18
results
for author:"Rump A."
in Literature Citations
| Dictyostelium myosin-5b is a conditional processive motor. Taft M.H., Hartmann F.K., Rump A., Keller H., Chizhov I., Manstein D.J., Tsiavaliaris G. J. Biol. Chem. 283:26902-26910(2008) · UniProtKB (1) |
| Identification and characterization of CaApe2 -- a neutral arginine/alanine/leucine-specific metallo-aminopeptidase from Candida albicans. Klinke T., Rump A., Poenisch R., Schellenberger W., Mueller E.-C., Otto A., Klimm W., Kriegel T.M. FEMS Yeast Res. 8:858-869(2008) · UniProtKB (2) · Mapped (2) |
| STAT3 is required for IL-6-gp130-dependent activation of hepcidin in vivo. Pietrangelo A., Dierssen U., Valli L., Garuti C., Rump A., Corradini E., Ernst M., Klein C., Trautwein C. Gastroenterology 132:294-300(2007) · Mapped (11) |
| Identification of a set of seven genes for the monitoring of minimal residual disease in pediatric acute myeloid leukemia. Steinbach D., Schramm A., Eggert A., Onda M., Dawczynski K., Rump A., Pastan I., Wittig S., Pfaffendorf N., Voigt A. et al. Clin. Cancer Res. 12:2434-2441(2006) · Mapped (1) |
| A splice-supporting intronic mutation in the last bp position of a cryptic exon within intron 6 of the CYBB gene induces its incorporation into the mRNA causing chronic granulomatous disease (CGD). Rump A., Rosen-Wolff A., Gahr M., Seidenberg J., Roos C., Walter L., Gunther V., Roesler J. Gene 371:174-181(2006) · Mapped (4) |
| In acute leukemia, the polymorphism -211C>T in the promoter region of the multidrug resistance-associated protein 3 (MRP3) does not determine the expression level of the gene. Doerfel C., Rump A., Sauerbrey A., Gruhn B., Zintl F., Steinbach D. Pharmacogenet. Genomics 16:149-150(2006) · Mapped (7) |
| Expression levels of the putative zinc transporter LIV-1 are associated with a better outcome of breast cancer patients. Kasper G., Weiser A.A., Rump A., Sparbier K., Dahl E., Hartmann A., Wild P., Schwidetzky U., Castanos-Velez E., Lehmann K. Int. J. Cancer 117:961-973(2005) · Mapped (4) |
| Neuronal leucine-rich repeat protein 4 functions in hippocampus-dependent long-lasting memory. Bando T., Sekine K., Kobayashi S., Watabe A.M., Rump A., Tanaka M., Suda Y., Kato S., Morikawa Y., Manabe T. et al. Mol. Cell. Biol. 25:4166-4175(2005) · UniProtKB (1) |
| Binding of ovarian cancer antigen CA125/MUC16 to mesothelin mediates cell adhesion. Rump A., Morikawa Y., Tanaka M., Minami S., Umesaki N., Takeuchi M., Miyajima A. J. Biol. Chem. 279:9190-9198(2004) · UniProtKB (3) · Mapped (3) |
| Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Mburu P., Mustapha M., Varela A., Weil D., El-Amraoui A., Holme R.H., Rump A., Hardisty R.E., Blanchard S., Coimbra R.S. et al. |
| Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis. Herr A., Meunier D., Muller I., Rump A., Fundele R., Ropers H.H., Nuber U.A. Dev. Dyn. 226:579-586(2003) · Mapped (11) |
| Different structural organization of the encephalopsin gene in man and mouse. Kasper G., Taudien S., Staub E., Mennerich D., Rieder M., Hinzmann B., Dahl E., Schwidetzky U., Rosenthal A., Rump A. |
| A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35. Hayes C., Rump A., Cadman M.R., Harrison M., Evans E.P., Lyon M.F., Morriss-Kay G.M., Rosenthal A., Brown S.D. Genomics 78:197-205(2001) · Mapped (10) |
| Complex arrangement of genes within a 220-kb region of double-duplicated DNA on human 2q37.1. Rump A., Kasper G., Hayes C., Wen G., Starke H., Liehr T., Lehmann R., Lagemann D., Rosenthal A. Genomics 73:50-55(2001) · UniProtKB (1) |
| Comparative genome sequence analysis of the Bpa/Str region in mouse and man. Mallon A.-M., Platzer M., Bate R., Gloeckner G., Botcherby M.R.M., Nordsiek G., Strivens M.A., Kioschis P., Dangel A., Cunningham D. et al. |
| The DNA sequence of human chromosome 21. Hattori M., Fujiyama A., Taylor T.D., Watanabe H., Yada T., Park H.-S., Toyoda A., Ishii K., Totoki Y., Choi D.-K. et al. Nature 405:311-319(2000) · UniProtKB (510) |
| Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Rao E., Weiss B., Fukami M., Rump A., Niesler B., Mertz A., Muroya K., Binder G., Kirsch S., Winkelmann M. et al. Nat. Genet. 16:54-63(1997) · UniProtKB (1) |
| Nucleotide sequence of a 24,206-base-pair DNA fragment carrying the entire nitrogen fixation gene cluster of Klebsiella pneumoniae. Arnold W., Rump A., Klipp W., Priefer U.B., Puehler A. J. Mol. Biol. 203:715-738(1988) · UniProtKB (21) |
