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Showing 1 to 12 of 20 entries
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[Pathogenesis of diabetic retinopathy].

Vnitrni lekarstvi

Pelikánová T.
PMID: 17642432
Vnitr Lek. 2007 May;53(5):498-505.

Diabetic retinopathy (DR) develops in patients with both type 1 and type 2 diabetes and is the major cause of vision loss and blindness in the working population. The main risk factor of DR is hyperglycemia accompanied by enhanced...

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Pelikánová T. Patogeneze diabetické retinopatie. [Pathogenesis of diabetic retinopathy]. Vnitr Lek. 2007;53(5):498-505
Pelikánová, T. (2007). Patogeneze diabetické retinopatie. [Pathogenesis of diabetic retinopathy]. Vnitrni lekarstvi, 53(5), 498-505.
Pelikánová, T. "Patogeneze diabetické retinopatie." [Pathogenesis of diabetic retinopathy]. Vnitrni lekarstvi vol. 53,5 (2007): 498-505.
Pelikánová T. Patogeneze diabetické retinopatie. [Pathogenesis of diabetic retinopathy]. Vnitr Lek. 2007 May;53(5):498-505. Czech. PMID: 17642432.
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Evaluation of Antioxidant and Wound Healing Effects of Alcoholic and Aqueous Extract of Ocimum sanctum Linn in Rats.

Evidence-based complementary and alternative medicine : eCAM

Shetty S, Udupa S, Udupa L.
PMID: 18317555
Evid Based Complement Alternat Med. 2008 Mar;5(1):95-101. doi: 10.1093/ecam/nem004.

In recent years, oxidative stress and free radicals have been implicated in impaired wound healing. Ocimum sanctum (O. sanctum), a plant widely used in Ayurveda, possesses anti-inflammatory and antioxidant properties. The present study was undertaken to assess the potential...

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Shetty S, Udupa S, Udupa L. Evaluation of Antioxidant and Wound Healing Effects of Alcoholic and Aqueous Extract of Ocimum sanctum Linn in Rats. Evid Based Complement Alternat Med. 2008;5(1):95-101doi: 10.1093/ecam/nem004.
Shetty, S., Udupa, S., & Udupa, L. (2008). Evaluation of Antioxidant and Wound Healing Effects of Alcoholic and Aqueous Extract of Ocimum sanctum Linn in Rats. Evidence-based complementary and alternative medicine : eCAM, 5(1), 95-101. https://doi.org/10.1093/ecam/nem004
Shetty, Somashekar, et al. "Evaluation of Antioxidant and Wound Healing Effects of Alcoholic and Aqueous Extract of Ocimum sanctum Linn in Rats." Evidence-based complementary and alternative medicine : eCAM vol. 5,1 (2008): 95-101. doi: https://doi.org/10.1093/ecam/nem004
Shetty S, Udupa S, Udupa L. Evaluation of Antioxidant and Wound Healing Effects of Alcoholic and Aqueous Extract of Ocimum sanctum Linn in Rats. Evid Based Complement Alternat Med. 2008 Mar;5(1):95-101. doi: 10.1093/ecam/nem004. PMID: 18317555; PMCID: PMC2249741.
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Laminar Flow on Endothelial Cells Suppresses eNOS O-GlcNAcylation to Promote eNOS Activity.

Circulation research

Basehore SE, Bohlman S, Weber C, Swaminathan S, Zhang Y, Jang C, Arany Z, Clyne AM.
PMID: 34605247
Circ Res. 2021 Nov 12;129(11):1054-1066. doi: 10.1161/CIRCRESAHA.121.318982. Epub 2021 Oct 04.

[Figure: see text].

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Basehore SE, Bohlman S, Weber C, et al. Laminar Flow on Endothelial Cells Suppresses eNOS O-GlcNAcylation to Promote eNOS Activity. Circ Res. 2021;129(11):1054-1066doi: 10.1161/CIRCRESAHA.121.318982.
Basehore, S. E., Bohlman, S., Weber, C., Swaminathan, S., Zhang, Y., Jang, C., Arany, Z., & Clyne, A. M. (2021). Laminar Flow on Endothelial Cells Suppresses eNOS O-GlcNAcylation to Promote eNOS Activity. Circulation research, 129(11), 1054-1066. https://doi.org/10.1161/CIRCRESAHA.121.318982
Basehore, Sarah E, et al. "Laminar Flow on Endothelial Cells Suppresses eNOS O-GlcNAcylation to Promote eNOS Activity." Circulation research vol. 129,11 (2021): 1054-1066. doi: https://doi.org/10.1161/CIRCRESAHA.121.318982
Basehore SE, Bohlman S, Weber C, Swaminathan S, Zhang Y, Jang C, Arany Z, Clyne AM. Laminar Flow on Endothelial Cells Suppresses eNOS O-GlcNAcylation to Promote eNOS Activity. Circ Res. 2021 Nov 12;129(11):1054-1066. doi: 10.1161/CIRCRESAHA.121.318982. Epub 2021 Oct 04. PMID: 34605247; PMCID: PMC8653916.
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Vibrational Signatures of Isomeric Lithiated N-acetyl-D-hexosamines by Gas-Phase Infrared Multiple-Photon Dissociation (IRMPD) Spectroscopy.

Journal of the American Society for Mass Spectrometry

Tan Y, Zhao N, Liu J, Li P, Stedwell CN, Yu L, Polfer NC.
PMID: 28050874
J Am Soc Mass Spectrom. 2017 Mar;28(3):539-550. doi: 10.1007/s13361-016-1575-x. Epub 2017 Jan 03.

Three lithiated N-acetyl-D-hexosamine (HexNAc) isomers, N-acetyl-D-glucosamine (GlcNAc), N-acetyl-D-galactosamine (GalNAc), and N-acetyl-D-mannosamine (ManNAc) are investigated as model monosaccharide derivatives by gas-phase infrared multiple-photon dissociation (IRMPD) spectroscopy. The hydrogen stretching region, which is attributed to OH and NH stretching modes, reveals...

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Tan Y, Zhao N, Liu J, et al. Vibrational Signatures of Isomeric Lithiated N-acetyl-D-hexosamines by Gas-Phase Infrared Multiple-Photon Dissociation (IRMPD) Spectroscopy. J Am Soc Mass Spectrom. 2017;28(3):539-550doi: 10.1007/s13361-016-1575-x.
Tan, Y., Zhao, N., Liu, J., Li, P., Stedwell, C. N., Yu, L., & Polfer, N. C. (2017). Vibrational Signatures of Isomeric Lithiated N-acetyl-D-hexosamines by Gas-Phase Infrared Multiple-Photon Dissociation (IRMPD) Spectroscopy. Journal of the American Society for Mass Spectrometry, 28(3), 539-550. https://doi.org/10.1007/s13361-016-1575-x
Tan, Yanglan, et al. "Vibrational Signatures of Isomeric Lithiated N-acetyl-D-hexosamines by Gas-Phase Infrared Multiple-Photon Dissociation (IRMPD) Spectroscopy." Journal of the American Society for Mass Spectrometry vol. 28,3 (2017): 539-550. doi: https://doi.org/10.1007/s13361-016-1575-x
Tan Y, Zhao N, Liu J, Li P, Stedwell CN, Yu L, Polfer NC. Vibrational Signatures of Isomeric Lithiated N-acetyl-D-hexosamines by Gas-Phase Infrared Multiple-Photon Dissociation (IRMPD) Spectroscopy. J Am Soc Mass Spectrom. 2017 Mar;28(3):539-550. doi: 10.1007/s13361-016-1575-x. Epub 2017 Jan 03. PMID: 28050874.
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Serum glycoconjugates and ceruloplasmin in cancer of uterine cervix.

Indian journal of clinical biochemistry : IJCB

Upadhya S, Upadhya S, Prabhu KS.
PMID: 23105331
Indian J Clin Biochem. 2002 Jan;17(1):20-4. doi: 10.1007/BF02867936.

The present study was done to assess the levels of glycoconjugates and ceruloplasmin in sera of patients with cervical cancer. Serum hexoses, hexosamines, sialic acid and fucose are elevated in a variety of inflammatory and neoplastic conditions. All the...

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Upadhya S, Upadhya S, Prabhu KS. Serum glycoconjugates and ceruloplasmin in cancer of uterine cervix. Indian J Clin Biochem. 2002;17(1):20-4doi: 10.1007/BF02867936.
Upadhya, S., Upadhya, S., & Prabhu, K. S. (2002). Serum glycoconjugates and ceruloplasmin in cancer of uterine cervix. Indian journal of clinical biochemistry : IJCB, 17(1), 20-4. https://doi.org/10.1007/BF02867936
Upadhya, Sharmila, et al. "Serum glycoconjugates and ceruloplasmin in cancer of uterine cervix." Indian journal of clinical biochemistry : IJCB vol. 17,1 (2002): 20-4. doi: https://doi.org/10.1007/BF02867936
Upadhya S, Upadhya S, Prabhu KS. Serum glycoconjugates and ceruloplasmin in cancer of uterine cervix. Indian J Clin Biochem. 2002 Jan;17(1):20-4. doi: 10.1007/BF02867936. PMID: 23105331; PMCID: PMC3453716.
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Composition of High Molecular Weight Excretions-Secretions from Infective Larvae of Meloidogyne javanica.

Journal of nematology

Bacic A, Felton Z, Bird AF.
PMID: 19287641
J Nematol. 1989 Oct;21(4):477-82.

Infective larvae (J2) of Meloidogyne javanica were incubated in distilled water for up to 14 days, and their high molecular weight (> 1,000 daltons) excretions-secretions (ES) were isolated and partially characterized. The ES consisted of a mixture of proteins,...

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Bacic A, Felton Z, Bird AF. Composition of High Molecular Weight Excretions-Secretions from Infective Larvae of Meloidogyne javanica. J Nematol. 1989;21(4):477-82
Bacic, A., Felton, Z., & Bird, A. F. (1989). Composition of High Molecular Weight Excretions-Secretions from Infective Larvae of Meloidogyne javanica. Journal of nematology, 21(4), 477-82.
Bacic, A, et al. "Composition of High Molecular Weight Excretions-Secretions from Infective Larvae of Meloidogyne javanica." Journal of nematology vol. 21,4 (1989): 477-82.
Bacic A, Felton Z, Bird AF. Composition of High Molecular Weight Excretions-Secretions from Infective Larvae of Meloidogyne javanica. J Nematol. 1989 Oct;21(4):477-82. PMID: 19287641; PMCID: PMC2618972.
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Histochemical staining and characterization of glycoproteins in Acid-secreting cells of frog stomach.

The Journal of cell biology

Forte TM, Forte JG.
PMID: 19866742
J Cell Biol. 1970 Nov 01;47(2):437-52. doi: 10.1083/jcb.47.2.437.

Glycoproteins were histochemically localized in oxyntic cells of the frog stomach by staining with periodic acid-silver methenamine. Reduction of silver was most intense on (a) the outer aspect of the apical plasmalemma, (b) within the tubular smooth membrane system...

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Forte TM, Forte JG. Histochemical staining and characterization of glycoproteins in Acid-secreting cells of frog stomach. J Cell Biol. 1970;47(2):437-52doi: 10.1083/jcb.47.2.437.
Forte, T. M., & Forte, J. G. (1970). Histochemical staining and characterization of glycoproteins in Acid-secreting cells of frog stomach. The Journal of cell biology, 47(2), 437-52. https://doi.org/10.1083/jcb.47.2.437
Forte, T M, and Forte, J G. "Histochemical staining and characterization of glycoproteins in Acid-secreting cells of frog stomach." The Journal of cell biology vol. 47,2 (1970): 437-52. doi: https://doi.org/10.1083/jcb.47.2.437
Forte TM, Forte JG. Histochemical staining and characterization of glycoproteins in Acid-secreting cells of frog stomach. J Cell Biol. 1970 Nov 01;47(2):437-52. doi: 10.1083/jcb.47.2.437. PMID: 19866742; PMCID: PMC2108089.
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Synthesis and in vitro cytotoxicity of acetylated 3-fluoro, 4-fluoro and 3,4-difluoro analogs of D-glucosamine and D-galactosamine.

Beilstein journal of organic chemistry

Horník Š, Červenková Šťastná L, Cuřínová P, Sýkora J, Káňová K, Hrstka R, Císařová I, Dračínský M, Karban J.
PMID: 27340467
Beilstein J Org Chem. 2016 Apr 20;12:750-9. doi: 10.3762/bjoc.12.75. eCollection 2016.

BACKGROUND: Derivatives of D-glucosamine and D-galactosamine represent an important family of the cell surface glycan components and their fluorinated analogs found use as metabolic inhibitors of complex glycan biosynthesis, or as probes for the study of protein-carbohydrate interactions. This...

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Horník Š, Červenková Šťastná L, Cuřínová P, et al. Synthesis and in vitro cytotoxicity of acetylated 3-fluoro, 4-fluoro and 3,4-difluoro analogs of D-glucosamine and D-galactosamine. Beilstein J Org Chem. 2016;12:750-9doi: 10.3762/bjoc.12.75.
Horník, �. �., Červenková Šťastná, L., Cuřínová, P., Sýkora, J., Káňová, K., Hrstka, R., Císařová, I., Dračínský, M., & Karban, J. (2016). Synthesis and in vitro cytotoxicity of acetylated 3-fluoro, 4-fluoro and 3,4-difluoro analogs of D-glucosamine and D-galactosamine. Beilstein journal of organic chemistry, 12750-9. https://doi.org/10.3762/bjoc.12.75
Horník, Štěpán, et al. "Synthesis and in vitro cytotoxicity of acetylated 3-fluoro, 4-fluoro and 3,4-difluoro analogs of D-glucosamine and D-galactosamine." Beilstein journal of organic chemistry vol. 12 (2016): 750-9. doi: https://doi.org/10.3762/bjoc.12.75
Horník Š, Červenková Šťastná L, Cuřínová P, Sýkora J, Káňová K, Hrstka R, Císařová I, Dračínský M, Karban J. Synthesis and in vitro cytotoxicity of acetylated 3-fluoro, 4-fluoro and 3,4-difluoro analogs of D-glucosamine and D-galactosamine. Beilstein J Org Chem. 2016 Apr 20;12:750-9. doi: 10.3762/bjoc.12.75. eCollection 2016. PMID: 27340467; PMCID: PMC4901990.
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Retraction of: Cooperation between subunits is essential for high-affinity binding of N-acetyl-D-hexosamines to dimeric soluble and dimeric cellular forms of human CD69.

Biochemistry

[No authors listed]
PMID: 24730519
Biochemistry. 2014 May 06;53(17):2864. doi: 10.1021/bi500367g. Epub 2014 Apr 15.

No abstract available.

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Retraction of: Cooperation between subunits is essential for high-affinity binding of N-acetyl-D-hexosamines to dimeric soluble and dimeric cellular forms of human CD69. Biochemistry. 2014;53(17):2864doi: 10.1021/bi500367g.
(2014). Retraction of: Cooperation between subunits is essential for high-affinity binding of N-acetyl-D-hexosamines to dimeric soluble and dimeric cellular forms of human CD69. Biochemistry, 53(17), 2864. https://doi.org/10.1021/bi500367g
"Retraction of: Cooperation between subunits is essential for high-affinity binding of N-acetyl-D-hexosamines to dimeric soluble and dimeric cellular forms of human CD69." Biochemistry vol. 53,17 (2014): 2864. doi: https://doi.org/10.1021/bi500367g
Retraction of: Cooperation between subunits is essential for high-affinity binding of N-acetyl-D-hexosamines to dimeric soluble and dimeric cellular forms of human CD69. Biochemistry. 2014 May 06;53(17):2864. doi: 10.1021/bi500367g. Epub 2014 Apr 15. PMID: 24730519.
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An efficient synthetic route to l-γ-methyleneglutamine and its amide derivatives, and their selective anticancer activity.

RSC advances

Hossain MI, Thomas AG, Mahdi F, Adam AT, Akins NS, Woodard MM, Paris JJ, Slusher BS, Le HV.
PMID: 33777357
RSC Adv. 2021 Feb 24;11(13):7115-7128. doi: 10.1039/d0ra08249j. Epub 2021 Feb 10.

In cancer cells, glutaminolysis is the primary source of biosynthetic precursors, fueling the TCA cycle with glutamine-derived α-ketoglutarate. The enhanced production of α-ketoglutarate is critical to cancer cells as it provides carbons for the TCA cycle to produce glutathione,...

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Hossain MI, Thomas AG, Mahdi F, et al. An efficient synthetic route to l-γ-methyleneglutamine and its amide derivatives, and their selective anticancer activity. RSC Adv. 2021;11(13):7115-7128doi: 10.1039/d0ra08249j.
Hossain, M. I., Thomas, A. G., Mahdi, F., Adam, A. T., Akins, N. S., Woodard, M. M., Paris, J. J., Slusher, B. S., & Le, H. V. (2021). An efficient synthetic route to l-γ-methyleneglutamine and its amide derivatives, and their selective anticancer activity. RSC advances, 11(13), 7115-7128. https://doi.org/10.1039/d0ra08249j
Hossain, Md Imran, et al. "An efficient synthetic route to l-γ-methyleneglutamine and its amide derivatives, and their selective anticancer activity." RSC advances vol. 11,13 (2021): 7115-7128. doi: https://doi.org/10.1039/d0ra08249j
Hossain MI, Thomas AG, Mahdi F, Adam AT, Akins NS, Woodard MM, Paris JJ, Slusher BS, Le HV. An efficient synthetic route to l-γ-methyleneglutamine and its amide derivatives, and their selective anticancer activity. RSC Adv. 2021 Feb 24;11(13):7115-7128. doi: 10.1039/d0ra08249j. Epub 2021 Feb 10. PMID: 33777357; PMCID: PMC7968037.
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Sodium N-Chlorobenzenesulfonamide as a Selective Oxidant for Hexosamines in Alkaline Medium: A Kinetic and Mechanistic Study.

The Journal of organic chemistry

Rangappa KS, Raghavendra MP, Mahadevappa DS, Channegowda D.
PMID: 11672041
J Org Chem. 1998 Feb 06;63(3):531-536. doi: 10.1021/jo971398t.

Oxidation of D-mannosamine (1), D-glucosamine (2), and D-galctosamine (3) by sodium N-chlorobenzenesulfonamide or chloramine-B (CAB) at 313 K is followed by a shortening of carbon chain and obeys the rate law, rate = k[CAB][sugar][HO(-)](x)(), where x is less than...

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Rangappa KS, Raghavendra MP, Mahadevappa DS, et al. Sodium N-Chlorobenzenesulfonamide as a Selective Oxidant for Hexosamines in Alkaline Medium: A Kinetic and Mechanistic Study. J Org Chem. 1998;63(3):531-536doi: 10.1021/jo971398t.
Rangappa, K. S., Raghavendra, M. P., Mahadevappa, D. S., & Channegowda, D. (1998). Sodium N-Chlorobenzenesulfonamide as a Selective Oxidant for Hexosamines in Alkaline Medium: A Kinetic and Mechanistic Study. The Journal of organic chemistry, 63(3), 531-536. https://doi.org/10.1021/jo971398t
Rangappa, Kanchugarakoppal S., et al. "Sodium N-Chlorobenzenesulfonamide as a Selective Oxidant for Hexosamines in Alkaline Medium: A Kinetic and Mechanistic Study." The Journal of organic chemistry vol. 63,3 (1998): 531-536. doi: https://doi.org/10.1021/jo971398t
Rangappa KS, Raghavendra MP, Mahadevappa DS, Channegowda D. Sodium N-Chlorobenzenesulfonamide as a Selective Oxidant for Hexosamines in Alkaline Medium: A Kinetic and Mechanistic Study. J Org Chem. 1998 Feb 06;63(3):531-536. doi: 10.1021/jo971398t. PMID: 11672041.
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Glycoprotein components, sialic acid and hexosamines, bound to inner and outer mitochondrial membranes.

FEBS letters

de Bernard B, Pugliarello MC, Sandri G, Sottocasa GL, Vittur F.
PMID: 11945557
FEBS Lett. 1971 Jan 12;12(3):125-128. doi: 10.1016/0014-5793(71)80049-2.

No abstract available.

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de Bernard B, Pugliarello MC, Sandri G, et al. Glycoprotein components, sialic acid and hexosamines, bound to inner and outer mitochondrial membranes. FEBS Lett. 1971;12(3):125-128doi: 10.1016/0014-5793(71)80049-2.
de Bernard, B., Pugliarello, M. C., Sandri, G., Sottocasa, G. L., & Vittur, F. (1971). Glycoprotein components, sialic acid and hexosamines, bound to inner and outer mitochondrial membranes. FEBS letters, 12(3), 125-128. https://doi.org/10.1016/0014-5793(71)80049-2
de Bernard, B, et al. "Glycoprotein components, sialic acid and hexosamines, bound to inner and outer mitochondrial membranes." FEBS letters vol. 12,3 (1971): 125-128. doi: https://doi.org/10.1016/0014-5793(71)80049-2
de Bernard B, Pugliarello MC, Sandri G, Sottocasa GL, Vittur F. Glycoprotein components, sialic acid and hexosamines, bound to inner and outer mitochondrial membranes. FEBS Lett. 1971 Jan 12;12(3):125-128. doi: 10.1016/0014-5793(71)80049-2. PMID: 11945557.
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Showing 1 to 12 of 20 entries