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Siying Lin

Showing results (61-70 of 102) with videos related to

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European Journal of Human Genetics : EJHG|May 20, 2021
Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiencySiying Lin, James Fasham, Fida' Al-Hijawi, et al.
International Journal of Ophthalmology|December 20, 2021
Novel mutations in <i>PDE6A</i> and <i>CDHR1</i> cause retinitis pigmentosa in Pakistani familiesMuhammad Dawood, Siying Lin, Taj Ud Din, et al.
Investigative Ophthalmology & Visual Science|May 3, 2024
Sex Distributions in Non-ABCA4 Autosomal Macular DystrophiesAmit V Mishra, Sandra Vermeirsch, Siying Lin, et al.
Clinical Genetics|June 12, 2024
Non-syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activitySiying Lin, Anthony G Robson, Dorothy A Thompson, et al.
Eye (London, England)|April 9, 2026
Retinopathy caused by a primary immune regulatory disorder - the spectrum of AIRE-associated retinopathy: case series and literature reviewMohammad Anas, Andrew C Browning, Siying Lin, et al.
Retina (Philadelphia, Pa.)|September 2, 2025
Novel method of detection of birefringent ocular amyloidosis deposits using monochromatic wavelengths of scanning laser ophthalmoscopySidra Zafar, Ari August, Siying Lin, et al.
JAMA Ophthalmology|September 26, 2024
Biallelic Loss-of-Function Variants in UBAP1L and Nonsyndromic Retinal DystrophiesEhsan Ullah, Siying Lin, Jiaxiong Lu, et al.
Nature Immunology|August 23, 2025
SATB1 is a key regulator of quiescence in stem-like CD8<sup>+</sup> T cellsSiying Lin, Hongshen Niu, Yuqi Zhang, et al.
Ophthalmology. Retina|January 14, 2024
Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom CohortSiying Lin, Sandra Vermeirsch, Nikolas Pontikos, et al.
Investigative Ophthalmology & Visual Science|August 29, 2025
Sex Distributions in the Most Frequent Autosomal Genetic Causes of Retinitis PigmentosaMark J Hughes, Tina Lamey, Elena R Schiff, et al.
Pageof 11

Showing results (61-70 of 102) with videos related to

Sort By:
Pageof 11
European Journal of Human Genetics : EJHG|May 20, 2021
Consolidating biallelic SDHD variants as a cause of mitochondrial complex II deficiencySiying Lin, James Fasham, Fida' Al-Hijawi, et al.
International Journal of Ophthalmology|December 20, 2021
Novel mutations in <i>PDE6A</i> and <i>CDHR1</i> cause retinitis pigmentosa in Pakistani familiesMuhammad Dawood, Siying Lin, Taj Ud Din, et al.
Investigative Ophthalmology & Visual Science|May 3, 2024
Sex Distributions in Non-ABCA4 Autosomal Macular DystrophiesAmit V Mishra, Sandra Vermeirsch, Siying Lin, et al.
Clinical Genetics|June 12, 2024
Non-syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activitySiying Lin, Anthony G Robson, Dorothy A Thompson, et al.
Eye (London, England)|April 9, 2026
Retinopathy caused by a primary immune regulatory disorder - the spectrum of AIRE-associated retinopathy: case series and literature reviewMohammad Anas, Andrew C Browning, Siying Lin, et al.
Retina (Philadelphia, Pa.)|September 2, 2025
Novel method of detection of birefringent ocular amyloidosis deposits using monochromatic wavelengths of scanning laser ophthalmoscopySidra Zafar, Ari August, Siying Lin, et al.
JAMA Ophthalmology|September 26, 2024
Biallelic Loss-of-Function Variants in UBAP1L and Nonsyndromic Retinal DystrophiesEhsan Ullah, Siying Lin, Jiaxiong Lu, et al.
Nature Immunology|August 23, 2025
SATB1 is a key regulator of quiescence in stem-like CD8<sup>+</sup> T cellsSiying Lin, Hongshen Niu, Yuqi Zhang, et al.
Ophthalmology. Retina|January 14, 2024
Spectrum of Genetic Variants in the Most Common Genes Causing Inherited Retinal Disease in a Large Molecularly Characterized United Kingdom CohortSiying Lin, Sandra Vermeirsch, Nikolas Pontikos, et al.
Investigative Ophthalmology & Visual Science|August 29, 2025
Sex Distributions in the Most Frequent Autosomal Genetic Causes of Retinitis PigmentosaMark J Hughes, Tina Lamey, Elena R Schiff, et al.
Pageof 11