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Prognostic value of some tumor markers in unresectable stage IV oropharyngeal carcinoma patients treated with concomitant radiochemotherapy.

Radiology and oncology

Soba E, Budihna M, Smid L, Gale N, Lesnicar H, Zakotnik B, Strojan P.
PMID: 26834523
Radiol Oncol. 2015 Nov 27;49(4):365-70. doi: 10.2478/raon-2014-0048. eCollection 2015 Dec.

BACKGROUND: The aim of the study was to investigate how the expression of tumor markers p21, p27, p53, cyclin D1, EGFR, Ki-67, and CD31 influenced the outcome of advanced inoperable oropharyngeal carcinoma patients, treated with concomitant radiochemotherapy.PATIENTS AND METHODS:...

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Soba E, Budihna M, Smid L, et al. Prognostic value of some tumor markers in unresectable stage IV oropharyngeal carcinoma patients treated with concomitant radiochemotherapy. Radiol Oncol. 2015;49(4):365-70doi: 10.2478/raon-2014-0048.
Soba, E., Budihna, M., Smid, L., Gale, N., Lesnicar, H., Zakotnik, B., & Strojan, P. (2015). Prognostic value of some tumor markers in unresectable stage IV oropharyngeal carcinoma patients treated with concomitant radiochemotherapy. Radiology and oncology, 49(4), 365-70. https://doi.org/10.2478/raon-2014-0048
Soba, Erika, et al. "Prognostic value of some tumor markers in unresectable stage IV oropharyngeal carcinoma patients treated with concomitant radiochemotherapy." Radiology and oncology vol. 49,4 (2015): 365-70. doi: https://doi.org/10.2478/raon-2014-0048
Soba E, Budihna M, Smid L, Gale N, Lesnicar H, Zakotnik B, Strojan P. Prognostic value of some tumor markers in unresectable stage IV oropharyngeal carcinoma patients treated with concomitant radiochemotherapy. Radiol Oncol. 2015 Nov 27;49(4):365-70. doi: 10.2478/raon-2014-0048. eCollection 2015 Dec. PMID: 26834523; PMCID: PMC4722927.
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endo/exo isomerism in norcarane and 2-norcaranol hydrotrioxides (ROOOH).

The Journal of organic chemistry

Erzen E, Cerkovnik J, Plesnicar B.
PMID: 14604395
J Org Chem. 2003 Nov 14;68(23):9129-31. doi: 10.1021/jo035154m.

Ozonation of norcarane (1) yielded endo and exo norcarane hydrotrioxides (2a, 2b), as characterized by (1)H and (13)C NMR spectroscopy. Further ozonation of the primary decomposition products of these hydrotrioxides, i.e., 2-norcaranols (3), produced the corresponding isomeric 2-norcaranol hydrotrioxides...

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Erzen E, Cerkovnik J, Plesnicar B. endo/exo isomerism in norcarane and 2-norcaranol hydrotrioxides (ROOOH). J Org Chem. 2003;68(23):9129-31doi: 10.1021/jo035154m.
Erzen, E., Cerkovnik, J., & Plesnicar, B. (2003). endo/exo isomerism in norcarane and 2-norcaranol hydrotrioxides (ROOOH). The Journal of organic chemistry, 68(23), 9129-31. https://doi.org/10.1021/jo035154m
Erzen, Evgen, et al. "endo/exo isomerism in norcarane and 2-norcaranol hydrotrioxides (ROOOH)." The Journal of organic chemistry vol. 68,23 (2003): 9129-31. doi: https://doi.org/10.1021/jo035154m
Erzen E, Cerkovnik J, Plesnicar B. endo/exo isomerism in norcarane and 2-norcaranol hydrotrioxides (ROOOH). J Org Chem. 2003 Nov 14;68(23):9129-31. doi: 10.1021/jo035154m. PMID: 14604395.
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EFFECT OF SODIUM IODIDE, MAGNESIUM SULFATE, THYROXIN, AND THYROTROPIC HORMONE ON THE BLOOD MAGNESIUM PARTITION.

The Journal of clinical investigation

Soffer LJ, Cohn C, Lesnick G, Sobotka H, Jacobs M.
PMID: 16695100
J Clin Invest. 1944 Mar;23(2):263-6. doi: 10.1172/JCI101489.

No abstract available.

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Soffer LJ, Cohn C, Lesnick G, et al. EFFECT OF SODIUM IODIDE, MAGNESIUM SULFATE, THYROXIN, AND THYROTROPIC HORMONE ON THE BLOOD MAGNESIUM PARTITION. J Clin Invest. 1944;23(2):263-6doi: 10.1172/JCI101489.
Soffer, L. J., Cohn, C., Lesnick, G., Sobotka, H., & Jacobs, M. (1944). EFFECT OF SODIUM IODIDE, MAGNESIUM SULFATE, THYROXIN, AND THYROTROPIC HORMONE ON THE BLOOD MAGNESIUM PARTITION. The Journal of clinical investigation, 23(2), 263-6. https://doi.org/10.1172/JCI101489
Soffer, L J, et al. "EFFECT OF SODIUM IODIDE, MAGNESIUM SULFATE, THYROXIN, AND THYROTROPIC HORMONE ON THE BLOOD MAGNESIUM PARTITION." The Journal of clinical investigation vol. 23,2 (1944): 263-6. doi: https://doi.org/10.1172/JCI101489
Soffer LJ, Cohn C, Lesnick G, Sobotka H, Jacobs M. EFFECT OF SODIUM IODIDE, MAGNESIUM SULFATE, THYROXIN, AND THYROTROPIC HORMONE ON THE BLOOD MAGNESIUM PARTITION. J Clin Invest. 1944 Mar;23(2):263-6. doi: 10.1172/JCI101489. PMID: 16695100; PMCID: PMC435337.
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Attitudes of midwifery students towards teaching breast-self examination.

Radiology and oncology

Plesnicar A, Golicnik M, Fazarinc IK, Kralj B, Kovac V, Plesnicar BK.
PMID: 22933891
Radiol Oncol. 2010 Mar;44(1):52-6. doi: 10.2478/v10019-010-0009-9. Epub 2010 Mar 18.

BACKGROUND: The purpose of this study was to asses the attitude of undergraduate midwifery students towards teaching other women in methods of breast self-examination (BSE). PARTICIPANTS AND METHODS.: The study was performed at the beginning and at the end...

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Plesnicar A, Golicnik M, Fazarinc IK, et al. Attitudes of midwifery students towards teaching breast-self examination. Radiol Oncol. 2010;44(1):52-6doi: 10.2478/v10019-010-0009-9.
Plesnicar, A., Golicnik, M., Fazarinc, I. K., Kralj, B., Kovac, V., & Plesnicar, B. K. (2010). Attitudes of midwifery students towards teaching breast-self examination. Radiology and oncology, 44(1), 52-6. https://doi.org/10.2478/v10019-010-0009-9
Plesnicar, Andrej, et al. "Attitudes of midwifery students towards teaching breast-self examination." Radiology and oncology vol. 44,1 (2010): 52-6. doi: https://doi.org/10.2478/v10019-010-0009-9
Plesnicar A, Golicnik M, Fazarinc IK, Kralj B, Kovac V, Plesnicar BK. Attitudes of midwifery students towards teaching breast-self examination. Radiol Oncol. 2010 Mar;44(1):52-6. doi: 10.2478/v10019-010-0009-9. Epub 2010 Mar 18. PMID: 22933891; PMCID: PMC3423671.
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THE UTILIZATION OF INTRAVENOUSLY INJECTED SALT IN NORMALS AND IN PATIENTS WITH CUSHING'S SYNDROME BEFORE AND AFTER ADMINISTRATION OF DESOXYCORTICOSTERONE ACETATE.

The Journal of clinical investigation

Soffer LJ, Lesnick G, Sorkin SZ, Sobotka HH, Jacobs M.
PMID: 16695083
J Clin Invest. 1944 Jan;23(1):51-4. doi: 10.1172/JCI101472.

No abstract available.

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Soffer LJ, Lesnick G, Sorkin SZ, et al. THE UTILIZATION OF INTRAVENOUSLY INJECTED SALT IN NORMALS AND IN PATIENTS WITH CUSHING'S SYNDROME BEFORE AND AFTER ADMINISTRATION OF DESOXYCORTICOSTERONE ACETATE. J Clin Invest. 1944;23(1):51-4doi: 10.1172/JCI101472.
Soffer, L. J., Lesnick, G., Sorkin, S. Z., Sobotka, H. H., & Jacobs, M. (1944). THE UTILIZATION OF INTRAVENOUSLY INJECTED SALT IN NORMALS AND IN PATIENTS WITH CUSHING'S SYNDROME BEFORE AND AFTER ADMINISTRATION OF DESOXYCORTICOSTERONE ACETATE. The Journal of clinical investigation, 23(1), 51-4. https://doi.org/10.1172/JCI101472
Soffer, L J, et al. "THE UTILIZATION OF INTRAVENOUSLY INJECTED SALT IN NORMALS AND IN PATIENTS WITH CUSHING'S SYNDROME BEFORE AND AFTER ADMINISTRATION OF DESOXYCORTICOSTERONE ACETATE." The Journal of clinical investigation vol. 23,1 (1944): 51-4. doi: https://doi.org/10.1172/JCI101472
Soffer LJ, Lesnick G, Sorkin SZ, Sobotka HH, Jacobs M. THE UTILIZATION OF INTRAVENOUSLY INJECTED SALT IN NORMALS AND IN PATIENTS WITH CUSHING'S SYNDROME BEFORE AND AFTER ADMINISTRATION OF DESOXYCORTICOSTERONE ACETATE. J Clin Invest. 1944 Jan;23(1):51-4. doi: 10.1172/JCI101472. PMID: 16695083; PMCID: PMC435316.
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An efficient methyltrioxorhenium(VII)-catalyzed transformation of hydrotrioxides (ROOOH) into dihydrogen trioxide (HOOOH).

Journal of the American Chemical Society

Bergant A, Cerkovnik J, Plesnicar B, Tuttle T.
PMID: 18834116
J Am Chem Soc. 2008 Oct 29;130(43):14086-7. doi: 10.1021/ja806411a. Epub 2008 Oct 04.

Dihydrogen trioxide (HOOOH) is formed nearly quantitatively in the low-temperature (-70 degrees C) methyltrioxorhenium(VII) (MTO)-catalyzed transformation of silyl hydrotrioxides (R3SiOOOH), and some acetal hydrotrioxides, in various solvents, as confirmed by 1H, and 17O NMR spectroscopy. The calculated energetics (B3LYP)...

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Bergant A, Cerkovnik J, Plesnicar B, et al. An efficient methyltrioxorhenium(VII)-catalyzed transformation of hydrotrioxides (ROOOH) into dihydrogen trioxide (HOOOH). J Am Chem Soc. 2008;130(43):14086-7doi: 10.1021/ja806411a.
Bergant, A., Cerkovnik, J., Plesnicar, B., & Tuttle, T. (2008). An efficient methyltrioxorhenium(VII)-catalyzed transformation of hydrotrioxides (ROOOH) into dihydrogen trioxide (HOOOH). Journal of the American Chemical Society, 130(43), 14086-7. https://doi.org/10.1021/ja806411a
Bergant, Ana, et al. "An efficient methyltrioxorhenium(VII)-catalyzed transformation of hydrotrioxides (ROOOH) into dihydrogen trioxide (HOOOH)." Journal of the American Chemical Society vol. 130,43 (2008): 14086-7. doi: https://doi.org/10.1021/ja806411a
Bergant A, Cerkovnik J, Plesnicar B, Tuttle T. An efficient methyltrioxorhenium(VII)-catalyzed transformation of hydrotrioxides (ROOOH) into dihydrogen trioxide (HOOOH). J Am Chem Soc. 2008 Oct 29;130(43):14086-7. doi: 10.1021/ja806411a. Epub 2008 Oct 04. PMID: 18834116.
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Hemiortho esters and hydrotrioxides as the primary products in the low-temperature ozonation of cyclic acetals: an experimental and theoretical investigation.

Journal of the American Chemical Society

Tuttle T, Cerkovnik J, Plesnicar B, Cremer D.
PMID: 15584745
J Am Chem Soc. 2004 Dec 15;126(49):16093-104. doi: 10.1021/ja0450511.

Low-temperature ozonation (-78 degrees C) of 1,3-dioxolanes 1a-1f and 1,3-dioxanes 1g and h in acetone-d6, methyl acetate, and tert-butyl methyl ether produced both the corresponding hemiortho esters (2a-h, ROH) and acetal hydrotrioxides (3a-h, ROOOH) in molar ratios ROH/ROOOH ranging...

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Tuttle T, Cerkovnik J, Plesnicar B, et al. Hemiortho esters and hydrotrioxides as the primary products in the low-temperature ozonation of cyclic acetals: an experimental and theoretical investigation. J Am Chem Soc. 2004;126(49):16093-104doi: 10.1021/ja0450511.
Tuttle, T., Cerkovnik, J., Plesnicar, B., & Cremer, D. (2004). Hemiortho esters and hydrotrioxides as the primary products in the low-temperature ozonation of cyclic acetals: an experimental and theoretical investigation. Journal of the American Chemical Society, 126(49), 16093-104. https://doi.org/10.1021/ja0450511
Tuttle, Tell, et al. "Hemiortho esters and hydrotrioxides as the primary products in the low-temperature ozonation of cyclic acetals: an experimental and theoretical investigation." Journal of the American Chemical Society vol. 126,49 (2004): 16093-104. doi: https://doi.org/10.1021/ja0450511
Tuttle T, Cerkovnik J, Plesnicar B, Cremer D. Hemiortho esters and hydrotrioxides as the primary products in the low-temperature ozonation of cyclic acetals: an experimental and theoretical investigation. J Am Chem Soc. 2004 Dec 15;126(49):16093-104. doi: 10.1021/ja0450511. PMID: 15584745.
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Dihydrogen trioxide clusters, (HOOOH)n (n = 2-4), and the hydrogen-bonded complexes of HOOOH with acetone and dimethyl ether: implications for the decomposition of HOOOH.

The journal of physical chemistry. A

Kovacic S, Koller J, Cerkovnik J, Tuttle T, Plesnicar B.
PMID: 18698743
J Phys Chem A. 2008 Sep 04;112(35):8129-35. doi: 10.1021/jp8036928. Epub 2008 Aug 13.

Hydrogen-bonded gas-phase molecular clusters of dihydrogen trioxide (HOOOH) have been investigated using DFT (B3LYP/6-311++G(3df,3pd)) and MP2/6-311++G(3df,3pd) methods. The binding energies, vibrational frequencies, and dipole moments for the various dimer, trimer, and tetramer structures, in which HOOOH acts as a...

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Kovacic S, Koller J, Cerkovnik J, et al. Dihydrogen trioxide clusters, (HOOOH)n (n = 2-4), and the hydrogen-bonded complexes of HOOOH with acetone and dimethyl ether: implications for the decomposition of HOOOH. J Phys Chem A. 2008;112(35):8129-35doi: 10.1021/jp8036928.
Kovacic, S., Koller, J., Cerkovnik, J., Tuttle, T., & Plesnicar, B. (2008). Dihydrogen trioxide clusters, (HOOOH)n (n = 2-4), and the hydrogen-bonded complexes of HOOOH with acetone and dimethyl ether: implications for the decomposition of HOOOH. The journal of physical chemistry. A, 112(35), 8129-35. https://doi.org/10.1021/jp8036928
Kovacic, Sasa, et al. "Dihydrogen trioxide clusters, (HOOOH)n (n = 2-4), and the hydrogen-bonded complexes of HOOOH with acetone and dimethyl ether: implications for the decomposition of HOOOH." The journal of physical chemistry. A vol. 112,35 (2008): 8129-35. doi: https://doi.org/10.1021/jp8036928
Kovacic S, Koller J, Cerkovnik J, Tuttle T, Plesnicar B. Dihydrogen trioxide clusters, (HOOOH)n (n = 2-4), and the hydrogen-bonded complexes of HOOOH with acetone and dimethyl ether: implications for the decomposition of HOOOH. J Phys Chem A. 2008 Sep 04;112(35):8129-35. doi: 10.1021/jp8036928. Epub 2008 Aug 13. PMID: 18698743.
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Production of a self-activating CBM-factor X fusion protein in a stable transformed Sf9 insect cell line using high cell density perfusion culture.

Cytotechnology

Gorenflo VM, Pfeifer TA, Lesnicki G, Kwan EM, Grigliatti TA, Kilburn DG, Piret JM.
PMID: 19003232
Cytotechnology. 2004 Mar;44(3):93-102. doi: 10.1007/s10616-005-0703-4.

Factor Xa is a serine protease, whose high selectivity can be used to cleave protein tags from recombinant proteins. A fusion protein comprised of a self-activating form of factor X linked to a cellulose-binding module, saCBMFX, was produced in...

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Gorenflo VM, Pfeifer TA, Lesnicki G, et al. Production of a self-activating CBM-factor X fusion protein in a stable transformed Sf9 insect cell line using high cell density perfusion culture. Cytotechnology. 2004;44(3):93-102doi: 10.1007/s10616-005-0703-4.
Gorenflo, V. M., Pfeifer, T. A., Lesnicki, G., Kwan, E. M., Grigliatti, T. A., Kilburn, D. G., & Piret, J. M. (2004). Production of a self-activating CBM-factor X fusion protein in a stable transformed Sf9 insect cell line using high cell density perfusion culture. Cytotechnology, 44(3), 93-102. https://doi.org/10.1007/s10616-005-0703-4
Gorenflo, Volker M, et al. "Production of a self-activating CBM-factor X fusion protein in a stable transformed Sf9 insect cell line using high cell density perfusion culture." Cytotechnology vol. 44,3 (2004): 93-102. doi: https://doi.org/10.1007/s10616-005-0703-4
Gorenflo VM, Pfeifer TA, Lesnicki G, Kwan EM, Grigliatti TA, Kilburn DG, Piret JM. Production of a self-activating CBM-factor X fusion protein in a stable transformed Sf9 insect cell line using high cell density perfusion culture. Cytotechnology. 2004 Mar;44(3):93-102. doi: 10.1007/s10616-005-0703-4. PMID: 19003232; PMCID: PMC3449484.
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The role of the HOOO(-) anion in the ozonation of alcohols: large differences in the gas-phase and in the solution-phase mechanism.

Journal of the American Chemical Society

Wu A, Cremer D, Plesnicar B.
PMID: 12889970
J Am Chem Soc. 2003 Aug 06;125(31):9395-402. doi: 10.1021/ja030245m.

The mechanism of the ozonation of isopropyl alcohol was investigated for the gas and the solution phase using second-order many body perturbation theory and density functional theory (DFT) with the hybrid functional B3LYP and a 6-311++G(3df,3pd) basis set. A...

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Wu A, Cremer D, Plesnicar B. The role of the HOOO(-) anion in the ozonation of alcohols: large differences in the gas-phase and in the solution-phase mechanism. J Am Chem Soc. 2003;125(31):9395-402doi: 10.1021/ja030245m.
Wu, A., Cremer, D., & Plesnicar, B. (2003). The role of the HOOO(-) anion in the ozonation of alcohols: large differences in the gas-phase and in the solution-phase mechanism. Journal of the American Chemical Society, 125(31), 9395-402. https://doi.org/10.1021/ja030245m
Wu, Anan, et al. "The role of the HOOO(-) anion in the ozonation of alcohols: large differences in the gas-phase and in the solution-phase mechanism." Journal of the American Chemical Society vol. 125,31 (2003): 9395-402. doi: https://doi.org/10.1021/ja030245m
Wu A, Cremer D, Plesnicar B. The role of the HOOO(-) anion in the ozonation of alcohols: large differences in the gas-phase and in the solution-phase mechanism. J Am Chem Soc. 2003 Aug 06;125(31):9395-402. doi: 10.1021/ja030245m. PMID: 12889970.
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17O NMR spectroscopic characterization and the mechanism of formation of alkyl hydrotrioxides (ROOOH) and hydrogen trioxide (HOOOH) in the low-temperature ozonation of isopropyl alcohol and isopropyl methyl ether: water-assisted decomposition.

Chemistry (Weinheim an der Bergstrasse, Germany)

Plesnicar B, Cerkovnik J, Tekavec T, Koller J.
PMID: 10826603
Chemistry. 2000 Mar 03;6(5):809-19. doi: 10.1002/(sici)1521-3765(20000303)6:5<809::aid-chem809>3.0.co;2-8.

Low-temperature ozonation of isopropyl alcohol (1a) and isopropyl methyl ether (1b) in [D6]acetone, methyl acetate, and tert-butyl methyl ether at -78 degrees C produced the corresponding hydrotrioxides, Me2C(OH)(OOOH) (2a) and Me2C(OMe)(OOOH) (2b), along with hydrogen trioxide (HOOOH). All the...

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Plesnicar B, Cerkovnik J, Tekavec T, et al. 17O NMR spectroscopic characterization and the mechanism of formation of alkyl hydrotrioxides (ROOOH) and hydrogen trioxide (HOOOH) in the low-temperature ozonation of isopropyl alcohol and isopropyl methyl ether: water-assisted decomposition. Chemistry. 2000;6(5):809-19doi: 10.1002/(sici)1521-3765(20000303)6:5<809::aid-chem809>3.0.co;2-8.
Plesnicar, B., Cerkovnik, J., Tekavec, T., & Koller, J. (2000). 17O NMR spectroscopic characterization and the mechanism of formation of alkyl hydrotrioxides (ROOOH) and hydrogen trioxide (HOOOH) in the low-temperature ozonation of isopropyl alcohol and isopropyl methyl ether: water-assisted decomposition. Chemistry (Weinheim an der Bergstrasse, Germany), 6(5), 809-19. https://doi.org/10.1002/(sici)1521-3765(20000303)6:5<809::aid-chem809>3.0.co;2-8
Plesnicar, et al. "17O NMR spectroscopic characterization and the mechanism of formation of alkyl hydrotrioxides (ROOOH) and hydrogen trioxide (HOOOH) in the low-temperature ozonation of isopropyl alcohol and isopropyl methyl ether: water-assisted decomposition." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 6,5 (2000): 809-19. doi: https://doi.org/10.1002/(sici)1521-3765(20000303)6:5<809::aid-chem809>3.0.co;2-8
Plesnicar B, Cerkovnik J, Tekavec T, Koller J. 17O NMR spectroscopic characterization and the mechanism of formation of alkyl hydrotrioxides (ROOOH) and hydrogen trioxide (HOOOH) in the low-temperature ozonation of isopropyl alcohol and isopropyl methyl ether: water-assisted decomposition. Chemistry. 2000 Mar 03;6(5):809-19. doi: 10.1002/(sici)1521-3765(20000303)6:5<809::aid-chem809>3.0.co;2-8. PMID: 10826603.
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Very high-level production and export in Escherichia coli of a cellulose binding domain for use in a generic secretion-affinity fusion system.

Biotechnology and bioengineering

Hasenwinkle D, Jervis E, Kops O, Liu C, Lesnicki G, Haynes CA, Kilburn DG.
PMID: 18636596
Biotechnol Bioeng. 1997 Sep 20;55(6):854-63. doi: 10.1002/(SICI)1097-0290(19970920)55:6<854::AID-BIT4>3.0.CO;2-F.

A novel expression vector pTugA, previously constructed in our laboratory, was modified to provide kanamycin resistance (pTugK) and used to direct the synthesis of polypeptides as fusions with the C- or N-terminus of a cellulose binding domain which serves...

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Hasenwinkle D, Jervis E, Kops O, et al. Very high-level production and export in Escherichia coli of a cellulose binding domain for use in a generic secretion-affinity fusion system. Biotechnol Bioeng. 1997;55(6):854-63doi: 10.1002/(SICI)1097-0290(19970920)55:6<854::AID-BIT4>3.0.CO;2-F.
Hasenwinkle, D., Jervis, E., Kops, O., Liu, C., Lesnicki, G., Haynes, C. A., & Kilburn, D. G. (1997). Very high-level production and export in Escherichia coli of a cellulose binding domain for use in a generic secretion-affinity fusion system. Biotechnology and bioengineering, 55(6), 854-63. https://doi.org/10.1002/(SICI)1097-0290(19970920)55:6<854::AID-BIT4>3.0.CO;2-F
Hasenwinkle, D, et al. "Very high-level production and export in Escherichia coli of a cellulose binding domain for use in a generic secretion-affinity fusion system." Biotechnology and bioengineering vol. 55,6 (1997): 854-63. doi: https://doi.org/10.1002/(SICI)1097-0290(19970920)55:6<854::AID-BIT4>3.0.CO;2-F
Hasenwinkle D, Jervis E, Kops O, Liu C, Lesnicki G, Haynes CA, Kilburn DG. Very high-level production and export in Escherichia coli of a cellulose binding domain for use in a generic secretion-affinity fusion system. Biotechnol Bioeng. 1997 Sep 20;55(6):854-63. doi: 10.1002/(SICI)1097-0290(19970920)55:6<854::AID-BIT4>3.0.CO;2-F. PMID: 18636596.
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