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Naushin H Waseem

Showing results (1-10 of 21) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|May 17, 2002
Mutation detection in factor VIII cDNA from lymphocytes of hemophilia A patients by solid phase fluorescent chemical cleavage of mismatchNaushin H Waseem, Richard Bagnall, Peter M Green, et al.
Ophthalmic Genetics|June 28, 2018
Identification and characterization of the VAX2 p.Leu139Arg variant: possible involvement of VAX2 in cone dystrophyGiovanna Alfano, Naushin H Waseem, Andrew R Webster, et al.
Investigative Ophthalmology & Visual Science|July 1, 2011
A 112 kb deletion in chromosome 19q13.42 leads to retinitis pigmentosaAnna M Rose, Rajarshi Mukhopadhyay, Andrew R Webster, et al.
Biochemistry|February 6, 2004
Conformational changes in the rod domain of human keratin 8 following heterotypic association with keratin 18 and its implication for filament stabilityAhmad Waseem, Uwe Karsten, Irene M Leigh, et al.
Molecular Vision|June 3, 2011
A novel 1-bp deletion in PITX3 causing congenital posterior polar cataractVanita Berry, Peter J Francis, Quincy Prescott, et al.
Investigative Ophthalmology & Visual Science|February 28, 2007
Mutations in the gene coding for the pre-mRNA splicing factor, PRPF31, in patients with autosomal dominant retinitis pigmentosaNaushin H Waseem, Veronika Vaclavik, Andrew Webster, et al.
Cancers|October 13, 2021
Vimentin Is at the Heart of Epithelial Mesenchymal Transition (EMT) Mediated MetastasisSaima Usman, Naushin H Waseem, Thuan Khanh Ngoc Nguyen, et al.
Cells|December 23, 2022
Transcriptome Analysis Reveals Vimentin-Induced Disruption of Cell-Cell Associations Augments Breast Cancer Cell MigrationSaima Usman, Ahmad Jamal, Antesar Bushaala, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, et al.
Human Molecular Genetics|June 23, 2012
Expression of PRPF31 and TFPT: regulation in health and retinal diseaseAnna M Rose, Amna Z Shah, Naushin H Waseem, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Methods in Molecular Biology (Clifton, N.J.)|May 17, 2002
Mutation detection in factor VIII cDNA from lymphocytes of hemophilia A patients by solid phase fluorescent chemical cleavage of mismatchNaushin H Waseem, Richard Bagnall, Peter M Green, et al.
Ophthalmic Genetics|June 28, 2018
Identification and characterization of the VAX2 p.Leu139Arg variant: possible involvement of VAX2 in cone dystrophyGiovanna Alfano, Naushin H Waseem, Andrew R Webster, et al.
Investigative Ophthalmology & Visual Science|July 1, 2011
A 112 kb deletion in chromosome 19q13.42 leads to retinitis pigmentosaAnna M Rose, Rajarshi Mukhopadhyay, Andrew R Webster, et al.
Biochemistry|February 6, 2004
Conformational changes in the rod domain of human keratin 8 following heterotypic association with keratin 18 and its implication for filament stabilityAhmad Waseem, Uwe Karsten, Irene M Leigh, et al.
Molecular Vision|June 3, 2011
A novel 1-bp deletion in PITX3 causing congenital posterior polar cataractVanita Berry, Peter J Francis, Quincy Prescott, et al.
Investigative Ophthalmology & Visual Science|February 28, 2007
Mutations in the gene coding for the pre-mRNA splicing factor, PRPF31, in patients with autosomal dominant retinitis pigmentosaNaushin H Waseem, Veronika Vaclavik, Andrew Webster, et al.
Cancers|October 13, 2021
Vimentin Is at the Heart of Epithelial Mesenchymal Transition (EMT) Mediated MetastasisSaima Usman, Naushin H Waseem, Thuan Khanh Ngoc Nguyen, et al.
Cells|December 23, 2022
Transcriptome Analysis Reveals Vimentin-Induced Disruption of Cell-Cell Associations Augments Breast Cancer Cell MigrationSaima Usman, Ahmad Jamal, Antesar Bushaala, et al.
Investigative Ophthalmology & Visual Science|November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, et al.
Human Molecular Genetics|June 23, 2012
Expression of PRPF31 and TFPT: regulation in health and retinal diseaseAnna M Rose, Amna Z Shah, Naushin H Waseem, et al.
Pageof 3