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The binding sites for Escherichia coli RNA polymerase on lambda phage DNA: Characteristics of binding sites on sonicated lambda DNA.

FEBS letters

Nakano E, Sakaguchi K.
PMID: 11945740
FEBS Lett. 1971 Apr 30;14(3):139-142. doi: 10.1016/0014-5793(71)80088-1.

No abstract available.

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Nakano E, Sakaguchi K. The binding sites for Escherichia coli RNA polymerase on lambda phage DNA: Characteristics of binding sites on sonicated lambda DNA. FEBS Lett. 1971;14(3):139-142doi: 10.1016/0014-5793(71)80088-1.
Nakano, E., & Sakaguchi, K. (1971). The binding sites for Escherichia coli RNA polymerase on lambda phage DNA: Characteristics of binding sites on sonicated lambda DNA. FEBS letters, 14(3), 139-142. https://doi.org/10.1016/0014-5793(71)80088-1
Nakano, E, and Sakaguchi, K. "The binding sites for Escherichia coli RNA polymerase on lambda phage DNA: Characteristics of binding sites on sonicated lambda DNA." FEBS letters vol. 14,3 (1971): 139-142. doi: https://doi.org/10.1016/0014-5793(71)80088-1
Nakano E, Sakaguchi K. The binding sites for Escherichia coli RNA polymerase on lambda phage DNA: Characteristics of binding sites on sonicated lambda DNA. FEBS Lett. 1971 Apr 30;14(3):139-142. doi: 10.1016/0014-5793(71)80088-1. PMID: 11945740.
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Development of a new enzyme-linked immunosorbent assay for the detection of anti-M2 in primary biliary cirrhosis.

Hepatology research : the official journal of the Japan Society of Hepatology

Jong-Hon K, Yajima R, Karino Y, Yoshida J, Tsuji K, Watanabe S, Horada K, Itoh Y, Sekiguchi K, Toyoda S, Maekubo H.
PMID: 11470623
Hepatol Res. 2001 Sep;21(1):1-7. doi: 10.1016/s1386-6346(01)00075-4.

We developed a new enzyme-linked immunosorbent assay (ELISA) for the detection of antimitochondrial antibody (AMA)-M2 in sera from patients with primary biliary cirrhosis (PBC), using 2-oxo-acid dehydrogenase complex (2-OADC) purified from porcine myocardium as the antigen source. The immunoreactivity...

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Jong-Hon K, Yajima R, Karino Y, et al. Development of a new enzyme-linked immunosorbent assay for the detection of anti-M2 in primary biliary cirrhosis. Hepatol Res. 2001;21(1):1-7doi: 10.1016/s1386-6346(01)00075-4.
Jong-Hon, K., Yajima, R., Karino, Y., Yoshida, J., Tsuji, K., Watanabe, S., Horada, K., Itoh, Y., Sekiguchi, K., Toyoda, S., & Maekubo, H. (2001). Development of a new enzyme-linked immunosorbent assay for the detection of anti-M2 in primary biliary cirrhosis. Hepatology research : the official journal of the Japan Society of Hepatology, 21(1), 1-7. https://doi.org/10.1016/s1386-6346(01)00075-4
Jong-Hon, K, et al. "Development of a new enzyme-linked immunosorbent assay for the detection of anti-M2 in primary biliary cirrhosis." Hepatology research : the official journal of the Japan Society of Hepatology vol. 21,1 (2001): 1-7. doi: https://doi.org/10.1016/s1386-6346(01)00075-4
Jong-Hon K, Yajima R, Karino Y, Yoshida J, Tsuji K, Watanabe S, Horada K, Itoh Y, Sekiguchi K, Toyoda S, Maekubo H. Development of a new enzyme-linked immunosorbent assay for the detection of anti-M2 in primary biliary cirrhosis. Hepatol Res. 2001 Sep;21(1):1-7. doi: 10.1016/s1386-6346(01)00075-4. PMID: 11470623.
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Collision-induced dissociation spectra versus collision energy (collision-induced dissociation curve) using a quadrupole ion trap mass spectrometer. II.(1) loss of CO from ionized o-, m- and p-anisoyl fluoride, CH(3)OC(6)H(4)COF(+.).

Journal of mass spectrometry : JMS

Tajima S, Siang LF, Fujishige M, Nakajima S, Sekiguchi O.
PMID: 11006609
J Mass Spectrom. 2000 Sep;35(9):1144-6. doi: 10.1002/1096-9888(200009)35:9<1144::AID-JMS43>3.0.CO;2-Q.

No abstract available.

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Tajima S, Siang LF, Fujishige M, et al. Collision-induced dissociation spectra versus collision energy (collision-induced dissociation curve) using a quadrupole ion trap mass spectrometer. II.(1) loss of CO from ionized o-, m- and p-anisoyl fluoride, CH(3)OC(6)H(4)COF(+.). J Mass Spectrom. 2000;35(9):1144-6doi: 10.1002/1096-9888(200009)35:9<1144::AID-JMS43>3.0.CO;2-Q.
Tajima, S., Siang, L. F., Fujishige, M., Nakajima, S., & Sekiguchi, O. (2000). Collision-induced dissociation spectra versus collision energy (collision-induced dissociation curve) using a quadrupole ion trap mass spectrometer. II.(1) loss of CO from ionized o-, m- and p-anisoyl fluoride, CH(3)OC(6)H(4)COF(+.). Journal of mass spectrometry : JMS, 35(9), 1144-6. https://doi.org/10.1002/1096-9888(200009)35:9<1144::AID-JMS43>3.0.CO;2-Q
Tajima, et al. "Collision-induced dissociation spectra versus collision energy (collision-induced dissociation curve) using a quadrupole ion trap mass spectrometer. II.(1) loss of CO from ionized o-, m- and p-anisoyl fluoride, CH(3)OC(6)H(4)COF(+.)." Journal of mass spectrometry : JMS vol. 35,9 (2000): 1144-6. doi: https://doi.org/10.1002/1096-9888(200009)35:9<1144::AID-JMS43>3.0.CO;2-Q
Tajima S, Siang LF, Fujishige M, Nakajima S, Sekiguchi O. Collision-induced dissociation spectra versus collision energy (collision-induced dissociation curve) using a quadrupole ion trap mass spectrometer. II.(1) loss of CO from ionized o-, m- and p-anisoyl fluoride, CH(3)OC(6)H(4)COF(+.). J Mass Spectrom. 2000 Sep;35(9):1144-6. doi: 10.1002/1096-9888(200009)35:9<1144::AID-JMS43>3.0.CO;2-Q. PMID: 11006609.
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Stepwise charge separation and charge recombination in ferrocene-meso,meso-linked porphyrin dimer-fullerene triad.

Journal of the American Chemical Society

Imahori H, Tamaki K, Araki Y, Sekiguchi Y, Ito O, Sakata Y, Fukuzumi S.
PMID: 11982381
J Am Chem Soc. 2002 May 08;124(18):5165-74. doi: 10.1021/ja016655x.

A meso,meso-linked porphyrin dimer [(ZnP)(2)] as a light-harvesting chromophore has been incorporated into a photosynthetic multistep electron-transfer model for the first time, including ferrocene (Fc), as an electron donor and fullerene (C(60)) as an electron acceptor to construct the...

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Imahori H, Tamaki K, Araki Y, et al. Stepwise charge separation and charge recombination in ferrocene-meso,meso-linked porphyrin dimer-fullerene triad. J Am Chem Soc. 2002;124(18):5165-74doi: 10.1021/ja016655x.
Imahori, H., Tamaki, K., Araki, Y., Sekiguchi, Y., Ito, O., Sakata, Y., & Fukuzumi, S. (2002). Stepwise charge separation and charge recombination in ferrocene-meso,meso-linked porphyrin dimer-fullerene triad. Journal of the American Chemical Society, 124(18), 5165-74. https://doi.org/10.1021/ja016655x
Imahori, Hiroshi, et al. "Stepwise charge separation and charge recombination in ferrocene-meso,meso-linked porphyrin dimer-fullerene triad." Journal of the American Chemical Society vol. 124,18 (2002): 5165-74. doi: https://doi.org/10.1021/ja016655x
Imahori H, Tamaki K, Araki Y, Sekiguchi Y, Ito O, Sakata Y, Fukuzumi S. Stepwise charge separation and charge recombination in ferrocene-meso,meso-linked porphyrin dimer-fullerene triad. J Am Chem Soc. 2002 May 08;124(18):5165-74. doi: 10.1021/ja016655x. PMID: 11982381.
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Isolable silyl and germyl radicals lacking conjugation with pi-bonds: synthesis, characterization, and reactivity.

Journal of the American Chemical Society

Sekiguchi A, Fukawa T, Nakamoto M, Lee VY, Ichinohe M.
PMID: 12175246
J Am Chem Soc. 2002 Aug 21;124(33):9865-9. doi: 10.1021/ja0126780.

The one-electron oxidation reaction of tris[di-tert-butyl(methyl)silyl]silyl and -germyl anions with dichlorogermylene-dioxane complex results in the formation of stable tris[di-tert-butyl(methyl)silyl]silyl and -germyl radicals 1 and 2, representing the first isolable radical species of heavier Group 14 elements lacking stabilization by...

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Sekiguchi A, Fukawa T, Nakamoto M, et al. Isolable silyl and germyl radicals lacking conjugation with pi-bonds: synthesis, characterization, and reactivity. J Am Chem Soc. 2002;124(33):9865-9doi: 10.1021/ja0126780.
Sekiguchi, A., Fukawa, T., Nakamoto, M., Lee, V. Y., & Ichinohe, M. (2002). Isolable silyl and germyl radicals lacking conjugation with pi-bonds: synthesis, characterization, and reactivity. Journal of the American Chemical Society, 124(33), 9865-9. https://doi.org/10.1021/ja0126780
Sekiguchi, Akira, et al. "Isolable silyl and germyl radicals lacking conjugation with pi-bonds: synthesis, characterization, and reactivity." Journal of the American Chemical Society vol. 124,33 (2002): 9865-9. doi: https://doi.org/10.1021/ja0126780
Sekiguchi A, Fukawa T, Nakamoto M, Lee VY, Ichinohe M. Isolable silyl and germyl radicals lacking conjugation with pi-bonds: synthesis, characterization, and reactivity. J Am Chem Soc. 2002 Aug 21;124(33):9865-9. doi: 10.1021/ja0126780. PMID: 12175246.
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1,4,5-trigermabicyclo[2.1.0]pent-2-en-5-ylium: the isolable bishomocyclopropenylium ion containing a heavier group 14 element.

Journal of the American Chemical Society

Ishida Y, Sekiguchi A, Kabe Y.
PMID: 13129328
J Am Chem Soc. 2003 Sep 24;125(38):11468-9. doi: 10.1021/ja030327a.

The isolable bishomoaromatic cation containing a heavier Group 14 element, (2,3,5-deloc)-2-phenyl-1,4,5-tris(tri-tert-butylsilyl)-1,4,5-trigermabicyclo[2.1.0]pent-2-en-5-ylium TPFPB- (2+.TPFPB-; TPFPB- = tetrakis(pentafluorophenyl)borate) was synthesized by the reaction of 5-bromo-2-phenyl-1,4,5-tris(tri-tert-butylsilyl)-1,4,5-trigermabicyclo[2.1.0]pent-2-ene (1) with [Et3Si(benzene)]+.TPFPB- in benzene at room temperature. The characteristic bishomoaromatic structure was unambiguously determined by...

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Ishida Y, Sekiguchi A, Kabe Y. 1,4,5-trigermabicyclo[2.1.0]pent-2-en-5-ylium: the isolable bishomocyclopropenylium ion containing a heavier group 14 element. J Am Chem Soc. 2003;125(38):11468-9doi: 10.1021/ja030327a.
Ishida, Y., Sekiguchi, A., & Kabe, Y. (2003). 1,4,5-trigermabicyclo[2.1.0]pent-2-en-5-ylium: the isolable bishomocyclopropenylium ion containing a heavier group 14 element. Journal of the American Chemical Society, 125(38), 11468-9. https://doi.org/10.1021/ja030327a
Ishida, Yutaka, et al. "1,4,5-trigermabicyclo[2.1.0]pent-2-en-5-ylium: the isolable bishomocyclopropenylium ion containing a heavier group 14 element." Journal of the American Chemical Society vol. 125,38 (2003): 11468-9. doi: https://doi.org/10.1021/ja030327a
Ishida Y, Sekiguchi A, Kabe Y. 1,4,5-trigermabicyclo[2.1.0]pent-2-en-5-ylium: the isolable bishomocyclopropenylium ion containing a heavier group 14 element. J Am Chem Soc. 2003 Sep 24;125(38):11468-9. doi: 10.1021/ja030327a. PMID: 13129328.
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Observation of the predicted negative Faraday A MCD term in a cyclobutadiene dianion.

Journal of the American Chemical Society

Ishii K, Kobayashi N, Matsuo T, Tanaka M, Sekiguchi A.
PMID: 11457402
J Am Chem Soc. 2001 Jun 06;123(22):5356-7. doi: 10.1021/ja004285r.

No abstract available.

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Ishii K, Kobayashi N, Matsuo T, et al. Observation of the predicted negative Faraday A MCD term in a cyclobutadiene dianion. J Am Chem Soc. 2001;123(22):5356-7doi: 10.1021/ja004285r.
Ishii, K., Kobayashi, N., Matsuo, T., Tanaka, M., & Sekiguchi, A. (2001). Observation of the predicted negative Faraday A MCD term in a cyclobutadiene dianion. Journal of the American Chemical Society, 123(22), 5356-7. https://doi.org/10.1021/ja004285r
Ishii, K, et al. "Observation of the predicted negative Faraday A MCD term in a cyclobutadiene dianion." Journal of the American Chemical Society vol. 123,22 (2001): 5356-7. doi: https://doi.org/10.1021/ja004285r
Ishii K, Kobayashi N, Matsuo T, Tanaka M, Sekiguchi A. Observation of the predicted negative Faraday A MCD term in a cyclobutadiene dianion. J Am Chem Soc. 2001 Jun 06;123(22):5356-7. doi: 10.1021/ja004285r. PMID: 11457402.
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The first silastannene >si=sn<: a new doubly-bonded system of heavier group 14 elements.

Journal of the American Chemical Society

Sekiguchi A, Izumi R, Lee VY, Ichinohe M.
PMID: 12475304
J Am Chem Soc. 2002 Dec 18;124(50):14822-3. doi: 10.1021/ja021077l.

The reaction of bis[di-tert-butyl(methyl)silyl]dilithiosilane 1 with dichlorobis(2,4,6-triisopropylphenyl)stannane in THF at room temperature yielded highly air- and moisture-sensitive deep violet crystals of 1,1-bis[di-tert-butyl(methyl)silyl]-2,2-bis(2,4,6-triisopropylphenyl)-1-sila-2-stannaethene 2 with a Si=Sn double bond. The molecular structure of 2 was established by X-ray crystallography, which...

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Sekiguchi A, Izumi R, Lee VY, et al. The first silastannene >si=sn<: a new doubly-bonded system of heavier group 14 elements. J Am Chem Soc. 2002;124(50):14822-3doi: 10.1021/ja021077l.
Sekiguchi, A., Izumi, R., Lee, V. Y., & Ichinohe, M. (2002). The first silastannene >si=sn<: a new doubly-bonded system of heavier group 14 elements. Journal of the American Chemical Society, 124(50), 14822-3. https://doi.org/10.1021/ja021077l
Sekiguchi, Akira, et al. "The first silastannene >si=sn<: a new doubly-bonded system of heavier group 14 elements." Journal of the American Chemical Society vol. 124,50 (2002): 14822-3. doi: https://doi.org/10.1021/ja021077l
Sekiguchi A, Izumi R, Lee VY, Ichinohe M. The first silastannene >si=sn<: a new doubly-bonded system of heavier group 14 elements. J Am Chem Soc. 2002 Dec 18;124(50):14822-3. doi: 10.1021/ja021077l. PMID: 12475304.
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Tin-centered radical and cation: stable and free.

Journal of the American Chemical Society

Sekiguchi A, Fukawa T, Lee VY, Nakamoto M.
PMID: 12889927
J Am Chem Soc. 2003 Aug 06;125(31):9250-1. doi: 10.1021/ja030156+.

The first stable stannyl radical (tBu2MeSi)3Sn* (1) has been synthesized by the reaction of tBu2MeSiNa with SnCl2-dioxane in diethyl ether. The X-ray crystal structure and electron paramagnetic resonance (EPR) data of this radical show that 1 has a planar...

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Sekiguchi A, Fukawa T, Lee VY, et al. Tin-centered radical and cation: stable and free. J Am Chem Soc. 2003;125(31):9250-1doi: 10.1021/ja030156+.
Sekiguchi, A., Fukawa, T., Lee, V. Y., & Nakamoto, M. (2003). Tin-centered radical and cation: stable and free. Journal of the American Chemical Society, 125(31), 9250-1. https://doi.org/10.1021/ja030156+
Sekiguchi, Akira, et al. "Tin-centered radical and cation: stable and free." Journal of the American Chemical Society vol. 125,31 (2003): 9250-1. doi: https://doi.org/10.1021/ja030156+
Sekiguchi A, Fukawa T, Lee VY, Nakamoto M. Tin-centered radical and cation: stable and free. J Am Chem Soc. 2003 Aug 06;125(31):9250-1. doi: 10.1021/ja030156+. PMID: 12889927.
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Radical cytoreductive surgery combined with platinums-carboplatin and cisplatin chemotherapy for advanced ovarian cancer.

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society

Suzuki M, Ohwara M, Sekiguchi I, Sato I.
PMID: 11240743
Int J Gynecol Cancer. 1999 Jan;9(1):54-60. doi: 10.1046/j.1525-1438.1999.09890.x.

In an attempt to improve the therapeutic outcome for patients with advanced ovarian cancer, primary radical cytoreductive surgery consisting of hysterectomy, bilateral salpingo-oophorectomy, omentectomy and retroperitoneal lymph node resection, with optimal cytoreduction in case of metastatic lesions, was followed...

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Suzuki M, Ohwara M, Sekiguchi I, et al. Radical cytoreductive surgery combined with platinums-carboplatin and cisplatin chemotherapy for advanced ovarian cancer. Int J Gynecol Cancer. 1999;9(1):54-60doi: 10.1046/j.1525-1438.1999.09890.x.
Suzuki, M., Ohwara, M., Sekiguchi, I., & Sato, I. (1999). Radical cytoreductive surgery combined with platinums-carboplatin and cisplatin chemotherapy for advanced ovarian cancer. International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 9(1), 54-60. https://doi.org/10.1046/j.1525-1438.1999.09890.x
Suzuki, M., et al. "Radical cytoreductive surgery combined with platinums-carboplatin and cisplatin chemotherapy for advanced ovarian cancer." International journal of gynecological cancer : official journal of the International Gynecological Cancer Society vol. 9,1 (1999): 54-60. doi: https://doi.org/10.1046/j.1525-1438.1999.09890.x
Suzuki M, Ohwara M, Sekiguchi I, Sato I. Radical cytoreductive surgery combined with platinums-carboplatin and cisplatin chemotherapy for advanced ovarian cancer. Int J Gynecol Cancer. 1999 Jan;9(1):54-60. doi: 10.1046/j.1525-1438.1999.09890.x. PMID: 11240743.
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Unimolecular metastable decompositions of gem-dimethoxyalkanes (RR'C(OCH(3))(2)) upon electron impact. I. Dimethoxymethane and 1, 1-dimethoxyethane.

Rapid communications in mass spectrometry : RCM

Takahashi Y, Higuchi T, Sekiguchi O, Fujizuka A, Nakajima S, Tajima S.
PMID: 10623930
Rapid Commun Mass Spectrom. 2000;14(2):61-7. doi: 10.1002/(SICI)1097-0231(20000130)14:2<61::AID-RCM834>3.0.CO;2-J.

The unimolecular metastable decompositions of dimethoxymethane (CH(2)(OCH(3))(2), 1) and 1,1-dimethoxyethane (CH(3)CH(OCH(3))(2), 2) upon electron impact have been investigated by means of mass-analyzed ion kinetic energy (MIKE) spectrometry, collision-induced dissociation (CID) spectrometry and D-labeling techniques. Both molecular ions are formed...

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Takahashi Y, Higuchi T, Sekiguchi O, et al. Unimolecular metastable decompositions of gem-dimethoxyalkanes (RR'C(OCH(3))(2)) upon electron impact. I. Dimethoxymethane and 1, 1-dimethoxyethane. Rapid Commun Mass Spectrom. 2000;14(2):61-7doi: 10.1002/(SICI)1097-0231(20000130)14:2<61::AID-RCM834>3.0.CO;2-J.
Takahashi, Y., Higuchi, T., Sekiguchi, O., Fujizuka, A., Nakajima, S., & Tajima, S. (2000). Unimolecular metastable decompositions of gem-dimethoxyalkanes (RR'C(OCH(3))(2)) upon electron impact. I. Dimethoxymethane and 1, 1-dimethoxyethane. Rapid communications in mass spectrometry : RCM, 14(2), 61-7. https://doi.org/10.1002/(SICI)1097-0231(20000130)14:2<61::AID-RCM834>3.0.CO;2-J
Takahashi, et al. "Unimolecular metastable decompositions of gem-dimethoxyalkanes (RR'C(OCH(3))(2)) upon electron impact. I. Dimethoxymethane and 1, 1-dimethoxyethane." Rapid communications in mass spectrometry : RCM vol. 14,2 (2000): 61-7. doi: https://doi.org/10.1002/(SICI)1097-0231(20000130)14:2<61::AID-RCM834>3.0.CO;2-J
Takahashi Y, Higuchi T, Sekiguchi O, Fujizuka A, Nakajima S, Tajima S. Unimolecular metastable decompositions of gem-dimethoxyalkanes (RR'C(OCH(3))(2)) upon electron impact. I. Dimethoxymethane and 1, 1-dimethoxyethane. Rapid Commun Mass Spectrom. 2000;14(2):61-7. doi: 10.1002/(SICI)1097-0231(20000130)14:2<61::AID-RCM834>3.0.CO;2-J. PMID: 10623930.
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Enantioselective ring cleavage of dioxane acetals mediated by a chiral Lewis acid: application to asymmetric desymmetrization of meso-1,3-diols.

Organic letters

Harada T, Sekiguchi K, Nakamura T, Suzuki J, Oku A.
PMID: 11594821
Org Lett. 2001 Oct 18;3(21):3309-12. doi: 10.1021/ol0165286.

[reaction: see text]. Phenylalanine-derived B-aryl-N-tosyloxazaborolidinones selectively activate one of two enantiotopic oxygen atoms in prochiral anti dioxane acetals derived from meso-1,3-diols, leading to enantioselective formation of ring-cleavage products. The reaction is utilized as a key step in asymmetric desymmetrization...

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Harada T, Sekiguchi K, Nakamura T, et al. Enantioselective ring cleavage of dioxane acetals mediated by a chiral Lewis acid: application to asymmetric desymmetrization of meso-1,3-diols. Org Lett. 2001;3(21):3309-12doi: 10.1021/ol0165286.
Harada, T., Sekiguchi, K., Nakamura, T., Suzuki, J., & Oku, A. (2001). Enantioselective ring cleavage of dioxane acetals mediated by a chiral Lewis acid: application to asymmetric desymmetrization of meso-1,3-diols. Organic letters, 3(21), 3309-12. https://doi.org/10.1021/ol0165286
Harada, T, et al. "Enantioselective ring cleavage of dioxane acetals mediated by a chiral Lewis acid: application to asymmetric desymmetrization of meso-1,3-diols." Organic letters vol. 3,21 (2001): 3309-12. doi: https://doi.org/10.1021/ol0165286
Harada T, Sekiguchi K, Nakamura T, Suzuki J, Oku A. Enantioselective ring cleavage of dioxane acetals mediated by a chiral Lewis acid: application to asymmetric desymmetrization of meso-1,3-diols. Org Lett. 2001 Oct 18;3(21):3309-12. doi: 10.1021/ol0165286. PMID: 11594821.
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