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1.

001-es BibID:BIBFORM058446
Első szerző:Balázs Margit (sejtbiológus, molekuláris genetikus)
Cím:A biophysical approach of cell surface phenomena and transmembrane signaling / Margit Balázs, L. Mátyus, J. Szöllősi, L. Trón, S. Damjanovich
Dátum:1991
ISBN:963 05 5926 9
Tárgyszavak:Orvostudományok Elméleti orvostudományok könyvfejezet
Cell
Surface
Transmembrane
Megjelenés:The Physical Aspect of the Living Cell / ed. by József Tigyi, Miklós Kellermayer, Carlton F. Hazlewood. - p. 271-298. -
További szerzők:Mátyus László (1956-) (biofizikus) Szöllősi János (1953-) (biofizikus) Trón Lajos (1941-) (biofizikus) Damjanovich Sándor (1936-2017) (biofizikus)
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
Borító:

2.

001-es BibID:BIBFORM006025
Első szerző:Balázs Margit (sejtbiológus, molekuláris genetikus)
Cím:Fluorescent tetradecanoylphorbol acetate : a novel probe of phorbol ester binding domains / Balázs, M., Szöllösi, J., Lee, W. C., Haugland, R. P., Guzikowski, A. P., Fulwyler, M. J., Damjanovich, S., Feuerstein, B. G., Pershadsingh, H. A.
Dátum:1991
Megjegyzések:Protein kinase C (PKC) has a prominent role in signal transduction of many bioactive substances. We synthesized the fluorescent derivative, phorbol-13-acetate-12-N-methyl-N-4-(N,N'-di(2-hydroxyethyl)amino)-7-n itr obenz-2-oxa-1,3-diazole-aminododecanoate (N-C12-Ac(13)) of 12-O-tetradecanoylphorbol-13-acetate (TPA) to monitor the location of phorbol ester binding sites and evaluate its potential use as a probe of PKC in viable cells. The excitation maximum wavelength of N-C12-Ac(13) is close to 488 nm, facilitating its use in argon-ion laser flow and imaging cytometry. When incubated with 100 nM N-C12-Ac(13) at 25 degrees C, P3HR-1 Burkitt lymphoma cells accumulated the dye rapidly, reaching maximum fluorescence within 25 min, 20-fold above autofluorescence. Addition of unlabeled TPA significantly decreased the fluorescence of N-C12-Ac(13) stained cells in a dose-dependent manner indicating specific displacement of the bound fluoroprobe. Competitive displacement of [3H]-phorbol-12,13-dibutyrate ([3H]-PBu2) from rat brain cytosol with N-C12-Ac(13) gave an apparent dissociation constant (Kd) of 11 nM. N-C12-Ac(13) possessed biological activity similar to TPA. Like TPA (final concentration 65 nM) N-C12-Ac(13), at a lower concentration (51 nM), induced expression of Epstein-Barr viral glycoprotein in P3HR-1 cells, differentiation of promyelocytic HL60 cells, and caused predicted changes in the mitotic cycle of histiocytic DD cells. Microspectrofluorometric images of single cells labeled with N-C12-Ac(13) showed bright fluorescence localized intracellularly and dim fluorescence in the nuclear region, consistent with dye binding mainly to cytoplasmic structures and/or organelles and being mostly excluded from the nucleus. Because of the high level of non-specific binding of N-C12-Ac(13), this probe is not ideal for visualizing PKC in intact cells, but would be a valuable fluoroprobe to investigate the kinetic properties of purified PKC. Also, knowledge gained from these studies allows us to predict structures of fluorescent phorbols likely to have less non-specific binding and, consequently, be potentially useful for monitoring PKC in viable cells.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
analysis
Animal
Antigens,Viral
Binding Sites
Brain Chemistry
Cell Cycle
chemical synthesis
Cytosol
Dyes
Female
Flow Cytometry
Fluorescence
Fluorescence Polarization
Fluorescent Dyes
Gene Expression
Herpesvirus 4,Human
Image Processing,Computer-Assisted
immunology
metabolism
Oxadiazoles
pharmacology
Phorbol Esters
Protein Kinase C
Rats
Rats,Inbred Strains
Signal Transduction
Support,Non-U.S.Gov't
Support,U.S.Gov't,P.H.S.
Tetradecanoylphorbol Acetate
Tumor Cells,Cultured
Megjelenés:Journal of Cellular Biochemistry. - 46 : 3 (1991), p. 266-276. -
További szerzők:Szöllősi János (1953-) (biofizikus) Lee, W. C. Haugland, R. P. Guzikowski, A. P. Fulwyler, Mack J. Damjanovich Sándor (1936-2017) (biofizikus) Feuerstein, Burt G. Pershadsingh, Harrihar A.
Internet cím:elektronikus változat
Borító:

3.

001-es BibID:BIBFORM005965
Első szerző:Balázs Margit (sejtbiológus, molekuláris genetikus)
Cím:Accessibility of cell surface thiols in human lymphocytes is altered by ionophores or OKT-3 antibody / Margit Balázs, János Matkó, János Szöllösi, László Mátyus, Mack J. Fulwyler, Sándor Damjanovich
Dátum:1986
Megjegyzések:The accessibility of cell surface sulfhydryl groups in human peripheral lymphocytes was investigated with 5,5'-dithiobis-(2-nitrobenzoic acid) in the presence and absence of ionophore antibiotics and the monoclonal antibody, OKT-3. Only a few accessible protein thiols have been found on the cells as demonstrated by labeling with a fluorescent non-penetrating thiol-marker, monobromotrimethyl-ammoniobimane and the subsequent gel electrophoretic analysis of the protein pattern. Difference spectrophotometric measurement of thiol-DTNB reaction revealed that ionophores altering the transmembrane potential induced an enhanced cell surface thiol-exposure on the minute time scale. The effect showed a dependence on the external concentration of the cations. The binding of monoclonal antibody, OKT-3, directed against T3 complexes, resulted in a similar, concentration-dependent increase of thiol-accessibility. These data are interpreted as early membrane-effects of ionophores and the specific antibody including changes in the conformational equilibrium or vertical displacements of certain membrane proteins. These events are likely to be coupled to the changes in the transmembrane potential of the lymphocytes.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Ammonium Compounds
analysis
Antibiotics
Antibodies,Monoclonal
blood
Cell Membrane
Dithionitrobenzoic Acid
drug effects
Electrophoresis,Polyacrylamide Gel
Human
Ionophores
Lymphocytes
Membrane Proteins
metabolism
pharmacology
Spectrometry,Fluorescence
Sulfhydryl Compounds
Support,Non-U.S.Gov't
Support,U.S.Gov't,P.H.S.
Megjelenés:Biochemical and Biophysical Research Communications. - 140 : 3 (1986), p. 999-1006. -
További szerzők:Matkó János (1952-) (biológus) Szöllősi János (1953-) (biofizikus) Mátyus László (1956-) (biofizikus) Fulwyler, Mack J. Damjanovich Sándor (1936-2017) (biofizikus)
Internet cím:elektronikus változat
Intézményi repozitóriumban (DEA) tárolt változa
DOI
Borító:

4.

001-es BibID:BIBFORM005928
Első szerző:Balázs Margit (sejtbiológus, molekuláris genetikus)
Cím:Effect of specific antibodies on membrane microviscosity of human lymphocytes / Balazs Margit, Szöllösi Janos, Somogyi Béla, Damjanovich Sándor
Dátum:1979
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény hazai lapban
Antibodies
Cell Membrane
drug effects
Globulins
Human
Hungary
immunology
Lymphocytes
ultrastructure
Viscosity
Megjelenés:Acta Biochimica et Biophysica Academiae Scientiarum Hungaricae. - 14 : 4 (1979), p. 213-216. -
További szerzők:Szöllősi János (1953-) (biofizikus) Somogyi Béla (1945-2006) (biofizikus) Damjanovich Sándor (1936-2017) (biofizikus)
Borító:

5.

001-es BibID:BIBFORM005173
035-os BibID:(scopus)77954466624 (wos)000257919000450
Első szerző:Balázs Margit (sejtbiológus, molekuláris genetikus)
Cím:Genomic and gene expression characterization of a novel trastuzumab-resistant breast cancer cell line / M. Balázs, M. Barok, V. Lázár, Z. Rákosy, E. Toth, J. Park, J. Szöllosi
Dátum:2008
Tárgyszavak:Orvostudományok Elméleti orvostudományok idézhető absztrakt
folyóiratcikk
Cell Line
Gene Expression
Biophysics
Hungary
Megjelenés:European Journal of Cancer. Supplements. - 6 : 9 (2008), p. 119. -
További szerzők:Barok Márk (1976-) (biofizikus) Lázár Viktória (1981-) (molekuláris biológus) Rákosy Zsuzsa (1978-) (sejtbiológus, molekuláris biológus, genetikus) Toth E. Park J. Szöllősi János (1953-) (biofizikus)
Internet cím:elektronikus változat
DOI
Borító:

6.

001-es BibID:BIBFORM015664
Első szerző:Barok Márk (biofizikus)
Cím:Characterization of a novel, trastuzumab resistant human breast cancer cell line / Barok Mark, Balazs Margit, Lazar Viktoria, Rakosy Zsuzsa, Toth Eniko, Treszl Andrea, Vereb Gyorgy, Colbern G. T., Park J. W., Szollosi Janos
Dátum:2010
ISSN:1945-0508
Megjegyzések:HER2-positive breast cancers represent a distinct phenotype and are intrinsically more aggressive than HER2-negative tumors. Although HER2-targeted therapies have been rationally developed, resistance to these treatments represents a process understood poorly. There are few experimental models that allow studying the molecular mechanism of resistance. Our aim was to characterize a trastuzumab resistant breast cancer cell line (B585) that was established from an invasive ductal carcinoma. B585 grows only in immunodeficient mice as a xenograft. CGH and FISH were used to define cytogenetic alterations, gene-expression analysis and immunohistochemistry were applied to detect RNA and protein expression. By array-CGH focused amplifications were identified for C-MYC, EGFR, ErbB2, CCND1 and TOP2-A oncogenes. ErbB2 was co-amplified with TOP2-A. mRNA overexpression was detected for the amplified genes. ErbB2 protein was overexpressed and showed heterogeneous distribution. In summary, molecular cytogenetic analysis and expression profiling of B585 revealed several new alterations. Based on the experiments performed in SCID mice and the genotypic/phenotypic characteristics, this new in vivo breast cancer xenograft is a valuable model to investigate molecular mechanism of trastuzumab resistance
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
analysis
Animals
Antibodies
Antibodies,Monoclonal
Antineoplastic Agents
article
Biophysics
Breast Neoplasms
Carcinoma
Carcinoma,Ductal,Breast
Cell Line
Cell Line,Tumor
Comparative Genomic Hybridization
Disease Models,Animal
Drug Resistance,Neoplasm
drug therapy
EGFR
ErbB2
Female
Gene Expression
Gene Expression Profiling
genetics
Human
Humans
Hungary
Immunohistochemistry
In Situ Hybridization,Fluorescence
metabolism
Mice
Mice,Scid
Oncogenes
Phenotype
Receptor,erbB-2
Research
Research Support
rna
Support
therapeutic use
therapy
Trastuzumab resistance
OTKA::1
MAB::3.1
Megjelenés:Frontiers In Bioscience (elite edition). - 1 : 2 (2010), p. 627-640. -
További szerzők:Balázs Margit (1952-) (sejtbiológus, molekuláris genetikus) Lázár Viktória (1981-) (molekuláris biológus) Rákosy Zsuzsa (1978-) (sejtbiológus, molekuláris biológus, genetikus) Tóth Enikő Treszl Andrea (1974-) (molekuláris biológus) Vereb György (1965-) (biofizikus, orvos) Colbern, Gail T. Park, John W. Szöllősi János (1953-) (biofizikus)
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
Borító:

7.

001-es BibID:BIBFORM005174
035-os BibID:(scopus)38349044364 (wos)000253278400023
Első szerző:Barok Márk (biofizikus)
Cím:Trastuzumab decreases the number of circulating and disseminated tumor cells despite trastuzumab resistance of the primary tumor / Márk Barok, Margit Balázs, Péter Nagy, Zsuzsa Rákosy, Andrea Treszl, Enikő Tóth, István Juhász, John W. Park, Jorma Isola, György Vereb, János Szöllősi
Dátum:2008
ISSN:304-3835 (Print)
Megjegyzések:We have recently shown that despite of the fact that the ErbB2-positive JIMT-1 human breast cancer cells intrinsically resistant to trastuzumab in vitro, trastuzumab inhibited the outgrowth of early phase JIMT-1 xenografts in SCID mice via antibody-dependent cellular cytotoxicity (ADCC). Here we show that trastuzumab significantly reduces the number of circulating and disseminated tumor cells (CTCs and DTCs) in this xenograft model system at a time when the primary tumor is already unresponsive to trastuzumab. This observation suggests that ErbB2 positive CTCs and DTCs might be sensitive to trastuzumab-mediated ADCC even if when the primary tumor is already non-responsive. Thus, trastuzumab treatment might also be beneficial in the case of patients with breast cancer that is already trastuzumab resistant.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
analysis
Animals
antagonists and inhibitors
Antibodies
Antibodies, Monoclonal
Antigens
Antigens, CD45
Antineoplastic Agents
article
Biophysics
blood
Bone Marrow
Breast Neoplasms
Cell Line, Tumor
Cells
Chromosomes, Human,X
drug effects
Drug Resistance, Neoplasm
drug therapy
EGFR
Epidermal Growth Factor
ErbB2
Female
genetics
Histocompatibility Antigens
Histocompatibility Antigens Class I
Human
Humans
Hungary
Immunohistochemistry
immunology
In Situ Hybridization,Fluorescence
In Vitro
metabolism
Mice
Mice, Scid
mouse
Neoplasm Circulating Cells
Neoplasm Metastasis
pathology
pharmacology
Receptor, Epidermal Growth Factor
Research
Research Support
Support
therapeutic use
Time Factors
Trastuzumab resistance
Xenograft Model Antitumor Assays
egyetemen (Magyarországon) készült közlemény
Megjelenés:Cancer Letters. - 260 : 1-2 (2008), p. 198-208. -
További szerzők:Balázs Margit (1952-) (sejtbiológus, molekuláris genetikus) Nagy Péter (1971-) (biofizikus) Rákosy Zsuzsa (1978-) (sejtbiológus, molekuláris biológus, genetikus) Treszl Andrea (1974-) (molekuláris biológus) Tóth Enikő Juhász István (1956-) (bőrgyógyász, bőrsebész, kozmetológus, klinikai onkológus) Park, John W. Isola, Jorma Vereb György (1965-) (biofizikus, orvos) Szöllősi János (1953-) (biofizikus)
Internet cím:elektronikus változat
DOI
Borító:

8.

001-es BibID:BIBFORM006027
Első szerző:Bene László (biofizikus)
Cím:Lateral organization of the ICAM-1 molecule at the surface of human lymphoblasts : a possible model for its co-distribution with the IL-2 receptor, class I and class II HLA molecules / Bene L., Balázs M., Matkó J., Möst J., Dierich M. P., Szöllösi J., Damjanovich S.
Dátum:1994
Megjegyzések:Lateral distribution of the ICAM-1 molecule and its topological relationship (mutual proximity) to the heavy and light chains of class I HLA molecules, HLA-DR and interleukin-2 receptor alpha-chain (IL-2R alpha) were studied in the plasma membrane of HUT-102B2 T and JY B lymphoblastoid cell lines by the technique of flow cytometric energy transfer (FCET). Effects of adherency and treatments with recombinant interferon-gamma or tumor necrosis factor-alpha on the relative expression level of ICAM-1 to the above cell surface proteins were also investigated. While the cytokines did not significantly affect the ICAM-1 level of either cell line, an increased ICAM-1 expression was found on adherent JY cells. The ICAM-1 expression varied significantly with the cell cycle and culture conditions, as well. The statistical analysis of the differences observed in the energy transfer efficiency histograms resulted in a possible model of lateral co-distribution of these proteins in the plasma membrane. These two-dimensional patterns proved to be different for T and B lymphoma lines. ICAM-1 molecules showed a high degree of self-association on HUT-102B2 (T) cells, while they were mainly expressed as monomers on the surface of JY (B) cells. Both cells showed a significant (ca. 30%) difference between densities of the heavy and light chains of class I HLA antigen, suggesting a substantial amount of beta 2-microglobulin free heavy chains on these cell lines. The class I HLA molecules also showed partial self-association, but on both cell lines. The beta 2-microglobulin and the heavy chain of the class I HLA showed strongly different proximities to the IL-2R alpha, HLA-DR and ICAM-1 molecules, indicating that their orientations relative to the other proteins are dissimilar. IL-2R alpha molecules of the HUT-102B2 (T) cells are located mostly in the vicinity of the beta 2-microglobulin. In contrast, the local density of HLA-DR antigens is higher in the proximity of the heavy chain than in the vicinity of the beta 2-microglobulin. The possible functional significance of these protein patterns is also discussed herein.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
analysis
Antibodies,Monoclonal
B-Lymphocyte Subsets
beta 2-Microglobulin
Cell Adhesion
Cell Adhesion Molecules
Cell Cycle
Cell Line
Energy Transfer
Flow Cytometry
Histocompatibility Antigens Class I
HLA Antigens
HLA-D Antigens
HLA-DR Antigens
Human
Hungary
immunology
Intercellular Adhesion Molecule-1
Interferon Type II
Interleukin-2
Light
physiology
Receptors,Interleukin-2
Support,Non-U.S.Gov't
Support,U.S.Gov't,Non-P.H.S.
T-Lymphocyte Subsets
Tumor Necrosis Factor
Megjelenés:European Journal of Immunology. - 24 : 9 (1994), p. 2115-2123. -
További szerzők:Balázs Margit (1952-) (sejtbiológus, molekuláris genetikus) Matkó János (1952-) (biológus) Most, J. Dierich, Manfred P. Szöllősi János (1953-) (biofizikus) Damjanovich Sándor (1936-2017) (biofizikus)
Internet cím:DOI
Borító:

9.

001-es BibID:BIBFORM004939
Első szerző:Bene László (biofizikus)
Cím:Major histocompatibility complex class I protein conformation altered by transmembrane potential changes / Bene, L., Szollosi, J., Balazs, M., Matyus, L., Gaspar, R., Ameloot, M., Dale, R. E., Damjanovich, S.
Dátum:1997
ISSN:0196-4763
Megjegyzések:The nature of charge distributions in membrane-bound macromolecular structures renders them susceptible to interaction with transmembrane potential fields. As a result, conformational changes in such species may be expected to occur when this potential is altered. We have detected reversible conformational change in the major histocompatibility complex (MHC) class I antigen in the plasma membrane of human JY cells, as monitored by flow-cytometric resonance energy-transfer, upon reduction of the transmembrane potential (depolarization). This change increased the intramolecular energy-transfer efficiency between fluorescent donor- and acceptor-labeled monoclonal antibodies directed, respectively, to epitopes on the light (beta 2-microglobulin) and the heavy chains of the MHC class I antigen. Repolarization of the depolarized samples restored the energy-transfer efficiency to the original values measured before depolarization. Depolarization caused similar relative changes in fluorescence resonance energy-transfer efficiency when Fab fragments were used for labeling MHC class I complex, suggesting that the observed phenomenon is not restricted to whole monoclonal antibodies.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
Antibodies, Monoclonal
Antigen Presentation
B-Lymphocytes
beta 2-Microglobulin
Cell Membrane
chemistry
cytology
Dyes
Energy Transfer
Enzyme Activation
Flow Cytometry
Fluorescein-5-isothiocyanate
Fluorescence
Fluorescent Dyes
Histocompatibility Antigens Class I
Human
Hungary
immunology
Light
Major Histocompatibility Complex
Membrane Potentials
metabolism
methods
Na(+)-K(+)-Exchanging ATPase
Patch-Clamp Techniques
physiology
Protein Conformation
Rhodamines
Surface Properties
Megjelenés:Cytometry. - 27 : 4 (1997), p. 353-357. -
További szerzők:Szöllősi János (1953-) (biofizikus) Balázs Margit (1952-) (sejtbiológus, molekuláris genetikus) Mátyus László (1956-) (biofizikus) Gáspár Rezső (1944-) (biofizikus) Ameloot, Marcel Dale, Robert E. Damjanovich Sándor (1936-2017) (biofizikus)
Internet cím:elektronikus változat
Borító:

10.

001-es BibID:BIBFORM081015
Első szerző:Damjanovich Sándor (biofizikus)
Cím:Are lymphocytes excitable cells? / S. Damjanovich, Margit Balázs, J. Szöllősi
Dátum:1989
ISSN:0231-4428
Megjegyzések:Nerve and muscle cells are defined traditionally as excitable cells, due to their capacity to react to external stimuli with subsequent electric and/or mechanical responses. Another category of cells, eminently among them the round-shaped blood cells, in particular the best studied lymphocytes, are classified as non-excitable cells. We try to present evidence that lymphocytes may also be accepted as excitable cells. A bit far-reaching, further generalization could be formulated claiming that every cell can be considered as an excitable one.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény hazai lapban
folyóiratcikk
Megjelenés:Acta Physica Hungarica. - 65 : 2-3 (1989), p. 349-353. -
További szerzők:Balázs Margit (1952-) (sejtbiológus, molekuláris genetikus) Szöllősi János (1953-) (biofizikus)
Internet cím:DOI
Intézményi repozitóriumban (DEA) tárolt változat
Borító:

11.

001-es BibID:BIBFORM033287
Első szerző:Damjanovich Sándor (biofizikus)
Cím:Protein dynamics and function / Sándor Damjanovich, Margit Balázs, János Szöllősi, Lajos Trón, Béla Somogyi
Dátum:1988
Tárgyszavak:Orvostudományok Egészségtudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
egyetemen (Magyarországon) készült közlemény
Megjelenés:Journal of Molecular Catalysis. - 47 : 2-3 (1988), p. 155-163. -
További szerzők:Balázs Margit (1952-) (sejtbiológus, molekuláris genetikus) Szöllősi János (1953-) (biofizikus) Trón Lajos (1941-) (biofizikus) Somogyi Béla (1945-2006) (biofizikus)
Internet cím:Intézményi repozitóriumban (DEA) tárolt változat
Borító:

12.

001-es BibID:BIBFORM006028
Első szerző:Damjanovich Sándor (biofizikus)
Cím:Dynamic physical interactions of plasma membrane molecules generate cell surface patterns and regulate cell activation processes / Damjanovich S., Mátyus L., Balázs, M., Gáspár R., Krasznai Z., Pieri C., Szöllösi J., Trón L.
Dátum:1992
Megjegyzések:Molecular interaction and transmembrane signal transducing events generate a very dynamic and ever changing "pattern" in the plasma membranes. Lymphocytes, the key functional elements of the immune system, are eminently suited to be the primary targets to investigate these proximity, mobility, or other physical-chemical changes in their plasma membranes. Recently, a number of experiments suggested that processed peptides from antigens can bind specific components of MHC molecules (Elliott et al., 1991). This is certainly a way to alter their structure. Cell surface patterns of topological nature, assembly and disassembly of oligomeric receptor structure like the IL-2 receptor have been investigated by sophisticated biophysical techniques. The dynamic changes in the two-dimensional cell surface pattern and intramolecular conformational changes within this "larger" macro-pattern may have a strong regulatory role in signal transducing and intercellular recognition processes. Recent data on these problems are presented together with brief and critical discussions.
Tárgyszavak:Orvostudományok Elméleti orvostudományok idegen nyelvű folyóiratközlemény külföldi lapban
folyóiratcikk
Animal
Cell Membrane
Human
Hungary
immunology
Lymphocyte Transformation
Lymphocytes
Membrane Proteins
Peptides
Signal Transduction
Megjelenés:Immunobiology. - 185 : 2-4 (1992), p. 337-349. -
További szerzők:Mátyus László (1956-) (biofizikus) Balázs Margit (1952-) (sejtbiológus, molekuláris genetikus) Gáspár Rezső (1944-) (biofizikus) Krasznai Zoltán (1950-) (biofizikus) Pieri, Carlo Szöllősi János (1953-) (biofizikus) Trón Lajos (1941-) (biofizikus)
Internet cím:Intézményi repozitóriumban (DEA) tárolt változa
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