Search research articles
Contact Us
Filters
Showing results (1-10 of 12) with videos related to
Page
of 2
Sort By:
Experimental Eye Research
|
May 16, 2016
First insights into the expression of VAX2 in humans and its localization in the adult primate retina
Giovanna 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 penetrance
Giulia 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 Gene
Barbara 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 pigmentosa
Anna 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 Cones
Giovanna 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 disease
Anna 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 Cancer
Matthew 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 disease
Sophia-Martha Kleine Holthaus, Saul Herranz-Martin, Giulia Massaro, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Experimental Eye Research
|
May 16, 2016
First insights into the expression of VAX2 in humans and its localization in the adult primate retina
Giovanna 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 penetrance
Giulia 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 Gene
Barbara 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 pigmentosa
Anna 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 Cones
Giovanna 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 disease
Anna 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 Cancer
Matthew 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 disease
Sophia-Martha Kleine Holthaus, Saul Herranz-Martin, Giulia Massaro, et al.
Page
of 2