Authors:
LOBENTANZ EM
KRASZNAI K
GRUBER A
BRUNNER C
MULLER HJ
SATTLER J
KRAFT HG
UTERMANN G
DIEPLINGER H
Citation: Em. Lobentanz et al., INTRACELLULAR METABOLISM OF HUMAN APOLIPOPROTEIN(A) IN STABLY TRANSFECTED HEP G2 CELLS, Biochemistry, 37(16), 1998, pp. 5417-5425
Authors:
VERHAGEN HJM
BLANKENSTEIJN JD
DEGROOT PG
HEIJNENSNYDER GJ
PRONK A
VROOM TM
MULLER HJ
NICOLAY K
VANVROONHOVEN TJMV
SIXMA JJ
EIKELBOOM BC
Citation: Hjm. Verhagen et al., IN-VIVO EXPERIMENTS WITH MESOTHELIAL CELL SEEDED EPTFE VASCULAR GRAFTS, European journal of vascular and endovascular surgery, 15(6), 1998, pp. 489-496
Citation: Z. Dobbie et Hj. Muller, MUTATION ANALYSIS OF THE BETA-CATENIN GENE IN FAP PATIENTS WITHOUT ANAPC MUTATION, European journal of human genetics, 6, 1998, pp. 4103-4103
Citation: Hj. Muller, EXTRAORDINARILY THICK WATER FILMS ON HYDROPHILIC SOLIDS - A RESULT OFHYDROPHOBIC REPULSION, Langmuir, 14(24), 1998, pp. 6789-6792
Citation: R. Krustev et al., THE THICKNESS AND CONTACT-ANGLE OF SODIUM DODECYL-SULFATE FOAM FILMS DEPENDING ON THE CONCENTRATION OF LICL, Colloid and polymer science, 276(6), 1998, pp. 518-523
Authors:
HEINIMANN K
MULLHAUPT B
WEBER W
ATTENHOFER M
SCOTT RJ
FRIED M
MARTINOLI S
MULLER HJ
DOBBIE Z
Citation: K. Heinimann et al., PHENOTYPIC DIFFERENCES IN FAMILIAL ADENOMATOUS POLYPOSIS BASED ON APCGENE MUTATION STATUS, Gut, 43(5), 1998, pp. 675-679
Authors:
THART BA
BAUER J
MULLER HJ
MELCHERS B
NICOLAY K
BROK H
BONTROP RE
LASSMANN H
MASSACESI L
Citation: Ba. Thart et al., HISTOPATHOLOGICAL CHARACTERIZATION OF MAGNETIC-RESONANCE IMAGING-DETECTABLE BRAIN WHITE-MATTER LESIONS IN A PRIMATE MODEL OF MULTIPLE-SCLEROSIS - A CORRELATIVE STUDY IN THE EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS MODEL IN COMMON MARMOSETS (CALLITHRIX-JACCHUS), The American journal of pathology, 153(2), 1998, pp. 649-663
Citation: C. Klauck et Hj. Muller, FORMAL BUSINESS PROCESS ENGINEERING BASED ON GRAPH-GRAMMARS, International journal of production economics, 50(2-3), 1997, pp. 129-140
Authors:
SANNER BM
KONERMANN M
STURM A
MULLER HJ
ZIDEK W
Citation: Bm. Sanner et al., RIGHT-VENTRICULAR DYSFUNCTION IN PATIENTS WITH OBSTRUCTIVE SLEEP-APNEA SYNDROME, The European respiratory journal, 10(9), 1997, pp. 2079-2083
Citation: C. Kang et al., THE AFFINITY OF APO(A) ISOFORMS FOR FIBRIN DECREASES UPON FORMATION OF LP(A) WITH AN LDL, Thrombosis and haemostasis, 1997, pp. 1331-1331
Citation: Hj. Duckers et al., LONGITUDINAL IN-VIVO MAGNETIC-RESONANCE-IMAGING STUDIES IN EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS - EFFECT OF A NEUROTROPHIC TREATMENT ON CORTICAL LESION DEVELOPMENT, Neuroscience, 77(4), 1997, pp. 1163-1173
Authors:
VANDORSTEN FA
REESE T
GELLERICH JF
VANECHTELD GJA
NEDERHOFF MGJ
MULLER HJ
VANVLIET G
NICOLAY K
Citation: Fa. Vandorsten et al., FLUXES THROUGH CYTOSOLIC AND MITOCHONDRIAL CREATINE-KINASE, MEASURED BY P-31 NMR, Molecular and cellular biochemistry, 174(1-2), 1997, pp. 33-42
Authors:
STEMPKA L
GIROD A
MULLER HJ
RINCKE G
MARKS F
GSCHWENDT M
BOSSEMEYER D
Citation: L. Stempka et al., PHOSPHORYLATION OF PROTEIN-KINASE-C-DELTA (PKC-DELTA) AT THREONINE-505 IS NOT A PREREQUISITE FOR ENZYMATIC-ACTIVITY - EXPRESSION OF RAT PKC-DELTA AND AN ALANINE-505 MUTANT IN BACTERIA IN A FUNCTIONAL FORM, The Journal of biological chemistry, 272(10), 1997, pp. 6805-6811
Authors:
KANG C
LOYAU S
SOULAT T
MULLER HJ
ANGLESCANO E
Citation: C. Kang et al., IDENTIFICATION OF KRINGLES OF APOLIPOPROTEIN(A) THAT ENABLE ITS BINDING TO FIBRIN AND MONOCYTIC CELLS, Atherosclerosis, 134(1-2), 1997, pp. 141-141
Citation: C. Kang et al., BINDING OF APO(A) ISOFORMS TO FIBRIN IS MODIFIED BY THEIR INCORPORATION INTO AN LDL LIPOPARTICLE, Atherosclerosis, 134(1-2), 1997, pp. 142-142
Authors:
ACQUATI F
RONICKE V
TARAMELLI R
MULLER HJ
Citation: F. Acquati et al., REPORTER GENE ANALYSIS OF 4 DNASEI HYPERSENSITIVE SITES IN THE PLASMINOGEN APOLIPOPROTEIN(A) INTERGENIC REGION/, Clinical genetics, 52(5), 1997, pp. 303-307
Authors:
BERGE KE
DJUROVIC S
MULLER HJ
ALESTROM P
BERG K
Citation: Ke. Berge et al., STUDIES ON EFFECTS OF LP(A) LIPOPROTEIN ON GENE-EXPRESSION IN ENDOTHELIAL-CELLS IN-VITRO, Clinical genetics, 52(5), 1997, pp. 314-325