Vimentin Is at the Heart of Epithelial Mesenchymal Transition (EMT) Mediated Metastasis
Usman, Saima, Waseem, Naushin H., Nguyen, Thuan Khanh Ngoc, Mohsin, Sahar, Jamal, Ahmad, Teh, Muy-Teck, Waseem, Ahmad
Published in Cancers (05.10.2021)
Published in Cancers (05.10.2021)
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Journal Article
Transcriptome Analysis Reveals Vimentin-Induced Disruption of Cell-Cell Associations Augments Breast Cancer Cell Migration
Usman, Saima, Jamal, Ahmad, Bushaala, Antesar, Waseem, Naushin H, Al-Dehlawi, Hebah, Yeudall, William Andrew, Teh, Muy-Teck, Tummala, Hemanth, Waseem, Ahmad
Published in Cells (Basel, Switzerland) (13.12.2022)
Published in Cells (Basel, Switzerland) (13.12.2022)
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Journal Article
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma
Waseem, Naushin H, Low, Sancy, Shah, Amna Z, Avisetti, Deepa, Ostergaard, Pia, Simpson, Michael, Niemiec, Katarzyna A, Martin-Martin, Belen, Aldehlawi, Hebah, Usman, Saima, Lee, Pak Sang, Khawaja, Anthony P, Ruddle, Jonathan B, Shah, Ameet, Sackey, Ege, Day, Alexander, Jiang, Yuzhen, Swinfield, Geoff, Viswanathan, Ananth, Alfano, Giovanna, Chakarova, Christina, Cordell, Heather J, Garway-Heath, David F, Khaw, Peng T, Bhattacharya, Shomi S, Waseem, Ahmad, Foster, Paul J
Published in PLoS genetics (01.04.2020)
Published in PLoS genetics (01.04.2020)
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Journal Article
Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa
Davidson, Alice E., Schwarz, Nele, Zelinger, Lina, Stern-Schneider, Gabriele, Shoemark, Amelia, Spitzbarth, Benjamin, Gross, Menachem, Laxer, Uri, Sosna, Jacob, Sergouniotis, Panagiotis I., Waseem, Naushin H., Wilson, Robert, Kahn, Richard A., Plagnol, Vincent, Wolfrum, Uwe, Banin, Eyal, Hardcastle, Alison J., Cheetham, Michael E., Sharon, Dror, Webster, Andrew R.
Published in American journal of human genetics (08.08.2013)
Published in American journal of human genetics (08.08.2013)
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Journal Article
A Splice-Site Mutation in a Retina-Specific Exon of BBS8 Causes Nonsyndromic Retinitis Pigmentosa
Riazuddin, S. Amer, Iqbal, Muhammad, Wang, Yue, Masuda, Tomohiro, Chen, Yuhng, Bowne, Sara, Sullivan, Lori S., Waseem, Naushin H., Bhattacharya, Shomi, Daiger, Stephen P., Zhang, Kang, Khan, Shaheen N., Riazuddin, Sheikh, Hejtmancik, J. Fielding, Sieving, Paul A., Zack, Donald J., Katsanis, Nicholas
Published in American journal of human genetics (14.05.2010)
Published in American journal of human genetics (14.05.2010)
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Journal Article
Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in rd11 mice
Friedman, James S., Chang, Bo, Krauth, Daniel S., Lopez, Irma, Waseem, Naushin H., Hurd, Ron E., Feathers, Kecia L., Branham, Kari E., Shaw, Manessa, Thomas, George E., Brooks, Matthew J., Liu, Chunqiao, Bakeri, Hirva A., Campos, Maria M., Maubaret, Cecilia, Webster, Andrew R., Rodriguez, Ignacio R., Thompson, Debra A., Bhattacharya, Shomi S., Koenekoop, Robert K., Heckenlively, John R., Swaroop, Anand, Nathans, Jeremy
Published in Proceedings of the National Academy of Sciences - PNAS (31.08.2010)
Published in Proceedings of the National Academy of Sciences - PNAS (31.08.2010)
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Journal Article
Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports
Audo, Isabelle, Bujakowska, Kinga, Mohand-Saïd, Saddek, Lancelot, Marie-Elise, Moskova-Doumanova, Veselina, Waseem, Naushin H, Antonio, Aline, Sahel, José-Alain, Bhattacharya, Shomi S, Zeitz, Christina
Published in BMC genetics (12.10.2010)
Published in BMC genetics (12.10.2010)
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Journal Article
Expression of PRPF31 and TFPT: regulation in health and retinal disease
ROSE, Anna M, SHAH, Amna Z, WASEEM, Naushin H, CHAKAROVA, Christina F, ALFANO, Giovanna, COUSSA, Razek G, AJLAN, Radwan, KOENEKOOP, Robert K, BHATTACHARYA, Shomi S
Published in Human molecular genetics (15.09.2012)
Published in Human molecular genetics (15.09.2012)
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Journal Article
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development
Simcoe, Mark J., Shah, Ameet, Fan, Baojian, Choquet, Hélène, Weisschuh, Nicole, Waseem, Naushin H., Jiang, Chen, Melles, Ronald B., Ritch, Robert, Mahroo, Omar A., Wissinger, Bernd, Jorgenson, Eric, Wiggs, Janey L., Garway-Heath, David F., Hysi, Pirro G., Hammond, Christopher J.
Published in Ophthalmology (Rochester, Minn.) (01.06.2022)
Published in Ophthalmology (Rochester, Minn.) (01.06.2022)
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Journal Article
NMNAT1 mutations cause Leber congenital amaurosis
FALK, Marni J, QI ZHANG, STANISZEWSKA, Magdalena, SHUKLA, Rachna, PALAVALLI, Lakshmi, MOHAND-SAID, Saddek, WASEEM, Naushin H, JALALI, Subhadra, PERIN, Juan C, PLACE, Emily, OSTROVSKY, Julian, RUI XIAO, NAKAMARU-OGISO, Eiko, BHATTACHARYA, Shomi S, CONSUGAR, Mark, WEBSTER, Andrew R, SAHEL, José-Alain, MOORE, Anthony T, BERSON, Eliot L, QIN LIU, XIAOWU GAI, PIERCE, Eric A, KANNABIRAN, Chitra, FONSECA-KELLY, Zoe, CHAKAROVA, Christina, AUDO, Isabelle, MACKAY, Donna S, ZEITZ, Christina, DEV BORMAN, Arundhati
Published in Nature genetics (01.09.2012)
Published in Nature genetics (01.09.2012)
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Journal Article
RP1L1 Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy
Davidson, Alice E., Sergouniotis, Panagiotis I., Mackay, Donna S., Wright, Genevieve A., Waseem, Naushin H., Michaelides, Michel, Holder, Graham E., Robson, Anthony G., Moore, Anthony T., Plagnol, Vincent, Webster, Andrew R.
Published in Human mutation (01.03.2013)
Published in Human mutation (01.03.2013)
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Journal Article
A Homozygous Mutation in the TUB Gene Associated with Retinal Dystrophy and Obesity
Borman, Arundhati Dev, Pearce, Laura R., Mackay, Donna S., Nagel-Wolfrum, Kerstin, Davidson, Alice E., Henderson, Robert, Garg, Sumedha, Waseem, Naushin H., Webster, Andrew R., Plagnol, Vincent, Wolfrum, Uwe, Farooqi, I. Sadaf, Moore, Anthony T.
Published in Human mutation (01.03.2014)
Published in Human mutation (01.03.2014)
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Journal Article
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8
Maubaret, Cécilia G, Vaclavik, Veronika, Mukhopadhyay, Rajarshi, Waseem, Naushin H, Churchill, Amanda, Holder, Graham E, Moore, Anthony T, Bhattacharya, Shomi S, Webster, Andrew R
Published in Investigative ophthalmology & visual science (02.12.2011)
Published in Investigative ophthalmology & visual science (02.12.2011)
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Journal Article
Mutations in the Gene Coding for the Pre-mRNA Splicing Factor, PRPF31, in Patients with Autosomal Dominant Retinitis Pigmentosa
Waseem, Naushin H, Vaclavik, Veronika, Webster, Andrew, Jenkins, Sharon A, Bird, Alan C, Bhattacharya, Shomi S
Published in Investigative ophthalmology & visual science (01.03.2007)
Published in Investigative ophthalmology & visual science (01.03.2007)
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Journal Article
Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma
Vishal, Mansi, Sharma, Anchal, Kaurani, Lalit, Alfano, Giovanna, Mookherjee, Suddhasil, Narta, Kiran, Agrawal, Jyoti, Bhattacharya, Iman, Roychoudhury, Susanta, Ray, Jharna, Waseem, Naushin H, Bhattacharya, Shomi S, Basu, Analabha, Sen, Abhijit, Ray, Kunal, Mukhopadhyay, Arijit
Published in BMC medical genomics (22.03.2016)
Published in BMC medical genomics (22.03.2016)
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Conformational Changes in the Rod Domain of Human Keratin 8 following Heterotypic Association with Keratin 18 and Its Implication for Filament Stability
Waseem, Ahmad, Karsten, Uwe, Leigh, Irene M, Purkis, Patricia, Waseem, Naushin H, Lane, E. Birgitte
Published in Biochemistry (Easton) (10.02.2004)
Published in Biochemistry (Easton) (10.02.2004)
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