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Dive into the research topics where Mohd Wahid is active.

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Featured researches published by Mohd Wahid.


RSC Advances | 2013

Entrapment of Chlorella vulgaris cells within graphene oxide layers

Mohd Wahid; Ela Eroglu; Xianjue Chen; Steven M. Smith; Colin L. Raston

Confinement of microalgae cells within layers of graphene oxide (GO) effectively reduces the rate of cell division, with the microalgal wrapping being more efficient in a vortex fluidic device than using mild sonication, as determined by the cell growth and the level of nitrate removal from the liquid effluent.


Chemical Communications | 2013

Nitrate uptake by p-phosphonic acid calix[8]arene stabilized graphene

Ela Eroglu; Wenzhe Zang; Paul K. Eggers; Xianjue Chen; Ramiz A. Boulos; Mohd Wahid; Steven M. Smith; Colin L. Raston

In situ sonic probe exfoliated graphene sheets in the presence of various concentrations of p-phosphonic acid calix[8]arene are effective in removing nitrate from aquatic effluents, with the efficiency increasing for higher ratios of calixarene to graphite. Mild sonication of the nitrate-adsorbed material releases some nitrate ions back to the effluent.


Biophysical Chemistry | 2008

Sequence and stability of the goat cytochrome c

Hamidur Rahaman; Khurshid Alam Khan; Imtaiyaz Hassan; Mohd Wahid; S. Baskar Singh; Tej P. Singh; Ali Akbar Moosavi-Movahedi; Faizan Ahmad

We have determined the sequence of mitochondrial cytochrome c (cyt-c) from the goat heart, and it was found to have a unique amino acid sequence among all amino acid sequences of cyt-c reported till date. Its sequence alignment with the bovine cytochrome c (b-cyt-c) led us to conclude that the goat cytochrome c (g-cyt-c) differs in amino acid sequence from b-cyt-c at only one position, i.e., Pro44(bovine) --> Ala44(goat). It has been observed that guanidinium chloride (GdmCl) induces a two-state transition between the native (N) and denatured (D) states of g-cyt-c. This conclusion is reached from the coincidence of GdmCl-induced transition curves monitored by measurements of absorbance at 405, 530 and 695 nm and circular dichroism (CD) at 222, 416 and 405 nm. Analysis of denaturation curves for the Gibbs energy of stabilization suggests that the stability of g-cyt-c is, within experimental errors, identical to that of b-cyt-c. We have also measured the effect of temperature on the equilibrium, N state <--> D state of g-cyt-c in the presence of different GdmCl concentrations. These measurements gave values of transition temperature (T(m)), changes in enthalpy (DeltaH(m)) and heat capacity (DeltaC(p)) of g-cyt-c in the absence of GdmCl, which are compared with those of b-cyt-c. We have used crystal structure coordinates of b-cyt-c to predict the structure and stability of g-cyt-c, which are compared with those of the bovine protein.


Critical Reviews in Oncology Hematology | 2016

Vismodegib, itraconazole and sonidegib as hedgehog pathway inhibitors and their relative competencies in the treatment of basal cell carcinomas.

Mohd Wahid; Arshad Jawed; Raju K. Mandal; Sajad A. Dar; Saif Khan; Naseem Akhter; Shafiul Haque

The advent of more sophisticated studies published has clarified the understating of the root cause of various skin cancers or basal cell carcinomas (BCCs). The remarkable role is played by the comprehensive work done on unraveling the mechanism controlling the function of hedgehog (Hh) pathway. The defective Hh pathway has been found as the major cause for BCCs as activated Hh signaling within primary cilia plays a key role in the pathogenesis of BCCs. The BCC accounts for up to 40% of all cancers in the US, with growing incidences in other countries as well. Thus, it is considered to be utmost important by the researchers all over the world developing drugs for the treatment of skin cancers targeting Hh pathway. Fewer drugs like vismodegib, itraconazole and sonidegib have shown promising results inhibiting the awry function of Hh pathway resulting in treatment of different forms of skin cancers. These drugs have shown positive results but failed to prove their potential as expected. Vismodegib and sonidegib are better but fail in case of resistant tumors. This review article describes the mechanism of actions of these Hh pathway inhibitors and provides the rationale for their effectiveness/non-effectiveness for the treatment of metastatic or locally advanced BCC.


Transactions of Nonferrous Metals Society of China | 2018

Review on underwater friction stir welding: A variant of friction stir welding with great potential of improving joint properties

Mohd Wahid; Zahid A. Khan; Arshad Noor Siddiquee

Abstract Friction stir welding (FSW) is a solid-state welding process which is capable of joining materials which are relatively difficult to be welded by fusion welding process. Further, this process is highly energy-efficient and environmental-friendly as compared to the fusion welding. Despite several advantages of FSW over fusion welding, the thermal cycles involved in FSW cause softening in joints generally in heat-treatable aluminum alloys (AAs) due to the dissolution or coarsening of the strengthening precipitates leading to decrease in mechanical properties. Underwater friction stir welding (UFSW) can be a process of choice to overcome these limitations. This process is suitable for alloys that are sensitive to heating during the welding and is widely used for heat-treatable AAs. The purpose of this article is to provide comprehensive literature review on current status and development of UFSW and its importance in comparison to FSW with an aim to discuss and summarize different aspects of UFSW. Specific attention is given to basic principle including material flow, temperature generation, process parameters, microstructure and mechanical properties. From the review, it is concluded that UFSW is an improved method compared with FSW for improving joint strength. Academicians, researchers and practitioners would be benefitted from this article as it compiles significantly important knowledge pertaining to UFSW.


Autoimmunity | 2017

Interleukin-6-174G > C (rs1800795) polymorphism distribution and its association with rheumatoid arthritis: A case-control study and meta-analysis.

Sajad Ahmad Dar; Shafiul Haque; Raju K. Mandal; Taru Singh; Mohd Wahid; Arshad Jawed; Aditya K. Panda; Naseem Akhter; Mohtashim Lohani; Mohammed Y. Areeshi; Gargi Rai; Shyama Datt; Sambit Nath Bhattacharya; Shukla Das

Abstract The association of interleukin-6 (IL-6)-174G > C (rs1800795) single nucleotide polymorphism (SNP) with the risk of acquiring rheumatoid arthritis (RA) is a relevant issue because of conflicting and consensus lacking reports published in literature. We investigated IL-6-174G > C promoter polymorphism in 34 RA patients, attending a tertiary care hospital in north India. We also performed a meta-analysis, of the previously published studies reporting this genetic relationship, in overall population, and independently in Asian and Caucasian ethnicities to further elucidate this association. A total of 13 studies, including the current one, involving 3291 RA cases and 3812 controls were analyzed. Out of the 13 studies, 6 were from Asian, 6 from Caucasian and 1 from a mixed population. Our case-control study showed significant association of IL-6-174G > C SNP with increased RA risk: allelic (OR = 3.750, 95% CI = 1.800–7.813, p < 0.001); dominant (OR = 2.800, 95% CI = 1.167–6.721, p = 0.021); and recessive (OR = 36.72, 95% CI = 2.004–672.7, p = 0.015). The meta-analysis revealed the increased RA risk associated with IL-6-174G > C SNP in overall population: allelic (OR = 1.650, 95% CI = 1.169–2.329, p = 0.004); homozygous (OR = 1.380, 95% CI = 0.906–2.101, p = 0.133); heterozygous (OR = 1.559, 95% CI = 1.001–2.428, p = 0.049); dominant (OR = 1.663, 95% CI = 1.078–2.567, p = 0.022); and recessive (OR = 1.366, 95% CI = 0.964–1.935, p = 0.079). Subgroup analysis also showed this polymorphism to be associated with increased RA risk in Asian population: allelic (OR = 3.724, 95% CI = 1.361–10.190, p = 0.010); dominant (OR = 3.823, 95% CI = 1.320–11.074, p = 0.013); and recessive (OR = 4.357, 95% CI = 1.634–11.623, p = 0.003), but not in Caucasian population. This meta-analysis shows that IL-6-174G > C SNP is significantly associated with increased RA risk in overall, and specifically in Asian population.


RSC Advances | 2016

Modeling and optimization of a continuous bead milling process for bacterial cell lysis using response surface methodology

Shafiul Haque; Saif A. Khan; Mohd Wahid; Raju K. Mandal; Dileep Tiwari; Sajad A. Dar; Debarati Paul; Mohammed Y. Areeshi; Arshad Jawed

Efficient cell lysis for intracellular protein recovery is a major bottleneck in the economics and commercial feasibility of any biotechnological process. Grinding of cells with abrasive beads, also known as bead milling remains a method of choice, as it can handle a large volume of cells. Bead mills when operated in a continuous mode substantiate to be economical, and more productive as compared to a batch mode process. In this study, the recovery of recombinant cholesterol oxidase (COD) was investigated and optimized using response surface methodology (RSM) based on Central Composite Design (CCD) in a continuous bead milling process. Process parameters, viz. slurry feed rate (A), bead loading (B), cell loading (C) and process time (D) were found to be significant during the continuous bead milling process. A polynomial model was developed to correlate the participating factors for efficient cell disruption. Optimized conditions yielded 3.20 g L−1 (∼90%) of COD with A = 300.6 mL h−1, B = 77.5% (v/v), C = 69.9 (OD600 nm) and D = 29.7 (min), when compared to existing batch mode operations (3.56 g L−1). This is the very first study that attempts to optimize a continuous bead milling process using RSM to maximize the intracellular protein (COD in this case) recovery with minimum inputs to make the process economical and scalable to industrial levels. The developed model in this study can be scaled-up to large-scale for efficient recovery of intracellular proteins in similar expression systems.


Critical Reviews in Oncology Hematology | 2016

Therapeutic potential and critical analysis of trastuzumab and bevacizumab in combination with different chemotherapeutic agents against metastatic breast/colorectal cancer affecting various endpoints

Mohd Wahid; Raju K. Mandal; Sajad A. Dar; Arshad Jawed; Mohtashim Lohani; Mohammad Y. Areeshi; Naseem Akhter; Shafiul Haque

Researchers are working day and night across the globe to eradicate or at least lessen the menace of cancer faced by the mankind. The two very frequently occurring cancers faced by the human beings are metastatic breast cancer and metastatic colorectal cancer. The various chemotherapeutic agents like anthracycline, cyclophosphamide, paclitaxel, irinotecan, fluorouracil and leucovorin etc., have been used impressively for long. But the obstinate character of metastatic breast cancer and metastatic colorectal cancer needs more to tackle the threat. So, the scientists found the use of monoclonal antibodies trastuzumab (Herceptin(®)) and bevacizumab (Avastin(®)) for the same. The current study critically investigates the therapeutic potential of trastuzumab and bevacizumab in combination with various chemotherapeutic agents against metastatic breast cancer and metastatic colorectal cancer. To the best of our knowledge, this is the very first critical analysis showing percent wise increase in various positive endpoints like median time to disease progression, median survival, and progression free survival etc. for the treatment of metastatic breast/colorectal cancer using trastuzumab and bevacizumab in combination with different chemotherapeutic agents and provides the rational for the success and failure of the selected monoclonal antibodies.


Scientific Reports | 2016

TNF-α -308 G > A (rs1800629) Polymorphism is Associated with Celiac Disease: A Meta-analysis of 11 Case-Control Studies.

Saif A. Khan; Raju K. Mandal; Arshad Jawed; Sajad Ahmad Dar; Mohd Wahid; Aditya K. Panda; Mohammed Y. Areeshi; Md. Ekhlaque Ahmed Khan; Shafiul Haque

Celiac disease (CD) remains one of the most significant autoimmune diseases worldwide. The pathogenesis of CD is not clearly understood and is probably attributed to genomic variations and host genetic make-up. Case-control and cohort studies of the association between the TNF-α -308 G > A (rs1800629) polymorphism and CD susceptibility have yielded inconsistent results. In this study, PubMed, EMBASE, and Google Scholar web-databases were searched for pertinent reports showing association of TNF-α -308 G > A gene with CD risk. A total of eleven reports involving 1774 controls and 1147 CD cases were included. Significant associations in four genetic models, viz. variant allele (A vs. G: p = 0.001; OR = 2.051, 95% CI = 1.452–2.895), variant homozygous (AA vs. GG: p = 0.001; OR = 6.626, 95% CI = 3.569–12.300), recessive (AA vs. GG + AG: p = 0.001; OR = 4.766, 95% CI = 3.177–7.152) and dominant (AA + AG vs. GG: p = 0.008; OR = 1.910, 95% CI = 1.181–3.088) were found in comparison with wild type homozygous GG genotype. However, heterozygous genetic model did not show any association. Sensitivity analysis revealed stable and statistically robust results. Our results suggest that TNF-α -308 G > A gene polymorphism significantly contributes to CD susceptibility.


Microbial Pathogenesis | 2018

Cytomegalovirus aggravates the autoimmune phenomenon in systemic autoimmune diseases

Essam Mohammed Janahi; Shukla Das; Sambit Nath Bhattacharya; Shafiul Haque; Naseem Akhter; Arshad Jawed; Mohd Wahid; Raju K. Mandal; Mohtashim Lohani; Mohammed Y. Areeshi; Shaia Saleh R. Almalki; Sajad Ahmad Dar

BACKGROUND Human Cytomegalovirus (CMV), because of its ability to extensively manipulate host immunity during active infection, has been suggested to be involved in autoimmunity. However, its influence on T-cells and cytokines in systemic autoimmune diseases like systemic lupus erythematosus (SLE) and systemic sclerosis (SSc) is indistinct. METHODS We investigated the in-vitro response of T lymphocytes from SLE and SSc patients to CMV antigen. Functional activity of T lymphocytes was determined by estimating Th1 (IL-2 and IFN-γ) and Th2 (IL-4 and IL-10) cytokines. RESULTS We observed that CMV antigen stimulation in-vitro resulted in significant increase in CD4:CD8 T-cell ratio in peripheral blood mononuclear cells (PBMCs) from SLE and SSc patients; response dominated by CD4+ than CD8+ memory T-cells. SSc T-cell response was differentiated by aberrant increase in CD4+CD25+ T-cells. CMV antigen caused elevation in IL-4 and IFN-γ production in both patient PBMCs, whereas IL-2 was also raised in SLE PBMCs. The development of large pool of memory T-cells and overproduction of IFN-γ may result in flare-up of autoimmunity in these patients. CONCLUSION Our study provides an insight into the immunopathological potential of CMV-reactive immune cells to develop new potential strategies for targeted therapeutic intervention.

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Sajad Ahmad Dar

University College of Medical Sciences

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Aditya K. Panda

Regional Medical Research Centre

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