Search Results - "Perveen, R."

Green versus sol-gel synthesis of ZnO nanoparticles and antimicrobial activity evaluation against panel of pathogens by Perveen, R, Shujaat, S, Qureshi, Z, Nawaz, S, Khan, M.I., Iqbal, M.

“…Green versus sol-gel synthesis of zinc oxide nanoparticles (ZnO NPs) were carried out and antimicrobial activity was evaluated against a wide panel of…”
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Response of salt stressed okra (Abelmoschus esculentus Moench) plants to foliar-applied glycine betaine and glycine betaine containing sugarbeet extract by Habib, N., Ashraf, M., Ali, Q., Perveen, R.

“…The present experiment was aimed at examining the ameliorative effect of foliar-applied glycine betaine (50mM GB) and glycine betaine containing sugarbeet…”
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Thermophoretic diffusion and nonlinear radiative heat transfer due to a contracting cylinder in a nanofluid with generalized slip condition by Abbas, Z., Perveen, R., Sheikh, M., Pop, I.

“…An analysis is carried out to study the generalized slip condition and MHD flow of a nanofluid due to a contracting cylinder in the presence of non-linear…”
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Mode of presentation and mortality amongst patients hospitalized with heart failure? A report from the First Euro Heart Failure Survey by Shoaib, Ahmad, Farag, M., Nolan, J., Rigby, A., Patwala, A., Rashid, M., Kwok, C. S., Perveen, R., Clark, A. L., Komajda, M., Cleland, J. G. F.

“…Background Heart failure is heterogeneous in aetiology, pathophysiology, and presentation. Despite this diversity, clinical trials of patients hospitalized for…”
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Genotype-phenotype correlation in Costello syndrome: HRAS mutation analysis in 43 cases by Kerr, B, Delrue, M-A, Sigaudy, S, Perveen, R, Marche, M, Burgelin, I, Stef, M, Tang, B, Eden, O B, O’Sullivan, J, De Sandre-Giovannoli, A, Reardon, W, Brewer, C, Bennett, C, Quarell, O, M’Cann, E, Donnai, D, Stewart, F, Hennekam, R, Cavé, H, Verloes, A, Philip, N, Lacombe, D, Levy, N, Arveiler, B, Black, G

“…Background: Costello syndrome (CS) is a rare multiple congenital abnormality syndrome, associated with failure to thrive and developmental delay. One of the…”
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A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation by Perveen, R., Favor, J., Jamieson, R.V., Ray, D.W., Black, G.C.M.

“…MAF, one of a family of large Maf bZIP transcription factors, is mutated in human developmental ocular disorders that include congenital cataract, microcornea,…”
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De novo GLI3 mutation in acrocallosal syndrome: broadening the phenotypic spectrum of GLI3 defects and overlap with murine models by Elson, E, Perveen, R, Donnai, D, Wall, S, Black, G C M

“…Acrocallosal syndrome (ACS) is characterised by postaxial polydactyly, hallux duplication, macrocephaly, and absence of the corpus callosum, usually with…”
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The Bangladesh clubfoot project: audit of two-year outcomes of Ponseti treatment in 400 children by Evans, A, Perveen, R, Barker, S, Ford-Powell, V, Wade, P, Khan, S, Dietz, F

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Kinetic and thermodynamic properties of an immobilized endoglucanase from Arachniotus citrinus by Saleem, M., Rashid, M.H., Jabbar, A., Perveen, R., Khalid, A.M., Rajoka, M.I.

“…Purified endoglucanase (apparently to homogeneity) from Arachniotus citrinus was immobilized in polyacrylamide gel with 53.4% yield of immobilization…”
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A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding by Lyon, Mary F., Jamieson, Robyn V., Perveen, Rahat, Glenister, Peter H., Griffiths, Robert, Boyd, Yvonne, Glimcher, Laurie H., Favor, Jack, Munier, Francis L., Black, Graeme C. M.

“…The murine autosomal dominant cataract mutants created in mutagenesis experiments have proven to be a powerful resource for modelling the biological processes…”
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Constitutional delay of growth and puberty is not commonly associated with mutations in the acid labile subunit gene by Banerjee, I, Hanson, D, Perveen, R, Whatmore, A, Black, G C, Clayton, P E

“…ObjectivesConstitutional delay of growth and puberty (CDGP) is a common clinical condition that may be inherited as an autosomal dominant, recessive or…”
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A mutation in the RIEG1 gene associated with Peters’ anomaly by Doward, W, Perveen, R, Lloyd, I C, Ridgway, A E A, Wilson, L, Black, G C M

“…Mutations within the RIEG1 homeobox gene on chromosome 4q25 have previously been reported in association with Rieger syndrome. We report a 3′ splice site…”
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Phenotypic Variability and Asymmetry of Rieger Syndrome Associated with PITX2 Mutations by Perveen, Rahat, Lloyd, I. Christopher, Clayton-Smith, Jill, Churchill, Amanda, van Heyningen, Veronica, Hanson, Isabel, Taylor, David, McKeown, Carole, Super, Maurice, Kerr, Bronwyn, Winter, Robin, Black, Graeme C. M

“…Rieger syndrome is an autosomal dominant condition characterized by a variable combination of anterior segment dysgenesis, dental anomalies, and umbilical…”
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Pulverulent cataract with variably associated microcornea and iris coloboma in a MAF mutation family by Jamieson, R V, Munier, F, Balmer, A, Farrar, N, Perveen, R, Black, G C M

“…Aims: To report the detailed clinical findings in a three generation pedigree with autosomal dominant cataract, microcornea, and coloboma resulting from…”
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Ultrastructural and Molecular Analysis of Bowman's Layer Corneal Dystrophies: An Epithelial Origin? by Ridgway, Alan E. A, Akhtar, Saeed, Munier, Francis L, Schorderet, Daniel F, Stewart, Helen, Perveen, Ramat, Bonshek, Richard E, Odenthal, Monica T. P, Dixon, Michael, Barraquer, Rafael, Escoto, Remberto, Black, Graeme C. M

“…Two mutations (R555Q and R124L) in the BIGH3 gene have been described in anterior or Bowman's layer dystrophies (CDB). The clinical, molecular, and…”
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P2460Furosemide versus bumetanide; a deep dive into national heart failure audit (England & Wales) by Shoaib, A., Mamas, M., Thackray, S., Uddin, M., Perveen, R., Khan, R.U., McDonagh, T., Dargie, H., Hardman, S., Clark, A.L., Cleland, J.G.F.C.

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Problem based learning by Rahman, M E, Perveen, R, Chowhury, A M, Rouf, A

“…PBL, an educational format, stimulates active and life long learning. PBL improves the motivation of students, stimulates integration of disciplines, small…”
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Locus heterogeneity in autosomal dominant congenital external ophthalmoplegia (CFEOM) by Black, G C, Perveen, R, Hatchwell, E, Reck, A, Clayton-Smith, J

“…Congenital external ophthalmoplegia (CFEOM) is an uncommon autosomal dominant condition that has previously been mapped to the pericentromeric region of…”
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Systematic review on current antiviral therapy in COVID-19 pandemic by Perveen, R A, Nasir, M, Talha, K A, Selina, F, Islam, M A

“…Currently, there are several attempts to find an effective antiviral drugs against the COVID-19. Although majority of the COVID-19 patients have mild to…”
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Further delineation of the KAT6B molecular and phenotypic spectrum by Gannon, Tamsin, Perveen, Rahat, Schlecht, Hélene, Ramsden, Simon, Anderson, Beverley, Kerr, Bronwyn, Day, Ruth, Banka, Siddharth, Suri, Mohnish, Berland, Siren, Gabbett, Michael, Ma, Alan, Lyonnet, Stan, Cormier-Daire, Valerie, Yilmaz, Rüstem, Borck, Guntram, Wieczorek, Dagmar, Anderlid, Britt-Marie, Smithson, Sarah, Vogt, Julie, Moore-Barton, Heather, Simsek-Kiper, Pelin Ozlem, Maystadt, Isabelle, Destrée, Anne, Bucher, Jessica, Angle, Brad, Mohammed, Shehla, Wakeling, Emma, Price, Sue, Singer, Amihood, Sznajer, Yves, Toutain, Annick, Haye, Damien, Newbury-Ecob, Ruth, Fradin, Melanie, McGaughran, Julie, Tuysuz, Beyhan, Tein, Mark, Bouman, Katelijne, Dabir, Tabib, Van den Ende, Jenneke, Luk, Ho Ming, Pilz, Daniela T, Eason, Jacqueline, Davies, Sally, Reardon, Willie, Garavelli, Livia, Zuffardi, Orsetta, Devriendt, Koen, Armstrong, Ruth, Johnson, Diana, Doco-Fenzy, Martine, Bijlsma, Emilia, Unger, Sheila, Veenstra-Knol, Hermine E, Kohlhase, Jürgen, Lo, Ivan F M, Smith, Janine, Clayton-Smith, Jill

“…KAT6B sequence variants have been identified previously in both patients with the Say-Barber-Biesecker type of blepharophimosis mental retardation syndromes…”
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