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Nature Communications
|
September 9, 2025
Discovery of a selective alpha-kinase 1 inhibitor for the rare genetic disease ROSAH syndrome
Jieqing Fan, Danyang Liu, Zhu Ming, et al.
Plos One
|
December 7, 2013
PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders
Lily Paemka, Vinit B Mahajan, Jessica M Skeie, et al.
Human Mutation
|
May 16, 2013
Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles
Benjamin W Darbro, Vinit B Mahajan, Lokesh Gakhar, et al.
Plos Genetics
|
November 21, 2012
Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome
Rebecca E McIntyre, Pavithra Lakshminarasimhan Chavali, Ozama Ismail, et al.
Cell
|
July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes
Jacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
January 21, 2026
Oculomics and AI: The Eye as a biomarker for health span
Joy Le Yi Wong, Haoran Cheng, Wen Jun Peh, et al.
Lancet (London, England)
|
July 18, 2017
Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial
Stephen Russell, Jean Bennett, Jennifer A Wellman, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
May 22, 2026
Corrigendum to "Oculomics and AI: The eye as a biomarker for health span" [Asia-Pac J Ophthalmol 15 (1) (2026) 100282]
Joy Le Yi Wong, Haoran Cheng, Wen Jun Peh, et al.
American Journal of Human Genetics
|
February 1, 2011
Mutations in prickle orthologs cause seizures in flies, mice, and humans
Hirotaka Tao, J Robert Manak, Levi Sowers, et al.
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Search research articles
Search
Showing results (251-260 of 259) with videos related to
Sort By:
Page
of 26
You have reached the last page of results.
This site can display upto 259 results.
Nature Communications
|
September 9, 2025
Discovery of a selective alpha-kinase 1 inhibitor for the rare genetic disease ROSAH syndrome
Jieqing Fan, Danyang Liu, Zhu Ming, et al.
Plos One
|
December 7, 2013
PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders
Lily Paemka, Vinit B Mahajan, Jessica M Skeie, et al.
Human Mutation
|
May 16, 2013
Mutations in extracellular matrix genes NID1 and LAMC1 cause autosomal dominant Dandy-Walker malformation and occipital cephaloceles
Benjamin W Darbro, Vinit B Mahajan, Lokesh Gakhar, et al.
Plos Genetics
|
November 21, 2012
Disruption of mouse Cenpj, a regulator of centriole biogenesis, phenocopies Seckel syndrome
Rebecca E McIntyre, Pavithra Lakshminarasimhan Chavali, Ozama Ismail, et al.
Cell
|
July 23, 2013
Genome-wide generation and systematic phenotyping of knockout mice reveals new roles for many genes
Jacqueline K White, Anna-Karin Gerdin, Natasha A Karp, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
January 21, 2026
Oculomics and AI: The Eye as a biomarker for health span
Joy Le Yi Wong, Haoran Cheng, Wen Jun Peh, et al.
Lancet (London, England)
|
July 18, 2017
Efficacy and safety of voretigene neparvovec (AAV2-hRPE65v2) in patients with RPE65-mediated inherited retinal dystrophy: a randomised, controlled, open-label, phase 3 trial
Stephen Russell, Jean Bennett, Jennifer A Wellman, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)
|
May 22, 2026
Corrigendum to "Oculomics and AI: The eye as a biomarker for health span" [Asia-Pac J Ophthalmol 15 (1) (2026) 100282]
Joy Le Yi Wong, Haoran Cheng, Wen Jun Peh, et al.
American Journal of Human Genetics
|
February 1, 2011
Mutations in prickle orthologs cause seizures in flies, mice, and humans
Hirotaka Tao, J Robert Manak, Levi Sowers, et al.
Page
of 26