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Ehsan Ullah

Showing results (221-230 of 233) with videos related to

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Cell Death & Disease|July 26, 2022
The crosstalk between endothelial cells and vascular smooth muscle cells aggravates high phosphorus-induced arterial calcificationXiao Lin, Su-Kang Shan, Feng Xu, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Variants in <i>NR6A1</i> cause a novel oculo-vertebral-renal (OVR) syndromeUma M Neelathi, Ehsan Ullah, Aman George, et al.
Human Genetics|September 1, 2018
Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disabilityRegie Lyn P Santos-Cortez, Valeed Khan, Falak Sher Khan, et al.
Research Square|November 28, 2024
Variants in <i>NR6A1</i> cause a novel oculo-vertebral-renal (OVR) syndromeUma M Neelathi, Ehsan Ullah, Aman George, et al.
Frontiers in Endocrinology|July 5, 2022
Histone Lysine Methylation Modification and Its Role in Vascular CalcificationYe-Chi Cao, Su-Kang Shan, Bei Guo, 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.
Cardiovascular Diabetology|September 9, 2024
MiRNA-132/212 encapsulated by adipose tissue-derived exosomes worsen atherosclerosis progressionBei Guo, Tong-Tian Zhuang, Chang-Chun Li, et al.
Scientific Reports|November 18, 2020
Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohortLev Prasov, Bin Guan, Ehsan Ullah, et al.
NPJ Genomic Medicine|October 29, 2024
SLC16A8 is a causal contributor to age-related macular degeneration riskNavid Nouri, Bailey Hannon Gussler, Amy Stockwell, et al.
Pageof 24

Showing results (221-230 of 233) with videos related to

Sort By:
Pageof 24
Cell Death & Disease|July 26, 2022
The crosstalk between endothelial cells and vascular smooth muscle cells aggravates high phosphorus-induced arterial calcificationXiao Lin, Su-Kang Shan, Feng Xu, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
Medrxiv : the Preprint Server for Health Sciences|November 28, 2024
Variants in <i>NR6A1</i> cause a novel oculo-vertebral-renal (OVR) syndromeUma M Neelathi, Ehsan Ullah, Aman George, et al.
Human Genetics|September 1, 2018
Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disabilityRegie Lyn P Santos-Cortez, Valeed Khan, Falak Sher Khan, et al.
Research Square|November 28, 2024
Variants in <i>NR6A1</i> cause a novel oculo-vertebral-renal (OVR) syndromeUma M Neelathi, Ehsan Ullah, Aman George, et al.
Frontiers in Endocrinology|July 5, 2022
Histone Lysine Methylation Modification and Its Role in Vascular CalcificationYe-Chi Cao, Su-Kang Shan, Bei Guo, 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.
Cardiovascular Diabetology|September 9, 2024
MiRNA-132/212 encapsulated by adipose tissue-derived exosomes worsen atherosclerosis progressionBei Guo, Tong-Tian Zhuang, Chang-Chun Li, et al.
Scientific Reports|November 18, 2020
Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohortLev Prasov, Bin Guan, Ehsan Ullah, et al.
NPJ Genomic Medicine|October 29, 2024
SLC16A8 is a causal contributor to age-related macular degeneration riskNavid Nouri, Bailey Hannon Gussler, Amy Stockwell, et al.
Pageof 24