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Amna Z Shah

Showing results (1-10 of 12) with videos related to

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Experimental Eye Research|May 16, 2016
First insights into the expression of VAX2 in humans and its localization in the adult primate retinaGiovanna Alfano, Amna Z Shah, Glen Jeffery, et al.
Plos Genetics|November 13, 2012
CNOT3 is a modifier of PRPF31 mutations in retinitis pigmentosa with incomplete penetranceGiulia Venturini, Anna M Rose, Amna Z Shah, et al.
Annals of Human Genetics|October 15, 2013
Dominant PRPF31 mutations are hypostatic to a recessive CNOT3 polymorphism in retinitis pigmentosa: a novel phenomenon of "linked trans-acting epistasis"Anna M Rose, Amna Z Shah, Giulia Venturini, et al.
Plos One|February 13, 2016
TOPORS, a Dual E3 Ubiquitin and Sumo1 Ligase, Interacts with 26 S Protease Regulatory Subunit 4, Encoded by the PSMC1 GeneBarbara Czub, Amna Z Shah, Giovanna Alfano, et al.
Scientific Reports|January 20, 2016
Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosaAnna M Rose, Amna Z Shah, Giulia Venturini, et al.
Plos One|November 16, 2016
EYS Is a Protein Associated with the Ciliary Axoneme in Rods and ConesGiovanna Alfano, Przemyslaw M Kruczek, Amna Z Shah, 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.
Journal of Molecular and Genetic Medicine : an International Journal of Biomedical Research|March 3, 2015
A Study into the Evolutionary Divergence of the Core Promoter Elements of <i>PRPF31</i> and <i>TFPT.</i>Anna M Rose, Amna Z Shah, Giovanna Alfano, et al.
Cancer Research|June 24, 2026
Virtual Tumors Enable Prediction of Personalized Therapeutic Combinations for Non-Small Cell Lung CancerMatthew A Clarke, Charlie George Barker, Ashley Nicholls, et al.
Human Molecular Genetics|December 7, 2019
Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten diseaseSophia-Martha Kleine Holthaus, Saul Herranz-Martin, Giulia Massaro, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Experimental Eye Research|May 16, 2016
First insights into the expression of VAX2 in humans and its localization in the adult primate retinaGiovanna Alfano, Amna Z Shah, Glen Jeffery, et al.
Plos Genetics|November 13, 2012
CNOT3 is a modifier of PRPF31 mutations in retinitis pigmentosa with incomplete penetranceGiulia Venturini, Anna M Rose, Amna Z Shah, et al.
Annals of Human Genetics|October 15, 2013
Dominant PRPF31 mutations are hypostatic to a recessive CNOT3 polymorphism in retinitis pigmentosa: a novel phenomenon of "linked trans-acting epistasis"Anna M Rose, Amna Z Shah, Giulia Venturini, et al.
Plos One|February 13, 2016
TOPORS, a Dual E3 Ubiquitin and Sumo1 Ligase, Interacts with 26 S Protease Regulatory Subunit 4, Encoded by the PSMC1 GeneBarbara Czub, Amna Z Shah, Giovanna Alfano, et al.
Scientific Reports|January 20, 2016
Transcriptional regulation of PRPF31 gene expression by MSR1 repeat elements causes incomplete penetrance in retinitis pigmentosaAnna M Rose, Amna Z Shah, Giulia Venturini, et al.
Plos One|November 16, 2016
EYS Is a Protein Associated with the Ciliary Axoneme in Rods and ConesGiovanna Alfano, Przemyslaw M Kruczek, Amna Z Shah, 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.
Journal of Molecular and Genetic Medicine : an International Journal of Biomedical Research|March 3, 2015
A Study into the Evolutionary Divergence of the Core Promoter Elements of <i>PRPF31</i> and <i>TFPT.</i>Anna M Rose, Amna Z Shah, Giovanna Alfano, et al.
Cancer Research|June 24, 2026
Virtual Tumors Enable Prediction of Personalized Therapeutic Combinations for Non-Small Cell Lung CancerMatthew A Clarke, Charlie George Barker, Ashley Nicholls, et al.
Human Molecular Genetics|December 7, 2019
Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten diseaseSophia-Martha Kleine Holthaus, Saul Herranz-Martin, Giulia Massaro, et al.
Pageof 2