Biological Chemistry Hoppe-seyler
Overview
Biological Chemistry Hoppe-seyler is a scientific journal, published since 1985 in English and German. The journal's country of origin is Germany and its primary focus area is biochemistry.
Details
Details
Abbr.
Biol Chem Hoppe Seyler
Start
1985
End
1996
Frequency
Monthly
p-ISSN
0177-3593
Country
Germany
Languages
English
German
German
Specialty
Biochemistry
Recent Articles
1.
Schneider H, Barth W, Bohme H
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):399-402.
PMID: 8839987
Lignin peroxidase (LiP) isozymes of Phanerochaete chrysosporium are encoded by a large family of closely related genes, whose total number is still unknown. Among genomic clones, obtained using the polymerase...
2.
Gololobov M, Wang W, Bateman Jr R
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):395-8.
PMID: 8839986
This paper reports a systematic study of the substrate and inhibitor specificity of papaya latex glutamine cyclotransferase (QC). The results showed that the second amino acid residue in N-terminal glutaminyl...
3.
Dehrmann F, Elliott E, Dennison C
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):391-4.
PMID: 8839985
Cathepsins B and L are thought to function extracellularly in pathological conditions. pH-Activity profiles of cathepsin B, measured in phosphate and acetate-Mes-Tris buffers of constant ionic strength, indicated that cathepsin...
4.
Budihna M, Strojan P, Smid L, Skrk J, Vrhovec I, Zupevc A, et al.
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):385-90.
PMID: 8839984
To estimate the prognostic value of cathepsins B, H, L, D and stefins A and B in head and neck carcinoma, their concentrations in cytosols of primary tumours and adjacent...
5.
Lu Z, Quazi N, Deady L, Polya G
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):373-84.
PMID: 8839983
A large series of isoquinoline derivatives was synthesised including derivatives of isoquinoline, isoquinolino[3,4-c]furazan, 1,2-dihydro-1-oxoisoquinoline, 6-oxopyrimido[1,2-d]isoquinoline, benzo[c][1,8]-naphthyridine, pyrazino[2,3-c]isoquinoline and benzimidazo[2,1-a]isoquinoline as well as further structurally related isoquinoline derivatives and pyrido-2,3-furazans. Representatives...
6.
Kehne J, Meyer H, Schurholz T
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):363-72.
PMID: 8839982
The voltage-gated chloride channel (CIC-0) from the electric organ of Torpedo californica was purified by immunoaffinity chromatography. A polyclonal antibody was shown to specifically recognize the CIC-0 channel (M(r) 85,000-90,000)...
7.
Becker J, Brendel M
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):357-62.
PMID: 8839981
Two distinct N-deoxyribosyltransferases of Lactobacillus leichmannii, designated as DRTase I and DRTase II, were separated and purified almost to homogeneity by one-step affinity chromatography. DRTase I is distinguished by specifically...
8.
Freist W, Logan D, Gauss D
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):343-56.
PMID: 8839980
Glycyl-tRNA synthetase, a class II aminoacyl-tRNA synthetase, catalyzes the synthesis of glycyl-tRNA, which is required to insert glycine into proteins. In a side reaction the enzyme also synthesizes dinuceloside polyphosphates,...
9.
Reuter G, Gabius H
Biol Chem Hoppe Seyler
. 1996 Jun;
377(6):325-42.
PMID: 8839979
Sialic acids are commonly positioned at non-reducing termini of complex carbohydrates. Steady refinements of analytical techniques have enabled detailed mapping of the complexity of sialic acids, unravelling a number of...
10.
Leonardi A, Turk B, Turk V
Biol Chem Hoppe Seyler
. 1996 May;
377(5):319-21.
PMID: 8828823
Inhibition of bovine cathepsins L and S by bovine stefin B, human stefins A and B and cystatin C was studied under pseudo-first-order conditions by continuous fluorimetric assay. All inhibitors...