Hansen TS - Search Results

1

Tetrahymena thermophila acidic ribosomal protein L37 contains an archaebacterial type of C-terminus.

Hansen TS, Andreasen PH, Dreisig H, Højrup P, Nielsen H, Engberg J, Kristiansen K. Hansen TS, et al. Gene. 1991 Sep 15;105(2):143-50. doi: 10.1016/0378-1119(91)90144-z. Gene. 1991. PMID: 1937011

2

The phosphorylated ribosomal protein S7 in Tetrahymena is homologous with mammalian S4 and the phosphorylated residues are located in the C-terminal region. Structural characterization of proteins separated by two-dimensional polyacrylamide gel electrophoresis.

Palm L, Andersen J, Rahbek-Nielsen H, Hansen TS, Kristiansen K, Højrup P. Palm L, et al. Among authors: hansen ts. J Biol Chem. 1995 Mar 17;270(11):6000-5. doi: 10.1074/jbc.270.11.6000. J Biol Chem. 1995. PMID: 7890730 Free article.

3

Detection and characterization of a novel splice mutation in the LDL receptor intron 12 resulting in two different mutant mRNA variants.

Nissen H, Hansen AB, Guldberg P, Petersen NE, Hansen TS, Hørder M. Nissen H, et al. Among authors: hansen ab, hansen ts. Atherosclerosis. 1997 Jan 3;128(1):75-83. doi: 10.1016/s0021-9150(96)05967-9. Atherosclerosis. 1997. PMID: 9051200

4

Mutation screening of the LDLR gene and ApoB gene in patients with a phenotype of familial hypercholesterolemia and normal values in a functional LDL receptor/apolipoprotein B assay.

Nissen H, Lestavel S, Hansen TS, Luc G, Bruckert E, Clavey V. Nissen H, et al. Among authors: hansen ts. Clin Genet. 1998 Jul;54(1):79-82. doi: 10.1111/j.1399-0004.1998.tb03699.x. Clin Genet. 1998. PMID: 9727746

5

Imipramine metabolism in relation to the sparteine oxidation polymorphism--a family study.

Madsen H, Hansen TS, Brøsen K. Madsen H, et al. Among authors: hansen ts. Pharmacogenetics. 1996 Dec;6(6):513-9. doi: 10.1097/00008571-199612000-00004. Pharmacogenetics. 1996. PMID: 9014200

6

A fast and robust dual-label nonradioactive oligonucleotide ligation assay for detection of factor V Leiden.

Chakravarty A, Hansen TS, Hørder M, Kristensen SR. Chakravarty A, et al. Among authors: hansen ts. Thromb Haemost. 1997 Oct;78(4):1234-6. Thromb Haemost. 1997. PMID: 9364990

7

Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein B.

Nissen H, Hansen AB, Guldberg P, Hansen TS, Petersen NE, Hørder M. Nissen H, et al. Among authors: hansen ab, hansen ts. Clin Genet. 1998 Jun;53(6):433-9. doi: 10.1111/j.1399-0004.1998.tb02591.x. Clin Genet. 1998. PMID: 9712531

8

Diagnostic strategy, genetic diagnosis and identification of new mutations in intermittent porphyria by denaturing gradient gel electrophoresis.

Nissen H, Petersen NE, Mustajoki S, Hansen TS, Mustajoki P, Kauppinen R, Hørder M. Nissen H, et al. Among authors: hansen ts. Hum Mutat. 1997;9(2):122-30. doi: 10.1002/(SICI)1098-1004(1997)9:2<122::AID-HUMU4>3.0.CO;2-B. Hum Mutat. 1997. PMID: 9067752

9

R325X mutation in exon 15 of the hydroxymethylbilane synthase gene identified in two Danish families with acute intermittent porphyria.

Petersen NE, Nissen H, Hansen TS, Rasmussen K, Brock A, Hørder M. Petersen NE, et al. Among authors: hansen ts. Clin Chem. 1996 Jan;42(1):106-7. Clin Chem. 1996. PMID: 8565205 No abstract available.

10

Vitamin D receptor alleles do not predict bone mineral density or bone loss in Danish perimenopausal women.

Hansen TS, Abrahamsen B, Henriksen FL, Hermann AP, Jensen LB, Hørder M, Gram J. Hansen TS, et al. Bone. 1998 May;22(5):571-5. doi: 10.1016/s8756-3282(98)00028-3. Bone. 1998. PMID: 9600794

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