17
results
for author:"Olsen A.S."
in Literature Citations
| Identification of a sigma B-dependent small noncoding RNA in Listeria monocytogenes. Nielsen J.S., Olsen A.S., Bonde M., Valentin-Hansen P., Kallipolitis B.H. J. Bacteriol. 190:6264-6270(2008) · Mapped (1) |
| The DNA sequence and biology of human chromosome 19. Grimwood J., Gordon L.A., Olsen A.S., Terry A., Schmutz J., Lamerdin J.E., Hellsten U., Goodstein D., Couronne O., Tran-Gyamfi M. et al. Nature 428:529-535(2004) · UniProtKB (1,180) |
| Inactivation of the EGF-TM7 receptor EMR4 after the Pan-Homo divergence. Hamann J., Kwakkenbos M.J., de Jong E.C., Heus H., Olsen A.S., van Lier R.A.W. Eur. J. Immunol. 33:1365-1371(2003) · UniProtKB (1) |
| Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints. Puttagunta R., Gordon L.A., Meyer G.E., Kapfhamer D., Lamerdin J.E., Kantheti P., Portman K.M., Chung W.K., Jenne D.E., Olsen A.S. et al. Genome Res. 10:1369-1380(2000) · Mapped (108) |
| A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome. Trettel F., Mantuano E., Calabresi V., Veneziano L., Olsen A.S., Georgescu A., Gordon L., Sabbadini G., Frontali M., Jodice C. Gene 241:45-50(2000) · UniProtKB (1) |
| Genomic organisation of the human cyclic AMP-specific phosphodiesterase PDE4C gene and its chromosomal localisation to 19p13.1, between RAB3A and JUND. Sullivan M., Olsen A.S., Houslay M.D. Cell. Signal. 11:735-742(1999) · UniProtKB (2) |
| Physical mapping of EMR1 and CD97 in human Chromosome 19 and assignment of Cd97 to mouse Chromosome 8 suggest an ancient genomic duplication. Carver E.A., Hamann J., Olsen A.S., Stubbs L. Mamm. Genome 10:1039-1040(1999) · Mapped (23) |
| Identification and characterization of the human homologue of the short PDE4A cAMP-specific phosphodiesterase 4A variant RD1 (PDE4A1) by analysis of the human HSPDE4A gene locus located at chromosome 19p13.2. Sullivan M., Rena G., Begg F., Gordon L., Olsen A.S., Houslay M.D. Biochem. J. 333:693-703(1998) · UniProtKB (11) |
| Localization and genomic structure of human deoxyhypusine synthase gene on chromosome 19p13.2-distal 19p13.1. Mantuano E., Trettel F., Olsen A.S., Lennin G., Frontali M., Jodice C. Gene 215:153-157(1998) · UniProtKB (1) |
| Location of mouse and human genes corresponding to conserved canine olfactory receptor gene subfamilies. Carver E.A., Issel-Tarver L., Rine J., Olsen A.S., Stubbs L. Mamm. Genome 9:349-354(1998) · Mapped (76) |
| A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Hemminki A., Markie D., Tomlinson I., Avizienyte E., Roth S., Loukola A., Bignell G., Warren W., Aminoff M., Hoeglund P. et al. |
| The human guanidinoacetate methyltransferase (GAMT) gene maps to a syntenic region on 19p13.3, homologous to band C of mouse chromosome 10, but GAMT is not mutated in jittery mice. Jenne D.E., Olsen A.S., Zimmer M. Biochem. Biophys. Res. Commun. 238:723-727(1997) · UniProtKB (2) |
| Chromosomal localization of the human and mouse hyaluronan synthase genes. Spicer A.P., Seldin M.F., Olsen A.S., Brown N., Wells D.E., Doggett N.A., Itano N., Kimata K., Inazawa J., McDonald J.A. Genomics 41:493-497(1997) · Mapped (22) |
| Physical mapping of receptor type protein tyrosine phosphatase sigma (PTPRS) to human chromosome 19p13.3. Wagner J., Gordon L.A., Heng H.H., Tremblay M.L., Olsen A.S. Genomics 38:76-78(1996) · Mapped (6) |
| Pseudoachondroplasia and multiple epiphyseal dysplasia due to mutations in the cartilage oligomeric matrix protein gene. Briggs M.D., Hoffman S.M.G., King L.M., Olsen A.S., Mohrenweiser H., Leroy J.G., Mortier G.R., Rimoin D.L., Lachman R.S., Gaines E.S. et al. Nat. Genet. 10:330-336(1995) · UniProtKB (1) |
| Transgenic mice that express a mini-gene version of the human gene for type I procollagen (COL1A1) develop a phenotype resembling a lethal form of osteogenesis imperfecta. Khillan J.S., Olsen A.S., Kontusaari S., Sokolov B., Prockop D.J. J. Biol. Chem. 266:23373-23379(1991) · Mapped (3) |
| Evolution of the mammalian G protein alpha subunit multigene family. Wilkie T.M., Gilbert D.J., Olsen A.S., Chen X.N., Amatruda T.T., Korenberg J.R., Trask B.J., de Jong P., Reed R.R., Simon M.I. Nat. Genet. 1:85-91(1992) · Mapped (135) |
