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Movement Disorders : Official Journal of the Movement Disorder Society
|
February 19, 2009
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
Greg T Sutherland, Glenda M Halliday, Peter A Silburn, et al.
Frontiers in Neuroscience
|
February 22, 2020
Structural Variants May Be a Source of Missing Heritability in sALS
Frances Theunissen, Loren L Flynn, Ryan S Anderton, et al.
Plos One
|
October 23, 2010
Fibulin-1 is increased in asthma--a novel mediator of airway remodeling?
Justine Y Lau, Brian G Oliver, Melissa Baraket, et al.
Stem Cell Research
|
July 1, 2021
Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene
Di Huang, Dan Zhang, Shang-Chih Chen, et al.
Stem Cell Research
|
July 2, 2021
Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene
Di Huang, Dan Zhang, Shang-Chih Chen, et al.
Frontiers in Genetics
|
April 25, 2022
Single Stranded Fully Modified-Phosphorothioate Oligonucleotides can Induce Structured Nuclear Inclusions, Alter Nuclear Protein Localization and Disturb the Transcriptome <i>In Vitro</i>
Loren L Flynn, Ruohan Li, Ianthe L Pitout, et al.
Ophthalmic Genetics
|
September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathy
Danial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Stem Cell Research
|
December 28, 2020
Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene
Khine Zaw, Elaine Y M Wong, Xiao Zhang, et al.
Molecular Genetics & Genomic Medicine
|
July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect
Di Huang, Jennifer A Thompson, Jason Charng, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 6, 2021
Antisense oligonucleotide-based drug development for Cystic Fibrosis patients carrying the 3849+10 kb C-to-T splicing mutation
Yifat S Oren, Michal Irony-Tur Sinai, Anita Golec, et al.
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Search research articles
Search
Showing results (91-100 of 109) with videos related to
Sort By:
Page
of 11
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 19, 2009
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease?
Greg T Sutherland, Glenda M Halliday, Peter A Silburn, et al.
Frontiers in Neuroscience
|
February 22, 2020
Structural Variants May Be a Source of Missing Heritability in sALS
Frances Theunissen, Loren L Flynn, Ryan S Anderton, et al.
Plos One
|
October 23, 2010
Fibulin-1 is increased in asthma--a novel mediator of airway remodeling?
Justine Y Lau, Brian G Oliver, Melissa Baraket, et al.
Stem Cell Research
|
July 1, 2021
Generation of two induced pluripotent stem cell lines from a patient with Stargardt disease caused by compound heterozygous mutations in the ABCA4 gene
Di Huang, Dan Zhang, Shang-Chih Chen, et al.
Stem Cell Research
|
July 2, 2021
Generation of an induced pluripotent stem cell line from a patient with Stargardt disease caused by biallelic c.[5461-10T>C;5603A>T];[6077T>C] mutations in the ABCA4 gene
Di Huang, Dan Zhang, Shang-Chih Chen, et al.
Frontiers in Genetics
|
April 25, 2022
Single Stranded Fully Modified-Phosphorothioate Oligonucleotides can Induce Structured Nuclear Inclusions, Alter Nuclear Protein Localization and Disturb the Transcriptome <i>In Vitro</i>
Loren L Flynn, Ruohan Li, Ianthe L Pitout, et al.
Ophthalmic Genetics
|
September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathy
Danial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Stem Cell Research
|
December 28, 2020
Generation of three induced pluripotent stem cell lines from a patient with Usher syndrome caused by biallelic c.949C > A and c.1256G > T mutations in the USH2A gene
Khine Zaw, Elaine Y M Wong, Xiao Zhang, et al.
Molecular Genetics & Genomic Medicine
|
July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defect
Di Huang, Jennifer A Thompson, Jason Charng, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
July 6, 2021
Antisense oligonucleotide-based drug development for Cystic Fibrosis patients carrying the 3849+10 kb C-to-T splicing mutation
Yifat S Oren, Michal Irony-Tur Sinai, Anita Golec, et al.
Page
of 11