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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 14, 2016
Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations
Kinga M Bujakowska, Rosario Fernandez-Godino, Emily Place, et al.
American Journal of Human Genetics
|
September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma
O J Lehmann, N D Ebenezer, T Jordan, et al.
Human Gene Therapy
|
November 26, 1998
Cationic phosphonolipids as nonviral gene transfer agents in the lungs of mice
C Guillaume-Gable, V Floch, B Mercier, et al.
Biochimica Et Biophysica Acta
|
May 30, 1998
Transgene expression kinetics after transfection with cationic phosphonolipids in hematopoietic non adherent cells
V Floch, M P Audrezet, C Guillaume, et al.
Toxicology Research
|
August 10, 2018
Systems toxicology meta-analysis of <i>in vitro</i> assessment studies: biological impact of a candidate modified-risk tobacco product aerosol compared with cigarette smoke on human organotypic cultures of the aerodigestive tract
A R Iskandar, B Titz, A Sewer, et al.
Therapeutic Advances in Ophthalmology
|
November 17, 2022
RNA-based therapies in inherited retinal diseases
Aniz Girach, Isabelle Audo, David G Birch, et al.
Ophthalmic Genetics
|
December 5, 2022
Fleck-like lesions in <i>CEP290-associated</i> leber congenital amaurosis: a case series
Tomas S Aleman, Erin C O'Neil, Katherine E Uyhazi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus
N B Romero, M Herasse, N Monnier, et al.
Brain Pathology (Zurich, Switzerland)
|
May 4, 2018
Pathogenic variants in the ABCC6 gene are associated with an increased risk for ischemic stroke
Eva Y G De Vilder, Stefanie Cardoen, Mohammad J Hosen, et al.
Human Mutation
|
October 28, 2014
An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients
Miriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, et al.
Page
of 44
Search research articles
Search
Showing results (331-340 of 438) with videos related to
Sort By:
Page
of 44
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 14, 2016
Copy-number variation is an important contributor to the genetic causality of inherited retinal degenerations
Kinga M Bujakowska, Rosario Fernandez-Godino, Emily Place, et al.
American Journal of Human Genetics
|
September 29, 2000
Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma
O J Lehmann, N D Ebenezer, T Jordan, et al.
Human Gene Therapy
|
November 26, 1998
Cationic phosphonolipids as nonviral gene transfer agents in the lungs of mice
C Guillaume-Gable, V Floch, B Mercier, et al.
Biochimica Et Biophysica Acta
|
May 30, 1998
Transgene expression kinetics after transfection with cationic phosphonolipids in hematopoietic non adherent cells
V Floch, M P Audrezet, C Guillaume, et al.
Toxicology Research
|
August 10, 2018
Systems toxicology meta-analysis of <i>in vitro</i> assessment studies: biological impact of a candidate modified-risk tobacco product aerosol compared with cigarette smoke on human organotypic cultures of the aerodigestive tract
A R Iskandar, B Titz, A Sewer, et al.
Therapeutic Advances in Ophthalmology
|
November 17, 2022
RNA-based therapies in inherited retinal diseases
Aniz Girach, Isabelle Audo, David G Birch, et al.
Ophthalmic Genetics
|
December 5, 2022
Fleck-like lesions in <i>CEP290-associated</i> leber congenital amaurosis: a case series
Tomas S Aleman, Erin C O'Neil, Katherine E Uyhazi, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
March 23, 2006
Clinical and histopathological aspects of central core disease associated and non-associated with RYR1 locus
N B Romero, M Herasse, N Monnier, et al.
Brain Pathology (Zurich, Switzerland)
|
May 4, 2018
Pathogenic variants in the ABCC6 gene are associated with an increased risk for ischemic stroke
Eva Y G De Vilder, Stefanie Cardoen, Mohammad J Hosen, et al.
Human Mutation
|
October 28, 2014
An augmented ABCA4 screen targeting noncoding regions reveals a deep intronic founder variant in Belgian Stargardt patients
Miriam Bauwens, Julie De Zaeytijd, Nicole Weisschuh, et al.
Page
of 44