Хайлтын үр дүнгүүд - Naushin Waseem

Үр дүнг сайжруулах
  1. 1
    Isolation and analysis of the fission yeast gene encoding polymerase delta accessory protein PCNA.

    Isolation and analysis of the fission yeast gene encoding polymerase delta accessory protein PCNA. -н Naushin Waseem, Karim Labib, Paul Nurse, David P. Lane

    Хэвлэсэн 1992
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    Artigo
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  2. 2
    Haemophilia A mutations in the UK: results of screening one‐third of the population

    Haemophilia A mutations in the UK: results of screening one‐third of the population -н P. M. Green, Richard D. Bagnall, Naushin Waseem, F. Giannelli

    Хэвлэсэн 2008
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    Artigo
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  3. 3
    Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A

    Recurrent inversion breaking intron 1 of the factor VIII gene is a frequent cause of severe hemophilia A -н Richard D. Bagnall, Naushin Waseem, Peter M. Green, F. Giannelli

    Хэвлэсэн 2002
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    Artigo
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  4. 4
    Prognostic value of proliferating cell nuclear antigen in gastric carcinoma.

    Prognostic value of proliferating cell nuclear antigen in gastric carcinoma. -н Sunjay Jain, M. I. Filipe, Peter A. Hall, Naushin Waseem, David P. Lane, David A. Levison

    Хэвлэсэн 1991
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    Artigo
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  5. 5
    Intracellular localization of the hepatitis B virus HBx protein

    Intracellular localization of the hepatitis B virus HBx protein -н Frank Henkler, Jonathan Hoare, Naushin Waseem, Robert Goldin, Michael J. McGarvey, Rajen Koshy, Ian A. King

    Хэвлэсэн 2001
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    Artigo
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  6. 6
    Vimentin Is at the Heart of Epithelial Mesenchymal Transition (EMT) Mediated Metastasis

    Vimentin Is at the Heart of Epithelial Mesenchymal Transition (EMT) Mediated Metastasis -н Saima Usman, Naushin Waseem, Thuan Khanh Ngoc Nguyen, Sahar Mohsin, Ahmad Jamal, Muy‐Teck Teh, Ahmad Waseem

    Хэвлэсэн 2021
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    Revisão
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  7. 7
    Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans

    Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans -н Vanita Berry, Cheryl Y. Gregory‐Evans, Warren Emmett, Naushin Waseem, Jacob Raby, Quincy Prescott, Anthony T. Moore, Shomi S. Bhattacharya

    Хэвлэсэн 2013
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    Artigo
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  8. 8
    <i>RP1L1</i>Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy

    <i>RP1L1</i>Variants are Associated with a Spectrum of Inherited Retinal Diseases Including Retinitis Pigmentosa and Occult Macular Dystrophy -н Alice E. Davidson, Panagiotis I. Sergouniotis, Donna S. Mackay, Genevieve Wright, Naushin Waseem, Michel Michaelides, Graham E. Holder, Anthony G. Robson, Anthony T. Moore, Vincent Plagnol, Andrew R. Webster

    Хэвлэсэн 2012
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    Artigo
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  9. 9
    A Homozygous Mutation in the<i><scp>TUB</scp></i>Gene Associated with Retinal Dystrophy and Obesity

    A Homozygous Mutation in the<i><scp>TUB</scp></i>Gene Associated with Retinal Dystrophy and Obesity -н Arundhati Dev Borman, Laura R. Pearce, Donna S. Mackay, Kerstin Nagel‐Wolfrum, Alice E. Davidson, Robert Henderson, Sumedha Garg, Naushin Waseem, Andrew R. Webster, Vincent Plagnol, Uwe Wolfrum, I. Sadaf Farooqi, Anthony T. Moore

    Хэвлэсэн 2013
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    Artigo
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  10. 10
    Molecular and Clinical Findings in Patients With Knobloch Syndrome

    Molecular and Clinical Findings in Patients With Knobloch Syndrome -н Sarah Hull, Gavin Arno, Cristy A. Ku, Zhongqi Ge, Naushin Waseem, Aman Chandra, Andrew R. Webster, Anthony G. Robson, Michel Michaelides, Richard G. Weleber, Indran Davagnanam, Rui Chen, Graham E. Holder, Mark E. Pennesi, Anthony T. Moore

    Хэвлэсэн 2016
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    Artigo
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  11. 11
    A Splice-Site Mutation in a Retina-Specific Exon of BBS8 Causes Nonsyndromic Retinitis Pigmentosa

    A Splice-Site Mutation in a Retina-Specific Exon of BBS8 Causes Nonsyndromic Retinitis Pigmentosa -н Sheikh Riazuddin, Muhammad Iqbal, Yue J. Wang, Tomohiro Masuda, Yuhng Chen, Sara J. Bowne, Lori S. Sullivan, Naushin Waseem, Shomi S. Bhattacharya, Stephen P. Daiger, Kang Zhang, Shaheen N. Khan, Sheikh Riazuddin, J. Fielding Hejtmancik, Paul A. Sieving, Donald J. Zack, Nicholas Katsanis

    Хэвлэсэн 2010
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    Artigo
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  12. 12
    A clinical and molecular characterisation of CRB1-associated maculopathy

    A clinical and molecular characterisation of CRB1-associated maculopathy -н Kamron Khan, Anthony G. Robson, Omar A. Mahroo, Gavin Arno, Chris F. Inglehearn, Monica Armengol, Naushin Waseem, Graham E. Holder, Keren Carss, Lucy F. Raymond, Andrew R. Webster, Anthony T. Moore, Martin McKibbin, Maria M. van Genderen, James A. Poulter, Michel Michaelides

    Хэвлэсэн 2018
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    Artigo
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  13. 13
    Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa

    Mutations in ARL2BP, Encoding ADP-Ribosylation-Factor-Like 2 Binding Protein, Cause Autosomal-Recessive Retinitis Pigmentosa -н Alice E. Davidson, Nele Schwarz, Lina Zelinger, Gabriele Stern-Schneider, Amelia Shoemark, Benjamin Spitzbarth, Menachem Gross, Uri Laxer, Jacob Sosna, Panagiotis I. Sergouniotis, Naushin Waseem, Robert Wilson, Richard Kahn, Vincent Plagnol, Uwe Wolfrum, Eyal Banin, Alison J. Hardcastle, Michael E. Cheetham, Dror Sharon, Andrew R. Webster

    Хэвлэсэн 2013
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    Artigo
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  14. 14
    Mucous Membrane Pemphigoid with Ocular Involvement

    Mucous Membrane Pemphigoid with Ocular Involvement -н Hon Shing Ong, Jane Setterfield, Darwin Minassian, John Dart, Debbie Booth, Elaina Reid, Nicole Carnt, Stefano Gugliemetti, Vijay Shanmuganathan, Martin Watson, Valerie Saw, Mark Wilkins, Vicky McCudden, Saj Ahmad, Virginia L. Calder, Naushin Waseem, Beverly Scott, Catey Bunce, William H. Gage, Mike Gleeson, Valerie J. Lund, Guri Sandhu

    Хэвлэсэн 2017
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    Artigo
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  15. 15
    Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in <i>rd11</i> mice

    Loss of lysophosphatidylcholine acyltransferase 1 leads to photoreceptor degeneration in <i>rd11</i> mice -н James S. Friedman, Bo Chang, Daniel S. Krauth, Irma López, Naushin Waseem, R.E. Hurd, Kecia L. Feathers, Kari Branham, Manessa Shaw, George E. Thomas, Matthew J. Brooks, Chunqiao Liu, Hirva Bakeri, Maria M Campos, C. Maubaret, Andrew R. Webster, Ignacio R. Rodríguez, Debra A. Thompson, Shomi S. Bhattacharya, Robert K. Koenekoop, John R. Heckenlively, Anand Swaroop

    Хэвлэсэн 2010
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    Artigo
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  16. 16
    Mutations in TOPORS Cause Autosomal Dominant Retinitis Pigmentosa with Perivascular Retinal Pigment Epithelium Atrophy

    Mutations in TOPORS Cause Autosomal Dominant Retinitis Pigmentosa with Perivascular Retinal Pigment Epithelium Atrophy -н Christina Chakarova, Myrto Papaioannou, Hemant Khanna, Irma López, Naushin Waseem, Amna Shah, Torsten Theis, James S. Friedman, C. Maubaret, Kinga M. Bujakowska, Brotati Kaur Veraitch, Mai M. Abd El-Aziz, Quincy Prescott, Sunil K. Parapuram, Wendy A. Bickmore, Peter Munro, Andreas Gal, Christian Hamel, Valeria Marigo, Chris P. Ponting, Bernd Wissinger, Eberhart Zrenner, Karl Matter, Anand Swaroop, Robert K. Koenekoop, Shomi S. Bhattacharya

    Хэвлэсэн 2007
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    Artigo
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  17. 17
    NMNAT1 mutations cause Leber congenital amaurosis

    NMNAT1 mutations cause Leber congenital amaurosis -н Marni J. Falk, Qi Zhang, Eiko Nakamaru‐Ogiso, Chitra Kannabiran, Zoë Fonseca-Kelly, Christina Chakarova, Isabelle Audo, Donna S. Mackay, Christina Zeitz, Arundhati Dev Borman, Magdalena Staniszewska, Rachna Shukla, Lakshmi Palavalli, Saddek Mohand‐Saïd, Naushin Waseem, Subhadra Jalali, Juan C. Perín, Emily Place, Julian Ostrovsky, Rui Xiao, Shomi S. Bhattacharya, Mark Consugar, Andrew R. Webster, José‐Alain Sahel, Anthony T. Moore, Eliot L. Berson, Qin Liu, Xiaowu Gai, Eric A. Pierce

    Хэвлэсэн 2012
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    Artigo
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  18. 18
    Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa

    Mutations in a BTB-Kelch Protein, KLHL7, Cause Autosomal-Dominant Retinitis Pigmentosa -н James S. Friedman, Joseph W. Ray, Naushin Waseem, Kory R. Johnson, Matthew J. Brooks, Therése Hugosson, Debra K. Breuer, Kari Branham, Daniel S. Krauth, Sara J. Bowne, Lori S. Sullivan, Vesna Ponjavic, Lotta Gränse, Ritu Khanna, Edward H. Trager, Linn Gieser, Dianna K. Hughbanks-Wheaton, Radu Cojocaru, Noor M. Ghiasvand, Christina Chakarova, Magnus Abrahamson, Harald H.H. Göring, Andrew R. Webster, David G. Birch, Gonçalo R. Abecasis, Yang C. Fann, Shomi S. Bhattacharya, Stephen P. Daiger, John R. Heckenlively, Sten Andréasson, Anand Swaroop

    Хэвлэсэн 2009
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    Artigo
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  19. 19
    Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement

    Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement -н Mohammed E. El‐Asrag, Panagiotis I. Sergouniotis, Martin McKibbin, Vincent Plagnol, Eamonn Sheridan, Naushin Waseem, Zakia Abdelhamed, Declan J. McKeefry, Kristof Van Schil, James A. Poulter, Colin A. Johnson, Ian Carr, Bart P. Leroy, Elfride De Baere, Chris F. Inglehearn, Andrew R. Webster, Carmel Toomes, Manir Ali, Graeme Black, Georgina Hall, Stuart Ingram, Rachel Gillespie, Simon Ramsden, Forbes D.C. Manson, Alison J. Hardcastle, Michel Michaelides, Michael E. Cheetham, Gavin Arno, Niclas Thomas, Shomi S. Bhattacharya, Tony Moore, Andrea H. Németh, Susan M. Downes, Stefano Lise, Emma Lord

    Хэвлэсэн 2015
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    Artigo
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  20. 20
    A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies

    A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies -н Hemant Khanna, Erica E. Davis, Carlos Murga‐Zamalloa, Alejandro Estrada‐Cuzcano, Irma López, Anneke I. den Hollander, Marijke N. Zonneveld, Mohammad Othman, Naushin Waseem, Christina Chakarova, C. Maubaret, Anna Dı́az-Font, Ian M. MacDonald, Donna M. Muzny, David A. Wheeler, Margaret Morgan, Lora Lewis, Clare V. Logan, Perciliz L. Tan, M Beer, Chris F. Inglehearn, Richard A. Lewis, Samuel G. Jacobson, Carsten Bergmann, Philip L. Beales, Tania Attié‐Bitach, Colin A. Johnson, Edgar A. Otto, Shomi S. Bhattacharya, Friedhelm Hildebrandt, Richard A. Gibbs, Robert K. Koenekoop, Anand Swaroop, Nicholas Katsanis

    Хэвлэсэн 2009
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    Artigo
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