Articles avec mandats d'accès public - Robert F MullinsEn savoir plus
Disponibles quelque part : 183
Retinal neurodegeneration may precede microvascular changes characteristic of diabetic retinopathy in diabetes mellitus
EH Sohn, HW van Dijk, C Jiao, PHB Kok, W Jeong, N Demirkaya, ...
Proceedings of the National Academy of Sciences 113 (19), E2655-E2664, 2016
Exigences : US National Institutes of Health, US Department of Veterans Affairs
T-cell immunoglobulin and mucin domain 1 (TIM-1) is a receptor for Zaire Ebolavirus and Lake Victoria Marburgvirus
AS Kondratowicz, NJ Lennemann, PL Sinn, RA Davey, CL Hunt, ...
Proceedings of the National Academy of Sciences 108 (20), 8426-8431, 2011
Exigences : US National Institutes of Health
Clinically focused molecular investigation of 1000 consecutive families with inherited retinal disease
EM Stone, JL Andorf, SS Whitmore, AP DeLuca, JC Giacalone, LM Streb, ...
Ophthalmology 124 (9), 1314-1331, 2017
Exigences : US National Institutes of Health
Choriocapillaris vascular dropout related to density of drusen in human eyes with early age-related macular degeneration
RF Mullins, MN Johnson, EA Faidley, JM Skeie, J Huang
Investigative ophthalmology & visual science 52 (3), 1606-1612, 2011
Exigences : US National Institutes of Health
Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degeneration
AP Voigt, K Mulfaul, NK Mullin, MJ Flamme-Wiese, JC Giacalone, ...
Proceedings of the National Academy of Sciences 116 (48), 24100-24107, 2019
Exigences : US National Institutes of Health, US Department of Veterans Affairs
Complement activation and choriocapillaris loss in early AMD: implications for pathophysiology and therapy
SS Whitmore, EH Sohn, KR Chirco, AV Drack, EM Stone, BA Tucker, ...
Progress in retinal and eye research 45, 1-29, 2015
Exigences : US National Institutes of Health
Exome sequencing and analysis of induced pluripotent stem cells identify the cilia-related gene male germ cell-associated kinase (MAK) as a cause of retinitis pigmentosa
BA Tucker, TE Scheetz, RF Mullins, AP DeLuca, JM Hoffmann, ...
Proceedings of the National Academy of Sciences 108 (34), E569-E576, 2011
Exigences : US National Institutes of Health
Copy number variations on chromosome 12q14 in patients with normal tension glaucoma
JH Fingert, AL Robin, JL Stone, BR Roos, LK Davis, TE Scheetz, ...
Human molecular genetics 20 (12), 2482-2494, 2011
Exigences : US National Institutes of Health
Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa
BA Tucker, RF Mullins, LM Streb, K Anfinson, ME Eyestone, E Kaalberg, ...
elife 2, e00824, 2013
Exigences : US National Institutes of Health, Howard Hughes Medical Institute
The membrane attack complex in aging human choriocapillaris: relationship to macular degeneration and choroidal thinning
RF Mullins, DP Schoo, EH Sohn, MJ Flamme-Wiese, G Workamelahu, ...
The American journal of pathology 184 (11), 3142-3153, 2014
Exigences : US National Institutes of Health, Howard Hughes Medical Institute, Doris …
Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease
TA Braun, RF Mullins, AH Wagner, JL Andorf, RM Johnston, BB Bakall, ...
Human molecular genetics 22 (25), 5136-5145, 2013
Exigences : US National Institutes of Health, Howard Hughes Medical Institute
Structural and molecular changes in the aging choroid: implications for age-related macular degeneration
KR Chirco, EH Sohn, EM Stone, BA Tucker, RF Mullins
Eye 31 (1), 10-25, 2017
Exigences : US National Institutes of Health
Association between the SERPING1 gene and age-related macular degeneration: a two-stage case–control study
S Ennis, C Jomary, R Mullins, A Cree, X Chen, A MacLeod, S Jones, ...
The Lancet 372 (9652), 1828-1834, 2008
Exigences : US National Institutes of Health, Howard Hughes Medical Institute
Using CRISPR-Cas9 to generate gene-corrected autologous iPSCs for the treatment of inherited retinal degeneration
ER Burnight, M Gupta, LA Wiley, KR Anfinson, A Tran, R Triboulet, ...
Molecular Therapy 25 (9), 1999-2013, 2017
Exigences : US National Institutes of Health
Automated segmentation of the choroid from clinical SD-OCT
L Zhang, K Lee, M Niemeijer, RF Mullins, M Sonka, MD Abramoff
Investigative ophthalmology & visual science 53 (12), 7510-7519, 2012
Exigences : US National Institutes of Health
CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype
ER Burnight, LA Wiley, AV Drack, TA Braun, KR Anfinson, EE Kaalberg, ...
Gene therapy 21 (7), 662-672, 2014
Exigences : US National Institutes of Health, Howard Hughes Medical Institute
Complement component C5a activates ICAM-1 expression on human choroidal endothelial cells
JM Skeie, JH Fingert, SR Russell, EM Stone, RF Mullins
Investigative ophthalmology & visual science 51 (10), 5336-5342, 2010
Exigences : US National Institutes of Health
Elevated membrane attack complex in human choroid with high risk complement factor H genotypes
RF Mullins, AD Dewald, LM Streb, K Wang, MH Kuehn, EM Stone
Experimental eye research 93 (4), 565-567, 2011
Exigences : US National Institutes of Health, Howard Hughes Medical Institute
North Carolina macular dystrophy is caused by dysregulation of the retinal transcription factor PRDM13
KW Small, AP DeLuca, SS Whitmore, T Rosenberg, R Silva-Garcia, ...
Ophthalmology 123 (1), 9-18, 2016
Exigences : US National Institutes of Health
Molecular characterization of foveal versus peripheral human retina by single-cell RNA sequencing
AP Voigt, SS Whitmore, MJ Flamme-Wiese, MJ Riker, LA Wiley, ...
Experimental eye research 184, 234-242, 2019
Exigences : US National Institutes of Health
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