Dagnaes-Hansen, F., Holst, H. U.
, Jensen, M. S., Vorup-Jensen, T., Flyvbjerg, A., Jensen, U. B. & Jensen, T. G. (2002).
Physiological effects of human growth hormone produced after hydrodynamic gene transfer of a plasmid vector containing the human ubiquitin promotor.
Journal of Molecular Medicine,
80(10), 665-70.
https://doi.org/10.1007/s00109-002-0371-1
Christensen, R., Jensen, U. B., Jensen, U. B. & Jensen, T. G. (2002).
Skin genetically engineered as a bioreactor or a 'metabolic sink'.
Cells, Tissues, Organs,
172(2), 96-104.
Børglum, A. D., Balslev, T., Haagerup, A., Birkebaek, N., Binderup, H., Kruse, T. A.
& Hertz, J. M. (2001).
A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
European Journal of Human Genetics,
9(10), 753-7.
https://doi.org/10.1038/sj.ejhg.5200701
Elkjær, M.-L.
, Nejsum, L. N., Gresz, V., Kwon, T. H.
, Jensen, U. B., Frøkiaer, J. & Nielsen, S. (2001).
Immunolocalization of aquaporin-8 in rat kidney, gastrointestinal tract, testis, and airways.
American Journal of Physiology: Renal Physiology,
281(6), F1047-57.
Westergaard, M., Henningsen, J.
, Svendsen, M. L., Johansen, C., Jensen, U. B., Schrøder, H. D., Kratchmarova - Blagoeva, I. H.
, Berge, R. K., Iversen, L., Bolund, L., Kragballe, K. & Kristiansen, K. (2001).
Modulation of keratinocyte gene expression and differentiation by PPAR-selective ligands and tetradecylthioacetic acid.
Journal of Investigative Dermatology,
116(5), 702-12.
https://doi.org/10.1046/j.0022-202x.2001.doc.x
Vogel, I., Glavind-Kristensen, M.
, Salvig, J. D., Secher, N. J., Thorsen, P., Sandager, K. P. & Uldbjerg, N. (2001).
Preterm delivery predicted by S-relaxin. In
Ikke angivet (pp. 518-4). Kluver Academic Press.
Vorup-Jensen, T., Sørensen, E. S., Jensen, U. B., Schwaeble, W., Kawasaki, T., Ma, Y., Uemura, K., Wakamiya, N.
, Suzuki, Y., Jensen, T. G., Takahashi, K., Ezekowitz, R. A.
, Thiel, S. & Jensenius, J. C. (2001).
Recombinant expression of human mannan-binding lectin.
International Immunopharmacology,
1(4), 677-87.
Vorup-Jensen, T., Jensen, U. B., Liu, H., Kawasaki, T., Uemura, K.
, Thiel, S., Dagnaes-Hansen, F. & Jensen, T. G. (2001).
Tail-vein injection of mannan-binding lectin DNA leads to high expression levels of multimeric protein in liver.
Molecular Therapy,
3(6), 867-74.
https://doi.org/10.1006/mthe.2001.0335
Kamperis, K., Siggaard, C.
, Herlin, T., Nathan, E., Hertz, J. M. & Rittig, S. (2000).
A novel splicing mutation in the V2 vasopressin receptor.
Pediatric Nephrology,
15(1-2), 43-9.
Elkjær, M.-L.
, Nejsum, L. N., Jensen, U. B., Kwon, T.-H.
, Frøkiær, J. & Nielsen, S. (2000).
Molecular Biology and Physiology of Water and Solute Transport: Aquaporin-8 and-9: tissue localization. In
Molecular Biology and Physiology of Water and Solute Transport: Aquaporin-8 and-9: tissue localization (pp. 85-89)
Jensen, U. B., Petersen, M. S., Lund, T. B., Jensen, T. G. & Bolund, L. (2000).
Transgene expression in human epidermal keratinocytes: cell cycle arrest of productively transfected cells.
Experimental Dermatology,
9(4), 298-310.
Gregersen, N., Winter, V. S., Corydon, M. J.
, Corydon, T. J., Rinaldo, P., Ribes, A., Martinez, G., Bennett, M. J., Vianey-Saban, C., Bhala, A., Hale, D. E., Lehnert, W., Kmoch, S., Roig, M., Riudor, E., Eiberg, H.
, Andresen, B. S., Bross, P., Bolund, L. A. & Kølvraa, S. (1998).
Identification of four new mutations in the short-chain acyl-CoA dehydrogenase (SCAD) gene in two patients: One of the variant alleles, 511C→T, is present at an unexpectedly high frequency in the general population, as was the case for 625G→A, together conferring susceptibility to ethylmalonic aciduria.
Human Molecular Genetics,
7(4), 619-627.
https://doi.org/10.1093/hmg/7.4.619
Corydon, T. J., Bross, P., Jensen, T. G., Corydon, M. J., Lund, T. B., Jensen, U. B., Kim, J. J.
, Gregersen, N. & Bolund, L. (1998).
Rapid degradation of short-chain acyl-CoA dehydrogenase variants with temperature-sensitive folding defects occurs after import into mitochondria.
Journal of Biological Chemistry,
273(21), 13065-71.
Tomiuk, J., Bachmann, L., Leipoldt, M., Ganzhorn, J. U., Ries, R., Weis, M.
& Loeschcke, V. (1997).
Genetic diversity of Lepilemur mustelinus ruficaudatus, a nocturnal lemur of Madagascar.
Conservation Biology,
11(2), 491-497.
https://doi.org/10.1046/j.1523-1739.1997.95290.x
Schrõck, E., Veldman, T., Padilla-Nash, H., Ning, Y., Spurbeck, J., Jalal, S., Shaffer, L. G., Papenhausen, P., Kozma, C., Phelan, M. C.
, Kjeldsen, E., Schonberg, S. A., O'Brien, P., Biesecker, L., Du Manoir, S. & Ried, T. (1997).
Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities.
Human Genetics,
101(3), 255-262.
https://doi.org/10.1007/s004390050626
Corydon, M. J.
, Andresen, B. S., Bross, P., Kjeldsen, M., Andreasen, P. H., Eiberg, H.
, Kølvraa, S. & Gregersen, N. (1997).
Structural organization of the human short-chain acyl-CoA dehydrogenase gene.
Mammalian Genome,
8(12), 922-926.
https://doi.org/10.1007/s003359900612
Hasle, H., Brandt, C., Kerndrup, G.
, Kjeldsen, E. & Sorensen, A. G. (1996).
Haemophagocytic lymphohistiocytosis associated with constitutional inversion of chromosome 9.
British Journal of Haematology,
93(4), 808-809.
https://doi.org/10.1046/j.1365-2141.1996.d01-1718.x
Orntoft, T. F.
, Vestergaard, E. M., Holmes, E.
, Jakobsen, J. S., Grunnet, N., Mortensen, M., Johnson, P.
, Bross, P., Gregersen, N., Andresen, K. S.
, Jensen, U. B., Bolund, L. & Wolf, H. (1996).
Influence of Lewis alpha1-3/4-L-fucosyltransferase (FUT3) gene mutations on enzyme activity, erythrocyte phenotyping, and circulating tumor marker sialyl-Lewis a levels.
Journal of Biological Chemistry,
271(50), 32260-8.
Jensen, T. G., Andresen, B. S., Jensen, H. K., Jensen, L. G., Heath, F.
, Pedersen, S., Nielsen, V., Jensen, U. B., Lund, T. B., Gregersen, N., Kølvraa, S. & Bolund, L. (1996).
Rapid characterization of disease-causing mutations in the low density lipoprotein receptor (LDL-R) gene by overexpression in COS cells.
Zeitschrift fuer Gastroenterologie,
34 Suppl 3, 9-11.
Hertz, J. M., Heiskari, N., Zhou, J.
, Jensen, U. B. & Tryggvason, K. (1995).
A nonsense mutation in the COL4A5 collagen gene in a family with X-linked juvenile Alport syndrome.
Kidney International,
47(1), 327-32.
Jensen, T. G., Bross, P., Andresen, B. S., Lund, T. B., Kristensen, T. J., Jensen, U. B., Jensen, U. B., Winther, V.
, Kølvraa, S., Gregersen, N. & Bolund, L. (1995).
Comparison between medium-chain acyl-CoA dehydrogenase mutant proteins overexpressed in bacterial and mammalian cells.
Human Mutation,
6(3), 226-31.
https://doi.org/10.1002/humu.1380060305
Hertz, J. M., Tommerup, N.
, Sørensen, F. B., Henriques, U. V.
, Nielsen, A. & Therkelsen, A. J. (1995).
Partial deletion 11q.
Clinical Genetics,
47(5), 231-235.
Hertz, J. M., Børglum, A. D., Brandt, C. A.
, Flint, T. & Bisgaard, C. (1994).
Charcot-Marie-Tooth disease type 1A: the parental origin of a de novo 17p11.2-p12 duplication.
Clinical Genetics,
46(4), 291-4.
Jensen, U. B., Jensen, T. G., Jensen, P. K., Rygaard, J., Hansen, B. S., Fogh, J.
, Kølvraa, S. & Bolund, L. (1994).
Gene transfer into cultured human epidermis and its transplantation onto immunodeficient mice: an experimental model for somatic gene therapy.
Journal of Investigative Dermatology,
103(3), 391-4.
Andresen, B. S., Bross, P., Jensen, T. G., Winter, V.
, Knudsen, I., Kølvraa, S., Jensen, U. B., Bolund, L., Duran, M. & Kim, J. J. (1993).
A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD).
American Journal of Human Genetics,
53(3), 730-9.
Jensen, T. G., Jensen, U. B., Jensen, P. K., Ibsen, H. H., Brandrup, F., Ballabio, A.
& Bolund, L. (1993).
Correction of steroid sulfatase deficiency by gene transfer into basal cells of tissue-cultured epidermis from patients with recessive X-linked ichthyosis.
Experimental Cell Research,
209(2), 392-7.
https://doi.org/10.1006/excr.1993.1326
Sunde, L., Vejerslev, L. O., Jensen, M. P.
, Pedersen, S., Hertz, J. M. & Bolund, L. (1993).
Genetic analysis of repeated, biparental, diploid, hydatidiform moles.
Cancer Genetics and Cytogenetics,
66(1), 16-22.
Jensen, T. G., Andresen, B. S., Bross, P., Jensen, U. B., Holme, E.
, Kølvraa, S., Gregersen, N. & Bolund, L. (1992).
Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cells.
BBA General Subjects,
1180(1), 65-72.
Koch, J., Kølvraa, S., Hobolt, N., Petersen, G. B., Willard, H. F., Waye, J. S.
, Gregersen, N. & Bolund, L. (1990).
A case of 46,XX,r(X) (p1q1) diagnosed by in situ hybridization.
Clinical Genetics,
37(3), 216-220.
https://doi.org/10.1111/j.1399-0004.1990.tb03505.x
Jensen, P. K., Hertz, J. M., Hahnemann, N., Smidt-Jensen, S. & Therkelsen, A. J. (1987).
Praenatal cytogenetisk diagnostik i første trimester.
Ugeskrift for Laeger,
149(11), 718-21.