simpson J.C., Wellenreuther R., Poustka A., Pepperkok R., Wiemann S. EMBO Rep. 1:287-292(2000) · UniProtKB (10) |
| 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) |
| Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. Smahi A., Courtois G., Vabres P., Yamaoka S., Heuertz S., Munnich A., Israel A., Heiss N.S., Klauck S.M., Kioschis P. et al. Nature 405:466-472(2000) · UniProtKB (1) |
| DMBT1 encodes a protein involved in the immune defense and in epithelial differentiation and is highly unstable in cancer. Mollenhauer J., Herbertz S., Holmskov U., Tolnay M., Krebs I., Merlo A., Schroder H.D., Maier D., Breitling F., Wiemann S. et al. Cancer Res. 60:1704-1710(2000) · UniProtKB (1) |
| The genomic structure of the DMBT1 gene: evidence for a region with susceptibility to genomic instability. Mollenhauer J., Holmskov U., Wiemann S., Krebs I., Herbertz S., Madsen J., Kioschis P., Coy J.F., Poustka A. Oncogene 18:6233-6240(1999) · UniProtKB (1) |
| DelGEF, an RCC1-related protein encoded by a gene on chromosome 11p14 critical for two forms of hereditary deafness. Uhlmann J., Wiemann S., Ponstingl H. FEBS Lett. 460:153-160(1999) · UniProtKB (2) |
| Dyskerin localizes to the nucleolus and its mislocalization is unlikely to play a role in the pathogenesis of dyskeratosis congenita. Heiss N.S., Girod A., Salowsky R., Wiemann S., Pepperkok R., Poustka A. Hum. Mol. Genet. 8:2515-2524(1999) · UniProtKB (1) |
