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Human Gene Therapy
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April 4, 2023
Gene Supplementation in Mice Heterozygous for the D477G RPE65 Variant Implicated in Autosomal Dominant Retinitis Pigmentosa
Kecia L Feathers, Lin Jia, Naheed W Khan, et al.
Gene Therapy
|
March 7, 2003
Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2Rd2/Rd2 model of retinal degeneration
F C Schlichtenbrede, A MacNeil, J W B Bainbridge, et al.
Experimental Eye Research
|
April 28, 2004
Minocycline delays photoreceptor death in the rds mouse through a microglia-independent mechanism
Edward H Hughes, Frank C Schlichtenbrede, Conor C Murphy, et al.
Engineering Analysis with Boundary Elements
|
November 7, 2022
A mathematical model of coronavirus transmission by using the heuristic computing neural networks
Zulqurnain Sabir, Adi Asmara, Sanaullah Dehraj, et al.
Metabolic Brain Disease
|
September 18, 2014
Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay
Salma Ben-Salem, Joseph G Gleeson, Aisha M Al-Shamsi, et al.
RSC Advances
|
June 27, 2022
Graphitic carbon nitride and APTES modified advanced electrochemical biosensor for detection of 17β-estradiol in spiked food samples
M S Bacchu, M R Ali, M N Hasan, et al.
Scientific Reports
|
December 5, 2020
Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populations
Zeina N Al-Mahayri, George P Patrinos, Sukanya Wattanapokayakit, et al.
Orphanet Journal of Rare Diseases
|
October 23, 2016
A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement
Nadia A Akawi, Salma Ben-Salem, Jozef Hertecant, et al.
Scientific Reports
|
January 24, 2017
Hypoxia inducible factors are dispensable for myeloid cell migration into the inflamed mouse eye
Peter J Gardner, Sidath E Liyanage, Enrico Cristante, et al.
Plos One
|
March 21, 2015
Müller glia activation in response to inherited retinal degeneration is highly varied and disease-specific
Claire Hippert, Anna B Graca, Amanda C Barber, et al.
Page
of 120
Search research articles
Search
Showing results (691-700 of 1,192) with videos related to
Sort By:
Page
of 120
Human Gene Therapy
|
April 4, 2023
Gene Supplementation in Mice Heterozygous for the D477G RPE65 Variant Implicated in Autosomal Dominant Retinitis Pigmentosa
Kecia L Feathers, Lin Jia, Naheed W Khan, et al.
Gene Therapy
|
March 7, 2003
Intraocular gene delivery of ciliary neurotrophic factor results in significant loss of retinal function in normal mice and in the Prph2Rd2/Rd2 model of retinal degeneration
F C Schlichtenbrede, A MacNeil, J W B Bainbridge, et al.
Experimental Eye Research
|
April 28, 2004
Minocycline delays photoreceptor death in the rds mouse through a microglia-independent mechanism
Edward H Hughes, Frank C Schlichtenbrede, Conor C Murphy, et al.
Engineering Analysis with Boundary Elements
|
November 7, 2022
A mathematical model of coronavirus transmission by using the heuristic computing neural networks
Zulqurnain Sabir, Adi Asmara, Sanaullah Dehraj, et al.
Metabolic Brain Disease
|
September 18, 2014
Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay
Salma Ben-Salem, Joseph G Gleeson, Aisha M Al-Shamsi, et al.
RSC Advances
|
June 27, 2022
Graphitic carbon nitride and APTES modified advanced electrochemical biosensor for detection of 17β-estradiol in spiked food samples
M S Bacchu, M R Ali, M N Hasan, et al.
Scientific Reports
|
December 5, 2020
Variation in 100 relevant pharmacogenes among emiratis with insights from understudied populations
Zeina N Al-Mahayri, George P Patrinos, Sukanya Wattanapokayakit, et al.
Orphanet Journal of Rare Diseases
|
October 23, 2016
A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement
Nadia A Akawi, Salma Ben-Salem, Jozef Hertecant, et al.
Scientific Reports
|
January 24, 2017
Hypoxia inducible factors are dispensable for myeloid cell migration into the inflamed mouse eye
Peter J Gardner, Sidath E Liyanage, Enrico Cristante, et al.
Plos One
|
March 21, 2015
Müller glia activation in response to inherited retinal degeneration is highly varied and disease-specific
Claire Hippert, Anna B Graca, Amanda C Barber, et al.
Page
of 120