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American Journal of Human Genetics
|
March 26, 1999
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study
A J Hardcastle, D L Thiselton, L Van Maldergem, et al.
The Gerontologist
|
April 1, 1988
A job diagnostic survey of nursing home caregivers: implications for job redesign
D Brannon, M A Smyer, M D Cohn, et al.
The Journal of Gene Medicine
|
May 26, 2026
In Vivo Assessment of dbDNA GNE<sup>wt</sup>/bi-shRNA-GNE<sup>M743T</sup> Lipoplex for GNE Myopathy: Improved Potency and Safety
Christopher M Jay, Fabienne Kerneis, Donald Rao, et al.
Current Biology : CB
|
June 15, 2022
Post-trauma behavioral phenotype predicts the degree of vulnerability to fear relapse after extinction in male rats
Fanny Demars, Ralitsa Todorova, Gabriel Makdah, et al.
Immunohorizons
|
September 22, 2020
Extracellular miR-146a-5p Induces Cardiac Innate Immune Response and Cardiomyocyte Dysfunction
Briana K Shimada, Yang Yang, Jing Zhu, et al.
American Journal of Human Genetics
|
October 1, 1987
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14
A F Wright, S S Bhattacharya, J F Clayton, et al.
European Urology Open Science
|
August 2, 2021
Features and Management of Late Relapse of Nonseminomatous Germ Cell Tumour
Alexander P M Jay, Mohammed Aldiwani, Michael E O'Callaghan, et al.
American Journal of Human Genetics
|
November 1, 1991
Risk calculation in retinitis pigmentosa
S M Holloway, L Strain, A E Shrimpton, et al.
The British Journal of Ophthalmology
|
May 1, 1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site
S L Owens, F W Fitzke, C F Inglehearn, et al.
Psychiatry Research
|
February 1, 1992
Clinical subtypes and age at onset in schizophrenic siblings
M Leboyer, M J Filteau, M Jay, et al.
Page
of 71
Search research articles
Search
Showing results (561-570 of 703) with videos related to
Sort By:
Page
of 71
American Journal of Human Genetics
|
March 26, 1999
Mutations in the RP2 gene cause disease in 10% of families with familial X-linked retinitis pigmentosa assessed in this study
A J Hardcastle, D L Thiselton, L Van Maldergem, et al.
The Gerontologist
|
April 1, 1988
A job diagnostic survey of nursing home caregivers: implications for job redesign
D Brannon, M A Smyer, M D Cohn, et al.
The Journal of Gene Medicine
|
May 26, 2026
In Vivo Assessment of dbDNA GNE<sup>wt</sup>/bi-shRNA-GNE<sup>M743T</sup> Lipoplex for GNE Myopathy: Improved Potency and Safety
Christopher M Jay, Fabienne Kerneis, Donald Rao, et al.
Current Biology : CB
|
June 15, 2022
Post-trauma behavioral phenotype predicts the degree of vulnerability to fear relapse after extinction in male rats
Fanny Demars, Ralitsa Todorova, Gabriel Makdah, et al.
Immunohorizons
|
September 22, 2020
Extracellular miR-146a-5p Induces Cardiac Innate Immune Response and Cardiomyocyte Dysfunction
Briana K Shimada, Yang Yang, Jing Zhu, et al.
American Journal of Human Genetics
|
October 1, 1987
Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14
A F Wright, S S Bhattacharya, J F Clayton, et al.
European Urology Open Science
|
August 2, 2021
Features and Management of Late Relapse of Nonseminomatous Germ Cell Tumour
Alexander P M Jay, Mohammed Aldiwani, Michael E O'Callaghan, et al.
American Journal of Human Genetics
|
November 1, 1991
Risk calculation in retinitis pigmentosa
S M Holloway, L Strain, A E Shrimpton, et al.
The British Journal of Ophthalmology
|
May 1, 1994
Ocular manifestations in autosomal dominant retinitis pigmentosa with a Lys-296-Glu rhodopsin mutation at the retinal binding site
S L Owens, F W Fitzke, C F Inglehearn, et al.
Psychiatry Research
|
February 1, 1992
Clinical subtypes and age at onset in schizophrenic siblings
M Leboyer, M J Filteau, M Jay, et al.
Page
of 71