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Siying Lin

Showing results (71-80 of 102) with videos related to

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Immunity|March 28, 2026
Krüppel-like factors 2 and 3 regulate T cell exhaustion by directing T cell residency and migrationJian Shen, Ryan J Brown, Yuqi Zhang, et al.
JCI Insight|August 16, 2019
Adoptive lymphocyte transfer to an HIV-infected progressor from an elite controllerStephen A Migueles, Cheryl Chairez, Siying Lin, et al.
Acta Ophthalmologica|June 29, 2026
Radial outer retina reflectivity (RORR) sign in LAMP2-associated retinopathyRachael C Heath Jeffery, Bohdan Kousal, Ulrike Grünert, et al.
Journal of Medical Genetics|June 28, 2022
Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approachSunayna Best, Jing Yu, Jenny Lord, et al.
Genes|August 28, 2025
Genetic Insights and Diagnostic Challenges in Highly Attenuated Lysosomal Storage DisordersElena Urizar, Eamon P McCarron, Chaitanya Gadepalli, et al.
American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.
JAMA Ophthalmology|April 11, 2024
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-AnalysisStéphanie S Cornelis, Joanna IntHout, Esmee H Runhart, et al.
NPJ Genomic Medicine|January 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie, et al.
American Journal of Medical Genetics. Part A|June 14, 2019
Delineating the expanding phenotype associated with SCAPER gene mutationJames Fasham, Gavin Arno, Siying Lin, et al.
Nature Communications|July 3, 2025
Variants in NR6A1 cause a novel oculo vertebral renal syndromeUma M Neelathi, Ehsan Ullah, Aman George, et al.
Pageof 11

Showing results (71-80 of 102) with videos related to

Sort By:
Pageof 11
Immunity|March 28, 2026
Krüppel-like factors 2 and 3 regulate T cell exhaustion by directing T cell residency and migrationJian Shen, Ryan J Brown, Yuqi Zhang, et al.
JCI Insight|August 16, 2019
Adoptive lymphocyte transfer to an HIV-infected progressor from an elite controllerStephen A Migueles, Cheryl Chairez, Siying Lin, et al.
Acta Ophthalmologica|June 29, 2026
Radial outer retina reflectivity (RORR) sign in LAMP2-associated retinopathyRachael C Heath Jeffery, Bohdan Kousal, Ulrike Grünert, et al.
Journal of Medical Genetics|June 28, 2022
Uncovering the burden of hidden ciliopathies in the 100 000 Genomes Project: a reverse phenotyping approachSunayna Best, Jing Yu, Jenny Lord, et al.
Genes|August 28, 2025
Genetic Insights and Diagnostic Challenges in Highly Attenuated Lysosomal Storage DisordersElena Urizar, Eamon P McCarron, Chaitanya Gadepalli, et al.
American Journal of Human Genetics|January 25, 2024
Mutations in SAMD7 cause autosomal-recessive macular dystrophy with or without cone dysfunctionMiriam Bauwens, Elifnaz Celik, Dinah Zur, et al.
JAMA Ophthalmology|April 11, 2024
Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-AnalysisStéphanie S Cornelis, Joanna IntHout, Esmee H Runhart, et al.
NPJ Genomic Medicine|January 14, 2022
Evidence that the Ser192Tyr/Arg402Gln in cis Tyrosinase gene haplotype is a disease-causing allele in oculocutaneous albinism type 1B (OCA1B)Siying Lin, Aida Sanchez-Bretaño, Joseph S Leslie, et al.
American Journal of Medical Genetics. Part A|June 14, 2019
Delineating the expanding phenotype associated with SCAPER gene mutationJames Fasham, Gavin Arno, Siying Lin, et al.
Nature Communications|July 3, 2025
Variants in NR6A1 cause a novel oculo vertebral renal syndromeUma M Neelathi, Ehsan Ullah, Aman George, et al.
Pageof 11