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Effect of workforce diversity on employee's job performance: the empirical assessment of education sector, Jalalabad, Afghanistan

workforce diversity

Qasim M.
GSID: ONXect9LpRUJ GSID: ONXect9LpRUJ

… The purpose of the study is to establish the effect of workforce diversity on employee’s performance in Afghanistan, Jalalabad based … the effect of workforce diversity on employee’s job performance in education sector, Jalalabad, Afghanistan. The term workforce...

Validation of a prognostic scoring system for critically ill patients with cirrhosis admitted to ICU.

Journal of the Intensive Care Society

Campbell J, McPeake J, Shaw M, Puxty A, Emerson P, Thomson SJ, Rahman TM, Quasim T, Kinsella J.
PMID: 28979418
J Intensive Care Soc. 2015 Aug;16(3):240. doi: 10.1177/1751143715584779. Epub 2015 Jul 23.

No abstract available.

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Campbell J, McPeake J, Shaw M, et al. Validation of a prognostic scoring system for critically ill patients with cirrhosis admitted to ICU. J Intensive Care Soc. 2015;16(3):240doi: 10.1177/1751143715584779.
Campbell, J., McPeake, J., Shaw, M., Puxty, A., Emerson, P., Thomson, S. J., Rahman, T. M., Quasim, T., & Kinsella, J. (2015). Validation of a prognostic scoring system for critically ill patients with cirrhosis admitted to ICU. Journal of the Intensive Care Society, 16(3), 240. https://doi.org/10.1177/1751143715584779
Campbell, J, et al. "Validation of a prognostic scoring system for critically ill patients with cirrhosis admitted to ICU." Journal of the Intensive Care Society vol. 16,3 (2015): 240. doi: https://doi.org/10.1177/1751143715584779
Campbell J, McPeake J, Shaw M, Puxty A, Emerson P, Thomson SJ, Rahman TM, Quasim T, Kinsella J. Validation of a prognostic scoring system for critically ill patients with cirrhosis admitted to ICU. J Intensive Care Soc. 2015 Aug;16(3):240. doi: 10.1177/1751143715584779. Epub 2015 Jul 23. PMID: 28979418; PMCID: PMC5606448.
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Characteristics and outcomes of lung cancer patients after intensive care admission.

Journal of the Intensive Care Society

Hulse K, Quasim T, Morrison D, MacLoone P, Sloane B, Kinsella J, Puxty K.
PMID: 28979417
J Intensive Care Soc. 2015 Aug;16(3):239. doi: 10.1177/1751143715583857. Epub 2015 Jul 23.

No abstract available.

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Hulse K, Quasim T, Morrison D, et al. Characteristics and outcomes of lung cancer patients after intensive care admission. J Intensive Care Soc. 2015;16(3):239doi: 10.1177/1751143715583857.
Hulse, K., Quasim, T., Morrison, D., MacLoone, P., Sloane, B., Kinsella, J., & Puxty, K. (2015). Characteristics and outcomes of lung cancer patients after intensive care admission. Journal of the Intensive Care Society, 16(3), 239. https://doi.org/10.1177/1751143715583857
Hulse, K, et al. "Characteristics and outcomes of lung cancer patients after intensive care admission." Journal of the Intensive Care Society vol. 16,3 (2015): 239. doi: https://doi.org/10.1177/1751143715583857
Hulse K, Quasim T, Morrison D, MacLoone P, Sloane B, Kinsella J, Puxty K. Characteristics and outcomes of lung cancer patients after intensive care admission. J Intensive Care Soc. 2015 Aug;16(3):239. doi: 10.1177/1751143715583857. Epub 2015 Jul 23. PMID: 28979417; PMCID: PMC5606447.
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Genome-Edited T Cell Therapies.

Current stem cell reports

Delhove JMKM, Qasim W.
PMID: 28596938
Curr Stem Cell Rep. 2017;3(2):124-136. doi: 10.1007/s40778-017-0077-5. Epub 2017 Apr 18.

PURPOSE OF REVIEW: Alternative approaches to conventional drug-based cancer treatments have seen T cell therapies deployed more widely over the last decade. This is largely due to their ability to target and kill specific cell types based on receptor...

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Delhove JMKM, Qasim W. Genome-Edited T Cell Therapies. Curr Stem Cell Rep. 2017;3(2):124-136doi: 10.1007/s40778-017-0077-5.
Delhove, J. M. K. M., & Qasim, W. (2017). Genome-Edited T Cell Therapies. Current stem cell reports, 3(2), 124-136. https://doi.org/10.1007/s40778-017-0077-5
Delhove, Juliette M K M, and Qasim, Waseem. "Genome-Edited T Cell Therapies." Current stem cell reports vol. 3,2 (2017): 124-136. doi: https://doi.org/10.1007/s40778-017-0077-5
Delhove JMKM, Qasim W. Genome-Edited T Cell Therapies. Curr Stem Cell Rep. 2017;3(2):124-136. doi: 10.1007/s40778-017-0077-5. Epub 2017 Apr 18. PMID: 28596938; PMCID: PMC5445182.
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Bilateral asymmetrical duplicated origin of vertebral arteries: Multidetector row CT angiographic study.

The Indian journal of radiology & imaging

Rameshbabu C, Gupta OP, Gupta KK, Qasim M.
PMID: 24851007
Indian J Radiol Imaging. 2014 Jan;24(1):61-5. doi: 10.4103/0971-3026.130699.

Bilateral duplicated origin of V-1 segment of vertebral arteries is an extremely rare vascular variant and only two such cases have been reported so far. Presence of this vascular abnormality was observed incidentally in a 36-year-old male patient, with...

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Rameshbabu C, Gupta OP, Gupta KK, et al. Bilateral asymmetrical duplicated origin of vertebral arteries: Multidetector row CT angiographic study. Indian J Radiol Imaging. 2014;24(1):61-5doi: 10.4103/0971-3026.130699.
Rameshbabu, C., Gupta, O. P., Gupta, K. K., & Qasim, M. (2014). Bilateral asymmetrical duplicated origin of vertebral arteries: Multidetector row CT angiographic study. The Indian journal of radiology & imaging, 24(1), 61-5. https://doi.org/10.4103/0971-3026.130699
Rameshbabu, Cs, et al. "Bilateral asymmetrical duplicated origin of vertebral arteries: Multidetector row CT angiographic study." The Indian journal of radiology & imaging vol. 24,1 (2014): 61-5. doi: https://doi.org/10.4103/0971-3026.130699
Rameshbabu C, Gupta OP, Gupta KK, Qasim M. Bilateral asymmetrical duplicated origin of vertebral arteries: Multidetector row CT angiographic study. Indian J Radiol Imaging. 2014 Jan;24(1):61-5. doi: 10.4103/0971-3026.130699. PMID: 24851007; PMCID: PMC4028918.
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Ortner's syndrome: Cardiovocal syndrome caused by aortic arch pseudoaneurysm.

Journal of the Saudi Heart Association

Al Kindi AH, Al Kindi FA, Al Abri QS, Al Kemyani NA.
PMID: 27688676
J Saudi Heart Assoc. 2016 Oct;28(4):266-9. doi: 10.1016/j.jsha.2016.02.006. Epub 2016 Feb 23.

72-year-old hypertensive presented with two weeks history of left sided chest pain and hoarseness. Workup demonstrated a pseudoaneurysm in the lesser curvature of the distal aortic arch opposite the origin of the left subclavian artery from a penetrating atherosclerotic...

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Al Kindi AH, Al Kindi FA, Al Abri QS, et al. Ortner's syndrome: Cardiovocal syndrome caused by aortic arch pseudoaneurysm. J Saudi Heart Assoc. 2016;28(4):266-9doi: 10.1016/j.jsha.2016.02.006.
Al Kindi, A. H., Al Kindi, F. A., Al Abri, Q. S., & Al Kemyani, N. A. (2016). Ortner's syndrome: Cardiovocal syndrome caused by aortic arch pseudoaneurysm. Journal of the Saudi Heart Association, 28(4), 266-9. https://doi.org/10.1016/j.jsha.2016.02.006
Al Kindi, Adil H, et al. "Ortner's syndrome: Cardiovocal syndrome caused by aortic arch pseudoaneurysm." Journal of the Saudi Heart Association vol. 28,4 (2016): 266-9. doi: https://doi.org/10.1016/j.jsha.2016.02.006
Al Kindi AH, Al Kindi FA, Al Abri QS, Al Kemyani NA. Ortner's syndrome: Cardiovocal syndrome caused by aortic arch pseudoaneurysm. J Saudi Heart Assoc. 2016 Oct;28(4):266-9. doi: 10.1016/j.jsha.2016.02.006. Epub 2016 Feb 23. PMID: 27688676; PMCID: PMC5034482.
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Immunosuppressant MPA Modulates Tight Junction through Epigenetic Activation of MLCK/MLC-2 Pathway via p38MAPK.

Frontiers in physiology

Khan N, Pantakani DV, Binder L, Qasim M, Asif AR.
PMID: 26733876
Front Physiol. 2015 Dec 22;6:381. doi: 10.3389/fphys.2015.00381. eCollection 2015.

BACKGROUND: Mycophenolic acid (MPA) is an important immunosuppressive drug (ISD) prescribed to prevent graft rejection in the organ transplanted patients, however, its use is also associated with adverse side effects like sporadic gastrointestinal (GI) disturbances. Recently, we reported the...

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Khan N, Pantakani DV, Binder L, et al. Immunosuppressant MPA Modulates Tight Junction through Epigenetic Activation of MLCK/MLC-2 Pathway via p38MAPK. Front Physiol. 2015;6:381doi: 10.3389/fphys.2015.00381.
Khan, N., Pantakani, D. V., Binder, L., Qasim, M., & Asif, A. R. (2015). Immunosuppressant MPA Modulates Tight Junction through Epigenetic Activation of MLCK/MLC-2 Pathway via p38MAPK. Frontiers in physiology, 6381. https://doi.org/10.3389/fphys.2015.00381
Khan, Niamat, et al. "Immunosuppressant MPA Modulates Tight Junction through Epigenetic Activation of MLCK/MLC-2 Pathway via p38MAPK." Frontiers in physiology vol. 6 (2015): 381. doi: https://doi.org/10.3389/fphys.2015.00381
Khan N, Pantakani DV, Binder L, Qasim M, Asif AR. Immunosuppressant MPA Modulates Tight Junction through Epigenetic Activation of MLCK/MLC-2 Pathway via p38MAPK. Front Physiol. 2015 Dec 22;6:381. doi: 10.3389/fphys.2015.00381. eCollection 2015. PMID: 26733876; PMCID: PMC4687409.
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Molecular diagnosis and phylogenetic analysis of human papillomavirus type-16 from suspected patients in Pakistan.

Infectious agents and cancer

Abdullah A, Qasim M, Shafiq M, Ijaz M, Parveen S, Murtaza S, Javed Q, Malik SA, Tarar SH, Mehmood S, Sami A, Naqvi SM, Hyder MZ.
PMID: 26766963
Infect Agent Cancer. 2016 Jan 12;11:1. doi: 10.1186/s13027-016-0047-z. eCollection 2016.

BACKGROUND: Human Papillomavirus (HPV) is well known pathogen that can cause benign and malignant tumors in humans, yet there is very little information regarding HPV types prevalent in Pakistan.METHODS: A total of 92 cervical secretions were collected from suspected...

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Abdullah A, Qasim M, Shafiq M, et al. Molecular diagnosis and phylogenetic analysis of human papillomavirus type-16 from suspected patients in Pakistan. Infect Agent Cancer. 2016;11:1doi: 10.1186/s13027-016-0047-z.
Abdullah, A., Qasim, M., Shafiq, M., Ijaz, M., Parveen, S., Murtaza, S., Javed, Q., Malik, S. A., Tarar, S. H., Mehmood, S., Sami, A., Naqvi, S. M., & Hyder, M. Z. (2016). Molecular diagnosis and phylogenetic analysis of human papillomavirus type-16 from suspected patients in Pakistan. Infectious agents and cancer, 111. https://doi.org/10.1186/s13027-016-0047-z
Abdullah, Abdullah, et al. "Molecular diagnosis and phylogenetic analysis of human papillomavirus type-16 from suspected patients in Pakistan." Infectious agents and cancer vol. 11 (2016): 1. doi: https://doi.org/10.1186/s13027-016-0047-z
Abdullah A, Qasim M, Shafiq M, Ijaz M, Parveen S, Murtaza S, Javed Q, Malik SA, Tarar SH, Mehmood S, Sami A, Naqvi SM, Hyder MZ. Molecular diagnosis and phylogenetic analysis of human papillomavirus type-16 from suspected patients in Pakistan. Infect Agent Cancer. 2016 Jan 12;11:1. doi: 10.1186/s13027-016-0047-z. eCollection 2016. PMID: 26766963; PMCID: PMC4711104.
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Design of new and potent diethyl thiobarbiturates as urease inhibitors: a computational approach.

Bioinformation

Wadood A, Riaz M, Mulk AU, Khan M, Haleem SA, Shams S, Gul S, Ahmed A, Qasim M, Ali F, Ul-Haq Z.
PMID: 24966538
Bioinformation. 2014 May 20;10(5):299-307. doi: 10.6026/97320630010299. eCollection 2014.

Urease is an important enzyme both in agriculture and medicine research. Strategies based on urease inhibition is critically considered as the first line treatment of infections caused by urease producing bacteria. Since, urease possess agro-chemical and medicinal importance, thus,...

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Wadood A, Riaz M, Mulk AU, et al. Design of new and potent diethyl thiobarbiturates as urease inhibitors: a computational approach. Bioinformation. 2014;10(5):299-307doi: 10.6026/97320630010299.
Wadood, A., Riaz, M., Mulk, A. U., Khan, M., Haleem, S. A., Shams, S., Gul, S., Ahmed, A., Qasim, M., Ali, F., & Ul-Haq, Z. (2014). Design of new and potent diethyl thiobarbiturates as urease inhibitors: a computational approach. Bioinformation, 10(5), 299-307. https://doi.org/10.6026/97320630010299
Wadood, Abdul, et al. "Design of new and potent diethyl thiobarbiturates as urease inhibitors: a computational approach." Bioinformation vol. 10,5 (2014): 299-307. doi: https://doi.org/10.6026/97320630010299
Wadood A, Riaz M, Mulk AU, Khan M, Haleem SA, Shams S, Gul S, Ahmed A, Qasim M, Ali F, Ul-Haq Z. Design of new and potent diethyl thiobarbiturates as urease inhibitors: a computational approach. Bioinformation. 2014 May 20;10(5):299-307. doi: 10.6026/97320630010299. eCollection 2014. PMID: 24966538; PMCID: PMC4070040.
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The mechanism of unimolecular decomposition of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane. A computational DFT study.

The journal of physical chemistry. A

Okovytyy S, Kholod Y, Qasim M, Fredrickson H, Leszczynski J.
PMID: 16833616
J Phys Chem A. 2005 Mar 31;109(12):2964-70. doi: 10.1021/jp045292v.

By using the B3LYP level of density functional theory, possible decomposition reaction pathways of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (CL-20) in the gas phase have been investigated. We have found several types of reactions for this process: homolytic cleavage of an N-N bond...

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Okovytyy S, Kholod Y, Qasim M, et al. The mechanism of unimolecular decomposition of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane. A computational DFT study. J Phys Chem A. 2005;109(12):2964-70doi: 10.1021/jp045292v.
Okovytyy, S., Kholod, Y., Qasim, M., Fredrickson, H., & Leszczynski, J. (2005). The mechanism of unimolecular decomposition of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane. A computational DFT study. The journal of physical chemistry. A, 109(12), 2964-70. https://doi.org/10.1021/jp045292v
Okovytyy, Sergiy, et al. "The mechanism of unimolecular decomposition of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane. A computational DFT study." The journal of physical chemistry. A vol. 109,12 (2005): 2964-70. doi: https://doi.org/10.1021/jp045292v
Okovytyy S, Kholod Y, Qasim M, Fredrickson H, Leszczynski J. The mechanism of unimolecular decomposition of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane. A computational DFT study. J Phys Chem A. 2005 Mar 31;109(12):2964-70. doi: 10.1021/jp045292v. PMID: 16833616.
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Enzymatic activities of some snake venoms from families Elapidae and Viperidae.

Pakistan journal of pharmaceutical sciences

Alam JM, Qasim R, Alam SM.
PMID: 16414774
Pak J Pharm Sci. 1996 Jan;9(1):37-41.

Alkaline phosphomonoesterase, phosphodiesterase, L-amino acid oxidase, hyaluronidase, 5'-nucleotidase, arginine ester hydrolase, phospholipase A2 and proteinase activities were determined in eight snake venoms, including three from sea snake, of families Elapidae and Viperidae from Pakistan. The species includes three sea...

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Alam JM, Qasim R, Alam SM. Enzymatic activities of some snake venoms from families Elapidae and Viperidae. Pak J Pharm Sci. 1996;9(1):37-41
Alam, J. M., Qasim, R., & Alam, S. M. (1996). Enzymatic activities of some snake venoms from families Elapidae and Viperidae. Pakistan journal of pharmaceutical sciences, 9(1), 37-41.
Alam, J M, et al. "Enzymatic activities of some snake venoms from families Elapidae and Viperidae." Pakistan journal of pharmaceutical sciences vol. 9,1 (1996): 37-41.
Alam JM, Qasim R, Alam SM. Enzymatic activities of some snake venoms from families Elapidae and Viperidae. Pak J Pharm Sci. 1996 Jan;9(1):37-41. PMID: 16414774.
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Amino acid composition of some common seaweeds.

Pakistan journal of pharmaceutical sciences

Qasim R.
PMID: 16414681
Pak J Pharm Sci. 1991 Jan;4(1):49-54.

The nutritive evaluation of seaweed proteins on the basis of amino acid composition has been reported in the present communication. Seventeen of the common amino acids including almost all essential amino acids have been detected in the protein hydrolysate...

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Qasim R. Amino acid composition of some common seaweeds. Pak J Pharm Sci. 1991;4(1):49-54
Qasim, R. (1991). Amino acid composition of some common seaweeds. Pakistan journal of pharmaceutical sciences, 4(1), 49-54.
Qasim, R. "Amino acid composition of some common seaweeds." Pakistan journal of pharmaceutical sciences vol. 4,1 (1991): 49-54.
Qasim R. Amino acid composition of some common seaweeds. Pak J Pharm Sci. 1991 Jan;4(1):49-54. PMID: 16414681.
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Showing 1 to 12 of 449 entries