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Muscle Fatigue in the Three Heads of the Triceps Brachii During a Controlled Forceful Hand Grip Task with Full Elbow Extension Using Surface Electromyography.

Journal of human kinetics

Ali A, Sundaraj K, Badlishah Ahmad R, Ahamed NU, Islam A, Sundaraj S.
PMID: 26240650
J Hum Kinet. 2015 Jul 10;46:69-76. doi: 10.1515/hukin-2015-0035. eCollection 2015 Jun 27.

The objective of the present study was to investigate the time to fatigue and compare the fatiguing condition among the three heads of the triceps brachii muscle using surface electromyography during an isometric contraction of a controlled forceful hand...

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Ali A, Sundaraj K, Badlishah Ahmad R, et al. Muscle Fatigue in the Three Heads of the Triceps Brachii During a Controlled Forceful Hand Grip Task with Full Elbow Extension Using Surface Electromyography. J Hum Kinet. 2015;46:69-76doi: 10.1515/hukin-2015-0035.
Ali, A., Sundaraj, K., Badlishah Ahmad, R., Ahamed, N. U., Islam, A., & Sundaraj, S. (2015). Muscle Fatigue in the Three Heads of the Triceps Brachii During a Controlled Forceful Hand Grip Task with Full Elbow Extension Using Surface Electromyography. Journal of human kinetics, 4669-76. https://doi.org/10.1515/hukin-2015-0035
Ali, Asraf, et al. "Muscle Fatigue in the Three Heads of the Triceps Brachii During a Controlled Forceful Hand Grip Task with Full Elbow Extension Using Surface Electromyography." Journal of human kinetics vol. 46 (2015): 69-76. doi: https://doi.org/10.1515/hukin-2015-0035
Ali A, Sundaraj K, Badlishah Ahmad R, Ahamed NU, Islam A, Sundaraj S. Muscle Fatigue in the Three Heads of the Triceps Brachii During a Controlled Forceful Hand Grip Task with Full Elbow Extension Using Surface Electromyography. J Hum Kinet. 2015 Jul 10;46:69-76. doi: 10.1515/hukin-2015-0035. eCollection 2015 Jun 27. PMID: 26240650; PMCID: PMC4519223.
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Vocal coselection in rat pup ultrasonic vocalizations.

Ecology and evolution

Spence HR, Aslam AM, Hofer MA, Brunelli SA, Shair HN.
PMID: 27066218
Ecol Evol. 2016 Feb 24;6(7):1922-9. doi: 10.1002/ece3.1907. eCollection 2016 Apr.

Selective breeding and natural selection that select for one trait often bring along other correlated traits via coselection. Selective breeding for an infantile trait, high or low call rates of isolation-induced ultrasonic vocalization of rat pups, also alters functions...

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Spence HR, Aslam AM, Hofer MA, et al. Vocal coselection in rat pup ultrasonic vocalizations. Ecol Evol. 2016;6(7):1922-9doi: 10.1002/ece3.1907.
Spence, H. R., Aslam, A. M., Hofer, M. A., Brunelli, S. A., & Shair, H. N. (2016). Vocal coselection in rat pup ultrasonic vocalizations. Ecology and evolution, 6(7), 1922-9. https://doi.org/10.1002/ece3.1907
Spence, Heather R, et al. "Vocal coselection in rat pup ultrasonic vocalizations." Ecology and evolution vol. 6,7 (2016): 1922-9. doi: https://doi.org/10.1002/ece3.1907
Spence HR, Aslam AM, Hofer MA, Brunelli SA, Shair HN. Vocal coselection in rat pup ultrasonic vocalizations. Ecol Evol. 2016 Feb 24;6(7):1922-9. doi: 10.1002/ece3.1907. eCollection 2016 Apr. PMID: 27066218; PMCID: PMC4767333.
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Protonated Carboxyl Anchor for Stable Adsorption of Ru N749 Dye (Black Dye) on a TiO2 Anatase (101) Surface.

The journal of physical chemistry letters

Sodeyama K, Sumita M, O'Rourke C, Terranova U, Islam A, Han L, Bowler DR, Tateyama Y.
PMID: 26286049
J Phys Chem Lett. 2012 Feb 16;3(4):472-7. doi: 10.1021/jz201583n. Epub 2012 Jan 30.

We have investigated the adsorption stability of ruthenium N749 dye [black dye (BD)], a highly efficient dye for dye-sensitized solar cells (DSCs), through protonated and deprotonated carboxyl group anchors on a TiO2 anatase (101) surface by using first-principles calculations....

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Sodeyama K, Sumita M, O'Rourke C, et al. Protonated Carboxyl Anchor for Stable Adsorption of Ru N749 Dye (Black Dye) on a TiO2 Anatase (101) Surface. J Phys Chem Lett. 2012;3(4):472-7doi: 10.1021/jz201583n.
Sodeyama, K., Sumita, M., O'Rourke, C., Terranova, U., Islam, A., Han, L., Bowler, D. R., & Tateyama, Y. (2012). Protonated Carboxyl Anchor for Stable Adsorption of Ru N749 Dye (Black Dye) on a TiO2 Anatase (101) Surface. The journal of physical chemistry letters, 3(4), 472-7. https://doi.org/10.1021/jz201583n
Sodeyama, Keitaro, et al. "Protonated Carboxyl Anchor for Stable Adsorption of Ru N749 Dye (Black Dye) on a TiO2 Anatase (101) Surface." The journal of physical chemistry letters vol. 3,4 (2012): 472-7. doi: https://doi.org/10.1021/jz201583n
Sodeyama K, Sumita M, O'Rourke C, Terranova U, Islam A, Han L, Bowler DR, Tateyama Y. Protonated Carboxyl Anchor for Stable Adsorption of Ru N749 Dye (Black Dye) on a TiO2 Anatase (101) Surface. J Phys Chem Lett. 2012 Feb 16;3(4):472-7. doi: 10.1021/jz201583n. Epub 2012 Jan 30. PMID: 26286049.
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Conserved antigenic sites between MERS-CoV and Bat-coronavirus are revealed through sequence analysis.

Source code for biology and medicine

Sharmin R, Islam AB.
PMID: 26962326
Source Code Biol Med. 2016 Mar 09;11:3. doi: 10.1186/s13029-016-0049-7. eCollection 2016.

BACKGROUND: MERS-CoV is a newly emerged human coronavirus reported closely related with HKU4 and HKU5 Bat coronaviruses. Bat and MERS corona-viruses are structurally related. Therefore, it is of interest to estimate the degree of conserved antigenic sites among them....

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Sharmin R, Islam AB. Conserved antigenic sites between MERS-CoV and Bat-coronavirus are revealed through sequence analysis. Source Code Biol Med. 2016;11:3doi: 10.1186/s13029-016-0049-7.
Sharmin, R., & Islam, A. B. (2016). Conserved antigenic sites between MERS-CoV and Bat-coronavirus are revealed through sequence analysis. Source code for biology and medicine, 113. https://doi.org/10.1186/s13029-016-0049-7
Sharmin, Refat, and Islam, Abul B M M K. "Conserved antigenic sites between MERS-CoV and Bat-coronavirus are revealed through sequence analysis." Source code for biology and medicine vol. 11 (2016): 3. doi: https://doi.org/10.1186/s13029-016-0049-7
Sharmin R, Islam AB. Conserved antigenic sites between MERS-CoV and Bat-coronavirus are revealed through sequence analysis. Source Code Biol Med. 2016 Mar 09;11:3. doi: 10.1186/s13029-016-0049-7. eCollection 2016. PMID: 26962326; PMCID: PMC4784407.
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Treatment referral system for tuberculosis patients in Dhaka, Bangladesh.

Public health action

Islam S, Hirayama T, Islam A, Ishikawa N, Afsana K.
PMID: 26767176
Public Health Action. 2015 Dec 21;5(4):236-40. doi: 10.5588/pha.15.0052.

OBJECTIVE: To evaluate the referral system in an urban DOTS-based programme in Dhaka, Bangladesh, including the peri-urban area, and to identify opportunities to strengthen the system.DESIGN: This was a retrospective cohort study in which diagnosed tuberculosis (TB) patients and...

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Islam S, Hirayama T, Islam A, et al. Treatment referral system for tuberculosis patients in Dhaka, Bangladesh. Public Health Action. 2015;5(4):236-40doi: 10.5588/pha.15.0052.
Islam, S., Hirayama, T., Islam, A., Ishikawa, N., & Afsana, K. (2015). Treatment referral system for tuberculosis patients in Dhaka, Bangladesh. Public health action, 5(4), 236-40. https://doi.org/10.5588/pha.15.0052
Islam, S, et al. "Treatment referral system for tuberculosis patients in Dhaka, Bangladesh." Public health action vol. 5,4 (2015): 236-40. doi: https://doi.org/10.5588/pha.15.0052
Islam S, Hirayama T, Islam A, Ishikawa N, Afsana K. Treatment referral system for tuberculosis patients in Dhaka, Bangladesh. Public Health Action. 2015 Dec 21;5(4):236-40. doi: 10.5588/pha.15.0052. PMID: 26767176; PMCID: PMC4682614.
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Synthesis of Isomeric and Potent Impurities of the Triazole-Based Antifungal Drug Voriconazole.

Scientia pharmaceutica

Sundaram DT, Mitra J, Islam A, Prabahar KJ, Venkateswara Rao B, Paul Douglas S.
PMID: 26839829
Sci Pharm. 2015 Mar 06;83(3):445-52. doi: 10.3797/scipharm.1501-13. Print 2015.

We describe the synthesis of two positional isomers and a desfluoro impurity of Voriconazole starting with Friedel-Crafts acylation of mono- and difluorobenzene. These isomers are the crucial components in determining the quality of Voriconazole during its manufacturing from the...

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Sundaram DT, Mitra J, Islam A, et al. Synthesis of Isomeric and Potent Impurities of the Triazole-Based Antifungal Drug Voriconazole. Sci Pharm. 2015;83(3):445-52doi: 10.3797/scipharm.1501-13.
Sundaram, D. T., Mitra, J., Islam, A., Prabahar, K. J., Venkateswara Rao, B., & Paul Douglas, S. (2015). Synthesis of Isomeric and Potent Impurities of the Triazole-Based Antifungal Drug Voriconazole. Scientia pharmaceutica, 83(3), 445-52. https://doi.org/10.3797/scipharm.1501-13
Sundaram, Dhanraj T S S, et al. "Synthesis of Isomeric and Potent Impurities of the Triazole-Based Antifungal Drug Voriconazole." Scientia pharmaceutica vol. 83,3 (2015): 445-52. doi: https://doi.org/10.3797/scipharm.1501-13
Sundaram DT, Mitra J, Islam A, Prabahar KJ, Venkateswara Rao B, Paul Douglas S. Synthesis of Isomeric and Potent Impurities of the Triazole-Based Antifungal Drug Voriconazole. Sci Pharm. 2015 Mar 06;83(3):445-52. doi: 10.3797/scipharm.1501-13. Print 2015. PMID: 26839829; PMCID: PMC4727777.
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In vitro thrombolytic potential of root extracts of four medicinal plants available in Bangladesh.

Ancient science of life

Hussain F, Islam A, Bulbul L, Moghal MR, Hossain MS.
PMID: 25538351
Anc Sci Life. 2014 Jan;33(3):162-4. doi: 10.4103/0257-7941.144620.

CONTEXT: Thrombus formation inside the blood vessels obstructs blood flow through the circulatory system leading hypertension, stroke to the heart, anoxia, and so on. Thrombolytic drugs are widely used for the management of cerebral venous sinus thrombosis patients, but...

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Hussain F, Islam A, Bulbul L, et al. In vitro thrombolytic potential of root extracts of four medicinal plants available in Bangladesh. Anc Sci Life. 2014;33(3):162-4doi: 10.4103/0257-7941.144620.
Hussain, F., Islam, A., Bulbul, L., Moghal, M. R., & Hossain, M. S. (2014). In vitro thrombolytic potential of root extracts of four medicinal plants available in Bangladesh. Ancient science of life, 33(3), 162-4. https://doi.org/10.4103/0257-7941.144620
Hussain, Fahad, et al. "In vitro thrombolytic potential of root extracts of four medicinal plants available in Bangladesh." Ancient science of life vol. 33,3 (2014): 162-4. doi: https://doi.org/10.4103/0257-7941.144620
Hussain F, Islam A, Bulbul L, Moghal MR, Hossain MS. In vitro thrombolytic potential of root extracts of four medicinal plants available in Bangladesh. Anc Sci Life. 2014 Jan;33(3):162-4. doi: 10.4103/0257-7941.144620. PMID: 25538351; PMCID: PMC4264304.
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Panchromatic donor-acceptor-donor conjugated oligomers for dye-sensitized solar cell applications.

ACS applied materials & interfaces

Stalder R, Xie D, Islam A, Han L, Reynolds JR, Schanze KS.
PMID: 24807377
ACS Appl Mater Interfaces. 2014 Jun 11;6(11):8715-22. doi: 10.1021/am501515s. Epub 2014 May 07.

We report on a sexithienyl and two donor-acceptor-donor oligothiophenes, employing benzothiadiazole and isoindigo as electron-acceptors, each functionalized with a phosphonic acid group for anchoring onto TiO2 substrates as light-harvesting molecules for dye sensitized solar cells (DSSCs). These dyes absorb...

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Stalder R, Xie D, Islam A, et al. Panchromatic donor-acceptor-donor conjugated oligomers for dye-sensitized solar cell applications. ACS Appl Mater Interfaces. 2014;6(11):8715-22doi: 10.1021/am501515s.
Stalder, R., Xie, D., Islam, A., Han, L., Reynolds, J. R., & Schanze, K. S. (2014). Panchromatic donor-acceptor-donor conjugated oligomers for dye-sensitized solar cell applications. ACS applied materials & interfaces, 6(11), 8715-22. https://doi.org/10.1021/am501515s
Stalder, Romain, et al. "Panchromatic donor-acceptor-donor conjugated oligomers for dye-sensitized solar cell applications." ACS applied materials & interfaces vol. 6,11 (2014): 8715-22. doi: https://doi.org/10.1021/am501515s
Stalder R, Xie D, Islam A, Han L, Reynolds JR, Schanze KS. Panchromatic donor-acceptor-donor conjugated oligomers for dye-sensitized solar cell applications. ACS Appl Mater Interfaces. 2014 Jun 11;6(11):8715-22. doi: 10.1021/am501515s. Epub 2014 May 07. PMID: 24807377.
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Novel acid-catalyzed rearrangement of methanofullerenes bearing an alpha-ylidic ester to cyclopentanofullerenes: a vinyl cyclopropane-type ring expansion.

The Journal of organic chemistry

Chuang SC, Islam A, Huang CW, Shih HT, Cheng CH.
PMID: 12737558
J Org Chem. 2003 May 16;68(10):3811-6. doi: 10.1021/jo030009u.

A novel acid-catalyzed ring expansion of methanofullerenes bearing an alpha-ylidic ester has been investigated. Treatment of dialkyl acetylenedicarboxylate and tricycloalkylphosphine with C(60) led to the isolation of a methanofullerene ylide after passing the reaction mixtures through a basic alumina...

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Chuang SC, Islam A, Huang CW, et al. Novel acid-catalyzed rearrangement of methanofullerenes bearing an alpha-ylidic ester to cyclopentanofullerenes: a vinyl cyclopropane-type ring expansion. J Org Chem. 2003;68(10):3811-6doi: 10.1021/jo030009u.
Chuang, S. C., Islam, A., Huang, C. W., Shih, H. T., & Cheng, C. H. (2003). Novel acid-catalyzed rearrangement of methanofullerenes bearing an alpha-ylidic ester to cyclopentanofullerenes: a vinyl cyclopropane-type ring expansion. The Journal of organic chemistry, 68(10), 3811-6. https://doi.org/10.1021/jo030009u
Chuang, Shih-Ching, et al. "Novel acid-catalyzed rearrangement of methanofullerenes bearing an alpha-ylidic ester to cyclopentanofullerenes: a vinyl cyclopropane-type ring expansion." The Journal of organic chemistry vol. 68,10 (2003): 3811-6. doi: https://doi.org/10.1021/jo030009u
Chuang SC, Islam A, Huang CW, Shih HT, Cheng CH. Novel acid-catalyzed rearrangement of methanofullerenes bearing an alpha-ylidic ester to cyclopentanofullerenes: a vinyl cyclopropane-type ring expansion. J Org Chem. 2003 May 16;68(10):3811-6. doi: 10.1021/jo030009u. PMID: 12737558.
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The isomerisation of carotene by means of antimony trichloride.

The Biochemical journal

Gillam AE, Heilbron IM, Morton RA.
PMID: 16744921
Biochem J. 1932;26(4):1174-7. doi: 10.1042/bj0261174.

No abstract available.

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Gillam AE, Heilbron IM, Morton RA. The isomerisation of carotene by means of antimony trichloride. Biochem J. 1932;26(4):1174-7doi: 10.1042/bj0261174.
Gillam, A. E., Heilbron, I. M., & Morton, R. A. (1932). The isomerisation of carotene by means of antimony trichloride. The Biochemical journal, 26(4), 1174-7. https://doi.org/10.1042/bj0261174
Gillam, A E, et al. "The isomerisation of carotene by means of antimony trichloride." The Biochemical journal vol. 26,4 (1932): 1174-7. doi: https://doi.org/10.1042/bj0261174
Gillam AE, Heilbron IM, Morton RA. The isomerisation of carotene by means of antimony trichloride. Biochem J. 1932;26(4):1174-7. doi: 10.1042/bj0261174. PMID: 16744921; PMCID: PMC1261019.
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Aminonaphthalic anhydrides as red-emitting materials: electroluminescence, crystal structure, and photophysical properties.

The journal of physical chemistry. B

Islam A, Cheng CC, Chi SH, Lee SJ, Hela PG, Chen IC, Cheng CH.
PMID: 16851591
J Phys Chem B. 2005 Mar 31;109(12):5509-17. doi: 10.1021/jp044669u.

The red and orange emitters (ANA-1-3) consisting of a 4-amino-1,8-naphthalic anhydride group were synthesized. The lowest absorption band of these ANA molecules centered at approximately 450 nm is assigned to be a charge-transfer transition with emission at 514-536 nm...

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Islam A, Cheng CC, Chi SH, et al. Aminonaphthalic anhydrides as red-emitting materials: electroluminescence, crystal structure, and photophysical properties. J Phys Chem B. 2005;109(12):5509-17doi: 10.1021/jp044669u.
Islam, A., Cheng, C. C., Chi, S. H., Lee, S. J., Hela, P. G., Chen, I. C., & Cheng, C. H. (2005). Aminonaphthalic anhydrides as red-emitting materials: electroluminescence, crystal structure, and photophysical properties. The journal of physical chemistry. B, 109(12), 5509-17. https://doi.org/10.1021/jp044669u
Islam, Aminul, et al. "Aminonaphthalic anhydrides as red-emitting materials: electroluminescence, crystal structure, and photophysical properties." The journal of physical chemistry. B vol. 109,12 (2005): 5509-17. doi: https://doi.org/10.1021/jp044669u
Islam A, Cheng CC, Chi SH, Lee SJ, Hela PG, Chen IC, Cheng CH. Aminonaphthalic anhydrides as red-emitting materials: electroluminescence, crystal structure, and photophysical properties. J Phys Chem B. 2005 Mar 31;109(12):5509-17. doi: 10.1021/jp044669u. PMID: 16851591.
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Column chromatographic separation of metal ions on 1-(2-pyridylazo)-2-napthol modified amberlite IR-120 resin.

Journal of separation science

Nabi S, Alim A, Islam A, Amjad M.
PMID: 16405175
J Sep Sci. 2005 Dec;28(18):2463-7. doi: 10.1002/jssc.200500170.

Cation exchange resin, Amberlite IR-120, has been modified by the sorption of 1-(2-pyridylazo)-2-napthol (PAN) at pH 6.0. The optimum conditions for the sorption of PAN on the resin have been established. The maximum sorption of PAN was found to...

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Nabi S, Alim A, Islam A, et al. Column chromatographic separation of metal ions on 1-(2-pyridylazo)-2-napthol modified amberlite IR-120 resin. J Sep Sci. 2005;28(18):2463-7doi: 10.1002/jssc.200500170.
Nabi, S., Alim, A., Islam, A., & Amjad, M. (2005). Column chromatographic separation of metal ions on 1-(2-pyridylazo)-2-napthol modified amberlite IR-120 resin. Journal of separation science, 28(18), 2463-7. https://doi.org/10.1002/jssc.200500170
Nabi, Syed, et al. "Column chromatographic separation of metal ions on 1-(2-pyridylazo)-2-napthol modified amberlite IR-120 resin." Journal of separation science vol. 28,18 (2005): 2463-7. doi: https://doi.org/10.1002/jssc.200500170
Nabi S, Alim A, Islam A, Amjad M. Column chromatographic separation of metal ions on 1-(2-pyridylazo)-2-napthol modified amberlite IR-120 resin. J Sep Sci. 2005 Dec;28(18):2463-7. doi: 10.1002/jssc.200500170. PMID: 16405175.
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Showing 1 to 12 of 562 entries