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Vox Sanguinis International Forum on donor notification and counselling strategies for markers of transfusion-transmissible infections: summary.

Vox sanguinis

Sharma RR, Lozano M, Fearon M, Bigham M, Djoudi R, Gallian P, Woimant G, Lee C, Leung JNS, Tsoi WC, Marwaha N, Sachdev S, Tadokoro K, Tani Y, Matsukura H, Shantseva N, Zhiburt E, Hindawi S, Chay J, Huang T, Teo D, Moleli N, Oyonarte S, Jayasekara SBA, Bokhorst A, van den Burg P, Hewitt P, Bianco C, Kessler D.
PMID: 28318027
Vox Sang. 2017 May;112(4):388-396. doi: 10.1111/vox.12469. Epub 2017 Mar 20.

No abstract available.

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Sharma RR, Lozano M, Fearon M, et al. Vox Sanguinis International Forum on donor notification and counselling strategies for markers of transfusion-transmissible infections: summary. Vox Sang. 2017;112(4):388-396doi: 10.1111/vox.12469.
Sharma, R. R., Lozano, M., Fearon, M., Bigham, M., Djoudi, R., Gallian, P., Woimant, G., Lee, C., Leung, J. N. S., Tsoi, W. C., Marwaha, N., Sachdev, S., Tadokoro, K., Tani, Y., Matsukura, H., Shantseva, N., Zhiburt, E., Hindawi, S., Chay, J., Huang, T., Teo, D., Moleli, N., Oyonarte, S., Jayasekara, S. B. A., Bokhorst, A., van den Burg, P., Hewitt, P., Bianco, C., & Kessler, D. (2017). Vox Sanguinis International Forum on donor notification and counselling strategies for markers of transfusion-transmissible infections: summary. Vox sanguinis, 112(4), 388-396. https://doi.org/10.1111/vox.12469
Sharma, R R, et al. "Vox Sanguinis International Forum on donor notification and counselling strategies for markers of transfusion-transmissible infections: summary." Vox sanguinis vol. 112,4 (2017): 388-396. doi: https://doi.org/10.1111/vox.12469
Sharma RR, Lozano M, Fearon M, Bigham M, Djoudi R, Gallian P, Woimant G, Lee C, Leung JNS, Tsoi WC, Marwaha N, Sachdev S, Tadokoro K, Tani Y, Matsukura H, Shantseva N, Zhiburt E, Hindawi S, Chay J, Huang T, Teo D, Moleli N, Oyonarte S, Jayasekara SBA, Bokhorst A, van den Burg P, Hewitt P, Bianco C, Kessler D. Vox Sanguinis International Forum on donor notification and counselling strategies for markers of transfusion-transmissible infections: summary. Vox Sang. 2017 May;112(4):388-396. doi: 10.1111/vox.12469. Epub 2017 Mar 20. PMID: 28318027.
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Orthosteric and Allosteric Ligands of Nicotinic Acetylcholine Receptors for Smoking Cessation.

Frontiers in molecular neuroscience

Mohamed TS, Jayakar SS, Hamouda AK.
PMID: 26635524
Front Mol Neurosci. 2015 Nov 25;8:71. doi: 10.3389/fnmol.2015.00071. eCollection 2015.

Nicotine addiction, the result of tobacco use, leads to over six million premature deaths world-wide per year, a number that is expected to increase by a third within the next two decades. While more than half of smokers want...

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Mohamed TS, Jayakar SS, Hamouda AK. Orthosteric and Allosteric Ligands of Nicotinic Acetylcholine Receptors for Smoking Cessation. Front Mol Neurosci. 2015;8:71doi: 10.3389/fnmol.2015.00071.
Mohamed, T. S., Jayakar, S. S., & Hamouda, A. K. (2015). Orthosteric and Allosteric Ligands of Nicotinic Acetylcholine Receptors for Smoking Cessation. Frontiers in molecular neuroscience, 871. https://doi.org/10.3389/fnmol.2015.00071
Mohamed, Tasnim S, et al. "Orthosteric and Allosteric Ligands of Nicotinic Acetylcholine Receptors for Smoking Cessation." Frontiers in molecular neuroscience vol. 8 (2015): 71. doi: https://doi.org/10.3389/fnmol.2015.00071
Mohamed TS, Jayakar SS, Hamouda AK. Orthosteric and Allosteric Ligands of Nicotinic Acetylcholine Receptors for Smoking Cessation. Front Mol Neurosci. 2015 Nov 25;8:71. doi: 10.3389/fnmol.2015.00071. eCollection 2015. PMID: 26635524; PMCID: PMC4658446.
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Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes.

Chemical communications (Cambridge, England)

Tani Y, Kuga K, Fujihara T, Terao J, Tsuji Y.
PMID: 26179158
Chem Commun (Camb). 2015 Aug 21;51(65):13020-3. doi: 10.1039/c5cc03932k.

A highly selective carbon-carbon bond-forming transformation of carbon dioxide (CO2) to alcohol oxidation level has been disclosed. By employing a copper/bisphosphine catalyst system and hydrosilanes as mild and easy-to-handle reducing agents, various allenes can be reacted with CO2 to...

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Tani Y, Kuga K, Fujihara T, et al. Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes. Chem Commun (Camb). 2015;51(65):13020-3doi: 10.1039/c5cc03932k.
Tani, Y., Kuga, K., Fujihara, T., Terao, J., & Tsuji, Y. (2015). Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes. Chemical communications (Cambridge, England), 51(65), 13020-3. https://doi.org/10.1039/c5cc03932k
Tani, Yosuke, et al. "Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes." Chemical communications (Cambridge, England) vol. 51,65 (2015): 13020-3. doi: https://doi.org/10.1039/c5cc03932k
Tani Y, Kuga K, Fujihara T, Terao J, Tsuji Y. Copper-catalyzed C-C bond-forming transformation of CO2 to alcohol oxidation level: selective synthesis of homoallylic alcohols from allenes, CO2, and hydrosilanes. Chem Commun (Camb). 2015 Aug 21;51(65):13020-3. doi: 10.1039/c5cc03932k. PMID: 26179158.
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Single administration of vildagliptin attenuates postprandial hypertriglyceridemia and endothelial dysfunction in normoglycemic individuals.

Experimental and therapeutic medicine

Noguchi K, Hirota M, Miyoshi T, Tani Y, Noda Y, Ito H, Nanba S.
PMID: 25452780
Exp Ther Med. 2015 Jan;9(1):84-88. doi: 10.3892/etm.2014.2051. Epub 2014 Nov 05.

Postprandial hypertriglyceridemia impairs endothelial function and plays an important role in the development of atherosclerosis. The aim of the present study was to examine the postprandial effects of the dipeptidyl peptidase-4 inhibitor vildagliptin and the α-glucosidase inhibitor voglibose on...

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Noguchi K, Hirota M, Miyoshi T, et al. Single administration of vildagliptin attenuates postprandial hypertriglyceridemia and endothelial dysfunction in normoglycemic individuals. Exp Ther Med. 2014;9(1):84-88doi: 10.3892/etm.2014.2051.
Noguchi, K., Hirota, M., Miyoshi, T., Tani, Y., Noda, Y., Ito, H., & Nanba, S. (2015). Single administration of vildagliptin attenuates postprandial hypertriglyceridemia and endothelial dysfunction in normoglycemic individuals. Experimental and therapeutic medicine, 9(1), 84-88. https://doi.org/10.3892/etm.2014.2051
Noguchi, Kaoru, et al. "Single administration of vildagliptin attenuates postprandial hypertriglyceridemia and endothelial dysfunction in normoglycemic individuals." Experimental and therapeutic medicine vol. 9,1 (2015): 84-88. doi: https://doi.org/10.3892/etm.2014.2051
Noguchi K, Hirota M, Miyoshi T, Tani Y, Noda Y, Ito H, Nanba S. Single administration of vildagliptin attenuates postprandial hypertriglyceridemia and endothelial dysfunction in normoglycemic individuals. Exp Ther Med. 2015 Jan;9(1):84-88. doi: 10.3892/etm.2014.2051. Epub 2014 Nov 05. PMID: 25452780; PMCID: PMC4247303.
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Patents and literature.

Applied biochemistry and biotechnology

Kit M, Narasimhan MJ, Anderson JA, Zimmermann U, Pilwat G, Furuya T, Tani Y, Kolehmainen SE, Tarkkanen V, Barrett SP, Gestrelius SM, Belloc A, Florent J, Lunel J, Palla J, Mancy D, Bailey JE, Cho YK, Mouri T, Kayama H, Foley SE, Oriel PJ, Epstein CC, Kimura K, Spraker PW, Ljungdahl LG, Wieget JK, Levine DW, Thilly WG, Wang DI, Wong JS, Eisinger MG, Young FE, Wilson GA, Mottice SL, Green H, Kehinde O, Buhler M, Olofsson M, Osseux PF, Degen L, Branduzzi P, Olivieri R, Cimini N, Kang KS, Veeder GT, Latymer Z, Andersen G, Drobot W, Monsheimer R, Pfleiderer E, Hidaka H, Kohno T, Eida T, Weisrock WP, Stevens VC, Takezawa K, Hiratani H, Wandrey C, Wichmann R, Leuchtenberger W, Kula M, Buckmann A, Troller J, Koshugi J, Frommer W, Muller L, Schmidt D, Puls W, Krause H, Heber U, Cohen SN, Wahl GM, Stark GR, Collins J, Hohn B, Sugano H, Matsui Y.
PMID: 24234232
Appl Biochem Biotechnol. 1982 May;7(3):217-30. doi: 10.1007/BF02798299.

No abstract available.

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Kit M, Narasimhan MJ, Anderson JA, et al. Patents and literature. Appl Biochem Biotechnol. 1982;7(3):217-30doi: 10.1007/BF02798299.
Kit, M., Narasimhan, M. J., Anderson, J. A., Zimmermann, U., Pilwat, G., Furuya, T., Tani, Y., Kolehmainen, S. E., Tarkkanen, V., Barrett, S. P., Gestrelius, S. M., Belloc, A., Florent, J., Lunel, J., Palla, J., Mancy, D., Bailey, J. E., Cho, Y. K., Mouri, T., Kayama, H., Foley, S. E., Oriel, P. J., Epstein, C. C., Kimura, K., Spraker, P. W., Ljungdahl, L. G., Wieget, J. K., Levine, D. W., Thilly, W. G., Wang, D. I., Wong, J. S., Eisinger, M. G., Young, F. E., Wilson, G. A., Mottice, S. L., Green, H., Kehinde, O., Buhler, M., Olofsson, M., Osseux, P. F., Degen, L., Branduzzi, P., Olivieri, R., Cimini, N., Kang, K. S., Veeder, G. T., Latymer, Z., Andersen, G., Drobot, W., Monsheimer, R., Pfleiderer, E., Hidaka, H., Kohno, T., Eida, T., Weisrock, W. P., Stevens, V. C., Takezawa, K., Hiratani, H., Wandrey, C., Wichmann, R., Leuchtenberger, W., Kula, M., Buckmann, A., Troller, J., Koshugi, J., Frommer, W., Muller, L., Schmidt, D., Puls, W., Krause, H., Heber, U., Cohen, S. N., Wahl, G. M., Stark, G. R., Collins, J., Hohn, B., Sugano, H., & Matsui, Y. (1982). Patents and literature. Applied biochemistry and biotechnology, 7(3), 217-30. https://doi.org/10.1007/BF02798299
Kit, M, et al. "Patents and literature." Applied biochemistry and biotechnology vol. 7,3 (1982): 217-30. doi: https://doi.org/10.1007/BF02798299
Kit M, Narasimhan MJ, Anderson JA, Zimmermann U, Pilwat G, Furuya T, Tani Y, Kolehmainen SE, Tarkkanen V, Barrett SP, Gestrelius SM, Belloc A, Florent J, Lunel J, Palla J, Mancy D, Bailey JE, Cho YK, Mouri T, Kayama H, Foley SE, Oriel PJ, Epstein CC, Kimura K, Spraker PW, Ljungdahl LG, Wieget JK, Levine DW, Thilly WG, Wang DI, Wong JS, Eisinger MG, Young FE, Wilson GA, Mottice SL, Green H, Kehinde O, Buhler M, Olofsson M, Osseux PF, Degen L, Branduzzi P, Olivieri R, Cimini N, Kang KS, Veeder GT, Latymer Z, Andersen G, Drobot W, Monsheimer R, Pfleiderer E, Hidaka H, Kohno T, Eida T, Weisrock WP, Stevens VC, Takezawa K, Hiratani H, Wandrey C, Wichmann R, Leuchtenberger W, Kula M, Buckmann A, Troller J, Koshugi J, Frommer W, Muller L, Schmidt D, Puls W, Krause H, Heber U, Cohen SN, Wahl GM, Stark GR, Collins J, Hohn B, Sugano H, Matsui Y. Patents and literature. Appl Biochem Biotechnol. 1982 May;7(3):217-30. doi: 10.1007/BF02798299. PMID: 24234232.
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Allium sativum L. Improves Visual Memory and Attention in Healthy Human Volunteers.

Evidence-based complementary and alternative medicine : eCAM

Tasnim S, Haque PS, Bari MS, Hossain MM, Islam SM, Shahriar M, Bhuiyan MA, Bin Sayeed MS.
PMID: 26351508
Evid Based Complement Alternat Med. 2015;2015:103416. doi: 10.1155/2015/103416. Epub 2015 Aug 13.

Studies have shown that Allium sativum L. (AS) protects amyloid-beta peptide-induced apoptosis, prevents oxidative insults to neurons and synapses, and thus prevent Alzheimer's disease progression in experimental animals. However, there is no experimental evidence in human regarding its putative...

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Tasnim S, Haque PS, Bari MS, et al. Allium sativum L. Improves Visual Memory and Attention in Healthy Human Volunteers. Evid Based Complement Alternat Med. 2015;2015:103416doi: 10.1155/2015/103416.
Tasnim, S., Haque, P. S., Bari, M. S., Hossain, M. M., Islam, S. M., Shahriar, M., Bhuiyan, M. A., & Bin Sayeed, M. S. (2015). Allium sativum L. Improves Visual Memory and Attention in Healthy Human Volunteers. Evidence-based complementary and alternative medicine : eCAM, 2015103416. https://doi.org/10.1155/2015/103416
Tasnim, Sara, et al. "Allium sativum L. Improves Visual Memory and Attention in Healthy Human Volunteers." Evidence-based complementary and alternative medicine : eCAM vol. 2015 (2015): 103416. doi: https://doi.org/10.1155/2015/103416
Tasnim S, Haque PS, Bari MS, Hossain MM, Islam SM, Shahriar M, Bhuiyan MA, Bin Sayeed MS. Allium sativum L. Improves Visual Memory and Attention in Healthy Human Volunteers. Evid Based Complement Alternat Med. 2015;2015:103416. doi: 10.1155/2015/103416. Epub 2015 Aug 13. PMID: 26351508; PMCID: PMC4550798.
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Diastereoselective photochromism of a bisbenzothienylethene governed by steric as well as electronic interactions.

Journal of the American Chemical Society

Yokoyama Y, Shiraishi H, Tani Y, Yokoyama Y, Yamaguchi Y.
PMID: 12797790
J Am Chem Soc. 2003 Jun 18;125(24):7194-5. doi: 10.1021/ja029535d.

Introduction of an asymmetric center to C-2 of one of the benzothiophene rings of bisbenzothienylperfluorocyclopentene results in a highly diastereoselective photochromic system. The stereogenic center bears a hydrogen atom, a methyl group, and a methoxymethoxy group. The steric as...

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Yokoyama Y, Shiraishi H, Tani Y, et al. Diastereoselective photochromism of a bisbenzothienylethene governed by steric as well as electronic interactions. J Am Chem Soc. 2003;125(24):7194-5doi: 10.1021/ja029535d.
Yokoyama, Y., Shiraishi, H., Tani, Y., Yokoyama, Y., & Yamaguchi, Y. (2003). Diastereoselective photochromism of a bisbenzothienylethene governed by steric as well as electronic interactions. Journal of the American Chemical Society, 125(24), 7194-5. https://doi.org/10.1021/ja029535d
Yokoyama, Yasushi, et al. "Diastereoselective photochromism of a bisbenzothienylethene governed by steric as well as electronic interactions." Journal of the American Chemical Society vol. 125,24 (2003): 7194-5. doi: https://doi.org/10.1021/ja029535d
Yokoyama Y, Shiraishi H, Tani Y, Yokoyama Y, Yamaguchi Y. Diastereoselective photochromism of a bisbenzothienylethene governed by steric as well as electronic interactions. J Am Chem Soc. 2003 Jun 18;125(24):7194-5. doi: 10.1021/ja029535d. PMID: 12797790.
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Chemical force microscopy of microcontact-printed self-assembled monolayers by pulsed-force-mode atomic force microscopy.

Ultramicroscopy

Okabe Y, Furugori M, Tani Y, Akiba U, Fujihira M.
PMID: 10741671
Ultramicroscopy. 2000 Feb;82(1):203-12. doi: 10.1016/s0304-3991(99)00143-6.

A novel chemically sensitive imaging mode based on adhesive force detection by previously developed pulsed-force-mode atomic force microscopy (PFM-AFM) is presented. PFM-AFM enables simultaneous imaging of surface topography and adhesive force between tip and sample surfaces. Since the adhesive...

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Okabe Y, Furugori M, Tani Y, et al. Chemical force microscopy of microcontact-printed self-assembled monolayers by pulsed-force-mode atomic force microscopy. Ultramicroscopy. 2000;82(1):203-12doi: 10.1016/s0304-3991(99)00143-6.
Okabe, Y., Furugori, M., Tani, Y., Akiba, U., & Fujihira, M. (2000). Chemical force microscopy of microcontact-printed self-assembled monolayers by pulsed-force-mode atomic force microscopy. Ultramicroscopy, 82(1), 203-12. https://doi.org/10.1016/s0304-3991(99)00143-6
Okabe, et al. "Chemical force microscopy of microcontact-printed self-assembled monolayers by pulsed-force-mode atomic force microscopy." Ultramicroscopy vol. 82,1 (2000): 203-12. doi: https://doi.org/10.1016/s0304-3991(99)00143-6
Okabe Y, Furugori M, Tani Y, Akiba U, Fujihira M. Chemical force microscopy of microcontact-printed self-assembled monolayers by pulsed-force-mode atomic force microscopy. Ultramicroscopy. 2000 Feb;82(1):203-12. doi: 10.1016/s0304-3991(99)00143-6. PMID: 10741671.
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RHC/c genotyping based on polymorphism in the promoter region of the RHCE gene.

Legal medicine (Tokyo, Japan)

Tanaka M, Yamashita N, Takahashi J, Hirayama F, Kajii E, Tani Y.
PMID: 12935697
Leg Med (Tokyo). 2001 Dec;3(4):205-12. doi: 10.1016/s1344-6223(01)00035-9.

Designing of PCR tests for the RHC allele is difficult because of the high DNA sequence homology between RHC and RHD genes, which differ by only a one-nucleotide substitution at position 48 in exon 1 of the RHCE gene....

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Tanaka M, Yamashita N, Takahashi J, et al. RHC/c genotyping based on polymorphism in the promoter region of the RHCE gene. Leg Med (Tokyo). 2001;3(4):205-12doi: 10.1016/s1344-6223(01)00035-9.
Tanaka, M., Yamashita, N., Takahashi, J., Hirayama, F., Kajii, E., & Tani, Y. (2001). RHC/c genotyping based on polymorphism in the promoter region of the RHCE gene. Legal medicine (Tokyo, Japan), 3(4), 205-12. https://doi.org/10.1016/s1344-6223(01)00035-9
Tanaka, M, et al. "RHC/c genotyping based on polymorphism in the promoter region of the RHCE gene." Legal medicine (Tokyo, Japan) vol. 3,4 (2001): 205-12. doi: https://doi.org/10.1016/s1344-6223(01)00035-9
Tanaka M, Yamashita N, Takahashi J, Hirayama F, Kajii E, Tani Y. RHC/c genotyping based on polymorphism in the promoter region of the RHCE gene. Leg Med (Tokyo). 2001 Dec;3(4):205-12. doi: 10.1016/s1344-6223(01)00035-9. PMID: 12935697.
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Glycolaldehyde-forming route in Bacillus subtilis in relation to vitamin B6 biosynthesis.

Journal of bioscience and bioengineering

Sakai A, Katayama K, Katsuragi T, Tani Y.
PMID: 16232966
J Biosci Bioeng. 2001;91(2):147-52. doi: 10.1263/jbb.91.147.

Glycolaldehyde (GA) was shown to be a precursor of vitamin B6 (B6), and to be formed from glycolate by glycolaldehyde dehydrogenase (GADH) in Escherichia coli. In this study, we show the glycolaldehyde-forming route in B6 biosynthesis in Bacillus subtilis....

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Sakai A, Katayama K, Katsuragi T, et al. Glycolaldehyde-forming route in Bacillus subtilis in relation to vitamin B6 biosynthesis. J Biosci Bioeng. 2001;91(2):147-52doi: 10.1263/jbb.91.147.
Sakai, A., Katayama, K., Katsuragi, T., & Tani, Y. (2001). Glycolaldehyde-forming route in Bacillus subtilis in relation to vitamin B6 biosynthesis. Journal of bioscience and bioengineering, 91(2), 147-52. https://doi.org/10.1263/jbb.91.147
Sakai, A, et al. "Glycolaldehyde-forming route in Bacillus subtilis in relation to vitamin B6 biosynthesis." Journal of bioscience and bioengineering vol. 91,2 (2001): 147-52. doi: https://doi.org/10.1263/jbb.91.147
Sakai A, Katayama K, Katsuragi T, Tani Y. Glycolaldehyde-forming route in Bacillus subtilis in relation to vitamin B6 biosynthesis. J Biosci Bioeng. 2001;91(2):147-52. doi: 10.1263/jbb.91.147. PMID: 16232966.
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Polyol production by culture of methanol-utilizing yeast.

Journal of bioscience and bioengineering

Suryadi H, Katsuragi T, Yoshida N, Suzuki S, Tani Y.
PMID: 16232735
J Biosci Bioeng. 2000;89(3):236-40. doi: 10.1016/s1389-1723(00)88825-8.

Four methanol-utilizing yeasts, Candida boidinii, Hansenula polymorpha, Hansenula ofunaensis, and Pichia pinus, produced polyols from corresponding sugars in a methanol medium. H. polymorpha produced larger amounts of xylitol than the other yeasts. Productivity was the highest at pH 8...

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Suryadi H, Katsuragi T, Yoshida N, et al. Polyol production by culture of methanol-utilizing yeast. J Biosci Bioeng. 2000;89(3):236-40doi: 10.1016/s1389-1723(00)88825-8.
Suryadi, H., Katsuragi, T., Yoshida, N., Suzuki, S., & Tani, Y. (2000). Polyol production by culture of methanol-utilizing yeast. Journal of bioscience and bioengineering, 89(3), 236-40. https://doi.org/10.1016/s1389-1723(00)88825-8
Suryadi, H, et al. "Polyol production by culture of methanol-utilizing yeast." Journal of bioscience and bioengineering vol. 89,3 (2000): 236-40. doi: https://doi.org/10.1016/s1389-1723(00)88825-8
Suryadi H, Katsuragi T, Yoshida N, Suzuki S, Tani Y. Polyol production by culture of methanol-utilizing yeast. J Biosci Bioeng. 2000;89(3):236-40. doi: 10.1016/s1389-1723(00)88825-8. PMID: 16232735.
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Stereoselective oxidation of alkylbenzenes by fungi.

Journal of bioscience and bioengineering

Uzura A, Katsuragi T, Tani Y.
PMID: 16232978
J Biosci Bioeng. 2001;91(2):217-21. doi: 10.1263/jbb.91.217.

Oxygenase is useful when oxygen is to be introduced at a nonactivated carbon-hydrogen bond to give an optically active center. To obtain such an enzyme from microorganisms, we screened soil samples for organisms that assimilated methylethylketone as their sole...

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Uzura A, Katsuragi T, Tani Y. Stereoselective oxidation of alkylbenzenes by fungi. J Biosci Bioeng. 2001;91(2):217-21doi: 10.1263/jbb.91.217.
Uzura, A., Katsuragi, T., & Tani, Y. (2001). Stereoselective oxidation of alkylbenzenes by fungi. Journal of bioscience and bioengineering, 91(2), 217-21. https://doi.org/10.1263/jbb.91.217
Uzura, A, et al. "Stereoselective oxidation of alkylbenzenes by fungi." Journal of bioscience and bioengineering vol. 91,2 (2001): 217-21. doi: https://doi.org/10.1263/jbb.91.217
Uzura A, Katsuragi T, Tani Y. Stereoselective oxidation of alkylbenzenes by fungi. J Biosci Bioeng. 2001;91(2):217-21. doi: 10.1263/jbb.91.217. PMID: 16232978.
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