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P Blair

Showing results (371-380 of 396) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|November 7, 2019
Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 miceEmily P McCann, Jennifer A Fifita, Natalie Grima, et al.
Developmental Cell|December 15, 2020
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart DiseaseIrfan S Kathiriya, Kavitha S Rao, Giovanni Iacono, et al.
Ophthalmology. Retina|July 17, 2022
Late Vitreoretinal Complications of Regressed Retinopathy of Prematurity: Retinal Break, Vitreous Hemorrhage, and Retinal DetachmentHan-Tung Hsu, Eugene Yu-Chuan Kang, Michael P Blair, et al.
American Journal of Ophthalmology|October 24, 2025
Comparing Rhegmatogenous and Tractional Retinal Detachment in Regressed Retinopathy of Prematurity: An International, Multicenter StudyHan-Tung Hsu, Eugene Yu-Chuan Kang, Michael P Blair, et al.
Human Molecular Genetics|March 29, 2012
Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosisJulien Couthouis, Michael P Hart, Renske Erion, et al.
Ophthalmology. Retina|February 16, 2020
Late-Onset Retinal Findings and Complications in Untreated Retinopathy of PrematurityAbdualrahman E Hamad, Omar Moinuddin, Michael P Blair, et al.
Cell Reports|October 28, 2020
Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease GeneticsAlfredo Iacoangeli, Tian Lin, Ahmad Al Khleifat, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Ophthalmology. Retina|November 25, 2020
Traumatic Retinal Detachment in Patients with Self-Injurious Behavior: An International Multicenter StudyElizabeth J Rossin, Irena Tsui, Sui Chien Wong, et al.
NPJ Genomic Medicine|March 7, 2020
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosisMarta F Nabais, Tian Lin, Beben Benyamin, et al.
Pageof 40

Showing results (371-380 of 396) with videos related to

Sort By:
Pageof 40
Journal of Neurology, Neurosurgery, and Psychiatry|November 7, 2019
Genetic and immunopathological analysis of CHCHD10 in Australian amyotrophic lateral sclerosis and frontotemporal dementia and transgenic TDP-43 miceEmily P McCann, Jennifer A Fifita, Natalie Grima, et al.
Developmental Cell|December 15, 2020
Modeling Human TBX5 Haploinsufficiency Predicts Regulatory Networks for Congenital Heart DiseaseIrfan S Kathiriya, Kavitha S Rao, Giovanni Iacono, et al.
Ophthalmology. Retina|July 17, 2022
Late Vitreoretinal Complications of Regressed Retinopathy of Prematurity: Retinal Break, Vitreous Hemorrhage, and Retinal DetachmentHan-Tung Hsu, Eugene Yu-Chuan Kang, Michael P Blair, et al.
American Journal of Ophthalmology|October 24, 2025
Comparing Rhegmatogenous and Tractional Retinal Detachment in Regressed Retinopathy of Prematurity: An International, Multicenter StudyHan-Tung Hsu, Eugene Yu-Chuan Kang, Michael P Blair, et al.
Human Molecular Genetics|March 29, 2012
Evaluating the role of the FUS/TLS-related gene EWSR1 in amyotrophic lateral sclerosisJulien Couthouis, Michael P Hart, Renske Erion, et al.
Ophthalmology. Retina|February 16, 2020
Late-Onset Retinal Findings and Complications in Untreated Retinopathy of PrematurityAbdualrahman E Hamad, Omar Moinuddin, Michael P Blair, et al.
Cell Reports|October 28, 2020
Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease GeneticsAlfredo Iacoangeli, Tian Lin, Ahmad Al Khleifat, et al.
American Journal of Human Genetics|October 15, 2013
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, et al.
Ophthalmology. Retina|November 25, 2020
Traumatic Retinal Detachment in Patients with Self-Injurious Behavior: An International Multicenter StudyElizabeth J Rossin, Irena Tsui, Sui Chien Wong, et al.
NPJ Genomic Medicine|March 7, 2020
Significant out-of-sample classification from methylation profile scoring for amyotrophic lateral sclerosisMarta F Nabais, Tian Lin, Beben Benyamin, et al.
Pageof 40