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Trends in Genetics : TIG
|
January 22, 2005
Light in retinitis pigmentosa
Avril Kennan, Aileen Aherne, Pete Humphries
The Patient
|
November 29, 2014
Adopting a Sustainable Community of Practice Model when Developing a Service to Support Patients with Epidermolysis Bullosa (EB): A Stakeholder-Centered Approach
Rosemary Joan Gowran, Avril Kennan, Siobhán Marshall, et al.
Human Molecular Genetics
|
March 5, 2002
Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice
Avril Kennan, Aileen Aherne, Arpad Palfi, et al.
PEC Innovation
|
July 19, 2024
Prioritising Key Concepts for informed health choices in cancer: An evidence-based online educational programme
Mengqi Li, Declan Devane, Claire Beecher, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 22, 2005
Toward a gene therapy for dominant disease: validation of an RNA interference-based mutation-independent approach
Anna-Sophia Kiang, Arpad Palfi, Marius Ader, et al.
Plos One
|
October 9, 2025
Evaluating the feasibility and acceptability of the Informed Health Choices-Cancer programme: A pilot randomised trial protocol
Mengqi Li, Marie Tierney, Claire Beecher, et al.
Journal of Cancer Survivorship : Research and Practice
|
August 7, 2025
Developing critical thinking and decision-making skills for cancer information: the Informed Health Choice-Cancer online learning resource
Mengqi Li, Declan Devane, Claire Beecher, et al.
HRB Open Research
|
September 27, 2023
Prioritising Informed Health Choices Key Concepts for those impacted by cancer: a protocol
Mengqi Li, Declan Devane, Claire Beecher, et al.
Molecular Vision
|
May 2, 2003
Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene
Sara J Bowne, Stephen P Daiger, Kimberly A Malone, et al.
Human Molecular Genetics
|
April 4, 2008
Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10)
Lawrence C S Tam, Anna-Sophia Kiang, Avril Kennan, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Trends in Genetics : TIG
|
January 22, 2005
Light in retinitis pigmentosa
Avril Kennan, Aileen Aherne, Pete Humphries
The Patient
|
November 29, 2014
Adopting a Sustainable Community of Practice Model when Developing a Service to Support Patients with Epidermolysis Bullosa (EB): A Stakeholder-Centered Approach
Rosemary Joan Gowran, Avril Kennan, Siobhán Marshall, et al.
Human Molecular Genetics
|
March 5, 2002
Identification of an IMPDH1 mutation in autosomal dominant retinitis pigmentosa (RP10) revealed following comparative microarray analysis of transcripts derived from retinas of wild-type and Rho(-/-) mice
Avril Kennan, Aileen Aherne, Arpad Palfi, et al.
PEC Innovation
|
July 19, 2024
Prioritising Key Concepts for informed health choices in cancer: An evidence-based online educational programme
Mengqi Li, Declan Devane, Claire Beecher, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 22, 2005
Toward a gene therapy for dominant disease: validation of an RNA interference-based mutation-independent approach
Anna-Sophia Kiang, Arpad Palfi, Marius Ader, et al.
Plos One
|
October 9, 2025
Evaluating the feasibility and acceptability of the Informed Health Choices-Cancer programme: A pilot randomised trial protocol
Mengqi Li, Marie Tierney, Claire Beecher, et al.
Journal of Cancer Survivorship : Research and Practice
|
August 7, 2025
Developing critical thinking and decision-making skills for cancer information: the Informed Health Choice-Cancer online learning resource
Mengqi Li, Declan Devane, Claire Beecher, et al.
HRB Open Research
|
September 27, 2023
Prioritising Informed Health Choices Key Concepts for those impacted by cancer: a protocol
Mengqi Li, Declan Devane, Claire Beecher, et al.
Molecular Vision
|
May 2, 2003
Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene
Sara J Bowne, Stephen P Daiger, Kimberly A Malone, et al.
Human Molecular Genetics
|
April 4, 2008
Therapeutic benefit derived from RNAi-mediated ablation of IMPDH1 transcripts in a murine model of autosomal dominant retinitis pigmentosa (RP10)
Lawrence C S Tam, Anna-Sophia Kiang, Avril Kennan, et al.
Page
of 2